about
Substitution of a single amino acid (aspartic acid for histidine) converts the functional activity of human complement C4B to C4AStructural basis of the polymorphism of human complement components C4A and C4B: gene size, reactivity and antigenicity.Molecular characterization of the HLA-linked steroid 21-hydroxylase B gene from an individual with congenital adrenal hyperplasiaMajor histocompatibility complex class III genes and susceptibility to immunoglobulin A deficiency and common variable immunodeficiency.The phylogeny and evolution of the thioester bond-containing proteins C3, C4 and alpha 2-macroglobulin.Polymorphism of the human complement C4 and steroid 21-hydroxylase genes. Restriction fragment length polymorphisms revealing structural deletions, homoduplications, and size variants.Gene copy-number variation and associated polymorphisms of complement component C4 in human systemic lupus erythematosus (SLE): low copy number is a risk factor for and high copy number is a protective factor against SLE susceptibility in European AStructural differences between the two human complement C4 isotypes affect the humoral immune response.Genetic sophistication of human complement components C4A and C4B and RP-C4-CYP21-TNX (RCCX) modules in the major histocompatibility complexPhenotypes, genotypes and disease susceptibility associated with gene copy number variations: complement C4 CNVs in European American healthy subjects and those with systemic lupus erythematosus.Molecular pathology of congenital adrenal hyperplasia.Association between C4, C4A, and C4B copy number variations and susceptibility to autoimmune diseases: a meta-analysis.Human gene copy number variation and infectious disease.Molecular genetics of the fourth component of human complement and steroid 21-hydroxylase.Duplications of complement and non-complement genes of the H-2S region: evolutionary aspects of the C4 isotypes and molecular analysis of their expression variants.Molecular biology of the human and mouse MHC class III genes: phylogenetic conservation, genetics and regulation of expression.The complement components coded in the major histocompatibility complexes and their biological activities.Genetic basis of human complement C4A deficiency. Detection of a point mutation leading to nonexpression.Counterregulatory effects of interferon-gamma and endotoxin on expression of the human C4 genes.Genetic deficiencies of the complement system and association with disease--early components.The origin of the very variable haemolytic activities of the common human complement component C4 allotypes including C4-A6.Deletion of complement C4 and steroid 21-hydroxylase genes in the HLA class III region.The complement component C4 of mammals.The low C5 convertase activity of the C4A6 allotype of human complement component C4.Null alleles of human complement C4. Evidence for pseudogenes at the C4A locus and for gene conversion at the C4B locus.Polymorphism in the Human Complement C4 Genes and Genetic Susceptibility to Autoimmune Hepatitis
P2860
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P2860
description
1985 nî lūn-bûn
@nan
1985 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1985 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1985年の論文
@ja
1985年論文
@yue
1985年論文
@zh-hant
1985年論文
@zh-hk
1985年論文
@zh-mo
1985年論文
@zh-tw
1985年论文
@wuu
name
Polymorphism of human complement component C4.
@ast
Polymorphism of human complement component C4.
@en
Polymorphism of human complement component C4.
@nl
type
label
Polymorphism of human complement component C4.
@ast
Polymorphism of human complement component C4.
@en
Polymorphism of human complement component C4.
@nl
prefLabel
Polymorphism of human complement component C4.
@ast
Polymorphism of human complement component C4.
@en
Polymorphism of human complement component C4.
@nl
P2093
P356
P1433
P1476
Polymorphism of human complement component C4.
@en
P2093
P2888
P304
P356
10.1007/BF00364869
P407
P577
1985-01-01T00:00:00Z
P6179
1015029498