Search research articles
Contact Us
Filters
Showing results (1-10 of 152) with videos related to
Page
of 16
Sort By:
Clinical Genetics
|
September 12, 2019
Growth factor and receptor malfunctions associated with human genetic deafness
Sadaf Naz, Thomas B Friedman
Trends in Molecular Medicine
|
November 8, 2003
The genetic bases for syndromic and nonsyndromic deafness among Jews
Tamar Ben-Yosef, Thomas B Friedman
Archives of Otolaryngology--Head & Neck Surgery
|
January 12, 2002
Auditory function and the M34T allele of connexin 26
Andrew J Griffith, Thomas B Friedman
Annual Review of Genomics and Human Genetics
|
October 7, 2003
Human nonsyndromic sensorineural deafness
Thomas B Friedman, Andrew J Griffith
STAR Protocols
|
November 29, 2021
Fast-dissociating but highly specific antibodies are novel tools in biology, especially useful for multiplex super-resolution microscopy
Takushi Miyoshi, Thomas B Friedman, Naoki Watanabe
Advances in Experimental Medicine and Biology
|
May 27, 2020
Myosins and Hearing
Thomas B Friedman, Inna A Belyantseva, Gregory I Frolenkov
Proceedings of the National Academy of Sciences of the United States of America
|
November 12, 2003
Myosin XVa localizes to the tips of inner ear sensory cell stereocilia and is essential for staircase formation of the hair bundle
Inna A Belyantseva, Erich T Boger, Thomas B Friedman
Retina (Philadelphia, Pa.)
|
December 24, 2005
Usher syndrome type 1: genotype-phenotype relationships
Thomas B Friedman, Julie M Schultz, Zubair M Ahmed
Frontiers in Physiology
|
April 2, 2024
Pathophysiology of human hearing loss associated with variants in myosins
Takushi Miyoshi, Inna A Belyantseva, Mrudhula Sajeevadathan, et al.
Hearing Research
|
December 28, 2011
Actin in hair cells and hearing loss
Meghan C Drummond, Inna A Belyantseva, Karen H Friderici, et al.
Page
of 16
Search research articles
Search
Showing results (1-10 of 152) with videos related to
Sort By:
Page
of 16
Clinical Genetics
|
September 12, 2019
Growth factor and receptor malfunctions associated with human genetic deafness
Sadaf Naz, Thomas B Friedman
Trends in Molecular Medicine
|
November 8, 2003
The genetic bases for syndromic and nonsyndromic deafness among Jews
Tamar Ben-Yosef, Thomas B Friedman
Archives of Otolaryngology--Head & Neck Surgery
|
January 12, 2002
Auditory function and the M34T allele of connexin 26
Andrew J Griffith, Thomas B Friedman
Annual Review of Genomics and Human Genetics
|
October 7, 2003
Human nonsyndromic sensorineural deafness
Thomas B Friedman, Andrew J Griffith
STAR Protocols
|
November 29, 2021
Fast-dissociating but highly specific antibodies are novel tools in biology, especially useful for multiplex super-resolution microscopy
Takushi Miyoshi, Thomas B Friedman, Naoki Watanabe
Advances in Experimental Medicine and Biology
|
May 27, 2020
Myosins and Hearing
Thomas B Friedman, Inna A Belyantseva, Gregory I Frolenkov
Proceedings of the National Academy of Sciences of the United States of America
|
November 12, 2003
Myosin XVa localizes to the tips of inner ear sensory cell stereocilia and is essential for staircase formation of the hair bundle
Inna A Belyantseva, Erich T Boger, Thomas B Friedman
Retina (Philadelphia, Pa.)
|
December 24, 2005
Usher syndrome type 1: genotype-phenotype relationships
Thomas B Friedman, Julie M Schultz, Zubair M Ahmed
Frontiers in Physiology
|
April 2, 2024
Pathophysiology of human hearing loss associated with variants in myosins
Takushi Miyoshi, Inna A Belyantseva, Mrudhula Sajeevadathan, et al.
Hearing Research
|
December 28, 2011
Actin in hair cells and hearing loss
Meghan C Drummond, Inna A Belyantseva, Karen H Friderici, et al.
Page
of 16