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Inhibition of G protein-gated K + channels by tertiapin-Q rescues sinus node dysfunction and atrioventricular conduction in mouse models of primary bradycardia

Scientific reports, 2020-06, Vol.10 (1), p.9835-9835, Article 9835

2020

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Functional Impact of BeKm-1, a High-Affinity hERG Blocker, on Cardiomyocytes Derived from Human-Induced Pluripotent Stem Cells

International journal of molecular sciences, 2020-10, Vol.21 (19), p.7167

2020

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Chemical Synthesis of a Functional Fluorescent-Tagged α-Bungarotoxin

Toxins, 2022-01, Vol.14 (2), p.79

2022

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Efficient functional neutralization of lethal peptide toxins in vivo by oligonucleotides

Scientific reports, 2017-08, Vol.7 (1), p.7202-9, Article 7202

2017

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Maurocalcine as a Non Toxic Drug Carrier Overcomes Doxorubicin Resistance in the Cancer Cell Line MDA-MB 231

Pharmaceutical research, 2009-04, Vol.26 (4), p.836-845

2009

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Aptamer Efficacies for In Vitro and In Vivo Modulation of αC-Conotoxin PrXA Pharmacology

Molecules (Basel, Switzerland), 2019-01, Vol.24 (2), p.229

2019

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Generation of human induced pluripotent stem cell lines from three patients affected by Catecholaminergic Polymorphic ventricular tachycardia (CPVT) carrying heterozygous mutations in RYR2 gene

Stem cell research, 2022-04, Vol.60, p.102688-102688, Article 102688

2022

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The β4 subunit of the voltage-gated calcium channel (Cacnb4) regulates the rate of cell proliferation in Chinese Hamster Ovary cells

The international journal of biochemistry & cell biology, 2017-08, Vol.89, p.57-70

2017

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C-terminal splice variants of P/Q-type Ca2+ channel CaV2.1 α1 subunits are differentially regulated by Rab3-interacting molecule proteins

The Journal of biological chemistry, 2017-06, Vol.292 (22), p.9365-9381

2017

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Interaction between the Dihydropyridine Receptor Ca2+Channel$\beta-Subunit$and Ryanodine Receptor Type 1 Strengthens Excitation-Contraction Coupling

Proceedings of the National Academy of Sciences - PNAS, 2005-12, Vol.102 (52), p.19225-19230

2005

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In cellulo phosphorylation induces pharmacological reprogramming of maurocalcin, a cell-penetrating venom peptide

Proceedings of the National Academy of Sciences - PNAS, 2016-04, Vol.113 (17), p.E2460-E2468

2016

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Functional evolution of scorpion venom peptides with an inhibitor cystine knot fold

Bioscience reports, 2013-01, Vol.33 (3), p.e00047

2013

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Direct Peptide Interaction with Surface Glycosaminoglycans Contributes to the Cell Penetration of Maurocalcine

The Journal of biological chemistry, 2008-08, Vol.283 (35), p.24274-24284

2008

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Nuclear life of the voltage-gated Cacnb4 subunit and its role in gene transcription regulation

Channels (Austin, Tex.), 2013-03, Vol.7 (2), p.119-125

2013

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Junctate is a key element in calcium entry induced by activation of InsP3 receptors and/or calcium store depletion

The Journal of cell biology, 2004-08, Vol.166 (4), p.537-548

2004

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Cell penetration properties of a highly efficient mini maurocalcine Peptide

Pharmaceuticals (Basel, Switzerland), 2013-03, Vol.6 (3), p.320-339

2013

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SRP-35, a newly identified protein of the skeletal muscle sarcoplasmic reticulum, is a retinol dehydrogenase

Biochemical journal, 2012-01, Vol.441 (2), p.731-741

2012

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Design of a Disulfide-less, Pharmacologically Inert, and Chemically Competent Analog of Maurocalcine for the Efficient Transport of Impermeant Compounds into Cells

The Journal of biological chemistry, 2008-10, Vol.283 (40), p.27048-27056

2008

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The CD38-independent ADP-ribosyl cyclase from mouse brain synaptosomes: a comparative study of neonate and adult brain

Biochemical journal, 2006-04, Vol.395 (2), p.417-426

2006

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Transient loss of voltage control of Ca2+ release in the presence of maurocalcine in skeletal muscle

