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1 CF is characterized by repeated lung infections leading
2 CF MDMs demonstrate a nearly 60% reduction in superoxide
3 CF patients under corrector-potentiator therapy, which e
4 CF photographs of 30 eyes (20 patients) with diabetic ma
5 CF was inversely associated with clinical attachment lev
6 CF-ALF influences the P. aeruginosa cell wall by reducin
7 CF-related growth deficits can be improved via inhibitio
12 le KL levels were measured in plasma from 48 CF patients and in primary CF bronchial epithelial cells
16 s from 33 individuals: 11 with T2D and acute CF, 11 T2D patients with equivalent neuropathy and 11 no
19 plitude compared to patches containing adult CFs, while pure mESC-CM patches did not form functional
20 nic CFs is superior to co-culture with adult CFs for in vitro generation of functional myocardium.
24 ence, we conclude that CS30 is common among "CF negative" LT + STp isolates and is associated with ET
28 lar interactions through CF...S, CF...H, and CF...pi noncovalent interactions and enhance electron mo
29 bronchial epithelial cells from healthy and CF donors was assessed by surface biotinylation and subs
31 predicted ASL height under basal normal and CF conditions and the collapse of surface hydration due
33 onses to P. aeruginosa We used wild-type and CF mice, which we hormone manipulated, inoculated with P
34 3 (Meg3) was found to be mostly expressed by CFs and to undergo transcriptional downregulation during
35 ine mole fraction of lysine plus cadaverine (CF) indicated biofilm lysine decarboxylase activity.
38 e common groundwater contaminant chloroform (CF), this study investigated for the first time both car
41 designated anthocyanins (AF) and copigments (CF), was carried out using adsorptive membrane chromatog
43 n/coconut fibre/zinc oxide nanoparticles (CS/CF/nZnO) hybrid support to yield a polyamine sensing str
45 orage based on chlorophyll fluorescence (DCA-CF) and respiratory quotient (DCA-RQ) on the quality and
46 tate), as compared to fruit stored under DCA-CF, but fruit stored under DCA-RQ 1.5 and RQ 2.0 also sh
47 es ranked with student t-test discriminating CF antigens from healthy controls and LC at a False Disc
48 Of note, the current assemblies of the dog, CF 3.1 and the sheep, OA 3.1, genomes contain 264 and 59
51 hat 3D co-culture of mESC-CMs with embryonic CFs is superior to co-culture with adult CFs for in vitr
54 ntigenically different colonization factors (CFs) have been identified and characterized in ETEC at l
56 c juice and sputa from sixteen adult PEG fed CF patients and five replaced PEG tubes were studied.
60 ntal changes may induce cardiac fibroblasts (CF) pathological responses is far from being elucidated,
61 on assays, we show that cardiac fibroblasts (CFs) adopt an osteoblast cell-like fate and contribute d
63 opmental stage of mouse cardiac fibroblasts (CFs) influences the formation and function of engineered
66 flammation is a hallmark of cystic fibrosis (CF) and associated with increased production of transfor
67 pathogens in patients with cystic fibrosis (CF) and can cause severe necrotizing pneumonia, which is
69 RATIONALE: Individuals with cystic fibrosis (CF) experience frequent acute pulmonary exacerbations, w
70 ng disease in children with cystic fibrosis (CF) indicates that sensitive noninvasive outcome measure
74 tem, naturally occurring in cystic fibrosis (CF) isolates, have been previously shown to reverse this
80 BD2 mutations identified in cystic fibrosis (CF) patients, demonstrating that mutants such as N1303K
84 flammatory diseases such as cystic fibrosis (CF), and targeting ER stress may be useful for alleviati
86 rtant diagnostic marker for cystic fibrosis (CF), but the implementation of point-of-care systems for
87 gen killing is defective in cystic fibrosis (CF), despite abundant production of reactive oxygen spec
88 newborn screening (NBS) for cystic fibrosis (CF), the timing and magnitude of growth deficiency or it
89 onia, wound infections, and cystic fibrosis (CF), which is caused by mutations of the cystic fibrosis
103 abase representing the corrugated flamelets (CF), thin reaction zones (TRZ) and broken reaction zones
104 edictive of mortality after continuous flow (CF) left ventricular assist device (LVAD) implantation.
105 ve two cycles of cisplatin and fluorouracil (CF; two 3-weekly cycles of cisplatin [80 mg/m(2) intrave
106 (PPW), retinal folds (RF), choroidal folds (CF), and creases using transaxial and en face views.
116 and at 12 months and grouped as caries free (CF), caries active with enamel lesions (CAE), and caries
118 re able to detect PQS in sputum samples from CF patients infected with P. aeruginosa but not in sampl
121 of seven genes, csmA-G, related to the human CF operon CS18 and the porcine CF operon 987P (F6).
125 after chronic pressure overload to identify CF-enriched lncRNAs and investigate their function and c
126 lication, power, impedance drop [Delta-Imp], CF, force-time integral [FTI], and ablation index [AI])
129 indings support a role for CXCL1 and IL-8 in CF lung disease severity and identify STAT3 as a modulat
132 demonstrated reduced tubulin acetylation in CF cell models and tissue that is correctable by inhibit
133 channel openings, the dysfunction of CFTR in CF and the action of drugs that repair CFTR gating defec
136 poron species and Exophiala dermatitidis, in CF sputa using standard bacterial and selective fungal c
141 s may explain the sex-based mortality gap in CF and other inflammatory lung illnesses, and the ER blo
145 deria species can cause serious infection in CF and themselves affect key oxidase components in murin
150 y of the pathogenetic mechanisms involved in CF, which include impaired chloride permeability and per
151 egrin distribution and sphingosine levels in CF epithelial cells and prevents P. aeruginosa infection
153 , our study suggests that circulating MPs in CF disease have a high content of inflammatory cytokines
156 on of ENaC may have therapeutic potential in CF airways by reducing sodium hyperabsorption, restoring
157 hypothesis that such changes are present in CF pancreata before the development of lipofibrosis.
