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Showing results (181-190 of 235) with videos related to

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JCI Insight|June 18, 2026
Distal enhancer-insulator module of GDF6 is essential for cochlear formationMohammad Faraz Zafeer, Clemer Abad, Havva Ortabozkoyun, et al.
Hearing Research|January 17, 2017
Broadening the phenotype of DFNB28: Mutations in TRIOBP are associated with moderate, stable hereditary hearing impairmentMieke Wesdorp, Jiddeke M van de Kamp, Erik F Hensen, et al.
Journal of Medical Genetics|March 19, 2026
<i>CDK4</i> and <i>CDK6</i> variants in patients with primary microcephaly lead to cell cycle defects and mitochondria-induced apoptosisEsra Isik, Mohammad Faraz Zafeer, Guney Bademci, 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.
Annals of Human Genetics|November 22, 2016
Targeted Resequencing of Deafness Genes Reveals a Founder MYO15A Variant in Northeastern BrazilGabrielle N Manzoli, Guney Bademci, Angelina X Acosta, et al.
Human Genomics|November 23, 2023
Dispersed DNA variants underlie hearing loss in South Florida's minority populationLéShon Peart, Joanna Gonzalez, Dayna Morel Swols, et al.
Developmental Cell|January 6, 2015
Ankrd11 is a chromatin regulator involved in autism that is essential for neural developmentDenis Gallagher, Anastassia Voronova, Mark A Zander, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 6, 2019
Dysfunction of <i>GRAP</i>, encoding the GRB2-related adaptor protein, is linked to sensorineural hearing lossChong Li, Guney Bademci, Asli Subasioglu, et al.
American Journal of Human Genetics|October 7, 2008
Mutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndromeHyung-Goo Kim, Ingo Kurth, Fei Lan, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 25, 2014
FAM65B is a membrane-associated protein of hair cell stereocilia required for hearingOscar Diaz-Horta, Asli Subasioglu-Uzak, M'hamed Grati, et al.
Pageof 24

Showing results (181-190 of 235) with videos related to

Sort By:
Pageof 24
JCI Insight|June 18, 2026
Distal enhancer-insulator module of GDF6 is essential for cochlear formationMohammad Faraz Zafeer, Clemer Abad, Havva Ortabozkoyun, et al.
Hearing Research|January 17, 2017
Broadening the phenotype of DFNB28: Mutations in TRIOBP are associated with moderate, stable hereditary hearing impairmentMieke Wesdorp, Jiddeke M van de Kamp, Erik F Hensen, et al.
Journal of Medical Genetics|March 19, 2026
<i>CDK4</i> and <i>CDK6</i> variants in patients with primary microcephaly lead to cell cycle defects and mitochondria-induced apoptosisEsra Isik, Mohammad Faraz Zafeer, Guney Bademci, 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.
Annals of Human Genetics|November 22, 2016
Targeted Resequencing of Deafness Genes Reveals a Founder MYO15A Variant in Northeastern BrazilGabrielle N Manzoli, Guney Bademci, Angelina X Acosta, et al.
Human Genomics|November 23, 2023
Dispersed DNA variants underlie hearing loss in South Florida's minority populationLéShon Peart, Joanna Gonzalez, Dayna Morel Swols, et al.
Developmental Cell|January 6, 2015
Ankrd11 is a chromatin regulator involved in autism that is essential for neural developmentDenis Gallagher, Anastassia Voronova, Mark A Zander, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 6, 2019
Dysfunction of <i>GRAP</i>, encoding the GRB2-related adaptor protein, is linked to sensorineural hearing lossChong Li, Guney Bademci, Asli Subasioglu, et al.
American Journal of Human Genetics|October 7, 2008
Mutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndromeHyung-Goo Kim, Ingo Kurth, Fei Lan, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 25, 2014
FAM65B is a membrane-associated protein of hair cell stereocilia required for hearingOscar Diaz-Horta, Asli Subasioglu-Uzak, M'hamed Grati, et al.
Pageof 24