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Steve Brown

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Nellie Y Loh; Sian E Piret; Michael J Stechman; Paolo Tammaro; Sjoerd Verkaart; Bushra N Ahmad; Frances M Ashcroft; Ilaria Bellantuono; Liz Bentley; René J M Bindels; Steve D M Brown; Roger D Cox; Henrik Dimke; Holly Evans; William D Fraser; Caroline M Gorvin; Fadil M Hannan; Joost G J Hoenderop; Tertius A Hough; Rajesh V Thakker
Autosomal dominant hypercalciuria in a mouse model due to a mutation of the epithelial calcium channel, TRPV5.
Katherine R Bull; Edward M Bertram; Bruce Beutler; Steve D M Brown; Tanya L Crockford; Anselm Enders; Christopher C Goodnow; Gerton Lunter; Ann-Marie Mallon; Lisa A Miosge; Paul Potter; Andrew J Rimmer; Carla M Roots; Owen M Siggs; Michelle M Simon; Belinda Whittle; Richard J Cornall
Unlocking the bottleneck in forward genetics using whole-genome sequencing and identity by descent to isolate causative mutations.
Ann-Marie Mallon; David Melvin; Hugh Morgan; Helen Parkinson; Steve D M Brown; Paul Flicek; Vivek Iyer; William C Skarnes
Accessing data from the International Mouse Phenotyping Consortium: state of the art and future plans.

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All Publications

2013: Nellie Y Loh; Sian E Piret; Michael J Stechman; Paolo Tammaro; Sjoerd Verkaart; Bushra N Ahmad; Frances M Ashcroft; Ilaria Bellantuono; Liz Bentley; René J M Bindels; Steve D M Brown; Roger D Cox; Henrik Dimke; Holly Evans; William D Fraser; Caroline M Gorvin; Fadil M Hannan; Joost G J Hoenderop; Tertius A Hough; Rajesh V Thakker
Autosomal dominant hypercalciuria in a mouse model due to a mutation of the epithelial calcium channel, TRPV5.
PloS one 2013;8(1):e55412.
2013: Katherine R Bull; Edward M Bertram; Bruce Beutler; Steve D M Brown; Tanya L Crockford; Anselm Enders; Christopher C Goodnow; Gerton Lunter; Ann-Marie Mallon; Lisa A Miosge; Paul Potter; Andrew J Rimmer; Carla M Roots; Owen M Siggs; Michelle M Simon; Belinda Whittle; Richard J Cornall
Unlocking the bottleneck in forward genetics using whole-genome sequencing and identity by descent to isolate causative mutations.
PLoS genetics 2013;9(1):e1003219.
2012: Ann-Marie Mallon; David Melvin; Hugh Morgan; Helen Parkinson; Steve D M Brown; Paul Flicek; Vivek Iyer; William C Skarnes
Accessing data from the International Mouse Phenotyping Consortium: state of the art and future plans.
Mammalian genome : official journal of the International Mammalian Genome Society 2012;23(9-10):641-52.
2012: Steve D M Brown; Mark W Moore
The International Mouse Phenotyping Consortium: past and future perspectives on mouse phenotyping.
Mammalian genome : official journal of the International Mammalian Genome Society 2012;23(9-10):632-40.
2012: Xiangbin Xu; Chen Yan; Wenhong Zhang; Steve D M Brown; Michael T Cheeseman; Yuxian Huang; Anuhya S Konduru; Byung Cheol Lee; Jae Hyang Lim; Jinjiang Pang; Rachel R Steere; Chang-Hoon Woo; Jing Wu; Haidong Xu; Jian-Dong Li
EVI1 acts as an inducible negative-feedback regulator of NF-κB by inhibiting p65 acetylation.
Journal of immunology (Baltimore, Md. : 1950) 2012;188(12):6371-80.
2012: Steve D M Brown; Mark W Moore
Towards an encyclopaedia of mammalian gene function: the International Mouse Phenotyping Consortium.
Disease models & mechanisms 2012;5(3):289-92.
2012: Silvia Corrochano; Jose J Lucas; Maurizio Renna; David C Rubinsztein; Cristina Tomas-Zapico; Steve D M Brown; Abraham Acevedo-Arozena
α-Synuclein levels affect autophagosome numbers in vivo and modulate Huntington disease pathology.
Autophagy 2012;8(3):431-2.
2012: Christopher T Esapa; Holly Evans; Rosie A Head; Tertius A Hough; Peter G T Howell; Eugene G McNally; M Andrew Nesbit; Sarah Testori; J H Duncan Bassett; Alan Boyde; Matthew A Brown; Steve D M Brown; Andrew J Carr; Carol P S Chan; Michael T Cheeseman; Anne Clark; Roger D Cox; Elizabeth A Crane; Peter I Croucher; Przemko Tylzanowski; Graham R Williams; Rajesh V Thakker
A mouse model for spondyloepiphyseal dysplasia congenita with secondary osteoarthritis due to a Col2a1 mutation.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2012;27(2):413-28.
2012: Silvia Corrochano; Rose Kent; Maurizio Renna; David C Rubinsztein; Michelle Stewart; Steve D M Brown; Sarah Carter; Nichola Chrobot; Jason Cooper; Abraham Acevedo-Arozena
α-Synuclein levels modulate Huntington's disease in mice.
Human molecular genetics 2012;21(3):485-94.
2012: Sian E Piret; Gethin Thomas; Matthew Brown; Steve D M Brown; Roger Cox; Peter Croucher; Olivier Devuyst; Christopher T Esapa; Caroline M Gorvin; Rosie Head; Nellie Y Loh; Rajesh V Thakker
A mouse model of early-onset renal failure due to a xanthine dehydrogenase nonsense mutation.
PloS one 2012;7(9):e45217.
2012: Christopher T Esapa; Holly Evans; Rosie A Head; Tertius A Hough; Jeshmi Jeyabalan; Eugene G McNally; Matthew A Brown; Steve D M Brown; Andrew J Carr; Michael T Cheeseman; Roger D Cox; Peter I Croucher; Gethin P Thomas; Rajesh V Thakker
A mouse with an N-Ethyl-N-nitrosourea (ENU) Induced Trp589Arg Galnt3 mutation represents a model for hyperphosphataemic familial tumoural calcinosis.
PloS one 2012;7(8):e43205.
