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Mustafa Tekin

Showing results (201-210 of 235) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|May 11, 2016
ROR1 is essential for proper innervation of auditory hair cells and hearing in humans and miceOscar Diaz-Horta, Clemer Abad, Levent Sennaroglu, et al.
International Journal of Pediatric Otorhinolaryngology|February 4, 2009
Mutations in TMC1 contribute significantly to nonsyndromic autosomal recessive sensorineural hearing loss: a report of five novel mutationsAsli Sirmaci, Duygu Duman, Hatice Oztürkmen-Akay, et al.
American Journal of Human Genetics|May 15, 2012
GPSM2 mutations cause the brain malformations and hearing loss in Chudley-McCullough syndromeDan Doherty, Albert E Chudley, Gail Coghlan, et al.
Cell|June 14, 2016
Digestion of Chromatin in Apoptotic Cell Microparticles Prevents AutoimmunityVanja Sisirak, Benjamin Sally, Vivette D'Agati, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 21, 2022
Mutations in <i>MINAR2</i> encoding membrane integral NOTCH2-associated receptor 2 cause deafness in humans and miceGuney Bademci, María Lachgar-Ruiz, Mangesh Deokar, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 23, 2019
Correction: ClinGen expert clinical validity curation of 164 hearing loss gene-disease pairsMarina T DiStefano, Sarah E Hemphill, Andrea M Oza, et al.
Human Molecular Genetics|December 19, 2018
FOXF2 is required for cochlear development in humans and miceGuney Bademci, Clemer Abad, Armagan Incesulu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 22, 2019
ClinGen expert clinical validity curation of 164 hearing loss gene-disease pairsMarina T DiStefano, Sarah E Hemphill, Andrea M Oza, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 25, 2013
Mutation of the ATP-gated P2X(2) receptor leads to progressive hearing loss and increased susceptibility to noiseDenise Yan, Yan Zhu, Tom Walsh, et al.
Journal of Human Genetics|May 22, 2023
Genome sequencing identifies coding and non-coding variants for non-syndromic hearing lossMemoona Ramzan, Duygu Duman, LeShon Chere Peart Hendricks, et al.
Pageof 24

Showing results (201-210 of 235) with videos related to

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Pageof 24
Proceedings of the National Academy of Sciences of the United States of America|May 11, 2016
ROR1 is essential for proper innervation of auditory hair cells and hearing in humans and miceOscar Diaz-Horta, Clemer Abad, Levent Sennaroglu, et al.
International Journal of Pediatric Otorhinolaryngology|February 4, 2009
Mutations in TMC1 contribute significantly to nonsyndromic autosomal recessive sensorineural hearing loss: a report of five novel mutationsAsli Sirmaci, Duygu Duman, Hatice Oztürkmen-Akay, et al.
American Journal of Human Genetics|May 15, 2012
GPSM2 mutations cause the brain malformations and hearing loss in Chudley-McCullough syndromeDan Doherty, Albert E Chudley, Gail Coghlan, et al.
Cell|June 14, 2016
Digestion of Chromatin in Apoptotic Cell Microparticles Prevents AutoimmunityVanja Sisirak, Benjamin Sally, Vivette D'Agati, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 21, 2022
Mutations in <i>MINAR2</i> encoding membrane integral NOTCH2-associated receptor 2 cause deafness in humans and miceGuney Bademci, María Lachgar-Ruiz, Mangesh Deokar, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 23, 2019
Correction: ClinGen expert clinical validity curation of 164 hearing loss gene-disease pairsMarina T DiStefano, Sarah E Hemphill, Andrea M Oza, et al.
Human Molecular Genetics|December 19, 2018
FOXF2 is required for cochlear development in humans and miceGuney Bademci, Clemer Abad, Armagan Incesulu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 22, 2019
ClinGen expert clinical validity curation of 164 hearing loss gene-disease pairsMarina T DiStefano, Sarah E Hemphill, Andrea M Oza, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 25, 2013
Mutation of the ATP-gated P2X(2) receptor leads to progressive hearing loss and increased susceptibility to noiseDenise Yan, Yan Zhu, Tom Walsh, et al.
Journal of Human Genetics|May 22, 2023
Genome sequencing identifies coding and non-coding variants for non-syndromic hearing lossMemoona Ramzan, Duygu Duman, LeShon Chere Peart Hendricks, et al.
Pageof 24