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...

Progress in therapies for cystic fibrosis

The lancet respiratory medicine, 2016-08, Vol.4 (8), p.662-674

2016

Volltextzugriff (PDF)

What Role Does CFTR Play in Development, Differentiation, Regeneration and Cancer?

International journal of molecular sciences, 2020-04, Vol.21 (9), p.3133

2020

Volltextzugriff (PDF)

Defining the disease liability of variants in the cystic fibrosis transmembrane conductance regulator gene

Nature genetics, 2013-10, Vol.45 (10), p.1160-1167

2013

Volltextzugriff (PDF)

Rescuing mutant CFTR: a multi-task approach to a better outcome in treating cystic fibrosis

Current pharmaceutical design, 2013, Vol.19 (19), p.3497-3508

2013

Volltextzugriff (PDF)

CFTR, Cell Junctions and the Cytoskeleton

International journal of molecular sciences, 2022-02, Vol.23 (5), p.2688

2022

Volltextzugriff (PDF)

A genetic screening strategy identifies novel regulators of the proteostasis network

PLoS genetics, 2011-12, Vol.7 (12), p.e1002438-e1002438

2011

Volltextzugriff (PDF)

Synergy in Cystic Fibrosis Therapies: Targeting SLC26A9

International journal of molecular sciences, 2021-12, Vol.22 (23), p.13064

2021

Volltextzugriff (PDF)

Molecular targeting of CFTR as a therapeutic approach to cystic fibrosis

Trends in pharmacological sciences (Regular ed.), 2007-07, Vol.28 (7), p.334-341

2007

Volltextzugriff (PDF)

Mutation-class dependent signatures outweigh disease-associated processes in cystic fibrosis cells

Cell & bioscience, 2023-02, Vol.13 (1), p.26-26, Article 26

2023

Volltextzugriff (PDF)

What Can RNA-Based Therapy Do for Monogenic Diseases?

Pharmaceutics, 2023-01, Vol.15 (1), p.260

2023

Volltextzugriff (PDF)

Rare Trafficking CFTR Mutations Involve Distinct Cellular Retention Machineries and Require Different Rescuing Strategies

International journal of molecular sciences, 2021-12, Vol.23 (1), p.24

2021

Volltextzugriff (PDF)

High-Content siRNA Screen Reveals Global ENaC Regulators and Potential Cystic Fibrosis Therapy Targets

Cell, 2013-09, Vol.154 (6), p.1390-1400

2013

Volltextzugriff (PDF)

Impact of KLF4 on Cell Proliferation and Epithelial Differentiation in the Context of Cystic Fibrosis

International journal of molecular sciences, 2020-09, Vol.21 (18), p.6717

2020

Volltextzugriff (PDF)

Using the genome to correct the ion transport defect in cystic fibrosis

The Journal of physiology, 2023-05, Vol.601 (9), p.1573-1582

Amaral, Margarida D.

2023

Volltextzugriff (PDF)

A molecular switch in the scaffold NHERF1 enables misfolded CFTR to evade the peripheral quality control checkpoint

Science signaling, 2015-05, Vol.8 (377), p.ra48

2015

Volltextzugriff (PDF)

Precision medicine for rare diseases: The times they are A-Changin

Current opinion in pharmacology, 2022-04, Vol.63, p.102201-102201, Article 102201

Amaral, Margarida D.

2022

Volltextzugriff (PDF)

CyFi-MAP: an interactive pathway-based resource for cystic fibrosis

Scientific reports, 2021-11, Vol.11 (1), p.22223-22223, Article 22223

2021

Volltextzugriff (PDF)

Transcriptome meta-analysis reveals common differential and global gene expression profiles in cystic fibrosis and other respiratory disorders and identifies CFTR regulators

Genomics (San Diego, Calif.), 2015-11, Vol.106 (5), p.268-277

2015

Volltextzugriff (PDF)

Most F508del-CFTR Is Targeted to Degradation at an Early Folding Checkpoint and Independently of Calnexin

Molecular and Cellular Biology, 2005-06, Vol.25 (12), p.5242-5252

2005

Volltextzugriff (PDF)

How to determine the mechanism of action of CFTR modulator compounds: A gateway to theranostics

European journal of medicinal chemistry, 2021-01, Vol.210, p.112989-112989, Article 112989

Amaral, Margarida D.

