Works by Brown, Steve D. M.

Results: 66

EuroPhenome: a repository for high-throughput mouse phenotyping data.

Published in:

Nucleic Acids Research, 2010, v. 38, p. D577, doi. 10.1093/nar/gkp1007

By:

Morgan, Hugh;
Beck, Tim;
Blake, Andrew;
Gates, Hilary;
Adams, Niels;
Debouzy, Guillaume;
Leblanc, Sophie;
Lengger, Christoph;
Maier, Holger;
Melvin, David;
Meziane, Hamid;
Richardson, Dave;
Wells, Sara;
White, Jacqui;
Wood, Joe;
Hrabé de Angelis, Martin;
Brown, Steve D. M.;
Hancock, John M.;
Mallon, Ann-Marie

Publication type:

Article

MouseBook: an integrated portal of mouse resources.

Published in:

Nucleic Acids Research, 2010, v. 38, p. D593, doi. 10.1093/nar/gkp867

By:

Blake, Andrew;
Pickford, Karen;
Greenaway, Simon;
Thomas, Steve;
Pickard, Amanda;
Williamson, Christine M.;
Adams, Niels C.;
Walling, Alison;
Beck, Tim;
Fray, Martin;
Peters, Jo;
Weaver, Tom;
Brown, Steve D. M.;
Hancock, John M.;
Mallon, Ann-Marie

Publication type:

Article

Establishing normal plasma and 24-hour urinary biochemistry ranges in C3H, BALB/c and C57BL/6J mice following acclimatization in metabolic cages.

Published in:

Laboratory Animals, 2010, v. 44, n. 3, p. 218, doi. 10.1258/la.2010.009128

By:

Stechman, Michael J.;
Ahmad, Bushra N.;
Loh, Nellie Y.;
Reed, Anita A. C.;
Stewart, Michelle;
Wells, Sara;
Hough, Tertius;
Bentley, Liz;
Cox, Roger D.;
Brown, Steve D. M.;
Thakker, Rajesh V.

Publication type:

Article

Myringotomy in the Junbo mouse model of chronic otitis media alleviates inflammation and cellular hypoxia.

Published in:

Laryngoscope, 2014, v. 124, n. 9, p. E377, doi. 10.1002/lary.24698

By:

Bhutta, Mahmood F.;
Cheeseman, Michael T.;
Brown, Steve D. M.

Publication type:

Article

Genome-wide screening reveals the genetic basis of mammalian embryonic eye development.

Published in:

BMC Biology, 2023, p. 1, doi. 10.1186/s12915-022-01475-0

By:

Chee, Justine M.;
Lanoue, Louise;
Clary, Dave;
Higgins, Kendall;
Bower, Lynette;
Flenniken, Ann;
Guo, Ruolin;
Adams, David J.;
Bosch, Fatima;
Braun, Robert E.;
Brown, Steve D. M.;
Chin, H.-J. Genie;
Dickinson, Mary E.;
Hsu, Chih-Wei;
Dobbie, Michael;
Gao, Xiang;
Galande, Sanjeev;
Grobler, Anne;
Heaney, Jason D.;
Herault, Yann

Publication type:

Article

Silvia Garagna (ed) Mouse genetics after the mouse genome. Karger, ISBN 3-805-57783-4, hardcover.

Published in:

2005

By:

Brown, Steve D. M.

Publication type:

Book Review

Characterization of Usher syndrome type I gene mutations in an Usher syndrome patient population.

Published in:

Human Genetics, 2005, v. 116, n. 4, p. 292, doi. 10.1007/s00439-004-1227-2

By:

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

Publication type:

Article

Advances in mouse genetics for the study of human disease.

Published in:

Human Molecular Genetics, 2021, v. 30, n. 20, p. R274, doi. 10.1093/hmg/ddab153

By:

Brown, Steve D M

Publication type:

Article

Genetic landscape of auditory dysfunction.

Published in:

Human Molecular Genetics, 2018, v. 27, p. R130, doi. 10.1093/hmg/ddy158

By:

Bowl, Michael R;
Brown, Steve D M

Publication type:

Article

A genetic modifier suggests that endurance exercise exacerbates Huntington's disease.

