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Denise Yan

Showing results (71-80 of 103) with videos related to

Pageof 11
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Human Genetics|March 26, 2026
The involvement of TNFRSF25 in age-related hearing lossMarie Valerie Roche, Pei-Ciao Tang, Denise Yan, et al.
Ear and Hearing|May 27, 2021
Review of Genotype-Phenotype Correlations in Usher SyndromeEric Nisenbaum, Torin P Thielhelm, Aida Nourbakhsh, et al.
Human Genetics|September 25, 2003
Evidence of a founder effect for the 235delC mutation of GJB2 (connexin 26) in east AsiansDenise Yan, Hong-Joon Park, Xiao Mei Ouyang, et al.
Gene|August 2, 2020
Recent advancements in understanding the role of epigenetics in the auditory systemRahul Mittal, Nicole Bencie, George Liu, et al.
Mutation Research|May 28, 2016
Abnormal mRNA splicing but normal auditory brainstem response (ABR) in mice with the prestin (SLC26A5) IVS2-2A>G mutationJian Zhang, Ziyi Liu, Aoshuang Chang, et al.
Gene|April 19, 2020
Diagnostic and therapeutic applications of genomic medicine in progressive, late-onset, nonsyndromic sensorineural hearing lossJoaquin E Jimenez, Aida Nourbakhsh, Brett Colbert, et al.
Human Molecular Genetics|October 20, 2019
Elmod3 knockout leads to progressive hearing loss and abnormalities in cochlear hair cell stereociliaWu Li, Yong Feng, Anhai Chen, et al.
Human Genetics|June 4, 2018
A dominant variant in the PDE1C gene is associated with nonsyndromic hearing lossLi Wang, Yong Feng, Denise Yan, et al.
Frontiers in Neurology|February 22, 2021
Genetics and the Individualized Therapy of Vestibular DisordersChristine Mei, Hongsong Dong, Eric Nisenbaum, et al.
Journal of Assisted Reproduction and Genetics|April 24, 2023
Correction to: Preimplantation genetic testing for hereditary hearing loss in Chinese populationQingling Bi, Shasha Huang, Hui Wang, et al.
Pageof 11

Showing results (71-80 of 103) with videos related to

Sort By:
Pageof 11
Human Genetics|March 26, 2026
The involvement of TNFRSF25 in age-related hearing lossMarie Valerie Roche, Pei-Ciao Tang, Denise Yan, et al.
Ear and Hearing|May 27, 2021
Review of Genotype-Phenotype Correlations in Usher SyndromeEric Nisenbaum, Torin P Thielhelm, Aida Nourbakhsh, et al.
Human Genetics|September 25, 2003
Evidence of a founder effect for the 235delC mutation of GJB2 (connexin 26) in east AsiansDenise Yan, Hong-Joon Park, Xiao Mei Ouyang, et al.
Gene|August 2, 2020
Recent advancements in understanding the role of epigenetics in the auditory systemRahul Mittal, Nicole Bencie, George Liu, et al.
Mutation Research|May 28, 2016
Abnormal mRNA splicing but normal auditory brainstem response (ABR) in mice with the prestin (SLC26A5) IVS2-2A>G mutationJian Zhang, Ziyi Liu, Aoshuang Chang, et al.
Gene|April 19, 2020
Diagnostic and therapeutic applications of genomic medicine in progressive, late-onset, nonsyndromic sensorineural hearing lossJoaquin E Jimenez, Aida Nourbakhsh, Brett Colbert, et al.
Human Molecular Genetics|October 20, 2019
Elmod3 knockout leads to progressive hearing loss and abnormalities in cochlear hair cell stereociliaWu Li, Yong Feng, Anhai Chen, et al.
Human Genetics|June 4, 2018
A dominant variant in the PDE1C gene is associated with nonsyndromic hearing lossLi Wang, Yong Feng, Denise Yan, et al.
Frontiers in Neurology|February 22, 2021
Genetics and the Individualized Therapy of Vestibular DisordersChristine Mei, Hongsong Dong, Eric Nisenbaum, et al.
Journal of Assisted Reproduction and Genetics|April 24, 2023
Correction to: Preimplantation genetic testing for hereditary hearing loss in Chinese populationQingling Bi, Shasha Huang, Hui Wang, et al.
Pageof 11