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Thomas B Friedman

Showing results (81-90 of 153) with videos related to

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Molecular Therapy : the Journal of the American Society of Gene Therapy|March 4, 2017
Gene Therapy Restores Balance and Auditory Functions in a Mouse Model of Usher SyndromeKevin Isgrig, Jack W Shteamer, Inna A Belyantseva, et al.
Human Genetics|August 11, 2007
The autosomal recessive nonsyndromic deafness locus DFNB72 is located on chromosome 19p13.3Quratul Ain, Sabiha Nazli, Saima Riazuddin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 17, 2003
Early childhood hearing loss: clinical and molecular genetics. An educational slide set of the American College of Medical GeneticsRaye L Alford, Thomas B Friedman, Bronya J B Keats, et al.
Genes|July 27, 2024
Deafness DFNB128 Associated with a Recessive Variant of Human <i>MAP3K1</i> Recapitulates Hearing Loss of <i>Map3k1</i>-Deficient MiceRabia Faridi, Rizwan Yousaf, Sayaka Inagaki, et al.
Cell Reports|February 3, 2021
Semi-automated single-molecule microscopy screening of fast-dissociating specific antibodies directly from hybridoma culturesTakushi Miyoshi, Qianli Zhang, Takafumi Miyake, et al.
Ophthalmic Genetics|May 7, 2020
Atypical and ultra-rare Usher syndrome: a reviewRosalie M Nolen, Robert B Hufnagel, Thomas B Friedman, et al.
Nature Genetics|February 19, 2002
Beethoven, a mouse model for dominant, progressive hearing loss DFNA36Sarah Vreugde, Alexandra Erven, Corné J Kros, et al.
The Journal of Clinical Investigation|October 4, 2011
Mouse model of enlarged vestibular aqueducts defines temporal requirement of Slc26a4 expression for hearing acquisitionByung Yoon Choi, Hyoung-Mi Kim, Taku Ito, et al.
Elife|November 9, 2021
Proposed therapy, developed in a <i>Pcdh15</i>-deficient mouse, for progressive loss of vision in human Usher syndromeSaumil Sethna, Wadih M Zein, Sehar Riaz, et al.
American Journal of Human Genetics|December 23, 2006
Tricellulin is a tight-junction protein necessary for hearingSaima Riazuddin, Zubair M Ahmed, Alan S Fanning, et al.
Pageof 16

Showing results (81-90 of 153) with videos related to

Sort By:
Pageof 16
Molecular Therapy : the Journal of the American Society of Gene Therapy|March 4, 2017
Gene Therapy Restores Balance and Auditory Functions in a Mouse Model of Usher SyndromeKevin Isgrig, Jack W Shteamer, Inna A Belyantseva, et al.
Human Genetics|August 11, 2007
The autosomal recessive nonsyndromic deafness locus DFNB72 is located on chromosome 19p13.3Quratul Ain, Sabiha Nazli, Saima Riazuddin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 17, 2003
Early childhood hearing loss: clinical and molecular genetics. An educational slide set of the American College of Medical GeneticsRaye L Alford, Thomas B Friedman, Bronya J B Keats, et al.
Genes|July 27, 2024
Deafness DFNB128 Associated with a Recessive Variant of Human <i>MAP3K1</i> Recapitulates Hearing Loss of <i>Map3k1</i>-Deficient MiceRabia Faridi, Rizwan Yousaf, Sayaka Inagaki, et al.
Cell Reports|February 3, 2021
Semi-automated single-molecule microscopy screening of fast-dissociating specific antibodies directly from hybridoma culturesTakushi Miyoshi, Qianli Zhang, Takafumi Miyake, et al.
Ophthalmic Genetics|May 7, 2020
Atypical and ultra-rare Usher syndrome: a reviewRosalie M Nolen, Robert B Hufnagel, Thomas B Friedman, et al.
Nature Genetics|February 19, 2002
Beethoven, a mouse model for dominant, progressive hearing loss DFNA36Sarah Vreugde, Alexandra Erven, Corné J Kros, et al.
The Journal of Clinical Investigation|October 4, 2011
Mouse model of enlarged vestibular aqueducts defines temporal requirement of Slc26a4 expression for hearing acquisitionByung Yoon Choi, Hyoung-Mi Kim, Taku Ito, et al.
Elife|November 9, 2021
Proposed therapy, developed in a <i>Pcdh15</i>-deficient mouse, for progressive loss of vision in human Usher syndromeSaumil Sethna, Wadih M Zein, Sehar Riaz, et al.
American Journal of Human Genetics|December 23, 2006
Tricellulin is a tight-junction protein necessary for hearingSaima Riazuddin, Zubair M Ahmed, Alan S Fanning, et al.
Pageof 16