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Steve Brown
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26
Steel, Karen
14
Hunter, Jackie
11
Fisher, Elizabeth
10
Liu, Xue Zhong
10
Nolan, Patrick
9
Mburu, Philomena
9
Brockdorff, Neil
9
Vizor, Lucie
8
Strivens, Mark
8
Spurr, Nigel
7
Glenister, Peter
6
Gray, Ian
6
Hardisty, Rachel
6
Parkinson, Nick
5
Hough, Tertius
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All Publications
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2009: Alagramam Kumar N; Brown Steve D M; Davis Rickie R; Johnson Ken R; Jones Sherri M; Macauley John B; Zheng Qing Yin; Zuo Jian
Foreword for special issue: mouse models for hearing research.
Brain research 2009;1277():1-2.
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2009: Schofield Paul N; Brown Steve D M; Sundberg John P; Arends Mark; Warren Madhuri V; Dubus Pierre; Ellender Michele; Fiette Laurence; Rozell Bjorn; Quintanilla-Martinez Leticia; Raspa Marcello; Song Ji-Ying; van der Valk Martin; McKerlie Colin
PRIME importance of pathology expertise.
Nature biotechnology 2009;27(1):24-5.
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2008: Mandillo Silvia; Tucci Valter; Hölter Sabine M; Meziane Hamid; Banchaabouchi Mumna Al; Kallnik Magdalena; Lad Heena V; Nolan Patrick M; Ouagazzal Abdel-Mouttalib; Coghill Emma L; Gale Karin; Golini Elisabetta; Jacquot Sylvie; Krezel Wojtek; Parker Andy; Riet Fabrice; Schneider Ilka; Marazziti Daniela; Auwerx Johan; Brown Steve D M; Chambon Pierre; Rosenthal Nadia; Tocchini-Valentini Glauco; Wurst Wolfgang
Reliability, robustness, and reproducibility in mouse behavioral phenotyping: a cross-laboratory study.
Physiological genomics 2008;34(3):243-55.
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2008: Brown Steve D M; Hardisty-Hughes Rachel E; Mburu Philomena
Quiet as a mouse: dissecting the molecular and genetic basis of hearing.
Nature reviews. Genetics 2008;9(4):277-90.
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2008: Groszer Matthias; Keays David A; Deacon Robert M J; de Bono Joseph P; Prasad-Mulcare Shweta; Gaub Simone; Baum Muriel G; French Catherine A; Nicod Jérôme; Coventry Julie A; Enard Wolfgang; Fray Martin; Brown Steve D M; Nolan Patrick M; Pääbo Svante; Channon Keith M; Costa Rui M; Eilers Jens; Ehret Günter; Rawlins J Nicholas P; Fisher Simon E
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.
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2008: Barbaric Ivana; Perry Mark J; Dear T Neil; Rodrigues Da Costa Alexandra; Salopek Daniela; Marusic Ana; Hough Tertius; Wells Sara; Hunter A Jackie; Cheeseman Michael; Brown Steve D M
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.
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2008: Acevedo-Arozena Abraham; Wells Sara; Potter Paul; Kelly Michelle; Cox Roger D; Brown Steve D M
ENU mutagenesis, a way forward to understand gene function.
Annual review of genomics and human genetics 2008;9():49-69.
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2007: Hough Tertius A; Polewski Monika; Johnson Kristen; Cheeseman Michael; Nolan Patrick M; Vizor Lucie; Rastan Sohaila; Boyde Alan; Pritzker Kenneth; Hunter A Jackie; Fisher Elizabeth M C; Terkeltaub Robert; Brown Steve D M
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.
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2007: Keays David A; Tian Guoling; Poirier Karine; Huang Guo-Jen; Siebold Christian; Cleak James; Oliver Peter L; Fray Martin; Harvey Robert J; Molnár Zoltán; Piñon Maria C; Dear Neil; Valdar William; Brown Steve D M; Davies Kay E; Rawlins J Nicholas P; Cowan Nicholas J; Nolan Patrick; Chelly Jamel; Flint Jonathan
Mutations in alpha-tubulin cause abnormal neuronal migration in mice and lissencephaly in humans.
Cell 2007;128(1):45-57.
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2006: Tucci Valter; Lad Heena V; Parker Andy; Polley Sian; Brown Steve D M; Nolan Patrick M
Gene-environment interactions differentially affect mouse strain behavioral parameters.
