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Brian Schutte

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Elizabeth J Leslie; Sherri Bale; John Compton; Brian C Schutte; Jennifer Standley; Jeffrey C Murray
Comparative analysis of IRF6 variants in families with Van der Woude syndrome and popliteal pterygium syndrome using public whole-exome databases.
Gabriel de la Garza; Martine Dunnwald; Cindy F Fukazawa; Douglas W Houston; Youssef A Kousa; J Robert Manak; Anuj Mankad; Tamer A Mansour; Jack Robert Schleiffarth; Brian C Schutte; Daniel S Wagner; Jason L Weirather; Gregory Bonde; Stephen Butcher; Robert A Cornell
Interferon regulatory factor 6 promotes differentiation of the periderm by activating expression of Grainyhead-like 3.
James Blackburn; Michael J Dixon; Nigel L Hammond; Kenya Honda; Yinling Hu; Katsushige Kawasaki; Maiko Kawasaki; Akira Kinoshita; Bigang Liu; Atsushi Ohazama; Yoko Otsuka-Tanaka; Ryan B Rountree; Ruth Schmidt-Ullrich; Brian C Schutte; Walter Birchmeier; Paul T Sharpe
The role of Irf6 in tooth epithelial invagination.

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2013: Elizabeth J Leslie; Sherri Bale; John Compton; Brian C Schutte; Jennifer Standley; Jeffrey C Murray
Comparative analysis of IRF6 variants in families with Van der Woude syndrome and popliteal pterygium syndrome using public whole-exome databases.
Genetics in medicine : official journal of the American College of Medical Genetics 2013;15(5):338-44.
2013: Gabriel de la Garza; Martine Dunnwald; Cindy F Fukazawa; Douglas W Houston; Youssef A Kousa; J Robert Manak; Anuj Mankad; Tamer A Mansour; Jack Robert Schleiffarth; Brian C Schutte; Daniel S Wagner; Jason L Weirather; Gregory Bonde; Stephen Butcher; Robert A Cornell
Interferon regulatory factor 6 promotes differentiation of the periderm by activating expression of Grainyhead-like 3.
The Journal of investigative dermatology 2013;133(1):68-77.
2012: James Blackburn; Michael J Dixon; Nigel L Hammond; Kenya Honda; Yinling Hu; Katsushige Kawasaki; Maiko Kawasaki; Akira Kinoshita; Bigang Liu; Atsushi Ohazama; Yoko Otsuka-Tanaka; Ryan B Rountree; Ruth Schmidt-Ullrich; Brian C Schutte; Walter Birchmeier; Paul T Sharpe
The role of Irf6 in tooth epithelial invagination.
Developmental biology 2012;365(1):61-70.
2012: Neli P Ragina; Karianne Schlosser; Brian C Schutte; Patricia K Senagore; Pamela J Swiatek; Eun Ah Chang; Walid D Fakhouri; Matti Kiupel; Jason Glenn Knott; Jose B Cibelli
Downregulation of H19 improves the differentiation potential of mouse parthenogenetic embryonic stem cells.
Stem cells and development 2012;21(7):1134-44.
2012: Walid D Fakhouri; David Fitzpatrick; Harris Morrison; Lindsey Rhea; Tianli Du; Martine Dunnwald; Eileen Sweezer; Baoli Yang; Brian C Schutte
MCS9.7 enhancer activity is highly, but not completely, associated with expression of Irf6 and p63.
Developmental dynamics : an official publication of the American Association of Anatomists 2012;241(2):340-9.
2012: Karen Mitchell; Jeffrey C Murray; James O'Sullivan; Rose Richardson; Rose-Anne Romano; Brian C Schutte; Alan L Shanske; Satrajit Sinha; Beverley Anderson; Dario Antonini; Sanjeev S Bhaskar; Graeme C M Black; Ed Blair; Jill Dixon; Caterina Missero; Michael J Dixon
Exome sequence identifies RIPK4 as the Bartsocas-Papas syndrome locus.
American journal of human genetics 2012;90(1):69-75.
