Lista de obras - Isabelle Baró - Dominio Público Uruguay

14-3-3 is a regulator of the cardiac voltage-gated sodium channel Nav1.5

artículo científico publicado en 2006

2-Receptor Ligand-Mediated Inhibition of Inwardly Rectifying K+ Channels in the Heart

artículo científico publicado en 2007

A Dominant Negative Isoform of the Long QT Syndrome 1 Gene Product

artículo científico publicado en 1998

A common antitussive drug, clobutinol, precipitates the long QT syndrome 2

artículo científico publicado en 2004

A consistent arrhythmogenic trait in Brugada syndrome cellular phenotype

artículo científico publicado en 2021

A long QT mutation substitutes cholesterol for phosphatidylinositol-4,5-bisphosphate in KCNQ1 channel regulation

artículo científico publicado en 2014

A long lasting Ca2+ -activated outward current in guinea-pig atrial myocytes

artículo científico publicado en 1989

ATP-sensitive K+ channels regulated by intracellular Ca2+ and phosphorylation in normal (T84) and cystic fibrosis (CFPAC-1) epithelial cells.

artículo científico publicado en 1995

Atrial fibrillation: Is NO an answer for refractoriness?

artículo científico publicado en 2006

Barium- and calcium-permeable channels open at negative membrane potentials in rat ventricular myocytes.

artículo científico publicado en 1989

Complex Brugada syndrome inheritance in a family harbouring compound SCN5A and CACNA1C mutations

Delayed rectifier K(+) currents and cardiac repolarization.

scientific article published on 14 August 2009

Dual effect of phosphatidylinositol (4,5)-bisphosphate PIP(2) on Shaker K(+) [corrected] channels

artículo científico publicado en 2012

Dynamic analysis of the QT interval in long QT1 syndrome patients with a normal phenotype

artículo científico publicado en 2001

Dysfunction of the Voltage-Gated K+ Channel β2 Subunit in a Familial Case of Brugada Syndrome

scientific article published on 10 June 2016

Effects of sulphonylureas on cAMP-stimulated Cl- transport via the cystic fibrosis gene product in human epithelial cells.

artículo científico publicado en 1994

Guest Editors' Introduction

scientific article published on 01 January 2010

HIV-Tat induces a decrease in IKr and IKsvia reduction in phosphatidylinositol-(4,5)-bisphosphate availability

artículo científico publicado en 2016

Haploinsufficiency in combination with aging causes SCN5A-linked hereditary Lenègre disease

artículo científico publicado en 2003

Impaired KCNQ1-KCNE1 and phosphatidylinositol-4,5-bisphosphate interaction underlies the long QT syndrome

artículo científico publicado en 2005

Inactivating properties of recombinant ROMK2 channels expressed in mammalian cells

artículo científico publicado en 2001

KCNE1-KCNQ1 osmoregulation by interaction of phosphatidylinositol-4,5-bisphosphate with Mg2+ and polyamines

artículo científico publicado en 2010

KCNQ1 channels voltage dependence through a voltage-dependent binding of the S4-S5 linker to the pore domain.

artículo científico publicado en 2010

Kv7.1 (KCNQ1) properties and channelopathies.

artículo científico publicado en 2008

LQT1-associated mutations increase KCNQ1 proteasomal degradation independently of Derlin-1.

artículo científico publicado en 2008

Marine n-3 PUFAs modulate IKs gating, channel expression, and location in membrane microdomains.

artículo científico publicado en 2014

Microarray analysis reveals complex remodeling of cardiac ion channel expression with altered thyroid status: relation to cellular and integrated electrophysiology.

artículo científico publicado en 2003

Multifocal ectopic Purkinje-related premature contractions: a new SCN5A-related cardiac channelopathy

artículo científico publicado en 2012

Mutation in KCNQ1 that has both recessive and dominant characteristics

artículo científico publicado en 2002

Mutation in the KCNQ1 gene leading to the short QT-interval syndrome

artículo científico publicado en 2004

Na+ channel mutation leading to loss of function and non-progressive cardiac conduction defects

artículo científico publicado en 2003

Neural modulation of ion channels in cardiac arrhythmias: clinical implications and future investigations.

