Rescue of neural crest-derived phenotypes in a zebrafish CHARGE model by Sox10 downregulation

CHD7 mutations are implicated in a majority of cases of the congenital disorder, CHARGE syndrome. CHARGE, an autosomal dominant syndrome, is known to affect multiple tissues including eye, heart, ear, craniofacial nerves and skeleton and genital organs. Using a morpholino-antisense-oligonucleotide-b...

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Detalhes bibliográficos
Publicado no:Hum Mol Genet
Main Authors: Asad, Zainab, Pandey, Aditi, Babu, Aswini, Sun, Yuhan, Shevade, Kaivalya, Kapoor, Shruti, Ullah, Ikram, Ranjan, Shashi, Scaria, Vinod, Bajpai, Ruchi, Sachidanandan, Chetana
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2016
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Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5179949/
https://ncbi.nlm.nih.gov/pubmed/27418670
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddw198
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