2012: Mark Le; Jasmine Morrison; Rachelle Naridze; Lindsey Rhea; Brian C Schutte; Leah C Biggs; Vesa Kaartinen; Martine Dunnwald
Transforming growth factor Beta 3 is required for excisional wound repair in vivo.
PloS one 2012;7(10):e48040.
2012: Ariadne Letra; Andrew C Lidral; Mary L Marazita; Toby G McHenry; Renato Menezes; Lina Moreno; Jeffrey C Murray; Iêda M Orioli; Joanne L Prasad; Brian C Schutte; Eduardo E Castilla; Sandra Daack-Hirsch; Walid Fakhouri; Renata F Fonseca; Jose M Granjeiro; Inga Kempa; Baiba Lace; Alexandre R Vieira
Interaction between IRF6 and TGFA genes contribute to the risk of nonsyndromic cleft lip/palate.
PloS one 2012;7(9):e45441.
2012: Leah C Biggs; Brian C Schutte; Lindsey Rhea; Martine Dunnwald
Interferon regulatory factor 6 is necessary, but not sufficient, for keratinocyte differentiation.
The Journal of investigative dermatology 2012;132(1):50-8.
2011: Walter H A Kahr; Ling Li; Noeleen B Loughran; Jack Moseley; Brie Nixon; John Parkinson; Fred G Pluthero; Jesse W Rowley; Gi-Yung Ryu; Brian C Schutte; Hansjörg Schwertz; Mike Storck; Denisa Urban; Kai Wang; Andrew S Weyrich; Shay Fabbro; Rick Gadzinski; Jesse Hinckley; Shawn M Jobe; Hilary Christensen; Jorge Di Paola
Mutations in NBEAL2, encoding a BEACH protein, cause gray platelet syndrome.
Nature genetics 2011;43(8):738-40.
2011: Nicholas K Rorick; Akira Kinoshita; Jason L Weirather; Myriam Peyrard-Janvid; Renata L L Ferreira de Lima; Martine Dunnwald; Alan L Shanske; Danilo Moretti-Ferreira; Hannele Koillinen; Juha Kere; Maria A Mansilla; Jeffrey C Murray; Steve L Goudy; Brian C Schutte
Genomic strategy identifies a missense mutation in WD-repeat domain 65 (WDR65) in an individual with Van der Woude syndrome.
American journal of medical genetics. Part A 2011;155A(6):1314-21.
2011: Shay Fabbro; Walter H A Kahr; Jesse Hinckley; Kai Wang; Jack Moseley; Gi-Yung Ryu; Brie Nixon; James G White; Thomas Bair; Brian C Schutte; Jorge Di Paola
Homozygosity mapping with SNP arrays confirms 3p21 as a recessive locus for gray platelet syndrome and narrows the interval significantly.
Blood 2011;117(12):3430-4.
2010: Jodi L P Jones; John W Canady; James T Brookes; George L Wehby; Jamie L'Heureux; Brian C Schutte; Jeffrey C Murray; Martine Dunnwald
Wound complications after cleft repair in children with Van der Woude syndrome.
The Journal of craniofacial surgery 2010;21(5):1350-3.
2009: Caleb Bailey; Naira V Margaryan; Daniel E Abbott; Brian C Schutte; Baoli Yang; Zhila Khalkhali-Ellis; Mary J C Hendrix
Temporal and spatial expression patterns for the tumor suppressor Maspin and its binding partner interferon regulatory factor 6 during breast development.
Development, growth & differentiation 2009;51(5):473-81.
2009: Renata L L Ferreira de Lima; Sarah A Hoper; Michella Ghassibe; Margaret E Cooper; Nicholas K Rorick; Shinji Kondo; Lori Katz; Mary L Marazita; John Compton; Sherri Bale; Ute Hehr; Michael J Dixon; Sandra Daack-Hirsch; Odile Boute; Bénédicte Bayet; Nicole Revencu; Christine Verellen-Dumoulin; Miikka Vikkula; Antonio Richieri-Costa; Danilo Moretti-Ferreira; Jeffrey C Murray; Brian C Schutte
Prevalence and nonrandom distribution of exonic mutations in interferon regulatory factor 6 in 307 families with Van der Woude syndrome and 37 families with popliteal pterygium syndrome.
