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Revisiting CFTR inhibition: a comparative study of CFTRinh‐172 and GlyH‐101 inhibitors

British journal of pharmacology, 2014-08, Vol.171 (15), p.3716-3727

2014

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KCNQ1 Gain-of-Function Mutation in Familial Atrial Fibrillation

Science (American Association for the Advancement of Science), 2003-01, Vol.299 (5604), p.251-254

2003

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The inward rectifier potassium channel Kir2.1 is required for osteoblastogenesis

Human molecular genetics, 2015-01, Vol.24 (2), p.471-479

2015

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Identification of a KCNE2 Gain-of-Function Mutation in Patients with Familial Atrial Fibrillation

American journal of human genetics, 2004-11, Vol.75 (5), p.899-905

2004

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A Kir2.1 gain-of-function mutation underlies familial atrial fibrillation

Biochemical and biophysical research communications, 2005-07, Vol.332 (4), p.1012-1019

2005

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In vitro molecular interactions and distribution of KCNE family with KCNQ1 in the human heart

Cardiovascular research, 2005-08, Vol.67 (3), p.529-538

2005

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Revisiting CFTR inhibition: a comparative study of CFTR inh ‐172 and GlyH ‐101 inhibitors

British journal of pharmacology, 2014-08, Vol.171 (15), p.3716-3727

2014

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Proximal Renal Tubular Acidosis in TASK2 K+Channel-Deficient Mice Reveals a Mechanism for Stabilizing Bicarbonate Transport

Proceedings of the National Academy of Sciences - PNAS, 2004-05, Vol.101 (21), p.8215-8220

2004

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PIP2 binding residues of Kir2.1 are common targets of mutations causing Andersen syndrome

Neurology, 2003-06, Vol.60 (11), p.1811

2003

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ARF6-dependent interaction of the TWIK1 K+ channel with EFA6, a GDP/GTP exchange factor for ARF6

EMBO reports, 2004-12, Vol.5 (12), p.1171-1175

2004

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Impairment of slow inactivation as a common mechanism for periodic paralysis in DIIS4-S5

Neurology, 2002-04, Vol.58 (8), p.1266

2002

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Mechanisms underlying Andersen's syndrome pathology in skeletal muscle are revealed in human myotubes

American Journal of Physiology: Cell Physiology, 2009-10, Vol.297 (4), p.C876-C885

2009

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In vivo and in vitro functional characterization of Andersen's syndrome mutations

The Journal of physiology, 2005-06, Vol.565 (3), p.731-741

2005

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344 A cluster of the cystic fibrosis transmembrane regulator (CFTR) mutation S549R in the Sultanate of Oman

Journal of cystic fibrosis, 2012-06, Vol.11, p.S145-S145

2012

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Global surveillance of trends in cancer survival 2000–14 (CONCORD-3): analysis of individual records for 37 513 025 patients diagnosed with one of 18 cancers from 322 population-based registries in 71 countries

The Lancet (British edition), 2018-03, Vol.391 (10125), p.1023-1075

2018

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Le pyrophosphate, un additif alimentaire comme stratégie thérapeutique pour lutter contre certaines maladies calcifiantes d’origine héréditaire ou métabolique

Nutrition clinique et métabolisme, 2023-05, Vol.37 (2), p.e80-e81

2023

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Mutations in Kir2.1 Cause the Developmental and Episodic Electrical Phenotypes of Andersen's Syndrome

Cell, 2001-05, Vol.105 (4), p.511-519

2001

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Pathologies liées aux canaux à rectification entrante

Archives des maladies du coeur et des vaisseaux. Pratique, 2015-06, Vol.2015 (239), p.25-30

2015

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CHANNELOPATHIES AND RELATED DISORDERS: EP.221 Diagnostic delay and atypical phenotypes in a French cohort of Andersen-Tawil syndrome

Neuromuscular disorders : NMD, 2021-10, Vol.31, p.S116-S116

2021

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CHANNELOPATHIES AND RELATED DISORDERS

