These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

76 related articles for article (PubMed ID: 9455189)

  • 21. [Mapping allelic deletions on the short arm of human chromosome 3 in kidney neoplasms].
    Bazov IV; Kazubskaia TP; Ermilova VD; Gar'kavtseva RF; Loginov VI; Zabarovskiĭ ER; Braga EA
    Mol Biol (Mosk); 2001; 35(3):404-12. PubMed ID: 11443921
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A methylthioadenosine phosphorylase (MTAP) fusion transcript identifies a new gene on chromosome 9p21 that is frequently deleted in cancer.
    Schmid M; Sen M; Rosenbach MD; Carrera CJ; Friedman H; Carson DA
    Oncogene; 2000 Nov; 19(50):5747-54. PubMed ID: 11126361
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Cloning and characterization of human and mouse mitochondrial elongation factor G, GFM and Gfm, and mapping of GFM to human chromosome 3q25.1-q26.2.
    Gao J; Yu L; Zhang P; Jiang J; Chen J; Peng J; Wei Y; Zhao S
    Genomics; 2001 May; 74(1):109-14. PubMed ID: 11374907
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Molecular analysis of deletions in human chromosome 3p21 and the role of resident cancer genes in disease.
    Angeloni D
    Brief Funct Genomic Proteomic; 2007 Mar; 6(1):19-39. PubMed ID: 17525073
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A new strategy for genome sequencing.
    Venter JC; Smith HO; Hood L
    Nature; 1996 May; 381(6581):364-6. PubMed ID: 8632789
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Integrated genome-wide gene expression map and high-resolution analysis of aberrant chromosomal regions in squamous cell lung cancer.
    Zhang XY; Hu Y; Cui YP; Miao XP; Tian F; Xia YJ; Wu YQ; Liu X
    FEBS Lett; 2006 May; 580(11):2774-8. PubMed ID: 16674950
    [TBL] [Abstract][Full Text] [Related]  

  • 27. claudin-18, a novel downstream target gene for the T/EBP/NKX2.1 homeodomain transcription factor, encodes lung- and stomach-specific isoforms through alternative splicing.
    Niimi T; Nagashima K; Ward JM; Minoo P; Zimonjic DB; Popescu NC; Kimura S
    Mol Cell Biol; 2001 Nov; 21(21):7380-90. PubMed ID: 11585919
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Human cDNA project: functional analysis of novel genes].
    Horie M; Nishino N; Shimada Y; Saito A; Nagata M; Irie Y; Takahashi E
    Tanpakushitsu Kakusan Koso; 1997 Dec; 42(17 Suppl):2844-50. PubMed ID: 9455202
    [No Abstract]   [Full Text] [Related]  

  • 29. The microcell hybrid-based "elimination test" identifies a 1-Mb putative tumor-suppressor region at 3p22.2-p22.1 centromeric to the homozygous deletion region detected in lung cancer.
    Kholodnyuk ID; Kost-Alimova M; Yang Y; Kiss H; Fedorova L; Klein G; Imreh S
    Genes Chromosomes Cancer; 2002 Jul; 34(3):341-4. PubMed ID: 12007195
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Genetic alteration of the beta-catenin gene (CTNNB1) in human lung cancer and malignant mesothelioma and identification of a new 3p21.3 homozygous deletion.
    Shigemitsu K; Sekido Y; Usami N; Mori S; Sato M; Horio Y; Hasegawa Y; Bader SA; Gazdar AF; Minna JD; Hida T; Yoshioka H; Imaizumi M; Ueda Y; Takahashi M; Shimokata K
    Oncogene; 2001 Jul; 20(31):4249-57. PubMed ID: 11464291
    [TBL] [Abstract][Full Text] [Related]  

  • 31. The myosin light chain kinase gene is not duplicated in mouse: partial structure and chromosomal localization of Mylk.
    Giorgi D; Ferraz C; Mattéi MG; Demaille J; Rouquier S
    Genomics; 2001 Jul; 75(1-3):49-56. PubMed ID: 11472067
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Chromosome 3p14 alterations in lung cancer: evidence that FHIT exon deletion is a target of tobacco carcinogens and asbestos.
    Nelson HH; Wiencke JK; Gunn L; Wain JC; Christiani DC; Kelsey KT
    Cancer Res; 1998 May; 58(9):1804-7. PubMed ID: 9581816
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Positional cloning of genes responsible for epilepsy and autism using a patient with chromosomal translocation].
    Isomura M; Nakamura Y
    Tanpakushitsu Kakusan Koso; 1997 Dec; 42(17 Suppl):2786-90. PubMed ID: 9455194
    [No Abstract]   [Full Text] [Related]  

  • 34. Clinical description and genome wide linkage study of Y-sutural cataract and myopia in a Chinese family.
    Zhang Q; Guo X; Xiao X; Yi J; Jia X; Hejtmancik JF
    Mol Vis; 2004 Nov; 10():890-900. PubMed ID: 15570218
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Physical and functional mapping of a tumor suppressor locus for renal cell carcinoma within chromosome 3p12.
    Lott ST; Lovell M; Naylor SL; Killary AM
    Cancer Res; 1998 Aug; 58(16):3533-7. PubMed ID: 9721855
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Computational BAC clone contig assembly for comprehensive genome analysis.
    Lapuk A; Volik S; Vincent R; Chin K; Kuo WL; de Jong P; Collins C; Gray JW
    Genes Chromosomes Cancer; 2004 May; 40(1):66-71. PubMed ID: 15034871
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Identification of unstable sequences within the common fragile site at 3p14.2: implications for the mechanism of deletions within fragile histidine triad gene/common fragile site at 3p14.2 in tumors.
    Corbin S; Neilly ME; Espinosa R; Davis EM; McKeithan TW; Le Beau MM
    Cancer Res; 2002 Jun; 62(12):3477-84. PubMed ID: 12067991
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Cancer of the kidney in adults. Genetics].
    Prog Urol; 1997 Nov; 7(5):767-73. PubMed ID: 9458475
    [No Abstract]   [Full Text] [Related]  

  • 39. Frequent homozygous deletions in the FRA3B region in tumor cell lines still leave the FHIT exons intact.
    Wang L; Darling J; Zhang JS; Qian CP; Hartmann L; Conover C; Jenkins R; Smith DI
    Oncogene; 1998 Feb; 16(5):635-42. PubMed ID: 9482109
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A genomic region encompassing a cluster of olfactory receptor genes and a myosin light chain kinase (MYLK) gene is duplicated on human chromosome regions 3q13-q21 and 3p13.
    Brand-Arpon V; Rouquier S; Massa H; de Jong PJ; Ferraz C; Ioannou PA; Demaille JG; Trask BJ; Giorgi D
    Genomics; 1999 Feb; 56(1):98-110. PubMed ID: 10036190
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.