Genetics in medicine : official journal of the American College of Medical Genetics 2009;11(4):241-7.
2009: Hayley J Little; Nicholas K Rorick; Ling-I Su; Clair Baldock; Saimon Malhotra; Tom Jowitt; Lokesh Gakhar; Ramaswamy Subramanian; Brian C Schutte; Michael J Dixon; Paul Shore
Missense mutations that cause Van der Woude syndrome and popliteal pterygium syndrome affect the DNA-binding and transcriptional activation functions of IRF6.
Human molecular genetics 2009;18(3):535-45.
2009: Jaime L Sabel; Claudia d'Alençon; Erin K O'Brien; Eric Van Otterloo; Katie Lutz; Tawny N Cuykendall; Brian C Schutte; Douglas W Houston; Robert A Cornell
Maternal Interferon Regulatory Factor 6 is required for the differentiation of primary superficial epithelia in Danio and Xenopus embryos.
Developmental biology 2009;325(1):249-62.
2008: Fedik Rahimov; Mary L Marazita; Axel Visel; Margaret E Cooper; Michael J Hitchler; Michele Rubini; Frederick E Domann; Manika Govil; Kaare Christensen; Camille Bille; Mads Melbye; Astanand Jugessur; Rolv T Lie; Allen J Wilcox; David R Fitzpatrick; Eric Green; Peter Anthony Mossey; Julian Little; Regine P Steegers-Theunissen; Len A Pennacchio; Brian C Schutte; Jeffrey C Murray
Disruption of an AP-2alpha binding site in an IRF6 enhancer is associated with cleft lip.
Nature genetics 2008;40(11):1341-7.
2008: Kazutoyo Osoegawa; Gery M Vessere; K H Utami; M Adela Mansilla; M K Johnson; Bridget M Riley; J L'Heureux; Rolph Pfundt; Johan Staaf; Walter A Van Der Vliet; Andrew C Lidral; Eric F P M Schoenmakers; Ake Borg; Brian C Schutte; Edward J Lammer; Jeffrey C Murray; P J de Jong
Identification of novel candidate genes associated with cleft lip and palate using array comparative genomic hybridisation.
Journal of medical genetics 2008;45(2):81-6.
2008: B Del Frari; M Amort; A R Janecke; Brian C Schutte; H Piza-Katzer
[Van-der-Woude Syndrome].
Klinische Pädiatrie 2008;220(1):26-8.
2007: Peg Nopoulos; Lynn Richman; Nancy C Andreasen; Jeffrey C Murray; Brian C Schutte
Abnormal brain structure in adults with Van der Woude syndrome.
Clinical genetics 2007;71(6):511-7.
2007: Peg Nopoulos; Lynn Richman; Nancy Andreasen; Jeffrey C Murray; Brian C Schutte
Cognitive dysfunction in adults with Van der Woude syndrome.
Genetics in medicine : official journal of the American College of Medical Genetics 2007;9(4):213-8.
2006: Christopher R Ingraham; Akira Kinoshita; Shinji Kondo; Baoli Yang; Samin Sajan; Kurt J Trout; Margaret I Malik; Martine Dunnwald; Stephen L Goudy; Michael Lovett; Jeffrey C Murray; Brian C Schutte
Abnormal skin, limb and craniofacial morphogenesis in mice deficient for interferon regulatory factor 6 (Irf6).
Nature genetics 2006;38(11):1335-40.
2006: Alexandra S Knight; Brian C Schutte; Rulang Jiang; Michael J Dixon
Developmental expression analysis of the mouse and chick orthologues of IRF6: the gene mutated in Van der Woude syndrome.
Developmental dynamics : an official publication of the American Association of Anatomists 2006;235(5):1441-7.
2005: Caleb Bailey; Zhila Khalkhali-Ellis; Shinji Kondo; Naira V Margaryan; Richard E B Seftor; William W Wheaton; Sumaira Amir; Michael Pins; Brian C Schutte; Mary J C Hendrix
Mammary serine protease inhibitor (Maspin) binds directly to interferon regulatory factor 6: identification of a novel serpin partnership.