Published in:

Human Molecular Genetics, 2018, v. 27, n. 10, p. 1723, doi. 10.1093/hmg/ddy077

By:

Corrochano, Silvia;
Blanco, Gonzalo;
Williams, Debbie;
Wettstein, Jessica;
Simon, Michelle;
Kumar, Saumya;
Moir, Lee;
Agnew, Thomas;
Stewart, Michelle;
Landman, Allison;
Kotiadis, Vassilios N.;
Duchen, Michael R.;
Wackerhage, Henning;
Rubinsztein, David C.;
Brown, Steve D. M.;
Acevedo-Arozena, Abraham

Publication type:

Article

Improving laboratory animal genetic reporting: LAG-R guidelines.

Published in:

Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-49439-y

By:

Teboul, Lydia;
Amos-Landgraf, James;
Benavides, Fernando J.;
Birling, Marie-Christine;
Brown, Steve D. M.;
Bryda, Elizabeth;
Bunton-Stasyshyn, Rosie;
Chin, Hsian-Jean;
Crispo, Martina;
Delerue, Fabien;
Dobbie, Michael;
Franklin, Craig L.;
Fuchtbauer, Ernst-Martin;
Gao, Xiang;
Golzio, Christelle;
Haffner, Rebecca;
Hérault, Yann;
Hrabe de Angelis, Martin;
Lloyd, Kevin C. Kent;
Magnuson, Terry R.

Publication type:

Article

A novel stereocilia defect in sensory hair cells of the deaf mouse mutant Tasmanian devil.

Published in:

European Journal of Neuroscience, 2002, v. 16, n. 8, p. 1433, doi. 10.1046/j.1460-9568.2002.02213.x

By:

Erven, Alexandra;
Skynner, Michael J.;
Okumura, Katsuzumi;
Takebayashi, Shin‐ichiro;
Brown, Steve D. M.;
Steel, Karen P.;
Allen, Nicholas D.

Publication type:

Article

Mice with an N-Ethyl-N-Nitrosourea (ENU) Induced Tyr209Asn Mutation in Natriuretic Peptide Receptor 3 (NPR3) Provide a Model for Kyphosis Associated with Activation of the MAPK Signaling Pathway.

Published in:

PLoS ONE, 2016, v. 11, n. 12, p. 1, doi. 10.1371/journal.pone.0167916

By:

Esapa, Christopher T.;
Piret, Sian E.;
Nesbit, M. Andrew;
Loh, Nellie Y.;
Thomas, Gethin;
Croucher, Peter I.;
Brown, Matthew A.;
Brown, Steve D. M.;
Cox, Roger D.;
Thakker, Rajesh V.

Publication type:

Article

Absence of Neuroplastin-65 Affects Synaptogenesis in Mouse Inner Hair Cells and Causes Profound Hearing Loss.

Published in:

Journal of Neuroscience, 2016, v. 36, n. 1, p. 222, doi. 10.1523/JNEUROSCI.1808-15.2016

By:

Carrott, Leanne;
Bowl, Michael R.;
Aguilar, Carlos;
Johnson, Stuart L.;
Chessum, Lauren;
West, Melissa;
Morse, Susan;
Dorning, Joanne;
Smart, Elizabeth;
Hardisty-Hughes, Rachel;
Ball, Greg;
Parker, Andrew;
Barnard, Alun R.;
MacLaren, Robert E.;
Wells, Sara;
Marcotti, Walter;
Brown, Steve D. M.

Publication type:

Article

Dynein mutations impair autophagic clearance of aggregate-prone proteins.

Published in:

Nature Genetics, 2005, v. 37, n. 7, p. 771, doi. 10.1038/ng1591

By:

Ravikumar, Brinda;
Acevedo-Arozena, Abraham;
Imarisio, Sara;
Berger, Zdenek;
Vacher, Coralie;
O'Kane, Cahir J.;
Brown, Steve D. M.;
Rubinsztein, David C.

Publication type:

Article

A mutation in Nischarin causes otitis media via LIMK1 and NF-κB pathways.