artículo científico publicado en 2010

New KCNQ1 mutations leading to haploinsufficiency in a general population; Defective trafficking of a KvLQT1 mutant.

artículo científico publicado en 2004

Non-invasive testing of acquired long QT syndrome: evidence for multiple arrhythmogenic substrates

artículo científico publicado en 2001

Opposite Effects of the S4–S5 Linker and PIP2 on Voltage-Gated Channel Function: KCNQ1/KCNE1 and Other Channels ⬇️

artículo científico publicado el 5 de julio de 2012

Phosphatidylinositol-4,5-bisphosphate (PIP(2)) stabilizes the open pore conformation of the Kv11.1 (hERG) channel

artículo científico publicado en 2010

Phosphatidylinositol-4,5-bisphosphate, PIP2, controls KCNQ1/KCNE1 voltage-gated potassium channels: a functional homology between voltage-gated and inward rectifier K+ channels.

artículo científico publicado en 2003

Physiological and Pathophysiological Insights of Nav1.4 and Nav1.5 Comparison

artículo científico publicado en 2015

RRAD mutation causes electrical and cytoskeletal defects in cardiomyocytes derived from a familial case of Brugada syndrome

scientific article published on 01 October 2019

The KCNQ1 potassium channel is down-regulated by ubiquitylating enzymes of the Nedd4/Nedd4-like family

artículo científico publicado en 2007

The N-terminal juxtamembranous domain of KCNQ1 is critical for channel surface expression: implications in the Romano-Ward LQT1 syndrome

artículo científico publicado en 2006

The effects of thapsigargin on [Ca2+]i in isolated rat mesenteric artery vascular smooth muscle cells

artículo científico publicado en 1992

Torsades de pointes complicating atrioventricular block: evidence for a genetic predisposition

artículo científico publicado en 2007

Toward Personalized Medicine: Using Cardiomyocytes Differentiated From Urine-Derived Pluripotent Stem Cells to Recapitulate Electrophysiological Characteristics of Type 2 Long QT Syndrome

artículo científico publicado en 2015

Trafficking-deficient long QT syndrome mutation KCNQ1-T587M confers severe clinical phenotype by impairment of KCNH2 membrane localization: evidence for clinically significant IKr-IKs alpha-subunit interaction.

artículo científico publicado en 2009

Transforming growth factor β receptor inhibition prevents ventricular fibrosis in a mouse model of progressive cardiac conduction disease.

artículo científico publicado en 2017

Lista de obras de Isabelle Baró

14-3-3 is a regulator of the cardiac voltage-gated sodium channel Nav1.5

2-Receptor Ligand-Mediated Inhibition of Inwardly Rectifying K+ Channels in the Heart

A Dominant Negative Isoform of the Long QT Syndrome 1 Gene Product

A common antitussive drug, clobutinol, precipitates the long QT syndrome 2

A consistent arrhythmogenic trait in Brugada syndrome cellular phenotype

A long QT mutation substitutes cholesterol for phosphatidylinositol-4,5-bisphosphate in KCNQ1 channel regulation

A long lasting Ca2+ -activated outward current in guinea-pig atrial myocytes

ATP-sensitive K+ channels regulated by intracellular Ca2+ and phosphorylation in normal (T84) and cystic fibrosis (CFPAC-1) epithelial cells.

Atrial fibrillation: Is NO an answer for refractoriness?

Barium- and calcium-permeable channels open at negative membrane potentials in rat ventricular myocytes.

Complex Brugada syndrome inheritance in a family harbouring compound SCN5A and CACNA1C mutations

Delayed rectifier K(+) currents and cardiac repolarization.

