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Denise Yan

Showing results (81-90 of 103) with videos related to

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Journal of Assisted Reproduction and Genetics|April 5, 2023
Preimplantation genetic testing for hereditary hearing loss in Chinese populationQingling Bi, Shasha Huang, Hui Wang, et al.
Journal of Cellular Physiology|August 12, 2016
Neurotransmitters: The Critical Modulators Regulating Gut-Brain AxisRahul Mittal, Luca H Debs, Amit P Patel, et al.
Human Molecular Genetics|January 21, 2015
A missense mutation in DCDC2 causes human recessive deafness DFNB66, likely by interfering with sensory hair cell and supporting cell cilia length regulationM'hamed Grati, Imen Chakchouk, Qi Ma, et al.
Genetic Testing and Molecular Biomarkers|December 11, 2014
Prevalence of mutations in GJB2, SLC26A4, and mtDNA in children with severe or profound sensorineural hearing loss in southwestern ChinaJie Qing, Yuan Zhou, Ruosha Lai, et al.
Gene|January 15, 2018
Genetic basis of hearing loss in Spanish, Hispanic and Latino populationsRahul Mittal, Amit P Patel, Desiree Nguyen, et al.
Journal of Medical Microbiology|August 8, 2015
Current concepts in the pathogenesis and treatment of chronic suppurative otitis mediaRahul Mittal, Christopher V Lisi, Robert Gerring, et al.
The Journal of Gene Medicine|November 26, 2016
Functional characterization of a novel loss-of-function mutation of PRPS1 related to early-onset progressive nonsyndromic hearing loss in Koreans (DFNX1): Potential implications on future therapeutic interventionSo Young Kim, Ah Reum Kim, Nayoung K D Kim, et al.
Human Mutation|February 4, 2016
MYO3A Causes Human Dominant Deafness and Interacts with Protocadherin 15-CD2 IsoformM'hamed Grati, Denise Yan, Manmeet H Raval, et al.
Molecular Genetics and Genomics : MGG|January 31, 2015
Novel mutations confirm that COL11A2 is responsible for autosomal recessive non-syndromic hearing loss DFNB53Imen Chakchouk, M'hamed Grati, Guney Bademci, et al.
Journal of Human Genetics|December 15, 2010
Novel missense mutations in MYO7A underlying postlingual high- or low-frequency non-syndromic hearing impairment in two large families from ChinaYi Sun, Jing Chen, Hanjun Sun, et al.
Pageof 11

Showing results (81-90 of 103) with videos related to

Sort By:
Pageof 11
Journal of Assisted Reproduction and Genetics|April 5, 2023
Preimplantation genetic testing for hereditary hearing loss in Chinese populationQingling Bi, Shasha Huang, Hui Wang, et al.
Journal of Cellular Physiology|August 12, 2016
Neurotransmitters: The Critical Modulators Regulating Gut-Brain AxisRahul Mittal, Luca H Debs, Amit P Patel, et al.
Human Molecular Genetics|January 21, 2015
A missense mutation in DCDC2 causes human recessive deafness DFNB66, likely by interfering with sensory hair cell and supporting cell cilia length regulationM'hamed Grati, Imen Chakchouk, Qi Ma, et al.
Genetic Testing and Molecular Biomarkers|December 11, 2014
Prevalence of mutations in GJB2, SLC26A4, and mtDNA in children with severe or profound sensorineural hearing loss in southwestern ChinaJie Qing, Yuan Zhou, Ruosha Lai, et al.
Gene|January 15, 2018
Genetic basis of hearing loss in Spanish, Hispanic and Latino populationsRahul Mittal, Amit P Patel, Desiree Nguyen, et al.
Journal of Medical Microbiology|August 8, 2015
Current concepts in the pathogenesis and treatment of chronic suppurative otitis mediaRahul Mittal, Christopher V Lisi, Robert Gerring, et al.
The Journal of Gene Medicine|November 26, 2016
Functional characterization of a novel loss-of-function mutation of PRPS1 related to early-onset progressive nonsyndromic hearing loss in Koreans (DFNX1): Potential implications on future therapeutic interventionSo Young Kim, Ah Reum Kim, Nayoung K D Kim, et al.
Human Mutation|February 4, 2016
MYO3A Causes Human Dominant Deafness and Interacts with Protocadherin 15-CD2 IsoformM'hamed Grati, Denise Yan, Manmeet H Raval, et al.
Molecular Genetics and Genomics : MGG|January 31, 2015
Novel mutations confirm that COL11A2 is responsible for autosomal recessive non-syndromic hearing loss DFNB53Imen Chakchouk, M'hamed Grati, Guney Bademci, et al.
Journal of Human Genetics|December 15, 2010
Novel missense mutations in MYO7A underlying postlingual high- or low-frequency non-syndromic hearing impairment in two large families from ChinaYi Sun, Jing Chen, Hanjun Sun, et al.
Pageof 11