FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Miriam Meisler

Research Profile

Living Beings

Chemicals & Drugs

Procedures

Concepts & Ideas

Molecular Sequence Data

Physiology

Genes & Molecular Sequences

Anatomy

Pancreas

Co-author Network

Publications

TOP 3
Philippe Campeau; Laurence Faivre; Richard A Gibbs; Eric Haan; Yangjin Bae; Lindsay Burrage; Guy M Lenk; James T Lu; Miriam H Meisler; Marina Mora; Lucia Morandi; Heiko Reutter; Jorge Román Corona-Rivera; Peter Turnpenny; Anneke T Vulto-van Silfhout; Brendan H Lee
Yunis-Varón Syndrome Is Caused by Mutations in FIG4, Encoding a Phosphoinositide Phosphatase.
Miriam H Meisler; Peter K Todd; Roger L Albin; Adrienne E Grant; Fang He; Julie M Jones; Masoud Kamali; Scott A Langenecker; Guy M Lenk; Andrew P Lieberman; Melvin G McInnis
C9ORF72 expansion in a family with bipolar disorder.
Sergey N Zolov; Yanling Zhang; Roger L Albin; Dave Bridges; Kimber Converso-Baran; Wei-Wei Lee; Guy M Lenk; Miriam H Meisler; Ellen Riehle; Mark W Russell; Alan R Saltiel; Rakesh Verma; Thomas Weide; Lois S Weisman
In vivo, Pikfyve generates PI(3,5)P2, which serves as both a signaling lipid and the major precursor for PI5P.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Miriam Meisler (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2013: Philippe Campeau; Laurence Faivre; Richard A Gibbs; Eric Haan; Yangjin Bae; Lindsay Burrage; Guy M Lenk; James T Lu; Miriam H Meisler; Marina Mora; Lucia Morandi; Heiko Reutter; Jorge Román Corona-Rivera; Peter Turnpenny; Anneke T Vulto-van Silfhout; Brendan H Lee
Yunis-Varón Syndrome Is Caused by Mutations in FIG4, Encoding a Phosphoinositide Phosphatase.
American journal of human genetics 2013;92(5):781-91.
2013: Miriam H Meisler; Peter K Todd; Roger L Albin; Adrienne E Grant; Fang He; Julie M Jones; Masoud Kamali; Scott A Langenecker; Guy M Lenk; Andrew P Lieberman; Melvin G McInnis
C9ORF72 expansion in a family with bipolar disorder.
Bipolar disorders 2013;15(3):326-32.
2012: Sergey N Zolov; Yanling Zhang; Roger L Albin; Dave Bridges; Kimber Converso-Baran; Wei-Wei Lee; Guy M Lenk; Miriam H Meisler; Ellen Riehle; Mark W Russell; Alan R Saltiel; Rakesh Verma; Thomas Weide; Lois S Weisman
In vivo, Pikfyve generates PI(3,5)P2, which serves as both a signaling lipid and the major precursor for PI5P.
Proceedings of the National Academy of Sciences of the United States of America 2012;109(43):17472-7.
2012: Yanling Zhang; Sergey N Zolov; Cole J Ferguson; Amber J McCartney; Miriam H Meisler; Michael Mark Alexander Sutton; Lois S Weisman
Modulation of synaptic function by VAC14, a protein that regulates the phosphoinositides PI(3,5)P₂ and PI(5)P.
The EMBO journal 2012;31(16):3442-56.
2012: C J Ferguson; Roman J Giger; A E Grant; J M Jones; G M Lenk; James Dowling; J J Winters; Miriam H Meisler
Neuronal expression of Fig4 is both necessary and sufficient to prevent spongiform neurodegeneration.
Human molecular genetics 2012;21(16):3525-34.
2012: Anna C Need; Kelly Schoch; Vandana Shashi; Kevin V Shianna; Yuki Hitomi; Marie T McDonald; Miriam H Meisler; David B Goldstein
Clinical application of exome sequencing in undiagnosed genetic conditions.
Journal of medical genetics 2012;49(6):353-61.
2012: Janelle E O'Brien; Lisa M Sharkey; Christina N Vallianatos; Stephen G Waxman; Ting Yu; Julie C Blossom; Sulayman D Dib-Hajj; Chongyang Han; Miriam H Meisler
Interaction of voltage-gated sodium channel Nav1.6 (SCN8A) with microtubule-associated protein Map1b.
The Journal of biological chemistry 2012;287(22):18459-66.
2012: Daniel J Klionsky; Jochen Klucken; Erwin Knecht; Ben C B Ko; Jan C Koch; Hiroshi Koga; Jae-Young Koh; Young Ho Koh; Masato Koike; Masaaki Komatsu; Eiki Kominami; Hee Jeong Kong; Wei-Jia Kong; Viktor I Korolchuk; Yaichiro Kotake; Michael I Koukourakis; Juan B Kouri Flores; Attila L Kovács; Claudine Kraft; Dimitri Krainc; Helmut Krämer; Carole Kretz-Remy; Anna M Krichevsky; Guido Kroemer; Rejko Krüger; Oleg Krut; Nicholas T Ktistakis; Chia-Yi Kuan; Roza Kucharczyk; Ashok Kumar; Raj Kumar; Sharad Kumar; Mondira Kundu; Hsing-Jien Kung; Tino Kurz; Ho Jeong Kwon; Albert R La Spada; Frank Lafont; Trond Lamark; Jacques Landry; Jon D Lane; Pierre Lapaquette; Jocelyn F Laporte; Lajos László; Sergio Lavandero; Josée N Lavoie; Robert Layfield; Pedro A Lazo; Laurent Le Cam; Weidong Le; Daniel J Ledbetter; Alvin J X Lee; Byung-Wan Lee; Gyun Min Lee; Jongdae Lee; Ju-Hyun Lee; Michael Lee; Myung-Shik Lee; Sug Hyung Lee; Christiaan Leeuwenburgh; Patrick Legembre; Renaud Legouis; Michael Lehmann; Huan-Yao Lei; Qun-Ying Lei; David A Leib; José Leiro; John J Lemasters; Antoinette Lemoine; Maciej S Lesniak; Dina Lev; Victor V Levenson; Beth Levine; Efrat Levy; Faqiang Li; Jun-Lin Li; Lian Li; Sheng Li; Weijie Li; Xue-Jun Li; Yan-bo Li; Yi-Ping Li; Chengyu Liang; Qiangrong Liang; Yung-Feng Liao; Pawel P Liberski; Andrew P Lieberman; Hyunjung J Lim; Kyu Lim; Kah-Leong Lim; Chiou-Feng Lin; Fu-Cheng Lin; Jian Lin; Jiandie D Lin; Kui Lin; Weei-Chin Lin; Wan-Wan Lin; Yi-Ling Lin; Rafael Linden; Paul Lingor; Jennifer Lippincott-Schwartz; Michael P Lisanti; Paloma B Liton; Bo Liu; Chun-Feng Liu; Kaiyu Liu; Leyuan Liu; Qiong A Liu; Wei Liu; Yule Liu; Young-Chau Liu; Richard A Lockshin; Chun-Nam Lok; Sagar Lonial; Benjamin Loos; Gabriel Lopez-Berestein; Carlos López-Otín; Laura Lossi; Michael T Lotze; Peter Lőw; Binfeng Lu; Bingwei Lu; Bo Lu; Zhen Lu; Frédéric Luciano; Nicholas W Lukacs; Anders H Lund; Melinda A Lynch-Day; Yong Ma; Fernando Macian; Jeffrey P MacKeigan; Kay F Macleod; Frank Madeo; Luigi Maiuri; Maria Chiara Maiuri; Davide Malagoli; May Christine V Malicdan; Walter Malorni; Na Man; Eva-Maria Mandelkow; Stéphen Manon; Irena Manov; Kai Mao; Xiang Mao; Zixu Mao; Philippe Marambaud; Daniela Marazziti; Yves L Marcel; Katie Marchbank; Piero Marchetti; Stefan Marciniak; Mateus Marcondes; Mohsen Mardi; Gabriella Marfe; Guillermo Mariño; Maria Markaki; Mark R Marten; Seamus J Martin; Camille Martinand-Mari; Wim Martinet; Marta Martinez-Vicente; Matilde Masini; Paola Matarrese; Saburo Matsuo; Raffaele Matteoni; Andreas Mayer; Nathalie M Mazure; David J McConkey; Melanie J McConnell; Catherine McDermott; Christine McDonald; Gerald M McInerney; Sharon L McKenna; BethAnn McLaughlin; Pamela J McLean; Christopher R McMaster; G Angus McQuibban; Alfred J Meijer; Miriam H Meisler; Alicia Meléndez; Thomas J Melia; Gerry Melino; Maria A Mena; Javier A Menendez; Rubem F S Menna-Barreto; Manoj B Menon; Fiona M Menzies; Carol A Mercer; Adalberto Merighi; Diane E Merry; Stefania Meschini; Christian G Meyer; Thomas F Meyer; Chao-Yu Miao; Jun-Ying Miao; Paul A M Michels; Carine Michiels; Dalibor Mijaljica; Ana Milojkovic; Saverio Minucci; Clelia Miracco; Cindy Miranti; Ioannis Mitroulis; Keisuke Miyazawa; Noboru Mizushima; Baharia Mograbi; Simin Mohseni; Xavier Molero; Bertrand Mollereau; Faustino Mollinedo; Takashi Momoi; Iryna Monastyrska; Martha M Monick; Mervyn Monteiro; Michael N Moore; Rodrigo Mora; Kevin Moreau; Paula I Moreira; Yuji Moriyasu; Jorge Moscat; Serge Mostowy; Jeremy C Mottram; Tomasz Motyl; Charbel E-H Moussa; Sylviane Muller; Sylke Müller; Karl Münger; Christian Münz; Leon O Murphy; Maureen E Murphy; Antonio Musarò; Indira Mysorekar; Eiichiro Nagata; Kazuhiro Nagata; Aimable Nahimana; Usha Nair; Toshiyuki Nakagawa; Kiichi Nakahira; Hiroyasu Nakano; Hitoshi Nakatogawa; Meera Nanjundan; Naweed I Naqvi; Derek P Narendra; Masashi Narita; Miguel Navarro; Steffan Nawrocki; Taras Y Nazarko; Andriy Nemchenko; Mihai G Netea; Thomas P Neufeld; Paul A Ney; Ioannis P Nezis; Huu Phuc Nguyen; Daotai Nie; Ichizo Nishino; Corey Nislow; Ralph A Nixon; Takeshi Noda; Angelika A Noegel; Anna Nogalska; Satoru Noguchi; Lucia Notterpek; Ivana Novak; Tomoyoshi Nozaki; Nobuyuki Nukina; Thorsten Nürnberger; Beat Nyfeler; Keisuke Obara; Terry D Oberley; Salvatore Oddo; Michinaga Ogawa; Toya Ohashi; Koji Okamoto; Nancy L Oleinick; F Javier Oliver; Laura J Olsen; Stefan Olsson; Onya Opota; Timothy F Osborne; Gary K Ostrander; Kinya Otsu; Jing-hsiung James Ou; Mireille Ouimet; Michael Overholtzer; Bulent Ozpolat; Paolo Paganetti; Ugo Pagnini; Nicolas Pallet; Glen E