(Q50506362)

14 March 2018

title

Extraocular muscle is spared despite the absence of an intact sarcoglycan complex in gamma- or delta-sarcoglycan-deficient mice. (English)

1 reference

14 March 2018

author name string

Porter JD

1

1 reference

14 March 2018

Merriam AP

2

1 reference

14 March 2018

Hack AA

3

1 reference

14 March 2018

Andrade FH

4

1 reference

14 March 2018

McNally EM

5

1 reference

14 March 2018

publication date

1 March 2001

1 reference

14 March 2018

published in

Neuromuscular Disorders

1 reference

14 March 2018

volume

11

1 reference

14 March 2018

issue

2

1 reference

14 March 2018

page(s)

197-207

1 reference

14 March 2018

Three muscular dystrophies: loss of cytoskeleton-extracellular matrix linkage.

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

From dystrophinopathy to sarcoglycanopathy: evolution of a concept of muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

Dystrophin-glycoprotein complex: its role in the molecular pathogenesis of muscular dystrophies.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

Animal models for muscular dystrophy show different patterns of sarcolemmal disruption.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

Gamma-sarcoglycan deficiency leads to muscle membrane defects and apoptosis independent of dystrophin

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

Genomic screening for beta-sarcoglycan gene mutations: missense mutations may cause severe limb-girdle muscular dystrophy type 2E (LGMD 2E)

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

Mutations in the sarcoglycan genes in patients with myopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

β–sarcoglycan: characterization and role in limb–girdle muscular dystrophy linked to 4q12

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

Identification of the Syrian hamster cardiomyopathy gene.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

Mutations in the dystrophin-associated protein gamma-sarcoglycan in chromosome 13 muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

Muscular dystrophies and the dystrophin-glycoprotein complex

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

Loss of the sarcoglycan complex and sarcospan leads to muscular dystrophy in beta-sarcoglycan-deficient mice

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

Mutational diversity and hot spots in the alpha-sarcoglycan gene in autosomal recessive muscular dystrophy (LGMD2D)

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

Progressive muscular dystrophy in alpha-sarcoglycan-deficient mice

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

Mutations that disrupt the carboxyl-terminus of gamma-sarcoglycan cause muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

Abnormalities in alpha-, beta- and gamma-sarcoglycan in patients with limb-girdle muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

Ca2+-calmodulin binds to the carboxyl-terminal domain of dystrophin

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

Characterization of the tyrosine phosphorylation and distribution of dystrobrevin isoforms

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

Interaction of nitric oxide synthase with the postsynaptic density protein PSD-95 and alpha1-syntrophin mediated by PDZ domains

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

Role for alpha-dystrobrevin in the pathogenesis of dystrophin-dependent muscular dystrophies

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

beta-dystrobrevin, a new member of the dystrophin family. Identification, cloning, and protein associations

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

Specific interactions between the syntrophin PDZ domain and voltage-gated sodium channels

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

The 87K postsynaptic membrane protein from Torpedo is a protein-tyrosine kinase substrate homologous to dystrophin

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

SH3 domain-mediated interaction of dystroglycan and Grb2

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

Ecto-ATPase activity of alpha-sarcoglycan (adhalin)

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

Extraocular muscles are spared in advanced Duchenne dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

Small-caliber skeletal muscle fibers do not suffer deleterious consequences of dystrophic gene expression

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

Small-caliber skeletal muscle fibers do not suffer necrosis in mdx mouse dystrophy.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

Absence of extraocular muscle pathology in Duchenne's muscular dystrophy: role for calcium homeostasis in extraocular muscle sparing

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

Extraocular, limb and diaphragm muscle group-specific antioxidant enzyme activity patterns in control and mdx mice

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

Commentary: extraocular muscle sparing in muscular dystrophy: a critical evaluation of potential protective mechanisms

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

The oculomotor periphery: the clinician's focus is no longer a basic science stepchild

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

Progressive depletion of fast alpha-actinin-positive muscle fibers in Duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

Fast muscle fibers are preferentially affected in Duchenne muscular dystrophy.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

Muscles of a different 'color': the unusual properties of the extraocular muscles may predispose or protect them in neurogenic and myogenic disease

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

Membrane targeting and stabilization of sarcospan is mediated by the sarcoglycan subcomplex

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

Association of dystrophin-related protein with dystrophin-associated proteins in mdx mouse muscle

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

Visualization of dystrophic muscle fibers in mdx mouse by vital staining with Evans blue: evidence of apoptosis in dystrophin-deficient muscle.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

Spatial and temporal patterns of myosin heavy chain expression in developing rat extraocular muscle.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

Visual system maldevelopment disrupts extraocular muscle-specific myosin expression

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

The mdx mouse skeletal muscle myopathy: I. A histological, morphometric and biochemical investigation

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

Fiber regeneration is not persistent in dystrophic (MDX) mouse skeletal muscle

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

Fibres of intermediate type 1C and 2C are found continuously in mdx soleus muscle up to 52 weeks

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

Adaptations in myosin heavy chain expression and contractile function in dystrophic mouse diaphragm

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

Systematic variation in myosin expression along extraocular muscle fibres of the adult rat.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

Integrins (alpha7beta1) in muscle function and survival. Disrupted expression in merosin-deficient congenital muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

Disruption of the sarcoglycan-sarcospan complex in vascular smooth muscle: a novel mechanism for cardiomyopathy and muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

The clinical spectrum of sarcoglycanopathies

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

Morphologic changes in extraocular muscles of the dystrophic hamster

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

Mechanical properties of the isolated inferior oblique muscle of the rabbit

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

Dynamic properties of inferior rectus muscle of the rat

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

Utrophin-dystrophin-deficient mice as a model for Duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

Skeletal and cardiac myopathies in mice lacking utrophin and dystrophin: a model for Duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

Sparing of mdx extraocular muscles from dystrophic pathology is not attributable to normalized concentration or distribution of neuronal nitric oxide synthase

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

Mechanisms of resistance to pathogenesis in muscular dystrophies

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

Dystrophin-associated proteins are greatly reduced in skeletal muscle from mdx mice

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

A PDZ-containing scaffold related to the dystrophin complex at the basolateral membrane of epithelial cells

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

Biochemical evidence for association of dystrobrevin with the sarcoglycan-sarcospan complex as a basis for understanding sarcoglycanopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

Animal models of muscular dystrophy – what can they teach us?

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900171-1

7 January 2021

10.1016/S0960-8966(00)00171-1

Identifiers

DOI

1 reference

14 March 2018

1 reference

14 March 2018