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- CHD3 gene - MedlinePlus
The CHD3 gene provides instructions for making a protein that regulates gene activity (expression) by a process known as chromatin remodeling Learn about this gene and related health conditions
- CHD3 Gene - GeneCards | CHD3 Protein | CHD3 Antibody
CHD3 (Chromodomain Helicase DNA Binding Protein 3) is a Protein Coding gene Diseases associated with CHD3 include Snijders Blok-Campeau Syndrome and Autism Spectrum Disorder Among its related pathways are RNA Polymerase I Promoter Opening and PIP3 activates AKT signaling
- CHD3 Foundation
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 intellectual disability, developmental delays, hypotonia, impaired speech and language, and characteristic facial features
- CHD3 helicase domain mutations cause a neurodevelopmental . . . - Nature
Here, the authors identify missense variants in CHD3 that disturb its chromatin remodeling activities and cause a neurodevelopmental disorder with macrocephaly and speech and language impairment
- CHD3 chromodomain helicase DNA binding protein 3 [ (human)]
The tandem PHD fingers of CHD3 bind histone H3 tails CHD3 and CHD4 exhibit distinct nuclear localization patterns in unperturbed cells, revealing a subset of specific target genes Mutations in CHD3 gene is associated with cutaneous T cell lymphoma and Sezary syndrome
- CHROMODOMAIN HELICASE DNA-BINDING PROTEIN 3; CHD3 - OMIM
CHD3, together with CHD4 (603277) and CDH5 (610771), form the nucleosome remodeling and histone deacetylase (NURD) repressor complex, which is involved in genomic integrity, cell cycle progression, and cell differentiation
- CHD3 Syndrome: Causes, Symptoms, and Diagnosis
CHD3 syndrome, also known as Snijders Blok-Campeau syndrome, is a rare genetic condition that influences brain and body development It presents with a wide array of signs that can differ from person to person
- CHD3 - Simons Searchlight
CHD3-related syndrome happens when there are changes to the CHD3 gene Learn more about CHD3 and connect with other Simons Searchlight families with the resources on this page
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