2021

Volltextzugriff (PDF)

Protocol for Application, Standardization and Validation of the Forskolin-Induced Swelling Assay in Cystic Fibrosis Human Colon Organoids

STAR protocols, 2020-06, Vol.1 (1), p.100019-100019, Article 100019

2020

Volltextzugriff (PDF)

Targeting CFTR: how to treat cystic fibrosis by CFTR-repairing therapies

Current drug targets, 2011-05, Vol.12 (5), p.683-693

Amaral, Margarida D

2011

Volltextzugriff (PDF)

A central role of the endoplasmic reticulum in the cell emerges from its functional contact sites with multiple organelles

Cellular and molecular life sciences : CMLS, 2020-12, Vol.77 (23), p.4729-4745

2020

Volltextzugriff (PDF)

Full Rescue of F508del-CFTR Processing and Function by CFTR Modulators Can Be Achieved by Removal of Two Regulatory Regions

International journal of molecular sciences, 2020-06, Vol.21 (12), p.4524

2020

Volltextzugriff (PDF)

1 – 25 von 302

Suche als RSS-Feed

Aktive Filter

Zeitschrift / SerieThe Journal Of Biological Chemistry

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(175)
Mit Volltextzugriff
(239)

Publikationsform

Artikel
(228)
Buchkapitel
(73)
Bücher
(1)

Sprache

Englisch
(300)
Portugiesisch
(4)

Erscheinungsjahr

n.n

Thema

Science & Technology
(195)
Life Sciences & Biomedicine
(182)
Humans
(159)
Cystic Fibrosis Transmembrane Conductance Regulator - Genetics
(113)
Cystic Fibrosis
(108)
Cystic Fibrosis Transmembrane Conductance Regulator - Metabolism
(103)
Biochemistry & Molecular Biology
(96)
Mutation
(87)
Cystic Fibrosis - Genetics
(79)
Respiratory System
(76)
Animals
(70)
Cystic Fibrosis - Metabolism
(61)
Biochemical Research Methods
(55)
Cftr
(52)
Cell Line
(41)
Cell Biology
(36)
Cystic Fibrosis Transmembrane Conductance Regulator - Chemistry
(30)
Proteins
(27)
Mice
(26)
Protein Folding
(26)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)
... seit 90 Tagen
(4)

Menü

Weitere Dienste

Einstellungen

Progress in therapies for cystic fibrosis

What Role Does CFTR Play in Development, Differentiation, Regeneration and Cancer?

Defining the disease liability of variants in the cystic fibrosis transmembrane conductance regulator gene

Rescuing mutant CFTR: a multi-task approach to a better outcome in treating cystic fibrosis

CFTR, Cell Junctions and the Cytoskeleton

A genetic screening strategy identifies novel regulators of the proteostasis network

Synergy in Cystic Fibrosis Therapies: Targeting SLC26A9

Molecular targeting of CFTR as a therapeutic approach to cystic fibrosis

Mutation-class dependent signatures outweigh disease-associated processes in cystic fibrosis cells

What Can RNA-Based Therapy Do for Monogenic Diseases?

Rare Trafficking CFTR Mutations Involve Distinct Cellular Retention Machineries and Require Different Rescuing Strategies

High-Content siRNA Screen Reveals Global ENaC Regulators and Potential Cystic Fibrosis Therapy Targets

Impact of KLF4 on Cell Proliferation and Epithelial Differentiation in the Context of Cystic Fibrosis

Using the genome to correct the ion transport defect in cystic fibrosis

A molecular switch in the scaffold NHERF1 enables misfolded CFTR to evade the peripheral quality control checkpoint

Precision medicine for rare diseases: The times they are A-Changin

CyFi-MAP: an interactive pathway-based resource for cystic fibrosis

Transcriptome meta-analysis reveals common differential and global gene expression profiles in cystic fibrosis and other respiratory disorders and identifies CFTR regulators

Most F508del-CFTR Is Targeted to Degradation at an Early Folding Checkpoint and Independently of Calnexin

How to determine the mechanism of action of CFTR modulator compounds: A gateway to theranostics

Protocol for Application, Standardization and Validation of the Forskolin-Induced Swelling Assay in Cystic Fibrosis Human Colon Organoids

Human Epididymis Protein 4: A Novel Serum Inflammatory Biomarker in Cystic Fibrosis

Targeting CFTR: how to treat cystic fibrosis by CFTR-repairing therapies

A central role of the endoplasmic reticulum in the cell emerges from its functional contact sites with multiple organelles

Full Rescue of F508del-CFTR Processing and Function by CFTR Modulators Can Be Achieved by Removal of Two Regulatory Regions

Aktive Filter

Suchergebnisse filtern