Pages that link to "Q34242785"
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The following pages link to Hereditary Multiple Fibrofolliculomas With Trichodiscomas and Acrochordons (Q34242785):
Displaying 50 items.
- Crystal structure of folliculin reveals a hidDENN function in genetically inherited renal cancer (Q24298712) (← links)
- Folliculin encoded by the BHD gene interacts with a binding protein, FNIP1, and AMPK, and is involved in AMPK and mTOR signaling (Q24306277) (← links)
- Interaction of folliculin (Birt-Hogg-Dubé gene product) with a novel Fnip1-like (FnipL/Fnip2) protein (Q24318494) (← links)
- Identification and characterization of a novel folliculin-interacting protein FNIP2 (Q24318963) (← links)
- Inactivation of the FLCN tumor suppressor gene induces TFE3 transcriptional activity by increasing its nuclear localization (Q24324012) (← links)
- Tumor suppressor FLCN inhibits tumorigenesis of a FLCN-null renal cancer cell line and regulates expression of key molecules in TGF-beta signaling (Q24329165) (← links)
- Birt-Hogg-Dube syndrome: clinicopathological features of the lung (Q24606257) (← links)
- BHD mutations, clinical and molecular genetic investigations of Birt-Hogg-Dubé syndrome: a new series of 50 families and a review of published reports (Q24654382) (← links)
- Conserved regulators of Rag GTPases orchestrate amino acid-dependent TORC1 signaling (Q26741367) (← links)
- Review of renal cell carcinoma and its common subtypes in radiology (Q26744297) (← links)
- Amino acid management in cancer (Q26798087) (← links)
- Diagnosis and management of BHD-associated kidney cancer (Q26822677) (← links)
- The metabolic basis of kidney cancer (Q27023273) (← links)
- FLCN and AMPK Confer Resistance to Hyperosmotic Stress via Remodeling of Glycogen Stores (Q27310260) (← links)
- Folliculin regulates ampk-dependent autophagy and metabolic stress survival (Q27316476) (← links)
- Homozygous loss of BHD causes early embryonic lethality and kidney tumor development with activation of mTORC1 and mTORC2 (Q28508427) (← links)
- Kidney-targeted Birt-Hogg-Dube gene inactivation in a mouse model: Erk1/2 and Akt-mTOR activation, cell hyperproliferation, and polycystic kidneys (Q28513499) (← links)
- Deficiency of FLCN in mouse kidney led to development of polycystic kidneys and renal neoplasia (Q28587662) (← links)
- The role of the Birt-Hogg-Dubé protein in mTOR activation and renal tumorigenesis (Q28590041) (← links)
- Folliculin controls lung alveolar enlargement and epithelial cell survival through E-cadherin, LKB1, and AMPK. (Q30578909) (← links)
- A high-resolution comparative map of canine Chromosome 5q14.3-q33 constructed utilizing the 1.5x canine genome sequence (Q31111955) (← links)
- Loss of heterozygosity at the FLCN locus in early renal cystic lesions in dogs with renal cystadenocarcinoma and nodular dermatofibrosis (Q33433951) (← links)
- The women behind the names: Dermatology eponyms named after women. (Q33641196) (← links)
- Topical rapamycin as a treatment for fibrofolliculomas in Birt-Hogg-Dubé syndrome: a double-blind placebo-controlled randomized split-face trial (Q33728003) (← links)
- Clinical and genetic characteristics of chinese patients with Birt-Hogg-Dubé syndrome (Q33743437) (← links)
- Hereditary leiomyomatosis and renal cell carcinoma (Q33817755) (← links)
- Negative regulation of EGFR signalling by the human folliculin tumour suppressor protein (Q33861388) (← links)
- A 4-bp deletion in the Birt-Hogg-Dubé gene (FLCN) causes dominantly inherited spontaneous pneumothorax (Q33938690) (← links)
- Germline BHD-mutation spectrum and phenotype analysis of a large cohort of families with Birt-Hogg-Dubé syndrome (Q33938826) (← links)
- Birt-Hogg-Dubé syndrome, a genodermatosis associated with spontaneous pneumothorax and kidney neoplasia, maps to chromosome 17p11.2. (Q34020592) (← links)
- The genetic basis of kidney cancer: a metabolic disease (Q34087148) (← links)
- Non-clear cell renal cancer: disease-based management and opportunities for targeted therapeutic approaches (Q34194075) (← links)
- Franklin H. Epstein Lecture. Both ends of the leash--the human links to good dogs with bad genes (Q34294115) (← links)
- Clinical and genetic spectrum of Birt-Hogg-Dube syndrome patients in whom pneumothorax and/or multiple lung cysts are the presenting feature (Q34308406) (← links)
- Renal cell tumour characteristics in patients with the Birt-Hogg-Dubé cancer susceptibility syndrome: a retrospective, multicentre study (Q34447213) (← links)
- Familial adult renal neoplasia (Q34515955) (← links)
- Identification of intragenic deletions and duplication in the FLCN gene in Birt-Hogg-Dubé syndrome. (Q34785861) (← links)
- Human folliculin delays cell cycle progression through late S and G2/M-phases: effect of phosphorylation and tumor associated mutations (Q34846527) (← links)
- Origin of renal cell carcinomas. (Q34882260) (← links)
- A rare soft tissue tumor masquerading as a parathyroid adenoma in a patient with birt-hogg-dubé syndrome and multiple cervical endocrinopathies. (Q34913413) (← links)
- Birt–Hogg–Dubé syndrome: an inherited cause of spontaneous pneumothorax (Q35045100) (← links)
- The mutation for medullary thyroid carcinoma with parathyroid tumors (MTC with PTs) is closely linked to the centromeric region of chromosome 10 (Q35198614) (← links)
- An efficient strategy for gene mapping using multipoint linkage analysis: exclusion of the multiple endocrine neoplasia 2A (MEN2A) locus from chromosome 13. (Q35198930) (← links)
- Spontaneous pneumothorax as indicator for Birt-Hogg-Dubé syndrome in paediatric patients (Q35201156) (← links)
- The genetic basis of renal cell carcinoma (Q35210970) (← links)
- Folliculin-interacting proteins Fnip1 and Fnip2 play critical roles in kidney tumor suppression in cooperation with Flcn (Q35279496) (← links)
- Genetics of skin appendage neoplasms and related syndromes (Q35447362) (← links)
- Pulmonary manifestations of Birt-Hogg-Dubé syndrome. (Q35536837) (← links)
- Imaging of hereditary renal cancer (Q35548045) (← links)
- Clinical and genetic studies of Birt-Hogg-Dubé syndrome. (Q35559819) (← links)