2011: Michael T Cheeseman; Helen Hilton; Tertius A Hough; Andrew Parker; Paras Pathak; Paul Potter; Tom Purnell; Maria R Romero; Hayley E Tyrer; Lucie Vizor; Kate Vowell; Sara Wells; Debbie Williams; Sulzhan Bali; Mahmood F Bhutta; Steve D M Brown
HIF-VEGF pathways are critical for chronic otitis media in Junbo and Jeff mouse mutants.
PLoS genetics 2011;7(10):e1002336.
2011: Steve D M Brown
Disease model discovery and translation. Introduction.
Mammalian genome : official journal of the International Mammalian Genome Society 2011;22(7-8):361.
2011: Hilary Gates; Ann-Marie Mallon; Steve D M Brown
High-throughput mouse phenotyping.
Methods (San Diego, Calif.) 2011;53(4):394-404.
2011: Marie S Rye; Mahmood F Bhutta; Michael T Cheeseman; David Burgner; Jenefer M Blackwell; Steve D M Brown; Sarra E Jamieson
Unraveling the genetics of otitis media: from mouse to human and back again.
Mammalian genome : official journal of the International Mammalian Genome Society 2011;22(1-2):66-82.
2011: Sally H Cross; Lisa McKie; Katrine West; Emma L Coghill; Jack Favor; Shoumo Bhattacharya; Steve D M Brown; Ian J Jackson
The Opdc missense mutation of Pax2 has a milder than loss-of-function phenotype.
Human molecular genetics 2011;20(2):223-34.
2011: Maria Cristina D'Adamo; Lijun Shang; Paola Imbrici; Steve D M Brown; Mauro Pessia; Stephen J Tucker
Genetic inactivation of Kcnj16 identifies Kir5.1 as an important determinant of neuronal PCO2/pH sensitivity.
The Journal of biological chemistry 2011;286(1):192-8.
2010: Andrew Parker; Rachel E Hardisty-Hughes; Laura Wisby; Susan Joyce; Steve D M Brown
Melody, an ENU mutation in Caspase 3, alters the catalytic cysteine residue and causes sensorineural hearing loss in mice.
Mammalian genome : official journal of the International Mammalian Genome Society 2010;21(11-12):565-76.
2010: Michael J Stechman; Bushra N Ahmad; Nellie Y Loh; Anita A C Reed; Michelle Stewart; Sara Wells; Tertius Hough; Liz Bentley; Roger D Cox; Steve D M Brown; Rajesh V Thakker
Establishing normal plasma and 24-hour urinary biochemistry ranges in C3H, BALB/c and C57BL/6J mice following acclimatization in metabolic cages.
Laboratory animals 2010;44(3):218-25.
2010: Kazuhiro Okumura; Eiji Mochizuki; Michinari Yokohama; Hisashi Yamakawa; Hiroshi Shitara; Philomena Mburu; Hiromichi Yonekawa; Steve D M Brown; Yoshiaki Kikkawa
Protein 4.1 expression in the developing hair cells of the mouse inner ear.
Brain research 2010;1307():53-62.
2010: Philomena Mburu; María Rosario Romero; Helen Hilton; Andrew Parker; Stuart Townsend; Yoshiaki Kikkawa; Steve D M Brown
Gelsolin plays a role in the actin polymerization complex of hair cell stereocilia.
PloS one 2010;5(7):e11627.
2010: Rachel E Hardisty-Hughes; Andrew Parker; Steve D M Brown
A hearing and vestibular phenotyping pipeline to identify mouse mutants with hearing impairment.
Nature protocols 2010;5(1):177-90.
2010: Hugh Morgan; Tim Beck; Andrew Blake; Hilary Gates; Niels Adams; Guillaume Debouzy; Sophie Leblanc; Christoph Lengger; Holger Maier; David Melvin; Hamid Meziane; Dave Richardson; Sara Wells; Jacqui White; Joe Wood; Martin Hrabé De Angelis; Steve D M Brown; John M Hancock; Ann-Marie Mallon
EuroPhenome: a repository for high-throughput mouse phenotyping data.
Nucleic acids research 2010;38(Database issue):D577-85.
2010: Andrew Blake; Karen Pickford; Simon Greenaway; Steve Thomas; Amanda Pickard; Christine M Williamson; Niels C Adams; Alison Walling; Tim Beck; Martin Fray; Jo Peters; Tom Weaver; Steve D M Brown; John M Hancock; Ann-Marie Mallon
MouseBook: an integrated portal of mouse resources.
Nucleic acids research 2010;38(Database issue):D593-9.
2009: Kumar N Alagramam; Steve D M Brown; Rickie R Davis; Ken R Johnson; Sherri M Jones; John B Macauley; Qing Yin Zheng; Jian Zuo
Foreword for special issue: mouse models for hearing research.
Brain research 2009;1277():1-2.
2009: Steve D M Brown; Wolfgang Wurst; Ralf Kühn; John Hancock
The functional annotation of mammalian genomes: the challenge of phenotyping.
Annual review of genetics 2009;43():305-33.
2009: Paul N Schofield; Steve D M Brown; John P Sundberg; Mark Arends; Madhuri V Warren; Pierre Dubus; Michele Ellender; Laurence Fiette; Bjorn Rozell; Leticia Quintanilla-Martinez; Marcello Raspa; Ji-Ying Song; Martin van der Valk; Colin McKerlie
PRIME importance of pathology expertise.
Nature biotechnology 2009;27(1):24-5.
2008: silvia mandillo; Valter Tucci; Sabine M Hölter; Hamid Meziane; Mumna Banchaabouchi; Magdalena Kallnik; Heena V Lad; Patrick M Nolan; Abdel-Mouttalib Ouagazzal; Emma L Coghill; Karin Gale; Elisabetta Golini; Sylvie Jacquot; Wojtek Krezel; Andy Parker; Fabrice Riet; Ilka Schneider; Daniela Marazziti; Johan Auwerx; Steve D M Brown; Pierre Chambon; Nadia Rosenthal; Glauco Tocchini-Valentini; Wolfgang Wurst
Reliability, robustness, and reproducibility in mouse behavioral phenotyping: a cross-laboratory study.
Physiological genomics 2008;34(3):243-55.
2008: Steve D M Brown; Rachel E Hardisty-Hughes; Philomena Mburu
Quiet as a mouse: dissecting the molecular and genetic basis of hearing.
Nature reviews. Genetics 2008;9(4):277-90.