Biophysical journal, 2006-09, Vol.91 (6), p.2206-2215

2006

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Gene regulation by voltage-dependent calcium channels

Biochimica et biophysica acta, 2009-06, Vol.1793 (6), p.1096-1104

2009

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Cavβ-subunit displacement is a key step to induce the reluctant state of P/Q calcium channels by direct G protein regulation

Proceedings of the National Academy of Sciences - PNAS, 2004-04, Vol.101 (16), p.6267-6272

2004

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Maurocalcine and Peptide A Stabilize Distinct Subconductance States of Ryanodine Receptor Type 1, Revealing a Proportional Gating Mechanism

The Journal of biological chemistry, 2003-05, Vol.278 (18), p.16095-16106

2003

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Critical Amino Acid Residues Determine the Binding Affinity and the Ca2+ Release Efficacy of Maurocalcine in Skeletal Muscle Cells

The Journal of biological chemistry, 2003-09, Vol.278 (39), p.37822-37831

2003

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C-terminal splice variants of P/Q-type Ca(2+) channel CaV2.1 α1 subunits are differentially regulated by Rab3-interacting molecule proteins

The Journal of biological chemistry, 2017-06, Vol.292 (22), p.9365-9381

2017

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Inhibition of G protein-gated K + channels by tertiapin-Q rescues sinus node dysfunction and atrioventricular conduction in mouse models of primary bradycardia

Functional Impact of BeKm-1, a High-Affinity hERG Blocker, on Cardiomyocytes Derived from Human-Induced Pluripotent Stem Cells

Chemical Synthesis of a Functional Fluorescent-Tagged α-Bungarotoxin

Efficient functional neutralization of lethal peptide toxins in vivo by oligonucleotides

Maurocalcine as a Non Toxic Drug Carrier Overcomes Doxorubicin Resistance in the Cancer Cell Line MDA-MB 231

Aptamer Efficacies for In Vitro and In Vivo Modulation of αC-Conotoxin PrXA Pharmacology

Generation of human induced pluripotent stem cell lines from three patients affected by Catecholaminergic Polymorphic ventricular tachycardia (CPVT) carrying heterozygous mutations in RYR2 gene

The β4 subunit of the voltage-gated calcium channel (Cacnb4) regulates the rate of cell proliferation in Chinese Hamster Ovary cells

C-terminal splice variants of P/Q-type Ca2+ channel CaV2.1 α1 subunits are differentially regulated by Rab3-interacting molecule proteins

Interaction between the Dihydropyridine Receptor Ca2+Channel$\beta-Subunit$and Ryanodine Receptor Type 1 Strengthens Excitation-Contraction Coupling

In cellulo phosphorylation induces pharmacological reprogramming of maurocalcin, a cell-penetrating venom peptide

Functional evolution of scorpion venom peptides with an inhibitor cystine knot fold

Direct Peptide Interaction with Surface Glycosaminoglycans Contributes to the Cell Penetration of Maurocalcine

Nuclear life of the voltage-gated Cacnb4 subunit and its role in gene transcription regulation

Junctate is a key element in calcium entry induced by activation of InsP3 receptors and/or calcium store depletion

Cell penetration properties of a highly efficient mini maurocalcine Peptide

SRP-35, a newly identified protein of the skeletal muscle sarcoplasmic reticulum, is a retinol dehydrogenase

Design of a Disulfide-less, Pharmacologically Inert, and Chemically Competent Analog of Maurocalcine for the Efficient Transport of Impermeant Compounds into Cells

The CD38-independent ADP-ribosyl cyclase from mouse brain synaptosomes: a comparative study of neonate and adult brain

Transient loss of voltage control of Ca2+ release in the presence of maurocalcine in skeletal muscle

Gene regulation by voltage-dependent calcium channels

Cavβ-subunit displacement is a key step to induce the reluctant state of P/Q calcium channels by direct G protein regulation

Maurocalcine and Peptide A Stabilize Distinct Subconductance States of Ryanodine Receptor Type 1, Revealing a Proportional Gating Mechanism

Critical Amino Acid Residues Determine the Binding Affinity and the Ca2+ Release Efficacy of Maurocalcine in Skeletal Muscle Cells

C-terminal splice variants of P/Q-type Ca(2+) channel CaV2.1 α1 subunits are differentially regulated by Rab3-interacting molecule proteins

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