Isolation of a complementary DNA clone for the human complement protein C2 and its use in the identification of a restriction fragment length polymorphism

Isolation of a complementary DNA clone for the human complement protein C2 and its use in the identification of a restriction fragment length polymorphism

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http://www.wikidata.org/entity/Q36586617
Type II human complement C2 deficiency. Allele-specific amino acid substitutions (Ser189 --> Phe; Gly444 --> Arg) cause impaired C2 secretionPrimary structure of human complement component C2. Homology to two unrelated protein familiesIndividuals with IgA deficiency and common variable immunodeficiency share polymorphisms of major histocompatibility complex class III genesA variable number of tandem repeats locus within the human complement C2 gene is associated with a retroposon derived from a human endogenous retrovirusA restriction fragment of the C2 gene is a unique marker for C2 deficiency and the uncommon C2 allele C2*B (a marker for type 1 diabetes)Major histocompatibility complex class III genes and susceptibility to immunoglobulin A deficiency and common variable immunodeficiency.Pretranslational regulation of the synthesis of the third component of complement in human mononuclear phagocytes by the lipid A portion of lipopolysaccharideSynergism between gamma interferon and lipopolysaccharide for synthesis of factor B, but not C2, in human fibroblasts.Expression of complement proteins C2 and factor B in transfected L cells.The cellular defect in alpha 1-proteinase inhibitor (alpha 1-PI) deficiency is expressed in human monocytes and in Xenopus oocytes injected with human liver mRNA.Complement in the pathophysiology and diagnosis of human diseases.Allelic associations of multiple RFLPs of the gene encoding complement protein C2.Cachectin/tumor necrosis factor regulates hepatic acute-phase gene expression.Genetic deficiencies of complement.Human complement protein C2. Alternative splicing generates templates for secreted and intracellular C2 proteins.Molecular heterogeneity in deficiency of complement protein C2 type I.Further observations on the role of the MHC genes and certain hearing disorders.
P2860

Isolation of a complementary DNA clone for the human complement protein C2 and its use in the identification of a restriction fragment length polymorphism

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http://www.wikidata.org/entity/Q36586617
description
1984 nî lūn-bûn
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1984年の論文
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1984年論文
@yue
1984年論文
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1984年論文
@zh-hk
1984年論文
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1984年論文
@zh-tw
1984年论文
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1984年论文
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1984年论文
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name
Isolation of a complementary D ...... n fragment length polymorphism
@ast
Isolation of a complementary D ...... n fragment length polymorphism
@en
type
label
Isolation of a complementary D ...... n fragment length polymorphism
@ast
Isolation of a complementary D ...... n fragment length polymorphism
@en
prefLabel
Isolation of a complementary D ...... n fragment length polymorphism
@ast
Isolation of a complementary D ...... n fragment length polymorphism
@en
P1433
P1476
P2093
P2860
P304
P31
P356
P407
P433
P478
P577
P698
P932
P356
P1433
P1476
Isolation of a complementary D ...... n fragment length polymorphism
@en
P2093
P2860
P304
P31
P356
P407
P433
P478
P577
P698
P932