BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

109 related articles for article (PubMed ID: 15300858)

  • 1. Splice-site genetic polymorphism of the human kallikrein 12 (KLK12) gene correlates with no substantial expression of KLK12 protein having serine protease activity.
    Shinmura K; Tao H; Yamada H; Kataoka H; Sanjar R; Wang J; Yoshimura K; Sugimura H
    Hum Mutat; 2004 Sep; 24(3):273-4. PubMed ID: 15300858
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A novel splice-site variant of the base excision repair gene MYH is associated with production of an aberrant mRNA transcript encoding a truncated MYH protein not localized in the nucleus.
    Tao H; Shinmura K; Hanaoka T; Natsukawa S; Shaura K; Koizumi Y; Kasuga Y; Ozawa T; Tsujinaka T; Li Z; Yamaguchi S; Yokota J; Sugimura H; Tsugane S
    Carcinogenesis; 2004 Oct; 25(10):1859-66. PubMed ID: 15180946
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Familial adenomatous polyposis: aberrant splicing due to missense or silent mutations in the APC gene.
    Aretz S; Uhlhaas S; Sun Y; Pagenstecher C; Mangold E; Caspari R; Möslein G; Schulmann K; Propping P; Friedl W
    Hum Mutat; 2004 Nov; 24(5):370-80. PubMed ID: 15459959
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clinical significance of human kallikrein 10 gene expression in colorectal cancer and gastric cancer.
    Feng B; Xu WB; Zheng MH; Ma JJ; Cai Q; Zhang Y; Ji J; Lu AG; Qu Y; Li JW; Wang ML; Hu WG; Liu BY; Zhu ZG
    J Gastroenterol Hepatol; 2006 Oct; 21(10):1596-603. PubMed ID: 16928223
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Erosive vitreoretinopathy and wagner disease are caused by intronic mutations in CSPG2/Versican that result in an imbalance of splice variants.
    Mukhopadhyay A; Nikopoulos K; Maugeri A; de Brouwer AP; van Nouhuys CE; Boon CJ; Perveen R; Zegers HA; Wittebol-Post D; van den Biesen PR; van der Velde-Visser SD; Brunner HG; Black GC; Hoyng CB; Cremers FP
    Invest Ophthalmol Vis Sci; 2006 Aug; 47(8):3565-72. PubMed ID: 16877430
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Human kallikrein-related peptidase 12: antibody generation and immunohistochemical localization in prostatic tissues.
    Memari N; Diamandis EP; Earle T; Campbell A; Van Dekken H; Van der Kwast TH
    Prostate; 2007 Sep; 67(13):1465-74. PubMed ID: 17654496
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular basis of recessive congenital methemoglobinemia, types I and II: Exon skipping and three novel missense mutations in the NADH-cytochrome b5 reductase (diaphorase 1) gene.
    Kugler W; Pekrun A; Laspe P; Erdlenbruch B; Lakomek M
    Hum Mutat; 2001 Apr; 17(4):348. PubMed ID: 11295830
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Expression and single nucleotide polymorphisms of kallikrein 10 in colorectal cancer].
    Feng B; Zheng MH; Ma JJ; Cai Q; Zhang Y; Ji J; Qu Y; Li JW; Lu AG; Wang ML; Liu BY; Zhu ZG
    Zhonghua Wai Ke Za Zhi; 2006 May; 44(9):623-7. PubMed ID: 16784657
    [TBL] [Abstract][Full Text] [Related]  

