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Statins and fenofibrate affect skeletal muscle chloride conductance in rats by differently impairing ClC‐1 channel regulation and expression

British journal of pharmacology, 2009-04, Vol.156 (8), p.1206-1215

2009

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Proof-of-concept validation of the mechanism of action of Src tyrosine kinase inhibitors in dystrophic mdx mouse muscle: in vivo and in vitro studies

Pharmacological research, 2019-07, Vol.145, p.104260-104260, Article 104260

2019

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In vivo silencing of aquaporin-1 by RNA interference inhibits angiogenesis in the chick embryo chorioallantoic membrane assay

Cellular and molecular biology (Noisy-le-Grand, France), 2006-01, Vol.52 (7), p.51

2006

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T.P.37 Changes in muscle expression of PGC-1[alpha] and related signalling molecules in the mdx mouse: Possible impact on adaptive fiber phenotype transition and implication for drug studies

Neuromuscular disorders : NMD, 2012-10, Vol.22 (9-10), p.864-864

2012

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P4.26 Toward the identification of druggable pathways involved in disease-related fatigue in Duchenne muscular dystrophy: In vivo and ex vivo studies in dystrophic mdx mice

Neuromuscular disorders : NMD, 2011-10, Vol.21 (9), p.712-712

2011

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T.P.2.13 Evaluation of time-dependent effects of statins and fibrate ‘in vivo’ treatment on ClC-1 chloride channel expression and function and on proteomic profile of rat skeletal muscle

Neuromuscular disorders : NMD, 2009-09, Vol.19 (8), p.583-584

2009

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T-pattern detection and analysis for the discovery of hidden features of behaviour

Journal of neuroscience methods, 2018-12, Vol.310, p.24-32

2018

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Increased density and age‐related sharing of synapses at the cone to OFF bipolar cell synapse in the mouse retina

Journal of comparative neurology (1911), 2020-05, Vol.528 (7), p.1140-1156

2020

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Identifying and analyzing the construction and effectiveness of offensive plays in basketball by using systematic observation

Behavior research methods, 2009-08, Vol.41 (3), p.719-730

2009

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ClC‐1 mutations in myotonia congenita patients: insights into molecular gating mechanisms and genotype–phenotype correlation

The Journal of physiology, 2015-09, Vol.593 (18), p.4181-4199

2015

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Pathophysiological Consequences of KATP Channel Overactivity and Pharmacological Response to Glibenclamide in Skeletal Muscle of a Murine Model of Cantù Syndrome

Frontiers in pharmacology, 2020-11, Vol.11, p.604885-604885

2020

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Visceral Fat Dysfunctions in the Rat Social Isolation Model of Psychosis

Frontiers in pharmacology, 2017-11, Vol.8, p.787-787

2017

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Recovery of the soleus muscle after short- and long-term disuse induced by hindlimb unloading: effects on the electrical properties and myosin heavy chain profile

Neurobiology of disease, 2005-03, Vol.18 (2), p.356-365

2005

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448 RSPO1-mutated keratinocytes from palmoplantar keratoderma display impaired differentiation, alteration of cell-cell adhesion, EMT-like phenotype and invasiveness properties

Journal of investigative dermatology, 2022-12, Vol.142 (12), p.S258-S258

2022

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Identification of sites responsible for the potentiating effect of niflumic acid on ClC‐Ka kidney chloride channels

British journal of pharmacology, 2010-08, Vol.160 (7), p.1652-1661

2010

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A unified nomenclature system for the nuclear receptor superfamily

Cell, 1999-04, Vol.97 (2), p.161-163

1999

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Keto analogues and amino acids supplementation induces a decrease of white blood cell counts and a reduction of muscle damage during intense exercise under thermoneutral conditions

Food & function, 2017-04, Vol.8 (4), p.1519-1525

2017

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Different dehydration levels and their impact on blood ammonia, cognitive-motor performance, and muscle damage in acclimated runners

Journal of sports medicine and physical fitness, 2022-12, Vol.62 (12)

2022

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CHANNELOPATHIES AND RELATED DISORDERS: EP.224 Repurposing of niflumic acid for ClC-1 mutation-driven pharmacological approach in myotonia congenita

