162 related articles for article (PubMed ID: 16932376)
1. Cystic kidney disease, chromophobe renal cell carcinoma and TCF2 (HNF1 beta) mutations.
Lebrun G; Vasiliu V; Bellanné-Chantelot C; Bensman A; Ulinski T; Chrétien Y; Grünfeld JP
Nat Clin Pract Nephrol; 2005 Dec; 1(2):115-9. PubMed ID: 16932376
[TBL] [Abstract][Full Text] [Related]
2. Renal phenotypes related to hepatocyte nuclear factor-1beta (TCF2) mutations in a pediatric cohort.
Ulinski T; Lescure S; Beaufils S; Guigonis V; Decramer S; Morin D; Clauin S; Deschênes G; Bouissou F; Bensman A; Bellanné-Chantelot C
J Am Soc Nephrol; 2006 Feb; 17(2):497-503. PubMed ID: 16371430
[TBL] [Abstract][Full Text] [Related]
3. Massively enlarged polycystic kidneys in monozygotic twins with TCF2/HNF-1beta (hepatocyte nuclear factor-1beta) heterozygous whole-gene deletion.
Faguer S; Bouissou F; Dumazer P; Guitard J; Bellanné-Chantelot C; Chauveau D
Am J Kidney Dis; 2007 Dec; 50(6):1023-7. PubMed ID: 18037103
[TBL] [Abstract][Full Text] [Related]
4. [Abnormalities of hepatocyte nuclear factor (HNF)-1beta: biological mechanisms, phenotypes, and clinical consequences].
Ulinski T; Bensman A; Lescure S
Arch Pediatr; 2009 Jul; 16(7):1049-56. PubMed ID: 19361964
[TBL] [Abstract][Full Text] [Related]
5. Germline hepatocyte nuclear factor 1alpha and 1beta mutations in renal cell carcinomas.
Rebouissou S; Vasiliu V; Thomas C; Bellanné-Chantelot C; Bui H; Chrétien Y; Timsit J; Rosty C; Laurent-Puig P; Chauveau D; Zucman-Rossi J
Hum Mol Genet; 2005 Mar; 14(5):603-14. PubMed ID: 15649945
[TBL] [Abstract][Full Text] [Related]
6. Anomalies of the TCF2 gene are the main cause of fetal bilateral hyperechogenic kidneys.
Decramer S; Parant O; Beaufils S; Clauin S; Guillou C; Kessler S; Aziza J; Bandin F; Schanstra JP; Bellanné-Chantelot C
J Am Soc Nephrol; 2007 Mar; 18(3):923-33. PubMed ID: 17267738
[TBL] [Abstract][Full Text] [Related]
7. [Cystic kidney disease and diabetes--an underdiagnosed monogenic developmental disorder].
Merenmies J; Ala-Houhala M; Tuomi T
Duodecim; 2012; 128(19):1999-2006. PubMed ID: 23155751
[TBL] [Abstract][Full Text] [Related]
8. TCF2 gene mutation leads to nephro-urological defects of unequal severity: an open question.
Zaffanello M; Brugnara M; Franchini M; Fanos V
Med Sci Monit; 2008 Jun; 14(6):RA78-86. PubMed ID: 18509286
[TBL] [Abstract][Full Text] [Related]
9. Growth hormone therapy-related hyperglycaemia in a boy with renal cystic hypodysplasia and a new mutation of the HNF1 beta gene.
Giglio S; Contini E; Toni S; Pela I
Nephrol Dial Transplant; 2010 Sep; 25(9):3116-9. PubMed ID: 20543213
[TBL] [Abstract][Full Text] [Related]
10. Severe pancreas hypoplasia and multicystic renal dysplasia in two human fetuses carrying novel HNF1beta/MODY5 mutations.
Haumaitre C; Fabre M; Cormier S; Baumann C; Delezoide AL; Cereghini S
Hum Mol Genet; 2006 Aug; 15(15):2363-75. PubMed ID: 16801329
[TBL] [Abstract][Full Text] [Related]
11. Mutations in BHD and TP53 genes, but not in HNF1beta gene, in a large series of sporadic chromophobe renal cell carcinoma.
