about
Cationic antimicrobial peptides promote microbial mutagenesis and pathoadaptation in chronic infectionsSecondhand Smoke Is an Important Modifiable Risk Factor in Sickle Cell Disease: A Review of the Current Literature and Areas for Future ResearchIFN-γ stimulates autophagy-mediated clearance of Burkholderia cenocepacia in human cystic fibrosis macrophagesAutophagy stimulation by rapamycin suppresses lung inflammation and infection by Burkholderia cenocepacia in a model of cystic fibrosis.Inpatient healthcare trends among adult cystic fibrosis patients in the U.S.Surveillance transbronchial biopsies in infant lung and heart-lung transplant recipients.Comprehensive evaluation of lung allograft function in infants after lung and heart-lung transplantation.Polysomnographic differences associated with pulmonary hypertension in patients with advanced lung disease due to cystic fibrosis.Respiratory syncytial virus: current and emerging treatment optionsCharacteristics of invasive Acinetobacter species isolates recovered in a pediatric academic centerThe Geographic Impact on Hospitalization in Patients with Cystic Fibrosis.Transplant center volume and outcomes in lung transplantation for cystic fibrosis.Impact of Donor Arterial Partial Pressure of Oxygen on Outcomes After Lung Transplantation in Adult Cystic Fibrosis Recipients.Human Cystic Fibrosis Macrophages Have Defective Calcium-Dependent Protein Kinase C Activation of the NADPH Oxidase, an Effect Augmented by Burkholderia cenocepacia.Burkholderia cenocepacia O polysaccharide chain contributes to caspase-1-dependent IL-1beta production in macrophages.Cysteamine-mediated clearance of antibiotic-resistant pathogens in human cystic fibrosis macrophages.Diabetic myonecrosis in a cystic fibrosis patient.Metabolomic responses to lumacaftor/ivacaftor in cystic fibrosis.Impact of Presence of Children on Indoor Tobacco Restrictions in Households of Urban and Rural Adult Tobacco Users.Influence of graft ischemic time on survival in children with cystic fibrosis after lung transplantation.Cystic fibrosis transmembrane conductance regulator (CFTR) modulators have differential effects on cystic fibrosis macrophage functionPulmonary findings in infants with cystic fibrosis during the first year of life: Results from the Baby Observational and Nutrition Study (BONUS) cohort study.The BMPR2 missense mutation p.K230N and pulmonary arterial hypertensionBenefits of pulmonary rehabilitation in pediatric asthmaDysregulated Calcium Homeostasis in Cystic Fibrosis Neutrophils Leads to Deficient Antimicrobial ResponsesSecondhand smoke alters arachidonic acid metabolism and inflammation in infants and children with cystic fibrosisAge and environmental exposures influence the fecal bacteriome of young children with cystic fibrosis
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description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Benjamin T Kopp
@ast
Benjamin T Kopp
@en
Benjamin T Kopp
@es
Benjamin T Kopp
@nl
type
label
Benjamin T Kopp
@ast
Benjamin T Kopp
@en
Benjamin T Kopp
@es
Benjamin T Kopp
@nl
prefLabel
Benjamin T Kopp
@ast
Benjamin T Kopp
@en
Benjamin T Kopp
@es
Benjamin T Kopp
@nl
P106
P1153
41561551500
P31
P496
0000-0002-2021-7990