2008: Matthias Groszer; David A Keays; Robert M J Deacon; Joseph P de Bono; Shweta Prasad-Mulcare; Simone Gaub; Muriel G Baum; Catherine A French; Jérôme Nicod; Julie A Coventry; Wolfgang Enard; Martin Fray; Steve D M Brown; Patrick M Nolan; Svante Pääbo; Keith M Channon; Rui M Costa; Jens Eilers; Günter Ehret; J Nicholas P Rawlins; Simon E Fisher
Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits.
Current biology : CB 2008;18(5):354-62.
2008: Ivana Barbaric; Mark J Perry; T Neil Dear; Alexandra Rodrigues Da Costa; Daniela Salopek; Ana Marusic; Tertius A Hough; Sara Wells; A Jackie Hunter; Michael Cheeseman; Steve D M Brown
An ENU-induced mutation in the Ankrd11 gene results in an osteopenia-like phenotype in the mouse mutant Yoda.
Physiological genomics 2008;32(3):311-21.
2008: Abraham Acevedo-Arozena; Sara Wells; Paul Potter; Michelle Kelly; Roger D Cox; Steve D M Brown
ENU mutagenesis, a way forward to understand gene function.
Annual review of genomics and human genetics 2008;9():49-69.
2007: Tertius A Hough; Monika Polewski; Kristen Johnson; Michael Cheeseman; Patrick M Nolan; Lucie Vizor; Sohaila Rastan; Alan Boyde; Kenneth Pritzker; A Jackie Hunter; Elizabeth M C Fisher; Robert Terkeltaub; Steve D M Brown
Novel mouse model of autosomal semidominant adult hypophosphatasia has a splice site mutation in the tissue nonspecific alkaline phosphatase gene Akp2.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2007;22(9):1397-407.
2007: David A Keays; Guoling Tian; Karine Poirier; Guo-Jen Huang; Christian Siebold; James Cleak; Peter L Oliver; Martin Fray; Robert Justin Harvey; Zoltán Molnár; Maria C Piñon; Neil Dear; William Valdar; Steve D M Brown; Kay E Davies; J N P Rawlins; Nicholas J Cowan; Patrick Nolan; Jamel Chelly; Jonathan Flint
Mutations in alpha-tubulin cause abnormal neuronal migration in mice and lissencephaly in humans.
Cell 2007;128(1):45-57.
2006: Rachel E Hardisty-Hughes; Hilda Tateossian; Susan A Morse; M Rosario Romero; Alice Middleton; Zuzanna Tymowska-Lalanne; A Jackie Hunter; Michael Cheeseman; Steve D M Brown
A mutation in the F-box gene, Fbxo11, causes otitis media in the Jeff mouse.
Human molecular genetics 2006;15(22):3273-9.
2006: Valter Tucci; Heena V Lad; Andy Parker; Sian Polley; Steve D M Brown; Patrick M Nolan
Gene-environment interactions differentially affect mouse strain behavioral parameters.
Mammalian genome : official journal of the International Mammalian Genome Society 2006;17(11):1113-20.
2006: Nick Parkinson; Rachel E Hardisty-Hughes; Hilda Tateossian; Hsun-Tien Tsai; Debra Brooker; Sue Morse; Zuzanna Lalane; Francesca MacKenzie; Martin Fray; Peter Glenister; Anne-Marie Woodward; Sian Polley; Ivana Barbaric; Neil Dear; Tertius A Hough; A Jackie Hunter; Michael T Cheeseman; Steve D M Brown
Mutation at the Evi1 locus in Junbo mice causes susceptibility to otitis media.
PLoS genetics 2006;2(10):e149.
2006: Steve D M Brown; John Hancock; Hilary Gates
Understanding mammalian genetic systems: the challenge of phenotyping in the mouse.
PLoS genetics 2006;2(8):e118.
2006: Philomena Mburu; Yoshiaki Kikkawa; Stuart Townsend; Rosario Romero; Hiromichi Yonekawa; Steve D M Brown
Whirlin complexes with p55 at the stereocilia tip during hair cell development.
Proceedings of the National Academy of Sciences of the United States of America 2006;103(29):10973-8.
2006: Fernando Segade; Kathleen A Daly; Dax Allred; Pamela J Hicks; Miranda Cox; Mark Brown; Rachel E Hardisty-Hughes; Steve D M Brown; Stephen S Rich; Donald W Bowden
Association of the FBXO11 gene with chronic otitis media with effusion and recurrent otitis media: the Minnesota COME/ROM Family Study.
Archives of otolaryngology--head & neck surgery 2006;132(7):729-33.
2006: Qing Yin Zheng; Rachel Hardisty-Hughes; Steve D M Brown
Mouse models as a tool to unravel the genetic basis for human otitis media.
Brain research 2006;1091(1):9-15.
2005: David C Rubinsztein; Brinda Ravikumar; Abraham Acevedo-Arozena; Sara Imarisio; Cahir J O'Kane; Steve D M Brown
Dyneins, autophagy, aggregation and neurodegeneration.
Autophagy 2005;1(3):177-8.
2005: Debora Bogani; Catherine Willoughby; Jennifer Davies; Kulvinder Kaur; Ghazala Mirza; Anju Paudyal; Heather Haines; Richard McKeone; Matthew Cadman; Guido Pieles; Jürgen E Schneider; Shoumo Bhattacharya; Andrea Hardy; Patrick M Nolan; Nikos Tripodis; Michael J Depew; Ramya Chandrasekara; Gimara Duncan; Paul T Sharpe; Andy Greenfield; Paul Denny; Steve D M Brown; Jiannis Ragoussis; Ruth Arkell
Dissecting the genetic complexity of human 6p deletion syndromes by using a region-specific, phenotype-driven mouse screen.
Proceedings of the National Academy of Sciences of the United States of America 2005;102(35):12477-82.
2005: Brinda Ravikumar; Abraham Acevedo-Arozena; Sara Imarisio; Zdenek Berger; Coralie Vacher; Cahir J O'Kane; Steve D M Brown; David C Rubinsztein
Dynein mutations impair autophagic clearance of aggregate-prone proteins.
Nature genetics 2005;37(7):771-6.
2005: Fiona Oliver; Julian K Christians; Xiaojun Liu; Susan Rhind; Vinesh Verma; Claire Davison; Steve D M Brown; Paul Denny; Peter D Keightley
Regulatory variation at glypican-3 underlies a major growth QTL in mice.