163 in) is able to additionally induce increased CF release of inflammatory and pro-fibrotic cytokines an
168 ents had >/=10 mg/dL differences between LDL-CF and LDL-CD compared with 25% and 20% of patients, res
169 ents had differences >/=10 mg/dL between LDL-CF and LDL-CD, whereas only 2% and 3% of patients, respe
172 en LDL-CD and estimated LDL-C (LDL-CN or LDL-CF) was stratified by LDL-C and triglyceride categories.
178 t characterizing lncRNA expression in murine CFs after chronic pressure overload to identify CF-enric
180 to our understanding of Bcc infection in non-CF patients and highlight the need for interventions to
182 dstream infections (BSIs) in a cohort of non-CF patients from the US Veterans Health Administration (
190 CF formation with only approximately 10% of CF recovery while sarcosine (SAR) showed insignificant e
195 neoadjuvant ECX compared with two cycles of CF did not increase survival, and cannot be considered s
200 icroF cm(-2) ) from combined polarization of CF interface dipoles and electrical-double-layer formati
202 table MICs on a non-negligible proportion of CF isolates, explained by a wide diversity of mutations
203 R) all resulted in remarkable suppression of CF formation with only approximately 10% of CF recovery
206 TEC isolates revealed that 8.6% (n = 13) of "CF negative" (n = 152) and 19.4% (n = 13) of "CF negativ
207 F negative" (n = 152) and 19.4% (n = 13) of "CF negative" LT + STp (n = 67) expressing isolates analy
209 e structure of LPS in the presence of OligoG CF-5/20, however, isothermal titration calorimetry demon
214 o combined properties that favorably opposed CF symptomatology: it reduced inflammation and increased
215 hat Staphylococcus aureus acquisition in our CF population occurred outside the hospital environment
220 se tolerance, adolescents and adults with PI-CF have impairments in functional islet mass and associa
223 ide, and glucagon responses compared with PS-CF and normal control subjects, indicating reduced beta-
226 used in conjunction with data from a recent CF genome-wide association study (GWAS) meta-analysis to
228 l cohort study, was conducted during regular CF clinic visits in the first 12 months of life at 28 US
229 less, detailed reports on lncRNAs regulating CF biology and describing their implication in cardiac r
232 intermolecular interactions through CF...S, CF...H, and CF...pi noncovalent interactions and enhance
233 ative stabilization through sigmaCC -->sigma*CF interactions are the underlying driving force for the
235 g them co-fractionation / mass spectrometry (CF-MS), but it remains difficult to identify directly co
237 domonas aeruginosa Here, we demonstrate that CF mice are highly susceptible to pulmonary infections w
239 uld enhance P. aeruginosa clearance from the CF airway by activating PTEN-mediated anti-bacterial res
240 athway contributing to IL-8 secretion in the CF bronchial epithelium with KL functioning as an endocr
241 neutropenia: 74 [17%] of 446 patients in the CF group vs 101 [23%] of 441 people in the ECX group).
242 ere were 21022 individuals (52% male) in the CF patient cohort in 2003 comprised of 12702 children an
243 he development of glucose intolerance in the CF pediatric population, and to CFRD, later in life.
247 this study introduces the development of the CF-MIMS (conception for field experiments, membrane choi
248 also presents two field applications of the CF-MIMS involving the well-logging of dissolved gases an
251 requency analysis (1 measure every 2 s), the CF-MIMS (Continuous Flow Membrane Inlet Mass Spectromete
255 dy from January 2003 to March 2009 using the CF Foundation Patient Registry merged with Centers for D
259 improve intermolecular interactions through CF...S, CF...H, and CF...pi noncovalent interactions and
262 sk of colorectal cancer (CRC) in adults with CF is 5-10 times greater compared to the general populat
266 ed about early lung disease in children with CF and discusses the implications for future clinical pr
274 ficiency in beta-cell number in infants with CF may contribute to the development of glucose intolera
276 ify the multiple tissue defects in mice with CF as well as in cells from subjects with the p.Phe508de
277 over a prescreening cohort of newborns with CF from 20 years before the contemporary cohort (mean z
278 es in lung disease severity in patients with CF (n = 6365; IL8, P = .001; CXCL1, P = .001), confirmin
279 Materials and Methods Twenty patients with CF and 20 matched healthy volunteers underwent functiona
283 ctive analyses of samples from patients with CF supported the translational relevance of these precli
284 the entire lungs was lower for patients with CF than for control subjects (mean +/- standard deviatio
285 ower lung halves were lower in patients with CF than in control subjects (right, 0.84 +/- 0.2 vs 1.16
286 ntion of home monitoring among patients with CF was able to detect more exacerbations than usual care
288 monocytes sorted from healthy patients with CF-derived MPs during their differentiation into osteocl
296 with sweat from individuals with and without CF, demonstrating convenient sweat diagnostics with reli
299 The relative number of beta-cells in young CF tissues was reduced by 50% or more when compared to a
300 islet morphology in tissues from very young CF children (<4 years of age), and adult patients with C
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