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 *

115 related articles for article (PubMed ID: 14580778)

  • 1. Identification of a BAC clone overlapping the t(6p12.3) breakpoint in the cell line ESS-1 derived from an endometrial stromal sarcoma.
    Gunawan B; Schulten HJ; Füzesi L
    Cancer Genet Cytogenet; 2003 Nov; 147(1):84-6. PubMed ID: 14580778
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Consistent rearrangement of chromosomal band 6p21 with generation of fusion genes JAZF1/PHF1 and EPC1/PHF1 in endometrial stromal sarcoma.
    Micci F; Panagopoulos I; Bjerkehagen B; Heim S
    Cancer Res; 2006 Jan; 66(1):107-12. PubMed ID: 16397222
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Identification of a yeast artificial chromosome spanning the 8q12 translocation breakpoint in pleomorphic adenomas with t(3;8)(p21;q12).
    Röijer E; Kas K; Klawitz I; Bullerdiek J; Van de Ven W; Stenman G
    Genes Chromosomes Cancer; 1996 Nov; 17(3):166-71. PubMed ID: 8946195
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Characterization of a complex chromosome rearrangement involving 6q in a melanoma cell line by chromosome microdissection.
    Guan XY; Zhang HE; Zhou H; Sham JS; Fung JM; Trent JM
    Cancer Genet Cytogenet; 2002 Apr; 134(1):65-70. PubMed ID: 11996799
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Delineation of the breakpoint at 18q21.1 in a cell line (Karpas1106) derived from mediastinal B-cell lymphoma by fluorescence in situ hybridization with multiple YAC clones.
    Tamura A; Akagi T; Nakazawa N; Kashima K; Nakamura S; Karpas A; Silverman GA; Morishima Y; Taniwaki M; Seto M
    Int J Cancer; 1998 Sep; 78(1):100-5. PubMed ID: 9724100
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Sorting nexin 3 (SNX3) is disrupted in a patient with a translocation t(6;13)(q21;q12) and microcephaly, microphthalmia, ectrodactyly, prognathism (MMEP) phenotype.
    Vervoort VS; Viljoen D; Smart R; Suthers G; DuPont BR; Abbott A; Schwartz CE
    J Med Genet; 2002 Dec; 39(12):893-9. PubMed ID: 12471201
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Multicolor chromosome banding (MCB) with YAC/BAC-based probes and region-specific microdissection DNA libraries.
    Liehr T; Weise A; Heller A; Starke H; Mrasek K; Kuechler A; Weier HU; Claussen U
    Cytogenet Genome Res; 2002; 97(1-2):43-50. PubMed ID: 12438737
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Endometrial stromal sarcoma with a sole t(X;17) chromosome change: report of a case and review of the literature.
    Amant F; Moerman P; Cadron I; Hagemeijer A; Vergote I; Debiec-Rychter M
    Gynecol Oncol; 2003 Mar; 88(3):459-62. PubMed ID: 12648605
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Translocation breakpoint in two unrelated Tourette syndrome cases, within a region previously linked to the disorder.
    Crawford FC; Ait-Ghezala G; Morris M; Sutcliffe MJ; Hauser RA; Silver AA; Mullan MJ
    Hum Genet; 2003 Jul; 113(2):154-61. PubMed ID: 12698358
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Microdissection based cloning of a translocation breakpoint in a human malignant melanoma.
    Zhang J; Cui P; Glatfelter AA; Cummings LM; Meltzer PS; Trent JM
    Cancer Res; 1995 Oct; 55(20):4640-5. PubMed ID: 7553642
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Analysis of a t(18;21)(p11.1;p11.1) translocation in a family with schizophrenia.
    Meerabux JM; Ohba H; Iwayama Y; Maekawa M; Detera-Wadleigh SD; DeLisi LE; Yoshikawa T
    J Hum Genet; 2009 Jul; 54(7):386-91. PubMed ID: 19461657
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Characterization of 6q abnormalities in childhood acute myeloid leukemia and identification of a novel t(6;11)(q24.1;p15.5) resulting in a NUP98-C6orf80 fusion in a case of acute megakaryoblastic leukemia.
    Tosi S; Ballabio E; Teigler-Schlegel A; Boultwood J; Bruch J; Harbott J
    Genes Chromosomes Cancer; 2005 Nov; 44(3):225-32. PubMed ID: 16028218
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular definition of chromosome translocations involving 10q24 and 19q13 in human malignant glioma cells.
    Chernova O; Cowell JK
    Cancer Genet Cytogenet; 1998 Aug; 105(1):60-8. PubMed ID: 9689932
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Identification of a novel, recurrent MBTD1-CXorf67 fusion in low-grade endometrial stromal sarcoma.
    Dewaele B; Przybyl J; Quattrone A; Finalet Ferreiro J; Vanspauwen V; Geerdens E; Gianfelici V; Kalender Z; Wozniak A; Moerman P; Sciot R; Croce S; Amant F; Vandenberghe P; Cools J; Debiec-Rychter M
    Int J Cancer; 2014 Mar; 134(5):1112-22. PubMed ID: 23959973
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Characterization of the breakpoints in a t(8;13)(p11;q12) translocation from a patient with myeloproliferative disease using fluorescence in situ hybridization.
    Chernova O; Still I; Kalaycio M; Hoeltge G; Cowell JK
    Genes Chromosomes Cancer; 1998 Feb; 21(2):160-5. PubMed ID: 9491328
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Isolation of cosmids corresponding to the chromosome breakpoints of a de novo autosomal translocation, t(6;19)(p21;q13.1), in a patient with multicystic renal dysplasia.
    Groenen PM; Garcia E; Thoelen R; Aly M; Schoenmakers EF; Devriendt K; Fryns JP; Van de Ven WJ
    Cytogenet Cell Genet; 1996; 75(4):210-5. PubMed ID: 9067426
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Localization of the 17q breakpoint of a constitutional 1;17 translocation in a patient with neuroblastoma within a 25-kb segment located between the ACCN1 and TLK2 genes and near the distal breakpoints of two microdeletions in neurofibromatosis type 1 patients.
    Van Roy N; Vandesompele J; Berx G; Staes K; Van Gele M; De Smet E; De Paepe A; Laureys G; van der Drift P; Versteeg R; Van Roy F; Speleman F
    Genes Chromosomes Cancer; 2002 Oct; 35(2):113-20. PubMed ID: 12203774
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A palindrome-mediated mechanism distinguishes translocations involving LCR-B of chromosome 22q11.2.
    Gotter AL; Shaikh TH; Budarf ML; Rhodes CH; Emanuel BS
    Hum Mol Genet; 2004 Jan; 13(1):103-15. PubMed ID: 14613967
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Frequent amplification and rearrangement of chromosomal bands 6p12-p21 and 17p11.2 in osteosarcoma.
    Lau CC; Harris CP; Lu XY; Perlaky L; Gogineni S; Chintagumpala M; Hicks J; Johnson ME; Davino NA; Huvos AG; Meyers PA; Healy JH; Gorlick R; Rao PH
    Genes Chromosomes Cancer; 2004 Jan; 39(1):11-21. PubMed ID: 14603437
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mapping of the X-breakpoint involved in a balanced X;12 translocation in a female with mild mental retardation.
    Bienvenu T; Der-Sarkissian H; Billuart P; Tissot M; Des Portes V; Brüls T; Chabrolle JP; Chauveau P; Cherry M; Kahn A; Cohen D; Beldjord C; Chelly J; Cherif D
    Eur J Hum Genet; 1997; 5(2):105-9. PubMed ID: 9195162
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.