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Human Genetics
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March 26, 2026
The involvement of TNFRSF25 in age-related hearing loss
Marie Valerie Roche, Pei-Ciao Tang, Denise Yan, et al.
Ear and Hearing
|
May 27, 2021
Review of Genotype-Phenotype Correlations in Usher Syndrome
Eric 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 Asians
Denise Yan, Hong-Joon Park, Xiao Mei Ouyang, et al.
Gene
|
August 2, 2020
Recent advancements in understanding the role of epigenetics in the auditory system
Rahul 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 mutation
Jian 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 loss
Joaquin 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 stereocilia
Wu Li, Yong Feng, Anhai Chen, et al.
Human Genetics
|
June 4, 2018
A dominant variant in the PDE1C gene is associated with nonsyndromic hearing loss
Li Wang, Yong Feng, Denise Yan, et al.
Frontiers in Neurology
|
February 22, 2021
Genetics and the Individualized Therapy of Vestibular Disorders
Christine 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 population
Qingling Bi, Shasha Huang, Hui Wang, et al.
Page
of 11
Search research articles
Search
Showing results (71-80 of 103) with videos related to
Sort By:
Page
of 11
Human Genetics
|
March 26, 2026
The involvement of TNFRSF25 in age-related hearing loss
Marie Valerie Roche, Pei-Ciao Tang, Denise Yan, et al.
Ear and Hearing
|
May 27, 2021
Review of Genotype-Phenotype Correlations in Usher Syndrome
Eric 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 Asians
Denise Yan, Hong-Joon Park, Xiao Mei Ouyang, et al.
Gene
|
August 2, 2020
Recent advancements in understanding the role of epigenetics in the auditory system
Rahul 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 mutation
Jian 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 loss
Joaquin 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 stereocilia
Wu Li, Yong Feng, Anhai Chen, et al.
Human Genetics
|
June 4, 2018
A dominant variant in the PDE1C gene is associated with nonsyndromic hearing loss
Li Wang, Yong Feng, Denise Yan, et al.
Frontiers in Neurology
|
February 22, 2021
Genetics and the Individualized Therapy of Vestibular Disorders
Christine 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 population
Qingling Bi, Shasha Huang, Hui Wang, et al.
Page
of 11