The Journal of biological chemistry 2005;280(40):34210-7.
2004: Theresa M Zucchero; Margaret E Cooper; Brion S Maher; Sandra Daack-Hirsch; Buena Nepomuceno; Lucilene Ribeiro; Diana Caprau; Kaare Christensen; Yasushi Suzuki; Junichiro Machida; Nagato Natsume; Koh-ichiro Yoshiura; Alexandre R Vieira; Iêda M Orioli; Eduardo E Castilla; Lina Moreno; Mauricio Arcos-Burgos; Andrew C Lidral; L Leigh Field; You-e Liu; Ajit Ray; Toby Goldstein; Rebecca E Schultz; Min Shi; Marla K Johnson; Shinji Kondo; Brian C Schutte; Mary L Marazita; Jeffrey C Murray
Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate.
The New England journal of medicine 2004;351(8):769-80.
2004: Alan L Shanske; S A Hoper; K Krahn; Brian C Schutte
Mutations in IRF6 do not cause Bartsocas-Papas syndrome in a family with two affected sibs.
American journal of medical genetics. Part A 2004;128A(4):431-3.
2004: J Carter Ralphe; Jeffrey L Segar; Brian C Schutte; Thomas D Scholz
Localization and function of the brain excitatory amino acid transporter type 1 in cardiac mitochondria.
Journal of molecular and cellular cardiology 2004;37(1):33-41.
2004: Jeffrey C Murray; Brian C Schutte
Cleft palate: players, pathways, and pursuits.
The Journal of clinical investigation 2004;113(12):1676-8.
2004: Jorge Di Paola; Todd L Goldman; Qining Qian; Shivanand R Patil; Brian C Schutte; B C Schute
Breakpoint of a balanced translocation (X:14) (q27.1;q32.3) in a girl with severe hemophilia B maps proximal to the factor IX gene.
Journal of thrombosis and haemostasis : JTH 2004;2(3):437-40.
2003: Shuji Kayano; Shigeo Kure; Yoichi Suzuki; Kiyoshi Kanno; Yoko Aoki; Shinji Kondo; Brian C Schutte; Jeffrey C Murray; Atsushi Yamada; Yoichi Matsubara
Novel IRF6 mutations in Japanese patients with Van der Woude syndrome: two missense mutations (R45Q and P396S) and a 17-kb deletion.
Journal of human genetics 2003;48(12):622-8.
2002: Linda W Dickerson; Daniel J Bonthius; Brian C Schutte; Baoli Yang; Thomas J Barna; Melissa C Bailey; Keith Nehrke; Roger A Williamson; Fred Lamb
Altered GABAergic function accompanies hippocampal degeneration in mice lacking ClC-3 voltage-gated chloride channels.
Brain research 2002;958(2):227-50.
2002: Todd E Scheetz; Jennifer A Bartlett; Jesse D Walters; Brian C Schutte; Thomas L Casavant; Paul B McCray
Genomics-based approaches to gene discovery in innate immunity.
Immunological reviews 2002;190():137-45.
2002: Jorge Arreola; Ted Begenisich; Keith Nehrke; Ha-Van Nguyen; Keerang Park; Linda Richardson; Baoli Yang; Brian C Schutte; Fred Lamb; James E Melvin
Secretion and cell volume regulation by salivary acinar cells from mice lacking expression of the Clcn3 Cl- channel gene.
The Journal of physiology 2002;545(Pt 1):207-16.
2002: Shinji Kondo; Brian C Schutte; Rebecca J Richardson; Bryan Bjork; Alexandra S Knight; Yoriko Watanabe; Emma Howard; Renata L L Ferreira de Lima; Sandra Daack-Hirsch; Achim Sander; Donna M McDonald-McGinn; Elaine H Zackai; Edward J Lammer; Arthur S Aylsworth; Holly H Ardinger; Andrew C Lidral; Barbara R Pober; Lina Moreno; Mauricio Arcos-Burgos; Consuelo Valencia; Claude Houdayer; Michel Bahuau; Danilo Moretti-Ferreira; Antonio Richieri-Costa; Michael J Dixon; Jeffrey C Murray
Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes.
