BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

125 related articles for article (PubMed ID: 26133275)

  • 21. An HIV Vaccine Protective Allele in
    Ebonwu J; Lassaunière R; Paximadis M; Goosen M; Strehlau R; Gray GE; Kuhn L; Tiemessen CT
    Front Immunol; 2021; 12():760571. PubMed ID: 34917081
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Correlation between frequency of non-allelic homologous recombination and homology properties: evidence from homology-mediated CNV mutations in the human genome.
    Peng Z; Zhou W; Fu W; Du R; Jin L; Zhang F
    Hum Mol Genet; 2015 Mar; 24(5):1225-33. PubMed ID: 25324539
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A practical case-control association test for detecting a susceptibility allele at a copy number variation locus.
    Ohashi J
    J Hum Genet; 2009 Mar; 54(3):169-73. PubMed ID: 19197338
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Frequency distribution of autoimmunity associated FCGR3B gene copy number in Indian population.
    Almal SH; Padh H
    Int J Immunogenet; 2015 Feb; 42(1):26-30. PubMed ID: 25428402
    [TBL] [Abstract][Full Text] [Related]  

  • 25. The Fc gamma receptor IIa R131H polymorphism is associated with inhibitor development in severe hemophilia A.
    Eckhardt CL; Astermark J; Nagelkerke SQ; Geissler J; Tanck MW; Peters M; Fijnvandraat K; Kuijpers TW
    J Thromb Haemost; 2014 Aug; 12(8):1294-301. PubMed ID: 24916518
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Association of FCGR2A and FCGR2A-FCGR3A haplotypes with susceptibility to giant cell arteritis.
    Morgan AW; Robinson JI; Barrett JH; Martin J; Walker A; Babbage SJ; Ollier WE; Gonzalez-Gay MA; Isaacs JD
    Arthritis Res Ther; 2006; 8(4):R109. PubMed ID: 16846526
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Allelic and copy-number variations of FcγRs affect granulocyte function and susceptibility for autoimmune blistering diseases.
    Recke A; Vidarsson G; Ludwig RJ; Freitag M; Möller S; Vonthein R; Schellenberger J; Haase O; Görg S; Nebel A; Flachsbart F; Schreiber S; Lieb W; Gläser R; Benoit S; Sárdy M; Eming R; Hertl M; Zillikens D; König IR; Schmidt E; Ibrahim S;
    J Autoimmun; 2015 Jul; 61():36-44. PubMed ID: 26032265
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Mapping of bovine FcgammaR (FCGR) genes by sperm typing allows extended use of human map information.
    Klungland H; Gomez-Raya L; Howard CJ; Collins RA; Rogne S; Lien S
    Mamm Genome; 1997 Aug; 8(8):573-7. PubMed ID: 9250863
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Fc-gamma receptor polymorphisms differentially influence susceptibility to systemic lupus erythematosus and lupus nephritis.
    Tsang-A-Sjoe MW; Nagelkerke SQ; Bultink IE; Geissler J; Tanck MW; Tacke CE; Ellis JA; Zenz W; Bijl M; Berden JH; de Leeuw K; Derksen RH; Kuijpers TW; Voskuyl AE
    Rheumatology (Oxford); 2016 May; 55(5):939-48. PubMed ID: 26748351
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Duplication of chicken defensin7 gene generated by gene conversion and homologous recombination.
    Lee MO; Bornelöv S; Andersson L; Lamont SJ; Chen J; Womack JE
    Proc Natl Acad Sci U S A; 2016 Nov; 113(48):13815-13820. PubMed ID: 27849592
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Nonallelic homologous recombination events responsible for copy number variation within an RNA silencing locus.
    Cho YB; Jones SI; Vodkin LO
    Plant Direct; 2019 Aug; 3(8):e00162. PubMed ID: 31468028
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Characterization of the nonallelic homologous recombination hotspot PRS3 associated with type-3 NF1 deletions.
    Zickler AM; Hampp S; Messiaen L; Bengesser K; Mussotter T; Roehl AC; Wimmer K; Mautner VF; Kluwe L; Upadhyaya M; Pasmant E; Chuzhanova N; Kestler HA; Högel J; Legius E; Claes K; Cooper DN; Kehrer-Sawatzki H
    Hum Mutat; 2012 Feb; 33(2):372-83. PubMed ID: 22045503
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Genome-wide analyses of LINE-LINE-mediated nonallelic homologous recombination.
    Startek M; Szafranski P; Gambin T; Campbell IM; Hixson P; Shaw CA; Stankiewicz P; Gambin A
    Nucleic Acids Res; 2015 Feb; 43(4):2188-98. PubMed ID: 25613453
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Contribution of Fcgamma receptor IIIA gene 158V/F polymorphism and copy number variation to the risk of ACPA-positive rheumatoid arthritis.
    Thabet MM; Huizinga TW; Marques RB; Stoeken-Rijsbergen G; Bakker AM; Kurreeman FA; White SJ; Toes RE; van der Helm-van Mil AH
    Ann Rheum Dis; 2009 Nov; 68(11):1775-80. PubMed ID: 19019892
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Mechanisms for recurrent and complex human genomic rearrangements.
    Liu P; Carvalho CM; Hastings PJ; Lupski JR
    Curr Opin Genet Dev; 2012 Jun; 22(3):211-20. PubMed ID: 22440479
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Copy number variation in autoimmunity--importance hidden in complexity?
    Olsson LM; Holmdahl R
    Eur J Immunol; 2012 Aug; 42(8):1969-76. PubMed ID: 22865047
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Evaluation of High-Throughput Genomic Assays for the Fc Gamma Receptor Locus.
    Hargreaves CE; Iriyama C; Rose-Zerilli MJ; Nagelkerke SQ; Hussain K; Ganderton R; Lee C; Machado LR; Hollox EJ; Parker H; Latham KV; Kuijpers TW; Potter KN; Coupland SE; Davies A; Stackpole M; Oates M; Pettitt AR; Glennie MJ; Cragg MS; Strefford JC
    PLoS One; 2015; 10(11):e0142379. PubMed ID: 26545243
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Chimeric CYP21A1P/CYP21A2 genes identified in Czech patients with congenital adrenal hyperplasia.
    Vrzalová Z; Hrubá Z; Hrabincová ES; Vrábelová S; Votava F; Koloušková S; Fajkusová L
    Eur J Med Genet; 2011; 54(2):112-7. PubMed ID: 20970527
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Fine mapping of meiotic NAHR-associated crossovers causing large NF1 deletions.
    Hillmer M; Wagner D; Summerer A; Daiber M; Mautner VF; Messiaen L; Cooper DN; Kehrer-Sawatzki H
    Hum Mol Genet; 2016 Feb; 25(3):484-96. PubMed ID: 26614388
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Acetylcholine-metabolizing butyrylcholinesterase (BCHE) copy number and single nucleotide polymorphisms and their role in attention-deficit/hyperactivity syndrome.
    Jacob CP; Weber H; Retz W; Kittel-Schneider S; Heupel J; Renner T; Lesch KP; Reif A
    J Psychiatr Res; 2013 Dec; 47(12):1902-8. PubMed ID: 24041656
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.