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Helmut Fuchs

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Mugdha Deo; Helmut Fuchs; Jenny Li-Ying Huang; Martin Hrabe de Angelis; Catherine D van Raamsdonk
Differential effects of neurofibromin gene dosage on melanocyte development.
Helmut Fuchs; Valérie Gailus-Durner; Wolfgang Hans; Sabine M Hölter; Matthias Klaften; Martina Klempt; Martin Klingenspor; Thomas Klopstock; Birgit Rathkolb; Jan Rozman; Sibylle Sabrautzki; Ralf Schneider; Hartwig Seedorf; Eckhard Wolf; Wolfgang Wurst; Lore Becker; Ralf Elvert; Martin Hrabě de Angelis
Does enamelin have pleiotropic effects on organs other than the teeth? Lessons from a phenotyping screen of two enamelin-mutant mouse lines.
Martin Irmler; Magdalena Kallnik; Martin Klingenspor; Helmut E Meyer; Jan Rozman; Holger Schulz; Fred W Van Leeuwen; Ines Bolle; Jing Jun Cheng; Frank J A Dennissen; Nicole Ehrhardt; Helmut Fuchs; Valérie Gailus-Durner; Romina J G Gentier; Denise J H P Hermes; Sabine M Hölter; David A Hopkins; Martin Hrabě de Angelis; Johannes Beckers
Long-term proteasomal inhibition in transgenic mice by UBB(+1) expression results in dysfunction of central respiration control reminiscent of brainstem neuropathology in Alzheimer patients.

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2013: Mugdha Deo; Helmut Fuchs; Jenny Li-Ying Huang; Martin Hrabe de Angelis; Catherine D van Raamsdonk
Differential effects of neurofibromin gene dosage on melanocyte development.
The Journal of investigative dermatology 2013;133(1):49-58.
2012: Helmut Fuchs; Valérie Gailus-Durner; Wolfgang Hans; Sabine M Hölter; Matthias Klaften; Martina Klempt; Martin Klingenspor; Thomas Klopstock; Birgit Rathkolb; Jan Rozman; Sibylle Sabrautzki; Ralf Schneider; Hartwig Seedorf; Eckhard Wolf; Wolfgang Wurst; Lore Becker; Ralf Elvert; Martin Hrabě de Angelis
Does enamelin have pleiotropic effects on organs other than the teeth? Lessons from a phenotyping screen of two enamelin-mutant mouse lines.
European journal of oral sciences 2012;120(4):269-77.
2012: Martin Irmler; Magdalena Kallnik; Martin Klingenspor; Helmut E Meyer; Jan Rozman; Holger Schulz; Fred W Van Leeuwen; Ines Bolle; Jing Jun Cheng; Frank J A Dennissen; Nicole Ehrhardt; Helmut Fuchs; Valérie Gailus-Durner; Romina J G Gentier; Denise J H P Hermes; Sabine M Hölter; David A Hopkins; Martin Hrabě de Angelis; Johannes Beckers
Long-term proteasomal inhibition in transgenic mice by UBB(+1) expression results in dysfunction of central respiration control reminiscent of brainstem neuropathology in Alzheimer patients.
Acta neuropathologica 2012;124(2):187-97.
2012: Sibylle Sabrautzki; Hartwig Seedorf; Tim M Strom; Eckhard Wolf; Matthias Klaften; Bettina Lorenz-Depiereux; Birgit Rathkolb; Isabel Rubio-Aliaga; Ana Benet-Pagès; Julia Calzada-Wack; Christian M Cohrs; Sebastian Eck; Irene Esposito; Jack Favor; Helmut Fuchs; Wolfgang Hans; Martin Hrabě de Angelis
New mouse models for metabolic bone diseases generated by genome-wide ENU mutagenesis.
Mammalian genome : official journal of the International Mammalian Genome Society 2012;23(7-8):416-30.
2012: Heike Kollmus; Colin McKerlie; Lluis Montoliu; Pedro J Otaegui; Rainer Post; Manuel Rebelo; Hermann Riedesel; Jesús Ruberte; Markus Brielmeier; Martin Hrabé De Angelis; Julia Fernández; Helmut Fuchs; Radislav Sedlacek; Klaus Schughart
Structural and functional concepts in current mouse phenotyping and archiving facilities.
Journal of the American Association for Laboratory Animal Science : JAALAS 2012;51(4):418-35.
