(Q34775643)

4 August 2017

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title

Navigating the maze of complement genetics: a guide for clinicians (English)

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4 August 2017

Harvey R Colten

1

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4 August 2017

publication date

1 September 2002

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Current Allergy and Asthma Reports

4 August 2017

published in

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4 August 2017

volume

2

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4 August 2017

issue

5

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4 August 2017

page(s)

379-384

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Molecular basis of hereditary C1q deficiency

4 August 2017

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS11882-002-0070-6

Disruption of disulfide bonds is responsible for impaired secretion in human complement factor H deficiency

21 January 2018

1 reference

12 December 2020

Complement and innate immunity.

1 reference

12 December 2020

Systemic lupus erythematosus, complement deficiency, and apoptosis

1 reference

12 December 2020

Identification of human erythrocyte blood group antigens on decay-accelerating factor (DAF) and an erythrocyte phenotype negative for DAF

1 reference

12 December 2020

Deficiency of a Granulocyte-Membrane Glycoprotein (gp150) in a Boy with Recurrent Bacterial Infections

1 reference

12 December 2020

Treatment of hereditary angioedema with a vapor-heated C1 inhibitor concentrate

1 reference

12 December 2020

Relevance of lymphoproliferative disorders and of anti-C1 inhibitor autoantibodies in acquired angio-oedema

1 reference

12 December 2020

Type II human complement C2 deficiency. Allele-specific amino acid substitutions (Ser189 --> Phe; Gly444 --> Arg) cause impaired C2 secretion

1 reference

12 December 2020

Inherited complete deficiency of 20-kilodalton homologous restriction factor (CD59) as a cause of paroxysmal nocturnal hemoglobinuria

1 reference

12 December 2020

Inherited deficiency of the fourth component of human complement

1 reference

12 December 2020

Genetic deficiencies of complement

1 reference

12 December 2020

Estrogen regulation of tissue-specific expression of complement C3.

1 reference

12 December 2020

Type I human complement C2 deficiency. A 28-base pair gene deletion causes skipping of exon 6 during RNA splicing

1 reference

12 December 2020

Homozygous C1q deficiency causes glomerulonephritis associated with multiple apoptotic bodies

1 reference

12 December 2020

C3 nephritic factor and C4 nephritic factor in the serum of two patients with hypocomplementaemic membranoproliferative glomerulonephritis.

1 reference

12 December 2020

Transinhibition of C1 inhibitor synthesis in type I hereditary angioneurotic edema

1 reference

12 December 2020

Plasma bradykinin in angio-oedema.

1 reference

12 December 2020

C1q and systemic lupus erythematosus

1 reference

12 December 2020

Human factor H deficiency. Mutations in framework cysteine residues and block in H protein secretion and intracellular catabolism

1 reference

12 December 2020

Heterogeneous mutations in the beta subunit common to the LFA-1, Mac-1, and p150,95 glycoproteins cause leukocyte adhesion deficiency

1 reference

12 December 2020

Heterogeneity, polypeptide chain composition and antigenic reactivity of C3 nephritic factor

1 reference

12 December 2020

Complement. First of two parts

1 reference

12 December 2020

The molecular basis of hereditary complement factor I deficiency

1 reference

12 December 2020

Complement deficiencies

1 reference

12 December 2020

Apoptosis and autoimmunity: complement deficiency and systemic lupus erythematosus revisited

1 reference

12 December 2020

A role for the C3a anaphylatoxin receptor in the effector phase of asthma

1 reference

12 December 2020

Leukocyte adhesion deficiency: an inherited defect in the Mac-1, LFA-1, and p150,95 glycoproteins

1 reference

12 December 2020

A critical role for murine complement regulator crry in fetomaternal tolerance

1 reference

12 December 2020

The C5a chemoattractant receptor mediates mucosal defence to infection

1 reference

12 December 2020

The complement system and adaptive immunity

1 reference

12 December 2020

Complement and apoptosis

1 reference

12 December 2020

C1-inhibitor deficiency and angioedema.

1 reference

12 December 2020

The dual pathogenesis of paroxysmal nocturnal hemoglobinuria.

1 reference

12 December 2020

Complement deficiencies

1 reference

12 December 2020

Complement C3 deficiency: human, animal, and experimental models

1 reference

12 December 2020

Molecular pathogenesis of liver disease in alpha1-antitrypsin deficiency

1 reference

12 December 2020

Implications of recent insights into the pathophysiology of paroxysmal nocturnal haemoglobinuria.

1 reference

12 December 2020

Molecular heterogeneity of C2 deficiency

1 reference

12 December 2020

Complement: a critical test of its biological importance

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12 December 2020

Complement factors and their receptors

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12 December 2020

Complement-mediated adipocyte lysis by nephritic factor sera

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12 December 2020

Studies of group B streptococcal infection in mice deficient in complement component C3 or C4 demonstrate an essential role for complement in both innate and acquired immunity

1 reference

12 December 2020

Soluble human complement receptor type 1: in vivo inhibitor of complement suppressing post-ischemic myocardial inflammation and necrosis

1 reference

12 December 2020

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

1 reference

12 December 2020

10.1007/S11882-002-0070-6

Identifiers

DOI

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Dimensions Publication ID

4 August 2017

1043379035

0 references

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