Palmer; Camilla Palumbo; Tianhong Pan; Theocharis Panaretakis; Udai Bhan Pandey; Zuzana Papackova; Issidora Papassideri; Irmgard Paris; Junsoo Park; Ohkmae K Park; Jan B Parys; Katherine R Parzych; Susann Patschan; Cam Patterson; Sophie Pattingre; John M Pawelek; Jianxin Peng; David H Perlmutter; Ida Perrotta; George Perry; Shazib Pervaiz; Matthias Peter; Godefridus J Peters; Morten Petersen; Goran Petrovski; James M Phang; Mauro Piacentini; Philippe Pierre; Valérie Pierrefite-Carle; Gérard Pierron; Ronit Pinkas-Kramarski; Antonio Piras; Natik Piri; Leonidas C Platanias; Stefanie Pöggeler; Marc Poirot; Angelo Poletti; Christian Poüs; Mercedes Pozuelo-Rubio; Mette Prætorius-Ibba; Anil Prasad; Mark Prescott; Muriel Priault; Nathalie Produit-Zengaffinen; Ann Progulske-Fox; Tassula Proikas-Cezanne; Serge Przedborski; Karin Przyklenk; Rosa Puertollano; Julien Puyal; Shu-Bing Qian; Liang Qin; Zheng-Hong Qin; Susan E Quaggin; Nina Raben; Hannah Rabinowich; Simon W Rabkin; Irfan Rahman; Abdelhaq Rami; Georg Ramm; Glenn Randall; Felix Randow; V Ashutosh Rao; Jeffrey C Rathmell; Brinda Ravikumar; Swapan K Ray; Bruce H Reed; John C Reed; Fulvio Reggiori; Anne Régnier-Vigouroux; Andreas S Reichert; John J Reiners; Russel J Reiter; Jun Ren; José L Revuelta; Christopher J Rhodes; Konstantinos Ritis; Elizete Rizzo; Jeffrey Robbins; Michel Roberge; Hernan Roca; Maria C Roccheri; Stephane Rocchi; H Peter Rodemann; Santiago Rodríguez de Córdoba; Bärbel Rohrer; Igor B Roninson; Kirill Rosen; Magdalena M Rost-Roszkowska; Mustapha Rouis; Kasper M A Rouschop; Francesca Rovetta; Brian P Rubin; David C Rubinsztein; Klaus Ruckdeschel; Edmund B Rucker; Assaf Rudich; Emil Rudolf; Nelson Ruiz-Opazo; Rossella Russo; Tor Erik Rusten; Kevin M Ryan; Stefan W Ryter; David M Sabatini; Junichi Sadoshima; Tapas Saha; Tatsuya Saitoh; Hiroshi Sakagami; Yasuyoshi Sakai; Ghasem Hoseini Salekdeh; Paolo Salomoni; Paul M Salvaterra; Guy Salvesen; Rosa Salvioli; Anthony M J Sanchez; José A Sánchez-Alcázar; Ricardo Sánchez-Prieto; Marco Sandri; Uma Sankar; Poonam Sansanwal; Laura Santambrogio; Shweta Saran; Sovan Sarkar; Minnie Sarwal; Chihiro Sasakawa; Ausra Sasnauskiene; Miklós Sass; Ken Sato; Miyuki Sato; Anthony H V Schapira; Michael Scharl; Hermann M Schätzl; Wiep Scheper; Stefano Schiaffino; Claudio Schneider; Marion E Schneider; Regine Schneider-Stock; Patricia V Schoenlein; Daniel F Schorderet; Christoph Schüller; Gary K Schwartz; Luca Scorrano; Linda Sealy; Per O Seglen; Juan Segura-Aguilar; Iban Seiliez; Oleksandr Seleverstov; Christian Sell; Jong Bok Seo; Duska Separovic; Vijayasaradhi Setaluri; Takao Setoguchi; Carmine Settembre; John J Shacka; Mala Shanmugam; Irving M Shapiro; Eitan Shaulian; Reuben J Shaw; James H Shelhamer; Han-Ming Shen; Wei-Chiang Shen; Zu-Hang Sheng; Yang Shi; Kenichi Shibuya; Yoshihiro Shidoji; Jeng-Jer Shieh; Chwen-Ming Shih; Yohta Shimada; Shigeomi Shimizu; Takahiro Shintani; Orian S Shirihai; Gordon C Shore; Andriy A Sibirny; Stan B Sidhu; Beata Sikorska; Elaine Silva-Zacarin; Elaine C M Silva-Zacarin; Alison Simmons; Anna Katharina Simon; Hans-Uwe Simon; Cristiano Simone; Anne Simonsen; David A Sinclair; Rajat Singh; Debasish Sinha; Frank A Sinicrope; Agnieszka Sirko; Parco M Siu; Efthimios Sivridis; Vojtech Skop; Vladimir P Skulachev; Ruth S Slack; Soraya S Smaili; Duncan Smith; Maria S Soengas; Thierry Soldati; Xueqin Song; Anil K Sood; Tuck Wah Soong; Federica Sotgia; Stephen A Spector; Claudia D Spies; Wolfdieter Springer; Srinivasa M Srinivasula; Leonidas Stefanis; Joan S Steffan; Ruediger Stendel; Harald Stenmark; Anastasis Stephanou; Stephan T Stern; Cinthya Sternberg; Björn Stork; Peter Strålfors; Carlos S Subauste; Xinbing Sui; David Sulzer; Jiaren Sun; Shi-Yong Sun; Zhi-Jun Sun; Joseph J Y Sung; Kuninori Suzuki; Toshihiko Suzuki; Michele S Swanson; Charles Swanton; Sean T Sweeney; Lai-King Sy; Gyorgy Szabadkai; Ira Tabas; Heinrich Taegtmeyer; Marco Tafani; Krisztina Takács-Vellai; Yoshitaka Takano; Kaoru Takegawa; Genzou Takemura; Fumihiko Takeshita; Nicholas J Talbot; Kevin S W Tan; Keiji Tanaka; Kozo Tanaka; Daolin Tang; Dingzhong Tang; Isei Tanida; Bakhos A Tannous; Nektarios Tavernarakis; Gregory A Taylor; Graham S Taylor; J Paul Taylor; Lance S Terada; Alexei Terman; Gianluca Tettamanti; Karin Thevissen; Craig B Thompson; Andrew Thorburn; Michael Thumm; FengFeng Tian; Yuan Tian; Glauco Tocchini-Valentini; Aviva M Tolkovsky; Yasuhiko Tomino; Lars Tönges; Sharon A Tooze; Cathy Tournier; John Tower; Roberto Towns; Vladimir Trajkovic; Leonardo H Travassos; Ting-Fen Tsai; Mario P Tschan; Takeshi Tsubata; Allan Tsung; Boris Turk; Lorianne S Turner; Suresh C Tyagi; Yasuo Uchiyama; Takashi Ueno; Midori Umekawa; Rika Umemiya-Shirafuji; Vivek K Unni; Maria I Vaccaro; Enza Maria Valente; Greet Van den Berghe; Ida J van der Klei; Wouter van Doorn; Linda F van Dyk; Marjolein van Egmond; Leo A van Grunsven; Peter Vandenabeele; Wim P Vandenberghe; Ilse Vanhorebeek; Eva C Vaquero; Guillermo Velasco; Tibor Vellai; Jose Miguel Vicencio; Richard D Vierstra; Miquel Vila; Cécile Vindis; Giampietro Viola; Maria Teresa Viscomi; Olga V Voitsekhovskaja; Clarissa von Haefen; Marcela Votruba; Keiji Wada; Richard Wade-Martins; Cheryl L Walker; Craig M Walsh; Jochen Walter; Xiang-Bo Wan; Aimin Wang; Chenguang Wang; Dawei Wang; Fan Wang; Fen Wang; Guanghui Wang; Haichao Wang; Horng-Dar Wang; Hong-Gang Wang; Jin Wang; Ke Wang; Mei Wang; Richard C Wang; Xinglong Wang; Xuejun Wang; Yipeng Wang; Ying-Jan Wang; Zhen Wang; Zhinong Wang; Zhigang Charles Wang; Derick G Wansink; Diane M Ward; Hirotaka Watada; Sarah L Waters; Paul Webster; Lixin Wei; Conrad C Weihl; William A Weiss; Scott M Welford; Long-Ping Wen; Caroline A Whitehouse; J Lindsay Whitton; Alexander J Whitworth; Tom Wileman; John W Wiley; Simon Wilkinson; Dieter Willbold; Roger L Williams; Peter R Williamson; Bradly G Wouters; Chenghan Wu; Dao-Cheng Wu; William K K Wu; Andreas Wyttenbach; Ramnik J Xavier; Zhijun Xi; Pu Xia; Gengfu Xiao; Zhiping Xie; Zhonglin Xie; Da-zhi Xu; Jianzhen Xu; Liang Xu; Xiaolei Xu; Ai Yamamoto; Akitsugu Yamamoto; Shunhei Yamashina; Michiaki Yamashita; Xianghua Yan; Mitsuhiro Yanagida; Dun-Sheng Yang; Elizabeth Yang; Jin-Ming Yang; Shi Yu Yang; Wannian Yang; Wei Yuan Yang; Zhifen Yang; Meng-Chao Yao; Tso-Pang Yao; Behzad Yeganeh; Wei-Lien Yen; Jia-jing Yin; Xiao-Ming Yin; Ook-Joon Yoo; Gyesoon Yoon; Seung-Yong Yoon; Tomohiro Yorimitsu; Yuko Yoshikawa; Tamotsu Yoshimori; Kohki Yoshimoto; Ho Jin You; Richard J Youle; Anas Younes; Li Yu; Long Yu; Seong-Woon Yu; Wai Haung Yu; Zhi-Min Yuan; Zhenyu Yue; Cheol-Heui Yun; Michisuke Yuzaki; Olga Zabirnyk; David N Zacks; Eldad Zacksenhaus; Nadia Zaffaroni; Zahra Zakeri; Herbert J Zeh; Scott O Zeitlin; Hong Zhang; Hui-Ling Zhang; Jianhua Zhang; Jing-Pu Zhang; Lin Zhang; Long Zhang; Ming-Yong Zhang; Xu Dong Zhang; Mantong Zhao; Ying Zhao; Yi-Fang Zhao; Zhizhuang J Zhao; Xiaoxiang Zheng; Boris Zhivotovsky; Qing Zhong; Cong-Zhao Zhou; Changlian Zhu; Wei-Guo Zhu; Xiongwei Zhu; Xiao-Feng Zhu; Yuangang Zhu; Teresa Zoladek; Wei-Xing Zong; Antonio Zorzano; Jürgen Zschocke; Fabio C Abdalla; Hagai Abeliovich; Robert T Abraham; Abraham Acevedo-Arozena; Khosrow Adeli; Lotta Agholme; Maria Agnello; Patrizia Agostinis; Julio A Aguirre-Ghiso; Hyung Jun Ahn; Ouardia Ait-Mohamed; Slimane Ait-Si-Ali; Takahiko Akematsu; Shizuo Akira; Matthew L Albert; Roger L Albin; Javier Alegre-Abarrategui; Maria Francesca Aleo; Mehrdad Alirezaei; alex almasan; Maylin Almonte-Becerril; Hesham M Al-Younes; Munir A Al-Zeer; Atsuo Amano; Ravi Amaravadi; Shoba Amarnath; Amal O Amer; Vellareddy Anantharam; Nathalie Andrieu-Abadie; David K Ann; Shailendra Anoopkumar-Dukie; Hiroshi Aoki; Nadezda Apostolova; Patrick Auberger; Misuzu Baba; Steven K Backues; Eric H Baehrecke; Ben A Bahr; Xue-Yuan Bai; Yannick Bailly; Robert Baiocchi; Giulia Baldini; Walter Balduini; Andrea Ballabio; Bruce A Bamber; Edward T W Bampton; Gábor Bánhegyi; Clinton R Bartholomew; Diane C Bassham; Robert C Bast; Henri Batoko; Boon-Huat Bay; Isabelle Beau; Daniel M Béchet; Thomas J Begley; Christian Behl; Christian Behrends; Soumeya Bekri; Bryan Bellaire; Linda J Bendall; Luca Benetti; Laura