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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

101 related items for PubMed ID: 14506701

  • 1. Molecular cloning of a constitutional t(7;22) translocation associated with risk of hematological malignancy.
    Hill AS, MacCallum PK, Young BD, Lillington DM.
    Genes Chromosomes Cancer; 2003 Nov; 38(3):260-4. PubMed ID: 14506701
    [Abstract] [Full Text] [Related]

  • 2. [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 Nov; 57(5):389-422. PubMed ID: 8571670
    [Abstract] [Full Text] [Related]

  • 3. A novel sequence-based approach to localize translocation breakpoints identifies the molecular basis of a t(4;22).
    Nimmakayalu MA, Gotter AL, Shaikh TH, Emanuel BS.
    Hum Mol Genet; 2003 Nov 01; 12(21):2817-25. PubMed ID: 12952865
    [Abstract] [Full Text] [Related]

  • 4. BglII-based panhandle and reverse panhandle PCR approaches increase capability for cloning der(II) and der(other) genomic breakpoint junctions of MLL translocations.
    Robinson BW, Slater DJ, Felix CA.
    Genes Chromosomes Cancer; 2006 Aug 01; 45(8):740-53. PubMed ID: 16703585
    [Abstract] [Full Text] [Related]

  • 5. Molecular characterisation of the t(1;15)(p22;q22) translocation in the prostate cancer cell line LNCaP.
    Strefford JC, Lane TM, Hill A, LeRoux L, Foot NJ, Shipley J, Oliver RT, Lu YJ, Young BD.
    Cytogenet Genome Res; 2006 Aug 01; 112(1-2):45-52. PubMed ID: 16276089
    [Abstract] [Full Text] [Related]

  • 6. 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 15; 55(20):4640-5. PubMed ID: 7553642
    [Abstract] [Full Text] [Related]

  • 7. Molecular cloning of IGλ rearrangements using long-distance inverse PCR (LDI-PCR).
    Shimanuki M, Sonoki T, Hosoi H, Watanuki J, Murata S, Kawakami K, Matsuoka H, Hanaoka N, Nakakuma H.
    Eur J Haematol; 2013 Jan 15; 90(1):59-67. PubMed ID: 23113889
    [Abstract] [Full Text] [Related]

  • 8. A reciprocal translocation 46,XY,t(8;9)(p11.2;q13) in a bladder exstrophy patient disrupts CNTNAP3 and presents evidence of a pericentromeric duplication on chromosome 9.
    Boyadjiev SA, South ST, Radford CL, Patel A, Zhang G, Hur DJ, Thomas GH, Gearhart JP, Stetten G.
    Genomics; 2005 May 15; 85(5):622-9. PubMed ID: 15820314
    [Abstract] [Full Text] [Related]

  • 9. Genomic and functional map of the chromosome 14 t(12;14) breakpoint cluster region in uterine leiomyoma.
    Lynch RA, Piper M, Bankier A, Bhugra B, Surti U, Liu J, Buckler A, Dear PH, Menon AG.
    Genomics; 1998 Aug 15; 52(1):17-26. PubMed ID: 9740667
    [Abstract] [Full Text] [Related]

  • 10. High incidence of familial breast cancer segregates with constitutional t(11;22)(q23;q11).
    Wieland I, Muschke P, Volleth M, Röpke A, Pelz AF, Stumm M, Wieacker P.
    Genes Chromosomes Cancer; 2006 Oct 15; 45(10):945-9. PubMed ID: 16845657
    [Abstract] [Full Text] [Related]

  • 11. Cloning of a new familial t(3;8) translocation associated with conventional renal cell carcinoma reveals a 5 kb microdeletion and no gene involved in the rearrangement.
    Rodríguez-Perales S, Meléndez B, Gribble SM, Valle L, Carter NP, Santamaría I, Conde L, Urioste M, Benítez J, Cigudosa JC.
    Hum Mol Genet; 2004 May 01; 13(9):983-90. PubMed ID: 15016767
    [Abstract] [Full Text] [Related]