Mammalian genome : official journal of the International Mammalian Genome Society 2006;17(11):1113-20.
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2006: Hardisty-Hughes Rachel E; Tateossian Hilda; Morse Susan A; Romero M Rosario; Middleton Alice; Tymowska-Lalanne Zuzanna; Hunter A Jackie; Cheeseman Michael; Brown Steve D M
A mutation in the F-box gene, Fbxo11, causes otitis media in the Jeff mouse.
Human molecular genetics 2006;15(22):3273-9.
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2006: Parkinson Nicholas; Hardisty-Hughes Rachel E; Tateossian Hilda; Tsai Hsun-Tien; Brooker Debra; Morse Sue; Lalane Zuzanna; MacKenzie Francesca; Fray Martin; Glenister Pete; Woodward Anne-Marie; Polley Sian; Barbaric Ivana; Dear Neil; Hough Tertius A; Hunter A Jackie; Cheeseman Michael T; Brown Steve D M
Mutation at the Evi1 locus in Junbo mice causes susceptibility to otitis media.
PLoS genetics 2006;2(10):e149.
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2006: Brown Steve D M; Hancock John M; Gates Hilary
Understanding mammalian genetic systems: the challenge of phenotyping in the mouse.
PLoS genetics 2006;2(8):e118.
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2006: Segade Fernando; Daly Kathleen A; Allred Dax; Hicks Pamela J; Cox Miranda; Brown Mark; Hardisty-Hughes Rachel E; Brown Steve D M; Rich Stephen S; Bowden Donald W
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.
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2006: Mburu Philomena; Kikkawa Yoshiaki; Townsend Stuart; Romero Rosario; Yonekawa Hiromichi; Brown Steve D M
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.
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2006: Zheng Qing Yin; Hardisty-Hughes Rachel; Brown Steve D M
Mouse models as a tool to unravel the genetic basis for human otitis media.
Brain research 2006;1091(1):9-15.
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2005: Rubinsztein David C; Ravikumar Brinda; Acevedo-Arozena Abraham; Imarisio Sara; O'Kane Cahir J; Brown Steve D M
Dyneins, autophagy, aggregation and neurodegeneration.
Autophagy 2005;1(3):177-8.
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2005: Bogani Debora; Willoughby Catherine; Davies Jennifer; Kaur Kulvinder; Mirza Ghazala; Paudyal Anju; Haines Heather; McKeone Richard; Cadman Matthew; Pieles Guido; Schneider Jürgen E; Bhattacharya Shoumo; Hardy Andrea; Nolan Patrick M; Tripodis Nikos; Depew Michael J; Chandrasekara Ramya; Duncan Gimara; Sharpe Paul T; Greenfield Andy; Denny Paul; Brown Steve D M; Ragoussis Jiannis; Arkell Ruth M
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.
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2005: Ravikumar Brinda; Acevedo-Arozena Abraham; Imarisio Sara; Berger Zdenek; Vacher Coralie; O'Kane Cahir J; Brown Steve D M; Rubinsztein David C
Dynein mutations impair autophagic clearance of aggregate-prone proteins.
Nature genetics 2005;37(7):771-6.
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2005: Oliver Fiona; Christians Julian K; Liu Xiaojun; Rhind Susan; Verma Vinesh; Davison Claire; Brown Steve D M; Denny Paul; Keightley Peter D
Regulatory variation at glypican-3 underlies a major growth QTL in mice.
PLoS biology 2005;3(5):e135.
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2005: Ouyang Xiao Mei; Yan Denise; Du Li Lin; Hejtmancik J Fielding; Jacobson Samuel G; Nance Walter E; Li An Ren; Angeli Simon; Kaiser Muriel; Newton Valerie; Brown Steve D M; Balkany Thomas; Liu Xue Zhong
Characterization of Usher syndrome type I gene mutations in an Usher syndrome patient population.
Human genetics 2005;116(4):292-9.
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2005: Kikkawa Yoshiaki; Mburu Philomena; Morse Sue; Kominami Ryo; Townsend Stuart; Brown Steve D M
Mutant analysis reveals whirlin as a dynamic organizer in the growing hair cell stereocilium.
Human molecular genetics 2005;14(3):391-400.