Berliocchi; Henri Bernardi; Francesca Bernassola; Sébastien Besteiro; Ingrid Bhatia-Kissova; Xiaoning Bi; Martine Biard-Piechaczyk; Janice S Blum; Lawrence H Boise; Paolo Bonaldo; David L Boone; Beat C Bornhauser; Karina R Bortoluci; Ioannis Bossis; Frédéric Bost; Jean-Pierre Bourquin; Patricia Boya; Michaël Boyer-Guittaut; Peter V Bozhkov; Nathan R Brady; Claudio Brancolini; Andreas Brech; Jay E Brenman; Ana Brennand; Emery H Bresnick; Patrick Brest; Dave Bridges; Molly L Bristol; Paul S Brookes; Eric J Brown; John H Brumell; Nicola Brunetti-Pierri; Ulf T Brunk; Dennis E Bulman; Scott J Bultman; Geert Bultynck; Lena F Burbulla; Wilfried Bursch; Jonathan P Butchar; Wanda Buzgariu; Sergio P Bydlowski; Ken Cadwell; Monika Cahová; Dongsheng Cai; Jiyang Cai; Qian Cai; Bruno Calabretta; Javier Calvo-Garrido; Nadine Camougrand; Michelangelo Campanella; Jenny Campos-Salinas; Eleonora Candi; Lizhi Cao; Allan B Caplan; Simon R Carding; Sandra M Cardoso; Jennifer Carew; Cathleen R Carlin; Virginie Carmignac; Leticia A M Carneiro; Serena Carra; Rosario A Caruso; Giorgio Casari; Caty Casas; Roberta Castino; Eduardo Cebollero; Francesco Cecconi; Jean Celli; Hassan Chaachouay; Han-Jung Chae; Chee-Yin Chai; David C Chan; Edmond Y Chan; Raymond Chuen-Chung Chang; Chi-Ming Che; Ching-Chow Chen; Guang-Chao Chen; Guo-Qiang Chen; Min Chen; Quan Chen; Steve S-L Chen; WenLi Chen; Xi Chen; Xiangmei Chen; Xiequn Chen; Yingyu Chen; Yongqiang Chen; Ye-Guang Chen; Yu-Jen Chen; Zhixiang Chen; Alan Cheng; Christopher H K Cheng; Yan Cheng; Heesun Cheong; Jae-Ho Cheong; Sara Cherry; Russ Chess-Williams; Zelda H Cheung; Eric Chevet; Hui-Ling Chiang; Roberto Chiarelli; Tomoki Chiba; Lih-Shen Chin; Shih-Hwa Chiou; Francis V Chisari; Chi Hin Cho; Dong-Hyung Cho; Augustine M K Choi; DooSeok Choi; Kyeong Sook Choi; Mary E Choi; Salem Chouaib; Divaker Choubey; Vinay Choubey; Charleen T Chu; Tsung-Hsien Chuang; Sheau-Huei Chueh; Taehoon Chun; Yong-Joon Chwae; Mee-Len Chye; Roberto Ciarcia; Maria R Ciriolo; Michael J Clague; Robert S B Clark; Peter G H Clarke; Robert Clarke; Patrice Codogno; Hilary A Coller; María I Colombo; Sergio Comincini; Maria Condello; Fabrizio Condorelli; Mark R Cookson; Graham H Coombs; Isabelle Coppens; Ramon Corbalan; Pascale Cossart; Paola Costelli; Safia Costes; Ana Coto-Montes; Eduardo Couve; Fraser P Coxon; James M Cregg; José L Crespo; Marianne J Cronjé; Ana Maria Cuervo; Joseph J Cullen; Mark J Czaja; Marcello D'Amelio; Arlette Darfeuille-Michaud; Lester M Davids; Faith E Davies; Massimo De Felici; John F de Groot; Cornelis A M de Haan; Luisa De Martino; Angelo De Milito; Vincenzo De Tata; Jayanta Debnath; Alexei Degterev; Benjamin Dehay; Lea M D Delbridge; Francesca Demarchi; Yi Zhen Deng; Jörn Dengjel; Paul Dent; Donna Denton; Vojo Deretic; Shyamal D Desai; Rodney J Devenish; Mario Di Gioacchino; Gilbert Di Paolo; Chiara Di Pietro; Guillermo Díaz-Araya; Inés Díaz-Laviada; Maria T Diaz-Meco; Javier Diaz-Nido; Ivan Dikic; Savithramma P Dinesh-Kumar; Wen-Xing Ding; Clark W Distelhorst; Abhinav Diwan; Mojgan Djavaheri-Mergny; Svetlana Dokudovskaya; Zheng Dong; Frank C Dorsey; Victor Dosenko; James Dowling; Stephen Doxsey; Marlène Dreux; Mark E Drew; Qiuhong Duan; Michel A Duchosal; Karen Duff; Isabelle Dugail; Madeleine Durbeej; Michael Duszenko; Charles L Edelstein; Aimee L Edinger; Gustavo Egea; Ludwig Eichinger; N Tony Eissa; Suhendan Ekmekcioglu; Zvulun Elazar; Wafik S El-Deiry; Mohamed Elgendy; Lisa M Ellerby; Kai Er Eng; Anna-Mart Engelbrecht; Simone Engelender; Jekaterina Erenpreisa; Ricardo Escalante; Audrey Esclatine; Eeva-Liisa Eskelinen; Lucile Espert; Virginia Espina; Huizhou Fan; Jia Fan; Qi-Wen Fan; Zhen Fan; Shengyun Fang; Yongqi Fang; Manolis Fanto; Alessandro Fanzani; Thomas Farkas; Jean-Claude Farré; Mathias Faure; Marcus Fechheimer; Carl G Feng; Jian Feng; Qili Feng; Youji Feng; László Fésüs; Ralph Feuer; Maria E Figueiredo-Pereira; Gian Maria Fimia; Diane C Fingar; Steven Finkbeiner; TOREN FINKEL; Kim D Finley; Filomena Fiorito; Edward A Fisher; Paul B Fisher; Marc Flajolet; Maria L Florez-McClure; Salvatore Florio; Edward A Fon; Francesco Fornai; Franco Fortunato; Rati Fotedar; Daniel H Fowler; Howard S Fox; Rodrigo Franco; Lisa B Frankel; Marc Fransen; José M Fuentes; Juan Fueyo; Jun Fujii; Kozo Fujisaki; Eriko Fujita; Mitsunori Fukuda; Ruth H Furukawa; Matthias Gaestel; Philippe Gailly; Malgorzata Gajewska; Brigitte Galliot; Vincent Galy; Subramaniam Ganesh; Barry Ganetzky; Ian G Ganley; Fen-Biao Gao; George F Gao; Jinming Gao; Lorena Garcia; Guillermo Garcia-Manero; Mikel Garcia-Marcos; Marjan Garmyn; Andrei L Gartel; Evelina Gatti; Mathias Gautel; Thomas R Gawriluk; Matthew E Gegg; Jiefei Geng; Marc Germain; Jason E Gestwicki; David A Gewirtz; Saeid Ghavami; Pradipta Ghosh; Anna M Giammarioli; Alexandra N Giatromanolaki; Spencer B Gibson; Robert W Gilkerson; Michael L Ginger; Ebru Goncu; Céline Gongora; Claudio D Gonzalez; Ramon Gonzalez; Cristina González-Estévez; Rosa Ana González-Polo; Elena Gonzalez-Rey; Nikolai V Gorbunov; Sharon Gorski; Sandro Goruppi; Roberta A Gottlieb; Devrim Gozuacik; Giovanna Elvira Granato; Gary D Grant; Kim N Green; Aleš Gregorc; Frédéric Gros; Charles Grose; Thomas W Grunt; Philippe Gual; Jun-Lin Guan; Kun-Liang Guan; Sylvie M Guichard; Anna S Gukovskaya; Ilya Gukovsky; Jan Gunst; Asa B Gustafsson; Andrew J Halayko; Amber N Hale; Sandra K Halonen; Maho Hamasaki; Feng Han; Ting Han; Michael K Hancock; Malene Hansen; Hisashi Harada; Masaru Harada; Stefan E Hardt; J Wade Harper; Adrian L Harris; James Harris; Steven D Harris; Marie-Joseé Hébert; Kim A Heidenreich; Miep H Helfrich; Gudmundur V Helgason; Elizabeth P Henske; Brian Herman; Paul K Herman; Claudio Hetz; Sabine Hilfiker; Joseph A Hill; Lynne J Hocking; Paul Hofman; Thomas G Hofmann; Jörg Höhfeld; Tessa L Holyoake; Ming-Huang Hong; David A Hood; Gökhan S Hotamisligil; Ewout J Houwerzijl; Maria Høyer-Hansen; Bingren Hu; Chien-An A Hu; Hong-Ming Hu; Ya Hua; Canhua Huang; Ju Huang; Shengbing Huang; Wei-Pang Huang; Tobias B Huber; Won-Ki Huh; Tai-Ho Hung; Ted R Hupp; Gang Min Hur; James B Hurley; Sabah N A Hussain; Patrick J Hussey; Jung Jin Hwang; Seungmin Hwang; Atsuhiro Ichihara; Shirin Ilkhanizadeh; Ken Inoki; Takeshi Into; Valentina Iovane; Juan L Iovanna; Nancy Y Ip; Yoshitaka Isaka; Hiroyuki Ishida; Ciro Isidoro; Ken-ichi Isobe; Akiko Iwasaki; Marta Izquierdo; Yotaro Izumi; Panu M Jaakkola; Marja Jäättelä; George R Jackson; William T Jackson; Bassam Janji; Marina Jendrach; Ju-Hong Jeon; Eui-Bae Jeung; Hong Jiang; Hongchi Jiang; Jean X Jiang; Ming Jiang; Qing Jiang; Xuejun Jiang; Xuejun Jiang; Alberto Jiménez; Meiyan Jin; Shengkan Jin; Cheol O Joe; Terje Johansen; Daniel E Johnson; Gail V W Johnson; Nicola L Jones; Bertrand Joseph; Suresh K Joseph; Annie M Joubert; Gábor Juhász; Lucienne Juillerat-Jeanneret; Chang Hwa Jung; Yong-Keun Jung; Kai Kaarniranta; Allen Kaasik; Tomohiro Kabuta; Motoni Kadowaki; Katarina Kagedal; Yoshiaki Kamada; Vitaliy O Kaminskyy; Harm H Kampinga; Hiromitsu Kanamori; Chanhee Kang; Khong Bee Kang; Kwang Il Kang; Rui Kang; Yoon-A Kang; Tomotake Kanki; Thirumala-Devi Kanneganti; Haruo Kanno; Arthi Kanthasamy; Anumantha G Kanthasamy; Vassiliki Karantza; Gur P Kaushal; Susmita Kaushik; Yoshinori Kawazoe; Po-Yuan Ke; John H Kehrl; Ameeta Kelekar; Claus Kerkhoff; David Kessel; Hany Khalil; Jan A K W Kiel; Amy A Kiger; Akio Kihara; Do-Hyung Kim; Dong-Hou Kim; Deok Ryong Kim; Eun-Kyoung Kim; Hyung-Ryong Kim; Jin Cheon Kim; Jeong Hun Kim; John K Kim; Jae-Sung Kim; Peter K Kim; Seong Who Kim; Yonghyun Kim; Yong-Sun Kim; Adi Kimchi; Alec C Kimmelman; Jason S King; Timothy J Kinsella; Vladimir Kirkin; Lorrie A Kirshenbaum; Katsuhiko Kitamoto; Kaio Kitazato; Ludger Klein; Walter T Klimecki; Giuseppe Arancia; John P Aris; Katsuhiko Asanuma; Nana Y O Asare; Hisashi Ashida; Valerie Askanas; David S Askew; Henry N Ginsberg; Jakub Golab; Michael S Goligorsky; Pierre Golstein; Candelaria Gomez-Manzano; Makoto Hashimoto; Jeffrey A Haspel; Shin-ichiro Hayashi; Lori A Hazelhurst; Congcong He; You-Wen He; Brian Zuckerbraun
Guidelines for the use and interpretation of assays for monitoring autophagy.
