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Thomas B Friedman

Showing results (21-30 of 153) with videos related to

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Advances in Oto-Rhino-Laryngology|November 1, 2002
Genetic modifiers of hereditary hearing lossSaima Riazuddin, Zubair M Ahmed, Thomas B Friedman, et al.
Genomics|February 28, 2002
Identification of target genes regulated by PAX3 and PAX3-FKHR in embryogenesis and alveolar rhabdomyosarcomaThomas D Barber, Melisa C Barber, Oana Tomescu, et al.
Genomics|October 20, 2006
Signatures from tissue-specific MPSS libraries identify transcripts preferentially expressed in the mouse inner earLinda M Peters, Inna A Belyantseva, Ayala Lagziel, et al.
Developmental Biology|May 11, 2005
Spatiotemporal pattern and isoforms of cadherin 23 in wild type and waltzer mice during inner ear hair cell developmentAyala Lagziel, Zubair M Ahmed, Julie M Schultz, et al.
The Journal of Biological Chemistry|December 29, 2020
The ATPase mechanism of myosin 15, the molecular motor mutated in DFNB3 human deafnessFangfang Jiang, Yasuharu Takagi, Arik Shams, et al.
Neurogenetics|February 17, 2016
Recessive mutations of TMC1 associated with moderate to severe hearing lossAyesha Imtiaz, Azra Maqsood, Atteeq U Rehman, et al.
Advances in Oto-Rhino-Laryngology|November 1, 2002
Clinical presentation of DFNB12 and Usher syndrome type 1DJulie M Bork, Robert J Morell, Shaheen Khan, et al.
Elife|February 9, 2018
Bipolar filaments of human nonmuscle myosin 2-A and 2-B have distinct motile and mechanical propertiesLuca Melli, Neil Billington, Sara A Sun, et al.
Plos Genetics|March 29, 2018
Mutations in Diphosphoinositol-Pentakisphosphate Kinase PPIP5K2 are associated with hearing loss in human and mouseRizwan Yousaf, Chunfang Gu, Zubair M Ahmed, et al.
Human Genetics|May 30, 2007
A twin study of auditory processing indicates that dichotic listening ability is a strongly heritable traitRobert J Morell, Carmen C Brewer, Dongliang Ge, et al.
Pageof 16

Showing results (21-30 of 153) with videos related to

Sort By:
Pageof 16
Advances in Oto-Rhino-Laryngology|November 1, 2002
Genetic modifiers of hereditary hearing lossSaima Riazuddin, Zubair M Ahmed, Thomas B Friedman, et al.
Genomics|February 28, 2002
Identification of target genes regulated by PAX3 and PAX3-FKHR in embryogenesis and alveolar rhabdomyosarcomaThomas D Barber, Melisa C Barber, Oana Tomescu, et al.
Genomics|October 20, 2006
Signatures from tissue-specific MPSS libraries identify transcripts preferentially expressed in the mouse inner earLinda M Peters, Inna A Belyantseva, Ayala Lagziel, et al.
Developmental Biology|May 11, 2005
Spatiotemporal pattern and isoforms of cadherin 23 in wild type and waltzer mice during inner ear hair cell developmentAyala Lagziel, Zubair M Ahmed, Julie M Schultz, et al.
The Journal of Biological Chemistry|December 29, 2020
The ATPase mechanism of myosin 15, the molecular motor mutated in DFNB3 human deafnessFangfang Jiang, Yasuharu Takagi, Arik Shams, et al.
Neurogenetics|February 17, 2016
Recessive mutations of TMC1 associated with moderate to severe hearing lossAyesha Imtiaz, Azra Maqsood, Atteeq U Rehman, et al.
Advances in Oto-Rhino-Laryngology|November 1, 2002
Clinical presentation of DFNB12 and Usher syndrome type 1DJulie M Bork, Robert J Morell, Shaheen Khan, et al.
Elife|February 9, 2018
Bipolar filaments of human nonmuscle myosin 2-A and 2-B have distinct motile and mechanical propertiesLuca Melli, Neil Billington, Sara A Sun, et al.
Plos Genetics|March 29, 2018
Mutations in Diphosphoinositol-Pentakisphosphate Kinase PPIP5K2 are associated with hearing loss in human and mouseRizwan Yousaf, Chunfang Gu, Zubair M Ahmed, et al.
Human Genetics|May 30, 2007
A twin study of auditory processing indicates that dichotic listening ability is a strongly heritable traitRobert J Morell, Carmen C Brewer, Dongliang Ge, et al.
Pageof 16