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Folliculin interacting protein 1

WebFolliculin (FLCN) is a tumor-suppressor protein mutated in the Birt–Hogg–Dubé (BHD) syndrome, which associates with two paralogous proteins, folliculin-interacting protein (FNIP)1 and FNIP2, forming a complex that interacts with … WebFeb 2, 2024 · FNIP1 forms a complex with FNIP2 (612768) and folliculin (FLCN; 607273) that interacts with AMP-activated protein kinase (AMPK; see 602739). FLCN is a …

Folliculin Interacting Protein 1 Maintains Metabolic Homeostasis …

Folliculin (FLCN) functions as a binding partner and uncompetitive inhibitor of Lactate Dehydrogenase-A (LDHA). A flexible loop within the amino-terminus of FLCN controls movement of the LDHA active site loop, tightly regulating its enzyme activity and, consequently, metabolic homeostasis in normal cells. See more The tumor suppressor gene FLCN encodes the protein folliculin, also known as Birt–Hogg–Dubé syndrome protein, which functions as an inhibitor of Lactate Dehydrogenase-A and a regulator of the Warburg effect. … See more Structure The FLCN gene consists of 14 exons. Location Cytogenetic location: The FLCN gene is located on the short (p) arm of chromosome 17 at position 11.2. (17p11.2). See more • FLCN+protein,+human at the U.S. National Library of Medicine Medical Subject Headings (MeSH) • The BHD Foundation Archived 2024-06-11 at the Wayback Machine supports research into BHD syndrome and maintains the world's first website … See more Interactions FLCN has been shown to interact through its C-terminus with two new co-chaperones folliculin interacting protein 1 (FNIP1) and folliculin interacting … See more • Schmidt LS, Linehan WM (October 2015). "Molecular genetics and clinical features of Birt-Hogg-Dubé syndrome". Nature Reviews. Urology. 12 (10): 558–69. doi: • Tee AR, Pause A … See more WebOct 1, 2024 · The reported target of miR-499 is the folliculin interacting protein 1 (Fnip1), a negative regulator of AMP-activated protein kinase (AMPK). Consequently, AMPK is an activator of peroxisome proliferator-activated receptor gamma coactivator 1-alpha (PGC-1α). hotter shoes ladies wide fitting https://arenasspa.com

Folliculin - Wikipedia

WebJun 1, 2024 · For the genes involved in the PI3K-Akt signaling pathway, the gene–gene network ( Figure 5 A) showed that 51 genes interacted directly with each other. The results revealed that 53 genes were directly involved, and one gene was indirectly involved in the PI3K-Akt signaling pathway. WebRecent studies using murine models for FLCN, a protein encoded by the FLCN gene, and its two binding partners, folliculin-interacting protein 1 (FNIP1) and folliculin-interacting protein 2 (FNIP2), have uncovered important roles for FLCN, FNIP1 and FNIP2 in cell metabolism, which include AMP-activated protein kinase-mediated energy sensing, … WebLOC127985354 folliculin-interacting protein 1 [ (silver crucian carp)] Gene ID: 127985354, updated on 2-Mar-2024. Summary Other designations. folliculin … hotter shoes login

Fnip1 regulates skeletal muscle fiber type specification, …

Category:127985354 - Gene ResultLOC127985354 folliculin-interacting …

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Folliculin interacting protein 1

Birt-Hogg-Dubé syndrome: Clinical and molecular aspects of

WebDec 29, 2014 · Folliculin interacting protein-1 (Fnip1) is an intracellular protein known to interact with folliculin (a protein mutated in Birt Hogg Dube’ Syndrome) and the master … WebTitle: Folliculin Interacting Protein 1 Maintains Metabolic Homeostasis during B Cell Development by Modulating AMPK, mTORC1, and TFE3. Loss of Fnip1 alters kidney …

Folliculin interacting protein 1

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WebMar 21, 2024 · FNIP1 (Folliculin Interacting Protein 1) is a Protein Coding gene. Diseases associated with FNIP1 include Immunodeficiency 93 And Hypertrophic Cardiomyopathy … WebFolliculin (FLCN) is a tumor suppressor gene responsible for the inherited Birt-Hogg-Dubé (BHD) syndrome, which affects kidneys, skin and lungs. …

WebMay 2, 2024 · The folliculin interacting protein 1 (FNIP1) is implicated in controlling cellular metabolism via AMPK and mTORC1. However, whether and how FNIP1 … WebLOC127985354 folliculin-interacting protein 1 [ (silver crucian carp)] Gene ID: 127985354, updated on 2-Mar-2024. Summary Other designations. folliculin-interacting protein 1

WebApr 9, 2014 · Folliculin-interacting protein 1 (Fnip1) is an adaptor protein that physically interacts with AMPK, an energy-sensing kinase that stimulates mitochondrial biogenesis and autophagy in response to low …

WebDec 1, 2024 · Folliculin interacting protein 1 (Fnip1) is a cytoplasmic protein originally discovered through its interaction with the master metabolic sensor 5′ AMP-activated …

WebDec 24, 2024 · FNIP1 folliculin interacting protein 1. Gene ID: 96459, updated on 24-Dec-2024. Gene type: protein coding. Also known as: IMD93. See all available tests in GTR … hotter shoes measuring guideWebApr 7, 2024 · It has been demonstrated that PPP5C interacts with a diverse set of transcription factors and proteins. It participates in multiple signaling networks that govern various cellular activities. PPP5C is expressed in all mammalian tissues, exerting extremely high levels in the brain [ 9 ]. hotter shoes long eatonWebApr 9, 2024 · The tumor suppressor Folliculin also known as FLCN, functions as an intracellular uncompetitive inhibitor of Lactate Dehydrogenase-A and a regulator of the Warburg effect. Folliculin impairs breast tumor growth by repressing TFE3-dependent induction of the Warburg effect and angiogenesis. linen tablecloth kohlsWebJan 28, 2024 · FNIP1 deficiency is a novel inborn error of immunity characterized by early and severe B-cell development defect, agammaglobulinemia, variable neutropenia, and … linen tablecloth inc tigard orWebJan 27, 2024 · Other findings are unique to each disorder, including granuloma formation or inflammatory bowel disease with CGD; heart disease/defects in some patients with Barth syndrome, folliculin-interacting protein 1 deficiency (FNIP1) deficiency, and glucose-6-phosphatase catalytic subunit 3 (G6PC3) deficiency; and psychomotor retardation and … linen tablecloth ironWebBirt-Hogg-Dubé (BHD) syndrome is an autosomal dominant disorder characterized by cutaneous fibrofolliculomas, pulmonary cysts, and kidney malignancies. Affected individuals carry germ line mutations linen tablecloth john lewisWebViviana Loria Kohen posted images on LinkedIn linen tablecloth ivory