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Journal Abstract Search


1160 related items for PubMed ID: 17192196

  • 1. Alternative splicing and differential gene expression in colon cancer detected by a whole genome exon array.
    Gardina PJ, Clark TA, Shimada B, Staples MK, Yang Q, Veitch J, Schweitzer A, Awad T, Sugnet C, Dee S, Davies C, Williams A, Turpaz Y.
    BMC Genomics; 2006 Dec 27; 7():325. PubMed ID: 17192196
    [Abstract] [Full Text] [Related]

  • 2. A statistical framework for genome-wide discovery of biomarker splice variations with GeneChip Human Exon 1.0 ST Arrays.
    Yoshida R, Numata K, Imoto S, Nagasaki M, Doi A, Ueno K, Miyano S.
    Genome Inform; 2006 Dec 27; 17(1):88-99. PubMed ID: 17503359
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  • 3. Gene expression and isoform variation analysis using Affymetrix Exon Arrays.
    Bemmo A, Benovoy D, Kwan T, Gaffney DJ, Jensen RV, Majewski J.
    BMC Genomics; 2008 Nov 07; 9():529. PubMed ID: 18990248
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  • 4. Predicting splice variant from DNA chip expression data.
    Hu GK, Madore SJ, Moldover B, Jatkoe T, Balaban D, Thomas J, Wang Y.
    Genome Res; 2001 Jul 07; 11(7):1237-45. PubMed ID: 11435406
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  • 5. Identification of differentially regulated splice variants and novel exons in glial brain tumors using exon expression arrays.
    French PJ, Peeters J, Horsman S, Duijm E, Siccama I, van den Bent MJ, Luider TM, Kros JM, van der Spek P, Sillevis Smitt PA.
    Cancer Res; 2007 Jun 15; 67(12):5635-42. PubMed ID: 17575129
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  • 6. Revised genomic structure of the human ghrelin gene and identification of novel exons, alternative splice variants and natural antisense transcripts.
    Seim I, Collet C, Herington AC, Chopin LK.
    BMC Genomics; 2007 Aug 30; 8():298. PubMed ID: 17727735
    [Abstract] [Full Text] [Related]

  • 7. Exon-based clustering of murine breast tumor transcriptomes reveals alternative exons whose expression is associated with metastasis.
    Dutertre M, Lacroix-Triki M, Driouch K, de la Grange P, Gratadou L, Beck S, Millevoi S, Tazi J, Lidereau R, Vagner S, Auboeuf D.
    Cancer Res; 2010 Feb 01; 70(3):896-905. PubMed ID: 20103641
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  • 13. Alternative splicing in colon, bladder, and prostate cancer identified by exon array analysis.
    Thorsen K, Sørensen KD, Brems-Eskildsen AS, Modin C, Gaustadnes M, Hein AM, Kruhøffer M, Laurberg S, Borre M, Wang K, Brunak S, Krainer AR, Tørring N, Dyrskjøt L, Andersen CL, Orntoft TF.
    Mol Cell Proteomics; 2008 Jul 01; 7(7):1214-24. PubMed ID: 18353764
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  • 14. In silico identification of breast cancer genes by combined multiple high throughput analyses.
    Shen D, He J, Chang HR.
    Int J Mol Med; 2005 Feb 01; 15(2):205-12. PubMed ID: 15647832
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  • 15. Genomic organization and structure of the 5'-flanking region of the TEX101 gene: alternative promoter usage and splicing generate transcript variants with distinct 5'-untranslated region.
    Tsukamoto H, Takizawa T, Takamori K, Ogawa H, Araki Y.
    Mol Reprod Dev; 2007 Feb 01; 74(2):154-62. PubMed ID: 16941676
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  • 16. Alternative mRNA splicing in colon cancer causes loss of expression of neural cell adhesion molecule.
    Huerta S, Srivatsan ES, Venkatesan N, Peters J, Moatamed F, Renner S, Livingston EH.
    Surgery; 2001 Nov 01; 130(5):834-43. PubMed ID: 11685193
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  • 17. Identification of low-abundance alternatively spliced mRNA variants by exon exclusive reverse transcriptase polymerase chain reaction.
    Wang F, Zhao Y, Hao Y, Tan Z.
    Anal Biochem; 2008 Dec 15; 383(2):307-10. PubMed ID: 18817741
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  • 18. Expressed sequence tag analysis of human retina for the NEIBank Project: retbindin, an abundant, novel retinal cDNA and alternative splicing of other retina-preferred gene transcripts.
    Wistow G, Bernstein SL, Wyatt MK, Ray S, Behal A, Touchman JW, Bouffard G, Smith D, Peterson K.
    Mol Vis; 2002 Jun 15; 8():196-204. PubMed ID: 12107411
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  • 19. Folylpoly-gamma-glutamate synthetase gene mRNA splice variants and protein expression in primary human leukemia cells, cell lines, and normal human tissues.
    Leclerc GJ, Barredo JC.
    Clin Cancer Res; 2001 Apr 15; 7(4):942-51. PubMed ID: 11309345
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  • 20. An efficient and high-throughput approach for experimental validation of novel human gene predictions.
    Brzoska PM, Brown C, Cassel M, Ceccardi T, Di Francisco V, Dubman A, Evans J, Fang R, Harris M, Hoover J, Hu F, Larry C, Li P, Malicdem M, Maltchenko S, Shannon M, Perkins S, Poulter K, Webster-Laig M, Xiao C, Young S, Spier G, Guegler K, Gilbert D, Samaha RR.
    Genomics; 2006 Apr 15; 87(4):437-45. PubMed ID: 16406193
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