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Guy Richardson

Showing results (1-10 of 9) with videos related to

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Current Topics in Developmental Biology|September 19, 2025
PrefaceDoris Wu, Guy Richardson
Molecular and Cellular Neurosciences|July 3, 2003
An emilin family extracellular matrix protein identified in the cochlear basilar membraneLori L Amma, Richard Goodyear, Jonathan S Faris, et al.
American Journal of Human Genetics|May 16, 2007
A mutation in CCDC50, a gene encoding an effector of epidermal growth factor-mediated cell signaling, causes progressive hearing lossSilvia Modamio-Hoybjor, Angeles Mencia, Richard Goodyear, et al.
Human Molecular Genetics|December 14, 2004
Myosin XVa and whirlin, two deafness gene products required for hair bundle growth, are located at the stereocilia tips and interact directlyBenjamin Delprat, Vincent Michel, Richard Goodyear, et al.
Blood|July 16, 2005
Clinical factors predictive of outcome with bortezomib in patients with relapsed, refractory multiple myelomaPaul Gerard Guy Richardson, Bart Barlogie, James Berenson, et al.
Human Molecular Genetics|May 30, 2009
In vivo and in vitro effects of two novel gamma-actin (ACTG1) mutations that cause DFNA20/26 hearing impairmentMatías Morín, Keith E Bryan, Fernando Mayo-Merino, et al.
The EMBO Journal|December 18, 2002
Myosin VIIa, harmonin and cadherin 23, three Usher I gene products that cooperate to shape the sensory hair cell bundleBatiste Boëda, Aziz El-Amraoui, Amel Bahloul, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 25, 2002
Otoancorin, an inner ear protein restricted to the interface between the apical surface of sensory epithelia and their overlying acellular gels, is defective in autosomal recessive deafness DFNB22Ingrid Zwaenepoel, Mirna Mustapha, Michel Leibovici, et al.
EMBO Molecular Medicine|June 19, 2014
The CD2 isoform of protocadherin-15 is an essential component of the tip-link complex in mature auditory hair cellsElise Pepermans, Vincent Michel, Richard Goodyear, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Current Topics in Developmental Biology|September 19, 2025
PrefaceDoris Wu, Guy Richardson
Molecular and Cellular Neurosciences|July 3, 2003
An emilin family extracellular matrix protein identified in the cochlear basilar membraneLori L Amma, Richard Goodyear, Jonathan S Faris, et al.
American Journal of Human Genetics|May 16, 2007
A mutation in CCDC50, a gene encoding an effector of epidermal growth factor-mediated cell signaling, causes progressive hearing lossSilvia Modamio-Hoybjor, Angeles Mencia, Richard Goodyear, et al.
Human Molecular Genetics|December 14, 2004
Myosin XVa and whirlin, two deafness gene products required for hair bundle growth, are located at the stereocilia tips and interact directlyBenjamin Delprat, Vincent Michel, Richard Goodyear, et al.
Blood|July 16, 2005
Clinical factors predictive of outcome with bortezomib in patients with relapsed, refractory multiple myelomaPaul Gerard Guy Richardson, Bart Barlogie, James Berenson, et al.
Human Molecular Genetics|May 30, 2009
In vivo and in vitro effects of two novel gamma-actin (ACTG1) mutations that cause DFNA20/26 hearing impairmentMatías Morín, Keith E Bryan, Fernando Mayo-Merino, et al.
The EMBO Journal|December 18, 2002
Myosin VIIa, harmonin and cadherin 23, three Usher I gene products that cooperate to shape the sensory hair cell bundleBatiste Boëda, Aziz El-Amraoui, Amel Bahloul, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 25, 2002
Otoancorin, an inner ear protein restricted to the interface between the apical surface of sensory epithelia and their overlying acellular gels, is defective in autosomal recessive deafness DFNB22Ingrid Zwaenepoel, Mirna Mustapha, Michel Leibovici, et al.
EMBO Molecular Medicine|June 19, 2014
The CD2 isoform of protocadherin-15 is an essential component of the tip-link complex in mature auditory hair cellsElise Pepermans, Vincent Michel, Richard Goodyear, et al.
Pageof 1