Neuromuscular disorders : NMD, 2021-10, Vol.31, p.S116

2021

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Defective Potassium Channel Kir2.1 Trafficking Underlies Andersen-Tawil Syndrome

The Journal of biological chemistry, 2003-12, Vol.278 (51), p.51779-51785

2003

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Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome)

The Journal of clinical investigation, 2002-08, Vol.110 (3), p.381-388

2002

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MiRP2 Forms Potassium Channels in Skeletal Muscle with Kv3.4 and Is Associated with Periodic Paralysis

Cell, 2001-01, Vol.104 (2), p.217-231

2001

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Global survival trends for brain tumors, by histology: analysis of individual records for 556,237 adults diagnosed in 59 countries during 2000–2014 (CONCORD-3)

Neuro-oncology (Charlottesville, Va.), 2023-03, Vol.25 (3), p.580-592

2023

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The histology of brain tumors for 67 331 children and 671 085 adults diagnosed in 60 countries during 2000-2014: a global, population-based study (CONCORD-3)

Neuro-oncology (Charlottesville, Va.), 2021-10, Vol.23 (10), p.1765-1776

2021

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Revisiting CFTR inhibition: a comparative study of CFTRinh‐172 and GlyH‐101 inhibitors

KCNQ1 Gain-of-Function Mutation in Familial Atrial Fibrillation

The inward rectifier potassium channel Kir2.1 is required for osteoblastogenesis

Identification of a KCNE2 Gain-of-Function Mutation in Patients with Familial Atrial Fibrillation

A Kir2.1 gain-of-function mutation underlies familial atrial fibrillation

In vitro molecular interactions and distribution of KCNE family with KCNQ1 in the human heart

Revisiting CFTR inhibition: a comparative study of CFTR inh ‐172 and GlyH ‐101 inhibitors

Proximal Renal Tubular Acidosis in TASK2 K+Channel-Deficient Mice Reveals a Mechanism for Stabilizing Bicarbonate Transport

PIP2 binding residues of Kir2.1 are common targets of mutations causing Andersen syndrome

ARF6-dependent interaction of the TWIK1 K+ channel with EFA6, a GDP/GTP exchange factor for ARF6

Impairment of slow inactivation as a common mechanism for periodic paralysis in DIIS4-S5

Mechanisms underlying Andersen's syndrome pathology in skeletal muscle are revealed in human myotubes

In vivo and in vitro functional characterization of Andersen's syndrome mutations

344 A cluster of the cystic fibrosis transmembrane regulator (CFTR) mutation S549R in the Sultanate of Oman

Global surveillance of trends in cancer survival 2000–14 (CONCORD-3): analysis of individual records for 37 513 025 patients diagnosed with one of 18 cancers from 322 population-based registries in 71 countries

Le pyrophosphate, un additif alimentaire comme stratégie thérapeutique pour lutter contre certaines maladies calcifiantes d’origine héréditaire ou métabolique

Mutations in Kir2.1 Cause the Developmental and Episodic Electrical Phenotypes of Andersen's Syndrome

Pathologies liées aux canaux à rectification entrante

CHANNELOPATHIES AND RELATED DISORDERS: EP.221 Diagnostic delay and atypical phenotypes in a French cohort of Andersen-Tawil syndrome

CHANNELOPATHIES AND RELATED DISORDERS

Defective Potassium Channel Kir2.1 Trafficking Underlies Andersen-Tawil Syndrome

Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome)

MiRP2 Forms Potassium Channels in Skeletal Muscle with Kv3.4 and Is Associated with Periodic Paralysis

Global survival trends for brain tumors, by histology: analysis of individual records for 556,237 adults diagnosed in 59 countries during 2000–2014 (CONCORD-3)

The histology of brain tumors for 67 331 children and 671 085 adults diagnosed in 60 countries during 2000-2014: a global, population-based study (CONCORD-3)

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