(Q37886671)

24 August 2017

Molecular basis of hereditary C1q deficiency--revisited: identification of several novel disease-causing mutations (English)

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24 August 2017

P Garred

9

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author name string

L Schejbel

1

1 reference

24 August 2017

L Skattum

2

1 reference

24 August 2017

S Hagelberg

3

1 reference

24 August 2017

A Åhlin

4

1 reference

24 August 2017

B Schiller

5

1 reference

24 August 2017

S Berg

6

1 reference

24 August 2017

F Genel

7

1 reference

24 August 2017

L Truedsson

8

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24 August 2017

9 June 2011

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24 August 2017

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24 August 2017

12

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24 August 2017

8

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24 August 2017

626-634

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https://scigraph.springernature.com/pub.10.1038/gene.2011.39

24 August 2017

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cites work

Complement. First of two parts

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2011.39

Localization of ligand-binding sites on human C1q globular head region using recombinant globular head fragments and single-chain antibodies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2011.39

Structural and functional anatomy of the globular domain of complement protein C1q.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2011.39

Characterization and organization of the genes encoding the A-, B- and C-chains of human complement subcomponent C1q. The complete derived amino acid sequence of human C1q

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2011.39

C1q and tumor necrosis factor superfamily: modularity and versatility

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2011.39

The crystal structure of the globular head of complement protein C1q provides a basis for its versatile recognition properties

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2011.39

Structure and activation of the C1 complex of complement: unraveling the puzzle.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2011.39

Reconstitution of the Complement Function in C1q-Deficient (C1qa-/-) Mice with Wild-Type Bone Marrow Cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2011.39

Restoration of C1q levels by bone marrow transplantation attenuates autoimmune disease associated with C1q deficiency in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2011.39

The non-classical functions of the classical complement pathway recognition subcomponent C1q.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2011.39

Systemic lupus erythematosus, complement deficiency, and apoptosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2011.39

C1q, autoimmunity and apoptosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2011.39

Role of surfactant proteins A, D, and C1q in the clearance of apoptotic cells in vivo and in vitro: calreticulin and CD91 as a common collectin receptor complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2011.39

Complement deficiencies and systemic lupus erythematosus

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2011.39

Clinical variability and characteristic autoantibody profile in primary C1q complement deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2011.39

Molecular basis of hereditary C1q deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2011.39

Molecular basis of a new type of C1q-deficiency associated with a non-functional low molecular weight (LMW) C1q: parallels and differences to other known genetic C1q-defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2011.39

Hereditary C1q deficiency and secondary Sjögren's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2011.39

Multiple identification of a particular type of hereditary C1q deficiency in the Turkish population: review of the cases and additional genetic and functional analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2011.39

Molecular basis of hereditary C1q deficiency associated with SLE and IgA nephropathy in a Turkish family

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2011.39

Homozygous hereditary C1q deficiency and systemic lupus erythematosus. A new family and the molecular basis of C1q deficiency in three families

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2011.39

SLE with C1q deficiency treated with fresh frozen plasma: a 10-year experience

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2011.39

Molecular, genetic and epidemiologic studies on selective complete C1q deficiency in Turkey

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2011.39

C1q deficiency and autoimmunity: the effects of genetic background on disease expression.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2011.39

Pediatric systemic lupus erythematosus with C1q deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2011.39

C1q: structure, function, and receptors

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2011.39

7 January 2021

C1q inhibits immune complex-induced interferon-alpha production in plasmacytoid dendritic cells: a novel link between C1q deficiency and systemic lupus erythematosus pathogenesis

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2011.39

7 January 2021

Direct binding of C1q to apoptotic cells and cell blebs induces complement activation

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2011.39

7 January 2021

A homozygous point mutation results in a stop codon in the C1q B-chain of a C1q-deficient individual

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2011.39

7 January 2021

Complement C1q and C8 deficiency in an individual with recurrent bacterial meningitis and adult-onset systemic lupus erythematosus-like illness

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2011.39

7 January 2021

PCR-RFLP genotyping of C1q mutations and single nucleotide polymorphisms in Malaysian patients with systemic lupus erythematosus

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2011.39

7 January 2021

C1q deficiency in an Inuit family: Identification of a new class of C1q disease-causing mutations

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2011.39

7 January 2021

C1q and systemic lupus erythematosus

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2011.39

7 January 2021

Systemic lupus erythematosus with C1q deficiency

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2011.39

7 January 2021

Extensive ulcerations due to pyoderma gangrenosum in a child with juvenile systemic lupus erythematosus and C1q deficiency.

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2011.39

7 January 2021

Identifiers

DOI

10.1038/GENE.2011.39

1 reference

24 August 2017

1 reference