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2004: Mallon Ann-Marie; Wilming Laurens; Weekes Joseph; Gilbert James G R; Ashurst Jennifer; Peyrefitte Sandrine; Matthews Lucy; Cadman Matthew; McKeone Richard; Sellick Chris A; Arkell Ruth; Botcherby Marc R M; Strivens Mark A; Campbell R Duncan; Gregory Simon; Denny Paul; Hancock John M; Rogers Jane; Brown Steve D M
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.
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2004: Quwailid Mohamed Mohideen; Hugill Alison; Dear Neil; Vizor Lucie; Wells Sara; Horner Emma; Fuller Shelly; Weedon Jessica; McMath Hamish; Woodman Paul; Edwards David; Campbell David; Rodger Susan; Carey Joanne; Roberts Ann; Glenister Pete; Lalanne Zuzanna; Parkinson Nick; Coghill Emma L; McKeone Richard; Cox Sam; Willan John; Greenfield Andy; Keays David; Brady Saffron; Spurr Nigel; Gray Ian; Hunter Jackie; Brown Steve D M; Cox Roger D
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.
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2004: Blanco G; Pritchard C; Underhill P; Breeds S; Townsend K M F; Greenfield A; Brown Steve D M
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.
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2004: Tsipouri Vicky; Curtin John A; Nolan Pat M; Vizor Lucie; Parsons Claire A; Clapham Colin M; Latham Ian D; Rooke Lesley J; Martin Jo E; Peters Jo; Hunter A Jackie; Rogers Derek; Rastan Sohaila; Brown Steve D M; Fisher Elizabeth M C; Spurr Nigel K; Gray Ian C
Three Novel Pigmentation Mutants Generated by Genome-Wide Random ENU Mutagenesis in the Mouse.
Comparative and functional genomics 2004;5(2):123-7.
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2004: Holmes Chris; Brown Steve D M
All systems GO for understanding mouse gene function.
Journal of biology 2004;3(5):20.
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2003: Rhodes Charlotte R; Parkinson Nicholas; Tsai Hsun; Brooker Debra; Mansell Siobhan; Spurr Nigel; Hunter A Jackie; Steel Karen P; Brown Steve D M
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.
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2003: Mburu Philomena; Mustapha Mirna; Varela Anabel; Weil Dominique; El-Amraoui Aziz; Holme Ralph H; Rump Andreas; Hardisty Rachel E; Blanchard Stéphane; Coimbra Roney S; Perfettini Isabelle; Parkinson Nick; Mallon Ann-Marie; Glenister Pete; Rogers Mike J; Paige Adam J; Moir Lee; Clay Jo; Rosenthal Andre; Liu Xue Zhong; Blanco Gonzalo; Steel Karen P; Petit Christine; Brown Steve D M
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.
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2003: Denny Paul; Hopes Elaine; Gingles Neill; Broman Karl W; McPheat William; Morten John; Alexander Janet; Andrew Peter W; Brown Steve D M
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.
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2003: Curtin John A; Quint Elizabeth; Tsipouri Vicky; Arkell Ruth M; Cattanach Bruce; Copp Andrew J; Henderson Deborah J; Spurr Nigel; Stanier Philip; Fisher Elizabeth M; Nolan Patrick M; Steel Karen P; Brown Steve D M; Gray Ian C; Murdoch Jennifer N
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.
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2003: Hardisty Rachel E; Erven Alexandra; Logan Karen; Morse Susan; Guionaud Sylvia; Sancho-Oliver Sara; Hunter A Jackie; Brown Steve D M; Steel Karen P
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.
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2003: Cox Roger D; Brown Steve D M
Rodent models of genetic disease.
Current opinion in genetics & development 2003;13(3):278-83.
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2003: Isaacs Adrian M; Oliver Peter L; Jones Emma L; Jeans Alexander; Potter Allyson; Hovik Berit H; Nolan Patrick M; Vizor Lucie; Glenister Peter; Simon A Katharina; Gray Ian C; Spurr Nigel K; Brown Steve D M; Hunter A Jackie; Davies Kay E
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.
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2003: Brown Steve D M; Hardisty Rachel E
Mutagenesis strategies for identifying novel loci associated with disease phenotypes.
Seminars in cell & developmental biology 2003;14(1):19-24.