2012: Benedetta Pozzi; Birgit Rathkolb; Simona Ronzoni; Anna Sciullo; Irina Treise; Eckhard Wolf; Thure Adler; Stefania Amodio; Christer Betsholtz; Ingrid Holmberg Betsholtz; Dirk H Busch; Stefano Casola; Daniela Castelletti; Martin Hrabě de Angelis; Pier Paolo Di Fiore; Helmut Fuchs; Valérie Gailus-Durner; Caterina Lucano; Nina Offenhäuser
The endocytic adaptor Eps15 controls marginal zone B cell numbers.
PloS one 2012;7(11):e50818.
2012: Pawel K Olszewski; Birgit Rathkolb; Ulf Risérus; Jan Rozman; Helgi B Schiöth; Siv Strömberg; Eckhard Wolf; Wolfgang Wurst; Martin Hrabě de Angelis; Johan Alsiö; Lore Becker; Nicole Ehrhardt; Ralf Elvert; Robert Fredriksson; Helmut Fuchs; Valérie Gailus-Durner; Wolfgang Hans; Sabine M Hölter; Josefin A Jacobsson; Martin Klingenspor; Anica Klockars; Thomas Klopstock; Allen S Levine; Claude Marcus; Manfred W Kilimann
Neurobeachin, a regulator of synaptic protein targeting, is associated with body fat mass and feeding behavior in mice and body-mass index in humans.
PLoS genetics 2012;8(3):e1002568.
2011: Monika Jeub; Bruno Pradier; Omneya Taha; Andreas Zimmer; Heinz Beck; Martin Hrabe de Angelis; Michael Emrich; Helmut Fuchs; Valerie Gailus-Durner; Danny Huylebroeck; Ildiko Racz
The transcription factor Smad-interacting protein 1 controls pain sensitivity via modulation of DRG neuron excitability.
Pain 2011;152(10):2384-98.
2011: Koichiro Abe; Helmut Fuchs; Auke Boersma; Wolfgang Hans; Philipp Yu; Svetoslav Kalaydjiev; Matthias Klaften; Thure Adler; Julia Calzada-Wack; Ilona Mossbrugger; Birgit Rathkolb; Jan Rozman; Cornelia Prehn; Miriam Maraslioglu; Yoshie Kametani; Shin Shimada; Jerzy Adamski; Dirk H Busch; Irene Esposito; Martin Klingenspor; Eckhard Wolf; Wolfgang Wurst; Valerie Gailus-Durner; Matilda Katan; Susan Marschall; Dian Soewarto; Sibylle Wagner; Martin Hrabě de Angelis
A novel N-ethyl-N-nitrosourea-induced mutation in phospholipase Cγ2 causes inflammatory arthritis, metabolic defects, and male infertility in vitro in a murine model.
Arthritis and rheumatism 2011;63(5):1301-11.
2011: Monika Raab; Birgit Rathkolb; Jan Rozman; Nicole Sänger; Mourad Mohamed Sanhaji; Jost Seibler; Eckhard Wolf; Juping Yuan; Thure Adler; Martin Hrabě de Angelis; Martin Bergmann; Dirk H Busch; Julia Calzada-Wack; Irene Esposito; Helmut Fuchs; Valérie Gailus-Durner; Sven Kappel; Martin Klingenspor; Rainald Knecht; Andrea Krämer; Bertolt Kreft; Elisabeth Kurunci-Csacsko; Yves Matthess; Florian Prinz; Klaus Strebhardt
Toxicity modelling of Plk1-targeted therapies in genetically engineered mice and cultured primary mammalian cells.
Nature communications 2011;2():395.
2010: Elisabeth Kemter; Birgit Rathkolb; Lise Bankir; Anja Schrewe; Wolfgang Hans; Christina Landbrecht; Matthias Klaften; Boris Ivandic; Helmut Fuchs; Valérie Gailus-Durner; Martin Hrabé De Angelis; Eckhard Wolf; Rüdiger Wanke; Bernhard Aigner
Mutation of the Na(+)-K(+)-2Cl(-) cotransporter NKCC2 in mice is associated with severe polyuria and a urea-selective concentrating defect without hyperreninemia.
American journal of physiology. Renal physiology 2010;298(6):F1405-15.
