proline has been researched along with Cystic Fibrosis in 13 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (15.38) | 18.7374 |
| 1990's | 4 (30.77) | 18.2507 |
| 2000's | 2 (15.38) | 29.6817 |
| 2010's | 2 (15.38) | 24.3611 |
| 2020's | 3 (23.08) | 2.80 |
| Authors | Studies |
|---|---|
| Almond, LM; Beringer, PM; Chung, PS; Hong, E; Rao, AP | 1 |
| Altenbach, RJ; Balut, C; Bogdan, A; Fan, Y; Gao, W; Gfesser, GA; Greszler, S; Koenig, JR; Kym, P; Liu, B; Manelli, A; Scanio, MJC; Schrimpf, M; Searle, XB; Singh, A; Swensen, AM; Tse, C; Vortherms, T; Wang, X; Yong, H; Zhao, G | 1 |
| Alton, EWFW; Blalock, JE; Brown, S; Bush, A; Davies, JC; Gaggar, A; Hilliard, TN; Jackson, PL; Lloyd, CM; Mc Fie, M; Patel, DF; Pyle, CJ; Regamey, N; Short, C; Snelgrove, RJ; Tan, HL; Thursfield, R; Turnbull, AR | 1 |
| Cutello, S; Di Dio, G; La Rosa, M; Leonardi, S; Parisi, GF; Rotolo, N | 1 |
| Britz-McKibbin, P; Finan, TM; Gavina, JM; White, CE | 1 |
| GOULD, BS; SHWACHMAN, H | 1 |
| Dötsch, J; Korbmacher, C; Kraus, C; Naehrlich, L; Rauh, R; Reis, A | 1 |
| Blalock, JE; Clancy, JP; Gaggar, A; Jackson, PL; McQuaid, DB; Noerager, BD; O'Reilly, PJ; Rowe, SM | 1 |
| Ishihara, H; Sheppard, DN; Travis, SM; Welsh, MJ | 1 |
| Akcakaya, N; Apak, M; Camcioglu, Y; Cokugras, H; Gokgoz, N; Kayserili, H; Kirdar, B; Onay, T; Topaloglu, O; Tsui, LC; Zielenski, J | 1 |
| Bonduelle, M; Dab, I; Liebaers, I; Lissens, W; Malfroot, A | 1 |
| Hodson, ME; Pitt, TL; Taylor, RF | 1 |
| Ammitzbøll, T; Espersen, F; Pedersen, SS; Schiøler, H | 1 |
13 other study(ies) available for proline and Cystic Fibrosis
| Article | Year |
|---|---|
Physiologically-Based Pharmacokinetic-Led Guidance for Patients With Cystic Fibrosis Taking Elexacaftor-Tezacaftor-Ivacaftor With Nirmatrelvir-Ritonavir for the Treatment of COVID-19.
Topics: Aminophenols; Benzodioxoles; Chloride Channel Agonists; COVID-19 Drug Treatment; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Cytochrome P-450 CYP3A; Drug Combinations; Drug Interactions; Humans; Indoles; Lactams; Leucine; Mutation; Nitriles; Proline; Pyrazoles; Pyridines; Pyrrolidines; Quinolines; Quinolones; Ritonavir | 2022 |
Discovery and SAR of 4-aminopyrrolidine-2-carboxylic acid correctors of CFTR for the treatment of cystic fibrosis.
Topics: Benzodioxoles; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Humans; Mutation; Proline; Structure-Activity Relationship | 2022 |
Abnormal pro-gly-pro pathway and airway neutrophilia in pediatric cystic fibrosis.
Topics: Airway Remodeling; Bronchoalveolar Lavage Fluid; Bronchoscopy; Chemotaxis, Leukocyte; Child; Cystic Fibrosis; Female; Humans; Infant, Newborn; Inflammation; Leukocyte Elastase; Male; Matrix Metalloproteinase 9; Neutrophils; Oligopeptides; Proline; Prolyl Oligopeptidases; Sputum | 2020 |
Phenotypic expression of the p.Leu1077Pro CFTR mutation in Sicilian cystic fibrosis patients.
