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Denise Yan

Showing results (51-60 of 103) with videos related to

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Neural Plasticity|April 3, 2019
New Genotypes and Phenotypes in Patients with 3 Subtypes of Waardenburg Syndrome Identified by Diagnostic Next-Generation SequencingWu Li, Lingyun Mei, Hongsheng Chen, et al.
International Journal of Pediatric Otorhinolaryngology|April 9, 2008
Cochlear implantation in individuals with Usher type 1 syndromeXue Z Liu, Simon I Angeli, Kaukab Rajput, et al.
Brain Research|March 10, 2010
Ush1c gene expression levels in the ear and eye suggest different roles for Ush1c in neurosensory organs in a new Ush1c knockout mouseCong Tian, Xue Z Liu, Fengchan Han, et al.
Human Molecular Genetics|November 13, 2004
Digenic inheritance of deafness caused by mutations in genes encoding cadherin 23 and protocadherin 15 in mice and humansQing Yin Zheng, Denise Yan, Xiao Mei Ouyang, et al.
Gene Reports|January 2, 2019
Amino acid 118 in the Deafness Causing (DFNA20/26) <i>ACTG1</i> gene is a Mutational Hot SpotLi Wang, Denise Yan, Litao Qin, et al.
Journal of Cellular Physiology|November 22, 2016
Signaling in the Auditory System: Implications in Hair Cell Regeneration and Hearing FunctionRahul Mittal, Luca H Debs, Desiree Nguyen, et al.
Frontiers in Microbiology|December 6, 2016
Otopathogenic <i>Pseudomonas aeruginosa</i> Enters and Survives Inside MacrophagesRahul Mittal, Christopher V Lisi, Hansi Kumari, et al.
Anatomical Record (Hoboken, N.J. : 2007)|March 16, 2019
Zebrafish Model for Nonsyndromic X-Linked Sensorineural Deafness, DFNX1Alexandra A DeSmidt, Bing Zou, M'hamed Grati, et al.
Audiology & Neuro-Otology|June 18, 2023
Genotype-Phenotype Correlations in TMPRSS3 (DFNB10/DFNB8) with Emphasis on Natural HistoryEric Nisenbaum, Denise Yan, A Eliot Shearer, et al.
Journal of Otology|January 28, 2021
Electrophysiology and genetic testing in the precision medicine of congenital deafness: A reviewKevin Y Zhan, Oliver F Adunka, Adrien Eshraghi, et al.
Pageof 11

Showing results (51-60 of 103) with videos related to

Sort By:
Pageof 11
Neural Plasticity|April 3, 2019
New Genotypes and Phenotypes in Patients with 3 Subtypes of Waardenburg Syndrome Identified by Diagnostic Next-Generation SequencingWu Li, Lingyun Mei, Hongsheng Chen, et al.
International Journal of Pediatric Otorhinolaryngology|April 9, 2008
Cochlear implantation in individuals with Usher type 1 syndromeXue Z Liu, Simon I Angeli, Kaukab Rajput, et al.
Brain Research|March 10, 2010
Ush1c gene expression levels in the ear and eye suggest different roles for Ush1c in neurosensory organs in a new Ush1c knockout mouseCong Tian, Xue Z Liu, Fengchan Han, et al.
Human Molecular Genetics|November 13, 2004
Digenic inheritance of deafness caused by mutations in genes encoding cadherin 23 and protocadherin 15 in mice and humansQing Yin Zheng, Denise Yan, Xiao Mei Ouyang, et al.
Gene Reports|January 2, 2019
Amino acid 118 in the Deafness Causing (DFNA20/26) <i>ACTG1</i> gene is a Mutational Hot SpotLi Wang, Denise Yan, Litao Qin, et al.
Journal of Cellular Physiology|November 22, 2016
Signaling in the Auditory System: Implications in Hair Cell Regeneration and Hearing FunctionRahul Mittal, Luca H Debs, Desiree Nguyen, et al.
Frontiers in Microbiology|December 6, 2016
Otopathogenic <i>Pseudomonas aeruginosa</i> Enters and Survives Inside MacrophagesRahul Mittal, Christopher V Lisi, Hansi Kumari, et al.
Anatomical Record (Hoboken, N.J. : 2007)|March 16, 2019
Zebrafish Model for Nonsyndromic X-Linked Sensorineural Deafness, DFNX1Alexandra A DeSmidt, Bing Zou, M'hamed Grati, et al.
Audiology & Neuro-Otology|June 18, 2023
Genotype-Phenotype Correlations in TMPRSS3 (DFNB10/DFNB8) with Emphasis on Natural HistoryEric Nisenbaum, Denise Yan, A Eliot Shearer, et al.
Journal of Otology|January 28, 2021
Electrophysiology and genetic testing in the precision medicine of congenital deafness: A reviewKevin Y Zhan, Oliver F Adunka, Adrien Eshraghi, et al.
Pageof 11