2010: Arianna Tocchetti; Charlotte Blanche Ekalle Soppo; Fabio Zani; Fabrizio Bianchi; Maria Cristina Gagliani; Benedetta Pozzi; Jan Rozman; Ralf Elvert; Nicole Ehrhardt; Birgit Rathkolb; Corinna Moerth; Marion Horsch; Helmut Fuchs; Valérie Gailus-Durner; Johannes Beckers; Martin Klingenspor; Eckhard Wolf; Martin Hrabé de Angelis; Eugenio Scanziani; Carlo Tacchetti; Giorgio Scita; Pier Paolo Di Fiore; Nina Offenhäuser
Loss of the actin remodeler Eps8 causes intestinal defects and improved metabolic status in mice.
PloS one 2010;5(3):e9468.
2010: Christopher Bachran; Alexander Weng; D Bachran; S B Riese; Nicole Schellmann; Matthias F Melzig; Helmut Fuchs
The distribution of saponins in vivo affects their synergy with chimeric toxins against tumours expressing human epidermal growth factor receptors in mice.
British journal of pharmacology 2010;159(2):345-52.
2009: Elisabeth Kemter; Birgit Rathkolb; Jan Rozman; Wolfgang Hans; Anja Schrewe; Christina Landbrecht; Matthias Klaften; Boris Ivandic; Helmut Fuchs; Valérie Gailus-Durner; Martin Klingenspor; Martin Hrabé De Angelis; Eckhard Wolf; Rüdiger Wanke; Bernhard Aigner
Novel missense mutation of uromodulin in mice causes renal dysfunction with alterations in urea handling, energy, and bone metabolism.
American journal of physiology. Renal physiology 2009;297(5):F1391-8.
2009: Birgit Rathkolb; Harry Noyes; Andrew Brass; Paul Dark; Helmut Fuchs; Valérie Gailus-Durner; John Gibson; Martin Hrabé De Angelis; Moses Ogugo; Fuad A Iraqi; Stephen J Kemp; Jan Naessens; Mathew E Pope; Eckhard Wolf; Morris Agaba
Clinical chemistry of congenic mice with quantitative trait loci for predicted responses to Trypanosoma congolense infection.
Infection and immunity 2009;77(9):3948-57.
2009: Uwe Ahting; Thomas Floss; Nikolas Uez; Ilka Schneider-Lohmar; Lore Becker; Eva Kling; Arcangela Iuso; Andreas Bender; Martin Hrabé De Angelis; Valérie Gailus-Durner; Helmut Fuchs; Thomas Meitinger; Wolfgang Wurst; Holger Prokisch; Thomas Klopstock
Neurological phenotype and reduced lifespan in heterozygous Tim23 knockout mice, the first mouse model of defective mitochondrial import.
Biochimica et biophysica acta 2009;1787(5):371-6.
2009: Jörg Isensee; Luca Meoli; Valeria Zazzu; Christoph Nabzdyk; Henning Witt; Dian Soewarto; Karin Effertz; Helmut Fuchs; Valérie Gailus-Durner; Dirk Busch; Thure Adler; Martin Hrabé De Angelis; Markus Irgang; Christiane Otto; Patricia Ruiz Noppinger
Expression pattern of G protein-coupled receptor 30 in LacZ reporter mice.
Endocrinology 2009;150(4):1722-30.
2009: Isabel Rubio-Aliaga; Gerhard K H Przemeck; Helmut Fuchs; Valérie Gailus-Durner; Thure Adler; Wolfgang Hans; Marion Horsch; Birgit Rathkolb; Jan Rozman; Anja Schrewe; Sibylle Wagner; Sabine M Hoelter; Lore Becker; Thomas Klopstock; Wolfgang Wurst; Eckhard Wolf; Martin Klingenspor; Boris T Ivandic; Dirk H Busch; Johannes Beckers; Martin Hrabé De Angelis
Dll1 haploinsufficiency in adult mice leads to a complex phenotype affecting metabolic and immunological processes.
PloS one 2009;4(6):e6054.
2008: Kelly A McGowan; Jun Z Li; Christopher Park; Veronica Beaudry; Holly K Tabor; Amit J Sabnis; Weibin Zhang; Helmut Fuchs; Martin Hrabé De Angelis; Richard Myers; Laura D Attardi; Gregory S Barsh
Ribosomal mutations cause p53-mediated dark skin and pleiotropic effects.
Nature genetics 2008;40(8):963-70.
