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Journal Abstract Search

128 related items for PubMed ID: 12648279

  • 41. Association between early onset and organ manifestations of systemic lupus erythematosus (SLE) and a down-regulating promoter polymorphism in the MBL2 gene.
    Jakab L, Laki J, Sallai K, Temesszentandrási G, Pozsonyi T, Kalabay L, Varga L, Gombos T, Blaskó B, Bíró A, Madsen HO, Radics J, Gergely P, Füst G, Czirják L, Garred P, Fekete B.
    Clin Immunol; 2007 Dec; 125(3):230-6. PubMed ID: 17942372
    [Abstract] [Full Text] [Related]

  • 42. Characterization of polymorphisms in the mannose-binding lectin gene promoter among human immunodeficiency virus 1 infected subjects.
    Vallinoto AC, Muto NA, Alves AE, Machado LF, Azevedo VN, Souza LL, Ishak MO, Ishak R.
    Mem Inst Oswaldo Cruz; 2008 Nov; 103(7):645-9. PubMed ID: 19057812
    [Abstract] [Full Text] [Related]

  • 43. [Correlation of mannose-binding lectin gene promoter polymorphism and plasma MBL concentration with HIV susceptibility in northern Chinese Han population].
    Sheng AJ, Liu LX, Wu H, Wang YX, Peng XX, Wang W.
    Nan Fang Yi Ke Da Xue Xue Bao; 2008 Apr; 28(4):567-71. PubMed ID: 18495592
    [Abstract] [Full Text] [Related]

  • 44. Mild and moderate Mannose Binding Lectin deficiency are associated with systemic lupus erythematosus and lupus nephritis in Brazilian patients.
    Perazzio SF, Silva NP, Carneiro-Sampaio M, Andrade LE.
    Rev Bras Reumatol Engl Ed; 2016 Apr; 56(3):220-7. PubMed ID: 27267640
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  • 45. Mannose-binding lectin variant alleles and the risk of arterial thrombosis in systemic lupus erythematosus.
    Øhlenschlaeger T, Garred P, Madsen HO, Jacobsen S.
    N Engl J Med; 2004 Jul 15; 351(3):260-7. PubMed ID: 15254284
    [Abstract] [Full Text] [Related]

  • 46. Association of mannose binding lectin codon 54 polymorphism with predisposition to Henoch-Schönlein purpura in childhood.
    Durmaz B, Aykut A, Hursitoglu G, Bak M, Serdaroglu E, Onay H, Ozkinay F.
    Int J Rheum Dis; 2014 Mar 15; 17(3):317-20. PubMed ID: 24576294
    [Abstract] [Full Text] [Related]

  • 47. No association of complement mannose-binding lectin deficiency with cardiovascular disease in patients with Systemic Lupus Erythematosus.
    Kieninger-Gräfitsch A, Vogt S, Ribi C, Dubler D, Chizzolini C, Huynh-Do U, Osthoff M, Trendelenburg M.
    Sci Rep; 2020 Feb 28; 10(1):3693. PubMed ID: 32111865
    [Abstract] [Full Text] [Related]

  • 48. Genetically determined mannan-binding lectin deficiency is of minor importance in determining susceptibility to severe infections and vascular organ damage in systemic lupus erythematosus.
    Jönsen A, Gullstrand B, Güner N, Bengtsson AA, Nived O, Truedsson L, Sturfelt G.
    Lupus; 2007 Feb 28; 16(4):245-53. PubMed ID: 17439930
    [Abstract] [Full Text] [Related]

  • 49. Systemic lupus erythematosus as a first presentation of common variable immunodeficiency associated with infrequent mannose-binding lectin gene polymorphisms.
    Torres-Salido M, Cortés-Hernández J, Balada E, Tarrés MV, Ordi-Ros J.
    Rheumatol Int; 2011 Apr 28; 31(4):537-41. PubMed ID: 19851769
    [Abstract] [Full Text] [Related]

  • 50. Evaluation mannose-binding lectin gene and promoter polymorphism in renal transplant recipients.
    Bohlouli A, Ebrahimzadeh ME, Kafil HS, Asgharzadeh M.
    J Pak Med Assoc; 2008 Jun 28; 58(6):294-8. PubMed ID: 18988385
    [Abstract] [Full Text] [Related]

