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Current Opinion in Neurology
|
December 22, 2011
Usher syndrome (sensorineural deafness and retinitis pigmentosa): pathogenesis, molecular diagnosis and therapeutic approaches
Crystel Bonnet, Aziz El-Amraoui
Nature Reviews. Genetics
|
May 12, 2023
Deafness: from genetic architecture to gene therapy
Christine Petit, Crystel Bonnet, Saaïd Safieddine
European Journal of Medical Genetics
|
June 30, 2026
NEW INSIGHTS INTO THE COMPLEX GENETIC ARCHITECTURE OF AGE-RELATED HEARING LOSS
Crystel Bonnet, Salim Aiche, Sophie Boucher
Proceedings of the National Academy of Sciences of the United States of America
|
August 30, 2006
A mitotically inheritable unit containing a MAP kinase module
Sébastien Kicka, Crystel Bonnet, Andrew K Sobering, et al.
Human Molecular Genetics
|
June 9, 2012
Defect in the gene encoding the EAR/EPTP domain-containing protein TSPEAR causes DFNB98 profound deafness
Sedigheh Delmaghani, Asadollah Aghaie, Nicolas Michalski, et al.
Biochemical and Biophysical Research Communications
|
October 3, 2002
Interaction of STOP with neuronal tubulin is independent of polyglutamylation
Crystel Bonnet, Eric Denarier, Christophe Bosc, et al.
Frontiers in Aging Neuroscience
|
March 18, 2021
Contributions of Age-Related and Audibility-Related Deficits to Aided Consonant Identification in Presbycusis: A Causal-Inference Analysis
Léo Varnet, Agnès C Léger, Sophie Boucher, et al.
Molecular Microbiology
|
September 22, 2006
The peroxisomal import proteins PEX2, PEX5 and PEX7 are differently involved in Podospora anserina sexual cycle
Crystel Bonnet, Eric Espagne, Denise Zickler, et al.
Vision Research
|
September 25, 2012
Fundus autofluorescence and optical coherence tomography in relation to visual function in Usher syndrome type 1 and 2
Ana Fakin, Martina Jarc-Vidmar, Damjan Glavač, et al.
RNA (New York, N.Y.)
|
June 6, 2006
mRNA localization to the mitochondrial surface allows the efficient translocation inside the organelle of a nuclear recoded ATP6 protein
Valérie Kaltimbacher, Crystel Bonnet, Gaëlle Lecoeuvre, et al.
Page
of 8
Search research articles
Search
Showing results (1-10 of 72) with videos related to
Sort By:
Page
of 8
Current Opinion in Neurology
|
December 22, 2011
Usher syndrome (sensorineural deafness and retinitis pigmentosa): pathogenesis, molecular diagnosis and therapeutic approaches
Crystel Bonnet, Aziz El-Amraoui
Nature Reviews. Genetics
|
May 12, 2023
Deafness: from genetic architecture to gene therapy
Christine Petit, Crystel Bonnet, Saaïd Safieddine
European Journal of Medical Genetics
|
June 30, 2026
NEW INSIGHTS INTO THE COMPLEX GENETIC ARCHITECTURE OF AGE-RELATED HEARING LOSS
Crystel Bonnet, Salim Aiche, Sophie Boucher
Proceedings of the National Academy of Sciences of the United States of America
|
August 30, 2006
A mitotically inheritable unit containing a MAP kinase module
Sébastien Kicka, Crystel Bonnet, Andrew K Sobering, et al.
Human Molecular Genetics
|
June 9, 2012
Defect in the gene encoding the EAR/EPTP domain-containing protein TSPEAR causes DFNB98 profound deafness
Sedigheh Delmaghani, Asadollah Aghaie, Nicolas Michalski, et al.
Biochemical and Biophysical Research Communications
|
October 3, 2002
Interaction of STOP with neuronal tubulin is independent of polyglutamylation
Crystel Bonnet, Eric Denarier, Christophe Bosc, et al.
Frontiers in Aging Neuroscience
|
March 18, 2021
Contributions of Age-Related and Audibility-Related Deficits to Aided Consonant Identification in Presbycusis: A Causal-Inference Analysis
Léo Varnet, Agnès C Léger, Sophie Boucher, et al.
Molecular Microbiology
|
September 22, 2006
The peroxisomal import proteins PEX2, PEX5 and PEX7 are differently involved in Podospora anserina sexual cycle
Crystel Bonnet, Eric Espagne, Denise Zickler, et al.
Vision Research
|
September 25, 2012
Fundus autofluorescence and optical coherence tomography in relation to visual function in Usher syndrome type 1 and 2
Ana Fakin, Martina Jarc-Vidmar, Damjan Glavač, et al.
RNA (New York, N.Y.)
|
June 6, 2006
mRNA localization to the mitochondrial surface allows the efficient translocation inside the organelle of a nuclear recoded ATP6 protein
Valérie Kaltimbacher, Crystel Bonnet, Gaëlle Lecoeuvre, et al.
Page
of 8