Autophagy 2012;8(4):445-544.
2012: Krishna R Veeramah; Stephen G Waxman; Xiaoyang Cheng; Sulayman D Dib-Hajj; Evan E Eichler; Robert P Erickson; Santhosh Girirajan; Miriam H Meisler; Janelle E O'Brien; Linda L Restifo; Dinesh Talwar; Michael F Hammer
De novo pathogenic SCN8A mutation identified by whole-genome sequencing of a family quartet affected by infantile epileptic encephalopathy and SUDEP.
American journal of human genetics 2012;90(3):502-10.
2012: Lauren T Gehman; Pratap Meera; Miriam H Meisler; Janelle E O'Brien; Thomas S Otis; Lily Shiue; Peter Stoilov; Manuel Ares; Douglas L Black
The splicing regulator Rbfox2 is required for both cerebellar development and mature motor function.
Genes & development 2012;26(5):445-60.
2012: Janelle E O'Brien; Ben A Barres; Valerie L Drews; Jason C Dugas; Julie M Jones; Miriam H Meisler
Rbfox proteins regulate alternative splicing of neuronal sodium channel SCN8A.
Molecular and cellular neurosciences 2012;49(2):120-6.
2012: Sami F Noujaim; Julie M Jones; Philip Furspan; Daniel Jiang; Michelle Milstein; Miriam H Meisler; Todd J Herron; Kuljeet Kaur; David S Auerbach; Jose Jalife
A null mutation of the neuronal sodium channel NaV1.6 disrupts action potential propagation and excitation-contraction coupling in the mouse heart.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2012;26(1):63-72.
2011: Jesse J Winters; Cole J Ferguson; Vessela I Giger-Mateeva; Guy M Lenk; Miriam H Meisler; Peter Shrager; Roman J Giger
Congenital CNS hypomyelination in the Fig4 null mouse is rescued by neuronal expression of the PI(3,5)P(2) phosphatase Fig4.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2011;31(48):17736-51.
2011: Ilaria Vaccari; Lois S Weisman; Lawrence Wrabetz; Federica Cerri; Gaëtan Chicanne; Giorgia Dina; Emily Kaufman; Miriam H Meisler; Bernard Payrastre; Angelo Quattrini; Hélène Tronchère; Alessandra Bolino
Genetic interaction between MTMR2 and FIG4 phospholipid phosphatases involved in Charcot-Marie-Tooth neuropathies.
PLoS genetics 2011;7(10):e1002319.
2011: Garth Nicholson; Stephen W Reddel; Angela Scheuerle; Ericka Simpson; Charles F Towne; Michelle Yasick; Sat Dev Batish; Leslie G Biesecker; Randall Blouin; Carla Brandt; Giovanni Coppola; Cole J Ferguson; Adrienne E Grant; Stuart Hoffman; Guy M Lenk; Miriam H Meisler
Distinctive genetic and clinical features of CMT4J: a severe neuropathy caused by mutations in the PI(3,5)P₂ phosphatase FIG4.
Brain : a journal of neurology 2011;134(Pt 7):1959-71.
2011: Guy M Lenk; Lois S Weisman; Jesse J Winters; Sergey N Zolov; Clement Y Chow; James Dowling; Cole J Ferguson; Roman J Giger; Adrienne E Grant; Natsuko Jin; Julie M Jones; Miriam H Meisler
Pathogenic mechanism of the FIG4 mutation responsible for Charcot-Marie-Tooth disease CMT4J.
PLoS genetics 2011;7(6):e1002104.
2011: Emily R Freilich; Julie M Jones; William D Gaillard; Joan A Conry; Tammy N Tsuchida; Christine Reyes; Sulayman Dib-Hajj; Stephen G Waxman; Miriam H Meisler; Phillip L Pearl
Novel SCN1A mutation in a proband with malignant migrating partial seizures of infancy.
Archives of neurology 2011;68(5):665-71.
2010: Miriam H Meisler; Janelle E O'Brien; Lisa M Sharkey
Sodium channel gene family: epilepsy mutations, gene interactions and modifier effects.
The Journal of physiology 2010;588(Pt 11):1841-8.
2010: Melinda S Martin; Karoni Dutt; Ligia A Papale; Céline M Dubé; Stacey B Dutton; Georgius de Haan; Anupama Shankar; Sergio Tufik; Miriam H Meisler; Tallie Z Baram; Alan L Goldin; Andrew Escayg
Altered function of the SCN1A voltage-gated sodium channel leads to gamma-aminobutyric acid-ergic (GABAergic) interneuron abnormalities.
The Journal of biological chemistry 2010;285(13):9823-34.
2010: Nancy Osorio; Laurence Cathala; Miriam H Meisler; Marcel Crest; Jacopo Magistretti; Patrick Delmas
Persistent Nav1.6 current at axon initial segments tunes spike timing of cerebellar granule cells.
The Journal of physiology 2010;588(Pt 4):651-70.
2010: Cole J Ferguson; Guy M Lenk; Miriam H Meisler
PtdIns(3,5)P2 and autophagy in mouse models of neurodegeneration.
Autophagy 2010;6(1):170-1.
2009: Cole J Ferguson; Guy M Lenk; Miriam H Meisler
Defective autophagy in neurons and astrocytes from mice deficient in PI(3,5)P2.
Human molecular genetics 2009;18(24):4868-78.
2009: Ligia A Papale; Barbara Beyer; Julie M Jones; Lisa M Sharkey; Sergio Tufik; Michael Epstein; Verity A Letts; Miriam H Meisler; Wayne N Frankel; Andrew Escayg
Heterozygous mutations of the voltage-gated sodium channel SCN8A are associated with spike-wave discharges and absence epilepsy in mice.
Human molecular genetics 2009;18(9):1633-41.
2009: Lisa M Sharkey; Julie M Jones; Peter Hedera; Miriam H Meisler
Evaluation of SCN8A as a candidate gene for autosomal dominant essential tremor.
Parkinsonism & related disorders 2009;15(4):321-3.
2009: Lisa M Sharkey; Xiaoyang Cheng; Valerie Drews; David A Buchner; Julie M Jones; Monica J Justice; Stephen G Waxman; Sulayman D Dib-Hajj; Miriam H Meisler
The ataxia3 mutation in the N-terminal cytoplasmic domain of sodium channel Na(v)1.6 disrupts intracellular trafficking.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2009;29(9):2733-41.
2009: Federica Mastroiacovo; Carla L Busceti; Francesca Biagioni; Slavianka G Moyanova; Miriam H Meisler; Giuseppe Battaglia; Andrea Caricasole; Valeria Bruno; Ferdinando Nicoletti
Induction of the Wnt antagonist, Dickkopf-1, contributes to the development of neuronal death in models of brain focal ischemia.
Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism 2009;29(2):264-76.
2009: Clement Y Chow; John E Landers; Sarah K Bergren; Peter C Sapp; Adrienne E Grant; Julie M Jones; Lesley Everett; Guy M Lenk; Diane M McKenna-Yasek; Lois S Weisman; Denise Figlewicz; Robert H Brown; Miriam H Meisler
Deleterious variants of FIG4, a phosphoinositide phosphatase, in patients with ALS.
American journal of human genetics 2009;84(1):85-8.
2008: Natsuko Jin; Clement Y Chow; Li Liu; Sergey N Zolov; Roderick Bronson; Muriel Davisson; Jason L Petersen; Yanling Zhang; Sujin Park; Jason E Duex; Daniel Goldowitz; Miriam H Meisler; Lois S Weisman
VAC14 nucleates a protein complex essential for the acute interconversion of PI3P and PI(3,5)P(2) in yeast and mouse.
The EMBO journal 2008;27(24):3221-34.
2008: William A Catterall; Sulayman Dib-Hajj; Miriam H Meisler; Daniela Pietrobon
Inherited neuronal ion channelopathies: new windows on complex neurological diseases.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2008;28(46):11768-77.
2008: Viive M Howell; Georgius de Haan; Sarah Bergren; Julie M Jones; Cymbeline T Culiat; Edward J Michaud; Wayne N Frankel; Miriam H Meisler
A targeted deleterious allele of the splicing factor SCNM1 in the mouse.
Genetics 2008;180(3):1419-27.
2008: Xuebao Zhang; Clement Y Chow; Zarife Sahenk; chris hall; Miriam H Meisler; Jun Li
Mutation of FIG4 causes a rapidly progressive, asymmetric neuronal degeneration.
Brain : a journal of neurology 2008;131(Pt 8):1990-2001.
2008: B C McKinney; C Y Chow; Miriam H Meisler; Geoffrey G Murphy
Exaggerated emotional behavior in mice heterozygous null for the sodium channel Scn8a (Nav1.6).
Genes, brain, and behavior 2008;7(6):629-38.
2008: Miriam H Meisler; Carsten Russ; Kate T Montgomery; Matthew Greenway; Sean Ennis; Orla Hardiman; Denise A Figlewicz; Nicole R Quenneville; Elizabeth Conibear; Robert H Brown
Evaluation of the Golgi trafficking protein VPS54 (wobbler) as a candidate for ALS.
Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases 2008;9(3):141-8.
2008: Katherine D Holland; Jennifer A Kearney; Tracy A Glauser; Gerri Buck; Mehdi Keddache; John R Blankston; Ian W Glaaser; Robert Kass; Miriam H Meisler
Mutation of sodium channel SCN3A in a patient with cryptogenic pediatric partial epilepsy.
Neuroscience letters 2008;433(1):65-70.
2007: Yanling Zhang; Sergey N Zolov; Clement Y Chow; Shalom G Slutsky; Simon C Richardson; Robert C Piper; Baoli Yang; Johnathan J Nau; Randal J Westrick; Sean J Morrison; Miriam H Meisler; Lois S Weisman
Loss of Vac14, a regulator of the signaling lipid phosphatidylinositol 3,5-bisphosphate, results in neurodegeneration in mice.
Proceedings of the National Academy of Sciences of the United States of America 2007;104(44):17518-23.
2007: Viive M Howell; Julie M Jones; Sarah K Bergren; Li Li; Allison C Billi; Matthew R Avenarius; Miriam H Meisler
Evidence for a direct role of the disease modifier SCNM1 in splicing.
Human molecular genetics 2007;16(20):2506-16.
2007: Valerie L Drews; Kehui Shi; Georgius de Haan; Miriam H Meisler
Identification of evolutionarily conserved, functional noncoding elements in the promoter region of the sodium channel gene SCN8A.
Mammalian genome : official journal of the International Mammalian Genome Society 2007;18(10):723-31.
2007: Clement Y Chow; Yanling Zhang; James Dowling; Natsuko Jin; Maja Adamska; Kensuke Shiga; Kinga Szigeti; chris hall; Jun Li; Xuebao Zhang; James R Lupski; Lois S Weisman; Miriam H Meisler
Mutation of FIG4 causes neurodegeneration in the pale tremor mouse and patients with CMT4J.
Nature 2007;448(7149):68-72.
2006: Katherine D Holland; Michelle T Fleming; Susannah Cheek; Jennifer L Moran; David Beier; Miriam H Meisler
De novo exon duplication in a new allele of mouse Glra1 (spasmodic).
Genetics 2006;174(4):2245-7.
2006: Stephen I Levin; Zayd M Khaliq; Teresa K Aman; Tina M Grieco; Jennifer A Kearney; Indira M Raman; Miriam H Meisler
Impaired motor function in mice with cell-specific knockout of sodium channel Scn8a (NaV1.6) in cerebellar purkinje neurons and granule cells.
