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Editorial: Calcium homeostasis in skeletal muscle function, plasticity and disease, Volume II

Frontiers in physiology, 2023-01, Vol.14, p.1130073-1130073

2023

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Tissue-specific expression of TRP channel genes in the mouse and its variation in three different mouse strains

BMC genomics, 2006-06, Vol.7 (1), p.159-159, Article 159

2006

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Editorial: Calcium Homeostasis in Skeletal Muscle Function, Plasticity, and Disease

Frontiers in physiology, 2021-03, Vol.12, p.671292-671292

2021

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Congenital muscle dystrophy and diet consistency affect mouse skull shape differently

Journal of anatomy, 2017-11, Vol.231 (5), p.736-748

2017

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Proteomic profiling of the dystrophin complex and membrane fraction from dystrophic mdx muscle reveals decreases in the cytolinker desmoglein and increases in the extracellular matrix stabilizers biglycan and fibronectin

Journal of muscle research and cell motility, 2017-04, Vol.38 (2), p.251-268

2017

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Calcium Ion in Skeletal Muscle: Its Crucial Role for Muscle Function, Plasticity, and Disease

Physiological reviews, 2000-07, Vol.80 (3), p.1215-1265

2000

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Cardiac and Respiratory Dysfunction in Duchenne Muscular Dystrophy and the Role of Second Messengers

Medicinal research reviews, 2013-09, Vol.33 (5), p.1174-1213

2013

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50 years to diagnosis: Autosomal dominant tubular aggregate myopathy caused by a novel STIM1 mutation

Neuromuscular disorders : NMD, 2015-07, Vol.25 (7), p.577-584

2015

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Comparative proteomic profiling of soleus, extensor digitorum longus, flexor digitorum brevis and interosseus muscles from the mdx mouse model of Duchenne muscular dystrophy

International journal of molecular medicine, 2013-09, Vol.32 (3), p.544-556

2013

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Activation of serum/glucocorticoid‐induced kinase 1 (SGK1) is important to maintain skeletal muscle homeostasis and prevent atrophy

EMBO molecular medicine, 2013-01, Vol.5 (1), p.80-91

2013

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Long‐term human IgG treatment improves heart and muscle function in a mouse model of Duchenne muscular dystrophy

Journal of cachexia, sarcopenia and muscle, 2020-08, Vol.11 (4), p.1018-1031

2020

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Transient receptor potential cation channels in normal and dystrophic mdx muscle

Neuromuscular disorders : NMD, 2008-06, Vol.18 (6), p.501-513

2008

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Chaperoning heat shock proteins: Proteomic analysis and relevance for normal and dystrophin-deficient muscle

Proteomics. Clinical applications, 2014-12, Vol.8 (11-12), p.875-895

2014

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Immunoblot Analysis of DIGE-Based Proteomics

Methods in molecular biology (Clifton, N.J.), 2018, Vol.1664, p.287

2018

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Long-Term Blocking of Calcium Channels in mdx Mice Results in Differential Effects on Heart and Skeletal Muscle

The American journal of pathology, 2011, Vol.178 (1), p.273-283

2011

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TRP channels in skeletal muscle: gene expression, function and implications for disease

Advances in experimental medicine and biology, 2011, Vol.704, p.749

Brinkmeier, Heinrich

2011

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Methocarbamol blocks muscular Nav1.4 channels and decreases isometric force of mouse muscles

Muscle & nerve, 2021-01, Vol.63 (1), p.141-150

2021

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Functional TRPV4 channels are expressed in mouse skeletal muscle and can modulate resting Ca2+ influx and muscle fatigue

Pflügers Archiv, 2011-01, Vol.461 (1), p.115-122

2011

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Anti-GM1 antibodies can block neuronal voltage-gated sodium channels

Muscle & nerve, 2000-09, Vol.23 (9), p.1414-1420

2000

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Methocarbamol blocks muscular Na v 1.4 channels and decreases isometric force of mouse muscles

Muscle & nerve, 2021-01, Vol.63 (1), p.141-150

2021

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Impaired muscle spindle function in murine models of muscular dystrophy

The Journal of physiology, 2020-04, Vol.598 (8), p.1591-1609

2020

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Functional Expression of TRPC6 and TRPV4 Channels in Mouse Skeletal Muscle Fibers

Biophysical journal, 2015-01, Vol.108 (2), p.282a-282a

2015

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The Spider Toxin GsMTx-4 Blocks TRPV4 Cation Channels Expressed in HEK-293 Cells

Biophysical journal, 2015-01, Vol.108 (2), p.126a-126a

2015

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Treatment with human immunoglobulin G improves the early disease course in a mouse model of Duchenne muscular dystrophy

Journal of neurochemistry, 2016-01, Vol.136 (2), p.351-362

2016

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TRPC3 Channel Blockers but not TRPC6 Blockers Inhibit Background Calcium Influx and Modulate Calcium Transients in Mouse Muscle Fibers

Biophysical journal, 2012-01, Vol.102 (3), p.534a-534a

2012

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Editorial: Calcium homeostasis in skeletal muscle function, plasticity and disease, Volume II

Tissue-specific expression of TRP channel genes in the mouse and its variation in three different mouse strains

Editorial: Calcium Homeostasis in Skeletal Muscle Function, Plasticity, and Disease

Congenital muscle dystrophy and diet consistency affect mouse skull shape differently

Proteomic profiling of the dystrophin complex and membrane fraction from dystrophic mdx muscle reveals decreases in the cytolinker desmoglein and increases in the extracellular matrix stabilizers biglycan and fibronectin

Calcium Ion in Skeletal Muscle: Its Crucial Role for Muscle Function, Plasticity, and Disease

Cardiac and Respiratory Dysfunction in Duchenne Muscular Dystrophy and the Role of Second Messengers

50 years to diagnosis: Autosomal dominant tubular aggregate myopathy caused by a novel STIM1 mutation

Comparative proteomic profiling of soleus, extensor digitorum longus, flexor digitorum brevis and interosseus muscles from the mdx mouse model of Duchenne muscular dystrophy

Activation of serum/glucocorticoid‐induced kinase 1 (SGK1) is important to maintain skeletal muscle homeostasis and prevent atrophy

Long‐term human IgG treatment improves heart and muscle function in a mouse model of Duchenne muscular dystrophy

Transient receptor potential cation channels in normal and dystrophic mdx muscle

Chaperoning heat shock proteins: Proteomic analysis and relevance for normal and dystrophin-deficient muscle

Immunoblot Analysis of DIGE-Based Proteomics

Long-Term Blocking of Calcium Channels in mdx Mice Results in Differential Effects on Heart and Skeletal Muscle

TRP channels in skeletal muscle: gene expression, function and implications for disease

Methocarbamol blocks muscular Nav1.4 channels and decreases isometric force of mouse muscles

Functional TRPV4 channels are expressed in mouse skeletal muscle and can modulate resting Ca2+ influx and muscle fatigue

Anti-GM1 antibodies can block neuronal voltage-gated sodium channels

Methocarbamol blocks muscular Na v 1.4 channels and decreases isometric force of mouse muscles

Impaired muscle spindle function in murine models of muscular dystrophy

Functional Expression of TRPC6 and TRPV4 Channels in Mouse Skeletal Muscle Fibers

The Spider Toxin GsMTx-4 Blocks TRPV4 Cation Channels Expressed in HEK-293 Cells

Treatment with human immunoglobulin G improves the early disease course in a mouse model of Duchenne muscular dystrophy

TRPC3 Channel Blockers but not TRPC6 Blockers Inhibit Background Calcium Influx and Modulate Calcium Transients in Mouse Muscle Fibers

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