Genetic ablation of complement C3 attenuates muscle pathology in dysferlin-deficient mice (Q34360151)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21060153%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

title

Genetic ablation of complement C3 attenuates muscle pathology in dysferlin-deficient mice (English)

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16 January 2020

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16 January 2020

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16 January 2020

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16 January 2020

Ellie M Frett

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16 January 2020

Jennifer R Levy

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16 January 2020

Erik P Rader

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16 January 2020

John D Lueck

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16 January 2020

Dimple Bansal

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16 January 2020

Rainer Ng

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16 January 2020

Daniel Beltrán-Valero de Bernabé

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16 January 2020

John A Faulkner

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16 January 2020

language of work or name

English

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publication date

8 November 2010

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Journal of Clinical Investigation

16 January 2020

published in

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16 January 2020

volume

120

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16 January 2020

issue

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16 January 2020

page(s)

4366-4374

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Inflammasome up-regulation and activation in dysferlin-deficient skeletal muscle

16 January 2020

cites work

1 reference

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Extensive mononuclear infiltration and myogenesis characterize recovery of dysferlin-null skeletal muscle from contraction-induced injuries

6 July 2018

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Dysferlin deficiency and the development of cardiomyopathy in a mouse model of limb-girdle muscular dystrophy 2B.

6 July 2018

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Genetic manipulation of dysferlin expression in skeletal muscle: novel insights into muscular dystrophy

6 July 2018

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Basal lamina strengthens cell membrane integrity via the laminin G domain-binding motif of alpha-dystroglycan

6 July 2018

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Suicidal membrane repair regulates phosphatidylserine externalization during apoptosis

6 July 2018

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New aspects on patients affected by dysferlin deficient muscular dystrophy

6 July 2018

1 reference

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Membrane repair defects in muscular dystrophy are linked to altered interaction between MG53, caveolin-3, and dysferlin

6 July 2018

1 reference

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Attenuated muscle regeneration is a key factor in dysferlin-deficient muscular dystrophy

6 July 2018

1 reference

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Sarcolemma-localized nNOS is required to maintain activity after mild exercise

6 July 2018

1 reference

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Impaired recovery of dysferlin-null skeletal muscle after contraction-induced injury in vivo

6 July 2018

1 reference

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Dysferlin deficiency enhances monocyte phagocytosis: a model for the inflammatory onset of limb-girdle muscular dystrophy 2B.

6 July 2018

1 reference

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C1q binds phosphatidylserine and likely acts as a multiligand-bridging molecule in apoptotic cell recognition

6 July 2018

1 reference

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Phenotypic study in 40 patients with dysferlin gene mutations: high frequency of atypical phenotypes

6 July 2018

1 reference

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Proteomic analysis of plasma membrane and secretory vesicles from human neutrophils

6 July 2018

1 reference

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Dysferlin-mediated membrane repair protects the heart from stress-induced left ventricular injury

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2993587

The differential gene expression profiles of proximal and distal muscle groups are altered in pre-pathological dysferlin-deficient mice

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2993587

Expression profiling with progression of dystrophic change in dysferlin-deficient mice (SJL).

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2993587

Ultrastructural changes in dysferlinopathy support defective membrane repair mechanism

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2993587

Muscle inflammation and MHC class I up-regulation in muscular dystrophy with lack of dysferlin: an immunopathological study

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2993587

Dysferlin Interacts with Annexins A1 and A2 and Mediates Sarcolemmal Wound-healing

6 July 2018

1 reference

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Impaired membrane resealing and autoimmune myositis in synaptotagmin VII-deficient mice

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2993587

Defective membrane repair in dysferlin-deficient muscular dystrophy

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2993587

Gene expression profiling in dysferlinopathies using a dedicated muscle microarray.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2993587

Release of chromatin protein HMGB1 by necrotic cells triggers inflammation

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2993587

Heat shock protein 70 is a potent activator of the human complement system.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2993587

Plasma membrane repair is mediated by Ca(2+)-regulated exocytosis of lysosomes

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2993587

Distal anterior compartment myopathy: a dysferlin mutation causing a new muscular dystrophy phenotype

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2993587

Dysferlin is a plasma membrane protein and is expressed early in human development

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2993587

6 July 2018

1 reference

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Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2993587

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2993587

Contractile properties of skeletal muscles from young, adult and aged mice

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2993587

Complement membrane attack on nucleated cells: resistance, recovery and non-lethal effects

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2993587

Experimental autoimmune encephalomyelitis in mice: immunologic response to mouse spinal cord and myelin basic proteins

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2993587

The susceptibility to experimental autoimmune encephalomyelitis is not related to dysferlin-deficiency

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2993587

Insufficient membrane fusion in dysferlin-deficient muscle fibers after heavy-ion irradiation.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2993587

Lipid raft proteome of the human neutrophil azurophil granule

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2993587

Histological and immunohistological changes of the skeletal muscles in older SJL/J mice.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2993587

Absence of dysferlin alters myogenin expression and delays human muscle differentiation "in vitro".

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2993587

Increased susceptibility to complement attack due to down-regulation of decay-accelerating factor/CD55 in dysferlin-deficient muscular dystrophy.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2993587

Clinical heterogeneity in dysferlinopathy

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2993587

Inflammation in dysferlin myopathy: immunohistochemical characterization of 13 patients.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2993587

Dysferlinopathy (LGMD2B): a 23-year follow-up study of 10 patients homozygous for the same frameshifting dysferlin mutations.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2993587

Necrotic but not apoptotic cell death releases heat shock proteins, which deliver a partial maturation signal to dendritic cells and activate the NF-kappa B pathway

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2993587

Late onset in dysferlinopathy widens the clinical spectrum

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2993587

Dysferlin expression in monocytes: A source of mRNA for mutation analysis

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2993587

Dysferlin deletion in SJL mice (SJL-Dysf) defines a natural model for limb girdle muscular dystrophy 2B

9 December 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2993587

Muscle inflammation, autoimmune Addison's disease and sarcoidosis in a patient with dysferlin deficiency

9 December 2018

1 reference

12 December 2020

Experimental autoimmune myositis in SJL/J mice

1 reference

12 December 2020

A novel, blood-based diagnostic assay for limb girdle muscular dystrophy 2B and miyoshi myopathy

1 reference

12 December 2020

[A patient with limb girdle muscular dystrophy type 2B (LGMD2B) manifesting cardiomyopathy]

1 reference

12 December 2020

Tibialis anterior muscles in mdx mice are highly susceptible to contraction-induced injury

1 reference

12 December 2020

The molecular basis of muscular dystrophy in the mdx mouse: a point mutation

1 reference

12 December 2020

Muscle pathology in dysferlin deficiency

1 reference

12 December 2020

Identifiers

DOI

10.1172/JCI42390

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21060153%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21060153%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

PubMed publication ID

21060153

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21060153%20AND%20SRC:MED&resulttype=core&format=json