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 …

2006年10月2日 · CHD7 disorder is an autosomal dominant disorder typically caused by a de novo pathogenic variant. In rare instances, an individual with CHD7 disorder inherits a pathogenic …

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 …

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 …

We found chd-7 regulates tumor growth factor-β (TGF-β) signaling pathways both for dauer diapause and for development of the cuticle, a specialized extracellular matrix. In frog …

2025年2月9日 · CHARGE syndrome is a rare genetic disease characterized by numerous congenital abnormalities, mainly caused by de novo alterations of the CHD7 gene. Study using …

2022年4月12日 · Here we report that chd-7, the nematode ortholog of Chd7, is required for dauer morphogenesis, lifespan determination, stress response, and body size determination. …

2017年3月20日 · Mutations in the ATP-dependent chromatin remodeller chromodomain, helicase, DNA binding (CHD) 7 are the major cause of CHARGE syndrome, which is characterized by …

2022年9月29日 · <span><i>CHD7</i> disorder is an autosomal dominant disorder typically caused by a <i>de novo</i> pathogenic variant. In rare instances, an individual with …

Chromodomain and Helicase Domain protein. The CHARGE syndrome ortholog CHD-7 regulates TGF-beta pathways in Caenorhabditis elegans. Predicted to enable several functions, …