Cystic fibrosis lung environment and Pseudomonas aeruginosa infection.

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Cystic fibrosis lung environment and Pseudomonas aeruginosa infection. is …
instance of (P31):
review articleQ7318358
scholarly articleQ13442814

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P6179Dimensions Publication ID1037635435
P356DOI10.1186/S12890-016-0339-5
P932PMC publication ID5139081
P698PubMed publication ID27919253

P50authorAnjali Y BhagirathQ88231318
Kangmin DuanQ38803382
P2093author name stringYanqi Li
Sara Badr
Maryam Dadashi
Deepti Somayajula
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Effect of mutator P. aeruginosa on antibiotic resistance acquisition and respiratory function in cystic fibrosisQ84219534
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Immunocytochemical localization of the cystic fibrosis gene product CFTRQ37609030
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Bacterial hypermutation in cystic fibrosis, not only for antibiotic resistanceQ37794342
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The serous cellQ37876724
Microevolution of Pseudomonas aeruginosa to a chronic pathogen of the cystic fibrosis lungQ37981915
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Current concepts of immune dysregulation in cystic fibrosis.Q38185216
Detrimental effects of secondhand smoke exposure on infants with cystic fibrosisQ38194542
Architecture and assembly of the Type VI secretion system.Q38200408
The problems of antibiotic resistance in cystic fibrosis and solutionsQ38300820
Effect of azithromycin on pulmonary function in patients with cystic fibrosis uninfected with Pseudomonas aeruginosa: a randomized controlled trialQ38373785
CFTR, bicarbonate, and the pathophysiology of cystic fibrosisQ38579954
Update on host-pathogen interactions in cystic fibrosis lung diseaseQ38605085
Facilitating Structure-Function Studies of CFTR Modulator Sites with Efficiencies in Mutagenesis and Functional Screening.Q38962286
Purinergic regulation of CFTR and Ca(2+)-activated Cl(-) channels and K(+) channels in human pancreatic duct epitheliumQ39201947
Acquisition of Pseudomonas aeruginosa in children with cystic fibrosisQ39455047
Effect of Media Modified To Mimic Cystic Fibrosis Sputum on the Susceptibility of Aspergillus fumigatus, and the Frequency of Resistance at One CenterQ39514745
Effect of residential proximity to major roadways on cystic fibrosis exacerbationsQ39578759
Genotypic and phenotypic variation in Pseudomonas aeruginosa reveals signatures of secondary infection and mutator activity in certain cystic fibrosis patients with chronic lung infectionsQ39656697
Treatment burden in patients with at least one class IV or V CFTR mutationQ40352553
Pre-adapting parasitic phages to a pathogen leads to increased pathogen clearance and lowered resistance evolution with Pseudomonas aeruginosa cystic fibrosis bacterial isolatesQ40421266
Early infection and progression of cystic fibrosis lung diseaseQ40636854
Rheological Properties of Cystic Fibrosis Bronchial Secretion and in Vitro Drug Permeation Study: The Effect of Sodium BicarbonateQ40841860
Abnormal glutathione transport in cystic fibrosis airway epitheliaQ40941623
Oxygen limitation contributes to antibiotic tolerance of Pseudomonas aeruginosa in biofilms.Q40968095
Seasonal onset of initial colonisation and chronic infection with Pseudomonas aeruginosa in patients with cystic fibrosis in DenmarkQ41145157
Integrated biophysical studies implicate partial unfolding of NBD1 of CFTR in the molecular pathogenesis of F508del cystic fibrosisQ41148531
Thermal unfolding studies show the disease causing F508del mutation in CFTR thermodynamically destabilizes nucleotide‐binding domain 1Q41148574
Differential expression of ORCC and CFTR induced by low temperature in CF airway epithelial cellsQ41404505
Epidemiology of Pseudomonas aeruginosa infection and the role of contamination of the environment in a cystic fibrosis clinicQ41448149
Fine particulate matter exposure and initial Pseudomonas aeruginosa acquisition in cystic fibrosisQ41541158
Pseudomonas aeruginosa eradicates Staphylococcus aureus by manipulating the host immunity.Q41712968
CFTR is required for PKA-regulated ATP sensitivity of Kir1.1 potassium channels in mouse kidneyQ42018121
Naturally produced outer membrane vesicles from Pseudomonas aeruginosa elicit a potent innate immune response via combined sensing of both lipopolysaccharide and protein componentsQ42181392
Correction of both NBD1 energetics and domain interface is required to restore ΔF508 CFTR folding and functionQ42321930
Bile acids stimulate chloride secretion through CFTR and calcium-activated Cl- channels in Calu-3 airway epithelial cellsQ42461659
P275copyright licenseCreative Commons Attribution 4.0 InternationalQ20007257
P6216copyright statuscopyrightedQ50423863
P433issue1
P407language of work or nameEnglishQ1860
P921main subjectrespiratory systemQ7891
perinatal diseaseQ18968218
cystic fibrosisQ178194
Pseudomonas aeruginosaQ31856
host microbial interactionQ68260314
P5008on focus list of Wikimedia projectScienceSourceQ55439927
P304page(s)174
P577publication date2016-12-05
P1433published inBMC Pulmonary MedicineQ15755469
P1476titleCystic fibrosis lung environment and Pseudomonas aeruginosa infection
P478volume16

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