Published in:

PLoS Genetics, 2017, v. 13, n. 8, p. 1, doi. 10.1371/journal.pgen.1006969

By:

Crompton, Michael;
Purnell, Tom;
Tyrer, Hayley E.;
Parker, Andrew;
Ball, Greg;
Hardisty-Hughes, Rachel E.;
Gale, Richard;
Williams, Debbie;
Dean, Charlotte H.;
Simon, Michelle M.;
Mallon, Ann-Marie;
Wells, Sara;
Bhutta, Mahmood F.;
Burton, Martin J.;
Tateossian, Hilda;
Brown, Steve D. M.

Publication type:

Article

Regulatory Variation at Glypican-3 Underlies a Major Growth QTL in Mice.

Published in:

PLoS Biology, 2005, v. 3, n. 5, p. 872, doi. 10.1371/journal.pbio.0030135

By:

Oliver, Fiona;
Christians, Julian K.;
Xiaojun Liu;
Rhind, Susan;
Verma, Vinesh;
Davison, Claire;
Brown, Steve D. M.;
Denny, Paul;
Keightley, Peter D.

Publication type:

Article

Regulatory Variation at Glypican-3 Underlies a Major Growth QTL in Mice.

Published in:

PLoS Biology, 2005, v. 3, n. 4, p. 1, doi. 10.1371/journal.pbio.0030135

By:

Oliver, Fiona;
Christians, Julian K;
Liu, Xiaojun;
Rhind, Susan;
Verma, Vinesh;
Davison, Claire;
Brown, Steve D. M;
Denny, Paul;
Keightley, Peter D

Publication type:

Article

Identification of a new mutation of the myosin VII head region in Usher syndrome type 1.

Published in:

Human Mutation, 1997, v. 10, n. 2, p. 168, doi. 10.1002/(SICI)1098-1004(1997)10:2<168::AID-HUMU10>3.0.CO;2-Y

By:

Liu, Xue-zhong;
Newton, Valerie E.;
Steel, Karen P.;
Brown, Steve D. M.

Publication type:

Article

Modification of an aggressive model of Alport Syndrome reveals early differences in disease pathogenesis due to genetic background.

Published in:

Scientific Reports, 2019, v. 9, n. 1, p. 1, doi. 10.1038/s41598-019-56837-6

By:

Falcone, Sara;
Wisby, Laura;
Nicol, Thomas;
Blease, Andrew;
Starbuck, Becky;
Parker, Andrew;
Sanderson, Jeremy;
Brown, Steve D. M.;
Scudamore, Cheryl L.;
Pusey, Charles D.;
Tam, Frederick W. K.;
Potter, Paul K.

Publication type:

Article

Correction of the auditory phenotype in C57BL/6N mice via CRISPR/Cas9-mediated homology directed repair.

Published in:

Genome Medicine, 2016, v. 8, p. 1, doi. 10.1186/s13073-016-0273-4

By:

Mianné, Joffrey;
Chessum, Lauren;
Kumar, Saumya;
Aguilar, Carlos;
Codner, Gemma;
Hutchison, Marie;
Parker, Andrew;
Mallon, Ann-Marie;
Wells, Sara;
Simon, Michelle M.;
Teboul, Lydia;
Brown, Steve D. M.;
Bowl, Michael R.

Publication type:

Article

Corrigendum: Comparative visualization of genotype-phenotype relationships.

Published in:

Nature Methods, 2015, v. 12, n. 11, p. 1098, doi. 10.1038/nmeth1115-1098c

By:

Yaikhom, Gagarine;
Morgan, Hugh;
Sneddon, Duncan;
Retha, Ahmad;
Atienza-Herrero, Julian;
Blake, Andrew;
Brown, James;
Di Fenza, Armida;
Fiegel, Tanja;
Horner, Neil;
Ring, Natalie;
Santos, Luis;
Westerberg, Henrik;
Brown, Steve D M;
Mallon, Ann-Marie

Publication type:

Article

Comparative visualization of genotype-phenotype relationships.