2008: Oliver Puk; Jana Löster; Claudia Dalke; Dian Soewarto; Helmut Fuchs; Birgit Budde; Peter Nürnberg; Eckhard Wolf; Martin Hrabé De Angelis; Jochen Graw
Mutation in a novel connexin-like gene (Gjf1) in the mouse affects early lens development and causes a variable small-eye phenotype.
Investigative ophthalmology & visual science 2008;49(4):1525-32.
2008: K Abe; S Wechs; Svetoslav Kalaydjiev; T J Franz; Dirk H Busch; Helmut Fuchs; Dian Soewarto; Heidrun Behrendt; S Wagner; Thilo Jakob; Martin Hrabé De Angelis
Novel lymphocyte-independent mechanisms to initiate inflammatory arthritis via bone marrow-derived cells of Ali18 mutant mice.
Rheumatology (Oxford, England) 2008;47(3):292-300.
2008: Thomas S Lisse; Frank Thiele; Helmut Fuchs; Wolfgang Hans; Gerhard K H Przemeck; Koichiro Abe; Birgit Rathkolb; Leticia Quintanilla-Martinez; Gabriele Hoelzlwimmer; Miep Helfrich; Eckhard Wolf; Stuart H Ralston; Martin Hrabé De Angelis
ER stress-mediated apoptosis in a new mouse model of osteogenesis imperfecta.
PLoS genetics 2008;4(2):e7.
2008: Holger Maier; Christoph Lengger; Bruno Simic; Helmut Fuchs; Valérie Gailus-Durner; Martin Hrabé De Angelis
MausDB: an open source application for phenotype data and mouse colony management in large-scale mouse phenotyping projects.
BMC bioinformatics 2008;9():169.
2007: Carola W Meyer; Ralf Elvert; André Scherag; Nicole Ehrhardt; Valérie Gailus-Durner; Helmut Fuchs; Helmut Schäfer; Martin Hrabé De Angelis; Gerhard Heldmaier; Martin Klingenspor
Power matters in closing the phenotyping gap.
Die Naturwissenschaften 2007;94(5):401-6.
2007: Franz Vauti; Tobias Goller; Rafael Beine; Lore Becker; Thomas Klopstock; Sabine M Hölter; Wolfgang Wurst; Helmut Fuchs; Valérie Gailus-Durner; Martin Hrabé De Angelis; Hans-Henning Arnold
The mouse Trm1-like gene is expressed in neural tissues and plays a role in motor coordination and exploratory behaviour.
Gene 2007;389(2):174-85.
2007: Isabel Rubio-Aliaga; Dian Soewarto; Sibylle Wagner; Matthias Klaften; Helmut Fuchs; Svetoslav Kalaydjiev; Dirk H Busch; Martina Klempt; Birgit Rathkolb; Eckhard Wolf; Koichiro Abe; Stefan Zeiser; Gerhard K H Przemeck; Johannes Beckers; Martin Hrabé De Angelis
A genetic screen for modifiers of the delta1-dependent notch signaling function in the mouse.
Genetics 2007;175(3):1451-63.
2007: Laetitia Magnol; Marie-Clémence Chevallier; Valérie Nalesso; Stéphanie Retif; Helmut Fuchs; Martina Klempt; Patricia Pereira; Michel Riottot; Sandra Andrzejewski; Bich-Thuy Doan; Jean-Jacques Panthier; Anne Puech; Jean-Claude Beloeil; Martin Hrabé De Angelis; Yann Herault
KIT is required for hepatic function during mouse post-natal development.
BMC developmental biology 2007;7():81.
2007: Kelly A McGowan; Helmut Fuchs; Martin Hrabé De Angelis; Gregory S Barsh
Identification of a Keratin 4 mutation in a chemically induced mouse mutant that models white sponge nevus.
The Journal of investigative dermatology 2007;127(1):60-4.
2006: Fabian Runkel; Matthias Klaften; Kerstin Koch; Volker Böhnert; Heinrich Büssow; Helmut Fuchs; Thomas Franz; Martin Hrabé De Angelis
Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71rco12 and Krt71rco13.
Mammalian genome : official journal of the International Mammalian Genome Society 2006;17(12):1172-82.
2006: Ilka Schneider; Werner S Tirsch; Theresa Faus-Kessler; Lore Becker; Eva Kling; Rose-Leah Austin Busse; Andreas Bender; Berend Feddersen; Johannes Tritschler; Helmut Fuchs; Valérie Gailus-Durner; Karl-Hans Englmeier; Martin Hrabé De Angelis; Thomas Klopstock
Systematic, standardized and comprehensive neurological phenotyping of inbred mice strains in the German Mouse Clinic.