PLoS biology 2005;3(5):e135.
2005: Xiao Mei Ouyang; Denise Yan; Li Lin Du; J Fielding Hejtmancik; Samuel G Jacobson; Walter E Nance; An Ren Li; Simon I Angeli; Muriel Kaiser; Valerie Newton; Steve D M Brown; Thomas J Balkany; Xue Zhong Liu
Characterization of Usher syndrome type I gene mutations in an Usher syndrome patient population.
Human genetics 2005;116(4):292-9.
2005: Yoshiaki Kikkawa; Philomena Mburu; Sue Morse; Ryo Kominami; Stuart Townsend; Steve D M Brown
Mutant analysis reveals whirlin as a dynamic organizer in the growing hair cell stereocilium.
Human molecular genetics 2005;14(3):391-400.
2004: Ann-Marie Mallon; Laurens G Wilming; Joseph Weekes; James G R Gilbert; Jennifer L Ashurst; Sandrine Peyrefitte; Lucy Matthews; Matthew Cadman; Richard McKeone; Chris A Sellick; Ruth Arkell; Marc R M Botcherby; Mark A Strivens; R Duncan Campbell; Simon Gregory; Paul Denny; John Hancock; Jane Rogers; Steve D M Brown
Organization and evolution of a gene-rich region of the mouse genome: a 12.7-Mb region deleted in the Del(13)Svea36H mouse.
Genome research 2004;14(10A):1888-901.
2004: Mohamed Mohideen Quwailid; Alison Hugill; Neil Dear; Lucie Vizor; Sara Wells; Emma Horner; Shelly Fuller; Jessica Weedon; Hamish McMath; Paul Woodman; David Edwards; David Campbell; Susan Rodger; Joanne Carey; Ann Roberts; Peter Glenister; Zuzanna Lalanne; Nick Parkinson; Emma L Coghill; Richard McKeone; Sam Cox; John Willan; Andy Greenfield; David A Keays; Saffron Brady; Nigel K Spurr; Ian C Gray; Jackie Hunter; Steve D M Brown; Roger D Cox
A gene-driven ENU-based approach to generating an allelic series in any gene.
Mammalian genome : official journal of the International Mammalian Genome Society 2004;15(8):585-91.
2004: G Blanco; C Pritchard; P Underhill; S Breeds; K M F Townsend; Andy Greenfield; Steve D M Brown
Molecular phenotyping of the mouse ky mutant reveals UCP1 upregulation at the neuromuscular junctions of dystrophic soleus muscle.
Neuromuscular disorders : NMD 2004;14(3):217-28.
2004: Vicky Tsipouri; John A Curtin; Pat M Nolan; Lucie Vizor; Claire A Parsons; Colin M Clapham; Ian D Latham; Lesley J Rooke; Jo E Martin; Jo Peters; A Jackie Hunter; Derek Rogers; Sohaila Rastan; Steve D M Brown; Elizabeth M C Fisher; Nigel K Spurr; Ian C Gray
Three novel pigmentation mutants generated by genome-wide random ENU mutagenesis in the mouse.
Comparative and functional genomics 2004;5(2):123-7.
2004: Chris Holmes; Steve D M Brown
All systems GO for understanding mouse gene function.
Journal of biology 2004;3(5):20.
2003: Charlotte R Rhodes; Nick Parkinson; Hsun Tsai; Debra Brooker; Siobhan Mansell; Nigel K Spurr; A Jackie Hunter; Karen P Steel; Steve D M Brown
The homeobox gene Emx2 underlies middle ear and inner ear defects in the deaf mouse mutant pardon.
Journal of neurocytology 2003;32(9):1143-54.
2003: Philomena Mburu; Mirna Mustapha; Anabel Varela; Dominique Weil; Aziz El-Amraoui; Ralph H Holme; Andreas Rump; Rachel E Hardisty; Stéphane Blanchard; Roney Coimbra; Isabelle Perfettini; Nick Parkinson; Ann-Marie Mallon; Peter Glenister; Mike J Rogers; Adam J Paige; Lee Moir; Jo Clay; Andre Rosenthal; Xue Zhong Liu; Gonzalo Blanco; Karen P Steel; Christine Petit; Steve D M Brown
Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31.
Nature genetics 2003;34(4):421-8.
2003: Paul Denny; Elaine Hopes; Neill Gingles; Karl W Broman; William McPheat; John Morten; Janet Alexander; Peter W Andrew; Steve D M Brown
A major locus conferring susceptibility to infection by Streptococcus pneumoniae in mice.
Mammalian genome : official journal of the International Mammalian Genome Society 2003;14(7):448-53.
2003: John A Curtin; Elizabeth Quint; Vicky Tsipouri; Ruth Arkell; Bruce Cattanach; Andrew J Copp; Deborah J Henderson; Nigel K Spurr; Philip Stanier; Elizabeth M C Fisher; Patrick M Nolan; Karen P Steel; Steve D M Brown; Ian C Gray; Jennifer N Murdoch
Mutation of Celsr1 disrupts planar polarity of inner ear hair cells and causes severe neural tube defects in the mouse.
Current biology : CB 2003;13(13):1129-33.
2003: Rachel E Hardisty; Alexandra Erven; Karen Logan; Susan Morse; Sylvia Guionaud; Sara Sancho-Oliver; A Jackie Hunter; Steve D M Brown; Karen P Steel
The deaf mouse mutant Jeff (Jf) is a single gene model of otitis media.
Journal of the Association for Research in Otolaryngology : JARO 2003;4(2):130-8.
2003: Roger D Cox; Steve D M Brown
Rodent models of genetic disease.
Current opinion in genetics & development 2003;13(3):278-83.
2003: Adrian M Isaacs; Peter L Oliver; Emma L Jones; Alexander Jeans; Allyson Potter; Berit H Hovik; Patrick M Nolan; Lucie Vizor; Peter Glenister; A Katharina Simon; Ian C Gray; Nigel K Spurr; Steve D M Brown; A Jackie Hunter; Kay E Davies
A mutation in Af4 is predicted to cause cerebellar ataxia and cataracts in the robotic mouse.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2003;23(5):1631-7.
2003: Steve D M Brown; Rachel E Hardisty
Mutagenesis strategies for identifying novel loci associated with disease phenotypes.
Seminars in cell & developmental biology 2003;14(1):19-24.
