131 related articles for article (PubMed ID: 2220825)
1. Minisatellite allele diversification: the origin of rare alleles at the HRAS1 locus.
Kasperczyk A; DiMartino NA; Krontiris TG
Am J Hum Genet; 1990 Nov; 47(5):854-9. PubMed ID: 2220825
[TBL] [Abstract][Full Text] [Related]
2. An association between the risk of cancer and mutations in the HRAS1 minisatellite locus.
Krontiris TG; Devlin B; Karp DD; Robert NJ; Risch N
N Engl J Med; 1993 Aug; 329(8):517-23. PubMed ID: 8336750
[TBL] [Abstract][Full Text] [Related]
3. The HRAS1 minisatellite locus and risk of ovarian cancer.
Weitzel JN; Ding S; Larson GP; Nelson RA; Goodman A; Grendys EC; Ball HG; Krontiris TG
Cancer Res; 2000 Jan; 60(2):259-61. PubMed ID: 10667571
[TBL] [Abstract][Full Text] [Related]
4. Genetic susceptibility associated with rare HRAS1 variable number of tandem repeats alleles in Spanish non-small cell lung cancer patients.
Rosell R; Calvo R; Sánchez JJ; Maurel J; Guillot M; Monzó M; Núñez L; Barnadas A
Clin Cancer Res; 1999 Jul; 5(7):1849-54. PubMed ID: 10430091
[TBL] [Abstract][Full Text] [Related]
5. Detection of two TaqI polymorphisms in the VTR region of the human HRAS1 oncogene.
Pierotti MA; Radice P; Biunno I; Borrello MG; Cattadori MR; Della Porta G
Cytogenet Cell Genet; 1986; 43(3-4):174-80. PubMed ID: 2879707
[TBL] [Abstract][Full Text] [Related]
6. Rare HRAS1 alleles are a risk factor for the development of brain tumors.
Vega A; Sobrido MJ; Ruiz-Ponte C; Barros F; Carracedo A
Cancer; 2001 Dec; 92(11):2920-6. PubMed ID: 11753967
[TBL] [Abstract][Full Text] [Related]
7. Ovarian cancer risk in BRCA1 carriers is modified by the HRAS1 variable number of tandem repeat (VNTR) locus.
Phelan CM; Rebbeck TR; Weber BL; Devilee P; Ruttledge MH; Lynch HT; Lenoir GM; Stratton MR; Easton DF; Ponder BA; Cannon-Albright L; Larsson C; Goldgar DE; Narod SA
Nat Genet; 1996 Mar; 12(3):309-11. PubMed ID: 8589723
[TBL] [Abstract][Full Text] [Related]
8. Human hypervariable sequences in risk assessment: rare Ha-ras alleles in cancer patients.
Krontiris TG; DiMartino NA; Mitcheson HD; Lonergan JA; Begg C; Parkinson DR
Environ Health Perspect; 1987 Dec; 76():147-53. PubMed ID: 3329095
[TBL] [Abstract][Full Text] [Related]
9. Rare HRAS1 alleles outside the VTR region in lymph nodes from patients with malignant lymphoma.
Stul M; Baens M; Mecucci C; Van den Berghe H; Cassiman JJ
Cancer Genet Cytogenet; 1993 Aug; 69(1):60-4. PubMed ID: 8104094
[TBL] [Abstract][Full Text] [Related]
10. HRAS1 minisatellite alleles in colorectal carcinoma: relationship to microsatelite instability.
Vega A; Barros F; Lleonart ME; Ramon y Cajal S; Carracedo A
Anticancer Res; 2001; 21(4A):2855-60. PubMed ID: 11724366
[TBL] [Abstract][Full Text] [Related]
11. Allelic variation of reporter gene activation by the HRAS1 minisatellite.
Green M; Krontiris TG
Genomics; 1993 Aug; 17(2):429-34. PubMed ID: 8406494
[TBL] [Abstract][Full Text] [Related]
12. The HRAS1 variable number of tandem repeats and risk of breast cancer.
Tamimi RM; Hankinson SE; Ding S; Gagalang V; Larson GP; Spiegelman D; Colditz GA; Krontiris TG; Hunter DJ
Cancer Epidemiol Biomarkers Prev; 2003 Dec; 12(12):1528-30. PubMed ID: 14693748
[TBL] [Abstract][Full Text] [Related]
13. Allele-specific MVR-PCR analysis at minisatellite D1S8.
Monckton DG; Tamaki K; MacLeod A; Neil DL; Jeffreys AJ
Hum Mol Genet; 1993 May; 2(5):513-9. PubMed ID: 8518788
[TBL] [Abstract][Full Text] [Related]
14. Hras1 VNTR alleles as susceptibility markers for lung cancer: relationship to microsatellite instability in tumors.
Lindstedt BA; Ryberg D; Zienolddiny S; Khan H; Haugen A
Anticancer Res; 1999; 19(6C):5523-7. PubMed ID: 10697610
[TBL] [Abstract][Full Text] [Related]
15. Cloning a selected fragment from a human DNA 'fingerprint': isolation of an extremely polymorphic minisatellite.
Wong Z; Wilson V; Jeffreys AJ; Thein SL
Nucleic Acids Res; 1986 Jun; 14(11):4605-16. PubMed ID: 2423969
[TBL] [Abstract][Full Text] [Related]
16. Allele-specific deletion in exon I of the HRAS1 gene.
Kasperczyk A; Mermer BA; Parkinson DR; Lonergan JA; Krontiris TG
Am J Hum Genet; 1989 Nov; 45(5):689-96. PubMed ID: 2573274
[TBL] [Abstract][Full Text] [Related]
17. An allele of HRAS1 3'variable number of tandem repeats is a frailty allele: implication for an evolutionarily-conserved pathway involved in longevity.
Bonafè M; Barbi C; Olivieri F; Yashin A; Andreev KF; Vaupel JW; De Benedictis G; Rose G; Carrieri G; Jazwinski SM; Franceschi C
Gene; 2002 Mar; 286(1):121-6. PubMed ID: 11943467
[TBL] [Abstract][Full Text] [Related]
18. HRAS1 rare minisatellite alleles and breast cancer in Australian women under age forty years.
Firgaira FA; Seshadri R; McEvoy CR; Dite GS; Giles GG; McCredie MR; Southey MC; Venter DJ; Hopper JL
J Natl Cancer Inst; 1999 Dec; 91(24):2107-11. PubMed ID: 10601382
[TBL] [Abstract][Full Text] [Related]
19. Loss of allelic heterozygosity at the harvey ras locus in human oral carcinomas.
Saranath D; Bhoite LT; Mehta AR; Sanghavi V; Deo MG
J Cancer Res Clin Oncol; 1991; 117(5):484-8. PubMed ID: 1679760
[TBL] [Abstract][Full Text] [Related]
20. Human restriction fragment length polymorphisms and cancer risk assessment.
Krontiris TG; DiMartino NA; Colb M; Mitcheson HD; Parkinson DR
J Cell Biochem; 1986; 30(4):319-29. PubMed ID: 3011817
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]