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Chromogranin A pathway: from pathogenic molecule to renal disease

Journal of hypertension, 2020-03, Vol.38 (3), p.456

2020

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A new common functional coding variant at the DDC gene change renal enzyme activity and modify renal dopamine function

Scientific reports, 2019-03, Vol.9 (1), p.5055-5055, Article 5055

2019

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Urinary Exosomes Identify Inflammatory Pathways in Vancomycin Associated Acute Kidney Injury

International journal of molecular sciences, 2021-03, Vol.22 (6), p.2784

2021

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Hypertension from targeted ablation of chromogranin A can be rescued by the human ortholog

The Journal of clinical investigation, 2005-07, Vol.115 (7), p.1942-1952

2005

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Analysis and validation of traits associated with a single nucleotide polymorphism Gly364Ser in catestatin using humanized chromogranin A mouse models

Journal of hypertension, 2016-01, Vol.34 (1), p.68-78

2016

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Novel Pathway of Insulin Sensitivity in Chromogranin A Null Mice: A CRUCIAL ROLE FOR PANCREASTATIN IN GLUCOSE HOMEOSTASIS

The Journal of biological chemistry, 2009-10, Vol.284 (42), p.28498-28509

2009

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Author Correction: A new common functional coding variant at the DDC gene change renal enzyme activity and modify renal dopamine function

Scientific reports, 2020-02, Vol.10 (1), p.2996-2996, Article 2996

2020

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Discovery of common human genetic variants of GTP cyclohydrolase 1 (GCH1) governing nitric oxide, autonomic activity, and cardiovascular risk

The Journal of clinical investigation, 2007-09, Vol.117 (9), p.2658-2671

2007

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Furosemide stress test and interstitial fibrosis in kidney biopsies in chronic kidney disease

BMC nephrology, 2020-03, Vol.21 (1), p.87-87, Article 87

2020

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MicroRNA-22 and promoter motif polymorphisms at the Chga locus in genetic hypertension: functional and therapeutic implications for gene expression and the pathogenesis of hypertension

Human molecular genetics, 2013-09, Vol.22 (18), p.3624-3640

2013

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Molecular Mechanism for Hypertensive Renal Disease: Differential Regulation of Chromogranin A Expression at 3'-Untranslated Region Polymorphism C+87T by MicroRNA-107

Journal of the American Society of Nephrology, 2015-08, Vol.26 (8), p.1816-1825

2015

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Cathepsin L Colocalizes with Chromogranin A in Chromaffin Vesicles to Generate Active Peptides

Endocrinology (Philadelphia), 2009-08, Vol.150 (8), p.3547-3557

2009

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Proteolytic Cleavage of Human Chromogranin A Containing Naturally Occurring Catestatin Variants: Differential Processing at Catestatin Region by Plasmin

Endocrinology (Philadelphia), 2008-02, Vol.149 (2), p.749-757

2008

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Catecholamine release-inhibitory peptide catestatin (chromogranin A352_372) : Naturally occurring amino acid variant Gly364ser causes profound changes in human autonomic activity and alters risk for hypertension

Circulation (New York, N.Y.), 2007-05, Vol.115 (17), p.2271-2281

2007

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Uric Acid and Acute Kidney Injury in the Critically Ill

Kidney medicine, 2019-01, Vol.1 (1), p.21-30

2019

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PC-1 Nucleoside Triphosphate Pyrophosphohydrolase Deficiency in Idiopathic Infantile Arterial Calcification

The American journal of pathology, 2001-02, Vol.158 (2), p.543-554

2001

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Naturally Occurring Human Genetic Variation in the 3′-Untranslated Region of the Secretory Protein Chromogranin A Is Associated With Autonomic Blood Pressure Regulation and Hypertension in a Sex-Dependent Fashion

Journal of the American College of Cardiology, 2008-10, Vol.52 (18), p.1468-1481

2008

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Polymorphisms at the F12 and KLKB1 loci have significant trait association with activation of the renin-angiotensin system

BMC medical genetics, 2016-03, Vol.17 (1), p.21-21, Article 21

2016

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Stability of Fibroblast Growth Factor 23 in Human Plasma

The journal of applied laboratory medicine, 2017-05, Vol.1 (6), p.729-734

2017

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Effects of chromogranin A deficiency and excess in vivo: biphasic blood pressure and catecholamine responses

