Proteasome inhibition improves the muscle of laminin α2 chain-deficient mice. (Q54401460)

29 May 2018

title

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

1 reference

29 May 2018

author name string

Virginie Carmignac

series ordinal

1 reference

29 May 2018

Ronan Quéré

series ordinal

1 reference

29 May 2018

Madeleine Durbeej

series ordinal

1 reference

29 May 2018

publication date

17 November 2010

1 reference

29 May 2018

published in

Human Molecular Genetics

1 reference

29 May 2018

volume

1 reference

29 May 2018

issue

1 reference

29 May 2018

page(s)

541-552

1 reference

29 May 2018

Identification of ubiquitin ligases required for skeletal muscle atrophy

cites work

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ499

Atrogin-1, a muscle-specific F-box protein highly expressed during muscle atrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ499

Akt/mTOR pathway is a crucial regulator of skeletal muscle hypertrophy and can prevent muscle atrophy in vivo

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ499

A protein kinase B-dependent and rapamycin-sensitive pathway controls skeletal muscle growth but not fiber type specification

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ499

Selective control of skeletal muscle differentiation by Akt1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ499

Foxo transcription factors induce the atrophy-related ubiquitin ligase atrogin-1 and cause skeletal muscle atrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ499

IKKbeta/NF-kappaB activation causes severe muscle wasting in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ499

Laminin alpha2 chain-null mutant mice by targeted disruption of the Lama2 gene: a new model of merosin (laminin 2)-deficient congenital muscular dystrophy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ499

Schwann cell myelination occurred without basal lamina formation in laminin alpha2 chain-null mutant (dy3K/dy3K) mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ499

Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ499

H36-alpha 7 is a novel integrin alpha chain that is developmentally regulated during skeletal myogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ499

Dystrophin glycoprotein complex-associated Gbetagamma subunits activate phosphatidylinositol-3-kinase/Akt signaling in skeletal muscle in a laminin-dependent manner

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ499

Alpha7beta1-integrin regulates mechanotransduction and prevents skeletal muscle injury

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ499

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ499

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ499

Proteasome inhibitor (MG-132) treatment of mdx mice rescues the expression and membrane localization of dystrophin and dystrophin-associated proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ499

Pharmacological rescue of the dystrophin-glycoprotein complex in Duchenne and Becker skeletal muscle explants by proteasome inhibitor treatment

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ499

Effect of calpain and proteasome inhibition on Ca2+-dependent proteolysis and muscle histopathology in the mdx mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ499

Laminin alpha1 chain improves laminin alpha2 chain deficient peripheral neuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ499

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ499

Transgenic overexpression of laminin alpha1 chain in laminin alpha2 chain-deficient mice rescues the disease throughout the lifespan

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ499

FoxO3 controls autophagy in skeletal muscle in vivo

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ499

Downstream of Akt: FoxO3 and mTOR in the regulation of autophagy in skeletal muscle

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ499

PGC-1alpha protects skeletal muscle from atrophy by suppressing FoxO3 action and atrophy-specific gene transcription

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ499

The activation of Akt/PKB signaling pathway and cell survival.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ499

Involvement of Hsp90 in signaling and stability of 3-phosphoinositide-dependent kinase-1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ499

Modulation of Akt kinase activity by binding to Hsp90

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ499

Hsp90 functions to balance the phosphorylation state of Akt during C2C12 myoblast differentiation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ499

Expression of laminin alpha1, alpha2, alpha4, and alpha5 chains, fibronectin, and tenascin-C in skeletal muscle of dystrophic 129ReJ dy/dy mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ499

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ499

Distribution and function of laminins in the neuromuscular system of developing, adult, and mutant mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ499

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ499

Linker molecules between laminins and dystroglycan ameliorate laminin-alpha2-deficient muscular dystrophy at all disease stages

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ499

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ499

Pathology is alleviated by doxycycline in a laminin-alpha2-null model of congenital muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ499

Inhibition of dystroglycan binding to laminin disrupts the PI3K/AKT pathway and survival signaling in muscle cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ499

Merosin-integrin promotion of skeletal myofiber cell survival: Differentiation state-distinct involvement of p60Fyn tyrosine kinase and p38alpha stress-activated MAP kinase

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ499

Muscle-specific RING finger 1 is a bona fide ubiquitin ligase that degrades cardiac troponin I

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ499

The E3 Ligase MuRF1 degrades myosin heavy chain protein in dexamethasone-treated skeletal muscle

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ499

Mechanisms of skeletal muscle atrophy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ499

Distinct roles for laminin globular domains in laminin alpha1 chain mediated rescue of murine laminin alpha2 chain deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ499

Cardiac ankyrin repeat protein is a marker of skeletal muscle pathological remodelling

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ499

21 January 2018

Identifiers

DOI

10.1093/HMG/DDQ499

1 reference

29 May 2018

1 reference

29 May 2018