Genetic polymorphism in human glycine-rich beta-glycoprotein.
about
Penicillamine-induced myasthenia in rheumatoid arthritis: its clinical and genetic features.Genetics of the complement systemInternal homologies of the Ba fragment from human complement component Factor B, a class III MHC antigenMolecular cloning and characterization of the gene coding for human complement protein factor BIsolation of cDNA clones for the human complement protein factor B, a class III major histocompatibility complex gene productMajor histocompatibility complex susceptibility genes for dermatitis herpetiformis compared with those for gluten-sensitive enteropathyThe complotype: dictating risk for inflammation and infectionConstruction of a genetic linkage map in man using restriction fragment length polymorphismsPartial complement deficiencies in idiopathic thrombocytopenia of childhood.Antinuclear antibodies in the relatives and spouses of patients with systemic sclerosis.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.21-hydroxylase deficiency families with HLA identical affected and unaffected sibs.A reassessment of the risk of multiple sclerosis developing in patients with optic neuritis after extended follow-upPartial trisomy 6p: 46,XX, -10, der(10),t(6;10) (p22;q26)pat and HLA localisation.A linkage study between HLA and cutaneous malignant melanoma or precursor lesions or bothGenetics and biochemical variability of variants of 21 hydroxylase deficiency.C4 null phenotypes among lupus erythematosus patients are predominantly the result of deletions covering C4 and closely linked 21-hydroxylase A genes.Genetic regulation of a structural polymorphism of human C3b receptor.Major histocompatibility complex haplotype studies in Ashkenazi Jewish patients with pemphigus vulgaris.Susceptibility or resistance to lysis by alloreactive natural killer cells is governed by a gene in the human major histocompatibility complex between BF and HLA-BA 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)HLA antigens in Japanese patients with myasthenia gravisUniparental isodisomy 6 associated with deficiency of the fourth component of complement.Properdin anc C3 proactivator: alternate pathway components in human glomerulonephritis.Polymorphism of the human complement C4 and steroid 21-hydroxylase genes. Restriction fragment length polymorphisms revealing structural deletions, homoduplications, and size variants.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.Human C4 haplotypes with duplicated C4A or C4BAn unusual "morphologic" variant of BF SGenetic heterogeneity of insulin-dependent (type I) diabetes mellitus: evidence from a study of extended haplotypesThe human salivary protein complex (SPC): a large block of related genes.Genetic interrelationship between insulin-dependent diabetes mellitus, the autoimmune thyroid diseases, and rheumatoid arthritis.HLA linkage and B14, DR1, BfS haplotype association with the genes for late onset and cryptic 21-hydroxylase deficiencyAnalysis of active and inactive complement C4 complotypes associated with subtypes of HLA-B17 in different racial groupsAlzheimer disease: evidence for susceptibility loci on chromosomes 6 and 14Mapping of the structural gene for the second component of complement with respect to the human major histocompatibility complexFive new rare variants of the properdin factor B (BF) locus.
P2860
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P2860
Genetic polymorphism in human glycine-rich beta-glycoprotein.
description
1972 nî lūn-bûn
@nan
1972年の論文
@ja
1972年学术文章
@wuu
1972年学术文章
@zh-cn
1972年学术文章
@zh-hans
1972年学术文章
@zh-my
1972年学术文章
@zh-sg
1972年學術文章
@yue
1972年學術文章
@zh
1972年學術文章
@zh-hant
name
Genetic polymorphism in human glycine-rich beta-glycoprotein.
@ast
Genetic polymorphism in human glycine-rich beta-glycoprotein.
@en
type
label
Genetic polymorphism in human glycine-rich beta-glycoprotein.
@ast
Genetic polymorphism in human glycine-rich beta-glycoprotein.
@en
prefLabel
Genetic polymorphism in human glycine-rich beta-glycoprotein.
@ast
Genetic polymorphism in human glycine-rich beta-glycoprotein.
@en
P2093
P2860
P356
P1476
Genetic polymorphism in human glycine-rich beta-glycoprotein.
@en
P2093
P2860
P356
10.1084/JEM.135.1.68
P407
P577
1972-01-01T00:00:00Z