Nature genetics 2002;32(2):285-9.
2002: Piranit N Kantaputra; Yupa Sumitsawan; Brian C Schutte; Chintana Tochareontanaphol
Van der Woude syndrome with sensorineural hearing loss, large craniofacial sinuses, dental pulp stones, and minor limb anomalies: report of a four-generation Thai family.
American journal of medical genetics 2002;108(4):275-80.
2002: Brian C Schutte; Joseph P Mitros; Jennifer A Bartlett; Jesse D Walters; Hong Peng Jia; Michael J Welsh; Thomas L Casavant; Paul B McCray
Discovery of five conserved beta -defensin gene clusters using a computational search strategy.
Proceedings of the National Academy of Sciences of the United States of America 2002;99(4):2129-33.
2002: Brian C Schutte; Paul B McCray
[beta]-defensins in lung host defense.
Annual review of physiology 2002;64():709-48.
2001: L G Naimeh; Brian C Schutte; W S Hamilton; Eva Tsalikian
Ontogeny of the H19 gene in sheep and effect of maternal fasting on its expression in the fetus.
Endocrine research 2001;27(4):417-31.
2001: Yoriko Watanabe; Jeffrey C Murray; Bryan Bjork; C P Bird; Pei-Wen Chiang; Simon G Gregory; David M Kurnit; Brian C Schutte
Matroshka and ectopic polymorphisms: Two new classes of DNA sequence variation identified at the Van der Woude syndrome locus on 1q32-q41.
Human mutation 2001;18(5):422-34.
2001: Fred Lamb; R W Graeff; G H Clayton; R L Smith; Brian C Schutte; Paul B McCray
Ontogeny of CLCN3 chloride channel gene expression in human pulmonary epithelium.
American journal of respiratory cell and molecular biology 2001;24(4):376-81.
2001: Hong Peng Jia; Brian C Schutte; A Schudy; R Linzmeier; Janet Guthmiller; Georgia K Johnson; Brian F Tack; J P Mitros; A Rosenthal; Tomas Ganz; Paul B McCray
Discovery of new human beta-defensins using a genomics-based approach.
Gene 2001;263(1-2):211-8.
2001: Brian C Schutte; John D Carpten; Anne Forus; Simon G Gregory; A Horii; Peter White
Report and abstracts of the sixth international workshop on human chromosome 1 mapping 2000. Iowa City, Iowa, USA. 30 September-3 October 2000.
Cytogenetics and cell genetics 2001;92(1-2):23-41.
2000: B E Rupert; Jeffrey L Segar; Brian C Schutte; Thomas D Scholz
Metabolic adaptation of the hypertrophied heart: role of the malate/aspartate and alpha-glycerophosphate shuttles.
Journal of molecular and cellular cardiology 2000;32(12):2287-97.
2000: Hong Peng Jia; S A Wowk; Brian C Schutte; S K Lee; A Vivado; Brian F Tack; Charles L Bevins; Paul B McCray
A novel murine beta -defensin expressed in tongue, esophagus, and trachea.
The Journal of biological chemistry 2000;275(43):33314-20.
2000: Nancy Arbour; Eva Lorenz; Brian C Schutte; Joseph Zabner; Joel N Kline; M Jones; Kathy L Frees; Janet L Watt; David A Schwartz
TLR4 mutations are associated with endotoxin hyporesponsiveness in humans.
Nature genetics 2000;25(2):187-91.
2000: Fred Lamb; Thomas J Barna; C Goud; Ingo Marenholz; Dietmar Mischke; Brian C Schutte
Complex RNA processing of TDRKH, a novel gene encoding the putative RNA-binding tudor and KH domains.
Gene 2000;246(1-2):209-18.
2000: Thomas D Scholz; Cynthia J Teneyck; Brian C Schutte
Thyroid hormone regulation of the NADH shuttles in liver and cardiac mitochondria.
Journal of molecular and cellular cardiology 2000;32(1):1-10.
