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7. Renal cystic disease in tuberous sclerosis: role of the polycystic kidney disease 1 gene. Sampson JR; Maheshwar MM; Aspinwall R; Thompson P; Cheadle JP; Ravine D; Roy S; Haan E; Bernstein J; Harris PC Am J Hum Genet; 1997 Oct; 61(4):843-51. PubMed ID: 9382094 [TBL] [Abstract][Full Text] [Related]
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9. Polycystic kidney disease as a result of loss of the tuberous sclerosis 2 tumor suppressor gene during development. Cai S; Everitt JI; Kugo H; Cook J; Kleymenova E; Walker CL Am J Pathol; 2003 Feb; 162(2):457-68. PubMed ID: 12547704 [TBL] [Abstract][Full Text] [Related]
10. Suppression of tumorigenicity by the wild-type tuberous sclerosis 2 (Tsc2) gene and its C-terminal region. Jin F; Wienecke R; Xiao GH; Maize JC; DeClue JE; Yeung RS Proc Natl Acad Sci U S A; 1996 Aug; 93(17):9154-9. PubMed ID: 8799170 [TBL] [Abstract][Full Text] [Related]
11. Carboxy terminal tail of polycystin-1 regulates localization of TSC2 to repress mTOR. Dere R; Wilson PD; Sandford RN; Walker CL PLoS One; 2010 Feb; 5(2):e9239. PubMed ID: 20169078 [TBL] [Abstract][Full Text] [Related]
12. Tuberous sclerosis and polycystic kidney disease in a 3-month-old infant. Laass MW; Spiegel M; Jauch A; Hahn G; Rupprecht E; Vogelberg C; Bartsch O; Huebner A Pediatr Nephrol; 2004 Jun; 19(6):602-8. PubMed ID: 15007723 [TBL] [Abstract][Full Text] [Related]
13. Imaging features of tuberous sclerosis complex with autosomal-dominant polycystic kidney disease: a contiguous gene syndrome. Back SJ; Andronikou S; Kilborn T; Kaplan BS; Darge K Pediatr Radiol; 2015 Mar; 45(3):386-95. PubMed ID: 25355409 [TBL] [Abstract][Full Text] [Related]
14. Distinct subcellular expression of endogenous polycystin-2 in the plasma membrane and Golgi apparatus of MDCK cells. Scheffers MS; Le H; van der Bent P; Leonhard W; Prins F; Spruit L; Breuning MH; de Heer E; Peters DJ Hum Mol Genet; 2002 Jan; 11(1):59-67. PubMed ID: 11772999 [TBL] [Abstract][Full Text] [Related]
15. Deletion of the TSC2 and PKD1 genes associated with severe infantile polycystic kidney disease--a contiguous gene syndrome. Brook-Carter PT; Peral B; Ward CJ; Thompson P; Hughes J; Maheshwar MM; Nellist M; Gamble V; Harris PC; Sampson JR Nat Genet; 1994 Dec; 8(4):328-32. PubMed ID: 7894481 [TBL] [Abstract][Full Text] [Related]
16. The tuberin (TSC2), autosomal dominant polycystic kidney disease (PKD1), and somatostatin type V receptor (SSTR5) genes form a synteny group in the Fugu genome. Sandford R; Sgotto B; Burn T; Brenner S Genomics; 1996 Nov; 38(1):84-6. PubMed ID: 8954784 [TBL] [Abstract][Full Text] [Related]
17. Acrofacial dysostosis in a patient with the TSC2-PKD1 contiguous gene syndrome. Dauwerse JG; Bouman K; van Essen AJ; van Der Hout AH; Kolsters G; Breuning MH; Peters DJ J Med Genet; 2002 Feb; 39(2):136-41. PubMed ID: 11836366 [No Abstract] [Full Text] [Related]
18. The TSC2/PKD1 contiguous gene syndrome. Harris PC Contrib Nephrol; 1997; 122():76-82. PubMed ID: 9399043 [No Abstract] [Full Text] [Related]
19. A tuberous sclerosis patient with a large TSC2 and PKD1 gene deletion shows extrarenal signs of autosomal dominant polycystic kidney disease. Longa L; Brusco A; Carbonara C; Polidoro S; Scolari F; Valzorio B; Riegler P; Tardanico R; Migone N Contrib Nephrol; 1997; 122():91-5. PubMed ID: 9399046 [No Abstract] [Full Text] [Related]
20. Chromosomal assignment of canine TSC2, PKD1 and CLN3 genes by radiation hybrid- and linkage analyses. Jónasdóttir TJ; Mellersh CS; Moe L; Vignaux F; Ostrander EA; Lingaas F Anim Genet; 2000 Apr; 31(2):123-6. PubMed ID: 10782211 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]