2002: Tertius A Hough; Patrick M Nolan; Vicky Tsipouri; Ayo TOYE; Ian C Gray; Michelle Goldsworthy; Lee Moir; Roger D Cox; Sian Clements; Peter Glenister; John Wood; Rachael L Selley; Mark A Strivens; Lucie Vizor; Stefan L McCormack; Josephine Peters; Elizabeth M C Fisher; Nigel K Spurr; Sohaila Rastan; Joanne E Martin; Steve D M Brown; A Jackie Hunter
Novel phenotypes identified by plasma biochemical screening in the mouse.
Mammalian genome : official journal of the International Mammalian Genome Society 2002;13(10):595-602.
2002: Alexandra Erven; Michael J Skynner; Katsuzumi Okumura; Shin-ichiro Takebayashi; Steve D M Brown; Karen P Steel; Nicholas D Allen
A novel stereocilia defect in sensory hair cells of the deaf mouse mutant Tasmanian devil.
The European journal of neuroscience 2002;16(8):1433-41.
2002: Steve D M Brown
Whither the mouse genome?
Mammalian genome : official journal of the International Mammalian Genome Society 2002;13(9):481-2.
2002: Adrian M Isaacs; Alexander Jeans; Peter L Oliver; Lucie Vizor; Steve D M Brown; A Jackie Hunter; Kay E Davies
Identification of a new Pmp22 mouse mutant and trafficking analysis of a Pmp22 allelic series suggesting that protein aggregates may be protective in Pmp22-associated peripheral neuropathy.
Molecular and cellular neurosciences 2002;21(1):114-25.
2002: Ralph H Holme; Brent W Kiernan; Steve D M Brown; Karen P Steel
Elongation of hair cell stereocilia is defective in the mouse mutant whirler.
The Journal of comparative neurology 2002;450(1):94-102.
2002: Caroline Thaung; Katrine West; Brian J Clark; Lisa McKie; Joanne E Morgan; Karen Arnold; Patrick M Nolan; Jo Peters; A Jackie Hunter; Steve D M Brown; Ian J Jackson; Sally H Cross
Novel ENU-induced eye mutations in the mouse: models for human eye disease.
Human molecular genetics 2002;11(7):755-67.
2002: Joachim Klose; Christina Nock; Marion Herrmann; Kai Stühler; Katrin Marcus; Martin Blüggel; Eberhard Krause; Leonard C Schalkwyk; Sohaila Rastan; Steve D M Brown; Konrad Büssow; Heinz Himmelbauer; Hans Lehrach
Genetic analysis of the mouse brain proteome.
Nature genetics 2002;30(4):385-93.
2002: Amy E Kiernan; Alexandra Erven; Stéphanie Voegeling; Jo Peters; Pat Nolan; Jackie Hunter; Yvonne Bacon; Karen P Steel; Steve D M Brown; Jean-Louis Guénet
ENU mutagenesis reveals a highly mutable locus on mouse Chromosome 4 that affects ear morphogenesis.
Mammalian genome : official journal of the International Mammalian Genome Society 2002;13(3):142-8.
2002: Emma L Coghill; Alison Hugill; Nick Parkinson; Claire Davison; Peter Glenister; Sian Clements; Jackie Hunter; Roger D Cox; Steve D M Brown
A gene-driven approach to the identification of ENU mutants in the mouse.
Nature genetics 2002;30(3):255-6.
2002: Nick Parkinson; Steve D M Brown
Focusing on the genetics of hearing: you ain't heard nothin' yet.
Genome biology 2002;3(6):COMMENT2006.
2001: C Hayes; A Rump; Matthew Cadman; M Harrison; E P Evans; Mary F Lyon; Gillian M Morriss-Kay; A Rosenthal; Steve D M Brown
A high-resolution genetic, physical, and comparative gene map of the doublefoot (Dbf) region of mouse chromosome 1 and the region of conserved synteny on human chromosome 2q35.
Genomics 2001;78(3):197-205.
2001: Thomas J Hudson; Deanna M Church; S Greenaway; H Nguyen; A Cook; RG Steen; WJ Van Etten; A B Castle; Mark A Strivens; P Trickett; C Heuston; C Davison; A Southwell; R Hardisty; A Varela-Carver; AR Haynes; P Rodriguez-Tome; H Doi; Minoru S H Ko; Joan U Pontius; Lynn M Schriml; L Wagner; Donna R Maglott; Steve D M Brown; Eric S Lander; Gerold Schuler; Paul Denny
A radiation hybrid map of mouse genes.
Nature genetics 2001;29(2):201-5.
2001: Ruth Arkell; Matthew Cadman; T Marsland; A Southwell; Caroline Thaung; J R Davies; T Clay; Colin V Beechey; E P Evans; Mark A Strivens; Steve D M Brown; Paul Denny
Genetic, physical, and phenotypic characterization of the Del(13)Svea36H mouse.
Mammalian genome : official journal of the International Mammalian Genome Society 2001;12(9):687-94.
2001: Steve D M Brown; R Balling
Systematic approaches to mouse mutagenesis.
Current opinion in genetics & development 2001;11(3):268-73.
2001: Xiaojun Liu; Fiona Oliver; Steve D M Brown; Paul Denny; Peter D Keightley
High-resolution quantitative trait locus mapping for body weight in mice by recombinant progeny testing.
Genetical research 2001;77(2):191-7.
2001: H Tsai; Rachel E Hardisty; C Rhodes; Amy E Kiernan; P Roby; Zuzanna Tymowska-Lalanne; Philomena Mburu; Sohaila Rastan; A Jackie Hunter; Steve D M Brown; Karen P Steel
The mouse slalom mutant demonstrates a role for Jagged1 in neuroepithelial patterning in the organ of Corti.
Human molecular genetics 2001;10(5):507-12.
2001: P T Todorov; Rachel E Hardisty; Steve D M Brown
Myosin VIIA is specifically associated with calmodulin and microtubule-associated protein-2B (MAP-2B).
The Biochemical journal 2001;354(Pt 2):267-74.
2001: G Blanco; Gary Coulton; A Biggin; C Grainge; J Moss; M Barrett; A Berquin; G Maréchal; M Skynner; P van Mier; A Nikitopoulou; M Kraus; C P Ponting; R M Mason; Steve D M Brown
The kyphoscoliosis (ky) mouse is deficient in hypertrophic responses and is caused by a mutation in a novel muscle-specific protein.
Human molecular genetics 2001;10(1):9-16.