Published in:

Nature Methods, 2015, v. 12, n. 8, p. 698, doi. 10.1038/nmeth.3477

By:

Yaikhom, Gagarine;
Morgan, Hugh;
Sneddon, Duncan;
Retha, Ahmad;
Atienza-Herrero, Julian;
Blake, Andrew;
Brown, James;
Di Fenza, Armida;
Fiegel, Tanja;
Horner, Neil;
Ring, Natalie;
Santos, Luis;
Westerberg, Henrik;
Brown, Steve D M;
Mallon, Ann-Marie

Publication type:

Article

Neuroplastin genetically interacts with Cadherin 23 and the encoded isoform Np55 is sufficient for cochlear hair cell function and hearing.

Published in:

PLoS Genetics, 2022, v. 18, n. 1, p. 1, doi. 10.1371/journal.pgen.1009937

By:

Newton, Sherylanne;
Kong, Fanbo;
Carlton, Adam J.;
Aguilar, Carlos;
Parker, Andrew;
Codner, Gemma F.;
Teboul, Lydia;
Wells, Sara;
Brown, Steve D. M.;
Marcotti, Walter;
Bowl, Michael R.

Publication type:

Article

Quiet as a mouse: dissecting the molecular and genetic basis of hearing.

Published in:

Nature Reviews Genetics, 2008, v. 9, n. 4, p. 277, doi. 10.1038/nrg2309

By:

Brown, Steve D. M.;
Hardisty-Hughes, Rachel E.;
Mburu, Philomena

Publication type:

Article

Human-specific gene CT47 blocks PRMT5 degradation to lead to meiosis arrest.

Published in:

Cell Death Discovery, 2022, v. 8, n. 1, p. 1, doi. 10.1038/s41420-022-01139-6

By:

Li, Chao;
Feng, Yuming;
Fu, Zhenxin;
Deng, Junjie;
Gu, Yue;
Wang, Hanben;
Wu, Xin;
Huang, Zhengyun;
Zhu, Yichen;
Liu, Zhiwei;
Huang, Moli;
Wang, Tao;
Hu, Shijun;
Yao, Bing;
Zeng, Yizhun;
Zhou, Chengji J.;
Brown, Steve D. M.;
Liu, Yi;
Vidal-Puig, Antonio;
Dong, Yingying

Publication type:

Article

Correction to: The International Mouse Phenotyping Consortium (IMPC): a functional catalogue of the mammalian genome that informs conservation.

Published in:

2019

By:

Muñoz-Fuentes, Violeta;
Cacheiro, Pilar;
Meehan, Terrence F.;
Aguilar-Pimentel, Juan Antonio;
Beaudet, Arthur L.;
Brown, Steve D. M.;
Dickinson, Mary E.;
Flenniken, Ann M.;
Flicek, Paul;
Galli, Antonella;
Mashhadi, Hamed Haseli;
Heaney, Jason D.;
Hrabě de Angelis, Martin;
Kim, Jong Kyoung;
Lloyd, K. C. Kent;
McKerlie, Colin;
Morgan, Hugh;
Murray, Stephen A.;
Nutter, Lauryl M. J.;
Reilly, Patrick T.

Publication type:

Correction Notice

The International Mouse Phenotyping Consortium (IMPC): a functional catalogue of the mammalian genome that informs conservation.

Published in:

Conservation Genetics, 2018, v. 19, n. 4, p. 995, doi. 10.1007/s10592-018-1072-9

By:

Muñoz-Fuentes, Violeta;
Cacheiro, Pilar;
Meehan, Terrence F.;
Aguilar-Pimentel, Juan Antonio;
Brown, Steve D. M.;
Flenniken, Ann M.;
Flicek, Paul;
Galli, Antonella;
Mashhadi, Hamed Haseli;
Hrabě de Angelis, Martin;
Kim, Jong Kyoung;
Lloyd, K. C. Kent;
McKerlie, Colin;
Morgan, Hugh;
Murray, Stephen A.;
Nutter, Lauryl M. J.;
Reilly, Patrick T.;
Seavitt, John R.;
Seong, Je Kyung;
Simon, Michelle

Publication type:

Article

CIB2 interacts with TMC1 and TMC2 and is essential for mechanotransduction in auditory hair cells.

