Human genes for three complement components that regulate the activation of C3 are tightly linked.
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Human factor H deficiency. Mutations in framework cysteine residues and block in H protein secretion and intracellular catabolismIdentification of a partial cDNA clone for the human receptor for complement fragments C3b/C4bCloning and characterization of cDNAs encoding the complete sequence of decay-accelerating factor of human complementIdentification of a partial cDNA clone for the C3d/Epstein-Barr virus receptor of human B lymphocytes: homology with the receptor for fragments C3b and C4b of the third and fourth components of complementThe central portion of factor H (modules 10-15) is compact and contains a structurally deviant CCP moduleThe C3b/C4b receptor is recognized by the Knops, McCoy, Swain-langley, and York blood group antiseraStructure of the human CR1 gene. Molecular basis of the structural and quantitative polymorphisms and identification of a new CR1-like alleleIdentification of an alternative polyadenylation site in the human C3b/C4b receptor (complement receptor type 1) transcriptional unit and prediction of a secreted form of complement receptor type 1Chromosomal location of the genes encoding the leukocyte adhesion receptors LFA-1, Mac-1 and p150,95. Identification of a gene cluster involved in cell adhesionStructure of the human B lymphocyte receptor for C3d and the Epstein-Barr virus and relatedness to other members of the family of C3/C4 binding proteinsHuman C3b/C4b receptor (CR1). Demonstration of long homologous repeating domains that are composed of the short consensus repeats characteristics of C3/C4 binding proteinsAnalysis of multiple restriction fragment length polymorphisms of the gene for the human complement receptor type I. Duplication of genomic sequences occurs in association with a high molecular mass receptor allotypeUsing mutagenesis and structural biology to map the binding site for the Plasmodium falciparum merozoite protein PfRh4 on the human immune adherence receptor.Clustering of missense mutations in the C-terminal region of factor H in atypical hemolytic uremic syndrome.Factor H binds to washed human platelets.Modeling how CD46 deficiency predisposes to atypical hemolytic uremic syndromeTranslational mini-review series on complement factor H: genetics and disease associations of human complement factor H.Complement factor H: using atomic resolution structure to illuminate disease mechanisms.Human genes for the alpha and beta chains of complement C4b-binding protein are closely linked in a head-to-tail arrangement.Complement control protein factor H: the good, the bad, and the inadequate.Assignment of complement components C4 binding protein (C4BP) and factor H (FH) to human chromosome 1q, using cDNA probes.Human complement C3b/C4b receptor (CR1) mRNA polymorphism that correlates with the CR1 allelic molecular weight polymorphismFamily study on the polymorphisms of the sixth and seventh components (C6 and C7) of human complement: linkage and haplotype analyses.Murine protein H is comprised of 20 repeating units, 61 amino acids in length.Structure of the gene coding for the alpha polypeptide chain of the human complement component C4b-binding protein.Quantitative variations of the C3b/C4b receptor (CR1) in human erythrocytes are controlled by genes within the regulator of complement activation (RCA) gene clusterDecay-accelerating factor. Genetic polymorphism and linkage to the RCA (regulator of complement activation) gene cluster in humansA physical map of the human regulator of complement activation gene cluster linking the complement genes CR1, CR2, DAF, and C4BP.Organization of the genes encoding complement receptors type 1 and 2, decay-accelerating factor, and C4-binding protein in the RCA locus on human chromosome 1.Molecular cloning and chromosomal localization of human membrane cofactor protein (MCP). Evidence for inclusion in the multigene family of complement-regulatory proteinsCloning and characterization of a cDNA representing a putative complement-regulatory plasma protein from barred sand bass (Parablax neblifer).Characterization of a T-lymphocyte Epstein-Barr virus/C3d receptor (CD21).Subversion of complement by hematophagous parasites.The interaction between complement component C4b-binding protein and the vitamin K-dependent protein S forms a link between blood coagulation and the complement systemAge-related macular degeneration: genetic and clinical findings.Recent insights into C3 glomerulopathyA protein with characteristics of factor H is present on rodent platelets and functions as the immune adherence receptor.Protection of host cells by complement regulators.Regulation of complement.C3b and factor H: key components of the complement system.
P2860
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P2860
Human genes for three complement components that regulate the activation of C3 are tightly linked.
description
1985 nî lūn-bûn
@nan
1985年の論文
@ja
1985年学术文章
@wuu
1985年学术文章
@zh-cn
1985年学术文章
@zh-hans
1985年学术文章
@zh-my
1985年学术文章
@zh-sg
1985年學術文章
@yue
1985年學術文章
@zh
1985年學術文章
@zh-hant
name
Human genes for three compleme ...... tion of C3 are tightly linked.
@ast
Human genes for three compleme ...... tion of C3 are tightly linked.
@en
type
label
Human genes for three compleme ...... tion of C3 are tightly linked.
@ast
Human genes for three compleme ...... tion of C3 are tightly linked.
@en
prefLabel
Human genes for three compleme ...... tion of C3 are tightly linked.
@ast
Human genes for three compleme ...... tion of C3 are tightly linked.
@en
P2093
P2860
P356
P1476
Human genes for three compleme ...... tion of C3 are tightly linked.
@en
P2093
D M Lublin
J P Atkinson
P Rubinstein
S Rodriguez de Cordoba
P2860
P304
P356
10.1084/JEM.161.5.1189
P407
P577
1985-05-01T00:00:00Z