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Redox homeostasis, oxidative stress and disuse muscle atrophy

The Journal of physiology, 2011-05, Vol.589 (9), p.2147-2160

2011

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Skeletal muscle ClC-1 chloride channels in health and diseases

Pflügers Archiv, 2020-07, Vol.472 (7), p.961-975

2020

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Bioisosteric Modification of To042: Synthesis and Evaluation of Promising Use‐Dependent Inhibitors of Voltage‐Gated Sodium Channels

ChemMedChem, 2021-12, Vol.16 (23), p.3588-3599

2021

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The analysis of myotonia congenita mutations discloses functional clusters of amino acids within the CBS2 domain and the C‐terminal peptide of the ClC‐1 channel

Human mutation, 2018-09, Vol.39 (9), p.1273-1283

2018

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Synthesis and Evaluation of Voltage‐Gated Sodium Channel Blocking Pyrroline Derivatives Endowed with Both Antiarrhythmic and Antioxidant Activities

ChemMedChem, 2021-02, Vol.16 (3), p.578-588

2021

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Anti-Angiogenic Activity of Drugs in Multiple Myeloma

Cancers, 2023-03, Vol.15 (7), p.1990

2023

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Immersive and Non-Immersive Virtual Reality for Pain and Anxiety Management in Pediatric Patients with Hematological or Solid Cancer: A Systematic Review

Cancers, 2023-02, Vol.15 (3), p.985

2023

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Emerging Roles for Ion Channels in Ovarian Cancer: Pathomechanisms and Pharmacological Treatment

Cancers, 2021-02, Vol.13 (4), p.668

2021

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Long-Term Safety and Usefulness of Mexiletine in a Large Cohort of Patients Affected by Non-dystrophic Myotonias

Frontiers in neurology, 2020-05, Vol.11, p.300-300

2020

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Development of Riluzole Analogs with Improved Use-Dependent Inhibition of Skeletal Muscle Sodium Channels

ACS medicinal chemistry letters, 2023-07, Vol.14 (7), p.999-1008

2023

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Elucidating the Contribution of Skeletal Muscle Ion Channels to Amyotrophic Lateral Sclerosis in search of new therapeutic options

Scientific reports, 2019-02, Vol.9 (1), p.3185-3185, Article 3185

2019

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Therapeutic Approaches to Genetic Ion Channelopathies and Perspectives in Drug Discovery

Frontiers in pharmacology, 2016-05, Vol.7, p.121-121

2016

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Ion Channels in Multiple Myeloma: Pathogenic Role and Therapeutic Perspectives

International journal of molecular sciences, 2022-06, Vol.23 (13), p.7302

2022

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Adaptation of mouse skeletal muscle to long-term microgravity in the MDS mission

PloS one, 2012-03, Vol.7 (3), p.e33232-e33232

2012

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Chaperone activity of niflumic acid on ClC-1 chloride channel mutants causing myotonia congenita

Frontiers in pharmacology, 2022-08, Vol.13, p.958196-958196

2022

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Is oxidative stress a cause or consequence of disuse muscle atrophy in mice? A proteomic approach in hindlimb-unloaded mice

Experimental physiology, 2010-02, Vol.95 (2), p.331-350

2010

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N‑Aryl-2,6-dimethylbenzamides, a New Generation of Tocainide Analogues as Blockers of Skeletal Muscle Voltage-Gated Sodium Channels

Journal of medicinal chemistry, 2014-03, Vol.57 (6), p.2589-2600

2014

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Effects of Nandrolone in the Counteraction of Skeletal Muscle Atrophy in a Mouse Model of Muscle Disuse: Molecular Biology and Functional Evaluation

PloS one, 2015-06, Vol.10 (6), p.e0129686-e0129686

2015

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Pathomechanisms of a CLCN1 Mutation Found in a Russian Family Suffering From Becker's Myotonia

Frontiers in neurology, 2020-09, Vol.11, p.1019-1019

2020

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Disuse of rat muscle in vivo reduces protein kinase C activity controlling the sarcolemma chloride conductance