2000: Dónal O'Carroll; Harry Scherthan; Antoine H F M Peters; Susanne Opravil; AR Haynes; G Laible; S Rea; M Schmid; A Lebersorger; Martin Jerratsch; L Sattler; M G Mattei; Paul Denny; Steve D M Brown; Dieter Schweizer; Thomas Jenuwein
Isolation and characterization of Suv39h2, a second histone H3 methyltransferase gene that displays testis-specific expression.
Molecular and cellular biology 2000;20(24):9423-33.
2000: Adrian M Isaacs; Kay E Davies; A Jackie Hunter; Patrick M Nolan; Lucie Vizor; Jo Peters; D G Gale; David P Kelsell; I D Latham; J M Chase; Elizabeth M C Fisher; MM Bouzyk; Allyson Potter; M Masih; Frank S Walsh; M A Sims; K E Doncaster; C A Parsons; J Martin; Steve D M Brown; Sohaila Rastan; Nigel K Spurr; Ian C Gray
Identification of two new Pmp22 mouse mutants using large-scale mutagenesis and a novel rapid mapping strategy.
Human molecular genetics 2000;9(12):1865-71.
2000: Mark A Strivens; R L Selley; S J Greenaway; M Hewitt; X Liu; K Battershill; S L McCormack; K A Pickford; Lucie Vizor; Patrick M Nolan; A Jackie Hunter; Jo Peters; Steve D M Brown
Informatics for mutagenesis: the design of mutabase--a distributed data recording system for animal husbandry, mutagenesis, and phenotypic analysis.
Mammalian genome : official journal of the International Mammalian Genome Society 2000;11(7):577-83.
2000: Patrick M Nolan; Jo Peters; Lucie Vizor; Mark A Strivens; R Washbourne; Tertius A Hough; C Wells; Peter Glenister; C Thornton; J Martin; E Fisher; D Rogers; J Hagan; Charlie Reavill; Ian C Gray; John Wood; Nigel K Spurr; M Browne; Sohaila Rastan; Jackie Hunter; Steve D M Brown
Implementation of a large-scale ENU mutagenesis program: towards increasing the mouse mutant resource.
Mammalian genome : official journal of the International Mammalian Genome Society 2000;11(7):500-6.
2000: C Wells; Steve D M Brown
Genomics meets genetics: towards a mutant map of the mouse.
Mammalian genome : official journal of the International Mammalian Genome Society 2000;11(7):472-7.
2000: Xue Zhong Liu; Steve D M Brown
Sensorineural hearing impairment: non-syndromic, recessive DFNB2.
Advances in oto-rhino-laryngology 2000;56():124-30.
2000: A J Paige; Brent W Kiernan; A Varela; M J Rogers; D Hughes; Karen P Steel; Steve D M Brown
A deletion on chromosome 4 cosegregates with the whirler deafness mutation: exclusion of Orm1 as a candidate.
Mammalian genome : official journal of the International Mammalian Genome Society 2000;11(1):51-7.
2000: Xue Zhong Liu; Xia Juan Xia; Li Rong Xu; Arti Pandya; C Y Liang; S Blanton; Steve D M Brown; Karen P Steel; Walter E Nance
Mutations in connexin31 underlie recessive as well as dominant non-syndromic hearing loss.
Human molecular genetics 2000;9(1):63-7.
1999: Rachel E Hardisty; Philomena Mburu; Steve D M Brown
ENU mutagenesis and the search for deafness genes.
British journal of audiology 1999;33(5):279-83.
1999: X Y Liu; Andrew W Dangel; Richard I Kelley; W Zhao; Paul Denny; M Botcherby; Bruce Cattanach; Jo Peters; P R Hunsicker; Ann-Marie Mallon; Mark A Strivens; R Bate; Webb Miller; M Rhodes; Steve D M Brown; Gail E Herman
The gene mutated in bare patches and striated mice encodes a novel 3beta-hydroxysteroid dehydrogenase.
Nature genetics 1999;22(2):182-7.
1999: M J Rogers; J Fleming; Brent W Kiernan; Philomena Mburu; A Varela; Steve D M Brown; Karen P Steel
Genetic mapping of the whirler mutation.
Mammalian genome : official journal of the International Mammalian Genome Society 1999;10(5):513-9.
1999: Xue Zhong Liu; CI Hope; C Y Liang; J M Zou; Li Rong Xu; T Cole; Robert F Mueller; SE Bundey; Walter E Nance; Karen P Steel; Steve D M Brown
A mutation (2314delG) in the Usher syndrome type IIA gene: high prevalence and phenotypic variation.
American journal of human genetics 1999;64(4):1221-5.
1999: G Laible; AR Haynes; A Lebersorger; Dónal O'Carroll; M G Mattei; Paul Denny; Steve D M Brown; Thomas Jenuwein
The murine polycomb-group genes Ezh1 and Ezh2 map close to Hox gene clusters on mouse chromosomes 11 and 6.
Mammalian genome : official journal of the International Mammalian Genome Society 1999;10(3):311-4.
1998: G Blanco; A Nikitopoulou; M Kraus; R M Mason; Gary Coulton; Steve D M Brown
A STS content physical and transcription map across the ky, kyphoscoliosis, nonrecombinant region.
Genomics 1998;54(3):415-23.
1998: Xue Zhong Liu; CI Hope; J Walsh; VE Newton; X M Ke; C Y Liang; Li Rong Xu; J M Zhou; D Trump; Karen P Steel; SE Bundey; Steve D M Brown
Mutations in the myosin VIIA gene cause a wide phenotypic spectrum, including atypical Usher syndrome.
American journal of human genetics 1998;63(3):909-12.
1998: Steve D M Brown
Mouse models of genetic disease: new approaches, new paradigms.
Journal of inherited metabolic disease 1998;21(5):532-9.
1998: G Blanco; NG Irving; Steve D M Brown; Christopher C J Miller; Declan McLoughlin
Mapping of the human and murine X11-like genes (APBA2 and apba2), the murine Fe65 gene (Apbb1), and the human Fe65-like gene (APBB2): genes encoding phosphotyrosine-binding domain proteins that interact with the Alzheimer's disease amyloid precursor protein.
Mammalian genome : official journal of the International Mammalian Genome Society 1998;9(6):473-5.
1998: T Self; M Mahony; J Fleming; J Walsh; Steve D M Brown; Karen P Steel
Shaker-1 mutations reveal roles for myosin VIIA in both development and function of cochlear hair cells.
