Mối liên hệ giữa sin3a và các ứng dụng trong văn học và nghệ thuật (ví dụ, trong thơ ca, âm nhạc).

Feb 14, 2022 ... ... SIN3A protein. Suppression of focal adhesion kinase and SIN3A also induces apoptosis and prevents tumor progression, suggesting that they ... Witteveen-Kolk syndrome (WITKOS) is an autosomal dominant disorder with characteristic distinctive facial features, microcephaly, short stature, and mildly ... Feb 27, 2024 ... Provided the recent observation that the SIN3A histone deacetylase complex reduces transcription-replication conflicts, we explore the role of ... Apr 18, 2020 ... Share your videos with friends, family, and the world. 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 ... SIN3A (SIN3 Transcription Regulator Family Member A) is a protein coding gene located on human chromosome 15q24.2. SIN3A is also known as WITKOS. Sin3a plays a critical role in the maintenance of Treg identity and function and is essential for the expression and stability of Foxp3. SIN3ASIN3 transcription regulator family member A · SFARI Gene Score · Autism Reports / Total Reports · Rare Variants / Common Variants · Aliases · Associated ... HDAC1 activity [29] and the Sin3A complex [30] are also required for full transcriptional activity of interferon-α responsive genes and Nanog promoter, ... Aug 1, 2023 ... SIN3A defects associated with syndromic congenital hypogonadotropic hypogonadism: an overlap with Witteveen-Kolk syndrome.