UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

The EGFR-ADAM17 Axis in Chronic Obstructive Pulmonary Disease and Cystic Fibrosis Lung Pathology

Mediators of inflammation, 2018-01, Vol.2018 (2018), p.1-22

2018

Volltextzugriff (PDF)

A functional CFTR assay using primary cystic fibrosis intestinal organoids

Nature medicine, 2013-07, Vol.19 (7), p.939-945

2013

Volltextzugriff (PDF)

CFTR Correctors and Antioxidants Partially Normalize Lipid Imbalance but not Abnormal Basal Inflammatory Cytokine Profile in CF Bronchial Epithelial Cells

Frontiers in physiology, 2021-02, Vol.12, p.619442-619442

2021

Volltextzugriff (PDF)

Extracellular oxidation in cystic fibrosis airway epithelium causes enhanced EGFR/ADAM17 activity

American journal of physiology. Lung cellular and molecular physiology, 2018-04, Vol.314 (4), p.L555-L568

2018

Volltextzugriff (PDF)

Mouse models of cystic fibrosis: Phenotypic analysis and research applications

Journal of cystic fibrosis, 2011-06, Vol.10, p.S152-S171

2011

Volltextzugriff (PDF)

High-Throughput Screening for Modulators of CFTR Activity Based on Genetically Engineered Cystic Fibrosis Disease-Specific iPSCs

Stem cell reports, 2019-06, Vol.12 (6), p.1389-1403

2019

Volltextzugriff (PDF)

Determination of thiocyanate in exhaled breath condensate

Free radical biology & medicine, 2018-10, Vol.126, p.334-340

2018

Volltextzugriff (PDF)

Rescue of murine F508del CFTR activity in native intestine by low temperature and proteasome inhibitors

PloS one, 2012-12, Vol.7 (12), p.e52070-e52070

2012

Volltextzugriff (PDF)

Dysregulated proinflammatory and fibrogenic phenotype of fibroblasts in cystic fibrosis

PloS one, 2013-05, Vol.8 (5), p.e64341

2013

Volltextzugriff (PDF)

Cationic Geminoid Peptide Amphiphiles Inhibit DENV2 Protease, Furin, and Viral Replication

Molecules (Basel, Switzerland), 2022-05, Vol.27 (10), p.3217

2022

Volltextzugriff (PDF)

Carbachol-induced colonic mucus formation requires transport via NKCC1, K+ channels and CFTR

Pflügers Archiv, 2015-07, Vol.467 (7), p.1403-1415

2015

Volltextzugriff (PDF)

Role of IL-1β in experimental cystic fibrosis upon P. aeruginosa infection

PloS one, 2014-12, Vol.9 (12), p.e114884-e114884

2014

Volltextzugriff (PDF)

Lentiviral gene therapy of murine hematopoietic stem cells ameliorates the Pompe disease phenotype

Blood, 2010-07, Vol.115 (26), p.5329-5337

2010

Volltextzugriff (PDF)

Small hydrophobic protein of human metapneumovirus does not affect virus replication and host gene expression in vitro

PloS one, 2013-03, Vol.8 (3), p.e58572

2013

Volltextzugriff (PDF)

Azithromycin reduces spontaneous and induced inflammation in ΔF508 cystic fibrosis mice

Respiratory research, 2006-10, Vol.7 (1), p.134-134, Article 134

2006

Volltextzugriff (PDF)

Elastase Exocytosis by Airway Neutrophils Is Associated with Early Lung Damage in Children with Cystic Fibrosis

American journal of respiratory and critical care medicine, 2019-04, Vol.199 (7), p.873-881

2019

Volltextzugriff (PDF)

Myeloperoxidase oxidation of methionine associates with early cystic fibrosis lung disease

The European respiratory journal, 2018-10, Vol.52 (4), p.1801118

2018

Volltextzugriff (PDF)

Oxidative stress and abnormal bioactive lipids in early cystic fibrosis lung disease

Journal of cystic fibrosis, 2019-11, Vol.18 (6), p.781-789

2019

Volltextzugriff (PDF)

Correction of lung inflammation in a F508del CFTR murine cystic fibrosis model by the sphingosine-1-phosphate lyase inhibitor LX2931

American journal of physiology. Lung cellular and molecular physiology, 2016-11, Vol.311 (5), p.L1000-L1014

2016

Volltextzugriff (PDF)

Key inflammatory markers in bronchoalveolar lavage predict bronchiectasis progression in young children with CF

Journal of cystic fibrosis, 2024-05, Vol.23 (3), p.450-456

2024

Volltextzugriff (PDF)

Proteomic Analysis of Naphthalene-Induced Airway Epithelial Injury and Repair in a Cystic Fibrosis Mouse Model