2000: Brian C Schutte; Bryan Bjork; K B Coppage; M I Malik; Simon G Gregory; D J Scott; L M Brentzell; Yoriko Watanabe; Michael J Dixon; Jeffrey C Murray
A preliminary gene map for the Van der Woude syndrome critical region derived from 900 kb of genomic sequence at 1q32-q41.
Genome research 2000;10(1):81-94.
1999: M H Raymond; Brian C Schutte; James C Torner; Trudy L Burns; Marcia C Willing
Osteocalcin: genetic and physical mapping of the human gene BGLAP and its potential role in postmenopausal osteoporosis.
Genomics 1999;60(2):210-7.
1999: Joel N Kline; J D Cowden; Gary W Hunninghake; Brian C Schutte; Janet L Watt; Christine Wohlford-Lenane; Linda S Powers; M P Jones; David A Schwartz
Variable airway responsiveness to inhaled lipopolysaccharide.
American journal of respiratory and critical care medicine 1999;160(1):297-303.
1999: Thomas L'Ecuyer; Brian C Schutte; K A Mendel; E Morris; A B Fulton
Muscle-specific transcription factors in fibroblasts expressing the alpha-striated tropomyosin 3' untranslated region.
Molecular genetics and metabolism 1999;67(3):213-26.
1999: Brian C Schutte; AM Basart; Yoriko Watanabe; J J Laffin; K Coppage; Bryan Bjork; Sandra Daack-Hirsch; S Patil; Michael J Dixon; Jeffrey C Murray
Microdeletions at chromosome bands 1q32-q41 as a cause of Van der Woude syndrome.
American journal of medical genetics 1999;84(2):145-50.
1999: Fred Lamb; G H Clayton; B X Liu; R L Smith; Thomas J Barna; Brian C Schutte
Expression of CLCN voltage-gated chloride channel genes in human blood vessels.
Journal of molecular and cellular cardiology 1999;31(3):657-66.
1999: Peter White; Anne Forus; Tara C Matise; Brian C Schutte; N Spieker; P Stanier; Jeffery Vance; Simon G Gregory
Report of the fifth international workshop on human chromosome 1 mapping 1999.
Cytogenetics and cell genetics 1999;87(3-4):143-71.
1999: Brian C Schutte; Jeffrey C Murray
The many faces and factors of orofacial clefts.
Human molecular genetics 1999;8(10):1853-9.
1998: Lide Liu; L Wang; Hong Peng Jia; Chengquan Zhao; Hong-Qiang Heng; Brian C Schutte; Paul B McCray; Tomas Ganz
Structure and mapping of the human beta-defensin HBD-2 gene and its expression at sites of inflammation.
Gene 1998;222(2):237-44.
1998: Frederick D Goldman; Zuhair K Ballas; Brian C Schutte; J Kemp; Clay Hollenback; N Noraz; N Taylor
Defective expression of p56lck in an infant with severe combined immunodeficiency.
The Journal of clinical investigation 1998;102(2):421-9.
1998: Thomas D Scholz; SL Koppenhafer; Cynthia J Teneyck; Brian C Schutte
Ontogeny of malate-aspartate shuttle capacity and gene expression in cardiac mitochondria.
The American journal of physiology 1998;274(3 Pt 1):C780-8.
1998: T M H Brennan; Daniel Landau; Hanna Shalev; Fred Lamb; Brian C Schutte; Roxanne Y Walder; Allyn L Mark; Rivka Carmi; Val C Sheffield
Linkage of infantile Bartter syndrome with sensorineural deafness to chromosome 1p.
American journal of human genetics 1998;62(2):355-61.
1998: Debra L Schutte; J Williams; Brian C Schutte; Meridean Maas
Alzheimer's disease genetics. Practice and education implications for special care unit nurses.
Journal of gerontological nursing 1998;24(1):40-8; quiz 63.
1997: Martin J Tymms; Annie Y-N Ng; RS Thomas; Brian C Schutte; J Zhou; H J Eyre; G R Sutherland; Arun Seth; M Rosenberg; TS Papas; C Debouck; Ismail Kola
A novel epithelial-expressed ETS gene, ELF3: human and murine cDNA sequences, murine genomic organization, human mapping to 1q32.2 and expression in tissues and cancer.