Journal of hypertension, 2010-04, Vol.28 (4), p.817-825

2010

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Long human CHGA flanking chromosome 14 sequence required for optimal BAC transgenic "rescue" of disease phenotypes in the mouse Chga knockout

Physiological genomics, 2010-03, Vol.41 (1), p.91-101

2010

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Cardiac Electrical Activity in a Genomically “Humanized” Chromogranin A Monogenic Mouse Model with Hyperadrenergic Hypertension

Journal of cardiovascular translational research, 2014-07, Vol.7 (5), p.483-493

2014

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Biogenesis of the Secretory Granule: Chromogranin A Coiled-Coil Structure Results in Unusual Physical Properties and Suggests a Mechanism for Granule Core Condensation

Biochemistry (Easton), 2007-09, Vol.46 (38), p.10999-11012

2007

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Subcellular targeting and function of osteoblast nucleotide pyrophosphatase phosphodiesterase 1

American Journal of Physiology: Cell Physiology, 2004-05, Vol.286 (5), p.C1177-C1187

2004

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Naturally Occurring Genetic Variants in Human Chromogranin A (CHGA) Associated with Hypertension as well as Hypertensive Renal Disease

Cellular and molecular neurobiology, 2010-11, Vol.30 (8), p.1395-1400

2010

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Chromogranin A pathway: from pathogenic molecule to renal disease

A new common functional coding variant at the DDC gene change renal enzyme activity and modify renal dopamine function

Urinary Exosomes Identify Inflammatory Pathways in Vancomycin Associated Acute Kidney Injury

Hypertension from targeted ablation of chromogranin A can be rescued by the human ortholog

Analysis and validation of traits associated with a single nucleotide polymorphism Gly364Ser in catestatin using humanized chromogranin A mouse models

Novel Pathway of Insulin Sensitivity in Chromogranin A Null Mice: A CRUCIAL ROLE FOR PANCREASTATIN IN GLUCOSE HOMEOSTASIS

Author Correction: A new common functional coding variant at the DDC gene change renal enzyme activity and modify renal dopamine function

Discovery of common human genetic variants of GTP cyclohydrolase 1 (GCH1) governing nitric oxide, autonomic activity, and cardiovascular risk

Furosemide stress test and interstitial fibrosis in kidney biopsies in chronic kidney disease

MicroRNA-22 and promoter motif polymorphisms at the Chga locus in genetic hypertension: functional and therapeutic implications for gene expression and the pathogenesis of hypertension

Molecular Mechanism for Hypertensive Renal Disease: Differential Regulation of Chromogranin A Expression at 3'-Untranslated Region Polymorphism C+87T by MicroRNA-107

Cathepsin L Colocalizes with Chromogranin A in Chromaffin Vesicles to Generate Active Peptides

Proteolytic Cleavage of Human Chromogranin A Containing Naturally Occurring Catestatin Variants: Differential Processing at Catestatin Region by Plasmin

Catecholamine release-inhibitory peptide catestatin (chromogranin A352_372) : Naturally occurring amino acid variant Gly364ser causes profound changes in human autonomic activity and alters risk for hypertension

Uric Acid and Acute Kidney Injury in the Critically Ill

PC-1 Nucleoside Triphosphate Pyrophosphohydrolase Deficiency in Idiopathic Infantile Arterial Calcification

Naturally Occurring Human Genetic Variation in the 3′-Untranslated Region of the Secretory Protein Chromogranin A Is Associated With Autonomic Blood Pressure Regulation and Hypertension in a Sex-Dependent Fashion

Polymorphisms at the F12 and KLKB1 loci have significant trait association with activation of the renin-angiotensin system

Stability of Fibroblast Growth Factor 23 in Human Plasma

Effects of chromogranin A deficiency and excess in vivo: biphasic blood pressure and catecholamine responses

Long human CHGA flanking chromosome 14 sequence required for optimal BAC transgenic "rescue" of disease phenotypes in the mouse Chga knockout

Cardiac Electrical Activity in a Genomically “Humanized” Chromogranin A Monogenic Mouse Model with Hyperadrenergic Hypertension

Biogenesis of the Secretory Granule: Chromogranin A Coiled-Coil Structure Results in Unusual Physical Properties and Suggests a Mechanism for Granule Core Condensation

Subcellular targeting and function of osteoblast nucleotide pyrophosphatase phosphodiesterase 1

Naturally Occurring Genetic Variants in Human Chromogranin A (CHGA) Associated with Hypertension as well as Hypertensive Renal Disease

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