204 related articles for article (PubMed ID: 7849709)
1. The tuberous sclerosis gene on chromosome 9q34 acts as a growth suppressor.
Green AJ; Johnson PH; Yates JR
Hum Mol Genet; 1994 Oct; 3(10):1833-4. PubMed ID: 7849709
[TBL] [Abstract][Full Text] [Related]
2. Loss of heterozygosity on chromosome 16p13.3 in hamartomas from tuberous sclerosis patients.
Green AJ; Smith M; Yates JR
Nat Genet; 1994 Feb; 6(2):193-6. PubMed ID: 8162074
[TBL] [Abstract][Full Text] [Related]
3. Loss of heterozygosity in tuberous sclerosis hamartomas.
Sepp T; Yates JR; Green AJ
J Med Genet; 1996 Nov; 33(11):962-4. PubMed ID: 8950679
[TBL] [Abstract][Full Text] [Related]
4. 9q34 loss of heterozygosity in a tuberous sclerosis astrocytoma suggests a growth suppressor-like activity also for the TSC1 gene.
Carbonara C; Longa L; Grosso E; Borrone C; Garrè MG; Brisigotti M; Migone N
Hum Mol Genet; 1994 Oct; 3(10):1829-32. PubMed ID: 7849708
[TBL] [Abstract][Full Text] [Related]
5. Loss of heterozygosity in the tuberous sclerosis (TSC2) region of chromosome band 16p13 occurs in sporadic as well as TSC-associated renal angiomyolipomas.
Henske EP; Neumann HP; Scheithauer BW; Herbst EW; Short MP; Kwiatkowski DJ
Genes Chromosomes Cancer; 1995 Aug; 13(4):295-8. PubMed ID: 7547639
[TBL] [Abstract][Full Text] [Related]
6. Allelic loss is frequent in tuberous sclerosis kidney lesions but rare in brain lesions.
Henske EP; Scheithauer BW; Short MP; Wollmann R; Nahmias J; Hornigold N; van Slegtenhorst M; Welsh CT; Kwiatkowski DJ
Am J Hum Genet; 1996 Aug; 59(2):400-6. PubMed ID: 8755927
[TBL] [Abstract][Full Text] [Related]
7. Apparent preferential loss of heterozygosity at TSC2 over TSC1 chromosomal region in tuberous sclerosis hamartomas.
Carbonara C; Longa L; Grosso E; Mazzucco G; Borrone C; Garrè ML; Brisigotti M; Filippi G; Scabar A; Giannotti A; Falzoni P; Monga G; Garini G; Gabrielli M; Riegler P; Danesino C; Ruggieri M; Magro G; Migone N
Genes Chromosomes Cancer; 1996 Jan; 15(1):18-25. PubMed ID: 8824721
[TBL] [Abstract][Full Text] [Related]
8. Identification of the tuberous sclerosis gene TSC1 on chromosome 9q34.
van Slegtenhorst M; de Hoogt R; Hermans C; Nellist M; Janssen B; Verhoef S; Lindhout D; van den Ouweland A; Halley D; Young J; Burley M; Jeremiah S; Woodward K; Nahmias J; Fox M; Ekong R; Osborne J; Wolfe J; Povey S; Snell RG; Cheadle JP; Jones AC; Tachataki M; Ravine D; Sampson JR; Reeve MP; Richardson P; Wilmer F; Munro C; Hawkins TL; Sepp T; Ali JB; Ward S; Green AJ; Yates JR; Kwiatkowska J; Henske EP; Short MP; Haines JH; Jozwiak S; Kwiatkowski DJ
Science; 1997 Aug; 277(5327):805-8. PubMed ID: 9242607
[TBL] [Abstract][Full Text] [Related]
9. Novel 23-base-pair duplication mutation in TSC1 exon 15 in an infant presenting with cardiac rhabdomyomas.
Smith M; Sperling D
Am J Med Genet; 1999 Jun; 84(4):346-9. PubMed ID: 10340649
[TBL] [Abstract][Full Text] [Related]
