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ERp29 as a regulator of Insulin biosynthesis

PloS one, 2020-05, Vol.15 (5), p.e0233502-e0233502

2020

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Correction: ERp29 as a regulator of Insulin biosynthesis

PloS one, 2020-08, Vol.15 (8), p.e0238264-e0238264

2020

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The Probable, Possible, and Novel Functions of ERp29

Frontiers in physiology, 2020-09, Vol.11, p.574339-574339

2020

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IL-17A induces Pendrin expression and chloride-bicarbonate exchange in human bronchial epithelial cells

PloS one, 2014-08, Vol.9 (8), p.e103263

2014

Volltextzugriff (PDF)

Bitter taste receptor agonists regulate epithelial two-pore potassium channels via cAMP signaling

Respiratory research, 2021-01, Vol.22 (1), p.31-31, Article 31

2021

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Early-phase insulin secretion during mixed-meal tolerance testing predicts β-cell function and secretory capacity in cystic fibrosis

Frontiers in endocrinology (Lausanne), 2024-02, Vol.15, p.1340346-1340346

2024

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ERp29 regulates epithelial sodium channel functional expression by promoting channel cleavage

American Journal of Physiology: Cell Physiology, 2014-10, Vol.307 (8), p.C701-C709

2014

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Bone metabolism and incretin hormones following glucose ingestion in young adults with pancreatic insufficient cystic fibrosis

Journal of clinical & translational endocrinology, 2022-12, Vol.30, p.100304-100304, Article 100304

2022

Volltextzugriff (PDF)

Differential Effects of Hsc70 and Hsp70 on the Intracellular Trafficking and Functional Expression of Epithelial Sodium Channels

Proceedings of the National Academy of Sciences - PNAS, 2006-04, Vol.103 (15), p.5817-5822

2006

Volltextzugriff (PDF)

4-Phenylbutyrate Stimulates Hsp70 Expression through the Elp2 Component of Elongator and STAT-3 in Cystic Fibrosis Epithelial Cells

The Journal of biological chemistry, 2011-12, Vol.286 (52), p.45083-45092

2011

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Body composition and pulmonary function in cystic fibrosis

Frontiers in pediatrics, 2014-01, Vol.2, p.33-33

2014

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ERp29 restricts Connexin43 oligomerization in the endoplasmic reticulum

Molecular biology of the cell, 2009-05, Vol.20 (10), p.2593-2604

2009

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Infant Body Mass Index or Weight-for-Length and Risk of Undernutrition in Childhood Among Children with Cystic Fibrosis

The Journal of pediatrics, 2022-04, Vol.243, p.116-121.e3

2022

Volltextzugriff (PDF)

Molecular Chaperones as Targets to Circumvent the CFTR Defect in Cystic Fibrosis

Frontiers in pharmacology, 2012-01, Vol.3, p.137-137

2012

Volltextzugriff (PDF)

Microbial Sharing between Pediatric Patients and Therapy Dogs during Hospital Animal-Assisted Intervention Programs

Microorganisms (Basel), 2021-05, Vol.9 (5), p.1054

2021

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Murine nasal septa for respiratory epithelial air-liquid interface cultures

BioTechniques, 2007-08, Vol.43 (2), p.195-204

2007

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1548-P: GLP-1 and GIP Reduce Insulin Clearance in Individuals with Pancreatic-Insufficient Cystic Fibrosis (PI-CF)

Diabetes (New York, N.Y.), 2023-06, Vol.72 (Supplement_1), p.1

2023

Volltextzugriff (PDF)

Evidence of CFTR Function in Cystic Fibrosis after Systemic Administration of 4-Phenylbutyrate

Molecular therapy, 2002-07, Vol.6 (1), p.119-126

2002

Volltextzugriff (PDF)

Preservation of β-cell Function in Pancreatic Insufficient Cystic Fibrosis With Highly Effective CFTR Modulator Therapy

The journal of clinical endocrinology and metabolism, 2023-12, Vol.109 (1), p.151-160