Dual effect of phosphatidylinositol (4,5)-bisphosphate PIP(2) on Shaker K(+) [corrected] channels

Dynamic analysis of the QT interval in long QT1 syndrome patients with a normal phenotype

Dysfunction of the Voltage-Gated K+ Channel β2 Subunit in a Familial Case of Brugada Syndrome

Effects of sulphonylureas on cAMP-stimulated Cl- transport via the cystic fibrosis gene product in human epithelial cells.

Guest Editors' Introduction

HIV-Tat induces a decrease in IKr and IKsvia reduction in phosphatidylinositol-(4,5)-bisphosphate availability

Haploinsufficiency in combination with aging causes SCN5A-linked hereditary Lenègre disease

Impaired KCNQ1-KCNE1 and phosphatidylinositol-4,5-bisphosphate interaction underlies the long QT syndrome

Inactivating properties of recombinant ROMK2 channels expressed in mammalian cells

KCNE1-KCNQ1 osmoregulation by interaction of phosphatidylinositol-4,5-bisphosphate with Mg2+ and polyamines

KCNQ1 channels voltage dependence through a voltage-dependent binding of the S4-S5 linker to the pore domain.

Kv7.1 (KCNQ1) properties and channelopathies.

LQT1-associated mutations increase KCNQ1 proteasomal degradation independently of Derlin-1.

Marine n-3 PUFAs modulate IKs gating, channel expression, and location in membrane microdomains.

Microarray analysis reveals complex remodeling of cardiac ion channel expression with altered thyroid status: relation to cellular and integrated electrophysiology.

Multifocal ectopic Purkinje-related premature contractions: a new SCN5A-related cardiac channelopathy

Mutation in KCNQ1 that has both recessive and dominant characteristics

Mutation in the KCNQ1 gene leading to the short QT-interval syndrome

Na+ channel mutation leading to loss of function and non-progressive cardiac conduction defects

Neural modulation of ion channels in cardiac arrhythmias: clinical implications and future investigations.

New KCNQ1 mutations leading to haploinsufficiency in a general population; Defective trafficking of a KvLQT1 mutant.

Non-invasive testing of acquired long QT syndrome: evidence for multiple arrhythmogenic substrates

Opposite Effects of the S4–S5 Linker and PIP2 on Voltage-Gated Channel Function: KCNQ1/KCNE1 and Other Channels ⬇️

Phosphatidylinositol-4,5-bisphosphate (PIP(2)) stabilizes the open pore conformation of the Kv11.1 (hERG) channel

Phosphatidylinositol-4,5-bisphosphate, PIP2, controls KCNQ1/KCNE1 voltage-gated potassium channels: a functional homology between voltage-gated and inward rectifier K+ channels.

Physiological and Pathophysiological Insights of Nav1.4 and Nav1.5 Comparison

RRAD mutation causes electrical and cytoskeletal defects in cardiomyocytes derived from a familial case of Brugada syndrome

The KCNQ1 potassium channel is down-regulated by ubiquitylating enzymes of the Nedd4/Nedd4-like family

The N-terminal juxtamembranous domain of KCNQ1 is critical for channel surface expression: implications in the Romano-Ward LQT1 syndrome

The effects of thapsigargin on [Ca2+]i in isolated rat mesenteric artery vascular smooth muscle cells

Torsades de pointes complicating atrioventricular block: evidence for a genetic predisposition

Toward Personalized Medicine: Using Cardiomyocytes Differentiated From Urine-Derived Pluripotent Stem Cells to Recapitulate Electrophysiological Characteristics of Type 2 Long QT Syndrome

Trafficking-deficient long QT syndrome mutation KCNQ1-T587M confers severe clinical phenotype by impairment of KCNH2 membrane localization: evidence for clinically significant IKr-IKs alpha-subunit interaction.

Transforming growth factor β receptor inhibition prevents ventricular fibrosis in a mouse model of progressive cardiac conduction disease.