Hereditary multiple fibrofolliculomas with trichodiscomas and acrochordons.
about
Crystal structure of folliculin reveals a hidDENN function in genetically inherited renal cancerFolliculin encoded by the BHD gene interacts with a binding protein, FNIP1, and AMPK, and is involved in AMPK and mTOR signalingInteraction of folliculin (Birt-Hogg-Dubé gene product) with a novel Fnip1-like (FnipL/Fnip2) proteinIdentification and characterization of a novel folliculin-interacting protein FNIP2Inactivation of the FLCN tumor suppressor gene induces TFE3 transcriptional activity by increasing its nuclear localizationTumor suppressor FLCN inhibits tumorigenesis of a FLCN-null renal cancer cell line and regulates expression of key molecules in TGF-beta signalingBirt-Hogg-Dube syndrome: clinicopathological features of the lungBHD mutations, clinical and molecular genetic investigations of Birt-Hogg-Dubé syndrome: a new series of 50 families and a review of published reportsConserved regulators of Rag GTPases orchestrate amino acid-dependent TORC1 signalingReview of renal cell carcinoma and its common subtypes in radiologyAmino acid management in cancerDiagnosis and management of BHD-associated kidney cancerThe metabolic basis of kidney cancerFLCN and AMPK Confer Resistance to Hyperosmotic Stress via Remodeling of Glycogen StoresFolliculin regulates ampk-dependent autophagy and metabolic stress survivalHomozygous loss of BHD causes early embryonic lethality and kidney tumor development with activation of mTORC1 and mTORC2Kidney-targeted Birt-Hogg-Dube gene inactivation in a mouse model: Erk1/2 and Akt-mTOR activation, cell hyperproliferation, and polycystic kidneysDeficiency of FLCN in mouse kidney led to development of polycystic kidneys and renal neoplasiaThe role of the Birt-Hogg-Dubé protein in mTOR activation and renal tumorigenesisFolliculin controls lung alveolar enlargement and epithelial cell survival through E-cadherin, LKB1, and AMPK.The women behind the names: Dermatology eponyms named after women.Topical rapamycin as a treatment for fibrofolliculomas in Birt-Hogg-Dubé syndrome: a double-blind placebo-controlled randomized split-face trial.Clinical and genetic characteristics of chinese patients with Birt-Hogg-Dubé syndromeHereditary leiomyomatosis and renal cell carcinoma.Negative regulation of EGFR signalling by the human folliculin tumour suppressor proteinA 4-bp deletion in the Birt-Hogg-Dubé gene (FLCN) causes dominantly inherited spontaneous pneumothorax.Germline BHD-mutation spectrum and phenotype analysis of a large cohort of families with Birt-Hogg-Dubé syndromeBirt-Hogg-Dubé syndrome, a genodermatosis associated with spontaneous pneumothorax and kidney neoplasia, maps to chromosome 17p11.2.The genetic basis of kidney cancer: a metabolic diseaseNon-clear cell renal cancer: disease-based management and opportunities for targeted therapeutic approaches.Franklin H. Epstein Lecture. Both ends of the leash--the human links to good dogs with bad genes.Clinical and genetic spectrum of Birt-Hogg-Dube syndrome patients in whom pneumothorax and/or multiple lung cysts are the presenting featureRenal cell tumour characteristics in patients with the Birt-Hogg-Dubé cancer susceptibility syndrome: a retrospective, multicentre study.Familial adult renal neoplasiaIdentification of intragenic deletions and duplication in the FLCN gene in Birt-Hogg-Dubé syndrome.Human folliculin delays cell cycle progression through late S and G2/M-phases: effect of phosphorylation and tumor associated mutationsA rare soft tissue tumor masquerading as a parathyroid adenoma in a patient with birt-hogg-dubé syndrome and multiple cervical endocrinopathies.Birt-Hogg-Dubé syndrome: an inherited cause of spontaneous pneumothoraxThe mutation for medullary thyroid carcinoma with parathyroid tumors (MTC with PTs) is closely linked to the centromeric region of chromosome 10An efficient strategy for gene mapping using multipoint linkage analysis: exclusion of the multiple endocrine neoplasia 2A (MEN2A) locus from chromosome 13.
P2860
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P2860
Hereditary multiple fibrofolliculomas with trichodiscomas and acrochordons.
description
1977 nî lūn-bûn
@nan
1977 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1977 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
1977年の論文
@ja
1977年論文
@yue
1977年論文
@zh-hant
1977年論文
@zh-hk
1977年論文
@zh-mo
1977年論文
@zh-tw
1977年论文
@wuu
name
Hereditary multiple fibrofolliculomas with trichodiscomas and acrochordons.
@ast
Hereditary multiple fibrofolliculomas with trichodiscomas and acrochordons.
@en
Hereditary multiple fibrofolliculomas with trichodiscomas and acrochordons.
@nl
type
label
Hereditary multiple fibrofolliculomas with trichodiscomas and acrochordons.
@ast
Hereditary multiple fibrofolliculomas with trichodiscomas and acrochordons.
@en
Hereditary multiple fibrofolliculomas with trichodiscomas and acrochordons.
@nl
prefLabel
Hereditary multiple fibrofolliculomas with trichodiscomas and acrochordons.
@ast
Hereditary multiple fibrofolliculomas with trichodiscomas and acrochordons.
@en
Hereditary multiple fibrofolliculomas with trichodiscomas and acrochordons.
@nl
P2093
P1433
P1476
Hereditary multiple fibrofolliculomas with trichodiscomas and acrochordons.
@en
P2093
P304
P356
10.1001/ARCHDERM.113.12.1674
P577
1977-12-01T00:00:00Z