UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Sie befinden Sich nicht im Netzwerk der Universität Paderborn. Der Zugriff auf elektronische Ressourcen ist gegebenenfalls nur via VPN oder Shibboleth (DFN-AAI) möglich. mehr Informationen...

Emerging Concepts in Defective Macrophage Phagocytosis in Cystic Fibrosis

International journal of molecular sciences, 2022-07, Vol.23 (14), p.7750

2022

Link zum Volltext

Verfügbarkeit prüfen

IFN-γ stimulates autophagy-mediated clearance of Burkholderia cenocepacia in human cystic fibrosis macrophages

PloS one, 2014-05, Vol.9 (5), p.e96681-e96681

2014

Link zum Volltext

Verfügbarkeit prüfen

Cysteamine-mediated clearance of antibiotic-resistant pathogens in human cystic fibrosis macrophages

PloS one, 2017-10, Vol.12 (10), p.e0186169-e0186169

2017

Link zum Volltext

Verfügbarkeit prüfen

(R)-Roscovitine and CFTR modulators enhance killing of multi-drug resistant Burkholderia cenocepacia by cystic fibrosis macrophages

Scientific reports, 2020-12, Vol.10 (1), p.21700-21700, Article 21700

2020

Link zum Volltext

Verfügbarkeit prüfen

Description of a Colocated Comprehensive Care Model for People With Sickle Cell and Comorbid Pulmonary Disease

Journal of pediatric hematology/oncology, 2023-08, Vol.45 (6), p.e723

2023

Link zum Volltext

Verfügbarkeit prüfen

Cationic antimicrobial peptides promote microbial mutagenesis and pathoadaptation in chronic infections

PLoS pathogens, 2014-04, Vol.10 (4), p.e1004083

2014

Link zum Volltext

Verfügbarkeit prüfen

Consequences of CRISPR-Cas9-Mediated CFTR Knockout in Human Macrophages

Frontiers in immunology, 2020-08, Vol.11, p.1871-1871

2020

Link zum Volltext

Verfügbarkeit prüfen

Oral cysteamine as an adjunct treatment in cystic fibrosis pulmonary exacerbations: An exploratory randomized clinical trial

PloS one, 2020-12, Vol.15 (12), p.e0242945

2020

Link zum Volltext

Verfügbarkeit prüfen

Correction: IFN-γ Stimulates Autophagy-Mediated Clearance of Burkholderia cenocepacia in Human Cystic Fibrosis Macrophages

PloS one, 2019, Vol.14 (2), p.e0213092-e0213092

2019

Link zum Volltext

Verfügbarkeit prüfen

Influence of human leukocyte antigen mismatching on bronchiolitis obliterans syndrome in lung transplantation

The Journal of heart and lung transplantation, 2016-02, Vol.35 (2), p.186-194

2016

Link zum Volltext

Verfügbarkeit prüfen

Cystic fibrosis transmembrane conductance regulator (CFTR) modulators have differential effects on cystic fibrosis macrophage function

Scientific reports, 2018-11, Vol.8 (1), p.17066-10, Article 17066

2018

Link zum Volltext

Verfügbarkeit prüfen

AR-13 reduces antibiotic-resistant bacterial burden in cystic fibrosis phagocytes and improves cystic fibrosis transmembrane conductance regulator function

Journal of cystic fibrosis, 2019-09, Vol.18 (5), p.622-629

2019

Link zum Volltext

Verfügbarkeit prüfen

The Geographic Impact on Hospitalization in Patients with Cystic Fibrosis

The Journal of pediatrics, 2016-03, Vol.170, p.246-252.e4

2016

Link zum Volltext

Verfügbarkeit prüfen

Characteristics of invasive Acinetobacter species isolates recovered in a pediatric academic center

BMC infectious diseases, 2016-07, Vol.16 (1), p.346-346, Article 346

2016

Link zum Volltext

Verfügbarkeit prüfen

Mortality Risk and Pulmonary Function in Adults With Cystic Fibrosis at Time of Wait Listing for Lung Transplantation

The Annals of thoracic surgery, 2015-08, Vol.100 (2), p.474-479

2015

Link zum Volltext

Verfügbarkeit prüfen

Inpatient healthcare trends among adult cystic fibrosis patients in the U.S

Pediatric pulmonology, 2012-03, Vol.47 (3), p.245-251

2012

Link zum Volltext

Verfügbarkeit prüfen

Long‐term pulmonary sequelae in adolescents post‐SARS‐CoV‐2 infection

Pediatric pulmonology, 2022-10, Vol.57 (10), p.2455-2463

2022

Link zum Volltext

Verfügbarkeit prüfen

Cystic fibrosis macrophage function and clinical outcomes after elexacaftor/tezacaftor/ivacaftor

The European respiratory journal, 2023-04, Vol.61 (4), p.2102861

2023

Link zum Volltext

Verfügbarkeit prüfen

Comprehensive evaluation of lung allograft function in infants after lung and heart-lung transplantation

The Journal of heart and lung transplantation, 2014-05, Vol.33 (5), p.507-513

2014

Link zum Volltext

Verfügbarkeit prüfen

Impact of elexacaftor–tezacaftor–ivacaftor on bacterial colonization and inflammatory responses in cystic fibrosis