Development (Cambridge, England) 1998;125(4):557-66.
1998: Steve D M Brown; P M Nolan
Mouse mutagenesis-systematic studies of mammalian gene function.
Human molecular genetics 1998;7(10):1627-33.
1997: Mark A Strivens; P Middlehurst; Steve D M Brown; Paul Denny
HOSEpipe--a WWW-hosted data management and analysis system for STS content mapping projects.
Mammalian genome : official journal of the International Mammalian Genome Society 1997;8(7):467-71.
1997: Philomena Mburu; Xue Zhong Liu; J Walsh; D Saw; M J Cope; F Gibson; J Kendrick-Jones; Karen P Steel; Steve D M Brown
Mutation analysis of the mouse myosin VIIA deafness gene.
Genes and function 1997;1(3):191-203.
1997: Xue Zhong Liu; J Walsh; Philomena Mburu; J Kendrick-Jones; M J Cope; Karen P Steel; Steve D M Brown
Mutations in the myosin VIIA gene cause non-syndromic recessive deafness.
Nature genetics 1997;16(2):188-90.
1997: Karen P Steel; Philomena Mburu; F Gibson; J Walsh; A Varela; K Brown; T Self; M Mahony; J Fleming; A Pearce; D Harvey; J Cable; Steve D M Brown
Unravelling the genetics of deafness.
The Annals of otology, rhinology & laryngology. Supplement 1997;168():59-62.
1997: Xue Zhong Liu; VE Newton; Karen P Steel; Steve D M Brown
Identification of a new mutation of the myosin VII head region in Usher syndrome type 1.
Human mutation 1997;10(2):168-70.
1997: G Lévy; F Levi-Acobas; Stéphane Blanchard; S Gerber; D Larget-Piet; V Chenal; Xue Zhong Liu; VE Newton; Karen P Steel; Steve D M Brown; Arnold Munnich; J Kaplan; Christine Petit; Dominique Weil
Myosin VIIA gene: heterogeneity of the mutations responsible for Usher syndrome type IB.
Human molecular genetics 1997;6(1):111-6.
1996: Karen P Steel; Steve D M Brown
Genetics of deafness.
Current opinion in neurobiology 1996;6(4):520-5.
1996: B de Gouyon; A Chatterjee; A Monaco; N Quaderi; Steve D M Brown; Gail E Herman
Comparative mapping on the mouse X chromosome defines a myotubular myopathy equivalent region.
Mammalian genome : official journal of the International Mammalian Genome Society 1996;7(8):575-9.
1996: Maurizio D'Esposito; N A Quaderi; Alfredo Ciccodicola; P Bruni; Teresa Esposito; Michele D'Urso; Steve D M Brown
Isolation, physical mapping, and northern analysis of the X-linked human gene encoding methyl CpG-binding protein, MECP2.
Mammalian genome : official journal of the International Mammalian Genome Society 1996;7(7):533-5.
1996: J Fleming; A Pearce; Steve D M Brown; Karen P Steel
The Sp4H deletion may contain a new locus essential for postimplantation development.
Genomics 1996;34(2):205-12.
1996: S Matsuura; V Episkopou; R Hamvas; Steve D M Brown
Xist expression from an Xist YAC transgene carried on the mouse Y chromosome.
Human molecular genetics 1996;5(4):451-9.
1996: P Mileham; Steve D M Brown
YAC clone contigs covering 5 Mb of a repeat sequence island on the mouse X chromosome.
Mammalian genome : official journal of the International Mammalian Genome Society 1996;7(4):253-61.
1996: M K Maconochie; A H Simpkins; E Damien; G Coulton; A J Greenfield; Steve D M Brown
The cysteine-rich and C-terminal domains of dystrophin are not required for normal costameric localization in the mouse.
Transgenic research 1996;5(2):123-30.
1995: N A Quaderi; Fernando Gianfrancesco; Steve D M Brown; Michele D'Urso; Maurizio D'Esposito
Genetic mapping of a gene encoding an atypical protein kinase C, protein kinase C lambda, to the proximal region of mouse chromosome 3.
Genomics 1995;29(3):815-6.
1995: D A Adler; N A Quaderi; Steve D M Brown; Verne M Chapman; J Moore; P Tate; Christine M Disteche
The X-linked methylated DNA binding protein, Mecp2, is subject to X inactivation in the mouse.
Mammalian genome : official journal of the International Mammalian Genome Society 1995;6(8):491-2.
1995: F Gibson; J Walsh; Philomena Mburu; A Varela; K A Brown; M Antonio; K W Beisel; Karen P Steel; Steve D M Brown
A type VII myosin encoded by the mouse deafness gene shaker-1.
Nature 1995;374(6517):62-4.
1994: N A Quaderi; Richard Meehan; P H Tate; Sally H Cross; Adrian P Bird; A Chatterjee; G E Herman; Steve D M Brown
Genetic and physical mapping of a gene encoding a methyl CpG binding protein, Mecp2, to the mouse X chromosome.
Genomics 1994;22(3):648-51.
1994: J Fleming; M J Rogers; Steve D M Brown; Karen P Steel
Linkage analysis of the whirler deafness gene on mouse chromosome 4.
Genomics 1994;21(1):42-8.
1994: K A Brown; M J Sutcliffe; Karen P Steel; Steve D M Brown
Sequencing of the olfactory marker protein gene in normal and shaker-1 mutant mice.
Mammalian genome : official journal of the International Mammalian Genome Society 1994;5(1):11-4.
1994: Steve D M Brown; A H Carey
Chromosome dissection and cloning.
Methods in molecular biology (Clifton, N.J.) 1994;29():425-36.
1994: Steve D M Brown; K P Steel
Genetic deafness--progress with mouse models.
Human molecular genetics 1994;3 Spec No():1453-6.
1994: Gail E Herman; Y Boyd; Verne M Chapman; A Chatterjee; Steve D M Brown
Mouse X chromosome.
Mammalian genome : official journal of the International Mammalian Genome Society 1994;5 Spec No():S276-88.
1993: Steve D M Brown; F Chartier; K Johnson; J S Cavanna
Mapping the Hrc gene to proximal mouse chromosome 7: delineation of a conserved linkage group with human 19q.
Genomics 1993;18(2):459-61.
1993: R M Hamvas; Z Larin; Neil Brockdorff; S Rastan; H Lehrach; F L Chartier; Steve D M Brown
YAC clone contigs surrounding the Zfx and Pola loci on the mouse X chromosome.
