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1.
Loss of α-actinin-3 confers protection from eccentric contraction damage in fast-twitch EDL muscles from aged mdx dystrophic mice by reducing pathological fibre branching.
Hum Mol Genet
; 31(9): 1417-1429, 2022 05 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-34761268
2.
Calcium and strontium contractile activation properties of single skinned skeletal muscle fibres from elderly women 66-90 years of age.
J Muscle Res Cell Motil
; 43(4): 173-183, 2022 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-35987933
3.
Sarcoplasmic reticulum calcium handling in unbranched, immediately post-necrotic fast-twitch mdx fibres is similar to wild-type littermates.
Exp Physiol
; 107(6): 601-614, 2022 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-35471703
4.
Dystrophin-negative slow-twitch soleus muscles are not susceptible to eccentric contraction induced injury over the lifespan of the mdx mouse.
Am J Physiol Cell Physiol
; 321(4): C704-C720, 2021 10 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-34432537
5.
The Effect of ACTN3 Gene Doping on Skeletal Muscle Performance.
Am J Hum Genet
; 102(5): 845-857, 2018 05 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-29706347
6.
Branched fibers from old fast-twitch dystrophic muscles are the sites of terminal damage in muscular dystrophy.
Am J Physiol Cell Physiol
; 314(6): C662-C674, 2018 06 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-29412689
7.
Analysis of the ACTN3 heterozygous genotype suggests that α-actinin-3 controls sarcomeric composition and muscle function in a dose-dependent fashion.
Hum Mol Genet
; 25(5): 866-77, 2016 Mar 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-26681802
8.
Altered Ca2+ kinetics associated with α-actinin-3 deficiency may explain positive selection for ACTN3 null allele in human evolution.
PLoS Genet
; 11(2): e1004862, 2015.
Artículo
en Inglés
| MEDLINE | ID: mdl-25590636
9.
Deficiency of α-actinin-3 is associated with increased susceptibility to contraction-induced damage and skeletal muscle remodeling.
Hum Mol Genet
; 20(15): 2914-27, 2011 Aug 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-21536590
10.
Assessment of Cell Viability in Electrically Excitable Muscle Cells Through Intact Twitch Stimulation.
Methods Mol Biol
; 2644: 177-192, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-37142922
11.
Six weeks of N-acetylcysteine antioxidant in drinking water decreases pathological fiber branching in MDX mouse dystrophic fast-twitch skeletal muscle.
Front Physiol
; 14: 1109587, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-36866174
12.
Antioxidant therapy in a mouse model of Duchenne muscular dystrophy: some promising results but with a weighty caveat.
J Physiol
; 595(23): 7015, 2017 12 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-29034480
13.
Absence of the Z-disc protein α-actinin-3 impairs the mechanical stability of Actn3KO mouse fast-twitch muscle fibres without altering their contractile properties or twitch kinetics.
Skelet Muscle
; 12(1): 14, 2022 06 23.
Artículo
en Inglés
| MEDLINE | ID: mdl-35733150
14.
Properties of extensor digitorum longus muscle and skinned fibers from adult and aged male and female Actn3 knockout mice.
Muscle Nerve
; 43(1): 37-48, 2011 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-20886650
15.
Acute inhibitory effects of clenbuterol on force, Ca²âº transients and action potentials in rat soleus may not involve the ß2-adrenoceptor pathway.
Clin Exp Pharmacol Physiol
; 38(9): 638-46, 2011 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-21752065
16.
Minocycline Treatment Reduces Mass and Force Output From Fast-Twitch Mouse Muscles and Inhibits Myosin Production in C2C12 Myotubes.
Front Physiol
; 12: 696039, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-34290621
17.
Lifespan Analysis of Dystrophic mdx Fast-Twitch Muscle Morphology and Its Impact on Contractile Function.
Front Physiol
; 12: 771499, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-34950049
18.
An Actn3 knockout mouse provides mechanistic insights into the association between alpha-actinin-3 deficiency and human athletic performance.
Hum Mol Genet
; 17(8): 1076-86, 2008 Apr 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-18178581
19.
Branched fibres in old dystrophic mdx muscle are associated with mechanical weakening of the sarcolemma, abnormal Ca2+ transients and a breakdown of Ca2+ homeostasis during fatigue.
Exp Physiol
; 95(5): 641-56, 2010 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-20139167
20.
Enhanced homosynaptic LTD in cerebellar Purkinje cells of the dystrophic MDX mouse.
Muscle Nerve
; 41(3): 329-34, 2010 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-19722255