Journal of proteome research, 2009-07, Vol.8 (7), p.3606-3616

2009

Volltextzugriff (PDF)

Increased susceptibility of Cftr-/- mice to LPS-induced lung remodeling

American journal of physiology. Lung cellular and molecular physiology, 2016-04, Vol.310 (8), p.L711-L719

2016

Volltextzugriff (PDF)

Airway profile of bioactive lipids predicts early progression of lung disease in cystic fibrosis

Journal of cystic fibrosis, 2020-11, Vol.19 (6), p.902-909

2020

Volltextzugriff (PDF)

Macrophage PD-1 associates with neutrophilia and reduced bacterial killing in early cystic fibrosis airway disease

Journal of cystic fibrosis, 2022-11, Vol.21 (6), p.967-976

2022

Volltextzugriff (PDF)

Inflammation and host-pathogen interaction: Cause and consequence in cystic fibrosis lung disease

Journal of cystic fibrosis, 2018-03, Vol.17 (2), p.S40-S45

2018

Volltextzugriff (PDF)

1 – 25 von 93

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(92)
Mit Volltextzugriff
(83)

Publikationsform

Artikel
(91)
Reviews
(2)

Sprache

Englisch
(92)
Französisch
(1)

Erscheinungsjahr

n.n

Thema

Science & Technology
(63)
Life Sciences & Biomedicine
(56)
Humans
(37)
Animals
(34)
Cystic Fibrosis
(28)
Mice
(22)
Cystic Fibrosis - Genetics
(18)
Cystic Fibrosis Transmembrane Conductance Regulator - Genetics
(18)
Female
(14)
Cystic Fibrosis Transmembrane Conductance Regulator - Metabolism
(13)
Physiology
(13)
Biological And Medical Sciences
(12)
Cell Line
(12)
Cystic Fibrosis - Pathology
(12)
Male
(12)
Respiratory System
(12)
Cystic Fibrosis - Metabolism
(11)
Cells, Cultured
(10)
Disease Models, Animal
(10)
Mutation
(10)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

The EGFR-ADAM17 Axis in Chronic Obstructive Pulmonary Disease and Cystic Fibrosis Lung Pathology

A functional CFTR assay using primary cystic fibrosis intestinal organoids

CFTR Correctors and Antioxidants Partially Normalize Lipid Imbalance but not Abnormal Basal Inflammatory Cytokine Profile in CF Bronchial Epithelial Cells

Extracellular oxidation in cystic fibrosis airway epithelium causes enhanced EGFR/ADAM17 activity

Mouse models of cystic fibrosis: Phenotypic analysis and research applications

High-Throughput Screening for Modulators of CFTR Activity Based on Genetically Engineered Cystic Fibrosis Disease-Specific iPSCs

Determination of thiocyanate in exhaled breath condensate

Rescue of murine F508del CFTR activity in native intestine by low temperature and proteasome inhibitors

Dysregulated proinflammatory and fibrogenic phenotype of fibroblasts in cystic fibrosis

Cationic Geminoid Peptide Amphiphiles Inhibit DENV2 Protease, Furin, and Viral Replication

Carbachol-induced colonic mucus formation requires transport via NKCC1, K+ channels and CFTR

Role of IL-1β in experimental cystic fibrosis upon P. aeruginosa infection

Lentiviral gene therapy of murine hematopoietic stem cells ameliorates the Pompe disease phenotype

Small hydrophobic protein of human metapneumovirus does not affect virus replication and host gene expression in vitro

Azithromycin reduces spontaneous and induced inflammation in ΔF508 cystic fibrosis mice

Elastase Exocytosis by Airway Neutrophils Is Associated with Early Lung Damage in Children with Cystic Fibrosis

Myeloperoxidase oxidation of methionine associates with early cystic fibrosis lung disease

Oxidative stress and abnormal bioactive lipids in early cystic fibrosis lung disease

Correction of lung inflammation in a F508del CFTR murine cystic fibrosis model by the sphingosine-1-phosphate lyase inhibitor LX2931

Key inflammatory markers in bronchoalveolar lavage predict bronchiectasis progression in young children with CF

Proteomic Analysis of Naphthalene-Induced Airway Epithelial Injury and Repair in a Cystic Fibrosis Mouse Model

Increased susceptibility of Cftr-/- mice to LPS-induced lung remodeling

Airway profile of bioactive lipids predicts early progression of lung disease in cystic fibrosis

Macrophage PD-1 associates with neutrophilia and reduced bacterial killing in early cystic fibrosis airway disease

Inflammation and host-pathogen interaction: Cause and consequence in cystic fibrosis lung disease

Suchergebnisse filtern