A gain-of-function mutation in the CLCN2 chloride channel gene causes primary aldosteronism

Genetic Causes of Functional Adrenocortical Adenomas

(2017) Maria-Christina Zennaro et al.   ENDOCRINE REVIEWS

Worldwide trends in blood pressure from 1975 to 2015: a pooled analysis of 1479 population-based measurement studies with 19·1 million participants

(2017) Bin Zhou et al.   LANCET

The Management of Primary Aldosteronism: Case Detection, Diagnosis, and Treatment: An Endocrine Society Clinical Practice Guideline

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Role of voltage-gated calcium channels in the regulation of aldosterone production from zona glomerulosa cells of the adrenal cortex

(2016) Paula Q. Barrett et al.   JOURNAL OF PHYSIOLOGY-LONDON

CACNA1H Mutations Are Associated With Different Forms of Primary Aldosteronism

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Discovery of CLC transport proteins: cloning, structure, function and pathophysiology

(2015) Thomas J. Jentsch   JOURNAL OF PHYSIOLOGY-LONDON

Recurrent gain of function mutation in calcium channel CACNA1H causes early-onset hypertension with primary aldosteronism

(2015) Ute I Scholl et al.   eLife

Subclinical leukodystrophy and infertility in a man with a novel homozygous CLCN2 mutation

(2014) D. Di Bella et al.   NEUROLOGY

Cardiovascular Complications Associated With Primary Aldosteronism

(2013) Sébastien Savard et al.   HYPERTENSION

Brain white matter oedema due to ClC-2 chloride channel deficiency: an observational analytical study

(2013) Christel Depienne et al.   LANCET NEUROLOGY

Development of monoclonal antibodies against human CYP11B1 and CYP11B2

(2013) Celso E. Gomez-Sanchez et al.   MOLECULAR AND CELLULAR ENDOCRINOLOGY

Somatic mutations in ATP1A1 and CACNA1D underlie a common subtype of adrenal hypertension

(2013) Elena A B Azizan et al.   NATURE GENETICS

Somatic and germline CACNA1D calcium channel mutations in aldosterone-producing adenomas and primary aldosteronism

(2013) Ute I Scholl et al.   NATURE GENETICS

Somatic mutations in ATP1A1 and ATP2B3 lead to aldosterone-producing adenomas and secondary hypertension

(2013) Felix Beuschlein et al.   NATURE GENETICS

Hyperaldosteronism as a Common Cause of Resistant Hypertension

(2012) David A. Calhoun   Annual Review of Medicine

Comparison of Aldosterone Production Among Human Adrenocortical Cell Lines

(2012) T. Wang et al.   HORMONE AND METABOLIC RESEARCH

Prevalence, Clinical, and Molecular Correlates of KCNJ5 Mutations in Primary Aldosteronism

(2012) Sheerazed Boulkroun et al.   HYPERTENSION

Zona glomerulosa cells of the mouse adrenal cortex are intrinsic electrical oscillators

(2012) Changlong Hu et al.   JOURNAL OF CLINICAL INVESTIGATION

Prevalence of Primary Aldosteronism in Patient's Cohorts and in Population-based Studies - A Review of the Current Literature

(2011) A. Hannemann et al.   HORMONE AND METABOLIC RESEARCH

Mineralocorticoid Receptor Mutations and a Severe Recessive Pseudohypoaldosteronism Type 1

(2011) E.-L. Hubert et al.   JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY

K+ Channel Mutations in Adrenal Aldosterone-Producing Adenomas and Hereditary Hypertension

(2011) M. Choi et al.   SCIENCE

ClC-2 Voltage-Gated Channels Constitute Part of the Background Conductance and Assist Chloride Extrusion

(2010) I. Rinke et al.   JOURNAL OF NEUROSCIENCE

The MIQE Guidelines: Minimum Information for Publication of Quantitative Real-Time PCR Experiments

(2009) S. A. Bustin et al.   CLINICAL CHEMISTRY

Molecular Pharmacology of Human Cav3.2 T-Type Ca2+ Channels: Block by Antihypertensives, Antiarrhythmics, and Their Analogs

(2008) E. Perez-Reyes et al.   JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS