(Q92154147)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31341277%20AND%20SRC:MED&resulttype=core&format=json

27 April 2020

title

A mutation-independent approach for muscular dystrophy via upregulation of a modifier gene (English)

1 reference

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27 April 2020

1 reference

1

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27 April 2020

author name string

Prabhpreet S Bassi

2

1 reference

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27 April 2020

Steven Erwood

3

1 reference

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27 April 2020

Dhekra Al-Basha

4

1 reference

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27 April 2020

Kinga I Gawlik

5

1 reference

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27 April 2020

Kyle Lindsay

6

1 reference

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27 April 2020

Elzbieta Hyatt

7

1 reference

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27 April 2020

Rebekah Kember

8

1 reference

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27 April 2020

Kara M Place

9

1 reference

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27 April 2020

Ryan M Marks

10

1 reference

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27 April 2020

Madeleine Durbeej

11

1 reference

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27 April 2020

Steven A Prescott

12

1 reference

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27 April 2020

Evgueni A Ivakine

13

1 reference

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27 April 2020

Ronald D Cohn

14

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27 April 2020

language of work or name

English

0 references

publication date

24 July 2019

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27 April 2020

1 reference

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27 April 2020

volume

572

1 reference

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27 April 2020

issue

7767

1 reference

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27 April 2020

page(s)

125-130

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

27 April 2020

cites work

1 reference

https://api.crossref.org/works/10.1038%2FS41586-019-1430-X

7 January 2021

Correction of a splicing defect in a mouse model of congenital muscular dystrophy type 1A using a homology-directed-repair-independent mechanism

1 reference

https://api.crossref.org/works/10.1038%2FS41586-019-1430-X

7 January 2021

Identification of a novel mutant transcript of laminin alpha 2 chain gene responsible for muscular dystrophy and dysmyelination in dy2J mice

1 reference

https://api.crossref.org/works/10.1038%2FS41586-019-1430-X

7 January 2021

Laminin α1 reduces muscular dystrophy in dy2J mice.

1 reference

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7 January 2021

Laminin alpha1 chain improves laminin alpha2 chain deficient peripheral neuropathy

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7 January 2021

CRISPR RNA-guided activation of endogenous human genes

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7 January 2021

RNA-guided gene activation by CRISPR-Cas9-based transcription factors

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7 January 2021

Spell Checking Nature: Versatility of CRISPR/Cas9 for Developing Treatments for Inherited Disorders

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7 January 2021

In vivo genome editing using Staphylococcus aureus Cas9

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7 January 2021

Increased polyamines as protective disease modifiers in Congenital Muscular Dystrophy.

1 reference

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7 January 2021

Diagnostic approach to the congenital muscular dystrophies

1 reference

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FS41586-019-1430-X

7 January 2021

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

1 reference

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7 January 2021

A single point mutation in the LN domain of LAMA2 causes muscular dystrophy and peripheral amyelination

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7 January 2021

Expression of laminin receptors in schwann cell differentiation: evidence for distinct roles.

1 reference

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7 January 2021

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

1 reference

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FS41586-019-1430-X

7 January 2021

Chimeric protein repair of laminin polymerization ameliorates muscular dystrophy phenotype.

1 reference

https://api.crossref.org/works/10.1038%2FS41586-019-1430-X

7 January 2021

Laminin-111 protein therapy prevents muscle disease in the mdx mouse model for Duchenne muscular dystrophy

1 reference

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7 January 2021

Increased Expression of Laminin Subunit Alpha 1 Chain by dCas9-VP160.

1 reference

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7 January 2021

Genetic Modulation of RNA Splicing with a CRISPR-Guided Cytidine Deaminase

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7 January 2021

Treatment of a metabolic liver disease by in vivo genome base editing in adult mice

1 reference

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7 January 2021

Muscle-specific CRISPR/Cas9 dystrophin gene editing ameliorates pathophysiology in a mouse model for Duchenne muscular dystrophy

1 reference

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7 January 2021

In Vivo Target Gene Activation via CRISPR/Cas9-Mediated Trans-epigenetic Modulation.

1 reference

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7 January 2021

Highly specific epigenome editing by CRISPR-Cas9 repressors for silencing of distal regulatory elements

1 reference

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7 January 2021

Notch1 signaling plays a role in regulating precursor differentiation during CNS remyelination.

1 reference

https://api.crossref.org/works/10.1038%2FS41586-019-1430-X

7 January 2021

A Five-Repeat Micro-Dystrophin Gene Ameliorated Dystrophic Phenotype in the Severe DBA/2J-mdx Model of Duchenne Muscular Dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FS41586-019-1430-X

7 January 2021

10.1038/S41586-019-1430-X

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31341277%20AND%20SRC:MED&resulttype=core&format=json

27 April 2020

1 reference