Chứng minh đẳng thức lượng giác có chứa sin3a.

May 3, 2013 ... Establishment of this gene variant database (LSDB) was supported by the Leiden University Medical Center (LUMC), Leiden, Nederland. Date created ... The SIN3A histone deacetylase complex is required for a complete transcriptional response to hypoxia. SIN3A-related syndrome is a genetic condition, which means that it is caused by variants in genes. Our genes contain the instructions, or code, that tell our ... Description. Sin3A is encoded by this gene is a transcriptional regulatory protein. It contains paired amphipathic helix (PAH) domains, which are important ... May 25, 2024 ... Gene name - Sin3A. Synonyms - Cytological map position - 49B5-49B7. Function - Transcription factor; Chromatin protein. Recent study has identified that haploinsufficiency of SIN3A (chromosome 15q24.2) is associated with mild syndromic intellectual disability. This phenotype ... Jan 24, 2025 ... BAHCC1 antagonizes SIN3A histone deacetylation and positively regulates the expression of genes that are important for growth and migration-related processes. Witteveen-Kolk syndrome is a rare neurodevelopmental disorder comprising intellectual disability, developmental delay and dysmorphic facial features SIN3A antibody ... SIN3A antibody detects SIN3A protein at nucleus on rat fore brain by immunohistochemical analysis. Sample: Paraffin-embedded rat fore brain. Aug 1, 2023 ... SIN3A defects associated with syndromic congenital hypogonadotropic hypogonadism: an overlap with Witteveen-Kolk syndrome.