BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

837 related articles for article (PubMed ID: 15361296)

  • 21. A novel region of deletion on 13q33-q34 in esophageal squamous cell carcinoma.
    Guo GM; Huang XP; Dong JT; Caia Y; Xu X; Han YL; Wu M; Zhan QM; Wang MR
    Oncol Rep; 2005 Dec; 14(6):1639-46. PubMed ID: 16273270
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. Loss of heterozygosity of chromosome 9p21 and 7q31 is correlated with high incidence of recurrent tumor in head and neck squamous cell carcinoma.
    Matsuura K; Shiga K; Yokoyama J; Saijo S; Miyagi T; Takasaka T
    Anticancer Res; 1998; 18(1A):453-8. PubMed ID: 9568119
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Identification of new minimally lost regions on 18q in head and neck squamous cell carcinoma.
    Takebayashi S; Ogawa T; Jung KY; Muallem A; Mineta H; Fisher SG; Grenman R; Carey TE
    Cancer Res; 2000 Jul; 60(13):3397-403. PubMed ID: 10910046
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Lymph node metastasis is associated with allelic loss on chromosome 13q12-13 in esophageal squamous cell carcinoma.
    Harada H; Tanaka H; Shimada Y; Shinoda M; Imamura M; Ishizaki K
    Cancer Res; 1999 Aug; 59(15):3724-9. PubMed ID: 10446988
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Molecular genetic evidence for the independent origin of multifocal papillary tumors in patients with papillary renal cell carcinomas.
    Jones TD; Eble JN; Wang M; MacLennan GT; Delahunt B; Brunelli M; Martignoni G; Lopez-Beltran A; Bonsib SM; Ulbright TM; Zhang S; Nigro K; Cheng L
    Clin Cancer Res; 2005 Oct; 11(20):7226-33. PubMed ID: 16243792
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Molecular evidence supporting field effect in urothelial carcinogenesis.
    Jones TD; Wang M; Eble JN; MacLennan GT; Lopez-Beltran A; Zhang S; Cocco A; Cheng L
    Clin Cancer Res; 2005 Sep; 11(18):6512-9. PubMed ID: 16166427
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Aberrant p16 expression is correlated with hemizygous deletions at the 9p21-22 chromosome region in non-small cell lung carcinomas.
    Spanakis NE; Gorgoulis V; Mariatos G; Zacharatos P; Kotsinas A; Garinis G; Trigidou R; Karameris A; Tsimara-Papastamatiou H; Kouloukousa M; Manolis EN; Kittas C
    Anticancer Res; 1999; 19(3A):1893-9. PubMed ID: 10470133
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Allelic imbalance on chromosomes 3p, 9p and 17p in malignant progression of laryngeal mucosa.
    Guo T; Sun JW; Lv QP; Li XG
    J Laryngol Otol; 2008 Jan; 122(1):72-7. PubMed ID: 17498326
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Study on loss of heterozygosity at microsatellite locus in larynx and pharynx squamous cell carcinoma and neck lymph nodes].
    Li B; Xu Y
    Lin Chuang Er Bi Yan Hou Ke Za Zhi; 2004 Jun; 18(6):321-3. PubMed ID: 15354767
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Loss of heterozygosity and mutation analysis of the p16 (9p21) and p53 (17p13) genes in squamous cell carcinoma of the head and neck.
    González MV; Pello MF; López-Larrea C; Suárez C; Menéndez MJ; Coto E
    Clin Cancer Res; 1995 Sep; 1(9):1043-9. PubMed ID: 9816078
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Allelic loss on chromosome 1 is associated with tumor progression of cervical carcinoma.
    Cheung TH; Chung TK; Poon CS; Hampton GM; Wang VW; Wong YF
    Cancer; 1999 Oct; 86(7):1294-8. PubMed ID: 10506716
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Genetic alterations of chromosome band 9p21-22 in head and neck cancer are not restricted to p16INK4a.
    Waber P; Dlugosz S; Cheng QC; Truelson J; Nisen PD
    Oncogene; 1997 Oct; 15(14):1699-704. PubMed ID: 9349503
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Does loss of heterozygosity in critical genome regions predict a local relapse in patients after laryngectomy?
    Szukała K; Sowińska A; Wierzbicka M; Biczysko W; Szyfter W; Szyfter K
    Mutat Res; 2006 Aug; 600(1-2):67-76. PubMed ID: 16814812
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Analysis of FHIT allelic imbalance/loss of heterozygosity and FHIT expression in cutaneous squamous cell carcinomas.
    Gray SE; Kay E; Leader M; Mabruk M
    J Cutan Pathol; 2008 Sep; 35(9):816-25. PubMed ID: 18494825
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Loss of heterozygosity on chromosome 13 in squamous cell carcinomas of the larynx].
    Bai S; Zhang X; Wang J
    Zhonghua Zhong Liu Za Zhi; 1997 Jan; 19(1):35-7. PubMed ID: 10743052
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Studies of the deletion and expression of cytokeratin 13 gene in laryngeal squamous cell carcinoma].
    He G; Fu WN; Qiu GB; Zhao Z; Xu ZM; Sun XH; Sun KL
    Yi Chuan Xue Bao; 2002 May; 29(5):390-5. PubMed ID: 12043564
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Frequent loss of heterozygosity in human primary squamous cell and colon carcinomas at 7q31.1: evidence for a broad range tumor suppressor gene.
    Zenklusen JC; Thompson JC; Klein-Szanto AJ; Conti CJ
    Cancer Res; 1995 Mar; 55(6):1347-50. PubMed ID: 7882334
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Allele losses in squamous cell carcinomas of the larynx].
    Bockmühl U; Petersen I; Dietel M
    Laryngorhinootologie; 1996 Jan; 75(1):48-62. PubMed ID: 8851120
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Genetic progression and divergence in superficial esophageal squamous cell carcinoma by loss of heterozygosity analysis.
    Shima H; Hiyama T; Tanaka S; Yoshihara M; Arihiro K; Chayama K
    Oncol Rep; 2006 Oct; 16(4):685-91. PubMed ID: 16969480
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 42.