Journal of neuroscience methods 2006;157(1):82-90.
2006: Koichiro Abe; Helmut Fuchs; Thomas Lisse; Wolfgang Hans; Martin Hrabé De Angelis
New ENU-induced semidominant mutation, Ali18, causes inflammatory arthritis, dermatitis, and osteoporosis in the mouse.
Mammalian genome : official journal of the International Mammalian Genome Society 2006;17(9):915-26.
2006: Kelly A McGowan; Swaroop Aradhya; Helmut Fuchs; Martin Hrabé De Angelis; Gregory S Barsh
A mouse keratin 1 mutation causes dark skin and epidermolytic hyperkeratosis.
The Journal of investigative dermatology 2006;126(5):1013-6.
2006: Ivan del Barco Barrantes; Ana Montero-Pedrazuela; Ana Guadaño-Ferraz; Maria Jesus Obregón; Raquel Martinez de Mena; Valérie Gailus-Durner; Helmut Fuchs; Tobias J Franz; Svetoslav Kalaydjiev; Martina Klempt; Sabine Hölter; Birgit Rathkolb; Claudia Reinhard; Gabriella Morreale de Escobar; Juan Bernal; Dirk H Busch; Wolfgang Wurst; Eckhard Wolf; Holger Schulz; Svetlana Shtrom; Erich Greiner; Martin Hrabé De Angelis; Heiner Westphal; Christof Niehrs
Generation and characterization of dickkopf3 mutant mice.
Molecular and cellular biology 2006;26(6):2317-26.
2005: Jochen Graw; Jana Löster; Oliver Puk; Doris Münster; Nicole Haubst; Dian Soewarto; Helmut Fuchs; Birgit Meyer; Peter Nürnberg; Walter Pretsch; Paul Selby; Jack Favor; Eckhard Wolf; Martin Hrabé De Angelis
Three novel Pax6 alleles in the mouse leading to the same small-eye phenotype caused by different consequences at target promoters.
Investigative ophthalmology & visual science 2005;46(12):4671-83.
2005: Bastian Pasche; Svetoslav Kalaydjiev; Tobias J Franz; Elisabeth Kremmer; Valérie Gailus-Durner; Helmut Fuchs; Martin Hrabé De Angelis; Andreas Lengeling; Dirk H Busch
Sex-dependent susceptibility to Listeria monocytogenes infection is mediated by differential interleukin-10 production.
Infection and immunity 2005;73(9):5952-60.
2005: Claudia Reinhard; Birgit Meyer; Helmut Fuchs; Tobias Stoeger; Gunter Eder; Franz Rüschendorf; Joachim Heyder; Peter Nürnberg; Martin Hrabé De Angelis; Holger Schulz
Genomewide linkage analysis identifies novel genetic Loci for lung function in mice.
American journal of respiratory and critical care medicine 2005;171(8):880-8.
2004: Fabian Runkel; Andreas Marquardt; C Stoeger; E Kochmann; D Simon; B Kohnke; Dirk Korthaus; Frank Wattler; Helmut Fuchs; Martin Hrabé De Angelis; Gabriele Stumm; Michael Nehls; Sigrid Wattler; Thomas Franz; Martin Augustin
The dominant alopecia phenotypes Bareskin, Rex-denuded, and Reduced Coat 2 are caused by mutations in gasdermin 3.
Genomics 2004;84(5):824-35.
2004: Catherine D van Raamsdonk; Karen R Fitch; Helmut Fuchs; Martin Hrabé De Angelis; Gregory S Barsh
Effects of G-protein mutations on skin color.
Nature genetics 2004;36(9):961-8.
2004: Adalheidur Gígja Hansdottir; Karen Pálsdóttir; Jack Favor; Angelika Neuhäuser-Klaus; Helmut Fuchs; Martin Hrabé De Angelis; Eiríkur Steingrímsson
The novel mouse microphthalmia mutations Mitfmi-enu5 and Mitfmi-bcc2 produce dominant negative Mitf proteins.
Genomics 2004;83(5):932-5.