Published in:

Nature Communications, 2017, v. 8, n. 6, p. 1, doi. 10.1038/s41467-017-00061-1

By:

Giese, Arnaud P. J.;
Yi-Quan Tang;
Sinha, Ghanshyam P.;
Bowl, Michael R.;
Goldring, Adam C.;
Parker, Andrew;
Freeman, Mary J.;
Brown, Steve D. M.;
Riazuddin, Saima;
Fettiplace, Robert;
Schafer, William R.;
Frolenkov, Gregory I.;
Ahmed, Zubair M.

Publication type:

Article

The deaf mouse mutant Jeff (Jf) is a single gene model of otitis media.

Published in:

2003

By:

Hardisty, Rachel E.;
Erven, Alexandra;
Logan, Karen;
Morse, Susan;
Guionaud, Sylvia;
Sancho-Oliver, Sara;
Jackie Hunter, A.;
Brown, Steve D. M.;
Steel, Karen P.;
Hunter, A Jackie

Publication type:

journal article

The Jeff Mouse Mutant Model for Chronic Otitis Media Manifests Gain-of-Function as Well as Loss-of-Function Effects.

Published in:

Frontiers in Genetics, 2020, v. 11, p. 1, doi. 10.3389/fgene.2020.00498

By:

Kubinyecz, Oana;
Vikhe, Pratik P.;
Purnell, Thomas;
Brown, Steve D. M.;
Tateossian, Hilda

Publication type:

Article

N-ethyl-N-Nitrosourea (ENU) Induced Mutations within the Klotho Gene Lead to Ectopic Calcification and Reduced Lifespan in Mouse Models.

Published in:

PLoS ONE, 2015, v. 10, n. 4, p. 1, doi. 10.1371/journal.pone.0122650

By:

Esapa, Christopher T.;
Hannan, Fadil M.;
Babinsky, Valerie N.;
Potter, Paul;
Thomas, Gethin P.;
Croucher, Peter I.;
Brown, Matthew A.;
Brown, Steve D. M.;
Cox, Roger D.;
Thakker, Rajesh V.

Publication type:

Article

Reducing <i>Igf-1r</i> Levels Leads To Paradoxical and Sexually Dimorphic Effects in HD Mice.

Published in:

PLoS ONE, 2014, v. 9, n. 8, p. 1, doi. 10.1371/journal.pone.0105595

By:

Corrochano, Silvia;
Renna, Maurizio;
Osborne, Georgina;
Carter, Sarah;
Stewart, Michelle;
May, Joel;
Bates, Gillian P.;
Brown, Steve D. M.;
Rubinsztein, David C.;
Acevedo-Arozena, Abraham

Publication type:

Article

The Actin-Binding Proteins Eps8 and Gelsolin Have Complementary Roles in Regulating the Growth and Stability of Mechanosensory Hair Bundles of Mammalian Cochlear Outer Hair Cells.

Published in:

PLoS ONE, 2014, v. 9, n. 1, p. 1, doi. 10.1371/journal.pone.0087331

By:

Olt, Jennifer;
Mburu, Philomena;
Johnson, Stuart L.;
Parker, Andy;
Kuhn, Stephanie;
Bowl, Mike;
Marcotti, Walter;
Brown, Steve D. M.

Publication type:

Article

Autosomal Dominant Hypercalciuria in a Mouse Model Due to a Mutation of the Epithelial Calcium Channel, TRPV5.

Published in:

PLoS ONE, 2013, v. 8, n. 1, p. 1, doi. 10.1371/journal.pone.0055412

By:

Loh, Nellie Y.;
Bentley, Liz;
Dimke, Henrik;
Verkaart, Sjoerd;
Tammaro, Paolo;
Gorvin, Caroline M.;
Stechman, Michael J.;
Ahmad, Bushra N.;
Hannan, Fadil M.;
Piret, Sian E.;
Evans, Holly;
Bellantuono, Ilaria;
Hough, Tertius A.;
Fraser, William D.;
Hoenderop, Joost G. J.;
Ashcroft, Frances M.;
Brown, Steve D. M.;
Bindels, René J. M.;
Cox, Roger D.;
Thakker, Rajesh V.

