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...

Cystic Fibrosis: A Journey through Time and Hope

International journal of molecular sciences, 2024-09, Vol.25 (17), p.9599

2024

Volltextzugriff (PDF)

In silico search for modifier genes associated with pancreatic and liver disease in Cystic Fibrosis

PloS one, 2017-03, Vol.12 (3), p.e0173822-e0173822

2017

Volltextzugriff (PDF)

The Interplay between the Unfolded Protein Response, Inflammation and Infection in Cystic Fibrosis

Cells (Basel, Switzerland), 2021-11, Vol.10 (11), p.2980

2021

Volltextzugriff (PDF)

A missense mutation in the alpha-actinin 1 gene (ACTN1) is the cause of autosomal dominant macrothrombocytopenia in a large French family

PloS one, 2013-09, Vol.8 (9), p.e74728

2013

Volltextzugriff (PDF)

The Inhibition of the Membrane-Bound Transcription Factor Site-1 Protease (MBTP1) Alleviates the p.Phe508del-Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Defects in Cystic Fibrosis Cells

Cells (Basel, Switzerland), 2024-01, Vol.13 (2), p.185

2024

Volltextzugriff (PDF)

Biophysical characterisation of calumenin as a charged F508del-CFTR folding modulator

PloS one, 2014-08, Vol.9 (8), p.e104970-e104970

2014

Volltextzugriff (PDF)

Buserelin alleviates chloride transport defect in human cystic fibrosis nasal epithelial cells

PloS one, 2017-11, Vol.12 (11), p.e0187774

2017

Volltextzugriff (PDF)

The calpain, caspase 12, caspase 3 cascade leading to apoptosis is altered in F508del-CFTR expressing cells

PloS one, 2009-12, Vol.4 (12), p.e8436-e8436

2009

Volltextzugriff (PDF)

Role of Interaction and Nucleoside Diphosphate Kinase B in Regulation of the Cystic Fibrosis Transmembrane Conductance Regulator Function by cAMP-Dependent Protein Kinase A

PloS one, 2016-03, Vol.11 (3), p.e0149097-e0149097

2016

Volltextzugriff (PDF)

Proteomic identification of calumenin as a G551D-CFTR associated protein

PloS one, 2012-06, Vol.7 (6), p.e40173

2012

Volltextzugriff (PDF)

Coupling cystic fibrosis to endoplasmic reticulum stress: Differential role of Grp78 and ATF6

Biochimica et biophysica acta, 2007-12, Vol.1772 (11), p.1236-1249

2007

Volltextzugriff (PDF)

Improvement of chloride transport defect by gonadotropin-releasing hormone (GnRH) in cystic fibrosis epithelial cells

PloS one, 2014-02, Vol.9 (2), p.e88964

2014

Volltextzugriff (PDF)

Functional analysis of pancreatitis-associated missense mutations in the pancreatic secretory trypsin inhibitor ( ) gene

European journal of human genetics : EJHG, 2007-09, Vol.15 (9), p.936-942

2007

Volltextzugriff (PDF)

Evaluation of aminopyrrolidine amide to improve chloride transport in CFTR-defective cells

Bioorganic & medicinal chemistry letters, 2022-09, Vol.72, p.128866-128866, Article 128866

2022

Volltextzugriff (PDF)

Monoallelic pathogenic ALG5 variants cause atypical polycystic kidney disease and interstitial fibrosis

American journal of human genetics, 2022-08, Vol.109 (8), p.1484-1499

2022

Volltextzugriff (PDF)

GEMPROT: visualization of the impact on the protein of the genetic variants found on each haplotype

Bioinformatics, 2019-07, Vol.35 (14), p.2492-2494

2019

Volltextzugriff (PDF)

TIMP1 intron 3 retention is a marker of colon cancer progression controlled by hnRNPA1

Molecular biology reports, 2020-04, Vol.47 (4), p.3031-3040

2020

Volltextzugriff (PDF)

Calumenin contributes to ER-Ca2+ homeostasis in bronchial epithelial cells expressing WT and F508del mutated CFTR and to F508del-CFTR retention

Cell calcium (Edinburgh), 2017-03, Vol.62, p.47-59

2017

Volltextzugriff (PDF)

Externalization of endogenous annexin A5 participates in apoptosis of rat cardiomyocytes

