Birt-Hogg-Dubé renal tumors are genetically distinct from other renal neoplasias and are associated with up-regulation of mitochondrial gene expression.
about
Genome-wide matching of genes to cellular roles using guilt-by-association models derived from single sample analysisFolliculin interacts with p0071 (plakophilin-4) and deficiency is associated with disordered RhoA signalling, epithelial polarization and cytokinesisMetabolism of kidney cancer: from the lab to clinical practiceGenomics of chromophobe renal cell carcinoma: implications from a rare tumor for pan-cancer studiesMetastatic renal cell carcinoma: update on epidemiology, genetics, and therapeutic modalitiesFolliculin regulates ampk-dependent autophagy and metabolic stress survivalRegulation of mitochondrial oxidative metabolism by tumor suppressor FLCNRenal cell cancer: overview of the current therapeutic landscape.The tumor suppressor folliculin regulates AMPK-dependent metabolic transformation.Gene expression in archived newborn blood spots distinguishes infants who will later develop cerebral palsy from matched controls.Folliculin-interacting proteins Fnip1 and Fnip2 play critical roles in kidney tumor suppression in cooperation with Flcn.Pulmonary manifestations of Birt-Hogg-Dubé syndrome.Mitochondrial DNA mutations distinguish bilateral multifocal renal oncocytomas from familial Birt-Hogg-Dubé tumorsClinical Features, Genetics and Potential Therapeutic Approaches for Birt-Hogg-Dubé Syndrome.Flcn-deficient renal cells are tumorigenic and sensitive to mTOR suppression.Birt-Hogg-Dubé syndrome: from gene discovery to molecularly targeted therapies.Molecular genetics and clinical features of Birt-Hogg-Dubé syndrome.The PGC-1/ERR signaling axis in cancer.Tumour and patient factors in renal cell carcinoma-towards personalized therapy.Establishment and characterization of BHD-F59RSVT, an immortalized cell line derived from a renal cell carcinoma in a patient with Birt-Hogg-Dubé syndrome.Oncocytoma-like renal tumor with transformation toward high-grade oncocytic carcinoma: a unique case with morphologic, immunohistochemical, and genomic characterization.Genetic, epidemiologic and clinicopathologic studies of Japanese Asian patients with Birt-Hogg-Dubé syndrome.Functional aspects of primary cilia in signaling, cell cycle and tumorigenesis.Immunohistochemical characterization of renal tumors in patients with Birt-Hogg-Dubé syndrome.RNA sequencing reveals upregulation of RUNX1-RUNX1T1 gene signatures in clear cell renal cell carcinomaWhere Birt-Hogg-Dubé meets Cowden syndrome: mirrored genetic defects in two cases of syndromic oncocytic tumours.Loss of the Birt-Hogg-Dubé gene product folliculin induces longevity in a hypoxia-inducible factor-dependent manner.FLCN: The causative gene for Birt-Hogg-Dubé syndrome.Conserved and Divergent Features of Mesenchymal Progenitor Cell Types within the Cortical Nephrogenic Niche of the Human and Mouse Kidney.Loss of Fnip1 alters kidney developmental transcriptional program and synergizes with TSC1 loss to promote mTORC1 activation and renal cyst formation.
P2860
Q21199585-CCD3E631-CF21-4C3E-921E-D52EE452E179Q24298493-61DE7B9D-9936-447B-9020-DFAEA55A92F4Q24600512-CCB6BAD9-CBBE-4376-B904-A7B371D5D7E8Q26851787-2D798AC6-5E50-470A-87A6-0F53B5ED828FQ26852437-C5509DF5-0484-4478-B776-601C9DE6A3A1Q27316476-2B9A5AE9-DEFD-4247-86BB-34598A02032CQ28506632-286ABA70-83E3-42F8-8ED5-FBD5A2A6B2ADQ30248354-17863F09-EC95-4551-A798-03C3193838A4Q33685916-EF9E2D45-F7EB-4FB1-86C7-AA68831F6922Q35150986-FD25CCF1-F269-496C-85CA-C927F1E89CACQ35279496-C3CCE6A4-D63C-40C0-B032-06067F7B605AQ35536837-2CA836C9-E949-4B0C-B9E4-FA4F0FD60891Q36235955-CC3CA95F-4BDD-45A5-BE32-E86CC51A3F12Q36283086-38327ACC-F368-43FC-847F-0BC0BA558FD2Q36544967-5E1095EE-56F8-4FC2-BBC3-D91186E25AC9Q36799958-3647480F-512A-4B39-B7B1-244EAB81435BQ37429054-7A730829-CC4D-4989-B7FB-1EE60BB216D4Q38064784-488EF498-D5C1-43D6-BD81-7602A8CB05E3Q38418649-FDCB8D4C-B393-4FC1-B879-5DF4BD42BCEAQ38725502-00FBA21B-9BFB-471E-B1D9-D14A328BA45CQ39128955-0B317A93-0F8F-4ECB-85A4-EB9522949E67Q40519705-EA316888-0487-4DFE-BEE7-46A0C034A3A6Q40963789-0A400D3F-5120-47E2-94BC-70A7E5711814Q41566823-60F32F4F-E854-439D-A5DE-D16AD39D530DQ42361297-3B30D047-417A-4073-97BA-87FFB55737F2Q42642212-FDA6A869-6393-42A8-98DF-24A8FFA2CE5DQ44159799-AF336223-D0CB-46AF-A5B0-4FEDC74EF2F0Q47712748-68DCB6E3-E5C4-4D23-8C49-F7769C8DC581Q49959878-70B05FB8-E863-4FAD-8934-87AF9B25E09AQ55500213-7ADCCCBD-8276-48C6-8EFC-43603AC3C898
P2860
Birt-Hogg-Dubé renal tumors are genetically distinct from other renal neoplasias and are associated with up-regulation of mitochondrial gene expression.
description
2010 nî lūn-bûn
@nan
2010 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Birt-Hogg-Dubé renal tumors ar ...... mitochondrial gene expression.
@ast
Birt-Hogg-Dubé renal tumors ar ...... mitochondrial gene expression.
@en
type
label
Birt-Hogg-Dubé renal tumors ar ...... mitochondrial gene expression.
@ast
Birt-Hogg-Dubé renal tumors ar ...... mitochondrial gene expression.
@en
prefLabel
Birt-Hogg-Dubé renal tumors ar ...... mitochondrial gene expression.
@ast
Birt-Hogg-Dubé renal tumors ar ...... mitochondrial gene expression.
@en
P2093
P2860
P50
P356
P1433
P1476
Birt-Hogg-Dubé renal tumors ar ...... mitochondrial gene expression.
@en
P2093
Annika Sääf
Arnaud Méjean
David Petillo
Jeff A Klomp
Jindong Chen
Karl J Dykema
Kyle A Furge
Laurent Yonneau
Natalie M Niemi
Peter Zickert
P2860
P2888
P356
10.1186/1755-8794-3-59
P577
2010-12-16T00:00:00Z
P5875
P6179
1029792526