Gad S; Lefèvre SH; Khoo SK; Giraud S; Vieillefond A; Vasiliu V; Ferlicot S; Molinié V; Denoux Y; Thiounn N; Chrétien Y; Méjean A; Zerbib M; Benoît G; Hervé JM; Allègre G; Bressac-de Paillerets B; Teh BT; Richard S
Br J Cancer; 2007 Jan; 96(2):336-40. PubMed ID: 17133269
[TBL] [Abstract][Full Text] [Related]
12. Phenotype of a patient with a de novo mutation in the hepatocyte nuclear factor 1beta/maturity-onset diabetes of the young type 5 gene.
Mayer C; Böttcher Y; Kovacs P; Halbritter J; Stumvoll M
Metabolism; 2008 Mar; 57(3):416-20. PubMed ID: 18249217
[TBL] [Abstract][Full Text] [Related]
13. Over expression of hypoxia-inducible protein 2, hypoxia-inducible factor-1alpha and nuclear factor kappaB is putatively involved in acquired renal cyst formation and subsequent tumor transformation in patients with end stage renal failure.
Konda R; Sugimura J; Sohma F; Katagiri T; Nakamura Y; Fujioka T
J Urol; 2008 Aug; 180(2):481-5. PubMed ID: 18550099
[TBL] [Abstract][Full Text] [Related]
14. Hereditary leiomyomatosis and renal cell cancer: an unusual and aggressive form of hereditary renal carcinoma.
Refae MA; Wong N; Patenaude F; Bégin LR; Foulkes WD
Nat Clin Pract Oncol; 2007 Apr; 4(4):256-61. PubMed ID: 17392716
[TBL] [Abstract][Full Text] [Related]
15. Hepatocyte nuclear factor-1beta gene deletions--a common cause of renal disease.
Edghill EL; Oram RA; Owens M; Stals KL; Harries LW; Hattersley AT; Ellard S; Bingham C
Nephrol Dial Transplant; 2008 Feb; 23(2):627-35. PubMed ID: 17971380
[TBL] [Abstract][Full Text] [Related]
16. [HNF1B-related disease: paradigm of a developmental gene and unexpected recognition of a new renal disease].
Chauveau D; Faguer S; Bandin F; Guigonis V; Chassaing N; Decramer S
Nephrol Ther; 2013 Nov; 9(6):393-7. PubMed ID: 24119877
[TBL] [Abstract][Full Text] [Related]
17. Germline and somatic c-met mutations in multifocal/bilateral and sporadic papillary renal carcinomas of selected patients.
Salvi A; Marchina E; Benetti A; Grigolato P; De Petro G; Barlati S
Int J Oncol; 2008 Aug; 33(2):271-6. PubMed ID: 18636147
[TBL] [Abstract][Full Text] [Related]
18. A novel HNF1B mutation p.R177Q in autosomal dominant tubulointerstitial kidney disease and maturity-onset diabetes of the young type 5: A pedigree-based case report.
Tao T; Yang Y; Hu Z
Medicine (Baltimore); 2020 Jul; 99(31):e21438. PubMed ID: 32756155
[TBL] [Abstract][Full Text] [Related]
19. Renal cysts and diabetes due to a heterozygous HNF-1beta gene deletion.
Eller P; Kaser S; Lhotta K; Edghill EL; Ellard S; Ebenbichler C; Patsch JR
Nephrol Dial Transplant; 2007 Apr; 22(4):1271-2. PubMed ID: 17127696
[No Abstract] [Full Text] [Related]
20. [A case report of chromophobe cell renal carcinoma arising from atrophic kidney during long-term haemodialysis].
Onishi T; Igarashi T; Tobe T; Ichikawa T
Hinyokika Kiyo; 2006 Dec; 52(12):919-21. PubMed ID: 17252973
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
