Search research articles
Contact Us
Filters
Showing results (31-40 of 153) with videos related to
Page
of 16
Sort By:
Advances in Oto-Rhino-Laryngology
|
November 1, 2002
DFNB3, spectrum of MYO15A recessive mutant alleles and an emerging genotype-phenotype correlation
Thomas B Friedman, John T Hinnant, Manju Ghosh, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
December 30, 2020
Myosin 18Aα targets the guanine nucleotide exchange factor β-Pix to the dendritic spines of cerebellar Purkinje neurons and promotes spine maturation
Christopher J Alexander, Melanie Barzik, Ikuko Fujiwara, et al.
American Journal of Medical Genetics. Part A
|
September 15, 2005
A new locus for nonsyndromic deafness DFNB51 maps to chromosome 11p13-p12
Rehan Sadiq Shaikh, Khushnooda Ramzan, Sabiha Nazli, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
July 23, 2023
Combined AAV-mediated gene replacement therapy improves auditory function in a mouse model of human DFNB42 deafness
Kevin Isgrig, Alexander X Cartagena-Rivera, Hong Jun Wang, et al.
Cell
|
July 3, 2018
Defects in the Alternative Splicing-Dependent Regulation of REST Cause Deafness
Yoko Nakano, Michael C Kelly, Atteeq U Rehman, et al.
Journal of the Association for Research in Otolaryngology : JARO
|
September 1, 2011
TRPA1-mediated accumulation of aminoglycosides in mouse cochlear outer hair cells
Ruben S Stepanyan, Artur A Indzhykulian, A Catalina Vélez-Ortega, et al.
Biorxiv : the Preprint Server for Biology
|
May 20, 2024
Live-cell single-molecule fluorescence microscopy for protruding organelles reveals regulatory mechanisms of MYO7A-driven cargo transport in stereocilia of inner ear hair cells
Takushi Miyoshi, Harshad D Vishwasrao, Inna A Belyantseva, et al.
Hearing Research
|
March 27, 2013
A null mutation of mouse Kcna10 causes significant vestibular and mild hearing dysfunction
Sue I Lee, Travis Conrad, Sherri M Jones, et al.
The European Journal of Neuroscience
|
March 3, 2007
Lhx3, a LIM domain transcription factor, is regulated by Pou4f3 in the auditory but not in the vestibular system
Ronna Hertzano, Amiel A Dror, Mireille Montcouquiol, et al.
Clinical Genetics
|
March 8, 2024
Homozygous novel truncating variant of CLPP associated with severe Perrault syndrome
Rabia Faridi, Pamela Stratton, Noemi Salmeri, et al.
Page
of 16
Search research articles
Search
Showing results (31-40 of 153) with videos related to
Sort By:
Page
of 16
Advances in Oto-Rhino-Laryngology
|
November 1, 2002
DFNB3, spectrum of MYO15A recessive mutant alleles and an emerging genotype-phenotype correlation
Thomas B Friedman, John T Hinnant, Manju Ghosh, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
December 30, 2020
Myosin 18Aα targets the guanine nucleotide exchange factor β-Pix to the dendritic spines of cerebellar Purkinje neurons and promotes spine maturation
Christopher J Alexander, Melanie Barzik, Ikuko Fujiwara, et al.
American Journal of Medical Genetics. Part A
|
September 15, 2005
A new locus for nonsyndromic deafness DFNB51 maps to chromosome 11p13-p12
Rehan Sadiq Shaikh, Khushnooda Ramzan, Sabiha Nazli, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
July 23, 2023
Combined AAV-mediated gene replacement therapy improves auditory function in a mouse model of human DFNB42 deafness
Kevin Isgrig, Alexander X Cartagena-Rivera, Hong Jun Wang, et al.
Cell
|
July 3, 2018
Defects in the Alternative Splicing-Dependent Regulation of REST Cause Deafness
Yoko Nakano, Michael C Kelly, Atteeq U Rehman, et al.
Journal of the Association for Research in Otolaryngology : JARO
|
September 1, 2011
TRPA1-mediated accumulation of aminoglycosides in mouse cochlear outer hair cells
Ruben S Stepanyan, Artur A Indzhykulian, A Catalina Vélez-Ortega, et al.
Biorxiv : the Preprint Server for Biology
|
May 20, 2024
Live-cell single-molecule fluorescence microscopy for protruding organelles reveals regulatory mechanisms of MYO7A-driven cargo transport in stereocilia of inner ear hair cells
Takushi Miyoshi, Harshad D Vishwasrao, Inna A Belyantseva, et al.
Hearing Research
|
March 27, 2013
A null mutation of mouse Kcna10 causes significant vestibular and mild hearing dysfunction
Sue I Lee, Travis Conrad, Sherri M Jones, et al.
The European Journal of Neuroscience
|
March 3, 2007
Lhx3, a LIM domain transcription factor, is regulated by Pou4f3 in the auditory but not in the vestibular system
Ronna Hertzano, Amiel A Dror, Mireille Montcouquiol, et al.
Clinical Genetics
|
March 8, 2024
Homozygous novel truncating variant of CLPP associated with severe Perrault syndrome
Rabia Faridi, Pamela Stratton, Noemi Salmeri, et al.
Page
of 16