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Xianlin Liu

Showing results (21-30 of 26) with videos related to

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Plos One|September 14, 2023
Gene regulation analysis of patient-derived iPSCs and its CRISPR-corrected control provides a new tool for studying perturbations of ELMOD3 c.512A>G mutation during the development of inherited hearing lossXianlin Liu, Jie Wen, Xuezhong Liu, 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.
Nanoscale Research Letters|June 30, 2011
Investigation of cracks in GaN films grown by combined hydride and metal organic vapor-phase epitaxial methodJianming Liu, Xianlin Liu, Chengming Li, et al.
Frontiers in Genetics|August 6, 2019
Proband Whole-Exome Sequencing Identified Genes Responsible for Autosomal Recessive Non-Syndromic Hearing Loss in 33 Chinese Nuclear FamiliesShushan Sang, Jie Ling, Xuezhong Liu, et al.
Clinical and Experimental Otorhinolaryngology|October 11, 2023
A Novel EYA1 Mutation Causing Alternative RNA Splicing in a Chinese Family With Branchio-Oto Syndrome: Implications for Molecular Diagnosis and Clinical ApplicationAnhai Chen, Jie Ling, Xin Peng, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 29, 2021
A nonsense <i>TMEM43</i> variant leads to disruption of connexin-linked function and autosomal dominant auditory neuropathy spectrum disorderMinwoo Wendy Jang, Doo-Yi Oh, Eunyoung Yi, et al.
Pageof 3

Showing results (21-30 of 26) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 26 results.
Plos One|September 14, 2023
Gene regulation analysis of patient-derived iPSCs and its CRISPR-corrected control provides a new tool for studying perturbations of ELMOD3 c.512A>G mutation during the development of inherited hearing lossXianlin Liu, Jie Wen, Xuezhong Liu, 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.
Nanoscale Research Letters|June 30, 2011
Investigation of cracks in GaN films grown by combined hydride and metal organic vapor-phase epitaxial methodJianming Liu, Xianlin Liu, Chengming Li, et al.
Frontiers in Genetics|August 6, 2019
Proband Whole-Exome Sequencing Identified Genes Responsible for Autosomal Recessive Non-Syndromic Hearing Loss in 33 Chinese Nuclear FamiliesShushan Sang, Jie Ling, Xuezhong Liu, et al.
Clinical and Experimental Otorhinolaryngology|October 11, 2023
A Novel EYA1 Mutation Causing Alternative RNA Splicing in a Chinese Family With Branchio-Oto Syndrome: Implications for Molecular Diagnosis and Clinical ApplicationAnhai Chen, Jie Ling, Xin Peng, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 29, 2021
A nonsense <i>TMEM43</i> variant leads to disruption of connexin-linked function and autosomal dominant auditory neuropathy spectrum disorderMinwoo Wendy Jang, Doo-Yi Oh, Eunyoung Yi, et al.
Pageof 3