Genetically determined heterogeneity of the C1 esterase inhibitor in patients with hereditary angioneurotic edema.
about
Dysfunctional C1 inhibitor Ta: deletion of Lys-251 results in acquisition of an N-glycosylation siteType II hereditary angioneurotic edema that may result from a single nucleotide change in the codon for alanine-436 in the C1 inhibitor geneType I C1 inhibitor deficiency with a small messenger RNA resulting from deletion of one exonNonsense mutations affect C1 inhibitor messenger RNA levels in patients with type I hereditary angioneurotic edemaHypoxia-activated genes from early placenta are elevated in preeclampsia, but not in Intra-Uterine Growth Retardation.Self-administered C1 esterase inhibitor concentrates for the management of hereditary angioedema: usability and patient acceptanceTransinhibition of C1 inhibitor synthesis in type I hereditary angioneurotic edema.Inhibitors of kallikrein in human plasma.Synthesis of C1 inhibitor in fibroblasts from patients with type I and type II hereditary angioneurotic edemaPlasma levels of C1- inhibitor complexes and cleaved C1- inhibitor in patients with hereditary angioneurotic edema.Studies on human plasma C1 inactivator-enzyme interactions. II. Structural features of an abnormal C1 inactivator from a kindred with hereditary angioneurotic edemaPlasma inhibitors of the components of the fibrinolytic pathway in manInhibition by C1INH of Hagemann factor fragment activation of coagulation, fibrinolysis, and kinin generation.Inherited incomplete deficiency of the fourth component of complement (C4) determined by a gene not linked to human histocompatibility leukocyte antigens.Lupus erythematosus associated with C1 inhibitor deficiency.Behavior in vivo of normal and dysfunctional C1 inhibitor in normal subjects and patients with hereditary angioneurotic edema.Restriction fragment length polymorphism of the C1 inhibitor gene in hereditary angioneurotic edema.A mutation unique in serine protease inhibitors (serpins) identified in a family with type II hereditary angioneurotic edema.Hereditary angioedema: causes, manifestations and treatment.Human skin collagenase in recessive dystrophic epidermolysis bullosa. Purification of a mutant enzyme from fibroblast culturesEnhanced biosynthesis of human skin collagenase in fibroblast cultures from recessive dystrophic epidermolysis bullosa.Response of variant hereditary angioedema phenotypes to danazol therapy. Genetic implications.Hereditary angioedema: case report and review of management.Treatment of hereditary angioedema: a review (CME).HAE Pathophysiology and Underlying Mechanisms.The Story of Angioedema: from Quincke to Bradykinin.Acquired C1 inhibitor (C1-INH) deficiency type II. Replacement therapy with C1-INH and analysis of patients' C1-INH and anti-C1-INH autoantibodies.Recombinational biases in the rearranged C1-inhibitor genes of hereditary angioedema patients.C1-inhibitor and its genetic alterations in hereditary angioneurotic edema.Variability in purified dysfunctional C1(-)-inhibitor proteins from patients with hereditary angioneurotic edema. Functional and analytical gel studies.Molecular basis for the deficiency of complement 1 inhibitor in type I hereditary angioneurotic edema.Rapid and sensitive techniques for identification and analysis of 'reactive-centre' mutants of C1-inhibitor proteins contained in type II hereditary angio-oedema plasmas.Dysfunctional C1-inhibitor(At), isolated from a type II hereditary-angio-oedema plasma, contains a P1 'reactive centre' (Arg444----His) mutation.Chymotrypsin inhibitory activity of normal C1-inhibitor and a P1 Arg to His mutant: evidence for the presence of overlapping reactive centersAngioedema induced by a peptide derived from complement component C2.Inherited disorders of the skin and skin diseases due to a hereditary predisposition.Management of angiotensin-converting enzyme inhibitor-induced angioedema.The Pathophysiology of Hereditary Angioedema
P2860
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P2860
Genetically determined heterogeneity of the C1 esterase inhibitor in patients with hereditary angioneurotic edema.
description
1971 nî lūn-bûn
@nan
1971 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1971 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
1971年の論文
@ja
1971年学术文章
@wuu
1971年学术文章
@zh-cn
1971年学术文章
@zh-hans
1971年学术文章
@zh-my
1971年学术文章
@zh-sg
1971年學術文章
@yue
name
Genetically determined heterog ...... ereditary angioneurotic edema.
@ast
Genetically determined heterog ...... ereditary angioneurotic edema.
@en
Genetically determined heterog ...... ereditary angioneurotic edema.
@nl
type
label
Genetically determined heterog ...... ereditary angioneurotic edema.
@ast
Genetically determined heterog ...... ereditary angioneurotic edema.
@en
Genetically determined heterog ...... ereditary angioneurotic edema.
@nl
prefLabel
Genetically determined heterog ...... ereditary angioneurotic edema.
@ast
Genetically determined heterog ...... ereditary angioneurotic edema.
@en
Genetically determined heterog ...... ereditary angioneurotic edema.
@nl
P2093
P2860
P356
P1476
Genetically determined heterog ...... ereditary angioneurotic edema.
@en
P2093
M R Klemperer
V H Donaldson
P2860
P304
P356
10.1172/JCI106708
P407
P577
1971-10-01T00:00:00Z