Type I C1 inhibitor deficiency with a small messenger RNA resulting from deletion of one exon (Q24624048)

2

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N Ramesh

3

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R Parad

4

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M Cicardi

5

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A E Davis

Journal of Clinical Investigation

6

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language of work or name

English

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publication date

June 1989

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published in

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volume

83

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page(s)

1888-93

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issue

6

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ACTION OF COMPLEMENT IN HEREDITARY ANGIONEUROTIC EDEMA: THE ROLE OF C'1-ESTERASE

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27 September 2017

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Hereditary angioneurotic edema: a clinical survey

27 September 2017

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Genetically determined heterogeneity of the C1 esterase inhibitor in patients with hereditary angioneurotic edema

27 September 2017

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Variability in purified dysfunctional C1(-)-inhibitor proteins from patients with hereditary angioneurotic edema. Functional and analytical gel studies

27 September 2017

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27 September 2017

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27 September 2017

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Human inhibitor of the first component of complement, C1: characterization of cDNA clones and localization of the gene to chromosome 11

27 September 2017

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[21] Specific synthesis of DNA in vitro via a polymerase-catalyzed chain reaction

27 September 2017

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Genomic and cDNA cloning of the human C1 inhibitor. Intron-exon junctions and comparison with other serpins

27 September 2017

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27 September 2017

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Treatment of hereditary angioedema with danazol. Reversal of clinical and biochemical abnormalities

27 September 2017

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27 September 2017

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27 September 2017

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27 September 2017

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Detection and sequence of mutations in the factor VIII gene of haemophiliacs

30 May 2018

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Synthesis of the second component of complement by long-term primary cultures of human monocytes

30 May 2018

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Variability in the amount of beta-globin mRNA in beta0 thalassemia

30 May 2018

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Altered C1 inhibitor genes in type I hereditary angioedema

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12 December 2020

Unstable β-globin mRNA in mRNA-deficient β0 thalassemia

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12 December 2020

Hereditary angioneurotic edema. II. Deficiency of inhibitor for serum globulin permeability factor and/or plasma kallikrein

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12 December 2020

Hereditary Angioedema: the Clinical Syndrome and Its Management

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12 December 2020

Molecular Heterogeneity of Inherited Antithrombin III Deficiency

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12 December 2020

DNA polymorphism of the C4 genes. A new marker for analysis of the major histocompatibility complex

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12 December 2020

Intranuclear defect in beta-globin mRNA accumulation due to a premature translation termination codon

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12 December 2020

Beta O-39 thalassemia gene: a premature termination codon causes beta-mRNA deficiency without affecting cytoplasmic beta-mRNA stability

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12 December 2020