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8p23.1 Microdeletion syndrome and obstructing myxomatous heart valve nodules.

作者信息

Oh Kei Shing, Febres-Aldana Christopher Antonio, Pelaez Liset, Alexis John

机构信息

Mount Sinai Medical Center, AM Rywlin Department of Pathology and Laboratory Medicine. Miami Beach, FL, USA.

Nicklaus Children's Hospital, Department of Pathology and Clinical Laboratories. Miami, FL, USA.

出版信息

Autops Case Rep. 2020 Apr 2;10(2):e2020168. doi: 10.4322/acr.2020.168.

DOI:10.4322/acr.2020.168
PMID:33344285
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7703449/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e724/7703449/615f6b9a102d/autopsy-10-2-e2020168-gf01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e724/7703449/615f6b9a102d/autopsy-10-2-e2020168-gf01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e724/7703449/615f6b9a102d/autopsy-10-2-e2020168-gf01.jpg

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本文引用的文献

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Regulates Lineage Decisions in Cardiovascular Progenitor Cells.调控心血管祖细胞的谱系决定。
Stem Cells Dev. 2019 Aug 15;28(16):1089-1103. doi: 10.1089/scd.2019.0040. Epub 2019 Jul 17.
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Embryological origin of the endocardium and derived valve progenitor cells: from developmental biology to stem cell-based valve repair.心内膜及衍生瓣膜祖细胞的胚胎学起源：从发育生物学到基于干细胞的瓣膜修复
Biochim Biophys Acta. 2013 Apr;1833(4):917-22. doi: 10.1016/j.bbamcr.2012.09.013. Epub 2012 Oct 16.
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Chromosome 8p23.1 deletions as a cause of complex congenital heart defects and diaphragmatic hernia.
8号染色体p23.1缺失作为复杂先天性心脏缺陷和膈疝的一个病因
Am J Med Genet A. 2009 Aug;149A(8):1661-77. doi: 10.1002/ajmg.a.32896.
4
Tbx20 regulation of endocardial cushion cell proliferation and extracellular matrix gene expression.Tbx20对心内膜垫细胞增殖和细胞外基质基因表达的调控
Dev Biol. 2007 Feb 15;302(2):376-88. doi: 10.1016/j.ydbio.2006.09.047. Epub 2006 Oct 3.
5
Development of heart valves requires Gata4 expression in endothelial-derived cells.心脏瓣膜的发育需要在内皮来源的细胞中表达Gata4。
Development. 2006 Sep;133(18):3607-18. doi: 10.1242/dev.02519. Epub 2006 Aug 16.