Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Thomas B Friedman

Showing results (71-80 of 153) with videos related to

Pageof 16
Sort By:
Molecular Vision|December 6, 2008
Double homozygous waltzer and Ames waltzer mice provide no evidence of retinal degenerationZubair M Ahmed, Sten Kjellstrom, Ricky J L Haywood-Watson, et al.
Human Genetics|August 2, 2021
New insights into Perrault syndrome, a clinically and genetically heterogeneous disorderRabia Faridi, Alessandro Rea, Cristina Fenollar-Ferrer, et al.
Journal of the Association for Research in Otolaryngology : JARO|April 14, 2010
CD44 is a marker for the outer pillar cells in the early postnatal mouse inner earRonna Hertzano, Chandrakala Puligilla, Siaw-Lin Chan, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 6, 2009
Gamma-actin is required for cytoskeletal maintenance but not developmentInna A Belyantseva, Benjamin J Perrin, Kevin J Sonnemann, et al.
Journal of Human Genetics|June 3, 2011
Molecular and clinical studies of X-linked deafness among Pakistani familiesAli M Waryah, Zubair M Ahmed, Munir A Bhinder, et al.
American Journal of Human Genetics|February 23, 2010
Targeted capture and next-generation sequencing identifies C9orf75, encoding taperin, as the mutated gene in nonsyndromic deafness DFNB79Atteeq Ur Rehman, Robert J Morell, Inna A Belyantseva, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|January 22, 2022
Gene Therapy Restores Balance and Auditory Functions in a Mouse Model of Usher SyndromeKevin Isgrig, Jack W Shteamer, Inna A Belyantseva, et al.
Ear and Hearing|August 19, 2003
Recent advances in the understanding of syndromic forms of hearing lossThomas B Friedman, Julie M Schultz, Tamar Ben-Yosef, et al.
Human Genetics|July 11, 2002
Nonsyndromic recessive deafness DFNB18 and Usher syndrome type IC are allelic mutations of USHICZubair M Ahmed, Tenesha N Smith, Saima Riazuddin, et al.
Human Molecular Genetics|October 23, 2003
PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23Zubair M Ahmed, Saima Riazuddin, Jamil Ahmad, et al.
Pageof 16

Showing results (71-80 of 153) with videos related to

Sort By:
Pageof 16
Molecular Vision|December 6, 2008
Double homozygous waltzer and Ames waltzer mice provide no evidence of retinal degenerationZubair M Ahmed, Sten Kjellstrom, Ricky J L Haywood-Watson, et al.
Human Genetics|August 2, 2021
New insights into Perrault syndrome, a clinically and genetically heterogeneous disorderRabia Faridi, Alessandro Rea, Cristina Fenollar-Ferrer, et al.
Journal of the Association for Research in Otolaryngology : JARO|April 14, 2010
CD44 is a marker for the outer pillar cells in the early postnatal mouse inner earRonna Hertzano, Chandrakala Puligilla, Siaw-Lin Chan, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 6, 2009
Gamma-actin is required for cytoskeletal maintenance but not developmentInna A Belyantseva, Benjamin J Perrin, Kevin J Sonnemann, et al.
Journal of Human Genetics|June 3, 2011
Molecular and clinical studies of X-linked deafness among Pakistani familiesAli M Waryah, Zubair M Ahmed, Munir A Bhinder, et al.
American Journal of Human Genetics|February 23, 2010
Targeted capture and next-generation sequencing identifies C9orf75, encoding taperin, as the mutated gene in nonsyndromic deafness DFNB79Atteeq Ur Rehman, Robert J Morell, Inna A Belyantseva, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|January 22, 2022
Gene Therapy Restores Balance and Auditory Functions in a Mouse Model of Usher SyndromeKevin Isgrig, Jack W Shteamer, Inna A Belyantseva, et al.
Ear and Hearing|August 19, 2003
Recent advances in the understanding of syndromic forms of hearing lossThomas B Friedman, Julie M Schultz, Tamar Ben-Yosef, et al.
Human Genetics|July 11, 2002
Nonsyndromic recessive deafness DFNB18 and Usher syndrome type IC are allelic mutations of USHICZubair M Ahmed, Tenesha N Smith, Saima Riazuddin, et al.
Human Molecular Genetics|October 23, 2003
PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23Zubair M Ahmed, Saima Riazuddin, Jamil Ahmad, et al.
Pageof 16