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2002: Hough Tertius A; Nolan Patrick M; Tsipouri Vicky; Toye Ayo A; Gray Ian C; Goldsworthy Michelle; Moir Lee; Cox Roger D; Clements Sian; Glenister Peter H; Wood John; Selley Rachael L; Strivens Mark A; Vizor Lucie; McCormack Stefan L; Peters Josephine; Fisher Elizabeth M; Spurr Nigel; Rastan Sohaila; Martin Joanne E; Brown Steve D M; Hunter A Jacqueline
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.
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2002: Erven Alexandra; Skynner Michael J; Okumura Katsuzumi; Takebayashi Shin-ichiro; Brown Steve D M; Steel Karen P; Allen Nicholas D
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.
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2002: Brown Steve D M
Whither the mouse genome?
Mammalian genome : official journal of the International Mammalian Genome Society 2002;13(9):481-2.
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2002: Isaacs Adrian M; Jeans Alexander; Oliver Peter L; Vizor Lucie; Brown Steve D M; Hunter A Jackie; Davies Kay E
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.
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2002: Holme Ralph H; Kiernan Brent W; Brown Steve D M; Steel Karen P
Elongation of hair cell stereocilia is defective in the mouse mutant whirler.
The Journal of comparative neurology 2002;450(1):94-102.
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2002: Thaung Caroline; West Katrine; Clark Brian J; McKie Lisa; Morgan Joanne E; Arnold Karen; Nolan Patrick M; Peters Jo; Hunter A Jackie; Brown Steve D M; Jackson Ian J; Cross Sally H
Novel ENU-induced eye mutations in the mouse: models for human eye disease.
Human molecular genetics 2002;11(7):755-67.
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2002: Klose Joachim; Nock Christina; Herrmann Marion; Stühler Kai; Marcus Katrin; Blüggel Martin; Krause Eberhard; Schalkwyk Leonard C; Rastan Sohaila; Brown Steve D M; Büssow Konrad; Himmelbauer Heinz; Lehrach Hans
Genetic analysis of the mouse brain proteome.
Nature genetics 2002;30(4):385-93.
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2002: Kiernan Amy E; Erven Alexandra; Voegeling Stéphanie; Peters Jo; Nolan Pat; Hunter Jackie; Bacon Yvonne; Steel Karen P; Brown Steve D M; Guénet Jean-Louis
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.
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2002: Coghill Emma L; Hugill Alison; Parkinson Nick; Davison Claire; Glenister Peter; Clements Sian; Hunter Jackie; Cox Roger D; Brown Steve D M
A gene-driven approach to the identification of ENU mutants in the mouse.
Nature genetics 2002;30(3):255-6.
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2002: Parkinson Nick; Brown Steve D M
Focusing on the genetics of hearing: you ain't heard nothin' yet.
Genome biology 2002;3(6):COMMENT2006.
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2001: Hayes C; Rump A; Cadman M R; Harrison M; Evans E P; Lyon M F; Morriss-Kay G M; Rosenthal A; Brown S D
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.
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2001: Hudson T J; Church D M; Greenaway S; Nguyen H; Cook A; Steen R G; Van Etten W J; Castle A B; Strivens M A; Trickett P; Heuston C; Davison C; Southwell A; Hardisty R; Varela-Carver A; Haynes A R; Rodriguez-Tome P; Doi H; Ko M S; Pontius J; Schriml L; Wagner L; Maglott D; Brown S D; Lander E S; Schuler G; Denny P
A radiation hybrid map of mouse genes.
Nature genetics 2001;29(2):201-5.
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2001: Arkell R M; Cadman M; Marsland T; Southwell A; Thaung C; Davies J R; Clay T; Beechey C V; Evans E P; Strivens M A; Brown S D; Denny P
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.
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2001: Brown S D; Balling R
Systematic approaches to mouse mutagenesis.
Current opinion in genetics & development 2001;11(3):268-73.
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2001: Liu X; Oliver F; Brown S D; Denny P; Keightley P D
High-resolution quantitative trait locus mapping for body weight in mice by recombinant progeny testing.
Genetical research 2001;77(2):191-7.
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2001: Tsai H; Hardisty R E; Rhodes C; Kiernan A E; Roby P; Tymowska-Lalanne Z; Mburu P; Rastan S; Hunter A J; Brown S D; Steel K P
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.
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2001: Todorov P T; Hardisty R E; Brown S D
Myosin VIIA is specifically associated with calmodulin and microtubule-associated protein-2B (MAP-2B).
