Amelioration of Muscle and Nerve Pathology in LAMA2 Muscular Dystrophy by AAV9-Mini-Agrin. (Q54210538)

26 May 2018

title

Amelioration of Muscle and Nerve Pathology in LAMA2 Muscular Dystrophy by AAV9-Mini-Agrin. (English)

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26 May 2018

1 reference

Chunping Qiao

1

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26 May 2018

Yi Dai

2

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26 May 2018

Viktoriya D Nikolova

3

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26 May 2018

Quan Jin

4

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26 May 2018

Jianbin Li

5

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26 May 2018

Bin Xiao

6

1 reference

26 May 2018

Juan Li

7

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26 May 2018

Sheryl S Moy

8

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26 May 2018

Xiao Xiao

9

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26 May 2018

publication date

31 January 2018

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26 May 2018

Molecular Therapy. Methods & Clinical Development

published in

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26 May 2018

volume

9

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26 May 2018

page(s)

47-56

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26 May 2018

Chimeric protein repair of laminin polymerization ameliorates muscular dystrophy phenotype.

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Angiotensin II type 1 receptor antagonists alleviate muscle pathology in the mouse model for laminin-α2-deficient congenital muscular dystrophy (MDC1A)

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Peripheral nerve pathology, including aberrant Schwann cell differentiation, is ameliorated by doxycycline in a laminin-α2-deficient mouse model of congenital muscular dystrophy.

26 May 2018

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26 May 2018

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Omigapil ameliorates the pathology of muscle dystrophy caused by laminin-alpha2 deficiency

26 May 2018

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26 May 2018

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Construction and analysis of compact muscle-specific promoters for AAV vectors

26 May 2018

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A simple protocol for paraffin-embedded myelin sheath staining with osmium tetroxide for light microscope observation

26 May 2018

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The zebrafish candyfloss mutant implicates extracellular matrix adhesion failure in laminin alpha2-deficient congenital muscular dystrophy

26 May 2018

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Laminin alpha1 chain improves laminin alpha2 chain deficient peripheral neuropathy

26 May 2018

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Robust systemic transduction with AAV9 vectors in mice: efficient global cardiac gene transfer superior to that of AAV8.

26 May 2018

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Laminin {alpha}1 chain corrects male infertility caused by absence of laminin {alpha}2 chain

26 May 2018

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Amelioration of laminin-alpha2-deficient congenital muscular dystrophy by somatic gene transfer of miniagrin

26 May 2018

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Overexpression of mini-agrin in skeletal muscle increases muscle integrity and regenerative capacity in laminin-alpha2-deficient mice.

26 May 2018

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Inhibition of apoptosis improves outcome in a model of congenital muscular dystrophy

26 May 2018

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The use of lead citrate at high pH as an electron-opaque stain in electron microscopy

26 May 2018

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Novel adeno-associated viruses from rhesus monkeys as vectors for human gene therapy

26 May 2018

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An agrin minigene rescues dystrophic symptoms in a mouse model for congenital muscular dystrophy.

26 May 2018

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A novel laminin alpha2 isoform in severe laminin alpha2 deficient congenital muscular dystrophy

26 May 2018

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26 May 2018

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26 May 2018

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Merosin-deficient congenital muscular dystrophy. Partial genetic correction in two mouse models

26 May 2018

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26 May 2018

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Membrane organization of the dystrophin-glycoprotein complex

26 May 2018

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Linker proteins restore basement membrane and correct LAMA2-related muscular dystrophy in mice.

26 May 2018

1 reference

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The extracellular matrix protein agrin promotes heart regeneration in mice

13 August 2018

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Limb girdle muscular dystrophy due to LAMA2 mutations: diagnostic difficulties due to associated peripheral neuropathy

13 August 2018

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Functional priorities in daily life for children and young people with dystonic movement disorders and their families.

13 August 2018

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Proteasome inhibition improves the muscle of laminin α2 chain-deficient mice.

13 August 2018

1 reference

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High AAV vector purity results in serotype- and tissue-independent enhancement of transduction efficiency

13 August 2018

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Congenital muscular dystrophy: mini-agrin delivers in mice

13 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=8638311

Laminin alpha1 chain reduces muscular dystrophy in laminin alpha2 chain deficient mice

13 August 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=8638311

Is there selection in favour of heterozygotes in families with merosin-deficient congenital muscular dystrophy?

13 August 2018

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12 December 2020

Laminin alpha 2 (merosin)-deficient muscular dystrophy and demyelinating neuropathy in two cats

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12 December 2020

The muscular dystrophies

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12 December 2020

Merosin-deficient congenital muscular dystrophy, autosomal recessive (MDC1A, MIM#156225, LAMA2 gene coding for alpha2 chain of laminin)

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12 December 2020

Laminin α2 deficiency and muscular dystrophy; genotype-phenotype correlation in mutant mice

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12 December 2020

Muscle-specific BCL2 expression ameliorates muscle disease in laminin {alpha}2-deficient, but not in dystrophin-deficient, mice

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12 December 2020

Genotype–phenotype correlation in a large population of muscular dystrophy patients with LAMA2 mutations

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12 December 2020

Evidence-based guideline summary: Evaluation, diagnosis, and management of congenital muscular dystrophy: Report of the Guideline Development Subcommittee of the American Academy of Neurology and the Practice Issues Review Panel of the American Asso

1 reference

12 December 2020

10.1016/J.OMTM.2018.01.005

Identifiers

DOI

1 reference

26 May 2018

PMC publication ID

8638311

1 reference

26 May 2018

PubMed publication ID

29766020

1 reference

26 May 2018