Topics: Child; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Female; Gene Expression Regulation; Genotype; Heterozygote; Humans; Leucine; Male; Mutation; Phenotype; Proline; Pseudomonas aeruginosa; Pseudomonas Infections; Sicily; Young Adult | 2013 |
Determination of 4-hydroxyproline-2-epimerase activity by capillary electrophoresis: A stereoselective platform for inhibitor screening of amino acid isomerases.
Topics: Amino Acid Isomerases; Bacterial Proteins; Cystic Fibrosis; Electrophoresis, Capillary; Enzyme Inhibitors; Humans; Hydroxyproline; Kinetics; Proline; Pseudomonas aeruginosa; Sensitivity and Specificity | 2010 |
Studies in cystic fibrosis; determination of plasma proline following protein feeding as a diagnostic test for pancreatic insufficiency.
Topics: Blood; Cystic Fibrosis; Diagnostic Tests, Routine; Disease; Exocrine Pancreatic Insufficiency; Humans; Pancreas; Pancreatic Diseases; Proline | 1956 |
Functional characterization of a novel CFTR mutation P67S identified in a patient with atypical cystic fibrosis.
Topics: Action Potentials; Adolescent; Amino Acid Substitution; Base Sequence; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Female; Humans; Molecular Sequence Data; Proline; Serine | 2007 |
A novel proteolytic cascade generates an extracellular matrix-derived chemoattractant in chronic neutrophilic inflammation.
Topics: Animals; Chemotactic Factors; Chemotaxis, Leukocyte; Chronic Disease; Cystic Fibrosis; Extracellular Matrix; Extracellular Matrix Proteins; Humans; Inflammation; Matrix Metalloproteinase 8; Matrix Metalloproteinase 9; Mice; Neutrophil Activation; Neutrophils; Oligopeptides; Proline; Prolyl Oligopeptidases; Receptors, Interleukin-8A; Receptors, Interleukin-8B; Serine Endopeptidases; Sputum | 2008 |
Contribution of proline residues in the membrane-spanning domains of cystic fibrosis transmembrane conductance regulator to chloride channel function.
Topics: Adenosine Triphosphate; Amino Acid Sequence; Chloride Channels; Cyclic AMP; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Electrophysiology; HeLa Cells; Humans; Membrane Potentials; Models, Structural; Point Mutation; Proline; Protein Structure, Secondary; Recombinant Proteins | 1996 |
Analysis of the CFTR gene in Turkish cystic fibrosis patients: identification of three novel mutations (3172delAC, P1013L and M1028I).
Topics: Adenine; Amino Acid Substitution; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Cytosine; Frameshift Mutation; Humans; Isoleucine; Leucine; Methionine; Mutation; Polymorphism, Genetic; Proline; Sequence Deletion; Turkey | 1998 |
A serine to proline substitution (S1255P) in the second nucleotide binding fold of the cystic fibrosis gene.
Topics: Adenosine Triphosphate; Base Sequence; Binding Sites; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Exons; Gene Frequency; Humans; Infant, Newborn; Male; Membrane Proteins; Point Mutation; Polymerase Chain Reaction; Proline; Serine | 1992 |
Auxotrophy of Pseudomonas aeruginosa in cystic fibrosis.
Topics: Amino Acids; Arginine; Bronchiectasis; Cystic Fibrosis; Humans; Methionine; Proline; Pseudomonas aeruginosa; Sputum; Thiamine | 1992 |
Excretion of urinary collagen metabolites correlates to severity of pulmonary disease in cystic fibrosis.
Topics: Adolescent; Adult; Bronchitis; Cystic Fibrosis; Female; Forced Expiratory Volume; Humans; Hydroxylysine; Hydroxyproline; Male; Pneumonia; Proline; Pseudomonas aeruginosa; Pseudomonas Infections | 1988 |