BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

92 related articles for article (PubMed ID: 10463588)

  • 21. Retention of polysomy at 9p23-24 during karyotypic evolution in human breast cancer cell line COLO 824.
    Savelyeva L; Claas A; An H; Weber RG; Lichter P; Schwab M
    Genes Chromosomes Cancer; 1999 Jan; 24(1):87-93. PubMed ID: 9892114
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Lack of association between LOH in the 9p region and clinicopathologic parameters in primary breast cancer.
    Vieira de Oliveira SF; Oliveira MM; Urban CA; de Lima RS; Cavalli IJ; Ribeiro EM
    Cancer Genet Cytogenet; 2010 Jul; 200(1):23-7. PubMed ID: 20513530
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Allelic loss in esophageal squamous cell carcinoma patients with and without family history of upper gastrointestinal tract cancer.
    Hu N; Roth MJ; Emmert-Buck MR; Tang ZZ; Polymeropolous M; Wang QH; Goldstein AM; Han XY; Dawsey SM; Ding T; Giffen C; Taylor PR
    Clin Cancer Res; 1999 Nov; 5(11):3476-82. PubMed ID: 10589761
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Loss of heterozygosity on the long arm of human chromosome 7 in sporadic renal cell carcinomas.
    Shridhar V; Sun QC; Miller OJ; Kalemkerian GP; Petros J; Smith DI
    Oncogene; 1997 Nov; 15(22):2727-33. PubMed ID: 9400999
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 3p21, 5q21, and 9p21 allelic deletions are frequently found in normal bronchial cells adjacent to non-small-cell lung cancer, while they are unusual in patients with no evidence of malignancy.
    Sanz-Ortega J; Saez MC; Sierra E; Torres A; Balibrea JL; Hernando F; Sanz-Esponera J; Merino MJ
    J Pathol; 2001 Nov; 195(4):429-34. PubMed ID: 11745674
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Refinement of the LOH region 1 at 11q23.1 deleted in human breast carcinomas and sublocalization of 11 expressed sequence tags within the refined region.
    di Iasio MG; Calin G; Tibiletti MG; Vorechovsky I; Benediktsson KP; Taramelli R; Barbanti-Brodano G; Negrini M
    Oncogene; 1999 Feb; 18(8):1635-8. PubMed ID: 10102634
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Refined deletion mapping of loss of heterozygosity on 22q13 in sporadic colorectal carcinoma].
    Zheng HT; Tang HM; Peng ZH; Zhou CZ; He L
    Zhonghua Wei Chang Wai Ke Za Zhi; 2006 Mar; 9(2):157-60. PubMed ID: 16555160
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Identification of chromosome arm 9p as the most frequent target of homozygous deletions in lung cancer.
    Sato M; Takahashi K; Nagayama K; Arai Y; Ito N; Okada M; Minna JD; Yokota J; Kohno T
    Genes Chromosomes Cancer; 2005 Dec; 44(4):405-14. PubMed ID: 16114034
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Novel somatic mutations in the BRCA1 gene in sporadic breast tumors.
    Janatova M; Zikan M; Dundr P; Matous B; Pohlreich P
    Hum Mutat; 2005 Mar; 25(3):319. PubMed ID: 15712267
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A region of deletion on chromosome 22q13 is common to human breast and colorectal cancers.
    Castells A; Gusella JF; Ramesh V; Rustgi AK
    Cancer Res; 2000 Jun; 60(11):2836-9. PubMed ID: 10850424
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Allelic losses at 1p36 and 19q13 in gliomas: correlation with histologic classification, definition of a 150-kb minimal deleted region on 1p36, and evaluation of CAMTA1 as a candidate tumor suppressor gene.
    Barbashina V; Salazar P; Holland EC; Rosenblum MK; Ladanyi M
    Clin Cancer Res; 2005 Feb; 11(3):1119-28. PubMed ID: 15709179
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Detailed deletion mapping in sporadic breast cancer at chromosomal region 17p13 distal to the TP53 gene: association with clinicopathological parameters.
    Seitz S; Poppe K; Fischer J; Nothnagel A; Estévez-Schwarz L; Haensch W; Schlag PM; Scherneck S
    J Pathol; 2001 Jul; 194(3):318-26. PubMed ID: 11439364
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Genome-wide search for loss of heterozygosity shows extensive genetic diversity of human breast carcinomas.
    Kerangueven F; Noguchi T; Coulier F; Allione F; Wargniez V; Simony-Lafontaine J; Longy M; Jacquemier J; Sobol H; Eisinger F; Birnbaum D
    Cancer Res; 1997 Dec; 57(24):5469-74. PubMed ID: 9407952
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Deletion of chromosomes 9p and 17 associated with abnormal expression of p53, p16/MTS1 and p15/MTS2 gene protein in hepatocellular carcinomas.
    Shao J; Li Y; Li H; Wu Q; Hou J; Liew C
    Chin Med J (Engl); 2000 Sep; 113(9):817-22. PubMed ID: 11776078
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Deletions on chromosome 4 in sporadic and BRCA mutated tumors and association with pathological variables.
    Johannsdottir HK; Johannesdottir G; Agnarsson BA; Eerola H; Arason A; Johannsson OT; Heikkilä P; Egilsson V; Olsson H; Borg A; Nevanlinna H; Barkardottir RB
    Anticancer Res; 2004; 24(5A):2681-7. PubMed ID: 15521105
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Identification of three regions on chromosome 17q in primary human breast carcinomas which are frequently deleted.
    Cropp CS; Champeme MH; Lidereau R; Callahan R
    Cancer Res; 1993 Dec; 53(23):5617-9. PubMed ID: 8242614
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Discovery of frequent homozygous deletions in chromosome 3p21.3 LUCA and AP20 regions in renal, lung and breast carcinomas.
    Senchenko VN; Liu J; Loginov W; Bazov I; Angeloni D; Seryogin Y; Ermilova V; Kazubskaya T; Garkavtseva R; Zabarovska VI; Kashuba VI; Kisselev LL; Minna JD; Lerman MI; Klein G; Braga EA; Zabarovsky ER
    Oncogene; 2004 Jul; 23(34):5719-28. PubMed ID: 15208675
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Frequent silence of chromosome 9p, homozygous DOCK8, DMRT1 and DMRT3 deletion at 9p24.3 in squamous cell carcinoma of the lung.
    Kang JU; Koo SH; Kwon KC; Park JW
    Int J Oncol; 2010 Aug; 37(2):327-35. PubMed ID: 20596660
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Genome-wide amplification and allelotyping of sporadic pituitary adenomas identify novel regions of genetic loss.
    Simpson DJ; Bicknell EJ; Buch HN; Cutty SJ; Clayton RN; Farrell WE
    Genes Chromosomes Cancer; 2003 Jul; 37(3):225-36. PubMed ID: 12759921
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Loss of heterozygosity at microsatellite markers from region p11-21 of chromosome 8 in microdissected breast tumor but not in peritumoral cells.
    Charafe-Jauffret E; Moulin JF; Ginestier C; Bechlian D; Conte N; Geneix J; Adélaïde J; Noguchi T; Hassoun J; Jacquemier J; Birnbaum D
    Int J Oncol; 2002 Nov; 21(5):989-96. PubMed ID: 12370745
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.