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Clemer Abad

Showing results (21-30 of 27) 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.
The Journal of Clinical Investigation|May 6, 2020
Long-range cis-regulatory elements controlling GDF6 expression are essential for ear developmentGuney Bademci, Clemer Abad, Filiz B Cengiz, 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.
Human Molecular Genetics|December 19, 2018
FOXF2 is required for cochlear development in humans and miceGuney Bademci, Clemer Abad, Armagan Incesulu, et al.
Human Genetics|July 9, 2018
MPZL2 is a novel gene associated with autosomal recessive nonsyndromic moderate hearing lossGuney Bademci, Clemer Abad, Armagan Incesulu, et al.
Molecular Cell|February 7, 2026
Unbalanced chromatin binding of Polycomb complexes drives neurodevelopmental disordersRodrigo L Borges, Gretter González-Blanco, Harikumar Arigela, et al.
The Journal of Clinical Investigation|September 30, 2025
Carboxypeptidase D deficiency causes hearing loss amenable to treatmentMemoona Ramzan, Natalie Ortiz-Vega, Mohammad Faraz Zafeer, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
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.
The Journal of Clinical Investigation|May 6, 2020
Long-range cis-regulatory elements controlling GDF6 expression are essential for ear developmentGuney Bademci, Clemer Abad, Filiz B Cengiz, 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.
Human Molecular Genetics|December 19, 2018
FOXF2 is required for cochlear development in humans and miceGuney Bademci, Clemer Abad, Armagan Incesulu, et al.
Human Genetics|July 9, 2018
MPZL2 is a novel gene associated with autosomal recessive nonsyndromic moderate hearing lossGuney Bademci, Clemer Abad, Armagan Incesulu, et al.
Molecular Cell|February 7, 2026
Unbalanced chromatin binding of Polycomb complexes drives neurodevelopmental disordersRodrigo L Borges, Gretter González-Blanco, Harikumar Arigela, et al.
The Journal of Clinical Investigation|September 30, 2025
Carboxypeptidase D deficiency causes hearing loss amenable to treatmentMemoona Ramzan, Natalie Ortiz-Vega, Mohammad Faraz Zafeer, et al.
Pageof 3