10. Clonality of tuberous sclerosis harmatomas shown by non-random X-chromosome inactivation.
Green AJ; Sepp T; Yates JR
Hum Genet; 1996 Feb; 97(2):240-3. PubMed ID: 8566961
[TBL] [Abstract][Full Text] [Related]
11. Tuberous sclerosis-like lesions in epileptogenic human neocortex lack allelic loss at the TSC1 and TSC2 regions.
Wolf HK; Normann S; Green AJ; von Bakel I; Blümcke I; Pietsch T; Wiestler OD; von Deimling A
Acta Neuropathol; 1997 Jan; 93(1):93-6. PubMed ID: 9006662
[TBL] [Abstract][Full Text] [Related]
12. Tuberous sclerosis complex: genotype/phenotype correlation of retinal findings.
Aronow ME; Nakagawa JA; Gupta A; Traboulsi EI; Singh AD
Ophthalmology; 2012 Sep; 119(9):1917-23. PubMed ID: 22608477
[TBL] [Abstract][Full Text] [Related]
13. Survey of somatic mutations in tuberous sclerosis complex (TSC) hamartomas suggests different genetic mechanisms for pathogenesis of TSC lesions.
Niida Y; Stemmer-Rachamimov AO; Logrip M; Tapon D; Perez R; Kwiatkowski DJ; Sims K; MacCollin M; Louis DN; Ramesh V
Am J Hum Genet; 2001 Sep; 69(3):493-503. PubMed ID: 11468687
[TBL] [Abstract][Full Text] [Related]
14. Malignant tumors of the kidney, brain, and soft tissues in children and young adults with the tuberous sclerosis complex.
Al-Saleem T; Wessner LL; Scheithauer BW; Patterson K; Roach ES; Dreyer SJ; Fujikawa K; Bjornsson J; Bernstein J; Henske EP
Cancer; 1998 Nov; 83(10):2208-16. PubMed ID: 9827727
[TBL] [Abstract][Full Text] [Related]
15. Cosmid contigs from the tuberous sclerosis candidate region on chromosome 9q34.
van Slegtenhorst M; Janssen B; Nellist M; Ramlakhan S; Hermans C; Hesseling A; van den Ouweland A; Kwiatkowski D; Eussen B; Sampson J
Eur J Hum Genet; 1995; 3(2):78-86. PubMed ID: 7552145
[TBL] [Abstract][Full Text] [Related]
16. Refined localization of TSC1 by combined analysis of 9q34 and 16p13 data in 14 tuberous sclerosis families.
Janssen B; Sampson J; van der Est M; Deelen W; Verhoef S; Daniels I; Hesseling A; Brook-Carter P; Nellist M; Lindhout D
Hum Genet; 1994 Oct; 94(4):437-40. PubMed ID: 7927344
[TBL] [Abstract][Full Text] [Related]
17. Large deletion at the TSC1 locus in a family with tuberous sclerosis complex.
Nellist M; Sancak O; Goedbloed MA; van Veghel-Plandsoen M; Maat-Kievit A; Lindhout D; Eussen BH; de Klein A; Halley DJ; van den Ouweland AM
Genet Test; 2005; 9(3):226-30. PubMed ID: 16225402
[TBL] [Abstract][Full Text] [Related]
18. Tuberous sclerosis complex: tumors and tumorigenesis.
Borkowska J; Schwartz RA; Kotulska K; Jozwiak S
Int J Dermatol; 2011 Jan; 50(1):13-20. PubMed ID: 21182496
[TBL] [Abstract][Full Text] [Related]
19. Physical analysis of the tuberous sclerosis region in 9q34.
Zhou CY; Wu KY; Leversha MA; Furlong RA; Ferguson-Smith MA; Affara NA
Genomics; 1995 Jan; 25(1):304-8. PubMed ID: 7774937
[TBL] [Abstract][Full Text] [Related]
20. Multifocal renal cell carcinoma in sibs from a chromosome 9 linked (TSC1) tuberous sclerosis family.
Sampson JR; Patel A; Mee AD
J Med Genet; 1995 Nov; 32(11):848-50. PubMed ID: 8592324
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
