Inherited structural polymorphism of the fourth component of human complement
about
Genetic analysis of completely sequenced disease-associated MHC haplotypes identifies shuffling of segments in recent human history.Substitution of a single amino acid (aspartic acid for histidine) converts the functional activity of human complement C4B to C4APenicillamine-induced myasthenia in rheumatoid arthritis: its clinical and genetic features.Structural basis of the polymorphism of human complement components C4A and C4B: gene size, reactivity and antigenicity.Variation analysis and gene annotation of eight MHC haplotypes: the MHC Haplotype ProjectLow serum C4 concentrations: an inherited predisposition to insulin dependent diabetes?Major histocompatibility complex susceptibility genes for dermatitis herpetiformis compared with those for gluten-sensitive enteropathyEarly Components of the Complement Classical Activation Pathway in Human Systemic Autoimmune DiseasesA comparison of the properties of two classes, C4A and C4B, of the human complement component C4The internal thioester and the covalent binding properties of the complement proteins C3 and C4Infections of People with Complement Deficiencies and Patients Who Have Undergone SplenectomyGenetic susceptibility to early onset pauciarticular juvenile chronic arthritis: a study of HLA and complement markers in 158 British patients.Human parvovirus infection in early rheumatoid and inflammatory arthritis.Complement activation and HLA-B27HLA-B alleles and complotypes in Mexican patients with seronegative spondyloarthropathies.Diversity and pattern of inheritance of autoantibodies in families with multiple cases of systemic lupus erythematosus.C4 null phenotypes among lupus erythematosus patients are predominantly the result of deletions covering C4 and closely linked 21-hydroxylase A genes.Major histocompatibility complex haplotype studies in Ashkenazi Jewish patients with pemphigus vulgaris.Low serum haemolytic function of the fourth complement component (C4) in insulin dependent diabetesModular variations of the human major histocompatibility complex class III genes for serine/threonine kinase RP, complement component C4, steroid 21-hydroxylase CYP21, and tenascin TNX (the RCCX module). A mechanism for gene deletions and disease asLinks between complement abnormalities and systemic lupus erythematosus.Deficiencies of human complement component C4A and C4B and heterozygosity in length variants of RP-C4-CYP21-TNX (RCCX) modules in caucasians. The load of RCCX genetic diversity on major histocompatibility complex-associated disease.A 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)Uniparental isodisomy 6 associated with deficiency of the fourth component of complement.Polymorphism of the human complement C4 and steroid 21-hydroxylase genes. Restriction fragment length polymorphisms revealing structural deletions, homoduplications, and size variants.Autoantibody to the C3b/C4b receptor and absence of this receptor from erythrocytes of a patient with systemic lupus erythematosus.Low plasma C4 concentrations: association with microangiopathy in insulin dependent diabetes.Extended major histocompatibility complex haplotypes in patients with gluten-sensitive enteropathy.Inherited incomplete deficiency of the fourth component of complement (C4) determined by a gene not linked to human histocompatibility leukocyte antigens.Family study of the major histocompatibility complex in patients with systemic lupus erythematosus: importance of null alleles of C4A and C4B in determining disease susceptibility.Tight linkage of the gene for spinocerebellar ataxia to D6S89 on the short arm of chromosome 6 in a kindred for which close linkage to both HLA and F13A1 is excluded.Human C4 haplotypes with duplicated C4A or C4BAn unusual "morphologic" variant of BF SThe genetic polymorphism of alpha 2-HS glycoprotein: study by ultrathin-layer isoelectric focusing and immunoblot.The immunological detection of a 21-OH deficiency mutation HLA supratype.Analysis of active and inactive complement C4 complotypes associated with subtypes of HLA-B17 in different racial groupsMurine binding protein of the fourth component of complement: structural polymorphism and its linkage to the major histocompatibility complexA unique recombination event resulting in a C4A*Q0,C4B*Q0 double null haplotype.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 AThe immune response to hepatitis B vaccine in humans: inheritance patterns in families.
P2860
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P2860
Inherited structural polymorphism of the fourth component of human complement
description
1980 nî lūn-bûn
@nan
1980年の論文
@ja
1980年学术文章
@wuu
1980年学术文章
@zh-cn
1980年学术文章
@zh-hans
1980年学术文章
@zh-my
1980年学术文章
@zh-sg
1980年學術文章
@yue
1980年學術文章
@zh
1980年學術文章
@zh-hant
name
Inherited structural polymorphism of the fourth component of human complement
@ast
Inherited structural polymorphism of the fourth component of human complement
@en
type
label
Inherited structural polymorphism of the fourth component of human complement
@ast
Inherited structural polymorphism of the fourth component of human complement
@en
prefLabel
Inherited structural polymorphism of the fourth component of human complement
@ast
Inherited structural polymorphism of the fourth component of human complement
@en
P2860
P356
P1476
Inherited structural polymorphism of the fourth component of human complement
@en
P2093
P2860
P304
P356
10.1073/PNAS.77.6.3576
P407
P577
1980-06-01T00:00:00Z