BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

87 related articles for article (PubMed ID: 16980714)

  • 21. Williams-Beuren syndrome: determination of deletion size using quantitative real-time PCR.
    Schubert C; Laccone F
    Int J Mol Med; 2006 Nov; 18(5):799-806. PubMed ID: 17016608
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Validation of a targeted DNA microarray for the clinical evaluation of recurrent abnormalities in chronic lymphocytic leukemia.
    Patel A; Kang SH; Lennon PA; Li YF; Rao PN; Abruzzo L; Shaw C; Chinault AC; Cheung SW
    Am J Hematol; 2008 Jul; 83(7):540-6. PubMed ID: 18161787
    [TBL] [Abstract][Full Text] [Related]  

  • 23. AZFc somatic microdeletions and copy number polymorphism of the DAZ genes in human males exposed to natural background radiation.
    Premi S; Srivastava J; Chandy SP; Ali S
    Hum Genet; 2007 May; 121(3-4):337-46. PubMed ID: 17308897
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Identification of the origin of marker chromosome by comparative genomic hybridization].
    Zhou L; Wu LQ; Liang DS; Pan Q; Long ZG; Dai HP; Li J; Cai F; Xia K; Xia JH
    Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2007 Apr; 32(2):264-7. PubMed ID: 17478934
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Mapping of a deletion interval on 8p21-22 in prostate cancer by gene dosage PCR].
    Schmidt H; Semjonow A; Csiszar K; Korsching E; Brandt B; Eltze E
    Verh Dtsch Ges Pathol; 2007; 91():302-7. PubMed ID: 18314628
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Relative copy number gain of MYC in diagnostic needle biopsies is an independent prognostic factor for prostate cancer patients.
    Ribeiro FR; Henrique R; Martins AT; Jerónimo C; Teixeira MR
    Eur Urol; 2007 Jul; 52(1):116-25. PubMed ID: 17070983
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Comparative genome profiling across subtypes of low-grade B-cell lymphoma identifies type-specific and common aberrations that target genes with a role in B-cell neoplasia.
    Ferreira BI; García JF; Suela J; Mollejo M; Camacho FI; Carro A; Montes S; Piris MA; Cigudosa JC
    Haematologica; 2008 May; 93(5):670-9. PubMed ID: 18367492
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Accurate determination of copy number variations (CNVs): application to the alpha- and beta-defensin CNVs.
    Nuytten H; Wlodarska I; Nackaerts K; Vermeire S; Vermeesch J; Cassiman JJ; Cuppens H
    J Immunol Methods; 2009 May; 344(1):35-44. PubMed ID: 19298822
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Transmission of genomic instability from a single irradiated human chromosome to the progeny of unirradiated cells.
    Mukaida N; Kodama S; Suzuki K; Oshimura M; Watanabe M
    Radiat Res; 2007 Jun; 167(6):675-81. PubMed ID: 17523850
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Identification of cryptic microaberrations in osteosarcoma by high-definition oligonucleotide array comparative genomic hybridization.
    Selvarajah S; Yoshimoto M; Maire G; Paderova J; Bayani J; Squire JA; Zielenska M
    Cancer Genet Cytogenet; 2007 Nov; 179(1):52-61. PubMed ID: 17981215
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Gain of chromosome X in prostatic atrophy detected by CGH and FISH analyses.
    Yildiz-Sezer S; Verdorfer I; Schäfer G; Rogatsch H; Bartsch G; Mikuz G
    Prostate; 2007 Mar; 67(4):433-8. PubMed ID: 17219381
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Genomic mechanisms and measurement of structural and numerical instability in cancer cells.
    Bayani J; Selvarajah S; Maire G; Vukovic B; Al-Romaih K; Zielenska M; Squire JA
    Semin Cancer Biol; 2007 Feb; 17(1):5-18. PubMed ID: 17126026
    [TBL] [Abstract][Full Text] [Related]  

  • 33. The complicated copy number alterations in chromosome 7 of a lung cancer cell line is explained by a model based on repeated breakage-fusion-bridge cycles.
    Kitada K; Yamasaki T
    Cancer Genet Cytogenet; 2008 Aug; 185(1):11-9. PubMed ID: 18656688
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Copy number variations associated with idiopathic autism identified by whole-genome microarray-based comparative genomic hybridization.
    Cho SC; Yim SH; Yoo HK; Kim MY; Jung GY; Shin GW; Kim BN; Hwang JW; Kang JJ; Kim TM; Chung YJ
    Psychiatr Genet; 2009 Aug; 19(4):177-85. PubMed ID: 19407672
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Genomic profiles associated with early micrometastasis in lung cancer: relevance of 4q deletion.
    Wrage M; Ruosaari S; Eijk PP; Kaifi JT; Hollmén J; Yekebas EF; Izbicki JR; Brakenhoff RH; Streichert T; Riethdorf S; Glatzel M; Ylstra B; Pantel K; Wikman H
    Clin Cancer Res; 2009 Mar; 15(5):1566-74. PubMed ID: 19208797
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Sperm-fluorescence in situ hybridization analysis in patients with pericentric inversions of Y chromosome].
    Luo YQ; Qian YL; Lu HM; Xu CM; Jin F
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Feb; 26(1):54-6. PubMed ID: 19199252
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Establishment and characterization of a new human acute myelocytic leukemia cell line SH-2 with a loss of Y chromosome, a derivative chromosome 16 resulting from an unbalanced translocation between chromosomes 16 and 17, monosomy 17, trisomy 19, and p53 alteration.
    Qiu H; Xue Y; Zhang J; Pan J; Dai H; Wu Y; Wang Y; Chen S; Wu D
    Exp Hematol; 2008 Nov; 36(11):1487-95. PubMed ID: 18715689
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Integrative analysis of genomic aberrations associated with prostate cancer progression.
    Kim JH; Dhanasekaran SM; Mehra R; Tomlins SA; Gu W; Yu J; Kumar-Sinha C; Cao X; Dash A; Wang L; Ghosh D; Shedden K; Montie JE; Rubin MA; Pienta KJ; Shah RB; Chinnaiyan AM
    Cancer Res; 2007 Sep; 67(17):8229-39. PubMed ID: 17804737
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Molecular characterization of breast cancer with high-resolution oligonucleotide comparative genomic hybridization array.
    Andre F; Job B; Dessen P; Tordai A; Michiels S; Liedtke C; Richon C; Yan K; Wang B; Vassal G; Delaloge S; Hortobagyi GN; Symmans WF; Lazar V; Pusztai L
    Clin Cancer Res; 2009 Jan; 15(2):441-51. PubMed ID: 19147748
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Molecular identification of chromosome Y sequences in Brazilian patients with Turner syndrome.
    Araujo C; Galera MF; Galera BB; Silvestre FG; Medeiros SF
    Gynecol Endocrinol; 2008 Dec; 24(12):713-7. PubMed ID: 19172542
    [TBL] [Abstract][Full Text] [Related]  

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