The Biochemical journal 2001;354(Pt 2):267-74.
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2001: Blanco G; Coulton G R; Biggin A; Grainge C; Moss J; Barrett M; Berquin A; Maréchal G; Skynner M; van Mier P; Nikitopoulou A; Kraus M; Ponting C P; Mason R M; Brown S D
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.
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2000: O'Carroll D; Scherthan H; Peters A H; Opravil S; Haynes A R; Laible G; Rea S; Schmid M; Lebersorger A; Jerratsch M; Sattler L; Mattei M G; Denny P; Brown S D; Schweizer D; Jenuwein T
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.
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2000: Isaacs A M; Davies K E; Hunter A J; Nolan P M; Vizor L; Peters J; Gale D G; Kelsell D P; Latham I D; Chase J M; Fisher E M; Bouzyk M M; Potter A; Masih M; Walsh F S; Sims M A; Doncaster K E; Parsons C A; Martin J; Brown S D; Rastan S; Spurr N K; Gray I C
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.
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2000: Strivens M A; Selley R L; Greenaway S J; Hewitt M; Liu X; Battershill K; McCormack S L; Pickford K A; Vizor L; Nolan P M; Hunter A J; Peters J; Brown S D
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.
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2000: Nolan P M; Peters J; Vizor L; Strivens M; Washbourne R; Hough T; Wells C; Glenister P; Thornton C; Martin J; Fisher E; Rogers D; Hagan J; Reavill C; Gray I; Wood J; Spurr N; Browne M; Rastan S; Hunter J; Brown S D
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.
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2000: Wells C; Brown S D
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.
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2000: Paige A J; Kiernan B W; Varela A; Rogers M J; Hughes D; Steel K P; Brown S D
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.
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2000: Liu X Z; Xia X J; Xu L R; Pandya A; Liang C Y; Blanton S H; Brown S D; Steel K P; Nance W E
Mutations in connexin31 underlie recessive as well as dominant non-syndromic hearing loss.
Human molecular genetics 2000;9(1):63-7.
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2000: Liu X Z; Brown S D
Sensorineural hearing impairment: non-syndromic, recessive DFNB2.
Advances in oto-rhino-laryngology 2000;56():124-30.
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1999: Hardisty R E; Mburu P; Brown S D
ENU mutagenesis and the search for deafness genes.
British journal of audiology 1999;33(5):279-83.
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1999: Liu X Y; Dangel A W; Kelley R I; Zhao W; Denny P; Botcherby M; Cattanach B; Peters J; Hunsicker P R; Mallon A M; Strivens M A; Bate R; Miller W; Rhodes M; Brown S D; Herman G E
The gene mutated in bare patches and striated mice encodes a novel 3beta-hydroxysteroid dehydrogenase.
Nature genetics 1999;22(2):182-7.
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1999: Rogers M J; Fleming J; Kiernan B W; Mburu P; Varela A; Brown S D; Steel K P
Genetic mapping of the whirler mutation.
Mammalian genome : official journal of the International Mammalian Genome Society 1999;10(5):513-9.
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1999: Liu X Z; Hope C; Liang C Y; Zou J M; Xu L R; Cole T; Mueller R F; Bundey S; Nance W; Steel K P; Brown S D
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.
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1999: Laible G; Haynes A R; Lebersorger A; O'Carroll D; Mattei M G; Denny P; Brown S D; Jenuwein T
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.
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1998: Blanco G; Nikitopoulou A; Kraus M; Mason R M; Coulton G R; Brown S D
A STS content physical and transcription map across the ky, kyphoscoliosis, nonrecombinant region.
Genomics 1998;54(3):415-23.
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1998: Liu X Z; Hope C; Walsh J; Newton V; Ke X M; Liang C Y; Xu L R; Zhou J M; Trump D; Steel K P; Bundey S; Brown S D
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.
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1998: Brown S D
Mouse models of genetic disease: new approaches, new paradigms.
Journal of inherited metabolic disease 1998;21(5):532-9.
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1998: Blanco G; Irving N G; Brown S D; Miller C C; McLoughlin D M
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.
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1998: Self T; Mahony M; Fleming J; Walsh J; Brown S D; Steel K P
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.
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1998: Brown S D; Nolan P M
Mouse mutagenesis-systematic studies of mammalian gene function.
