Deletion of Lys224 in regulatory domain 4 of Factor H reveals a novel pathomechanism for dense deposit disease (MPGN II) (Q24317382)

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19 January 2020

title

Deletion of Lys224 in regulatory domain 4 of Factor H reveals a novel pathomechanism for dense deposit disease (MPGN II) (English)

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19 January 2020

3

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author name string

Licht C

1

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19 January 2020

Heinen S

2

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19 January 2020

Löschmann I

4

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19 January 2020

Saunders RE

5

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19 January 2020

Perkins SJ

6

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19 January 2020

Waldherr R

7

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19 January 2020

Skerka C

8

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19 January 2020

Kirschfink M

9

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19 January 2020

Hoppe B

10

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19 January 2020

Zipfel PF

11

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19 January 2020

language of work or name

English

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publication date

12 April 2006

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19 January 2020

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19 January 2020

volume

70

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19 January 2020

issue

1

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19 January 2020

page(s)

42-50

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Factor H and the pathogenesis of renal diseases

19 January 2020

cites work

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7 January 2021

Partial H (beta 1H) deficiency and glomerulonephritis in two families

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H deficiency in two brothers with atypical dense intramembranous deposit disease

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Hereditary, complete deficiency of complement factor H associated with recurrent meningococcal disease

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Heterozygous and homozygous factor H deficiency states in a Dutch family

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Combined homozygous factor H and heterozygous C2 deficiency in an Italian family

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Inherited factor H deficiency and collagen type III glomerulopathy

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Heterozygous and homozygous factor h deficiencies associated with hemolytic uremic syndrome or membranoproliferative glomerulonephritis: report and genetic analysis of 16 cases

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Activation of the alternative pathway of complement by monoclonal lambda light chains in membranoproliferative glomerulonephritis

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Complement-mediated adipocyte lysis by nephritic factor sera

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Hereditary porcine membranoproliferative glomerulonephritis type II is caused by factor H deficiency

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Uncontrolled C3 activation causes membranoproliferative glomerulonephritis in mice deficient in complement factor H

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

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The molecular basis for hereditary porcine membranoproliferative glomerulonephritis type II: point mutations in the factor H coding sequence block protein secretion

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Complement analysis in children with idiopathic membranoproliferative glomerulonephritis: a long-term follow-up

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Human anti-idiotypic antibody responses to autoantibody against the alternative pathway C3 convertase

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Haemolytic uraemic syndrome and mutations of the factor H gene: a registry-based study of German speaking countries

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7 January 2021

Mapping of the domains required for decay acceleration activity of the human factor H-like protein 1 and factor H.

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7 January 2021

Complement system on the attack in autoimmunity

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Crystal structure of two CD46 domains reveals an extended measles virus-binding surface

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Adhesion mechanism of human beta(2)-glycoprotein I to phospholipids based on its crystal structure.

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Successful plasma therapy for atypical hemolytic uremic syndrome caused by factor H deficiency owing to a novel mutation in the complement cofactor protein domain 15.

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Different regulation of factor H and FHL-1/reconectin by inflammatory mediators and expression of the two proteins in rheumatoid arthritis (RA).

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A new screening test for C3 nephritis factor based on a stable cell bound convertase on sheep erythrocytes

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Complement factor I deficiency in a family with recurrent infections

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The human factor H-related protein 4 (FHR-4). A novel short consensus repeat-containing protein is associated with human triglyceride-rich lipoproteins

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7 January 2021

Mutations in factor H reduce binding affinity to C3b and heparin and surface attachment to endothelial cells in hemolytic uremic syndrome

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7 January 2021

The yeast Candida albicans binds complement regulators factor H and FHL-1.

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Complement Resistance of Borrelia burgdorferi Correlates with the Expression of BbCRASP-1, a Novel Linear Plasmid-encoded Surface Protein That Interacts with Human Factor H and FHL-1 and Is Unrelated to Erp Proteins

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7 January 2021

Identifiers

DOI

10.1038/SJ.KI.5000269

2 references

Consolidated OpenCitations Corpus – April 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16612335%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

19 January 2020

1003749987

0 references

1 reference

Consolidated OpenCitations Corpus – April 2017

2 references

Consolidated OpenCitations Corpus – April 2017