Publication type:

Article

A Mouse Model of Early-Onset Renal Failure Due to a Xanthine Dehydrogenase Nonsense Mutation.

Published in:

PLoS ONE, 2012, v. 7, n. 9, p. 1, doi. 10.1371/journal.pone.0045217

By:

Piret, Sian E.;
Esapa, Christopher T.;
Gorvin, Caroline M.;
Head, Rosie;
Loh, Nellie Y.;
Devuyst, Olivier;
Thomas, Gethin;
Brown, Steve D. M.;
Brown, Matthew;
Croucher, Peter;
Cox, Roger;
Thakker, Rajesh V.;
Shree Ram Singh

Publication type:

Article

A Mouse with an N-Ethyl- N-Nitrosourea (ENU) Induced Trp589Arg Galnt3Mutation Represents a Model for Hyperphosphataemic Familial Tumoural Calcinosis.

Published in:

PLoS ONE, 2012, v. 7, n. 8, p. 1, doi. 10.1371/journal.pone.0043205

By:

Esapa, Christopher T.;
Head, Rosie A.;
Jeyabalan, Jeshmi;
Evans, Holly;
Hough, Tertius A.;
Cheeseman, Michael T.;
McNally, Eugene G.;
Carr, Andrew J.;
Thomas, Gethin P.;
Brown, Matthew A.;
Croucher, Peter I.;
Brown, Steve D. M.;
Cox, Roger D.;
Thakker, Rajesh V.;
Aprikyan, Andranik Andrew

Publication type:

Article

Gelsolin Plays a Role in the Actin Polymerization Complex of Hair Cell Stereocilia.

Published in:

PLoS ONE, 2010, v. 5, n. 7, p. 1, doi. 10.1371/journal.pone.0011627

By:

Mburu, Philomena;
Romero, María Rosario;
Hilton, Helen;
Parker, Andrew;
Townsend, Stuart;
Kikkawa, Yoshiaki;
Brown, Steve D. M.

Publication type:

Article

Unlocking the Bottleneck in Forward Genetics Using Whole-Genome Sequencing and Identity by Descent to Isolate Causative Mutations.

Published in:

PLoS Genetics, 2013, v. 9, n. 1, p. 1, doi. 10.1371/journal.pgen.1003219

By:

Bull, Katherine R.;
Rimmer, Andrew J.;
Siggs, Owen M.;
Miosge, Lisa A.;
Roots, Carla M.;
Enders, Anselm;
Bertram, Edward M.;
Crockford, Tanya L.;
Whittle, Belinda;
Potter, Paul K.;
Simon, Michelle M.;
Mallon, Ann-Marie;
Brown, Steve D. M.;
Beutler, Bruce;
Goodnow, Christopher C.;
Lunter, Gerton;
Cornall, Richard J.

Publication type:

Article

HIF--VEGF Pathways Are Critical for Chronic Otitis Media in Junbo and Jeff Mouse Mutants.

Published in:

PLoS Genetics, 2011, v. 7, n. 10, p. 1, doi. 10.1371/journal.pgen.1002336

By:

Cheeseman, Michael T.;
Tyrer, Hayley E.;
Williams, Debbie;
Hough, Tertius A.;
Pathak, Paras;
Romero, Maria R.;
Hilton, Helen;
Bali, Sulzhan;
Parker, Andrew;
Vizor, Lucie;
Purnell, Tom;
Vowell, Kate;
Wells, Sara;
Bhutta, Mahmood F.;
Potter, Paul K.;
Brown, Steve D. M.

Publication type:

Article

Loss of Baiap2l2 destabilizes the transducing stereocilia of cochlear hair cells and leads to deafness.

