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603 related items for PubMed ID: 8383093

  • 21. Coamplification of prostate stem cell antigen (PSCA) and MYC in locally advanced prostate cancer.
    Reiter RE, Sato I, Thomas G, Qian J, Gu Z, Watabe T, Loda M, Jenkins RB.
    Genes Chromosomes Cancer; 2000 Jan; 27(1):95-103. PubMed ID: 10564591
    [Abstract] [Full Text] [Related]

  • 22. Nonsyntenic amplification of MYC with CDK4 and MDM2 in a malignant mixed tumor of salivary gland.
    Rao PH, Murty VV, Louie DC, Chaganti RS.
    Cancer Genet Cytogenet; 1998 Sep; 105(2):160-3. PubMed ID: 9723034
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  • 23. Isolation of a cosmid sublibrary for a region of chromosome 12 frequently amplified in human cancers using a complex chromosome microdissection probe.
    Elkahloun AG, Meltzer PS, Guan XY, McNinch JS, Trent JM, de Jong PJ.
    Genomics; 1996 Feb 01; 31(3):343-7. PubMed ID: 8838316
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  • 24. Relationship between gene amplification and chromosomal deviations in malignant human gliomas.
    Bigner SH, Wong AJ, Mark J, Muhlbaier LH, Kinzler KW, Vogelstein B, Bigner DD.
    Cancer Genet Cytogenet; 1987 Nov 01; 29(1):165-70. PubMed ID: 3478127
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  • 25. Identification, molecular cloning, and characterization of the chromosome 12 breakpoint cluster region of uterine leiomyomas.
    Schoenmakers EF, Mols R, Wanschura S, Kools PF, Geurts JM, Bartnitzke S, Bullerdiek J, van den Berghe H, Van de Ven WJ.
    Genes Chromosomes Cancer; 1994 Oct 01; 11(2):106-18. PubMed ID: 7529547
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  • 26. Integration of viral sequences into the c-myc gene in two mammary adenocarcinomas induced by polyomavirus in athymic nude mice.
    Berebbi M, Cajean-Feroldi C, Apiou F, Couturier J, Garcette M, Emanoil-Ravier R, Cabannes J, Perricaudet M, Blangy D.
    J Virol; 1995 Oct 01; 69(10):5935-45. PubMed ID: 7666498
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  • 27. Detection of short repeated genomic sequences on metaphase chromosomes using padlock probes and target primed rolling circle DNA synthesis.
    Lohmann JS, Stougaard M, Koch J.
    BMC Mol Biol; 2007 Nov 13; 8():103. PubMed ID: 17997865
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  • 28. Non-syntenic amplification of MDM2 and MYCN in human neuroblastoma.
    Corvi R, Savelyeva L, Breit S, Wenzel A, Handgretinger R, Barak J, Oren M, Amler L, Schwab M.
    Oncogene; 1995 Mar 16; 10(6):1081-6. PubMed ID: 7700632
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  • 29. Partial chromosome 21 amplification in a child with acute lymphoblastic leukemia.
    Le Coniat M, Romana SP, Berger R.
    Genes Chromosomes Cancer; 1995 Nov 16; 14(3):204-9. PubMed ID: 8589037
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  • 30. Localization of amplified MYC gene sequences to double minute chromosomes in acute myelogenous leukemia.
    Slovak ML, Ho JP, Pettenati MJ, Khan A, Douer D, Lal S, Traweek ST.
    Genes Chromosomes Cancer; 1994 Jan 16; 9(1):62-7. PubMed ID: 7507702
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  • 31. Detection of c-myc amplification in uveal melanoma by fluorescent in situ hybridization.
    Parrella P, Caballero OL, Sidransky D, Merbs SL.
    Invest Ophthalmol Vis Sci; 2001 Jul 16; 42(8):1679-84. PubMed ID: 11431428
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  • 32. DNA sequence amplification in human prostate cancer identified by chromosome microdissection: potential prognostic implications.
    Van Den Berg C, Guan XY, Von Hoff D, Jenkins R, Bittner, Griffin C, Kallioniemi O, Visakorpi, McGill, Herath J.
    Clin Cancer Res; 1995 Jan 16; 1(1):11-8. PubMed ID: 9815882
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  • 33. Refined localization of the erbB-3 proto-oncogene by direct visualization of FISH signals on LUT-inverted and contrast-enhanced digital images of DAPI-banded chromosomes.
    Zimonjic DB, Rezanka L, DiPaolo JA, Popescu NC.
    Cancer Genet Cytogenet; 1995 Apr 16; 80(2):100-2. PubMed ID: 7736422
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  • 34. Extrachromosomal gene amplification in acute myeloid leukemia; characterization by metaphase analysis, comparative genomic hybridization, and semi-quantitative PCR.
    Mohamed AN, Macoska JA, Kallioniemi A, Kallioniemi OP, Waldman F, Ratanatharathorn V, Wolman SR.
    Genes Chromosomes Cancer; 1993 Nov 16; 8(3):185-9. PubMed ID: 7509627
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  • 35. Isolation of amplified DNA sequences from IMR-32 human neuroblastoma cells: facilitation by fluorescence-activated flow sorting of metaphase chromosomes.
    Kanda N, Schreck R, Alt F, Bruns G, Baltimore D, Latt S.
    Proc Natl Acad Sci U S A; 1983 Jul 16; 80(13):4069-73. PubMed ID: 6575396
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  • 36. Molecular characterization of MAR, a multiple aberration region on human chromosome segment 12q13-q15 implicated in various solid tumors.
    Van de Ven WJ, Schoenmakers EF, Wanschura S, Kazmierczak B, Kools PF, Geurts JM, Bartnitzke S, Van den Berghe H, Bullerdiek J.
    Genes Chromosomes Cancer; 1995 Apr 16; 12(4):296-303. PubMed ID: 7539285
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  • 37. Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors.
    Kallioniemi A, Kallioniemi OP, Sudar D, Rutovitz D, Gray JW, Waldman F, Pinkel D.
    Science; 1992 Oct 30; 258(5083):818-21. PubMed ID: 1359641
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  • 38. From amplification to gene in thyroid cancer: a high-resolution mapped bacterial-artificial-chromosome resource for cancer chromosome aberrations guides gene discovery after comparative genome hybridization.
    Chen X, Knauf JA, Gonsky R, Wang M, Lai EH, Chissoe S, Fagin JA, Korenberg JR.
    Am J Hum Genet; 1998 Aug 30; 63(2):625-37. PubMed ID: 9683604
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  • 39. Chromosomal location and structure of amplicons in two human cell lines with coamplification of c-myc and Ki-ras oncogenes.
    Fukumoto M, Suzuki A, Inazawa J, Yoshimura T, Arao S, Takahashi T, Nomura H, Hiai H.
    Somat Cell Mol Genet; 1993 Jan 30; 19(1):21-8. PubMed ID: 8460396
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  • 40. Detection of amplified sequences at 5q11-->q13 in a homogenously staining region found by fluorescent in situ hybridization in a case of B-cell non-Hodgkin's lymphoma.
    Wlodarska I, De Wolf-Peeters C, Dierick H, Hilliker C, Thomas J, Mecucci C, Cassiman JJ, Van den Berghe H.
    Cytogenet Cell Genet; 1994 Jan 30; 65(3):179-83. PubMed ID: 8222756
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