The Journal of physiology, 2007-11, Vol.584 (3), p.983-995

2007

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Synthesis and Toxicopharmacological Evaluation of m-Hydroxymexiletine, the First Metabolite of Mexiletine More Potent Than the Parent Compound on Voltage-Gated Sodium Channels

Journal of medicinal chemistry, 2012-02, Vol.55 (3), p.1418-1422

2012

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Risk of Myopathy in Patients in Therapy with Statins: Identification of Biological Markers in a Pilot Study

Frontiers in pharmacology, 2017-07, Vol.8, p.500-500

2017

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A large cohort of myotonia congenita probands: novel mutations and a high-frequency mutation region in exons 4 and 5 of the CLCN1 gene

Journal of human genetics, 2013-09, Vol.58 (9), p.581-587

2013

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Redox homeostasis, oxidative stress and disuse muscle atrophy

Skeletal muscle ClC-1 chloride channels in health and diseases

Bioisosteric Modification of To042: Synthesis and Evaluation of Promising Use‐Dependent Inhibitors of Voltage‐Gated Sodium Channels

The analysis of myotonia congenita mutations discloses functional clusters of amino acids within the CBS2 domain and the C‐terminal peptide of the ClC‐1 channel

Synthesis and Evaluation of Voltage‐Gated Sodium Channel Blocking Pyrroline Derivatives Endowed with Both Antiarrhythmic and Antioxidant Activities

Anti-Angiogenic Activity of Drugs in Multiple Myeloma

Immersive and Non-Immersive Virtual Reality for Pain and Anxiety Management in Pediatric Patients with Hematological or Solid Cancer: A Systematic Review

Emerging Roles for Ion Channels in Ovarian Cancer: Pathomechanisms and Pharmacological Treatment

Long-Term Safety and Usefulness of Mexiletine in a Large Cohort of Patients Affected by Non-dystrophic Myotonias

Development of Riluzole Analogs with Improved Use-Dependent Inhibition of Skeletal Muscle Sodium Channels

Elucidating the Contribution of Skeletal Muscle Ion Channels to Amyotrophic Lateral Sclerosis in search of new therapeutic options

Therapeutic Approaches to Genetic Ion Channelopathies and Perspectives in Drug Discovery

Ion Channels in Multiple Myeloma: Pathogenic Role and Therapeutic Perspectives

Adaptation of mouse skeletal muscle to long-term microgravity in the MDS mission

Chaperone activity of niflumic acid on ClC-1 chloride channel mutants causing myotonia congenita

Is oxidative stress a cause or consequence of disuse muscle atrophy in mice? A proteomic approach in hindlimb-unloaded mice

N‑Aryl-2,6-dimethylbenzamides, a New Generation of Tocainide Analogues as Blockers of Skeletal Muscle Voltage-Gated Sodium Channels

Effects of Nandrolone in the Counteraction of Skeletal Muscle Atrophy in a Mouse Model of Muscle Disuse: Molecular Biology and Functional Evaluation

Pathomechanisms of a CLCN1 Mutation Found in a Russian Family Suffering From Becker's Myotonia

Disuse of rat muscle in vivo reduces protein kinase C activity controlling the sarcolemma chloride conductance

Uptake-Dependent and -Independent Effects of Fibroblasts-Derived Extracellular Vesicles on Bone Marrow Endothelial Cells from Patients with Multiple Myeloma: Therapeutic and Clinical Implications

Synthesis and Toxicopharmacological Evaluation of m-Hydroxymexiletine, the First Metabolite of Mexiletine More Potent Than the Parent Compound on Voltage-Gated Sodium Channels

Risk of Myopathy in Patients in Therapy with Statins: Identification of Biological Markers in a Pilot Study

A large cohort of myotonia congenita probands: novel mutations and a high-frequency mutation region in exons 4 and 5 of the CLCN1 gene

Paracrine effects of IGF-1 overexpression on the functional decline due to skeletal muscle disuse: molecular and functional evaluation in hindlimb unloaded MLC/mIgf-1 transgenic mice

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