Oncogene 1997;15(20):2449-62.
1997: S Peiffer-Schneider; Brian C Schutte; Jeffrey C Murray; Kathy L Frees; K Williamson; NJ Leysens; David A Schwartz
Exclusion of Ifa and Ifb as the Lps gene and mapping of three markers near the Lps locus.
Mammalian genome : official journal of the International Mammalian Genome Society 1997;8(10):785-6.
1997: Thomas D Scholz; SL Koppenhafer; Cynthia J Teneyck; Brian C Schutte
Developmental regulation of the alpha-glycerophosphate shuttle in porcine myocardium.
Journal of molecular and cellular cardiology 1997;29(6):1605-13.
1997: Dianne L Atkins; P A Krumm; Brian C Schutte; J D Harrison; Steven H Green
Regulation of rat cardiac myocyte growth by a neuronal factor secreted by PC12 cells.
Pediatric research 1997;41(6):832-41.
1997: Jeffery Vance; Tara C Matise; R Wooster; Brian C Schutte; G A Bruns; N van Roy; Garrett M Brodeur; Y X Tao; S Gregory; A Weith; M Vaudin; P White
Report and abstracts of the third international workshop on human chromosome 1 mapping 1997.
Cytogenetics and cell genetics 1997;78(3-4):154-82.
1997: Brian C Schutte; K Ranade; Jonathan A Pruessner; Nicholas C Dracopoli
Optimized conditions for cloning PCR products into an XcmI T-vector.
BioTechniques 1997;22(1):40-2, 44.
1996: Brian C Schutte; A Sander; M Malik; Jeffrey C Murray
Refinement of the Van der Woude gene location and construction of a 3.5-Mb YAC contig and STS map spanning the critical region in 1q32-q41.
Genomics 1996;36(3):507-14.
1995: Josée Robillard; W V Page; M S Mathews; Brian C Schutte; Anne Monique Nuyt; Jeffrey L Segar
Differential gene expression and regulation of renal angiotensin II receptor subtypes (AT1 and AT2) during fetal life in sheep.
Pediatric research 1995;38(6):896-904.
1994: Josée Robillard; Brian C Schutte; W V Page; J A Fedderson; C C Porter; Jeffrey L Segar
Ontogenic changes and regulation of renal angiotensin II type 1 receptor gene expression during fetal and newborn life.
Pediatric research 1994;36(6):755-62.
1994: B Weiffenbach; J Dubois; S Manning; N S Ma; Brian C Schutte; Sara T Winokur; M R Altherr; S J Jacobsen; V P Stanton; K Yokoyama
YAC contigs for 4q35 in the region of the facioscapulohumeral muscular dystrophy (FSHD) gene.
Genomics 1994;19(3):532-41.
1993: Sara T Winokur; Brian C Schutte; B Weiffenbach; S S Washington; D McElligott; Aravinda Chakravarti; J H Wasmuth; M R Altherr
A radiation hybrid map of 15 loci on the distal long arm of chromosome 4, the region containing the gene responsible for facioscapulohumeral muscular dystrophy (FSHD).
American journal of human genetics 1993;53(4):874-80.
1989: B F Pugh; Brian C Schutte; Michael M Cox
Extent of duplex DNA underwinding induced by RecA protein binding in the presence of ATP.
Journal of molecular biology 1989;205(3):487-92.
1988: Brian C Schutte; Michael M Cox
Homology-dependent underwinding of duplex DNA in recA protein generated paranemic complexes.
Biochemistry 1988;27(20):7886-94.
1987: Brian C Schutte; Michael M Cox
Homology-dependent changes in adenosine 5'-triphosphate hydrolysis during recA protein promoted DNA strand exchange: evidence for long paranemic complexes.
Biochemistry 1987;26(18):5616-25.
1987: S L Brenner; R S Mitchell; S W Morrical; S K Neuendorf; Brian C Schutte; M M Cox
recA protein-promoted ATP hydrolysis occurs throughout recA nucleoprotein filaments.
The Journal of biological chemistry 1987;262(9):4011-6.