Results 231 to 240 of about 159,192 (287)

Urgent diagnosis of hereditary angioedema in the ICU and ED: the critical role of rapid complement testing - a case report. [PDF]

Int J Emerg Med
Dungan LS, Khalib K, Curley D, Keogan M.
europepmc   +1 more source

Functional Diversity of Complement C4 Isotypes in Bony Fish Complement

Functional Diversity of Complement C4 Isotypes in Bony Fish Complement
openaire  

Some of the next articles are maybe not open access.

Related searches:

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, Beckman, G, Franzén, L, Jacobsson, L, Lindström   +4 more
openaire   +2 more sources

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 T, Belt, C Y, Yu, M C, Carroll, R R, Porter   +3 more
openaire   +2 more sources

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.
S A, Robb, A H, Fielder, C E, Saunders, N J, Davey, M W, Burley, D H, Lord, J R, Batchelor, V, Dubowitz   +7 more
openaire   +2 more sources

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, I J, Sørensen, L, Buskjaer, L U, Lamm   +3 more
openaire   +2 more sources

Complement components (C3, C4) in childhood asthma

The Indian Journal of Pediatrics, 2005
To assess the involvement of complements (C3, C4) in the pathophysiology of bronchial asthma.Selection of patients (n = 64) were made according to the recommended international criteria for diagnosis and classification of asthma. Serum levels of complement components (C3, C4) were measured by radial immunodiffusion technique in 64 Libyan children (age:
F I E, Najam, A S M, Giasuddin, A H, Shembesh   +2 more
openaire   +2 more sources

Genetics of complement C4. Two homoduplication haplotypes C4S C4S and C4F C4F in a family

Human Genetics, 1982
A family in which two homoduplicated C4 haplotypes (or supergenes) segregate is described. One haplotype C4F*3 C4F*2.2 is composed of two C4F alleles and the other C4S*5.1 C4S*1 of two C4S alleles. The C4F duplication haplotype is a partial inhibitor of the Rodgers antigen, and judged from our family and population material, it seems to be rather ...
G, Bruun-Petersen, L U, Lamm, B K, Jacobsen, T, Kristensen   +3 more
openaire   +2 more sources