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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Detaylı Bibliyografya
Asıl Yazarlar: Liu, Zhihui, Li, Wenling, Ma, Xuefei, Ding, Nancy, Spallotta, Francesco, Southon, Eileen, Tessarollo, Lino, Gaetano, Carlo, Mukouyama, Yoh-suke, Thiele, Carol J.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: American Society for Biochemistry and Molecular Biology 2014
Konular:
Developmental Biology
Online Erişim: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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