2004: Carola W Meyer; Dirk Korthaus; Wolfgang Jagla; Emmanuelle Cornali; Johannes Grosse; Helmut Fuchs; Martin Klingenspor; Stephanie Roemheld; Matthias H Tschöp; Gerhard Heldmaier; Martin Hrabé De Angelis; Michael Nehls
A novel missense mutation in the mouse growth hormone gene causes semidominant dwarfism, hyperghrelinemia, and obesity.
Endocrinology 2004;145(5):2531-41.
2004: Claudia Dalke; Jana Löster; Helmut Fuchs; Valérie Gailus-Durner; Dian Soewarto; Jack Favor; Angelika Neuhäuser-Klaus; Walter Pretsch; Florian Gekeler; Kei Shinoda; Eberhart Zrenner; Thomas Meitinger; Martin Hrabé De Angelis; Jochen Graw
Electroretinography as a screening method for mutations causing retinal dysfunction in mice.
Investigative ophthalmology & visual science 2004;45(2):601-9.
2003: T Peters; Reinhard Sedlmeier; Heinrich Büssow; Fabian Runkel; Georg H Lüers; Dirk Korthaus; Helmut Fuchs; Martin Hrabé De Angelis; Gabriele Stumm; Andreas Russ; Rebecca M Porter; Martin Augustin; Thomas Franz
Alopecia in a novel mouse model RCO3 is caused by mK6irs1 deficiency.
The Journal of investigative dermatology 2003;121(4):674-80.
2003: Karen R Fitch; Kelly A McGowan; Catherine D van Raamsdonk; Helmut Fuchs; Daekee Lee; Anne Puech; Yann Herault; David Threadgill; Martin Hrabé De Angelis; Gregory S Barsh
Genetics of dark skin in mice.
Genes & development 2003;17(2):214-28.
2002: Jochen Graw; Jana Löster; Dian Soewarto; Helmut Fuchs; André Reis; Eckhard Wolf; Rudi Balling; Martin Hrabé De Angelis
V76D mutation in a conserved gD-crystallin region leads to dominant cataracts in mice.
Mammalian genome : official journal of the International Mammalian Genome Society 2002;13(8):452-5.
2002: Claudia Reinhard; Gunter Eder; Helmut Fuchs; Axel Ziesenis; Joachim Heyder; Holger Schulz
Inbred strain variation in lung function.
Mammalian genome : official journal of the International Mammalian Genome Society 2002;13(8):429-37.
2001: Jochen Graw; Jana Löster; Dian Soewarto; Helmut Fuchs; Birgit Meyer; André Reis; Eckhard Wolf; Rudi Balling; Martin Hrabé De Angelis
Characterization of a mutation in the lens-specific MP70 encoding gene of the mouse leading to a dominant cataract.
Experimental eye research 2001;73(6):867-76.
2001: Jochen Graw; Jana Löster; Dian Soewarto; Helmut Fuchs; Birgit Meyer; André Reis; Eckhard Wolf; Rudi Balling; Martin Hrabé De Angelis
Characterization of a new, dominant V124E mutation in the mouse alphaA-crystallin-encoding gene.
Investigative ophthalmology & visual science 2001;42(12):2909-15.
2001: Jochen Graw; Jana Löster; Dian Soewarto; Helmut Fuchs; A Reis; E Wolf; Rudi Balling; Martin Hrabé De Angelis
Aey2, a new mutation in the betaB2-crystallin-encoding gene of the mouse.
Investigative ophthalmology & visual science 2001;42(7):1574-80.
2001: Jochen Graw; Norman Klopp; Jana Löster; Dian Soewarto; Helmut Fuchs; J Becker-Follmann; André Reis; Eckhard Wolf; Rudi Balling; M Habré de Angelis
Ethylnitrosourea-induced mutation in mice leads to the expression of a novel protein in the eye and to dominant cataracts.
Genetics 2001;157(3):1313-20.
2000: W Pargent; S Heffner; K F Schäble; Dian Soewarto; Helmut Fuchs; Martin Hrabé De Angelis
MouseNet database: digital management of a large-scale mutagenesis project.
Mammalian genome : official journal of the International Mammalian Genome Society 2000;11(7):590-3.
1999: Jochen Graw; M Jung; Jana Löster; Norman Klopp; Dian Soewarto; C Fella; Helmut Fuchs; André Reis; Eckhard Wolf; Rudi Balling; Martin Hrabé De Angelis
Mutation in the betaA3/A1-crystallin encoding gene Cryba1 causes a dominant cataract in the mouse.
Genomics 1999;62(1):67-73.