2023

Volltextzugriff (PDF)

Quantification of Enteric Dysfunction in Cystic Fibrosis: Inter- and Intraindividual Variability

The Journal of pediatrics, 2024-02, Vol.265, p.113800-113800, Article 113800

2024

Volltextzugriff (PDF)

The EXTrauterine Environment for Neonatal Development Supports Normal Intestinal Maturation and Development

Cellular and molecular gastroenterology and hepatology, 2020-01, Vol.10 (3), p.623-637

2020

Volltextzugriff (PDF)

The KDEL receptor has a role in the biogenesis and trafficking of the epithelial sodium channel (ENaC)

The Journal of biological chemistry, 2019-11, Vol.294 (48), p.18324-18336

2019

Volltextzugriff (PDF)

Abnormal glucose tolerance and the 50-gram glucose challenge test in Cystic fibrosis

Journal of cystic fibrosis, 2020-09, Vol.19 (5), p.696-699

2020

Volltextzugriff (PDF)

Effect of VX-770 in Persons with Cystic Fibrosis and the G551D-CFTR Mutation

The New England journal of medicine, 2010-11, Vol.363 (21), p.1991-2003

2010

Volltextzugriff (PDF)

On preventing the extinction of the physician-scientist in pediatric pulmonology

Frontiers in pediatrics, 2014-01, Vol.2, p.4-4

2014

Volltextzugriff (PDF)

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ERp29 as a regulator of Insulin biosynthesis

Correction: ERp29 as a regulator of Insulin biosynthesis

The Probable, Possible, and Novel Functions of ERp29

IL-17A induces Pendrin expression and chloride-bicarbonate exchange in human bronchial epithelial cells

Bitter taste receptor agonists regulate epithelial two-pore potassium channels via cAMP signaling

Early-phase insulin secretion during mixed-meal tolerance testing predicts β-cell function and secretory capacity in cystic fibrosis

ERp29 regulates epithelial sodium channel functional expression by promoting channel cleavage

Bone metabolism and incretin hormones following glucose ingestion in young adults with pancreatic insufficient cystic fibrosis

Differential Effects of Hsc70 and Hsp70 on the Intracellular Trafficking and Functional Expression of Epithelial Sodium Channels

4-Phenylbutyrate Stimulates Hsp70 Expression through the Elp2 Component of Elongator and STAT-3 in Cystic Fibrosis Epithelial Cells

Body composition and pulmonary function in cystic fibrosis

ERp29 restricts Connexin43 oligomerization in the endoplasmic reticulum

Infant Body Mass Index or Weight-for-Length and Risk of Undernutrition in Childhood Among Children with Cystic Fibrosis

Molecular Chaperones as Targets to Circumvent the CFTR Defect in Cystic Fibrosis

Microbial Sharing between Pediatric Patients and Therapy Dogs during Hospital Animal-Assisted Intervention Programs

Murine nasal septa for respiratory epithelial air-liquid interface cultures

1548-P: GLP-1 and GIP Reduce Insulin Clearance in Individuals with Pancreatic-Insufficient Cystic Fibrosis (PI-CF)

Evidence of CFTR Function in Cystic Fibrosis after Systemic Administration of 4-Phenylbutyrate

Preservation of β-cell Function in Pancreatic Insufficient Cystic Fibrosis With Highly Effective CFTR Modulator Therapy

Quantification of Enteric Dysfunction in Cystic Fibrosis: Inter- and Intraindividual Variability

The EXTrauterine Environment for Neonatal Development Supports Normal Intestinal Maturation and Development

The KDEL receptor has a role in the biogenesis and trafficking of the epithelial sodium channel (ENaC)

Abnormal glucose tolerance and the 50-gram glucose challenge test in Cystic fibrosis

Effect of VX-770 in Persons with Cystic Fibrosis and the G551D-CFTR Mutation

On preventing the extinction of the physician-scientist in pediatric pulmonology

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