(Q46588754)

23 December 2017

title

Deficiency of alpha-sarcoglycan differently affects fast- and slow-twitch skeletal muscles (English)

1 reference

23 December 2017

author name string

Daniela Danieli-Betto

1

1 reference

23 December 2017

Alessandra Esposito

2

1 reference

23 December 2017

Elena Germinario

3

1 reference

23 December 2017

Dorianna Sandonà

4

1 reference

23 December 2017

Tiziana Martinello

5

1 reference

23 December 2017

Anna Jakubiec-Puka

6

1 reference

23 December 2017

Donatella Biral

7

1 reference

23 December 2017

Romeo Betto

8

1 reference

23 December 2017

publication date

7 July 2005

1 reference

23 December 2017

American Journal of Physiology - Regulatory, Integrative and Comparative Physiology

published in

1 reference

23 December 2017

volume

289

1 reference

23 December 2017

issue

5

1 reference

23 December 2017

page(s)

R1328-37

1 reference

23 December 2017

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

cites work

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00673.2004

Function and genetics of dystrophin and dystrophin-related proteins in muscle

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00673.2004

Beta-sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00673.2004

Loss of sarcolemma nNOS in sarcoglycan-deficient muscle.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00673.2004

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00673.2004

Calcium sensitivity and myofibrillar protein isoforms of rat skinned skeletal muscle fibres.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00673.2004

Alteration of excitation-contraction coupling mechanism in extensor digitorum longus muscle fibres of dystrophic mdx mouse and potential efficacy of taurine

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00673.2004

Sarcoplasmic reticulum function in slow- and fast-twitch skeletal muscles from mdx mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00673.2004

Progressive muscular dystrophy in alpha-sarcoglycan-deficient mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00673.2004

Muscular dystrophies involving the dystrophin-glycoprotein complex: an overview of current mouse models.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00673.2004

Disruption of the beta-sarcoglycan gene reveals pathogenetic complexity of limb-girdle muscular dystrophy type 2E

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00673.2004

Actions of caffeine on fast- and slow-twitch muscles of the rat.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00673.2004

Effects of modulators of sarcoplasmic Ca2+ release on the development of skeletal muscle fatigue

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00673.2004

Early changes of type 2B fibers after denervation of rat EDL skeletal muscle

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00673.2004

Membrane abnormalities and Ca homeostasis in muscles of the mdx mouse, an animal model of the Duchenne muscular dystrophy: a review

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00673.2004

Muscle degeneration without mechanical injury in sarcoglycan deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00673.2004

Sarcoglycans in muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00673.2004

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00673.2004

Functional rescue of the sarcoglycan complex in the BIO 14.6 hamster using delta-sarcoglycan gene transfer

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00673.2004

Alpha1-syntrophin-deficient skeletal muscle exhibits hypertrophy and aberrant formation of neuromuscular junctions during regeneration.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00673.2004

The sarcoglycan complex in limb-girdle muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00673.2004

Sarcoglycan isoforms in skeletal muscle

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00673.2004

Dystrophin-glycoprotein complex: post-translational processing and dystroglycan function.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00673.2004

Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00673.2004

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00673.2004

Mechanical function of dystrophin in muscle cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00673.2004

Altered muscle force and stiffness of skeletal muscles in alpha-sarcoglycan-deficient mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00673.2004

Dystrophin protects the sarcolemma from stresses developed during muscle contraction

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00673.2004

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00673.2004

Contractile properties and susceptibility to exercise-induced damage of normal and mdx mouse tibialis anterior muscle

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00673.2004

Cell Therapy of -Sarcoglycan Null Dystrophic Mice Through Intra-Arterial Delivery of Mesoangioblasts

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00673.2004

Characterization of the ATP-hydrolysing activity of alpha-sarcoglycan

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00673.2004

Muscular dystrophies and the dystrophin-glycoprotein complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00673.2004

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00673.2004

Isometric contractile properties and caffeine sensitivity of the diaphragm, EDL and soleus in the mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00673.2004

Consequences of thyroxine treatment on diaphragm and EDL of normal and dystrophic hamsters

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00673.2004

Electrophoretic separation of rat skeletal muscle myosin heavy-chain isoforms.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00673.2004

Filamin 2 (FLN2): A muscle-specific sarcoglycan interacting protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00673.2004

Functional characteristics of dystrophic skeletal muscle: insights from animal models

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00673.2004

Fast muscle fibers are preferentially affected in Duchenne muscular dystrophy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00673.2004

Contractile properties of skinned muscle fibres from young and adult normal and dystrophic (mdx) mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00673.2004

Full functional rescue of a complete muscle (TA) in dystrophic hamsters by adeno-associated virus vector-directed gene therapy

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00673.2004

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00673.2004

Unloaded shortening velocity and myosin heavy chain and alkali light chain isoform composition in rat skeletal muscle fibres

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00673.2004

10.1152/AJPREGU.00673.2004

21 January 2018

Identifiers

DOI

1 reference

23 December 2017

1 reference

23 December 2017