Journal of neurophysiology 2006;96(2):785-93.
2006: M M Trudeau; Joline C Dalton; John W Day; Laura P W Ranum; Miriam H Meisler
Heterozygosity for a protein truncation mutation of sodium channel SCN8A in a patient with cerebellar atrophy, ataxia, and mental retardation.
Journal of medical genetics 2006;43(6):527-30.
2006: Diana Woodruff-Pak; John T Green; Stephen I Levin; Miriam H Meisler
Inactivation of sodium channel Scn8A (Na-sub(v)1.6) in Purkinje neurons impairs learning in Morris water maze and delay but not trace eyeblink classical conditioning.
Behavioral neuroscience 2006;120(2):229-40.
2006: Miriam H Meisler; M M Trudeau; Joline C Dalton; John W Day; Laura P W Ranum
Gene symbol: SCN8A. Disease: Ataxia. Accession #Hd0520.
Human genetics 2006;118(6):776.
2006: Jennifer A Kearney; Anna K Wiste; Ulrich Stephani; Michelle M Trudeau; Anne Siegel; Rajesh RamachandranNair; Roy D Elterman; Hiltrud Muhle; Juliane Reinsdorf; W Donald Shields; Miriam H Meisler; Andrew Escayg
Recurrent de novo mutations of SCN1A in severe myoclonic epilepsy of infancy.
Pediatric neurology 2006;34(2):116-20.
2005: Thomas Schmitt-John; Carsten Drepper; Anke Mussmann; Phillip Hahn; Melanie Kuhlmann; Cora Thiel; Martin Hafner; Andreas Lengeling; Peter Heimann; Julie M Jones; Miriam H Meisler; Harald Jockusch
Mutation of Vps54 causes motor neuron disease and defective spermiogenesis in the wobbler mouse.
Nature genetics 2005;37(11):1213-5.
2005: Julie Turnbull; Hannes Lohi; Jennifer A Kearney; Guy Rouleau; Antonio V Delgado-Escueta; Miriam H Meisler; Patrick Cossette; Berge A Minassian
Sacred disease secrets revealed: the genetics of human epilepsy.
Human molecular genetics 2005;14 Spec No. 2():2491-2500.
2005: Julie Turnbull; Hannes Lohi; Jennifer A Kearney; Guy Rouleau; Antonio V Delgado-Escueta; Miriam H Meisler; Patrick Cossette; Berge A Minassian
Sacred disease secrets revealed: the genetics of human epilepsy.
Human molecular genetics 2005;14(17):2491-500.
2005: Miriam H Meisler; Jennifer A Kearney
Sodium channel mutations in epilepsy and other neurological disorders.
The Journal of clinical investigation 2005;115(8):2010-7.
2005: Maja Adamska; Allison C Billi; Susannah Cheek; Miriam H Meisler
Genetic interaction between Wnt7a and Lrp6 during patterning of dorsal and posterior structures of the mouse limb.
Developmental dynamics : an official publication of the American Association of Anatomists 2005;233(2):368-72.
2005: Valerie L Drews; Andrew P Lieberman; Miriam H Meisler
Multiple transcripts of sodium channel SCN8A (Na(V)1.6) with alternative 5'- and 3'-untranslated regions and initial characterization of the SCN8A promoter.
Genomics 2005;85(2):245-57.
2004: Jay Spampanato; Jennifer A Kearney; G de Haan; Dyke P McEwen; Andrew Escayg; Ildiko Aradi; Bryan T MacDonald; Stephen I Levin; Ivan Soltesz; Paolo Benna; Elisa Montalenti; Lori L Isom; Alan L Goldin; Miriam H Meisler
A novel epilepsy mutation in the sodium channel SCN1A identifies a cytoplasmic domain for beta subunit interaction.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2004;24(44):10022-34.
2004: Sanjeev Gupta; Rajesh Singh; Pinaki Datta; Zhijia Zhang; Christopher Orr; Zhixian Lu; Garrett C DuBois; Antonis S Zervos; Miriam H Meisler; Srinivasa M Srinivasula; Teresa Fernandes-Alnemri; Emad S Alnemri
The C-terminal tail of presenilin regulates Omi/HtrA2 protease activity.
The Journal of biological chemistry 2004;279(44):45844-54.
2004: Miriam H Meisler; Nicholas W Plummer; Daniel L Burgess; David A Buchner; Leslie K Sprunger
Allelic mutations of the sodium channel SCN8A reveal multiple cellular and physiological functions.
Genetica 2004;122(1):37-45.
2004: Stephen I Levin; Miriam H Meisler
Floxed allele for conditional inactivation of the voltage-gated sodium channel Scn8a (NaV1.6).
Genesis (New York, N.Y. : 2000) 2004;39(4):234-9.
2004: Maja Adamska; Bryan T MacDonald; Zubair H Sarmast; Edward R Oliver; Miriam H Meisler
En1 and Wnt7a interact with Dkk1 during limb development in the mouse.
Developmental biology 2004;272(1):134-44.
2004: Bryan T MacDonald; Maja Adamska; Miriam H Meisler
Hypomorphic expression of Dkk1 in the doubleridge mouse: dose dependence and compensatory interactions with Lrp6.
Development (Cambridge, England) 2004;131(11):2543-52.
2004: David A Buchner; Kevin Seburn; Wayne N Frankel; Miriam H Meisler
Three ENU-induced neurological mutations in the pore loop of sodium channel Scn8a (Na(v)1.6) and a genetically linked retinal mutation, rd13.
Mammalian genome : official journal of the International Mammalian Genome Society 2004;15(5):344-51.
2003: Melanie Hamann; Miriam H Meisler; Angelika Richter
Motor disturbances in mice with deficiency of the sodium channel gene Scn8a show features of human dystonia.
Experimental neurology 2003;184(2):830-8.
2003: Julie M Jones; Pinaki Datta; Srinivasa M Srinivasula; Weizhen Ji; Sanjeev Gupta; ZhiJia Zhang; Erika Davies; Gyorgy Hajn\u2264czky; Thomas L Saunders; Margaret L Van Keuren; Teresa Fernandes-Alnemri; Miriam H Meisler; Emad S Alnemri
Loss of Omi mitochondrial protease activity causes the neuromuscular disorder of mnd2 mutant mice.
Nature 2003;425(6959):721-7.
2003: David A Buchner; Michelle Trudeau; Alfred L George; Leslie K Sprunger; Miriam H Meisler
High-resolution mapping of the sodium channel modifier Scnm1 on mouse chromosome 3 and identification of a 1.3-kb recombination hot spot.
Genomics 2003;82(4):452-9.
2003: David A Buchner; Michelle Trudeau; Miriam H Meisler
SCNM1, a putative RNA splicing factor that modifies disease severity in mice.
Science (New York, N.Y.) 2003;301(5635):967-9.
2003: Ying Wang; Shinji Matsuda; Valerie Drews; Takashi Torashima; Miriam H Meisler; Michisuke Yuzaki
A hot spot for hotfoot mutations in the gene encoding the delta2 glutamate receptor.
The European journal of neuroscience 2003;17(8):1581-90.
2003: David A Buchner; Miriam H Meisler
TSRC1, a widely expressed gene containing seven thrombospondin type I repeats.
Gene 2003;307():23-30.
2003: Maja Adamska; Bryan T MacDonald; Miriam H Meisler
Doubleridge, a mouse mutant with defective compaction of the apical ectodermal ridge and normal dorsal-ventral patterning of the limb.
Developmental biology 2003;255(2):350-62.
2003: Lauren A Weiss; Andrew Escayg; Jennifer A Kearney; M Trudeau; Bryan T MacDonald; M Mori; J Reichert; Joseph Buxbaum; Miriam H Meisler
Sodium channels SCN1A, SCN2A and SCN3A in familial autism.
Molecular psychiatry 2003;8(2):186-94.
2003: Jay Spampanato; Andrew Escayg; Miriam H Meisler; Alan L Goldin
Generalized epilepsy with febrile seizures plus type 2 mutation W1204R alters voltage-dependent gating of Na(v)1.1 sodium channels.
Neuroscience 2003;116(1):37-48.
2002: Jennifer A Kearney; David A Buchner; Georgius De Haan; Maja Adamska; Stephen I Levin; Amy R Furay; Roger L Albin; Julie M Jones; Mauricio Montal; Martin J Stevens; Leslie K Sprunger; Miriam H Meisler
Molecular and pathological effects of a modifier gene on deficiency of the sodium channel Scn8a (Na(v)1.6).
Human molecular genetics 2002;11(22):2765-75.
2002: Silvia Rathke-Hartlieb; Uwe Schlomann; Peter Heimann; Miriam H Meisler; Harald Jockusch; Joerg Walter Bartsch
Progressive loss of striatal neurons causes motor dysfunction in MND2 mutant mice and is not prevented by Bcl-2.
Experimental neurology 2002;175(1):87-97.
2002: Miriam H Meisler; Jennifer A Kearney; Leslie K Sprunger; Bryan T MacDonald; David A Buchner; Andrew Escayg
Mutations of voltage-gated sodium channels in movement disorders and epilepsy.
Novartis Foundation symposium 2002;241():72-81; discussion 82-6, 226-32.
2001: Miriam H Meisler
Evolutionarily conserved noncoding DNA in the human genome: how much and what for?
Genome research 2001;11(10):1617-8.
2001: Jay Spampanato; Andrew Escayg; Miriam H Meisler; Alan L Goldin
Functional effects of two voltage-gated sodium channel mutations that cause generalized epilepsy with febrile seizures plus type 2.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2001;21(19):7481-90.
2001: W Ji; F Chen; T Do; A Do; B A Roe; Miriam H Meisler
DQX1, an RNA-dependent ATPase homolog with a novel DEAQ box: expression pattern and genomic sequence comparison of the human and mouse genes.
Mammalian genome : official journal of the International Mammalian Genome Society 2001;12(6):456-61.
2001: Miriam H Meisler; J Kearney; Andrew Escayg; Bryan T MacDonald; Leslie K Sprunger
Sodium channels and neurological disease: insights from Scn8a mutations in the mouse.
The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry 2001;7(2):136-45.
2001: N Maurice; Tatiana Tkatch; Miriam H Meisler; L K Sprunger; Dalton Surmeier
D1/D5 dopamine receptor activation differentially modulates rapidly inactivating and persistent sodium currents in prefrontal cortex pyramidal neurons.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2001;21(7):2268-77.
2001: Andrew Escayg; Armin Heils; Bryan T MacDonald; Karsten Haug; Thomas Sander; Miriam H Meisler
A novel SCN1A mutation associated with generalized epilepsy with febrile seizures plus--and prevalence of variants in patients with epilepsy.
American journal of human genetics 2001;68(4):866-73.
2001: J H Nadeau; R Balling; G Barsh; D Beier; S D Brown; M Bucan; Sally A Camper; G Carlson; N Copeland; J Eppig; C Fletcher; W N Frankel; D Ganten; D Goldowitz; C Goodnow; Jean Louis GUENET; G Hicks; M Hrabe de Angelis; I Jackson; H J Jacob; N Jenkins; D Johnson; M Justice; S Kay; D Kingsley; H Lehrach; Terry Magnuson; Miriam H Meisler; A Poustka; E M Rinchik; J Rossant; L B Russell; J Schimenti; T Shiroishi; W C Skarnes; P Soriano; W Stanford; J S Takahashi; W Wurst; A Zimmer
Sequence interpretation. Functional annotation of mouse genome sequences.
Science (New York, N.Y.) 2001;291(5507):1251-5.
2001: Miriam H Meisler; J Kearney; R Ottman; Andrew Escayg
Identification of epilepsy genes in human and mouse.