Cardiovascular research, 2004-12, Vol.64 (3), p.496-506

2004

Volltextzugriff (PDF)

G551D-CFTR needs more bound actin than wild-type CFTR to maintain its presence in plasma membranes

Cell biology international, 2015-08, Vol.39 (8), p.978-985

2015

Volltextzugriff (PDF)

Surface plasmon resonance shows a gender difference in circulating annexin A5 in human

Talanta (Oxford), 2012-05, Vol.93, p.219-223

2012

Volltextzugriff (PDF)

Rapid detection of the mature form of cystic fibrosis transmembrane regulator by surface plasmon resonance

Analytical methods, 2015-01, Vol.7 (1), p.226-236

2015

Volltextzugriff (PDF)

Biological Determinants of Aldosterone-Induced Cardiac Fibrosis in Rats

Hypertension (Dallas, Tex. 1979), 1995-12, Vol.26 (6), p.971-978

1995

Volltextzugriff (PDF)

Annexin V is directly involved in cystic fibrosis transmembrane conductance regulator's chloride channel function

Biochimica et biophysica acta, 2007-10, Vol.1772 (10), p.1121-1133

2007

Volltextzugriff (PDF)

Annexin A5 increases the cell surface expression and the chloride channel function of the ΔF508-cystic fibrosis transmembrane regulator

Biochimica et biophysica acta. Molecular basis of disease, 2008-10, Vol.1782 (10), p.605-614

2008

Volltextzugriff (PDF)

1 – 25 von 53

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(50)
Mit Volltextzugriff
(50)

Publikationsform

Sprache

Englisch
(49)
Französisch
(4)

Erscheinungsjahr

n.n

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Cystic Fibrosis: A Journey through Time and Hope

In silico search for modifier genes associated with pancreatic and liver disease in Cystic Fibrosis

The Interplay between the Unfolded Protein Response, Inflammation and Infection in Cystic Fibrosis

A missense mutation in the alpha-actinin 1 gene (ACTN1) is the cause of autosomal dominant macrothrombocytopenia in a large French family

The Inhibition of the Membrane-Bound Transcription Factor Site-1 Protease (MBTP1) Alleviates the p.Phe508del-Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Defects in Cystic Fibrosis Cells

Biophysical characterisation of calumenin as a charged F508del-CFTR folding modulator

Buserelin alleviates chloride transport defect in human cystic fibrosis nasal epithelial cells

The calpain, caspase 12, caspase 3 cascade leading to apoptosis is altered in F508del-CFTR expressing cells

Role of Interaction and Nucleoside Diphosphate Kinase B in Regulation of the Cystic Fibrosis Transmembrane Conductance Regulator Function by cAMP-Dependent Protein Kinase A

Proteomic identification of calumenin as a G551D-CFTR associated protein

Coupling cystic fibrosis to endoplasmic reticulum stress: Differential role of Grp78 and ATF6

Improvement of chloride transport defect by gonadotropin-releasing hormone (GnRH) in cystic fibrosis epithelial cells

Functional analysis of pancreatitis-associated missense mutations in the pancreatic secretory trypsin inhibitor ( ) gene

Evaluation of aminopyrrolidine amide to improve chloride transport in CFTR-defective cells

Monoallelic pathogenic ALG5 variants cause atypical polycystic kidney disease and interstitial fibrosis

GEMPROT: visualization of the impact on the protein of the genetic variants found on each haplotype

TIMP1 intron 3 retention is a marker of colon cancer progression controlled by hnRNPA1

Calumenin contributes to ER-Ca2+ homeostasis in bronchial epithelial cells expressing WT and F508del mutated CFTR and to F508del-CFTR retention

Externalization of endogenous annexin A5 participates in apoptosis of rat cardiomyocytes

G551D-CFTR needs more bound actin than wild-type CFTR to maintain its presence in plasma membranes

Surface plasmon resonance shows a gender difference in circulating annexin A5 in human

Rapid detection of the mature form of cystic fibrosis transmembrane regulator by surface plasmon resonance

Biological Determinants of Aldosterone-Induced Cardiac Fibrosis in Rats

Annexin V is directly involved in cystic fibrosis transmembrane conductance regulator's chloride channel function

Annexin A5 increases the cell surface expression and the chloride channel function of the ΔF508-cystic fibrosis transmembrane regulator

Suchergebnisse filtern