246 related articles for article (PubMed ID: 7894115)
1. [Demonstration of two regions involved in chromosome 1p deletion in breast tumors].
Bièche I; Champème MH; Matifas F; Cropp C; Callahan R; Lidereau R
Bull Cancer; 1994 Feb; 81(2):108-13. PubMed ID: 7894115
[TBL] [Abstract][Full Text] [Related]
2. Two distinct regions involved in 1p deletion in human primary breast cancer.
Bièche I; Champème MH; Matifas F; Cropp CS; Callahan R; Lidereau R
Cancer Res; 1993 May; 53(9):1990-4. PubMed ID: 8097672
[TBL] [Abstract][Full Text] [Related]
3. Loss and gain of distinct regions of chromosome 1q in primary breast cancer.
Bièche I; Champème MH; Lidereau R
Clin Cancer Res; 1995 Jan; 1(1):123-7. PubMed ID: 9815894
[TBL] [Abstract][Full Text] [Related]
4. Genetic alteration mapping on chromosome 7 in primary breast cancer.
Bièche I; Khodja A; Driouch K; Lidereau R
Clin Cancer Res; 1997 Jun; 3(6):1009-16. PubMed ID: 9815778
[TBL] [Abstract][Full Text] [Related]
5. Frequent somatic imbalance of marker alleles for chromosome 1 in human primary breast carcinoma.
Devilee P; van Vliet M; Bardoel A; Kievits T; Kuipers-Dijkshoorn N; Pearson PL; Cornelisse CJ
Cancer Res; 1991 Feb; 51(3):1020-5. PubMed ID: 1670997
[TBL] [Abstract][Full Text] [Related]
6. A tumor suppressor gene on chromosome 1p32-pter controls the amplification of MYC family genes in breast cancer.
Bièche I; Champème MH; Lidereau R
Cancer Res; 1994 Aug; 54(16):4274-6. PubMed ID: 7913873
[TBL] [Abstract][Full Text] [Related]
7. Consistent association of 1p loss of heterozygosity with pheochromocytomas from patients with multiple endocrine neoplasia type 2 syndromes.
Moley JF; Brother MB; Fong CT; White PS; Baylin SB; Nelkin B; Wells SA; Brodeur GM
Cancer Res; 1992 Feb; 52(4):770-4. PubMed ID: 1346584
[TBL] [Abstract][Full Text] [Related]
8. Detection and cloning of a common region of loss of heterozygosity at chromosome 1p in breast cancer.
Nagai H; Negrini M; Carter SL; Gillum DR; Rosenberg AL; Schwartz GF; Croce CM
Cancer Res; 1995 Apr; 55(8):1752-7. PubMed ID: 7712484
[TBL] [Abstract][Full Text] [Related]
9. Deletion mapping of chromosomal region 1p32-pter in primary breast cancer.
Bièche I; Khodja A; Lidereau R
Genes Chromosomes Cancer; 1999 Mar; 24(3):255-63. PubMed ID: 10451706
[TBL] [Abstract][Full Text] [Related]
10. Detailed deletion mapping of chromosome 17q in ovarian and breast cancers: 2-cM region on 17q21.3 often and commonly deleted in tumors.
Saito H; Inazawa J; Saito S; Kasumi F; Koi S; Sagae S; Kudo R; Saito J; Noda K; Nakamura Y
Cancer Res; 1993 Jul; 53(14):3382-5. PubMed ID: 8100738
[TBL] [Abstract][Full Text] [Related]
11. Deletion mapping on the short arm of chromosome 1 in Merkel cell carcinoma.
Leonard JH; Cook AL; Nancarrow D; Hayward N; Van Gele M; Van Roy N; Speleman F
Cancer Detect Prev; 2000; 24(6):620-7. PubMed ID: 11198276
[TBL] [Abstract][Full Text] [Related]
12. A widely expressed transcription factor with multiple DNA sequence specificity, CTCF, is localized at chromosome segment 16q22.1 within one of the smallest regions of overlap for common deletions in breast and prostate cancers.
Filippova GN; Lindblom A; Meincke LJ; Klenova EM; Neiman PE; Collins SJ; Doggett NA; Lobanenkov VV
Genes Chromosomes Cancer; 1998 May; 22(1):26-36. PubMed ID: 9591631
[TBL] [Abstract][Full Text] [Related]
13. Localization of a tumor suppressor gene associated with the progression of human breast carcinoma within a 1-cM interval of 8p22-p23.1.
Yokota T; Yoshimoto M; Akiyama F; Sakamoto G; Kasumi F; Nakamura Y; Emi M
Cancer; 1999 Jan; 85(2):447-52. PubMed ID: 10023714
[TBL] [Abstract][Full Text] [Related]
14. Molecular analysis of genetic changes in the origin and development of renal cell carcinoma.
Anglard P; Tory K; Brauch H; Weiss GH; Latif F; Merino MJ; Lerman MI; Zbar B; Linehan WM
Cancer Res; 1991 Feb; 51(4):1071-7. PubMed ID: 1671754
[TBL] [Abstract][Full Text] [Related]
15. A detailed deletion mapping of the short arm of chromosome 3 in sporadic renal cell carcinoma.
Yamakawa K; Morita R; Takahashi E; Hori T; Ishikawa J; Nakamura Y
Cancer Res; 1991 Sep; 51(17):4707-11. PubMed ID: 1678685
[TBL] [Abstract][Full Text] [Related]
16. Deletion mapping of chromosomes 14q and 1p in human neuroblastoma.
Takayama H; Suzuki T; Mugishima H; Fujisawa T; Ookuni M; Schwab M; Gehring M; Nakamura Y; Sugimura T; Terada M
Oncogene; 1992 Jun; 7(6):1185-9. PubMed ID: 1594247
[TBL] [Abstract][Full Text] [Related]
17. Loss of heterozygosity identifies multiple sites of allelic deletions on chromosome 1 in human male germ cell tumors.
Mathew S; Murty VV; Bosl GJ; Chaganti RS
Cancer Res; 1994 Dec; 54(23):6265-9. PubMed ID: 7954476
[TBL] [Abstract][Full Text] [Related]
18. Allele loss on chromosome 16q24.2-qter occurs frequently in breast cancers irrespectively of differences in phenotype and extent of spread.
Tsuda H; Callen DF; Fukutomi T; Nakamura Y; Hirohashi S
Cancer Res; 1994 Jan; 54(2):513-7. PubMed ID: 8275489
[TBL] [Abstract][Full Text] [Related]
19. Evidence for two tumor suppressor loci associated with proximal chromosome 9p to q and distal chromosome 9q in bladder cancer and the initial screening for GAS1 and PTC mutations.
Simoneau AR; Spruck CH; Gonzalez-Zulueta M; Gonzalgo ML; Chan MF; Tsai YC; Dean M; Steven K; Horn T; Jones PA
Cancer Res; 1996 Nov; 56(21):5039-43. PubMed ID: 8895761
[TBL] [Abstract][Full Text] [Related]
20. Clinical investigation of neuroblastoma with partial deletion in the short arm of chromosome 1.
Ohtsu K; Hiyama E; Ichikawa T; Matsuura Y; Yokoyama T
Clin Cancer Res; 1997 Jul; 3(7):1221-8. PubMed ID: 9815803
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
