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Journal Abstract Search

201 related items for PubMed ID: 12480675

  • 1. Polymerase chain reaction based C4AQ0 and C4BQ0 genotyping: association with systemic lupus erythematosus in southwest Han Chinese.
    Man XY, Luo HR, Li XP, Yao YG, Mao CZ, Zhang YP.
    Ann Rheum Dis; 2003 Jan; 62(1):71-3. PubMed ID: 12480675
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  • 2. Complete deficiencies of complement C4A and C4B including 2-bp insertion in codon 1213 are genetic risk factors of systemic lupus erythematosus in Thai populations.
    Ittiprasert W, Kantachuvesiri S, Pavasuthipaisit K, Verasertniyom O, Chaomthum L, Totemchokchyakarn K, Kitiyanant Y.
    J Autoimmun; 2005 Aug; 25(1):77-84. PubMed ID: 15998580
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  • 3. The intricate role of complement component C4 in human systemic lupus erythematosus.
    Yang Y, Chung EK, Zhou B, Lhotta K, Hebert LA, Birmingham DJ, Rovin BH, Yu CY.
    Curr Dir Autoimmun; 2004 Aug; 7():98-132. PubMed ID: 14719377
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  • 4. Lack of evidence of a specific role for C4A gene deficiency in determining disease susceptibility among C4-deficient patients with systemic lupus erythematosus (SLE).
    Dragon-Durey MA, Rougier N, Clauvel JP, Caillat-Zucman S, Remy P, Guillevin L, Liote F, Blouin J, Ariey F, Lambert BU, Kazatchkine MD, Weiss L.
    Clin Exp Immunol; 2001 Jan; 123(1):133-9. PubMed ID: 11168010
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  • 5. Low copy numbers of complement C4 and homozygous deficiency of C4A may predispose to severe disease and earlier disease onset in patients with systemic lupus erythematosus.
    Jüptner M, Flachsbart F, Caliebe A, Lieb W, Schreiber S, Zeuner R, Franke A, Schröder JO.
    Lupus; 2018 Apr; 27(4):600-609. PubMed ID: 29050534
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  • 6. Impact of C4, C4A and C4B gene copy number variation in the susceptibility, phenotype and progression of systemic lupus erythematosus.
    Pereira KMC, Perazzio S, Faria AGA, Moreira ES, Santos VC, Grecco M, da Silva NP, Andrade LEC.
    Adv Rheumatol; 2019 Aug 06; 59(1):36. PubMed ID: 31387635
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  • 7. Low C4A copy numbers and higher HERV gene insertion contributes to increased risk of SLE, with absence of association with disease phenotype and disease activity.
    Mariaselvam CM, Seth G, Kavadichanda C, Boukouaci W, Wu CL, Costes B, Thabah MM, Krishnamoorthy R, Leboyer M, Negi VS, Tamouza R.
    Immunol Res; 2024 Aug 06; 72(4):697-706. PubMed ID: 38594415
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  • 8. Low C4, C4A and C4B gene copy numbers are stronger risk factors for juvenile-onset than for adult-onset systemic lupus erythematosus.
    Pereira KM, Faria AG, Liphaus BL, Jesus AA, Silva CA, Carneiro-Sampaio M, Andrade LE.
    Rheumatology (Oxford); 2016 May 06; 55(5):869-73. PubMed ID: 26800705
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  • 13. Complement allotyping in SLE: association with C4A null.
    Christiansen FT, Dawkins RL, Uko G, McCluskey J, Kay PH, Zilko PJ.
    Aust N Z J Med; 1983 Oct 06; 13(5):483-8. PubMed ID: 6606418
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  • 14. Impact of Homozygous C4A Deficiency on Clinical Presentation of Systemic Lupus Erythematosus.
    Ansari AA, Tipu HN, Ahmad D, Farhan M.
    J Coll Physicians Surg Pak; 2020 Aug 06; 30(8):790-795. PubMed ID: 32893787
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  • 17. Family study of the major histocompatibility complex in patients with systemic lupus erythematosus: importance of null alleles of C4A and C4B in determining disease susceptibility.
    Fielder AH, Walport MJ, Batchelor JR, Rynes RI, Black CM, Dodi IA, Hughes GR.
    Br Med J (Clin Res Ed); 1983 Feb 05; 286(6363):425-8. PubMed ID: 6401549
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  • 19. A study of the genetic basis of C4A protein deficiency. Detection of C4A gene deletion by long-range PCR and its associated haplotypes.
    Kristjánsdóttir H, Steinsson K.
    Scand J Rheumatol; 2004 Feb 05; 33(6):417-22. PubMed ID: 15794202
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