Pages that link to "Q37839809"

The following pages link to The Cystic Fibrosis Neutrophil: A Specialized Yet Potentially Defective Cell (Q37839809):

Displaying 32 items.

• Epithelial Anion Transport as Modulator of Chemokine Signaling (Q26744381) (← links)
• Animal Models of Cystic Fibrosis Pathology: Phenotypic Parallels and Divergences (Q26747210) (← links)
• The Role of Serine Proteases and Antiproteases in the Cystic Fibrosis Lung (Q26799771) (← links)
• Innate receptors and cellular defense against pulmonary infections (Q26996036) (← links)
• Airway Gland Structure and Function (Q28082284) (← links)
• Influence of neutrophil defects on Burkholderia cepacia complex pathogenesis (Q30425441) (← links)
• Harnessing Neutrophil Survival Mechanisms during Chronic Infection by Pseudomonas aeruginosa: Novel Therapeutic Targets to Dampen Inflammation in Cystic Fibrosis (Q33857503) (← links)
• Neutrophil Extracellular Trap (NET)-Mediated Killing of Pseudomonas aeruginosa: Evidence of Acquired Resistance within the CF Airway, Independent of CFTR (Q34016539) (← links)
• A neutrophil intrinsic impairment affecting Rab27a and degranulation in cystic fibrosis is corrected by CFTR potentiator therapy (Q34047949) (← links)
• Neutrophil-mediated phagocytic host defense defect in myeloid Cftr-inactivated mice (Q34128926) (← links)
• The mitochondrial complex I activity is reduced in cells with impaired cystic fibrosis transmembrane conductance regulator (CFTR) function (Q34489613) (← links)
• NOX2 As a Target for Drug Development: Indications, Possible Complications, and Progress (Q35985407) (← links)
• Novel cellular targets of AhR underlie alterations in neutrophilic inflammation and inducible nitric oxide synthase expression during influenza virus infection (Q36514344) (← links)
• Modulating Innate and Adaptive Immunity by (R)-Roscovitine: Potential Therapeutic Opportunity in Cystic Fibrosis (Q36709312) (← links)
• Cystic fibrosis transmembrane conductance regulator recruitment to phagosomes in neutrophils (Q37029698) (← links)
• Galectin-9 signaling through TIM-3 is involved in neutrophil-mediated Gram-negative bacterial killing: an effect abrogated within the cystic fibrosis lung (Q37203240) (← links)
• Mucosal and systemic antibody responses to potential Pseudomonas aeruginosa vaccine protein antigens in young children with cystic fibrosis following colonization and infection (Q37478266) (← links)
• Interactions between Neutrophils and Pseudomonas aeruginosa in Cystic Fibrosis (Q37727995) (← links)
• PPARγ as a therapeutic target in cystic fibrosis (Q38001841) (← links)
• Targeting cytosolic proliferating cell nuclear antigen in neutrophil-dominated inflammation (Q38062530) (← links)
• Pseudomonas aeruginosa: new insights into pathogenesis and host defenses (Q38101888) (← links)
• Ivacaftor: a review of its use in patients with cystic fibrosis (Q38136994) (← links)
• Neutrophils at work (Q38221176) (← links)
• Advanced Role of Neutrophils in Common Respiratory Diseases (Q38739370) (← links)
• Neutrophil-Expressed p21/waf1 Favors Inflammation Resolution in Pseudomonas aeruginosa Infection (Q38823607) (← links)
• Neutrophil Membrane Cholesterol Content is a Key Factor in Cystic Fibrosis Lung Disease (Q41688386) (← links)
• RNAi in Respiratory Diseases (Q58061971) (← links)
• Progression of Cystic Fibrosis Lung Disease from Childhood to Adulthood: Neutrophils, Neutrophil Extracellular Trap (NET) Formation, and NET Degradation (Q64101109) (← links)
• Modulators of Transient Receptor Potential (TRP) Channels as Therapeutic Options in Lung Disease (Q64230474) (← links)
• Neutrophils in the innate immunity conundrum of cystic fibrosis: a CFTR-related matter? (Q86523714) (← links)
• Neutrophils as a Potential Source of Chitinase-3-like Protein 1 in Cystic Fibrosis (Q88873934) (← links)
• Lights and Shadows in the Use of Mesenchymal Stem Cells in Lung Inflammation, a Poorly Investigated Topic in Cystic Fibrosis (Q92155494) (← links)