Annual review of genetics 2001;35():567-88.
2001: Evan Reid; Andrew Escayg; Andrew Dearlove; Miriam H Meisler; David C Rubinsztein
The spastic paraplegia SPG10 locus: narrowing of critical region and exclusion of sodium channel gene SCN8A as a candidate.
Journal of medical genetics 2001;38(1):65-7.
2001: Jennifer A Kearney; Nicholas W Plummer; M R Smith; J Kapur; T R Cummins; S G Waxman; Alan L Goldin; Miriam H Meisler
A gain-of-function mutation in the sodium channel gene Scn2a results in seizures and behavioral abnormalities.
Neuroscience 2001;102(2):307-17.
2000: Alan L Goldin; Robert L Barchi; John H Caldwell; F Hofmann; J R Howe; J C Hunter; RG Kallen; Gail Mandel; Miriam H Meisler; Y B Netter; M Noda; M M Tamkun; S G Waxman; J N Wood; W A Catterall
Nomenclature of voltage-gated sodium channels.
Neuron 2000;28(2):365-8.
2000: Andrew Escayg; M De Waard; D D Lee; D Bichet; P Wolf; T Mayer; J Johnston; Robert W Baloh; Thomas Sander; Miriam H Meisler
Coding and noncoding variation of the human calcium-channel beta4-subunit gene CACNB4 in patients with idiopathic generalized epilepsy and episodic ataxia.
American journal of human genetics 2000;66(5):1531-9.
2000: Andrew Escayg; Bryan T MacDonald; Miriam H Meisler; Stéphanie Baulac; Gilles Huberfeld; I An-Gourfinkel; Alexis Brice; Eric LeGuern; Bruno Moulard; D Chaigne; Catherine Buresi; Alain Malafosse
Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2.
Nature genetics 2000;24(4):343-5.
2000: Julie M Jones; J D Huang; Valerie Mermall; B A Hamilton; Mark S Mooseker; Andrew Escayg; N G Copeland; N A Jenkins; Miriam H Meisler
The mouse neurological mutant flailer expresses a novel hybrid gene derived by exon shuffling between Gnb5 and Myo5a.
Human molecular genetics 2000;9(5):821-8.
1999: Kejian Chen; Leslie K Sprunger; Miriam H Meisler; Hardress J Waller; Donald A Godfrey
Reduced spontaneous activity in the dorsal cochlear nucleus of Scn8a mutant mice.
Brain research 1999;847(1):85-9.
1999: W Lu; C L Phillips; Paul D Killen; T Hlaing; Wilbur R Harrison; Frederick F Elder; Jeffrey H Miner; P A Overbeek; Miriam H Meisler
Insertional mutation of the collagen genes Col4a3 and Col4a4 in a mouse model of Alport syndrome.
Genomics 1999;61(2):113-24.
1999: Sulayman D Dib-Hajj; Lynda Tyrrell; Andrew Escayg; Patrick M Wood; Miriam H Meisler; Stephen G Waxman
Coding sequence, genomic organization, and conserved chromosomal localization of the mouse gene Scn11a encoding the sodium channel NaN.
Genomics 1999;59(3):309-18.
1999: AJ Griffith; W Ji; Mark E Prince; Richard A Altschuler; Miriam H Meisler
Optic, olfactory, and vestibular dysmorphogenesis in the homozygous mouse insertional mutant Tg9257.
Journal of craniofacial genetics and developmental biology 1999;19(3):157-63.
1999: Nicholas W Plummer; Miriam H Meisler
Evolution and diversity of mammalian sodium channel genes.
Genomics 1999;57(2):323-31.
1999: W Ji; Bruce Herron; J M Jones; N A Jenkins; D J Gilbert; N G Copeland; R Swank; Lorraine Flaherty; Miriam H Meisler
Identification of genes within the Krd deletion on mouse chromosome 19.
Mammalian genome : official journal of the International Mammalian Genome Society 1999;10(4):399-401.
1999: Leslie K Sprunger; Andrew Escayg; Sara J Tallaksen-Greene; Roger L Albin; Miriam H Meisler
Dystonia associated with mutation of the neuronal sodium channel Scn8a and identification of the modifier locus Scnm1 on mouse chromosome 3.
Human molecular genetics 1999;8(3):471-9.
1999: W Jang; A Hua; Sandra V Spilson; Webb Miller; Bruce A Roe; Miriam H Meisler
Comparative sequence of human and mouse BAC clones from the mnd2 region of chromosome 2p13.
Genome research 1999;9(1):53-61.
1998: Nicholas W Plummer; J Galt; Julie M Jones; Daniel L Burgess; Leslie K Sprunger; David C Kohrman; Miriam H Meisler
Exon organization, coding sequence, physical mapping, and polymorphic intragenic markers for the human neuronal sodium channel gene SCN8A.
Genomics 1998;54(2):287-96.
1998: JS Weber; W Jang; K Simin; W Lu; J Yu; Miriam H Meisler
High-resolution genetic, physical, and transcript map of the mnd2 region of mouse chromosome 6.
Genomics 1998;54(1):107-15.
1998: H Nomura; A E Turco; Y Pei; Luba Kalaydjieva; Tina Schiavello; Stanislawa Weremowicz; W Ji; Cynthia C Morton; Miriam H Meisler; S T Reeders; Jing Zhou
Identification of PKDL, a novel polycystic kidney disease 2-like gene whose murine homologue is deleted in mice with kidney and retinal defects.
The Journal of biological chemistry 1998;273(40):25967-73.
1998: M R Smith; RD Smith; Nicholas W Plummer; Miriam H Meisler; Alan L Goldin
Functional analysis of the mouse Scn8a sodium channel.
The Journal of neuroscience : the official journal of the Society for Neuroscience 1998;18(16):6093-102.
1998: K D García; Leslie K Sprunger; Miriam H Meisler; Kurt G Beam
The sodium channel Scn8a is the major contributor to the postnatal developmental increase of sodium current density in spinal motoneurons.
The Journal of neuroscience : the official journal of the Society for Neuroscience 1998;18(14):5234-9.
1998: Andrew Escayg; Julie M Jones; Jennifer A Kearney; Peter F Hitchcock; Miriam H Meisler
Calcium channel beta 4 (CACNB4): human ortholog of the mouse epilepsy gene lethargic.
Genomics 1998;50(1):14-22.
1998: Miriam H Meisler; AJ Griffith; Matthew L Warman; George E Tiller; Leslie K Sprunger
Gene symbol: COL11A1. Disease: Marshall syndrome.
Human genetics 1998;102(4):498.
1998: AJ Griffith; Leslie K Sprunger; DA Sirko-Osadsa; George E Tiller; Miriam H Meisler; Matthew L Warman
Marshall syndrome associated with a splicing defect at the COL11A1 locus.
American journal of human genetics 1998;62(4):816-23.
1998: J M Jones; Elizabeth Bentley; Miriam H Meisler; Susan M Darling
Genetic mapping of the voltage-gated shaker potassium channel beta subunit Kcnab1 to mouse chromosome 3.
Mammalian genome : official journal of the International Mammalian Genome Society 1998;9(3):260.
1997: Miriam H Meisler; Leslie K Sprunger; Nicholas W Plummer; Andrew Escayg; Julie M Jones
Ion channel mutations in mouse models of inherited neurological disease.
Annals of medicine 1997;29(6):569-74.
1997: Indira M Raman; Leslie K Sprunger; Miriam H Meisler; Bruce P Bean
Altered subthreshold sodium currents and disrupted firing patterns in Purkinje neurons of Scn8a mutant mice.
Neuron 1997;19(4):881-91.
1997: Nicholas W Plummer; M W McBurney; Miriam H Meisler
Alternative splicing of the sodium channel SCN8A predicts a truncated two-domain protein in fetal brain and non-neuronal cells.
The Journal of biological chemistry 1997;272(38):24008-15.
1997: Miriam H Meisler
Mutation watch: PEX PLUS? Gene(s) for X-linked hypophosphatemia and deafness.
Mammalian genome : official journal of the International Mammalian Genome Society 1997;8(8):543-4.
1997: Sally A Camper; Miriam H Meisler
Meeting report: 10th International Mouse Genome Conference.
Mammalian genome : official journal of the International Mammalian Genome Society 1997;8(7):461-3.
1997: P Urbánek; I Fetka; Miriam H Meisler; Meinrad Busslinger
Cooperation of Pax2 and Pax5 in midbrain and cerebellum development.
Proceedings of the National Academy of Sciences of the United States of America 1997;94(11):5703-8.
1997: Miriam H Meisler
Mutation watch.
Mammalian genome : official journal of the International Mammalian Genome Society 1997;8(5):305-6.
1997: W Jang; JS Weber; E B Harkins; Miriam H Meisler
Localization of the rhotekin gene RTKN on the physical maps of mouse chromosome 6 and human chromosome 2p13 and exclusion as a candidate for mnd2 and LGMD2B.
Genomics 1997;40(3):506-7.
1997: W Jang; JS Weber; Mariko Tokito; Erika L F Holzbaur; Miriam H Meisler
Mouse p150Glued (dynactin 1) cDNA sequence and evaluation as a candidate for the neuromuscular disease mutation mnd2.
Biochemical and biophysical research communications 1997;231(2):344-7.
1997: Daniel L Burgess; Julie M Jones; Miriam H Meisler; Jeffrey L Noebels
Mutation of the Ca2+ channel beta subunit gene Cchb4 is associated with ataxia and seizures in the lethargic (lh) mouse.
Cell 1997;88(3):385-92.
1997: Miriam H Meisler
Mutation watch: mouse brachyury (T), the T-box gene family, and human disease.
Mammalian genome : official journal of the International Mammalian Genome Society 1997;8(11):799-800.
1996: M A Scarpetta; Michael D Uhler; Miriam H Meisler
The mouse Prkacn2 gene encoding protein kinase A inhibitor 2 is located on proximal chromosome 10.
Mammalian genome : official journal of the International Mammalian Genome Society 1996;7(12):921-2.
1996: David C Kohrman; M R Smith; A L Goldin; J Harris; Miriam H Meisler
A missense mutation in the sodium channel Scn8a is responsible for cerebellar ataxia in the mouse mutant jolting.
The Journal of neuroscience : the official journal of the Society for Neuroscience 1996;16(19):5993-9.
1996: Miriam H Meisler
The role of the laboratory mouse in the human genome project.
American journal of human genetics 1996;59(4):764-71.
1996: W Jang; J S Weber; R Bashir; K Bushby; Miriam H Meisler
Aup1, a novel gene on mouse chromosome 6 and human chromosome 2p13.
Genomics 1996;36(2):366-8.
1996: Julie M Jones; Barbara Ranscht; Erik O Berglund; S Gruenheid; P Gros; Miriam H Meisler
Close linkage of three neuronal genes on distal mouse chromosome 15.
Mammalian genome : official journal of the International Mammalian Genome Society 1996;7(9):696-7.
1996: Daniel L Burgess; Jill A Rafael-Fortney; Miriam H Meisler; Jeffrey S Chamberlain
Dlgh1, a mouse homolog of the drosophila discs-large gene, is located on chromosome 16.
Mammalian genome : official journal of the International Mammalian Genome Society 1996;7(8):623-4.
1996: David C Kohrman; J B Harris; Miriam H Meisler
Mutation detection in the med and medJ alleles of the sodium channel Scn8a. Unusual splicing due to a minor class AT-AC intron.
The Journal of biological chemistry 1996;271(29):17576-81.
1996: Andrew J Griffith; Daniel L Burgess; David C Kohrman; J Yu; J Blaschak; S Blanton; Michael Boehnke; J T Hecht; J Overhauser; Miriam H Meisler
Localization of the homolog of a mouse craniofacial mutant to human chromosome 18q11 and evaluation of linkage to human CLP and CPO.