Human molecular genetics 1998;7(10):1627-33.
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1997: Strivens M A; Middlehurst P; Brown S D; Denny P
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.
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1997: Mburu P; Liu X Z; Walsh J; Saw D; Cope M J; Gibson F; Kendrick-Jones J; Steel K P; Brown S D
Mutation analysis of the mouse myosin VIIA deafness gene.
Genes and function 1997;1(3):191-203.
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1997: Liu X Z; Walsh J; Mburu P; Kendrick-Jones J; Cope M J; Steel K P; Brown S D
Mutations in the myosin VIIA gene cause non-syndromic recessive deafness.
Nature genetics 1997;16(2):188-90.
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1997: Steel K P; Mburu P; Gibson F; Walsh J; Varela A; Brown K; Self T; Mahony M; Fleming J; Pearce A; Harvey D; Cable J; Brown S D
Unravelling the genetics of deafness.
The Annals of otology, rhinology & laryngology. Supplement 1997;168():59-62.
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1997: Lévy G; Levi-Acobas F; Blanchard S; Gerber S; Larget-Piet D; Chenal V; Liu X Z; Newton V; Steel K P; Brown S D; Munnich A; Kaplan J; Petit C; Weil D
Myosin VIIA gene: heterogeneity of the mutations responsible for Usher syndrome type IB.
Human molecular genetics 1997;6(1):111-6.
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1997: Liu X Z; Newton V E; Steel K P; Brown S D
Identification of a new mutation of the myosin VII head region in Usher syndrome type 1.
Human mutation 1997;10(2):168-70.
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1996: Steel K P; Brown S D
Genetics of deafness.
Current opinion in neurobiology 1996;6(4):520-5.
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1996: de Gouyon B; Chatterjee A; Monaco A; Quaderi N; Brown S D; Herman G E
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.
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1996: D'Esposito M; Quaderi N A; Ciccodicola A; Bruni P; Esposito T; D'Urso M; Brown S D
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.
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1996: Fleming J; Pearce A; Brown S D; Steel K P
The Sp4H deletion may contain a new locus essential for postimplantation development.
Genomics 1996;34(2):205-12.
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1996: Matsuura S; Episkopou V; Hamvas R; Brown S D
Xist expression from an Xist YAC transgene carried on the mouse Y chromosome.
Human molecular genetics 1996;5(4):451-9.
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1996: Mileham P; Brown S D
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.
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1996: Maconochie M K; Simpkins A H; Damien E; Coulton G; Greenfield A J; Brown S D
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.
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1995: Quaderi N A; Gianfrancesco F; Brown S D; D'Urso M; D'Esposito M
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.
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1995: Adler D A; Quaderi N A; Brown S D; Chapman V M; Moore J; Tate P; Disteche C M
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.
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1995: Gibson F; Walsh J; Mburu P; Varela A; Brown K A; Antonio M; Beisel K W; Steel K P; Brown S D
A type VII myosin encoded by the mouse deafness gene shaker-1.
Nature 1995;374(6517):62-4.
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1994: Quaderi N A; Meehan R R; Tate P H; Cross S H; Bird A P; Chatterjee A; Herman G E; Brown S D
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.
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1994: Fleming J; Rogers M J; Brown S D; Steel K P
Linkage analysis of the whirler deafness gene on mouse chromosome 4.
Genomics 1994;21(1):42-8.
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1994: Brown K A; Sutcliffe M J; Steel K P; Brown S D
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.
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1994: Brown S D; Carey A H
Chromosome dissection and cloning.
Methods in molecular biology (Clifton, N.J.) 1994;29():425-36.
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1994: Brown S D; Steel K P
Genetic deafness--progress with mouse models.
Human molecular genetics 1994;3 Spec No():1453-6.
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1994: Herman G E; Boyd Y; Chapman V; Chatterjee A; Brown S D
Mouse X chromosome.
Mammalian genome : official journal of the International Mammalian Genome Society 1994;5 Spec No():S276-88.
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1993: Brown S D; Chartier F; Johnson K; Cavanna J S
Mapping the Hrc gene to proximal mouse chromosome 7: delineation of a conserved linkage group with human 19q.
Genomics 1993;18(2):459-61.
