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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Bibliografiske detaljer
Main Authors: Liu, Zhihui, Li, Wenling, Ma, Xuefei, Ding, Nancy, Spallotta, Francesco, Southon, Eileen, Tessarollo, Lino, Gaetano, Carlo, Mukouyama, Yoh-suke, Thiele, Carol J.
Format: Artigo
Sprog:Inglês
Udgivet: American Society for Biochemistry and Molecular Biology 2014
Fag:
Developmental Biology
Online adgang: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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