Neuromuscular disorders : NMD, 2021-10, Vol.31, p.S117-S117

2021

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CHANNELOPATHIES AND RELATED DISORDERS

Neuromuscular disorders : NMD, 2021-10, Vol.31, p.S117

2021

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Activation of β-catenin signaling by Rspo1 controls differentiation of the mammalian ovary

Human molecular genetics, 2008-05, Vol.17 (9), p.1264-1277

2008

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Application of BioFire FilmArray Blood Culture Identification panel for rapid identification of the causative agents of ventilator-associated pneumonia

Clinical microbiology and infection, 2018-11, Vol.24 (11), p.1213.e1-1213.e4

2018

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In-vivo administration of CLC-K kidney chloride channels inhibitors increases water diuresis in rats: a new drug target for hypertension?

Journal of hypertension, 2012-01, Vol.30 (1), p.153-167

2012

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Prevalence study of muscle channelopathies in Italy

Neuromuscular disorders : NMD, 2016-10, Vol.26, p.S197-S197

2016

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Consequences of SUR2[A478V] Mutation in Skeletal Muscle of Murine Model of Cantu Syndrome

Cells (Basel, Switzerland), 2021-07, Vol.10 (7), p.1791

2021

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Statins and fenofibrate affect skeletal muscle chloride conductance in rats by differently impairing ClC‐1 channel regulation and expression

Proof-of-concept validation of the mechanism of action of Src tyrosine kinase inhibitors in dystrophic mdx mouse muscle: in vivo and in vitro studies

In vivo silencing of aquaporin-1 by RNA interference inhibits angiogenesis in the chick embryo chorioallantoic membrane assay

T.P.37 Changes in muscle expression of PGC-1[alpha] and related signalling molecules in the mdx mouse: Possible impact on adaptive fiber phenotype transition and implication for drug studies

P4.26 Toward the identification of druggable pathways involved in disease-related fatigue in Duchenne muscular dystrophy: In vivo and ex vivo studies in dystrophic mdx mice

T.P.2.13 Evaluation of time-dependent effects of statins and fibrate ‘in vivo’ treatment on ClC-1 chloride channel expression and function and on proteomic profile of rat skeletal muscle

T-pattern detection and analysis for the discovery of hidden features of behaviour

Increased density and age‐related sharing of synapses at the cone to OFF bipolar cell synapse in the mouse retina

Identifying and analyzing the construction and effectiveness of offensive plays in basketball by using systematic observation

ClC‐1 mutations in myotonia congenita patients: insights into molecular gating mechanisms and genotype–phenotype correlation

Pathophysiological Consequences of KATP Channel Overactivity and Pharmacological Response to Glibenclamide in Skeletal Muscle of a Murine Model of Cantù Syndrome

Visceral Fat Dysfunctions in the Rat Social Isolation Model of Psychosis

Recovery of the soleus muscle after short- and long-term disuse induced by hindlimb unloading: effects on the electrical properties and myosin heavy chain profile

448 RSPO1-mutated keratinocytes from palmoplantar keratoderma display impaired differentiation, alteration of cell-cell adhesion, EMT-like phenotype and invasiveness properties

Identification of sites responsible for the potentiating effect of niflumic acid on ClC‐Ka kidney chloride channels

A unified nomenclature system for the nuclear receptor superfamily

Keto analogues and amino acids supplementation induces a decrease of white blood cell counts and a reduction of muscle damage during intense exercise under thermoneutral conditions

Different dehydration levels and their impact on blood ammonia, cognitive-motor performance, and muscle damage in acclimated runners

CHANNELOPATHIES AND RELATED DISORDERS: EP.224 Repurposing of niflumic acid for ClC-1 mutation-driven pharmacological approach in myotonia congenita

CHANNELOPATHIES AND RELATED DISORDERS

Activation of β-catenin signaling by Rspo1 controls differentiation of the mammalian ovary

Application of BioFire FilmArray Blood Culture Identification panel for rapid identification of the causative agents of ventilator-associated pneumonia

In-vivo administration of CLC-K kidney chloride channels inhibitors increases water diuresis in rats: a new drug target for hypertension?

Prevalence study of muscle channelopathies in Italy

Consequences of SUR2[A478V] Mutation in Skeletal Muscle of Murine Model of Cantu Syndrome

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