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Journal Abstract Search

281 related items for PubMed ID: 2561058

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  • 3. The structure and function of the first component of complement: genetic engineering approach (a review).
    Gál P, Cseh S, Schumaker VN, Závodszky P.
    Acta Microbiol Immunol Hung; 1994; 41(4):361-80. PubMed ID: 7866721
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  • 6. C1, the first component of complement: structure-function-relationship of C1q and collectins (MBP, SP-A, SP-D, conglutinin), C1-esterases (C1r and C1s), and C1-inhibitor in health and disease.
    Loos M, Colomb M.
    Behring Inst Mitt; 1993 Dec; (93):1-5. PubMed ID: 8172555
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  • 7. Cutaneous manifestations of complement deficiencies.
    Lipsker D, Hauptmann G.
    Lupus; 2010 Aug; 19(9):1096-106. PubMed ID: 20693203
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  • 9. [Hereditary complement deficiencies].
    Fischer E.
    Hautarzt; 1982 Feb; 33(2):65-72. PubMed ID: 6281215
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  • 12. [C1r/C1s deficiency].
    Ohno T.
    Ryoikibetsu Shokogun Shirizu; 2000 Feb; (32):189-92. PubMed ID: 11212686
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  • 16. Expression of recombinant human complement C1q allows identification of the C1r/C1s-binding sites.
    Bally I, Ancelet S, Moriscot C, Gonnet F, Mantovani A, Daniel R, Schoehn G, Arlaud GJ, Thielens NM.
    Proc Natl Acad Sci U S A; 2013 May 21; 110(21):8650-5. PubMed ID: 23650384
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  • 19. C1 dissociation. Spontaneous generation in human serum of a trimer complex containing C1 inactivator, activated C1r, and zymogen C1s.
    Laurell AB, Mårtensson U, Sjöholm AG.
    J Immunol; 1987 Dec 15; 139(12):4145-51. PubMed ID: 2826582
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