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Asadollah Aghaie

Showing results (1-10 of 13) with videos related to

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Human Molecular Genetics|June 9, 2012
Defect in the gene encoding the EAR/EPTP domain-containing protein TSPEAR causes DFNB98 profound deafnessSedigheh Delmaghani, Asadollah Aghaie, Nicolas Michalski, et al.
European Journal of Human Genetics : EJHG|September 27, 2003
DFNB40, a recessive form of sensorineural hearing loss, maps to chromosome 22q11.21-12.1Sedigheh Delmaghani, Asadollah Aghaie, Sylvie Compain-Nouaille, et al.
The Journal of Biological Chemistry|March 28, 2008
New insights into the alternative D-glucarate degradation pathwayAsadollah Aghaie, Christophe Lechaplais, Peggy Sirven, et al.
The Journal of Cell Biology|May 13, 2017
Usher syndrome type 1-associated cadherins shape the photoreceptor outer segmentCataldo Schietroma, Karine Parain, Amrit Estivalet, et al.
International Journal of Molecular Medicine|September 12, 2006
crv4, a mouse model for human ataxia associated with kyphoscoliosis caused by an mRNA splicing mutation of the metabotropic glutamate receptor 1 (Grm1)Valerio Conti, Asadollah Aghaie, Michele Cilli, et al.
American Journal of Human Genetics|June 4, 2016
Mutations in CDC14A, Encoding a Protein Phosphatase Involved in Hair Cell Ciliogenesis, Cause Autosomal-Recessive Severe to Profound DeafnessSedigheh Delmaghani, Asadollah Aghaie, Yosra Bouyacoub, et al.
The Journal of Cell Biology|January 13, 2016
Class III myosins shape the auditory hair bundles by limiting microvilli and stereocilia growthAndrea Lelli, Vincent Michel, Jacques Boutet de Monvel, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 14, 2008
The mitochondrial protease AFG3L2 is essential for axonal developmentFrancesca Maltecca, Asadollah Aghaie, David G Schroeder, et al.
Nature Genetics|June 29, 2006
Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathySedigheh Delmaghani, Francisco J del Castillo, Vincent Michel, et al.
The Journal of Cell Biology|October 10, 2012
Localization of Usher 1 proteins to the photoreceptor calyceal processes, which are absent from miceIman Sahly, Eric Dufour, Cataldo Schietroma, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Human Molecular Genetics|June 9, 2012
Defect in the gene encoding the EAR/EPTP domain-containing protein TSPEAR causes DFNB98 profound deafnessSedigheh Delmaghani, Asadollah Aghaie, Nicolas Michalski, et al.
European Journal of Human Genetics : EJHG|September 27, 2003
DFNB40, a recessive form of sensorineural hearing loss, maps to chromosome 22q11.21-12.1Sedigheh Delmaghani, Asadollah Aghaie, Sylvie Compain-Nouaille, et al.
The Journal of Biological Chemistry|March 28, 2008
New insights into the alternative D-glucarate degradation pathwayAsadollah Aghaie, Christophe Lechaplais, Peggy Sirven, et al.
The Journal of Cell Biology|May 13, 2017
Usher syndrome type 1-associated cadherins shape the photoreceptor outer segmentCataldo Schietroma, Karine Parain, Amrit Estivalet, et al.
International Journal of Molecular Medicine|September 12, 2006
crv4, a mouse model for human ataxia associated with kyphoscoliosis caused by an mRNA splicing mutation of the metabotropic glutamate receptor 1 (Grm1)Valerio Conti, Asadollah Aghaie, Michele Cilli, et al.
American Journal of Human Genetics|June 4, 2016
Mutations in CDC14A, Encoding a Protein Phosphatase Involved in Hair Cell Ciliogenesis, Cause Autosomal-Recessive Severe to Profound DeafnessSedigheh Delmaghani, Asadollah Aghaie, Yosra Bouyacoub, et al.
The Journal of Cell Biology|January 13, 2016
Class III myosins shape the auditory hair bundles by limiting microvilli and stereocilia growthAndrea Lelli, Vincent Michel, Jacques Boutet de Monvel, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 14, 2008
The mitochondrial protease AFG3L2 is essential for axonal developmentFrancesca Maltecca, Asadollah Aghaie, David G Schroeder, et al.
Nature Genetics|June 29, 2006
Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathySedigheh Delmaghani, Francisco J del Castillo, Vincent Michel, et al.
The Journal of Cell Biology|October 10, 2012
Localization of Usher 1 proteins to the photoreceptor calyceal processes, which are absent from miceIman Sahly, Eric Dufour, Cataldo Schietroma, et al.
Pageof 2