WebTuberous sclerosis complex is a genetic disorder characterized by the growth of numerous noncancerous (benign) tumors in many parts of the body. These tumors can occur in the … WebLa sclérose tubéreuse de Bourneville (tuberous sclerosis complex) est un syndrome neurocutané qui se produit chez 1 enfant sur 6000; 85% des cas sont atteints de mutations du gène TSC1 (9q34), qui contrôle la production d'hamartine, ou du gène TSC2 (16p13.3), qui contrôle la production de tubérine. Ces protéines agissent comme des suppresseurs de …
TSC2 - an overview ScienceDirect Topics
WebMutations in TSC2 can cause Lymphangioleiomyomatosis, a disease caused by the enlargement of tissue in the lungs, creating cysts and tumours and causing difficulty … WebMar 4, 2024 · Tuberous sclerosis complex (TSC) is an autosomal dominant syndrome that presents with diverse and complex clinical features and involves multiple human systems. TSC-related neurological abnormalities and organ dysfunction greatly affect the quality of life and can even result in death in patients with TSC. It is widely accepted that most TSC … florida life jacket laws children
Trimble File Conversion
WebJan 14, 2024 · 结节性硬化症蛋白复合体(TuberousSclerosisComplex,简称TSC复合体)是mTORC1信号通路中重要的蛋白质复合体,其整合细胞外各种因素的刺激,负调控mTORC1复合体的活性,起到肿瘤抑制的作用。TSC复合体包含三个亚基:TSC1,TSC2以及TBC1D7。其中TSC2包含一个GTP酶活化蛋白(GTPaseactivatingprotein,简称GAP)结构域 ... WebAddgene Alerts. Receive email alerts when new plasmids with this gene become available. Log in to subscribe to Addgene Alerts. Description TSC complex subunit 2. Also known as LAM, PPP1R160, TSC4. Species Homo sapiens. Entrez ID 7249. MGC ID BC150300. WebMutation in either the TSC1 or TSC2 tumor suppressor gene is responsible for the inherited genetic disease of tuberous sclerosis complex. TSC1 and TSC2 form a physical and functional complex to regulate cell growth. Recently, it has been demonstrated that TSC1·TSC2 functions to inhibit ribosomal S6 kinase and negatively regulate cell size. … florida life insurance company