Genomics 1993;17(1):52-8.
1993: P Cooper; J T Keer; V M McCabe; R M Hamvas; Steve D M Brown; S Rastan; Neil Brockdorff
Physical mapping of 2000 kb of the mouse X chromosome in the vicinity of the Xist locus.
Genomics 1993;15(3):570-5.
1993: Steve D M Brown; Philip Avner; Y Boyd; Verne M Chapman; S Rastan; L Sefton; J D Thomas; G E Herman
Encyclopedia of the mouse genome III. October 1993. Mouse X chromosome.
Mammalian genome : official journal of the International Mammalian Genome Society 1993;4 Spec No():S269-81.
1993: U Gangadharan; M K Maconochie; K E Davies; Steve D M Brown
Isolation and characterization of a genomic clone from the murine utrophin locus.
Mammalian genome : official journal of the International Mammalian Genome Society 1993;4(10):608-11.
1992: Steve D M Brown
The Mouse Genome Project and human genetics. A report from the 5th International Mouse Genome Mapping Workshop, Lunteren, Holland.
Genomics 1992;13(2):490-2.
1992: K A Brown; M J Sutcliffe; Karen P Steel; Steve D M Brown
Close linkage of the olfactory marker protein gene to the mouse deafness mutation shaker-1.
Genomics 1992;13(1):189-93.
1992: F L Chartier; J T Keer; M J Sutcliffe; D A Henriques; P Mileham; Steve D M Brown
Construction of a mouse yeast artificial chromosome library in a recombination-deficient strain of yeast.
Nature genetics 1992;1(2):132-6.
1992: R M Hamvas; A Zinn; J T Keer; Elizabeth M C Fisher; P Beer-Romero; Steve D M Brown; David C Page
Rps4 maps near the inactivation center on the mouse X chromosome.
Genomics 1992;12(2):363-7.
1992: R M Hamvas; Wolf Reik; S J Gaunt; Steve D M Brown; P B Singh
Mapping of a mouse homolog of a heterochromatin protein gene the X chromosome.
Mammalian genome : official journal of the International Mammalian Genome Society 1992;2(1):72-5.
1992: M K Maconochie; Steve D M Brown; A J Greenfield
Sequence analysis of two exons from the murine dystrophin locus.
Mammalian genome : official journal of the International Mammalian Genome Society 1992;2(1):64-8.
1992: Steve D M Brown; Philip Avner; G E Herman
Mouse X chromosome.
Mammalian genome : official journal of the International Mammalian Genome Society 1992;3 Spec No():S274-88.
1991: N G Irving; Steve D M Brown
Mouse chromosome-specific markers generated by PCR and their mapping through interspecific backcrosses.
Genomics 1991;11(3):679-86.
1991: J Nasir; M K Maconochie; Steve D M Brown
Co-amplification of L1 line elements with localised low copy repeats in Giemsa dark bands: implications for genome organisation.
Nucleic acids research 1991;19(12):3255-60.
1991: Neil Brockdorff; G Kay; S Smith; J T Keer; R M Hamvas; Steve D M Brown; S Rastan
High-density molecular map of the central span of the mouse X chromosome.
Genomics 1991;10(1):17-22.
1991: N G Irving; John Hardy; Steve D M Brown
The multipoint genetic mapping of mouse chromosome 16.
Genomics 1991;9(2):386-9.
1991: Steve D M Brown; K A Brown; M J Sutcliffe; J S Cavanna; A J Greenfield; Karen P Steel
Reverse genetic approaches to cloning deafness genes.
Annals of the New York Academy of Sciences 1991;630():93-9.
1991: Steve D M Brown; Philip Avner; Verne M Chapman; R M Hamvas; G E Herman
Mouse X chromosome.
Mammalian genome : official journal of the International Mammalian Genome Society 1991;1 Spec No():S318-31.
1990: J T Keer; R M Hamvas; Neil Brockdorff; D Page; S Rastan; Steve D M Brown
Genetic mapping in the region of the mouse X-inactivation center.
Genomics 1990;7(4):566-72.
1990: J S Cavanna; A J Greenfield; keith jack johnson; A R Marks; B Nadal-Ginard; Steve D M Brown
Establishment of the mouse chromosome 7 region with homology to the myotonic dystrophy region of human chromosome 19q.
Genomics 1990;7(1):12-8.
1990: J Nasir; Elizabeth M C Fisher; Neil Brockdorff; C M Disteche; M F Lyon; Steve D M Brown
Unusual molecular characteristics of a repeat sequence island within a Giemsa-positive band on the mouse X chromosome.
Proceedings of the National Academy of Sciences of the United States of America 1990;87(1):399-403.
1989: N G Irving; John Hardy; N Bahary; J M Friedman; Steve D M Brown
The alpha 2 chain of type 1 collagen does not map to mouse chromosome 16 but maps close to the Met proto-oncogene on mouse chromosome 6.
Cytogenetics and cell genetics 1989;50(2-3):121-2.
1988: J S Cavanna; G Coulton; J E Morgan; Neil Brockdorff; S M Forrest; K E Davies; Steve D M Brown
Molecular and genetic mapping of the mouse mdx locus.
Genomics 1988;3(4):337-41.
1988: Neil Brockdorff; Elizabeth M C Fisher; Stuart H Orkin; M F Lyon; Steve D M Brown
Localization of the human X-linked gene for chronic granulomatous disease to the mouse X chromosome: implications for X-chromosome evolution.
Cytogenetics and cell genetics 1988;48(2):124-5.
1987: Neil Brockdorff; Elizabeth M C Fisher; J S Cavanna; M F Lyon; Steve D M Brown
Construction of a detailed molecular map of the mouse X chromosome by microcloning and interspecific crosses.
The EMBO journal 1987;6(11):3291-7.
1987: Neil Brockdorff; G S Cross; J S Cavanna; Elizabeth M C Fisher; M F Lyon; K E Davies; Steve D M Brown
The mapping of a cDNA from the human X-linked Duchenne muscular dystrophy gene to the mouse X chromosome.
Nature 1987;328(6126):166-8.
1985: Elizabeth M C Fisher; J S Cavanna; Steve D M Brown
Microdissection and microcloning of the mouse X chromosome.
Proceedings of the National Academy of Sciences of the United States of America 1985;82(17):5846-9.