BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

127 related articles for article (PubMed ID: 9216715)

  • 1. Band 1p36 abnormalities and t(1;17) in ovarian carcinoma.
    Thompson FH; Taetle R; Trent JM; Liu Y; Massey-Brown K; Scott KM; Weinstein RS; Emerson JC; Alberts DS; Nelson MA
    Cancer Genet Cytogenet; 1997 Jul; 96(2):106-10. PubMed ID: 9216715
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Rearrangements of chromosome band 1p36 in non-Hodgkin's lymphoma.
    Dave BJ; Hess MM; Pickering DL; Zaleski DH; Pfeifer AL; Weisenburger DD; Armitage JO; Sanger WG
    Clin Cancer Res; 1999 Jun; 5(6):1401-9. PubMed ID: 10389925
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Translocation breakpoint mapping and sequence analysis in three monosomy 1p36 subjects with der(1)t(1;1)(p36;q44) suggest mechanisms for telomere capture in stabilizing de novo terminal rearrangements.
    Ballif BC; Wakui K; Gajecka M; Shaffer LG
    Hum Genet; 2004 Jan; 114(2):198-206. PubMed ID: 14579147
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Characterization of the recurrent translocation t(1;1)(p36.3;q21.1-2) in non-Hodgkin lymphoma by multicolor banding and fluorescence in situ hybridization analysis.
    Lestou VS; Ludkovski O; Connors JM; Gascoyne RD; Lam WL; Horsman DE
    Genes Chromosomes Cancer; 2003 Apr; 36(4):375-81. PubMed ID: 12619161
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Maternal balanced translocation leading to partial duplication of 4q and partial deletion of 1p in a son: cytogenetic and FISH studies using band-specific painting probes generated by chromosome microdissection.
    Chen Z; Grebe TA; Guan XY; Notohamiprodjo M; Nutting PJ; Stone JF; Trent JM; Sandberg AA
    Am J Med Genet; 1997 Aug; 71(2):160-6. PubMed ID: 9217215
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Characterisation of the chromosome breakpoints in a patient with a constitutional translocation t(1;17)(p36.31-p36.13;q11.2-q12) and neuroblastoma.
    Laureys G; Versteeg R; Speleman F; van der Drift P; Francke U; Opdenakker G; Van Roy N
    Eur J Cancer; 1995; 31A(4):523-6. PubMed ID: 7576958
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Identification of the breakpoint-flanking markers on chromosomes 1 and 17 of a constitutional translocation T(1;17)(P36;Q12-21) in a patient with neuroblastoma].
    Laureys GG
    Verh K Acad Geneeskd Belg; 1995; 57(5):389-422. PubMed ID: 8571670
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Analysis of a whole arm translocation between chromosomes 18 and 20 using fluorescence in situ hybridization: detection of a break in the centromeric alpha-satellite sequences.
    Tümer Z; Berg A; Mikkelsen M
    Hum Genet; 1995 Mar; 95(3):299-302. PubMed ID: 7868122
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Characterization of chromosome 1 abnormalities in malignant melanomas.
    Smedley D; Sidhar S; Birdsall S; Bennett D; Herlyn M; Cooper C; Shipley J
    Genes Chromosomes Cancer; 2000 May; 28(1):121-5. PubMed ID: 10738310
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Cytogenetic and fluorescence in situ hybridization characterization of chromosome 1 rearrangements in head and neck carcinomas delineate a target region for deletions within 1p11-1p13.
    Jin Y; Jin C; Wennerberg J; Mertens F; Höglund M
    Cancer Res; 1998 Dec; 58(24):5859-65. PubMed ID: 9865746
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Rearrangement of chromosome 1 is a frequent finding in endometrial carcinoma. An in situ hybridization study in nine endometrial carcinomas.
    Ketter R; von Ballestrem CL; Lampel S; Seitz G; Zang KD; Romanakis K; Wullich B
    Cancer Genet Cytogenet; 1995 Jun; 81(2):109-14. PubMed ID: 7621405
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Detection of chromosome aberrations in paraffin sections of seven gonadal yolk sac tumors of childhood.
    Jenderny J; Köster E; Meyer A; Borchers O; Grote W; Harms D; Jänig U
    Hum Genet; 1995 Dec; 96(6):644-50. PubMed ID: 8522320
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Constitutional translocation t(1;17)(p36.31-p36.13;q11.2-q12.1) in a neuroblastoma patient. Establishment of somatic cell hybrids and identification of PND/A12M2 on chromosome 1 and NF1/SCYA7 on chromosome 17 as breakpoint flanking single copy markers.
    Laureys G; Speleman F; Versteeg R; van der Drift P; Chan A; Leroy J; Francke U; Opdenakker G; Van Roy N
    Oncogene; 1995 Mar; 10(6):1087-93. PubMed ID: 7700633
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Multicolor FISH analysis of chromosomal breaks, duplications, deletions, and numerical abnormalities in the sperm of healthy men.
    Sloter ED; Lowe X; Moore II DH; Nath J; Wyrobek AJ
    Am J Hum Genet; 2000 Oct; 67(4):862-72. PubMed ID: 10961911
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Centromeric alpha-satellite DNA break in reciprocal translocations.
    Wang JC; Hajianpour A; Habibian R
    Cytogenet Genome Res; 2009; 125(4):329-33. PubMed ID: 19864896
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Centromeric chromosomal translocations show tissue-specific differences between squamous cell carcinomas and adenocarcinomas.
    Hermsen M; Snijders A; Guervós MA; Taenzer S; Koerner U; Baak J; Pinkel D; Albertson D; van Diest P; Meijer G; Schrock E
    Oncogene; 2005 Feb; 24(9):1571-9. PubMed ID: 15674345
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Intratumor distribution of 1p deletions in human colorectal adenocarcinoma is commonly homogeneous: indirect evidence of early involvement in colorectal tumorigenesis.
    Di Vinci A; Infusini E; Nigro S; Monaco R; Giaretti W
    Cancer; 1998 Aug; 83(3):415-22. PubMed ID: 9690532
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Fluorescence in situ hybridization analysis using cosmid probes to define chromosome 6q abnormalities in ovarian carcinoma cell lines.
    Lastowska MA; Lillington DM; Shelling AN; Cooke I; Gibbons B; Young BD; Ganesan TS
    Cancer Genet Cytogenet; 1994 Oct; 77(2):99-105. PubMed ID: 7954328
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Interphase fluorescence in situ hybridization studies of ovarian adenocarcinomas using the midisatellite probe.
    Kalir T; Eisberg A; Dottino P; Cohen C
    Gynecol Oncol; 1999 Feb; 72(2):208-14. PubMed ID: 10021303
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Analysis of 1;17 translocation breakpoints in neuroblastoma: implications for mapping of neuroblastoma genes.
    Van Roy N; Laureys G; Van Gele M; Opdenakker G; Miura R; van der Drift P; Chan A; Versteeg R; Speleman F
    Eur J Cancer; 1997 Oct; 33(12):1974-8. PubMed ID: 9516836
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.