Mối liên hệ giữa sin3a và các vấn đề về tương lai và bền vững.

Witteveen-Kolk syndrome is a rare neurodevelopmental disorder comprising intellectual disability, developmental delay and dysmorphic facial features Jan 24, 2022 ... Conclusions. Our studies revealed that Sin3a was a novel mediator of MET during early reprogramming, where Sin3a functioned as an epigenetic ... Aug 1, 2023 ... SIN3A defects associated with syndromic congenital hypogonadotropic hypogonadism: an overlap with Witteveen-Kolk syndrome. The Effect of Sin3a Complex on Cell Cycle and Cell Death in Mouse Embryonic Stem Cells. Date. 2019-09-29. Author. Güven, Gözde Terzi Çizmecioğlu, Nihal. SIN3ASIN3 transcription regulator family member A · SFARI Gene Score · Autism Reports / Total Reports · Rare Variants / Common Variants · Aliases · Associated ... Unfollow This Gene ... Click here to learn more about how to cite ClinGen and to see a list of the external resources utilized. The information on this website is ... SIN3A antibody ... SIN3A antibody detects SIN3A protein at nucleus on rat fore brain by immunohistochemical analysis. Sample: Paraffin-embedded rat fore brain. View Sin3a /Sin3a<+> Trp53 /Trp53 involves: 129S2/SvPas * C57BL/6 * FVB: phenotypes, images, diseases, and references. Jan 24, 2025 ... BAHCC1 antagonizes SIN3A histone deacetylation and positively regulates the expression of genes that are important for growth and migration-related processes. Sin3A associated protein 30 [Source:HGNC Symbol;Acc:HGNC:10532]. Ensembl ID. ENSG00000164105. Bio databases IDs, NCBI: 8819 Ensembl: ENSG00000164105. Aliases ...