
CHD7 Gene - GeneCards | CHD7 Protein | CHD7 Antibody
2024年12月24日 · CHD7 (Chromodomain Helicase DNA Binding Protein 7) is a Protein Coding gene. Diseases associated with CHD7 include Charge Syndrome and Hypogonadotropic …
CHD7 Disorder - GeneReviews® - NCBI Bookshelf
2006年10月2日 · CHD7 encodes a chromodomain protein that is involved in the ATP-dependent remodeling of chromatin. CHD7 binds to more than 10,000 sites in the mammalian genome …
CHD7 - Wikipedia
Chromodomain-helicase-DNA-binding protein 7 is an ATP-dependent 'chromatin' or 'nucleosome' remodeling factor [5] that in humans is encoded by the CHD7 gene. [6] [7] CHD7 is an ATP …
CHARGE syndrome protein CHD7 regulates epigenomic activation …
2021年9月29日 · Haploinsufficiency of the chromatin remodeling enzyme CHD7 causes CHARGE syndrome, a genetic disorder that affects the development of the cerebellum. However, how …
CHD7 gene - MedlinePlus
The CHD7 gene provides instructions for making a protein called chromodomain helicase DNA binding protein 7. This protein is found in many parts of the body before birth, including the …
PNAS:新发现!CHD7基因或是人类胚胎正常发育的潜在关键因 …
2020年12月8日 · 文章中,研究人员成功失活了小鼠胚胎神经嵴细胞中名为CHD7的基因,随后追踪发育中的心脏神经嵴细胞中CHD7基因的失活如何诱发心脏右心室流出道 ...
CHD7 mutations and CHARGE syndrome: the clinical implications …
Finally, we give updated recommendations for clinical surveillance of patients with a CHD7 mutation, based on our exploration of the phenotypic spectrum and on our experience in a …
CHD7 Disorder - PubMed
2022年9月29日 · CHD7 disorder is an autosomal dominant disorder typically caused by a de novo pathogenic variant. In rare instances, an individual with <i>CHD7</i> disorder inherits a …
CHD7 regulates bone-fat balance by suppressing PPAR-γ …
2022年3月17日 · Chromodomain helicase DNA-binding protein 7 (CHD7), an ATP-dependent eukaryotic chromatin remodeling enzyme, is essential for the development of organs. The...
CHD7 chromodomain helicase DNA binding protein 7 [ (human)]
2025年2月9日 · CHD7 regulates otic lineage specification and hair cell differentiation in human inner ear organoids. [Analysis of CHD7 gene variants in 22 patients with idiopathic …