Published in:

Journal of Physiology, 2021, v. 599, n. 4, p. 1173, doi. 10.1113/JP280670

By:

Carlton, Adam J.;
Halford, Julia;
Underhill, Anna;
Jeng, Jing‐Yi;
Avenarius, Matthew R.;
Gilbert, Merle L.;
Ceriani, Federico;
Ebisine, Kimimuepigha;
Brown, Steve D. M.;
Bowl, Michael R.;
Barr‐Gillespie, Peter G.;
Marcotti, Walter

Publication type:

Article

Biophysical and morphological changes in inner hair cells and their efferent innervation in the ageing mouse cochlea.

Published in:

Journal of Physiology, 2021, v. 599, n. 1, p. 269, doi. 10.1113/JP280256

By:

Jeng, Jing‐Yi;
Carlton, Adam J.;
Johnson, Stuart L.;
Brown, Steve D. M.;
Holley, Matthew C.;
Bowl, Michael R.;
Marcotti, Walter

Publication type:

Article

Pathophysiological changes in inner hair cell ribbon synapses in the ageing mammalian cochlea.

Published in:

Journal of Physiology, 2020, v. 598, n. 19, p. 4339, doi. 10.1113/JP280018

By:

Jeng, Jing‐Yi;
Ceriani, Federico;
Olt, Jennifer;
Brown, Steve D. M.;
Holley, Matthew C.;
Bowl, Michael R.;
Johnson, Stuart L.;
Marcotti, Walter

Publication type:

Article

Age‐related changes in the biophysical and morphological characteristics of mouse cochlear outer hair cells.

Published in:

Journal of Physiology, 2020, v. 598, n. 18, p. 3891, doi. 10.1113/JP279795

By:

Jeng, Jing‐Yi;
Johnson, Stuart L.;
Carlton, Adam J;
De Tomasi, Lara;
Goodyear, Richard J.;
De Faveri, Francesca;
Furness, David N.;
Wells, Sara;
Brown, Steve D. M.;
Holley, Matthew C.;
Richardson, Guy P.;
Mustapha, Mirna;
Bowl, Michael R.;
Marcotti, Walter

Publication type:

Article

Analysis of genome-wide knockout mouse database identifies candidate ciliopathy genes.

Published in:

Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-19710-7

By:

Higgins, Kendall;
Moore, Bret A.;
Berberovic, Zorana;
Adissu, Hibret A.;
Eskandarian, Mohammad;
Flenniken, Ann M.;
Shao, Andy;
Imai, Denise M.;
Clary, Dave;
Lanoue, Louise;
Newbigging, Susan;
Nutter, Lauryl M. J.;
Adams, David J.;
Bosch, Fatima;
Braun, Robert E.;
Brown, Steve D. M.;
Dickinson, Mary E.;
Dobbie, Michael;
Flicek, Paul;
Gao, Xiang

Publication type:

Article

Novel ENU-induced eye mutations in the mouse: models for human eye disease.

Published in:

Human Molecular Genetics, 2002, v. 11, n. 7, p. 755, doi. 10.1093/hmg/11.7.755

By:

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.

Publication type:

Article

Mouse mutagenesis--systematic studies of mammalian gene function.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 10, p. 1627, doi. 10.1093/hmg/7.10.1627

By:

Brown, Steve D. M.;
Nolan, Patrick M.

Publication type:

Article

Mouse mutagenesis—systematic studies of mammalian gene function.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 10, p. 1627, doi. 10.1093/hmg/7.10.1627

By:

Brown, Steve D. M.;
Nolan, Patrick M.

Publication type:

Article

Myosin VIIA Gene: Heterogeneity of the Mutations Responsible for Usher Syndrome Type IB.

Published in:

Human Molecular Genetics, 1997, v. 6, n. 1, p. 111, doi. 10.1093/hmg/6.1.111

By:

Lévy, Gallia;
Levi-Acobas, Fabienne;
Blanchard, Stéphane;
Gerber, Sylvie;
Larget-Piet, Dominique;
Chenal, Viviane;
Liu, Xue-Zhong;
Newton, Valerie;
Steel, Karen P.;
Brown, Steve D. M.;
Munnich, Arnold;
Kaplan, Josseline;
Petit, Christine;
Weil, Dominique

Publication type:

Article

PRIME importance of pathology expertise.

Published in:

2009

By:

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

Publication type:

Letter