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Journal Abstract Search

215 related items for PubMed ID: 22387014

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  • 2. 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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  • 3. Effects of Complement C4 Gene Copy Number Variations, Size Dichotomy, and C4A Deficiency on Genetic Risk and Clinical Presentation of Systemic Lupus Erythematosus in East Asian Populations.
    Chen JY, Wu YL, Mok MY, Wu YJ, Lintner KE, Wang CM, Chung EK, Yang Y, Zhou B, Wang H, Yu D, Alhomosh A, Jones K, Spencer CH, Nagaraja HN, Lau YL, Lau CS, Yu CY.
    Arthritis Rheumatol; 2016 Jun; 68(6):1442-1453. PubMed ID: 26814708
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  • 5. 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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  • 8. Gene copy-number variations (CNVs) of complement C4 and C4A deficiency in genetic risk and pathogenesis of juvenile dermatomyositis.
    Lintner KE, Patwardhan A, Rider LG, Abdul-Aziz R, Wu YL, Lundström E, Padyukov L, Zhou B, Alhomosh A, Newsom D, White P, Jones KB, O'Hanlon TP, Miller FW, Spencer CH, Yu CY.
    Ann Rheum Dis; 2016 Sep; 75(9):1599-606. PubMed ID: 26493816
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  • 9. Human Complement C4B Allotypes and Deficiencies in Selected Cases With Autoimmune Diseases.
    Zhou D, Rudnicki M, Chua GT, Lawrance SK, Zhou B, Drew JL, Barbar-Smiley F, Armstrong TK, Hilt ME, Birmingham DJ, Passler W, Auletta JJ, Bowden SA, Hoffman RP, Wu YL, Jarjour WN, Mok CC, Ardoin SP, Lau YL, Yu CY.
    Front Immunol; 2021 Sep; 12():739430. PubMed ID: 34764957
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  • 10. Identification of two independent risk factors for lupus within the MHC in United Kingdom families.
    Fernando MM, Stevens CR, Sabeti PC, Walsh EC, McWhinnie AJ, Shah A, Green T, Rioux JD, Vyse TJ.
    PLoS Genet; 2007 Nov; 3(11):e192. PubMed ID: 17997607
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  • 11. 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 Nov; 7():98-132. PubMed ID: 14719377
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  • 12. Assessment of complement C4 gene copy number using the paralog ratio test.
    Fernando MM, Boteva L, Morris DL, Zhou B, Wu YL, Lokki ML, Yu CY, Rioux JD, Hollox EJ, Vyse TJ.
    Hum Mutat; 2010 Jul; 31(7):866-74. PubMed ID: 20506482
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  • 13. Insights on the relationship between complement component C4 serum concentrations and C4 gene copy numbers in a Western Australian systemic lupus erythematosus cohort.
    Margery-Muir AA, Bundell C, Wetherall JD, Whidborne R, Martinez P, Groth DM.
    Lupus; 2018 Sep; 27(10):1687-1696. PubMed ID: 30041577
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  • 14. C4A deficiency due to a 2 bp insertion is increased in patients with systemic lupus erythematosus.
    Sullivan KE, Kim NA, Goldman D, Petri MA.
    J Rheumatol; 1999 Oct; 26(10):2144-7. PubMed ID: 10529130
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  • 15. Complete complement components C4A and C4B deficiencies in human kidney diseases and systemic lupus erythematosus.
    Yang Y, Lhotta K, Chung EK, Eder P, Neumair F, Yu CY.
    J Immunol; 2004 Aug 15; 173(4):2803-14. PubMed ID: 15294999
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  • 16. 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 15; 55(5):869-73. PubMed ID: 26800705
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  • 17. HLA-DRB1 allele frequencies and C4 copy number variation in Finnish sarcoidosis patients and associations with disease prognosis.
    Wennerström A, Pietinalho A, Vauhkonen H, Lahtela L, Palikhe A, Hedman J, Purokivi M, Varkki E, Seppänen M, Lokki ML, Selroos O, Finnish Sarcoidosis Study Group.
    Hum Immunol; 2012 Jan 15; 73(1):93-100. PubMed ID: 22074998
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  • 18. Deficiencies of human complement component C4A and C4B and heterozygosity in length variants of RP-C4-CYP21-TNX (RCCX) modules in caucasians. The load of RCCX genetic diversity on major histocompatibility complex-associated disease.
    Blanchong CA, Zhou B, Rupert KL, Chung EK, Jones KN, Sotos JF, Zipf WB, Rennebohm RM, Yung Yu C.
    J Exp Med; 2000 Jun 19; 191(12):2183-96. PubMed ID: 10859342
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  • 19. 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 19; 123(1):133-9. PubMed ID: 11168010
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  • 20. Genetic, structural and functional diversities of human complement components C4A and C4B and their mouse homologues, Slp and C4.
    Blanchong CA, Chung EK, Rupert KL, Yang Y, Yang Z, Zhou B, Moulds JM, Yu CY.
    Int Immunopharmacol; 2001 Mar 19; 1(3):365-92. PubMed ID: 11367523
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