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Denise Yan

Showing results (91-100 of 103) with videos related to

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Human Genetics|January 22, 2005
Characterization of Usher syndrome type I gene mutations in an Usher syndrome patient populationXiao Mei Ouyang, Denise Yan, Li Lin Du, et al.
Plos One|March 9, 2017
Screening of deafness-causing DNA variants that are common in patients of European ancestry using a microarray-based approachDenise Yan, Guangxin Xiang, Xingping Chai, et al.
Human Genetics|December 4, 2008
Digenic inheritance of non-syndromic deafness caused by mutations at the gap junction proteins Cx26 and Cx31Xue-Zhong Liu, Yongyi Yuan, Denise Yan, et al.
Molecular Cancer Therapeutics|August 5, 2017
Combination Therapy with c-Met and Src Inhibitors Induces Caspase-Dependent Apoptosis of Merlin-Deficient Schwann Cells and Suppresses Growth of Schwannoma CellsMarisa A Fuse, Stephani Klingeman Plati, Sarah S Burns, et al.
Oncotarget|April 22, 2017
Ponatinib promotes a G1 cell-cycle arrest of merlin/NF2-deficient human schwann cellsAlejandra M Petrilli, Jeanine Garcia, Marga Bott, et al.
Human Genetics|March 30, 2016
A mutation in SLC22A4 encoding an organic cation transporter expressed in the cochlea strial endothelium causes human recessive non-syndromic hearing loss DFNB60Mariem Ben Said, M'hamed Grati, Takahiro Ishimoto, et al.
Human Molecular Genetics|April 30, 2003
Prestin, a cochlear motor protein, is defective in non-syndromic hearing lossXue Zhong Liu, Xiao Mei Ouyang, Xia Juan Xia, et al.
Human Genetics|May 2, 2018
ELMOD3, a novel causative gene, associated with human autosomal dominant nonsyndromic and progressive hearing lossWu Li, Jie Sun, Jie Ling, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 6, 2019
Extrusion pump ABCC1 was first linked with nonsyndromic hearing loss in humans by stepwise genetic analysisMeng Li, Lingyun Mei, Chufeng He, et al.
American Journal of Human Genetics|December 22, 2009
Loss-of-function mutations in the PRPS1 gene cause a type of nonsyndromic X-linked sensorineural deafness, DFN2Xuezhong Liu, Dongyi Han, Jianzhong Li, et al.
Pageof 11

Showing results (91-100 of 103) with videos related to

Sort By:
Pageof 11
Human Genetics|January 22, 2005
Characterization of Usher syndrome type I gene mutations in an Usher syndrome patient populationXiao Mei Ouyang, Denise Yan, Li Lin Du, et al.
Plos One|March 9, 2017
Screening of deafness-causing DNA variants that are common in patients of European ancestry using a microarray-based approachDenise Yan, Guangxin Xiang, Xingping Chai, et al.
Human Genetics|December 4, 2008
Digenic inheritance of non-syndromic deafness caused by mutations at the gap junction proteins Cx26 and Cx31Xue-Zhong Liu, Yongyi Yuan, Denise Yan, et al.
Molecular Cancer Therapeutics|August 5, 2017
Combination Therapy with c-Met and Src Inhibitors Induces Caspase-Dependent Apoptosis of Merlin-Deficient Schwann Cells and Suppresses Growth of Schwannoma CellsMarisa A Fuse, Stephani Klingeman Plati, Sarah S Burns, et al.
Oncotarget|April 22, 2017
Ponatinib promotes a G1 cell-cycle arrest of merlin/NF2-deficient human schwann cellsAlejandra M Petrilli, Jeanine Garcia, Marga Bott, et al.
Human Genetics|March 30, 2016
A mutation in SLC22A4 encoding an organic cation transporter expressed in the cochlea strial endothelium causes human recessive non-syndromic hearing loss DFNB60Mariem Ben Said, M'hamed Grati, Takahiro Ishimoto, et al.
Human Molecular Genetics|April 30, 2003
Prestin, a cochlear motor protein, is defective in non-syndromic hearing lossXue Zhong Liu, Xiao Mei Ouyang, Xia Juan Xia, et al.
Human Genetics|May 2, 2018
ELMOD3, a novel causative gene, associated with human autosomal dominant nonsyndromic and progressive hearing lossWu Li, Jie Sun, Jie Ling, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 6, 2019
Extrusion pump ABCC1 was first linked with nonsyndromic hearing loss in humans by stepwise genetic analysisMeng Li, Lingyun Mei, Chufeng He, et al.
American Journal of Human Genetics|December 22, 2009
Loss-of-function mutations in the PRPS1 gene cause a type of nonsyndromic X-linked sensorineural deafness, DFN2Xuezhong Liu, Dongyi Han, Jianzhong Li, et al.
Pageof 11