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Biorxiv : the Preprint Server for Biology
|
December 18, 2023
Sord deficient rats develop a motor-predominant peripheral neuropathy unveiling novel pathophysiological insights
Adriana P Rebelo, Clemer Abad, Maike F Dohrn, et al.
Biology
|
May 26, 2018
A Rare De Novo <i>RAI1</i> Gene Mutation Affecting BDNF-Enhancer-Driven Transcription Activity Associated with Autism and Atypical Smith-Magenis Syndrome Presentation
Clemer Abad, Melissa M Cook, Lei Cao, et al.
Brain : a Journal of Neurology
|
March 27, 2024
SORD-deficient rats develop a motor-predominant peripheral neuropathy unveiling novel pathophysiological insights
Adriana P Rebelo, Clemer Abad, Maike F Dohrn, et al.
JCI Insight
|
June 18, 2026
Distal enhancer-insulator module of GDF6 is essential for cochlear formation
Mohammad Faraz Zafeer, Clemer Abad, Havva Ortabozkoyun, et al.
Molecular Autism
|
June 7, 2020
Transcriptional consequences of MBD5 disruption in mouse brain and CRISPR-derived neurons
Catarina M Seabra, Tatsiana Aneichyk, Serkan Erdin, 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 loss
Chong Li, Guney Bademci, Asli Subasioglu, et al.
Developmental Cell
|
January 6, 2015
Ankrd11 is a chromatin regulator involved in autism that is essential for neural development
Denis Gallagher, Anastassia Voronova, Mark A Zander, 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 hearing
Oscar Diaz-Horta, Asli Subasioglu-Uzak, M'hamed Grati, et al.
JCI Insight
|
February 1, 2024
ADAMTSL2 mutations determine the phenotypic severity in geleophysic dysplasia
Vladimir Camarena, Monique M Williams, Alejo A Morales, et al.
Human Genetics
|
November 22, 2014
Characterization of ANKRD11 mutations in humans and mice related to KBG syndrome
Katherina Walz, Devon Cohen, Paul M Neilsen, et al.
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Search research articles
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Showing results (11-20 of 27) with videos related to
Sort By:
Page
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Biorxiv : the Preprint Server for Biology
|
December 18, 2023
Sord deficient rats develop a motor-predominant peripheral neuropathy unveiling novel pathophysiological insights
Adriana P Rebelo, Clemer Abad, Maike F Dohrn, et al.
Biology
|
May 26, 2018
A Rare De Novo <i>RAI1</i> Gene Mutation Affecting BDNF-Enhancer-Driven Transcription Activity Associated with Autism and Atypical Smith-Magenis Syndrome Presentation
Clemer Abad, Melissa M Cook, Lei Cao, et al.
Brain : a Journal of Neurology
|
March 27, 2024
SORD-deficient rats develop a motor-predominant peripheral neuropathy unveiling novel pathophysiological insights
Adriana P Rebelo, Clemer Abad, Maike F Dohrn, et al.
JCI Insight
|
June 18, 2026
Distal enhancer-insulator module of GDF6 is essential for cochlear formation
Mohammad Faraz Zafeer, Clemer Abad, Havva Ortabozkoyun, et al.
Molecular Autism
|
June 7, 2020
Transcriptional consequences of MBD5 disruption in mouse brain and CRISPR-derived neurons
Catarina M Seabra, Tatsiana Aneichyk, Serkan Erdin, 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 loss
Chong Li, Guney Bademci, Asli Subasioglu, et al.
Developmental Cell
|
January 6, 2015
Ankrd11 is a chromatin regulator involved in autism that is essential for neural development
Denis Gallagher, Anastassia Voronova, Mark A Zander, 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 hearing
Oscar Diaz-Horta, Asli Subasioglu-Uzak, M'hamed Grati, et al.
JCI Insight
|
February 1, 2024
ADAMTSL2 mutations determine the phenotypic severity in geleophysic dysplasia
Vladimir Camarena, Monique M Williams, Alejo A Morales, et al.
Human Genetics
|
November 22, 2014
Characterization of ANKRD11 mutations in humans and mice related to KBG syndrome
Katherina Walz, Devon Cohen, Paul M Neilsen, et al.
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of 3