Results 181 to 190 of about 158,583 (222)

In vitro synthesis of some complement components (C1q, C3 and C4) by lymphoid tissues and circulating leucocytes in man.

, 1975
R F Lai A Fat, R. van Furth
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Heterogeneous myocardial contraction detected by speckle tracking echocardiography in systemic lupus erythematosus is associated with complement protein C4: a cross-sectional study from a Swedish tertiary referral centre. [PDF]

Rheumatol Int
Shahab F, Zachrisson H, Svensson C, Åström Aneq M, Sjöwall C, Kylhammar D.   +5 more
europepmc   +1 more source

Complement C3 predicting acute-on-chronic liver failure in cirrhotic patients with bacterial infection within 90 days: a cohort study. [PDF]

Eur J Gastroenterol Hepatol
Chen S, Li R, Liu H, Feng X, Zhou H, Zeng W, Ren H, Xiong Q, Zhang C, Wang X, Yang Y.   +10 more
europepmc   +1 more source

A hidden clue behind angioedema in an elderly patient. [PDF]

Oxf Med Case Reports
Cetin O, Toprak ID, Kemec G, Erdem S, Yegen G, Demir S.   +5 more
europepmc   +1 more source

Left Ventricle Libman-Sacks Endocarditis Secondary to Systemic Lupus Erythematosus and Antiphospholipid Syndrome: A Case Report. [PDF]

Am J Case Rep
Yang ZH, Gong WQ, Liu Y, Zheng MJ.
europepmc   +1 more source

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Complement Factor C4 in Schizophrenia

Human Heredity, 1985
The complement factor C4 was studied in 165 schizophrenic patients and in 330 controls. A highly significant increase in the frequency of C4B deficiency (BQO) was found among the schizophrenic patients compared with controls (p less than 0.0005).
C. Rudduck, L. Lindström, G. Franzén, L. Beckman, L. Jacobsson   +4 more
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Polymorphism of human complement component C4

Immunogenetics, 1985
An assessment has been made of the polymorphism of human complement component C4 by comparing derived amino acid sequences of cDNA and genomic DNA with limited amino acid sequences. In all, one complete and six partial sequences have been obtained from material from three individuals and include two C4A and two C4B alleles.
K. Tertia Belt, Michael C. Carroll, Rodney R. Porter, C. Yung Yu   +3 more
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C4 complement allotypes in juvenile dermatomyositis

Human Immunology, 1988
Twenty probands with juvenile dermatomyositis and their relatives were studied to determine the inherited segregation patterns of class I, II, and III HLA region markers including C4A, C4B, Bf, and C2 complement polymorphisms. The extended haplotype B8, DR3, C4A*Q0, C4B*1, C2*C, and Bf*S was present in 13 of the 20 probands.
M.W. Burley, A.H.L. Fielder, V. Dubowitz, S.A. Robb, D.H. Lord, Nick Davey, C.E. Saunders, J. R. Batchelor   +7 more
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Genetic studies of complement C4 in man

Human Genetics, 1979
A C4 variant found in about 5% of the population is described. The fast-moving part of this variant is governed by an allele (Fx) codominant to F. The Fx allele is in very strong linkage disequilibrium with HLA-B17 as the linkage disequilibrium parameter accounted for nearly 100% of the haplotype frequency of B17,Fx.
G. B. Petersen, Inger Juncker Sørensen, L. U. Lamm, Lisbeth Buskjaer   +3 more
openaire   +3 more sources