Genomics 1996;34(3):299-303.
1996: Andrew J Griffith; G L Radice; Daniel L Burgess; David C Kohrman; Gwenn M Hansen; Monica J Justice; K R Johnson; M T Davisson; Miriam H Meisler
Location of the 9257 and ataxia mutations on mouse chromosome 18.
Mammalian genome : official journal of the International Mammalian Genome Society 1996;7(6):417-9.
1996: Julie M Jones; Miriam H Meisler; Lori L Isom
Scn2b, a voltage-gated sodium channel beta2 gene on mouse chromosome 9.
Genomics 1996;34(2):258-9.
1996: Rumaisa Bashir; Sharon M Keers; T Strachan; R Passos-Bueno; M Zatz; J Weissenbach; D Le Paslier; Miriam H Meisler; K Bushby
Genetic and physical mapping at the limb-girdle muscular dystrophy locus (LGMD2B) on chromosome 2p.
Genomics 1996;33(1):46-52.
1995: K J Abel; Jianfeng Xu; G Y Yin; Robert H Lyons Jr; Miriam H Meisler; Barbara L Weber
Mouse Brca1: localization sequence analysis and identification of evolutionarily conserved domains.
Human molecular genetics 1995;4(12):2265-73.
1995: Daniel L Burgess; David C Kohrman; J Galt; Nicholas W Plummer; Julie M Jones; B Spear; Miriam H Meisler
Mutation of a new sodium channel gene, Scn8a, in the mouse mutant 'motor endplate disease'.
Nature genetics 1995;10(4):461-5.
1995: David C Kohrman; Nicholas W Plummer; T Schuster; Julie M Jones; W Jang; Daniel L Burgess; J Galt; B T Spear; Miriam H Meisler
Insertional mutation of the motor endplate disease (med) locus on mouse chromosome 15.
Genomics 1995;26(2):171-7.
1995: Julie M Jones; Sicco Popma; M Mizuta; S Seino; Miriam H Meisler
Synaptotagmin genes on mouse chromosomes 1, 7, and 10 and human chromosome 19.
Mammalian genome : official journal of the International Mammalian Genome Society 1995;6(3):212-3.
1995: A Patel; J M Rochelle; J M Jones; Janos Sumegi; George R. Uhl; Michael F Seldin; Miriam H Meisler; P Gregor
Mapping of the taurine transporter gene to mouse chromosome 6 and to the short arm of human chromosome 3.
Genomics 1995;25(1):314-7.
1994: Miriam H Meisler; L L Barrow; C M Canessa; B C Rossier
SCNN1, an epithelial cell sodium channel gene in the conserved linkage group on mouse chromosome 6 and human chromosome 12.
Genomics 1994;24(1):185-6.
1994: S A Keller; Julie M Jones; A Boyle; L L Barrow; Paul D Killen; Daniel G Green; N V Kapousta; Peter F Hitchcock; Richard T Swank; Miriam H Meisler
Kidney and retinal defects (Krd), a transgene-induced mutation with a deletion of mouse chromosome 19 that includes the Pax2 locus.
Genomics 1994;23(2):309-20.
1994: Anand Swaroop; TL Yang-Feng; W Liu; L Gieser; L L Barrow; K C Chen; N Agarwal; Miriam H Meisler; David I Smith
Molecular characterization of a novel human gene, SEC13R, related to the yeast secretory pathway gene SEC13, and mapping to a conserved linkage group on human chromosome 3p24-p25 and mouse chromosome 6.
Human molecular genetics 1994;3(8):1281-6.
1994: L L Barrow; K Simin; Julie M Jones; D C Lee; Miriam H Meisler
Conserved linkage of early growth response 4, annexin 4, and transforming growth factor alpha on mouse chromosome 6.
Genomics 1994;19(2):388-90.
1994: J B Prins; Miriam H Meisler; Michael F Seldin
Mouse chromosome 3.
Mammalian genome : official journal of the International Mammalian Genome Society 1994;5 Spec No():S40-50.
1994: C N Ting; David C Kohrman; Daniel L Burgess; A Boyle; Richard A Altschuler; G Gholizadeh; Linda C Samuelson; W Jang; Miriam H Meisler
Insertional mutation on mouse chromosome 18 with vestibular and craniofacial abnormalities.
Genetics 1994;136(1):247-54.
1993: Julie M Jones; James T Elder; K Simin; S A Keller; Miriam H Meisler
Insertional mutation of the hairless locus on mouse chromosome 14.
Mammalian genome : official journal of the International Mammalian Genome Society 1993;4(11):639-43.
1993: C N Ting; Daniel L Burgess; Jeffrey S Chamberlain; T P Keith; K Falls; Miriam H Meisler
Phosphoenolpyruvate carboxykinase (GTP): characterization of the human PCK1 gene and localization distal to MODY on chromosome 20.
Genomics 1993;16(3):698-706.
1993: Julie M Jones; Roger L Albin; Eva L Feldman; K Simin; T G Schuster; Wesley A Dunnick; John T Collins; C E Chrisp; B A Taylor; Miriam H Meisler
mnd2: a new mouse model of inherited motor neuron disease.
Genomics 1993;16(3):669-77.
1993: P A Bain; Miriam H Meisler; B A Taylor; Anita H Payne
The genes encoding gonadal and nongonadal forms of 3 beta-hydroxysteroid dehydrogenase/delta 5-delta 4 isomerase are closely linked on mouse chromosome 3.
Genomics 1993;16(1):219-23.
1993: T M Johnson; M P Rosenberg; Miriam H Meisler
An insulin-responsive element in the pancreatic enhancer of the amylase gene.
The Journal of biological chemistry 1993;268(1):464-8.
1993: H Yu; R Thun; Settara C Chandrasekharappa; Jeffrey M. Trent; J Zhang; Miriam H Meisler
Human PCK1 encoding phosphoenolpyruvate carboxykinase is located on chromosome 20q13.2.
Genomics 1993;15(1):219-21.
1993: L L Barrow; K Simin; Karen L Mohlke; W C Nichols; David Ginsburg; Miriam H Meisler
Conserved linkage of neurotrophin-3 and von Willebrand factor on mouse chromosome 6.
Mammalian genome : official journal of the International Mammalian Genome Society 1993;4(6):343-5.
1993: Michael F Seldin; Johannes B Prins; NR Rodrigues; John A Todd; Miriam H Meisler
Encyclopedia of the mouse genome III. October 1993. Mouse chromosome 3.
Mammalian genome : official journal of the International Mammalian Genome Society 1993;4 Spec No():S47-57.
1993: Irina N Bespalova; Q Farjo; Douglas P Mortlock; A U Jackson; Miriam H Meisler; Anand Swaroop; Margit Burmeister
Mapping of the neural retina leucine zipper gene, Nrl, to mouse chromosome 14.
Mammalian genome : official journal of the International Mammalian Genome Society 1993;4(10):618-20.
1993: Miriam H Meisler; C N Ting
The remarkable evolutionary history of the human amylase genes.
Critical reviews in oral biology and medicine : an official publication of the American Association of Oral Biologists 1993;4(3-4):503-9.
1992: Miriam H Meisler
Insertional mutation of 'classical' and novel genes in transgenic mice.
Trends in genetics : TIG 1992;8(10):341-4.
1992: Julie M Jones; Miriam H Meisler; Michael F Seldin; B K Lee; E M Eicher
Localization of insulin-2 (Ins-2) and the obesity mutant tubby (tub) to distinct regions of mouse chromosome 7.
Genomics 1992;14(1):197-9.
1992: C N Ting; M P Rosenberg; C M Snow; Linda C Samuelson; Miriam H Meisler
Endogenous retroviral sequences are required for tissue-specific expression of a human salivary amylase gene.
Genes & development 1992;6(8):1457-65.
1992: Roland M Schmid; Miriam H Meisler
Dietary regulation of pancreatic amylase in transgenic mice mediated by a 126-base pair DNA fragment.
The American journal of physiology 1992;262(6 Pt 1):G971-6.
1992: Miriam H Meisler; J A Todd; N Rodrigues; E K Wakeland; Michael F Seldin
Mouse chromosome 3.
Mammalian genome : official journal of the International Mammalian Genome Society 1992;3 Spec No():S44-54.
1991: Linda C Samuelson; K Wiebauer; G Howard; Roland M Schmid; D Koeplin; Miriam H Meisler
Isolation of the murine ribonuclease gene Rib-1: structure and tissue specific expression in pancreas and parotid gland.
Nucleic acids research 1991;19(24):6935-41.
1991: K J Wu; Linda C Samuelson; G Howard; Miriam H Meisler; Gretchen Darlington
Transactivation of pancreas-specific gene sequences in somatic cell hybrids.
Molecular and cellular biology 1991;11(9):4423-30.
1991: J D Ceci; R M Kovatch; D A Swing; Julie M Jones; C M Snow; M P Rosenberg; Nancy A Jenkins; Neal G Copeland; Miriam H Meisler
Transgenic mice carrying a murine amylase 2.2/SV40 T antigen fusion gene develop pancreatic acinar cell and stomach carcinomas.
Oncogene 1991;6(2):323-32.
1991: Miriam H Meisler; Michael F Seldin
Mouse chromosome 3.
Mammalian genome : official journal of the International Mammalian Genome Society 1991;1 Spec No():S42-50.
1990: S A Keller; Susanne Liptay; Amiya K Hajra; Miriam H Meisler
Transgene-induced mutation of the murine steel locus.
Proceedings of the National Academy of Sciences of the United States of America 1990;87(24):10019-22.
1990: S A Keller; M P Rosenberg; T M Johnson; G Howard; Miriam H Meisler
Regulation of amylase gene expression in diabetic mice is mediated by a cis-acting upstream element close to the pancreas-specific enhancer.
Genes & development 1990;4(8):1316-21.
1990: T M Johnson; Miriam H Meisler; M I Bennett; G R Willsky
Vanadate induction of pancreatic amylase mRNA in diabetic rats.
Diabetes 1990;39(6):757-9.
1990: Linda C Samuelson; K Wiebauer; C M Snow; Miriam H Meisler
Retroviral and pseudogene insertion sites reveal the lineage of human salivary and pancreatic amylase genes from a single gene during primate evolution.
Molecular and cellular biology 1990;10(6):2513-20.
1990: N C Dracopoli; Miriam H Meisler
Mapping the human amylase gene cluster on the proximal short arm of chromosome 1 using a highly informative (CA)n repeat.
Genomics 1990;7(1):97-102.
1989: P C Groot; Willem H Mager; R R Frants; Miriam H Meisler; Linda C Samuelson
The human amylase-encoding genes amy2 and amy3 are identical to AMY2A and AMY2B.
Gene 1989;85(2):567-8.
1989: G Howard; P R Keller; T M Johnson; Miriam H Meisler
Binding of a pancreatic nuclear protein is correlated with amylase enhancer activity.
Nucleic acids research 1989;17(20):8185-95.
1989: Julie M Jones; S A Keller; Linda C Samuelson; L Osborn; M P Rosenberg; Miriam H Meisler
A salivary amylase transgene is efficiently expressed in liver but not in parotid gland of transgenic mice.
Nucleic acids research 1989;17(16):6613-23.
1989: Miriam H Meisler; G Howard
Effects of insulin on gene transcription.
Annual review of physiology 1989;51():701-14.
1988: L Osborn; M P Rosenberg; S A Keller; C N Ting; Miriam H Meisler
Insulin response of a hybrid amylase/CAT gene in transgenic mice.
The Journal of biological chemistry 1988;263(32):16519-22.
1988: Linda C Samuelson; K Wiebauer; Deborah L Gumucio; Miriam H Meisler
Expression of the human amylase genes: recent origin of a salivary amylase promoter from an actin pseudogene.
