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Volumn 199, Issue 2, 1998, Pages 286-294

Molecular basis of hereditary C1q deficiency

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENT COMPONENT C1Q;

EID: 0031687525     PISSN: 01712985     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0171-2985(98)80033-8     Document Type: Article
Times cited : (40)

References (20)
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  • 2
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  • 3
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    • SELLAR, G. C., D. J. BLAKE, and K. B. M. REID. 1981. Characterisation and organisation of the genes encoding the A, B and C chain of human C1q. The complete derived amino acid sequence of human C1q. Biochem. J. 274: 481.
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    • Sellar, G.C.1    Blake, D.J.2    Reid, K.B.M.3
  • 4
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  • 5
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    • Reid, K.B.M.1
  • 8
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    • Petry, F.1    Berkel, A.I.2    Loos, M.3
  • 9
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    • Non-sense and missense mutations in the structural genes of complement component C1q A and C chains are linked with two different types of complete selective C1q deficiencies
    • PETRY, F., D. T. LE, M. KIRSCHFINK, and M. LOOS. 1995. Non-sense and missense mutations in the structural genes of complement component C1q A and C chains are linked with two different types of complete selective C1q deficiencies. J. Immunol. 155: 4734.
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    • LOOS, M., A. B. LAURELL, A. G. SJÖRHOLM, U. MARTENSSON, and A. I. BERKEL. 1980. Immunochemical and functional analyses of a complete C1q deficiency in man: evidence that C1r and C1s are in the native form, and that they reassociate with purified C1q to form macromolecular C1. J. Immunol. 124: 59.
    • (1980) J. Immunol. , vol.124 , pp. 59
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  • 15
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  • 16
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    • SLINGSBY, J. H., P. NORSWORTHY, G. PEARCE, A. K. VAISHNAW, H. ISSLER, B. J. MORLEY, and M. J. WALPORT. 1996. Homozygous hereditary C1q deficiency and systemic lupus erythematosus. A new family and the molecular basis of C1q deficiency in three families. Arthritis Rheum. 39: 663.
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  • 18
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    • Molecular basis of a new type of C1q-deficiency associated with a non-functional low molecular weight (LMW) C1q - Parallels and differences to other known genetic C1q-defects
    • PETRY, F., G. HAUPTMANN, J. GOETZ, E. GROSSHANS, and M. LOOS. 1997. Molecular basis of a new type of C1q-deficiency associated with a non-functional low molecular weight (LMW) C1q - parallels and differences to other known genetic C1q-defects. Immunopharmacol. 38: 189.
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    • abstr.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.