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Complement C1 Inactivator Proteins
Known as:
Complement Component 1 Inactivator Proteins
, c1-inh
, Complement C1 Inactivator Proteins [Chemical/Ingredient]
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Serum proteins that inhibit, antagonize, or inactivate COMPLEMENT C1 or its subunits.
National Institutes of Health
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Related topics
Related topics
12 relations
Narrower (4)
C1 esterase inhibitor
C1 esterase inhibitor (human)
Complement C1s Esterase Inhibitor Proteins
SERPING1 protein, human
C1 esterase inhibitor (recombinant)
Process of secretion
agonists
aspects of radiation effects
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Broader (1)
Complement Inactivating Agents
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Hereditary angioedema type II combined with other allergic pathology-case report
S. Dermendzhiev
,
T. Dermendzhiev
,
A. Dzhambov
2018
Corpus ID: 81832048
Hereditary Angioedema (HAE) is a rare disease, and its incidence varies across different populations. HAE belongs to a group of…
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2014
2014
9 C 1-esterase inhibitor protects against early vein graft remodeling under arterial blood pressure
P. Krijnen
,
K. Kupreishvili
,
+11 authors
Niessen
2014
Corpus ID: 35754714
Objective Arterial pressure induced vein graft injury can result in endothelial loss, accelerated atherosclerosis and vein graft…
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Review
2014
Review
2014
Hereditary Angioedema due to C1 Inhibitor Deficiency: C1-INH Replacement Therapy
M. Cancian
2014
Corpus ID: 70989436
Hereditary angioedema (HAE) is a rare condition affecting about 1 in 50.000 individuals and caused by a mutation in the gene…
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Review
2011
Review
2011
Hereditary C1-inhibitor esterase deficiency: a rather well defined entity
D. Moldovan
,
E. Mihály
,
F. Popescu
,
Géza-Attila Szöllösi
,
M. Dobreanu
2011
Corpus ID: 55061123
Hereditary angioedema (HAE) is a rare disease, asso ciated with quantitative or qualitative genetic def iciency of C1-esterase…
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2002
2002
[Hereditary deficiency of C1-esterase inhibitor presenting with recurrent abdominal pain].
J. Steiss
,
P. Mayser
,
L. Gortner
,
G. Alzen
Klinische Pädiatrie
2002
Corpus ID: 32019085
Hereditary deficiency of C1-esterase inhibitor (C1-INH) which clinically manifests as hereditary angioedema is a rare disorder…
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Review
1982
Review
1982
Serum C1-esterase inhibitor (C1INH) levels in normal adults.
G. Ongaro
,
A. Calabró
,
M. Panunzio
Quaderni Sclavo di diagnostica clinica e di…
1982
Corpus ID: 30714237
1982
1982
Effect of treatment with 17 alpha-alkylated androgens on C4 conversion products in hereditary angioedema studied by crossed immunoelectrophoresis.
Luigi Bergamaschini
,
M. Cicardi
,
A. Tucci
,
A. Agostoni
Journal of Clinical Pathology
1982
Corpus ID: 37422091
During agarose electrophoresis C4 in the normal human serum is converted into cleavage products of Beta 1 and Beta 2 mobility. By…
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1976
1976
Plasmin inactivation in Plasma
E. Haselager
,
T. M. Goote
,
J. Vreeken
Thrombosis and Haemostasis
1976
Corpus ID: 223759
Summary Inhibition and inactivation of plasmin is ascribed to α2-macroglobulin, α1-antitrypsin and c1-esterase inhibitor. In an…
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