  • 51. Genetic variants of mannose-binding lectin 2 gene influence progression and prognosis of patients with hepatitis B virus infection in China.
    Gu X, Ji Q, Wang H, Jiang M, Yang J, Fang M, Wang M, Gao C.
    Clin Res Hepatol Gastroenterol; 2016 Nov 28; 40(5):614-621. PubMed ID: 26857650
    [Abstract] [Full Text] [Related]

  • 52. Interleukin 10 gene promoter polymorphisms (rs1800896, rs1800871 and rs1800872) and haplotypes are associated with the activity of systemic lupus erythematosus and IL10 levels in an Iranian population.
    Mohammadi S, Saghaeian Jazi M, Zare Ebrahimabad M, Eghbalpour F, Abdolahi N, Tabarraei A, Yazdani Y.
    Int J Immunogenet; 2019 Feb 28; 46(1):20-30. PubMed ID: 30430731
    [Abstract] [Full Text] [Related]

  • 53. Detection of structural gene mutations and promoter polymorphisms in the mannan-binding lectin (MBL) gene by polymerase chain reaction with sequence-specific primers.
    Steffensen R, Thiel S, Varming K, Jersild C, Jensenius JC.
    J Immunol Methods; 2000 Jul 31; 241(1-2):33-42. PubMed ID: 10915847
    [Abstract] [Full Text] [Related]

  • 54. Association of CD40 polymorphisms and haplotype with risk of systemic lupus erythematosus.
    Wu CJ, Guo J, Luo HC, Wei CD, Wang CF, Lan Y, Wei YS.
    Rheumatol Int; 2016 Jan 31; 36(1):45-52. PubMed ID: 26289938
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  • 55. Mannose-binding lectin serum levels in patients with systemic lupus erythematosus: association with thrombocytopaenia and seizure.
    Cieslinski JZ, Skare TL, Nisihara R, De Messias-Reason IJ, Utiyama SRR.
    Lupus; 2018 Mar 31; 27(3):372-379. PubMed ID: 28786770
    [Abstract] [Full Text] [Related]

  • 56. Restricted polymorphism of the mannose-binding lectin gene of indigenous Australians.
    Turner MW, Dinan L, Heatley S, Jack DL, Boettcher B, Lester S, McCluskey J, Roberton D.
    Hum Mol Genet; 2000 Jun 12; 9(10):1481-6. PubMed ID: 10888598
    [Abstract] [Full Text] [Related]

  • 57. A role for mannose-binding lectin dysfunction in generation of autoantibodies in systemic lupus erythematosus.
    Seelen MA, van der Bijl EA, Trouw LA, Zuiverloon TC, Munoz JR, Fallaux-van den Houten FC, Schlagwein N, Daha MR, Huizinga TW, Roos A.
    Rheumatology (Oxford); 2005 Jan 12; 44(1):111-9. PubMed ID: 15479757
    [Abstract] [Full Text] [Related]

  • 58. Clinical and genetic risk factors for pneumonia in systemic lupus erythematosus.
    Kinder BW, Freemer MM, King TE, Lum RF, Nititham J, Taylor K, Edberg JC, Bridges SL, Criswell LA.
    Arthritis Rheum; 2007 Aug 12; 56(8):2679-86. PubMed ID: 17665457
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  • 59. Mannose-binding lectin gene-2 polymorphisms and serum mannose-binding lectin levels in Behçet's disease.
    Kim J, Im CH, Kang EH, Lee EY, Lee YJ, Park KS, Song YW.
    Clin Exp Rheumatol; 2009 Aug 12; 27(2 Suppl 53):S13-7. PubMed ID: 19796526
    [Abstract] [Full Text] [Related]

  • 60. Mannose-binding lectin polymorphisms in common variable immunodeficiency.
    Aghamohammadi A, Foroughi F, Rezaei N, Dianat S, Solgi G, Amirzargar AA.
    Clin Exp Med; 2009 Dec 12; 9(4):285-90. PubMed ID: 19408100
    [Abstract] [Full Text] [Related]

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