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Arrhythmogenesis in a catecholaminergic polymorphic ventricular tachycardia mutation that depresses ryanodine receptor function

Proceedings of the National Academy of Sciences - PNAS, 2015-03, Vol.112 (13), p.E1669-E1677

2015

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Cardiac Kir2.1 and NaV1.5 Channels Traffic Together to the Sarcolemma to Control Excitability

Circulation research, 2018-05, Vol.122 (11), p.1501-1516

2018

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Supersolar metallicity in G0–G3 main-sequence stars with V < 15. II. An extension of the sample

Monthly notices of the Royal Astronomical Society, 2020-04, Vol.493 (4), p.5807-5815

2020

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Early science with the Large Millimetre Telescope: Deep LMT/AzTEC millimetre observations of ϵ Eridani and its surroundings

Monthly notices of the Royal Astronomical Society, 2016-11, Vol.462 (3), p.2285-2294

2016

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Arrhythmogenic mechanisms in ryanodine receptor channelopathies

Science China. Life sciences, 2015-01, Vol.58 (1), p.54-58

2015

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Regulation of secondary wall synthesis and cell death by NAC transcription factors in the monocot Brachypodium distachyon

Journal of experimental botany, 2013-03, Vol.64 (5), p.1333-1343

2013

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OpiCa1-PEG-PLGA nanomicelles antagonize acute heart failure induced by the cocktail of epinephrine and caffeine

Materials today bio, 2023-12, Vol.23, p.100859-100859, Article 100859

2023

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Increased late sodium current in myocytes from a canine heart failure model and from failing human heart

Journal of molecular and cellular cardiology, 2005-03, Vol.38 (3), p.475-483

2005

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Lithium abundance in a sample of solar-like stars

Monthly notices of the Royal Astronomical Society, 2015-08, Vol.451 (4), p.4368-4374

2015

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GPD1L links redox state to cardiac excitability by PKC-dependent phosphorylation of the sodium channel SCN5A

American journal of physiology. Heart and circulatory physiology, 2009-10, Vol.297 (4), p.H1446-H1452

2009

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Fluorescence-Based Isolation of Bacterial Genes Expressed Within Host Cells

Science (American Association for the Advancement of Science), 1997-09, Vol.277 (5334), p.2007-2011

1997

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Multi-filter Transit Observations of HAT-P-3b and TrES-3b with Multiple Northern Hemisphere Telescopes

Publications of the Astronomical Society of the Pacific, 2017-06, Vol.129 (976), p.64401

2017

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Three-dimensional displacement in multi-colored objects

Optics express, 2017-05, Vol.25 (10), p.11652-11672

2017

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Atrial Infarction-Induced Spontaneous Focal Discharges and Atrial Fibrillation in Sheep: Role of Dantrolene-Sensitive Aberrant Ryanodine Receptor Calcium Release

Circulation. Arrhythmia and electrophysiology, 2018-03, Vol.11 (3), p.e005659-e005659

2018

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A Ubiquitous Splice Variant and a Common Polymorphism Affect Heterologous Expression of Recombinant Human SCN5A Heart Sodium Channels

Circulation research, 2003-10, Vol.93 (9), p.821-828

2003

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Molecular and functional characterization of novel glycerol-3-phosphate dehydrogenase 1-like gene (GPD1-L) mutations in sudden infant death syndrome

Circulation (New York, N.Y.), 2007-11, Vol.116 (20), p.2253-2259

2007

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Drug‐induced long QT syndrome: hERG K+ channel block and disruption of protein trafficking by fluoxetine and norfluoxetine

British journal of pharmacology, 2006-11, Vol.149 (5), p.481-489

2006

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Terrorism and oil markets: A cross-sectional evaluation

Finance research letters, 2018-03, Vol.24, p.42-48

2018

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The pediatric clinical nurse specialist: A children's hospital journey

Journal of pediatric nursing, 2022-09, Vol.66, p.213-215

Valdivia, Hector R.

2022

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The Effect of Acidic Residues on the Binding between Opicalcin1 and Ryanodine Receptor from the Structure–Functional Analysis

Journal of natural products (Washington, D.C.), 2024-01, Vol.87 (1), p.104-112

2024

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Postmortem molecular analysis of SCN5A defects in sudden infant death syndrome

JAMA : the journal of the American Medical Association, 2001-11, Vol.286 (18), p.2264

2001

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Loss-of-function mutation of the SCN3B-encoded sodium channel {beta}3 subunit associated with a case of idiopathic ventricular fibrillation

Cardiovascular research, 2010-06, Vol.86 (3), p.392-400

2010

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Increasing PV solar collection using the upper edges in balconies

Journal of physics. Conference series, 2023-11, Vol.2600 (4), p.42009

Valdivia-Sisniegas, R H

2023

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A common human SCN5A polymorphism modifies expression of an arrhythmia causing mutation

Physiological genomics, 2003-02, Vol.12 (3), p.187-193

2003

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Sudden infant death syndrome–associated mutations in the sodium channel beta subunits

Heart rhythm, 2010-06, Vol.7 (6), p.771-778

2010

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Arrhythmogenesis in a catecholaminergic polymorphic ventricular tachycardia mutation that depresses ryanodine receptor function

Cardiac Kir2.1 and NaV1.5 Channels Traffic Together to the Sarcolemma to Control Excitability

Supersolar metallicity in G0–G3 main-sequence stars with V < 15. II. An extension of the sample

Early science with the Large Millimetre Telescope: Deep LMT/AzTEC millimetre observations of ϵ Eridani and its surroundings

Arrhythmogenic mechanisms in ryanodine receptor channelopathies

Regulation of secondary wall synthesis and cell death by NAC transcription factors in the monocot Brachypodium distachyon

OpiCa1-PEG-PLGA nanomicelles antagonize acute heart failure induced by the cocktail of epinephrine and caffeine

Increased late sodium current in myocytes from a canine heart failure model and from failing human heart

Lithium abundance in a sample of solar-like stars

GPD1L links redox state to cardiac excitability by PKC-dependent phosphorylation of the sodium channel SCN5A

Fluorescence-Based Isolation of Bacterial Genes Expressed Within Host Cells

Multi-filter Transit Observations of HAT-P-3b and TrES-3b with Multiple Northern Hemisphere Telescopes

Three-dimensional displacement in multi-colored objects

Atrial Infarction-Induced Spontaneous Focal Discharges and Atrial Fibrillation in Sheep: Role of Dantrolene-Sensitive Aberrant Ryanodine Receptor Calcium Release

A Ubiquitous Splice Variant and a Common Polymorphism Affect Heterologous Expression of Recombinant Human SCN5A Heart Sodium Channels

Molecular and functional characterization of novel glycerol-3-phosphate dehydrogenase 1-like gene (GPD1-L) mutations in sudden infant death syndrome

Drug‐induced long QT syndrome: hERG K+ channel block and disruption of protein trafficking by fluoxetine and norfluoxetine

Terrorism and oil markets: A cross-sectional evaluation

The pediatric clinical nurse specialist: A children's hospital journey

The Effect of Acidic Residues on the Binding between Opicalcin1 and Ryanodine Receptor from the Structure–Functional Analysis

Postmortem molecular analysis of SCN5A defects in sudden infant death syndrome

Loss-of-function mutation of the SCN3B-encoded sodium channel {beta}3 subunit associated with a case of idiopathic ventricular fibrillation

Increasing PV solar collection using the upper edges in balconies

A common human SCN5A polymorphism modifies expression of an arrhythmia causing mutation

Sudden infant death syndrome–associated mutations in the sodium channel beta subunits

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