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1993: Hamvas R M; Larin Z; Brockdorff N; Rastan S; Lehrach H; Chartier F L; Brown S D
YAC clone contigs surrounding the Zfx and Pola loci on the mouse X chromosome.
Genomics 1993;17(1):52-8.
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1993: Cooper P; Keer J T; McCabe V M; Hamvas R M; Brown S D; Rastan S; Brockdorff N
Physical mapping of 2000 kb of the mouse X chromosome in the vicinity of the Xist locus.
Genomics 1993;15(3):570-5.
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1993: Brown S D; Avner P; Boyd Y; Chapman V; Rastan S; Sefton L; Thomas J D; Herman G E
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.
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1993: Gangadharan U; Maconochie M K; Davies K E; Brown S D
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.
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1992: Brown S D
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.
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1992: Brown K A; Sutcliffe M J; Steel K P; Brown S D
Close linkage of the olfactory marker protein gene to the mouse deafness mutation shaker-1.
Genomics 1992;13(1):189-93.
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1992: Chartier F L; Keer J T; Sutcliffe M J; Henriques D A; Mileham P; Brown S D
Construction of a mouse yeast artificial chromosome library in a recombination-deficient strain of yeast.
Nature genetics 1992;1(2):132-6.
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1992: Hamvas R M; Zinn A; Keer J T; Fisher E M; Beer-Romero P; Brown S D; Page D C
Rps4 maps near the inactivation center on the mouse X chromosome.
Genomics 1992;12(2):363-7.
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1992: Hamvas R M; Reik W; Gaunt S J; Brown S D; Singh P B
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.
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1992: Maconochie M K; Brown S D; Greenfield A J
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.
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1992: Brown S D; Avner P; Herman G E
Mouse X chromosome.
Mammalian genome : official journal of the International Mammalian Genome Society 1992;3 Spec No():S274-88.
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1991: Irving N G; Brown S D
Mouse chromosome-specific markers generated by PCR and their mapping through interspecific backcrosses.
Genomics 1991;11(3):679-86.
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1991: Nasir J; Maconochie M K; Brown S D
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.
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1991: Brockdorff N; Kay G; Smith S; Keer J T; Hamvas R M; Brown S D; Rastan S
High-density molecular map of the central span of the mouse X chromosome.
Genomics 1991;10(1):17-22.
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1991: Irving N G; Hardy J A; Brown S D
The multipoint genetic mapping of mouse chromosome 16.
Genomics 1991;9(2):386-9.
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1991: Brown S D; Brown K A; Sutcliffe M J; Cavanna J S; Greenfield A J; Steel K P
Reverse genetic approaches to cloning deafness genes.
Annals of the New York Academy of Sciences 1991;630():93-9.
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1991: Brown S D; Avner P; Chapman V M; Hamvas R M; Herman G E
Mouse X chromosome.
Mammalian genome : official journal of the International Mammalian Genome Society 1991;1 Spec No():S318-31.
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1990: Keer J T; Hamvas R M; Brockdorff N; Page D; Rastan S; Brown S D
Genetic mapping in the region of the mouse X-inactivation center.
Genomics 1990;7(4):566-72.
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1990: Cavanna J S; Greenfield A J; Johnson K J; Marks A R; Nadal-Ginard B; Brown S D
Establishment of the mouse chromosome 7 region with homology to the myotonic dystrophy region of human chromosome 19q.
Genomics 1990;7(1):12-8.
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1990: Nasir J; Fisher E M; Brockdorff N; Disteche C M; Lyon M F; Brown S D
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.
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1989: Irving N G; Hardy J A; Bahary N; Friedman J M; Brown S D
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.
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1988: Cavanna J S; Coulton G; Morgan J E; Brockdorff N; Forrest S M; Davies K E; Brown S D
Molecular and genetic mapping of the mouse mdx locus.
Genomics 1988;3(4):337-41.
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1988: Brockdorff N; Fisher E M; Orkin S H; Lyon M F; Brown S D
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.
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1987: Brockdorff N; Fisher E M; Cavanna J S; Lyon M F; Brown S D
Construction of a detailed molecular map of the mouse X chromosome by microcloning and interspecific crosses.
The EMBO journal 1987;6(11):3291-7.
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1987: Brockdorff N; Cross G S; Cavanna J S; Fisher E M; Lyon M F; Davies K E; Brown S D
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.
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1985: Fisher E M; Cavanna J S; Brown S D
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.
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