Molecular basis of polymorphisms of human complement component C3.
about
Complement component 3: an assessment of association with AMD and analysis of gene-gene and gene-environment interactions in a Northern Irish cohortC3 R102G polymorphism increases risk of age-related macular degenerationR102G polymorphism of the C3 gene associated with exudative age-related macular degeneration in a French populationThe complex nature of serum C3 and C4 as biomarkers of lupus renal flare.Common polymorphisms in C3, factor B, and factor H collaborate to determine systemic complement activity and disease riskAllelic variants of complement genes associated with dense deposit disease.Clinical aspects and molecular basis of primary deficiencies of complement component C3 and its regulatory proteins factor I and factor H.New approaches to the treatment of dense deposit disease.Polymorphism of the complement receptor 1 gene correlates with the hematologic response to eculizumab in patients with paroxysmal nocturnal hemoglobinuriaPolymorphism of C3 complement in association with myocardial infarction in a sample of central TunisiaNew functional and structural insights from updated mutational databases for complement factor H, Factor I, membrane cofactor protein and C3.Association of polymorphisms in complement component 3 with age-related macular degeneration in an Iranian population.Complement C3F allotype synthesized by liver recipient modifies transplantation outcome independently from donor hepatic C3.The comorbid association of migraine with osteoarthritis and hypertension: complement C3F and Berkson's bias.Mannose-binding lectin 1 haplotypes influence serum MBL-A concentration, complement activity, and milk production traits in Chinese Holstein cattle.The investigation of allele and genotype frequencies of human C3 (rs2230199) in south Iranian population.C3F gene mutation is involved in the susceptibility to pre-eclampsia.Cooperation between C1q and DNase I in the clearance of necrotic cell-derived chromatin.C3 and C4 allotypes in anti-neutrophil cytoplasmic autoantibody (ANCA)-positive vasculitis.Human complement factor 3 polymorphism determination by capillary electrophoresis of serum.Complement in ANCA-associated glomerulonephritis.Haplotype-based association analysis of 56 functional candidate genes in the IBD6 locus on chromosome 19Analysis of C3 Gene Variants in Patients With Idiopathic Recurrent Spontaneous Pregnancy Loss
P2860
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P2860
Molecular basis of polymorphisms of human complement component C3.
description
1990 nî lūn-bûn
@nan
1990年の論文
@ja
1990年論文
@yue
1990年論文
@zh-hant
1990年論文
@zh-hk
1990年論文
@zh-mo
1990年論文
@zh-tw
1990年论文
@wuu
1990年论文
@zh
1990年论文
@zh-cn
name
Molecular basis of polymorphisms of human complement component C3.
@en
Molecular basis of polymorphisms of human complement component C3.
@nl
type
label
Molecular basis of polymorphisms of human complement component C3.
@en
Molecular basis of polymorphisms of human complement component C3.
@nl
prefLabel
Molecular basis of polymorphisms of human complement component C3.
@en
Molecular basis of polymorphisms of human complement component C3.
@nl
P2093
P2860
P356
P1476
Molecular basis of polymorphisms of human complement component C3.
@en
P2093
P2860
P304
P356
10.1084/JEM.172.4.1011
P407
P50
P577
1990-10-01T00:00:00Z