2022年6月1日 · We assembled a cohort of 21 families with inherited CHD3 variants and used a combination of objectified in-depth clinical analyses, cell-based expression studies, and large …

2024年12月24日 · CHD3 (Chromodomain Helicase DNA Binding Protein 3) is a Protein Coding gene. Diseases associated with CHD3 include Snijders Blok-Campeau Syndrome and Autism …

We mapped the CHD composition of NuRD complexes in mammalian cells and discovered that they are isoform-specific, containing either the monomeric CHD3 or CHD4 ATPase. Both …

Chromodomain-helicase-DNA-binding protein 3 is an enzyme that in humans is encoded by the CHD3 gene. [5][6][7] This gene encodes a member of the CHD family of proteins which are …

该基因编码 CHD 蛋白质家族的成员，其特征在于存在染色质 (染色质组织修饰剂) 结构域和 SNF2 相关解旋酶/ATP 酶结构域。 这种蛋白质是称为 Mi-2/NuRD 复合物的组蛋白去乙酰化酶复合 …

2006年2月7日 · Localizes to sites of DNA damage (PubMed: 28977666). An autosomal dominant neurodevelopmental disorder characterized by intellectual disability with a wide range of …

2024年8月15日 · chd3在laml（急性骨髓性白血病），paad（胰腺癌）和thym中表现出上调，而在cesc（宫颈癌），coad（结肠癌），gbm（胶质母细胞瘤），kich（肾嫌色细 …

1993年3月1日 · We introduce a joint treatment using one potential surface for a set of different isotopomers for both internal coordinate and normal coordinate models. The latter uses the …

Even small changes in CHD3 can disrupt that process, resulting in abnormal brain development and creating a variety of conditions that affect other parts of the body. Common traits are …

2017年10月13日 · CHD3 and CHD4 (Chromodomain Helicase DNA binding protein), two highly similar representatives of the Mi-2 subfamily of SF2 helicases, are coexpressed in many cell …