Essential Role of the Zinc Finger Transcription Factor Casz1 for Mammalian Cardiac Morphogenesis and Development

Chromosome 1p36 deletion syndrome is one of the most common terminal deletions observed in humans and is related to congenital heart disease (CHD). However, the 1p36 genes that contribute to heart disease have not been clearly delineated. Human CASZ1 gene localizes to 1p36 and encodes a zinc finger...

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Detalhes bibliográficos
Main Authors: Liu, Zhihui, Li, Wenling, Ma, Xuefei, Ding, Nancy, Spallotta, Francesco, Southon, Eileen, Tessarollo, Lino, Gaetano, Carlo, Mukouyama, Yoh-suke, Thiele, Carol J.
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Biochemistry and Molecular Biology 2014
Assuntos:
Developmental Biology
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4207993/
https://ncbi.nlm.nih.gov/pubmed/25190801
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M114.570416
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