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Journal Abstract Search

152 related items for PubMed ID: 24460793

  • 21. Genetic variants of the copy number polymorphic beta-defensin locus are associated with sporadic prostate cancer.
    Huse K, Taudien S, Groth M, Rosenstiel P, Szafranski K, Hiller M, Hampe J, Junker K, Schubert J, Schreiber S, Birkenmeier G, Krawczak M, Platzer M.
    Tumour Biol; 2008; 29(2):83-92. PubMed ID: 18515986
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  • 25. Quantitative PCR from human genomic DNA: The determination of gene copy numbers for congenital adrenal hyperplasia and RCCX copy number variation.
    Doleschall M, Darvasi O, Herold Z, Doleschall Z, Nyirő G, Somogyi A, Igaz P, Patócs A.
    PLoS One; 2022; 17(12):e0277299. PubMed ID: 36454796
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  • 29. A novel multiplex fluorescent competitive PCR for copy number variation detection.
    Chen K, Dong SS, Wu N, Wu ZH, Zhou YX, Li K, Zhang F, Xiao JH.
    Genomics; 2019 Dec; 111(6):1745-1751. PubMed ID: 30529537
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  • 30. Accurate, high-throughput typing of copy number variation using paralogue ratios from dispersed repeats.
    Armour JA, Palla R, Zeeuwen PL, den Heijer M, Schalkwijk J, Hollox EJ.
    Nucleic Acids Res; 2007 Dec; 35(3):e19. PubMed ID: 17175532
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  • 31. Extensive normal copy number variation of a beta-defensin antimicrobial-gene cluster.
    Hollox EJ, Armour JA, Barber JC.
    Am J Hum Genet; 2003 Sep; 73(3):591-600. PubMed ID: 12916016
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  • 32. Analysis of beta-defensin and Toll-like receptor gene copy number variation in celiac disease.
    Fernandez-Jimenez N, Castellanos-Rubio A, Plaza-Izurieta L, Gutierrez G, Castaño L, Vitoria JC, Bilbao JR.
    Hum Immunol; 2010 Aug; 71(8):833-6. PubMed ID: 20483368
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  • 35. Multiplex Ligation-Dependent Probe Amplification (MLPA) for Prenatal Diagnosis of Common Aneuploidies.
    Schouten J, van Vught P, Galjaard RJ.
    Methods Mol Biol; 2019 Aug; 1885():161-170. PubMed ID: 30506197
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  • 36. Identification and expression analysis of the β-defensin genes in the goat small intestine.
    Zhang L, Xiao H, Huang J, Ouyang L, Li S, Tang Y.
    Gene; 2021 Oct 30; 801():145846. PubMed ID: 34274482
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  • 37. Accurate determination of copy number variations (CNVs): application to the alpha- and beta-defensin CNVs.
    Nuytten H, Wlodarska I, Nackaerts K, Vermeire S, Vermeesch J, Cassiman JJ, Cuppens H.
    J Immunol Methods; 2009 May 15; 344(1):35-44. PubMed ID: 19298822
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  • 38. Use of the MLPA assay in the molecular diagnosis of gene copy number alterations in human genetic diseases.
    Stuppia L, Antonucci I, Palka G, Gatta V.
    Int J Mol Sci; 2012 May 15; 13(3):3245-3276. PubMed ID: 22489151
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  • 39. An MLPA-based approach for high-resolution genotyping of disease-related multi-allelic CNVs.
    Marcinkowska-Swojak M, Klonowska K, Figlerowicz M, Kozlowski P.
    Gene; 2014 Aug 10; 546(2):257-62. PubMed ID: 24942243
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  • 40. Multiplex Ligation-dependent Probe Amplification (MLPA®) for the detection of copy number variation in genomic sequences.
    Eijk-Van Os PG, Schouten JP.
    Methods Mol Biol; 2011 Aug 10; 688():97-126. PubMed ID: 20938835
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