  • 9. KLK12 is a novel serine protease and a new member of the human kallikrein gene family-differential expression in breast cancer.
    Yousef GM; Magklara A; Diamandis EP
    Genomics; 2000 Nov; 69(3):331-41. PubMed ID: 11056051
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Polymorphisms of the DNA repair gene XPA and XPC and its correlation with gastric cardiac adenocarcinoma in a high incidence population in North China.
    Dong Z; Guo W; Zhou R; Wan L; Li Y; Wang N; Kuang G; Wang S
    J Clin Gastroenterol; 2008 Sep; 42(8):910-5. PubMed ID: 18645534
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Concurrent expression of aryl hydrocarbon receptor and CYP1A1 but not CYP1A1 MspI polymorphism is correlated with gastric cancers raised in Dalian, China.
    Ma JX; Zhang KL; Liu X; Ma YL; Pei LN; Zhu YF; Zhou L; Chen XY; Kong QY; Li H; Liu J
    Cancer Lett; 2006 Aug; 240(2):253-60. PubMed ID: 16337337
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Correlation of XPC Ala499Val and Lys939Gln polymorphisms to risks of esophageal squamous cell carcinoma and gastric cardiac adenocarcinoma].
    Zhou RM; Li Y; Wang N; Zhang XJ; Dong XJ; Guo W
    Ai Zheng; 2006 Sep; 25(9):1113-9. PubMed ID: 16965652
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic characterization of protein C deficiency in Japanese subjects using a rapid and nonradioactive method for single-stand conformational polymorphism analysis and a model building.
    Miyata T; Sakata T; Zheng YZ; Tsukamoto H; Umeyama H; Uchiyama S; Ikusaka M; Yoshioka A; Imanaka Y; Fujimura H; Kambayashi J; Kato H
    Thromb Haemost; 1996 Sep; 76(3):302-11. PubMed ID: 8883262
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Inactivating mutations of the human base excision repair gene NEIL1 in gastric cancer.
    Shinmura K; Tao H; Goto M; Igarashi H; Taniguchi T; Maekawa M; Takezaki T; Sugimura H
    Carcinogenesis; 2004 Dec; 25(12):2311-7. PubMed ID: 15319300
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Association of GABA(B)R1 receptor gene polymorphism with obstructive sleep apnea syndrome.
    Bayazit YA; Yilmaz M; Kokturk O; Erdal ME; Ciftci T; Gokdogan T; Kemaloglu Y; Ileri F
    ORL J Otorhinolaryngol Relat Spec; 2007; 69(3):190-7. PubMed ID: 17264536
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Influences of chymase and angiotensin I-converting enzyme gene polymorphisms on gastric cancer risks in Japan.
    Sugimoto M; Furuta T; Shirai N; Ikuma M; Sugimura H; Hishida A
    Cancer Epidemiol Biomarkers Prev; 2006 Oct; 15(10):1929-34. PubMed ID: 17035401
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The association between the interleukin-1 polymorphisms and gastric cancer risk depends on the family history of gastric carcinoma in the study population.
    Starzyńska T; Ferenc K; Wex T; Kähne T; Lubiński J; Lawniczak M; Marlicz K; Malfertheiner P
    Am J Gastroenterol; 2006 Feb; 101(2):248-54. PubMed ID: 16454826
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Identification of a novel splice site mutation of the CSPG2 gene in a Japanese family with Wagner syndrome.
    Miyamoto T; Inoue H; Sakamoto Y; Kudo E; Naito T; Mikawa T; Mikawa Y; Isashiki Y; Osabe D; Shinohara S; Shiota H; Itakura M
    Invest Ophthalmol Vis Sci; 2005 Aug; 46(8):2726-35. PubMed ID: 16043844
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Allelic polymorphism of endothelial NO-synthase gene and its functional manifestations.
    Dosenko VE; Zagoriy VY; Haytovich NV; Gordok OA; Moibenko AA
    Acta Biochim Pol; 2006; 53(2):299-302. PubMed ID: 16733564
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Altered expression of the human base excision repair gene NTH1 in gastric cancer.
    Goto M; Shinmura K; Igarashi H; Kobayashi M; Konno H; Yamada H; Iwaizumi M; Kageyama S; Tsuneyoshi T; Tsugane S; Sugimura H
    Carcinogenesis; 2009 Aug; 30(8):1345-52. PubMed ID: 19414504
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.