  • 12. Mapping by chromosome sorting of several gene probes, including c-myc, to the derivative chromosomes of a 3;8 translocation associated with familial renal cancer.
    Harris P, Morton CC, Guglielmi P, Li F, Kelly K, Latt SA.
    Cytometry; 1986 Nov 01; 7(6):589-94. PubMed ID: 3536362
    [Abstract] [Full Text] [Related]

  • 13. Characterization of a recurrent t(1;2)(p36;p24) in human uterine leiomyoma.
    van Rijk A, Sweers M, Huys E, Kersten M, Merkx G, van Kessel AG, Debiec-Rychter M, Schoenmakers EF.
    Cancer Genet Cytogenet; 2009 Aug 01; 193(1):54-62. PubMed ID: 19602464
    [Abstract] [Full Text] [Related]

  • 14. Analysis of balanced rearrangements of chromosome 6 in acute leukemia: clustered breakpoints in q22-q23 and possible involvement of c-MYB in a new recurrent translocation, t(6;7)(q23;q32 through 36).
    Sinclair P, Harrison CJ, Jarosová M, Foroni L.
    Haematologica; 2005 May 01; 90(5):602-11. PubMed ID: 15921375
    [Abstract] [Full Text] [Related]

  • 15. WAVE3, an actin-polymerization gene, is truncated and inactivated as a result of a constitutional t(1;13)(q21;q12) chromosome translocation in a patient with ganglioneuroblastoma.
    Sossey-Alaoui K, Su G, Malaj E, Roe B, Cowell JK.
    Oncogene; 2002 Aug 29; 21(38):5967-74. PubMed ID: 12185600
    [Abstract] [Full Text] [Related]

  • 16. Fine mapping of the constitutional translocation t(11;22)(q23;q11).
    Tapia-Páez I, O'Brien KP, Kost-Alimova M, Sahlén S, Kedra D, Bruder CE, Andersson B, Roe BA, Hu P, Imreh S, Blennow E, Dumanski JP.
    Hum Genet; 2000 May 29; 106(5):506-16. PubMed ID: 10914680
    [Abstract] [Full Text] [Related]

  • 17. Cryptic insertion into 11q23 of MLLT10 not involved in t(1;15;11;10)(p36;q11;q23;q24) in infant acute biphenotypic leukemia.
    Matsuda K, Tanaka M, Araki S, Yanagisawa R, Yamauchi K, Koike K.
    Cancer Genet Cytogenet; 2009 Apr 15; 190(2):113-20. PubMed ID: 19380030
    [Abstract] [Full Text] [Related]

  • 18. Homozygous disruption of PDZD7 by reciprocal translocation in a consanguineous family: a new member of the Usher syndrome protein interactome causing congenital hearing impairment.
    Schneider E, Märker T, Daser A, Frey-Mahn G, Beyer V, Farcas R, Schneider-Rätzke B, Kohlschmidt N, Grossmann B, Bauss K, Napiontek U, Keilmann A, Bartsch O, Zechner U, Wolfrum U, Haaf T.
    Hum Mol Genet; 2009 Feb 15; 18(4):655-66. PubMed ID: 19028668
    [Abstract] [Full Text] [Related]

  • 19. Characterization of a familial t(16;22) balanced translocation associated with congenital cataract leads to identification of a novel gene, TMEM114, expressed in the lens and disrupted by the translocation.
    Jamieson RV, Farrar N, Stewart K, Perveen R, Mihelec M, Carette M, Grigg JR, McAvoy JW, Lovicu FJ, Tam PP, Scambler P, Lloyd IC, Donnai D, Black GC.
    Hum Mutat; 2007 Oct 15; 28(10):968-77. PubMed ID: 17492639
    [Abstract] [Full Text] [Related]

  • 20. The 9p24.3 breakpoint of a constitutional t(6;9)(p12;p24) in a patient with chronic lymphocytic leukemia maps close to the putative promoter region of the DMRT2 gene.
    Rüssel J, Dutta U, Wand D, Schlote D, Hansmann I.
    Cytogenet Genome Res; 2009 Oct 15; 125(2):81-6. PubMed ID: 19729909
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 6.