Pediatric pulmonology, 2023-03, Vol.58 (3), p.825-833

2023

Link zum Volltext

Verfügbarkeit prüfen

Dysregulated Calcium Homeostasis in Cystic Fibrosis Neutrophils Leads to Deficient Antimicrobial Responses

The Journal of immunology (1950), 2018-10, Vol.201 (7), p.2016-2027

2018

Link zum Volltext

Verfügbarkeit prüfen

Whole-blood transcriptomic responses to lumacaftor/ivacaftor therapy in cystic fibrosis

Journal of cystic fibrosis, 2020-03, Vol.19 (2), p.245-254

2020

Link zum Volltext

Verfügbarkeit prüfen

Not All Children with Cystic Fibrosis Have Abnormal Esophageal Neutralization during Chemical Clearance of Acid Reflux

Pediatric Gastroenterology, 2017, Hepatology & Nutrition, 20(3), , pp.153-159

2017

Link zum Volltext

Verfügbarkeit prüfen

Human Cystic Fibrosis Macrophages Have Defective Calcium-Dependent Protein Kinase C Activation of the NADPH Oxidase, an Effect Augmented by Burkholderia cenocepacia

The Journal of immunology (1950), 2017-03, Vol.198 (5), p.1985-1994

2017

Link zum Volltext

Verfügbarkeit prüfen

Sweat metabolomics before and after intravenous antibiotics for pulmonary exacerbation in people with cystic fibrosis

Respiratory medicine, 2022-01, Vol.191, p.106687-106687, Article 106687

2022

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 279

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(265)
Mit Volltextzugriff
(257)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(197)
Life Sciences & Biomedicine
(147)
Humans
(90)
Physical Sciences
(50)
Male
(47)
Female
(46)
Cystic Fibrosis
(37)
Respiratory System
(35)
Adult
(34)
Pediatrics
(27)
Sea Level
(26)
Child
(25)
Animals
(24)
Adolescent
(23)
Climate Change
(22)
Environmental Sciences
(21)
Multidisciplinary Sciences
(21)
Science & Technology - Other Topics
(21)
Environmental Sciences & Ecology
(20)
Geology
(19)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

Pediatric Pulmonology
(15)
Cancer Research
(10)
Plos One
(10)
Chest
(7)
Journal Of Cystic Fibrosis
(6)
Nature Communications
(6)
Quaternary Science Reviews
(6)
Earth's Future
(5)
Scientific Reports
(5)
Proceedings Of The National Academy Of Sciences
(4)

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(2)
... seit 90 Tagen
(6)

Menü

Weitere Dienste

Einstellungen

Emerging Concepts in Defective Macrophage Phagocytosis in Cystic Fibrosis

IFN-γ stimulates autophagy-mediated clearance of Burkholderia cenocepacia in human cystic fibrosis macrophages

Cysteamine-mediated clearance of antibiotic-resistant pathogens in human cystic fibrosis macrophages

(R)-Roscovitine and CFTR modulators enhance killing of multi-drug resistant Burkholderia cenocepacia by cystic fibrosis macrophages

Description of a Colocated Comprehensive Care Model for People With Sickle Cell and Comorbid Pulmonary Disease

Cationic antimicrobial peptides promote microbial mutagenesis and pathoadaptation in chronic infections

Consequences of CRISPR-Cas9-Mediated CFTR Knockout in Human Macrophages

Oral cysteamine as an adjunct treatment in cystic fibrosis pulmonary exacerbations: An exploratory randomized clinical trial

Correction: IFN-γ Stimulates Autophagy-Mediated Clearance of Burkholderia cenocepacia in Human Cystic Fibrosis Macrophages

Influence of human leukocyte antigen mismatching on bronchiolitis obliterans syndrome in lung transplantation

Cystic fibrosis transmembrane conductance regulator (CFTR) modulators have differential effects on cystic fibrosis macrophage function

AR-13 reduces antibiotic-resistant bacterial burden in cystic fibrosis phagocytes and improves cystic fibrosis transmembrane conductance regulator function

The Geographic Impact on Hospitalization in Patients with Cystic Fibrosis

Characteristics of invasive Acinetobacter species isolates recovered in a pediatric academic center

Mortality Risk and Pulmonary Function in Adults With Cystic Fibrosis at Time of Wait Listing for Lung Transplantation

Inpatient healthcare trends among adult cystic fibrosis patients in the U.S

Long‐term pulmonary sequelae in adolescents post‐SARS‐CoV‐2 infection

Cystic fibrosis macrophage function and clinical outcomes after elexacaftor/tezacaftor/ivacaftor

Comprehensive evaluation of lung allograft function in infants after lung and heart-lung transplantation

Impact of elexacaftor–tezacaftor–ivacaftor on bacterial colonization and inflammatory responses in cystic fibrosis

Dysregulated Calcium Homeostasis in Cystic Fibrosis Neutrophils Leads to Deficient Antimicrobial Responses

Whole-blood transcriptomic responses to lumacaftor/ivacaftor therapy in cystic fibrosis

Not All Children with Cystic Fibrosis Have Abnormal Esophageal Neutralization during Chemical Clearance of Acid Reflux

Human Cystic Fibrosis Macrophages Have Defective Calcium-Dependent Protein Kinase C Activation of the NADPH Oxidase, an Effect Augmented by Burkholderia cenocepacia

Sweat metabolomics before and after intravenous antibiotics for pulmonary exacerbation in people with cystic fibrosis

Suchergebnisse filtern