Nucleic acids research 1988;16(17):8261-76.
1988: Linda C Samuelson; P R Keller; G J Darlington; Miriam H Meisler
Glucocorticoid and developmental regulation of amylase mRNAs in mouse liver cells.
Molecular and cellular biology 1988;8(9):3857-63.
1988: Deborah L Gumucio; K Wiebauer; R M Caldwell; Linda C Samuelson; Miriam H Meisler
Concerted evolution of human amylase genes.
Molecular and cellular biology 1988;8(3):1197-205.
1987: John Stalvey; Miriam H Meisler; A H Payne
Evidence that the same structural gene encodes testicular and adrenal 3 beta-hydroxysteroid dehydrogenase-isomerase.
Biochemical genetics 1987;25(1-2):181-90.
1987: Miriam H Meisler; J E Spence; J E Dixon; R M Caldwell; C D Minth; Arthur L Beaudet
Exclusion of close linkage between the loci for cystic fibrosis and neuropeptide Y on human chromosome 7.
Cytogenetics and cell genetics 1987;44(2-3):175-6.
1987: T B Shows; P J McAlpine; C Boucheix; Francis S Collins; P M Conneally; J Frézal; H Gershowitz; P N Goodfellow; J G Hall; P Issitt; C A Jones; B B Knowles; M Lewis; Victor A McKusick; Miriam H Meisler; N E Morton; P Rubenstein; Moses Schanfield; R D Schmickel; M H Skolnick; M A Spence; G R Sutherland; M Traver; N Van Cong; H F Willard
Guidelines for human gene nomenclature. An international system for human gene nomenclature (ISGN, 1987).
Cytogenetics and cell genetics 1987;46(1-4):11-28.
1987: L Osborn; M P Rosenberg; S A Keller; Miriam H Meisler
Tissue-specific and insulin-dependent expression of a pancreatic amylase gene in transgenic mice.
Molecular and cellular biology 1987;7(1):326-34.
1986: Miriam H Meisler; T K Antonucci; L O Treisman; Deborah L Gumucio; Linda C Samuelson
Interstrain variation in amylase gene copy number and mRNA abundance in three mouse tissues.
Genetics 1986;113(3):713-22.
1986: G J Darlington; C C Tsai; Linda C Samuelson; Deborah L Gumucio; Miriam H Meisler
Simultaneous expression of salivary and pancreatic amylase genes in cultured mouse hepatoma cells.
Molecular and cellular biology 1986;6(4):969-75.
1986: T Takeuchi; Deborah L Gumucio; T Yamada; Miriam H Meisler; C D Minth; J E Dixon; R E Eddy; T B Shows
Genes encoding pancreatic polypeptide and neuropeptide Y are on human chromosomes 17 and 7.
The Journal of clinical investigation 1986;77(3):1038-41.
1986: R W Elliott; Linda C Samuelson; M S Lambert; Miriam H Meisler
Assignment of pancreatic ribonuclease gene to mouse chromosome 14.
Cytogenetics and cell genetics 1986;42(1-2):110-2.
1985: Deborah L Gumucio; K Wiebauer; A Dranginis; Linda C Samuelson; L O Treisman; R M Caldwell; T K Antonucci; Miriam H Meisler
Evolution of the amylase multigene family. YBR/Ki mice express a pancreatic amylase gene which is silent in other strains.
The Journal of biological chemistry 1985;260(25):13483-9.
1985: K Wiebauer; Deborah L Gumucio; J M Jones; R M Caldwell; H T Hartle; Miriam H Meisler
A 78-kilobase region of mouse chromosome 3 contains salivary and pancreatic amylase genes and a pseudogene.
Proceedings of the National Academy of Sciences of the United States of America 1985;82(16):5446-9.
1984: M Tosi; R Bovey; S Astolfi; S Bodary; Miriam H Meisler; P K Wellauer
Multiple non-allelic genes encoding pancreatic alpha-amylase of mouse are expressed in a strain-specific fashion.
The EMBO journal 1984;3(12):2809-16.
1984: A Dranginis; M Morley; M Nesbitt; B B Rosenblum; Miriam H Meisler
Independent regulation of nonallelic pancreatic amylase genes in diabetic mice.
The Journal of biological chemistry 1984;259(19):12216-9.
1984: T K Antonucci; O H Von Deimling; B B Rosenblum; L C Skow; Miriam H Meisler
Conserved linkage within a 4-cM region of mouse chromosome 9 and human chromosome 11.
Genetics 1984;107(3):463-75.
1984: Miriam H Meisler; L Wanner; J Strahler
Pigmentation and lysosomal phenotypes in mice doubly homozygous for both light-ear and pale-ear mutant alleles.
The Journal of heredity 1984;75(2):103-6.
1983: Miriam H Meisler; J Strahler; K Wiebauer; K K Thomsen
Multiple genes encode mouse pancreatic amylases.
Isozymes 1983;7():39-57.
1982: T K Antonucci; V C Chapman; Miriam H Meisler
Linkage of the structural gene for uroporphyrinogen I synthase to markers on mouse chromosome 9 in a cross between feral and inbred mice.
Biochemical genetics 1982;20(7-8):703-10.
1982: J R Strahler; Miriam H Meisler
Two distinct pancreatic amylase genes are active in YBR mice.
Genetics 1982;101(1):91-102.
1982: L A Wanner; J V Neel; Miriam H Meisler
Separation of allelic variants by two-dimensional electrophoresis.
American journal of human genetics 1982;34(2):209-15.
1981: R H McCluer; M A Williams; S K Gross; Miriam H Meisler
Testosterone effects on the induction and urinary excretion of mouse kidney glycosphingolipids associated with lysosomes.
The Journal of biological chemistry 1981;256(24):13112-20.
1981: J H Bloor; Miriam H Meisler; J T Nielsen
Genetic determination of amylase synthesis in the mouse.
The Journal of biological chemistry 1981;256(1):373-7.
1981: Miriam H Meisler; L Wanner; F T Kao; C Jones
Localization of the uroporphyrinogen I synthase locus to human chromosome region 11q13 leads to qter and interconversion of enzyme isomers.
Cytogenetics and cell genetics 1981;31(2):l24-8.
1980: Miriam H Meisler; J Levy; F Sansone; M Gordon
Morphologic and biochemical abnormalities of kidney lysosomes in mice with an inherited albinism.
The American journal of pathology 1980;101(3):581-93.
1980: J H Bloor; Miriam H Meisler
Additional evidence for the close linkage of amy-1 and amy-2 in the mouse.
The Journal of heredity 1980;71(6):449-51.
1980: J V Neel; Harvey W Mohrenweiser; Miriam H Meisler
Rate of spontaneous mutation at human loci encoding protein structure.
Proceedings of the National Academy of Sciences of the United States of America 1980;77(10):6037-41.
1980: Miriam H Meisler; L Wanner; R E Eddy; T B Shows
The UPS locus encoding uroporphyrinogen I synthase is located on human chromosome 11.
Biochemical and biophysical research communications 1980;95(1):170-6.
1980: Miriam H Meisler; M L Carter
Rare structural variants of human and murine uroporphyrinogen I synthase.
Proceedings of the National Academy of Sciences of the United States of America 1980;77(5):2848-52.
1980: E K Novak; Richard T Swank; Miriam H Meisler
Pigmentation and lysosome function in mice homozygous for both pale ear and beige-J pigment genes.
Genetical research 1980;35(2):195-204.
1980: T B Shows; C A Alper; D Bootsma; M Dorf; T Douglas; T Huisman; S Kit; H P Klinger; C Kozak; P A Lalley; D Lindsley; P J McAlpine; J K McDougall; P Meera Khan; Miriam H Meisler; N E Morton; J M Opitz; C W Partridge; R Payne; T H Roderick; P Rubinstein; F H Ruddle; M Shaw; J W Spranger; K Weiss
International System for Human Gene Nomenclature (1979) ISGN (1979).
Birth defects original article series 1980;15(11):96-116.
1979: Miriam H Meisler; C Reinke
A sensitive fluorescent assay for N-acetyltransferase activity in human lymphocytes from newborns and adults.
Clinica chimica acta; international journal of clinical chemistry 1979;96(1-2):91-6.
1979: Miriam H Meisler; C Orlowski; E Gross; J H Bloor
Cadmium metabolism in cdm/cdm mice.
Biochemical genetics 1979;17(7-8):731-6.
1979: J P Hjorth; Miriam H Meisler; J T Nielsen
Genetic variation in amount of salivary amylase in the bank vole, Clethrionomys glareola.
Genetics 1979;92(3):915-30.
1979: T B Shows; L R Scrafford-Wolff; J A Brown; Miriam H Meisler
GM1-gangliosidosis: chromosome 3 assignment of the beta-galactosidase-A gene (beta GALA).
Somatic cell genetics 1979;5(2):147-58.
1979: T B Shows; C A Alper; D Bootsma; M Dorf; T Douglas; T Huisman; S Kit; H P Klinger; C Kozak; P A Lalley; D Lindsley; P J McAlpine; J K McDougall; P Meera Khan; Miriam H Meisler; N E Morton; J M Opitz; C W Partridge; R Payne; T H Roderick; P Rubinstein; F H Ruddle; M Shaw; J W Spranger; K Weiss
International system for human gene nomenclature (1979) ISGN (1979).
Cytogenetics and cell genetics 1979;25(1-4):96-116.
1978: Miriam H Meisler
Synthesis and secretion of kidney beta-galactosidase in mutant le/le mice.
The Journal of biological chemistry 1978;253(9):3129-34.
1978: T B Shows; L Scrafford-Wolff; J A Brown; Miriam H Meisler
Assignment of a beta-galactosidase gene (beta GALA) to chromosome 3 in man.
Cytogenetics and cell genetics 1978;22(1-6):219-22.
1976: K Paigen; Miriam H Meisler; J Felton; Verne M Chapman
Genetic determination of the beta-galactosidase developmental program in mouse liver.
Cell 1976;9(4 Pt 1):533-9.
1976: Miriam H Meisler
Effects of the Bgs locus on mouse beta-galactosidase.
Biochemical genetics 1976;14(11-12):921-32.
1975: Miriam H Meisler
Inhibition of human liver beta-galactosidases and beta-glucosidase by n-bromoacetyl-beta-D-galactosylamine.
Biochimica et biophysica acta 1975;410(2):347-53.
1975: S Tomino; Miriam H Meisler
Biochemical and immunological studies of purified mouse beta-galactosidase.
The Journal of biological chemistry 1975;250(19):7752-8.
1975: H Tanaka; Miriam H Meisler; Kunihiko Suzuki
Activity of human hepatic beta-galactosidase toward natural glycosphingolipid substrates.
Biochimica et biophysica acta 1975;398(3):452-63.
1974: Miriam H Meisler; M C Rattazzi
Immunological studies of beta galactosidase in normal human liver and in GM1 gangliosidosis.
American journal of human genetics 1974;26(6):683-91.
1974: J Felton; Miriam H Meisler; K Paigen
A locus determining beta-galactosidase activity in the mouse.
The Journal of biological chemistry 1974;249(10):3267-72.
1972: Miriam H Meisler; K Paigen
Coordinated development of -glucuronidase and -galactosidase in mouse organs.
Science (New York, N.Y.) 1972;177(4052):894-6.
1969: Miriam H Meisler; T A Langan
Characterization of a phosphatase specific for phosphorylated histones and protamine.
The Journal of biological chemistry 1969;244(18):4961-8.
1966: Miriam H Meisler; R H McCluer
Nucleohistone dissociation by ganglioside micelles.
Science (New York, N.Y.) 1966;154(3751):896-7.
1966: R J Penick; Miriam H Meisler; R H McCluer
Thin-layer chromatographic studies of human brain gangliosides.
Biochimica et biophysica acta 1966;116(2):279-87.