UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 82

Sortiert nach

Correction: ERp29 as a regulator of Insulin biosynthesis

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

2020

Volltextzugriff (PDF)

The Probable, Possible, and Novel Functions of ERp29

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

2020

Volltextzugriff (PDF)

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)

Body composition and pulmonary function in cystic fibrosis

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

2014

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

Volltextzugriff (PDF)

Murine nasal septa for respiratory epithelial air-liquid interface cultures

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

2007

Volltextzugriff (PDF)

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)

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)

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

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

2014

Volltextzugriff (PDF)

828-P: Preservation of ß-Cell Function in Pancreatic Insufficient Cystic Fibrosis (CF) with Highly Effective CFTR Modulator Therapy

Diabetes (New York, N.Y.), 2022-06, Vol.71 (Supplement_1)

2022

Volltextzugriff (PDF)

Editorial Focus: CFTR‐dependent bicarbonate secretion by Calu‐3 cells

Physiological reports, 2018-05, Vol.6 (10), p.e13691-n/a

Rubenstein, Ronald C.

2018

Volltextzugriff (PDF)

The presence of Aspergillus fumigatus is associated with worse respiratory quality of life in cystic fibrosis

Journal of cystic fibrosis, 2020-01, Vol.19 (1), p.125-130

2020

Volltextzugriff (PDF)

Patient and parent perceptions of the diagnosis and management of cystic fibrosis-related diabetes

Journal of clinical & translational endocrinology, 2014-09, Vol.1 (3), p.100-107

2014

Volltextzugriff (PDF)

Sexual and reproductive health behaviors and experiences reported by young women with cystic fibrosis

Journal of cystic fibrosis, 2018-01, Vol.17 (1), p.57-63

2018

Volltextzugriff (PDF)

β‐Cell secretory defects are present in pancreatic insufficient cystic fibrosis with 1‐hour oral glucose tolerance test glucose ≥155 mg/dL

Pediatric diabetes, 2018-11, Vol.19 (7), p.1173-1182

2018

Volltextzugriff (PDF)

Safety and efficacy of treatment with lumacaftor in combination with ivacaftor in younger patients with cystic fibrosis

Expert review of respiratory medicine, 2019-05, Vol.13 (5), p.417-423

2019

Volltextzugriff (PDF)

Dysregulated insulin in pancreatic insufficient cystic fibrosis with post-prandial hypoglycemia

Journal of cystic fibrosis, 2020-03, Vol.19 (2), p.310-315

2020

Volltextzugriff (PDF)

Sexual and reproductive health care utilization and preferences reported by young women with cystic fibrosis

Journal of cystic fibrosis, 2018-01, Vol.17 (1), p.64-70

2018

Volltextzugriff (PDF)

1783-P: Effects of DPP-4 Inhibition on the Enteroinsular Axis in Pancreatic Insufficient Cystic Fibrosis

Diabetes (New York, N.Y.), 2020-06, Vol.69 (Supplement_1)

2020

Volltextzugriff (PDF)

The Clinical Association between Aspergillus fumigatus and Respiratory Outcomes in Adolescents and Adults with Cystic Fibrosis

Annals of the American Thoracic Society, 2023-07, Vol.20 (7), p.984-992

2023

Volltextzugriff (PDF)

Sodium 4-phenylbutyrate downregulates Hsc70: implications for intracellular trafficking of Delta F508-CFTR

American Journal of Physiology: Cell Physiology, 2000-02, Vol.278 (2), p.C259-C267

2000

Volltextzugriff (PDF)

Hsp70 Promotes Epithelial Sodium Channel Functional Expression by Increasing Its Association with Coat Complex II and Its Exit from Endoplasmic Reticulum

The Journal of biological chemistry, 2012-06, Vol.287 (23), p.19255-19265

2012

Volltextzugriff (PDF)

A pilot clinical trial of oral sodium 4-phenylbutyrate (buphenyl) in ΔF508-homozygous cystic fibrosis patients: Partial restoration of nasal epithelial CFTR function

American journal of respiratory and critical care medicine, 1998-02, Vol.157 (2), p.484-490

1998

Volltextzugriff (PDF)

Hsc70 negatively regulates epithelial sodium channel trafficking at multiple sites in epithelial cells

American Journal of Physiology: Cell Physiology, 2013-10, Vol.305 (7), p.C776-C787

2013

Volltextzugriff (PDF)

1 – 25 von 82

Suche als RSS-Feed

Aktive Filter

ThemaHumans

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(77)
Mit Volltextzugriff
(75)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

Life Sciences & Biomedicine
(30)
Science & Technology
(30)
Cystic Fibrosis
(23)
Biological And Medical Sciences
(14)
Animals
(10)
Respiratory System
(10)
Fundamental And Applied Biological Sciences. Psychology
(9)
Medical Sciences
(7)
Biochemistry & Molecular Biology
(6)
Glucose
(6)
Insulin Secretion
(6)
Physiology
(6)
Cells
(5)
Glucose Tolerance
(5)
Mice
(5)
Molecular And Cellular Biology
(5)
Proteins
(5)
Secretion
(5)
Diabetes
(4)
Dogs
(4)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Correction: ERp29 as a regulator of Insulin biosynthesis

The Probable, Possible, and Novel Functions of ERp29

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

Body composition and pulmonary function in 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)

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

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

828-P: Preservation of ß-Cell Function in Pancreatic Insufficient Cystic Fibrosis (CF) with Highly Effective CFTR Modulator Therapy

Editorial Focus: CFTR‐dependent bicarbonate secretion by Calu‐3 cells

The presence of Aspergillus fumigatus is associated with worse respiratory quality of life in cystic fibrosis

Patient and parent perceptions of the diagnosis and management of cystic fibrosis-related diabetes

Sexual and reproductive health behaviors and experiences reported by young women with cystic fibrosis

β‐Cell secretory defects are present in pancreatic insufficient cystic fibrosis with 1‐hour oral glucose tolerance test glucose ≥155 mg/dL

Safety and efficacy of treatment with lumacaftor in combination with ivacaftor in younger patients with cystic fibrosis

Dysregulated insulin in pancreatic insufficient cystic fibrosis with post-prandial hypoglycemia

Sexual and reproductive health care utilization and preferences reported by young women with cystic fibrosis

1783-P: Effects of DPP-4 Inhibition on the Enteroinsular Axis in Pancreatic Insufficient Cystic Fibrosis

The Clinical Association between Aspergillus fumigatus and Respiratory Outcomes in Adolescents and Adults with Cystic Fibrosis

Sodium 4-phenylbutyrate downregulates Hsc70: implications for intracellular trafficking of Delta F508-CFTR

Hsp70 Promotes Epithelial Sodium Channel Functional Expression by Increasing Its Association with Coat Complex II and Its Exit from Endoplasmic Reticulum

A pilot clinical trial of oral sodium 4-phenylbutyrate (buphenyl) in ΔF508-homozygous cystic fibrosis patients: Partial restoration of nasal epithelial CFTR function

Hsc70 negatively regulates epithelial sodium channel trafficking at multiple sites in epithelial cells

Aktive Filter

Suchergebnisse filtern