Výsledky vyhledávání - Steve D.M. Brown
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Advances in mouse genetics for the study of human disease Autor Steve D. M. Brown
Vydáno 2021Revisão -
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The search for the mouse X-chromosome inactivation centre Autor Sohaila Rastan, Steve D. M. Brown
Vydáno 1990Revisão -
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Otitis media in the Tgif knockout mouse implicates TGFβ signalling in chronic middle ear inflammatory disease Autor Hilda Tateossian, Susan Morse, Andrew Parker, Philomena Mburu, Nick Warr, Abraham Acevedo‐Arozena, Michael Cheeseman, Sara Wells, Steve D. M. Brown
Vydáno 2013Artigo -
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A mutation in the F-box gene, Fbxo11, causes otitis media in the Jeff mouse Autor Rachel E. Hardisty-Hughes, Hilda Tateossian, Susan Morse, M. Rosario Romero, Alice Middleton, Zuzanna Tymowska‐Lalanne, A. Jackie Hunter, Michael Cheeseman, Steve D. M. Brown
Vydáno 2006Artigo -
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Multiscale alterations in bone matrix quality increased fragility in steroid induced osteoporosis Autor Angelo Karunaratne, Xi Li, Liz Bentley, Dan Sykes, A. Boyde, Christopher T. Esapa, Nicholas J. Terrill, Steve D. M. Brown, Roger Cox, Rajesh V. Thakker, Himadri S. Gupta
Vydáno 2015Artigo -
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Modification of an aggressive model of Alport Syndrome reveals early differences in disease pathogenesis due to genetic background Autor Sara Falcone, Laura Wisby, T. NICOL, Andrew Blease, Becky Starbuck, Andrew Parker, Jeremy Sanderson, Steve D. M. Brown, Cheryl L. Scudamore, Charles D. Pusey, Frederick W.K. Tam, Paul Potter
Vydáno 2019Artigo -
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A Mutation (2314delG) in the Usher Syndrome Type IIA Gene: High Prevalence and Phenotypic Variation Autor Xuezhong Liu, Carolyn Hope, Chuan Yu Liang, Jiu Mu Zou, Li Rong Xu, Tim Cole, Robert F. Mueller, Sarah Bundey, Walter E. Nance, Karen P. Steel, Steve D. M. Brown
Vydáno 1999Carta -
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The Novel PMCA2 Pump Mutation Tommy Impairs Cytosolic Calcium Clearance in Hair Cells and Links to Deafness in Mice Autor Mario Bortolozzi, Marisa Brini, Nick Parkinson, Giulia Crispino, Pietro Scimemi, Romolo Daniele De Siati, Francesca Di Leva, Andrew Parker, Saida Ortolano, Edoardo Arslan, Steve D. M. Brown, Ernesto Carafoli, Fabio Mammano
Vydáno 2010Artigo -
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Correction of the auditory phenotype in C57BL/6N mice via CRISPR/Cas9-mediated homology directed repair Autor Joffrey Mianné, Lauren Chessum, Saumya Kumar, Carlos Aguilar, Gemma Codner, Marie Hutchison, Andrew Parker, Ann‐Marie Mallon, Sara Wells, Michelle M. Simon, Lydia Teboul, Steve D. M. Brown, Michael R. Bowl
Vydáno 2016Artigo -
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Mutations in the Myosin VIIA Gene Cause a Wide Phenotypic Spectrum, Including Atypical Usher Syndrome Autor Xue Zhong Liu, Carolyn Hope, James Walsh, Valerie Newton, Xiao Mei Ke, Chuan Yu Liang, Li Ron Xu, Jiu Mu Zhou, Dorothy Trump, Karen P. Steel, Sarah Bundey, Steve D. M. Brown
Vydáno 1998Carta
Vyhledávací nástroje:
Související témata
Biology
Genetics
Gene
Medicine
Phenotype
Computational biology
Cell biology
Mutation
Mutant
Anatomy
Genome
Chemistry
Pathology
Inner ear
Internal medicine
Biochemistry
Disease
Endocrinology
Mutagenesis
Audiology
Hair cell
Neuroscience
Otitis
Cochlea
Function (biology)
Hearing loss
Immunology
Receptor
Allele
Candidate gene