tyrosine and Cystic Fibrosis

tyrosine has been researched along with Cystic Fibrosis in 36 studies

Research

Studies (36)

Timeframe	Studies, this research(%)	All Research%
pre-1990	15 (41.67)	18.7374
1990's	3 (8.33)	18.2507
2000's	11 (30.56)	29.6817
2010's	7 (19.44)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Kitoko, JZ; Lopes-Pacheco, M; Morales, MM; Petrs-Silva, H; Rocco, PRM	1
Itokazu, Y; Limper, AH; Marks, DL; O'Grady, SM; Pagano, RE; Schroeder, AS	1
Cesaro, L; Donella-Deana, A; Marin, O; Pinna, LA; Venerando, A	1
Bienvenu, T; Burgel, PR; Chapron, J; Dusser, D; Gaitch, N; Génin, E; Girodon, E; Honoré, I; Hubert, D; Kanaan, R; Martinez, B; Viel, M	1
Gruenert, DC; Hanrahan, JW; LeSimple, P; Liao, J; Robert, R	1
Balding, E; Berry, LJ; Brennan, S; Carlin, JB; Carzino, R; Chapman, AL; de Klerk, N; Douglas, T; Foo, C; Gangell, CL; Garratt, LW; Hall, GL; Harrison, J; Kettle, AJ; Kicic, A; Laing, IA; Logie, KM; Massie, J; Mott, LS; Murray, C; Parsons, F; Pillarisetti, N; Poreddy, SR; Ranganathan, SC; Robertson, CF; Robins-Browne, R; Robinson, PJ; Senthilmohan, R; Skoric, B; Sly, PD; Stick, SM; Sutanto, EN; Thomson, E; Williamson, E	1
Bernevic, B; Döring, G; Moise, A; Petre, BA; Przybylski, M; Stumbaum, M; Ulrich, M	1
Morrissey, BM; Rodman, DM; Schilling, K; Silkoff, PE; Weil, JV	1
Bagu, J; Lacy, P; Man, SF; Mayes, DC; Moqbel, R; Musat-Marcu, S; Saude, EJ; Sykes, BD	1
Abraham, SN; Duncan, MJ; Li, G; Wright, JR; Zaas, DW	1
Di Stefano, A; Folkerts, G; Ricciardolo, FL; Sabatini, F	1
Celio, S; Chládek, J; Durka, SS; Heizmann, CW; Moeller, A; Sennhauser, FH; Troxler, H; Wildhaber, JH	1
Coward, RF; Smith, P	1
Mowat, AP	1
Holmberg, L; Kornfält, R; Kristoffersson, AC; Schaedel, C	1
Möhler, M; Stremmel, W; Wagner, V	1
Dunsmore, SE; Matrisian, LM; Parks, WC; Roby, JD; Saarialho-Kere, UK; Welgus, HG; Wilson, CL	1
Bradbury, NA; Weixel, KM	1
Ambrosioni, A; Cantù-Rajnoldi, A; Costantini, D; Fiori, S; Giunta, A; Padoan, R; Prandoni, S; Russo, MC; Seia, M	1
Grisham, MB; Hegab, AH; Hillman, BC; Jinkins, PA; Jones, KL; Owens, MW; Robbins, RA; Sato, E; Simpson, KL	1
Cross, CE; Eiserich, JP; Marelich, GP; Nguyen, MN; Shigenaga, MK; Van Der Vliet, A	1
Hadeli, K; Hoyt, JC; Nelson, D; Robbins, RA; Sato, E	1
Balint, B; Barnes, PJ; Donnelly, LE; Hanazawa, T; Hodson, ME; Kharitonov, SA; Shah, PL	1
Bernaudin, F	1
Fric, P; Jodl, J; Kasafírek, E; Malis, F; Slabý, J; Vávrová, V	1
Dimmick, JE; Hardwick, DF	1
Rigilano, JC; Stevens, MB; Wilson, CC	1
Ersser, RS; Gibbons, IS; Seakins, JW	1
Davidson, M; Silverberg, M	1
Seakins, JW	1
Lowman, JT; Ulstrom, RA; Walker, WA	1
Applegarth, DA; Israels, S; Ross, P; Zack, P	2
Barbero, GJ; Braddock, LI	1
Robinson, R	1

Reviews

6 review(s) available for tyrosine and Cystic Fibrosis

Article	Year
Reactive nitrogen species in the respiratory tract. European journal of pharmacology, 2006, Mar-08, Volume: 533, Issue:1-3 Topics: Animals; Asthma; Cystic Fibrosis; Humans; Nitric Oxide; Oxidative Stress; Pulmonary Disease, Chronic Obstructive; Reactive Nitrogen Species; Reactive Oxygen Species; Respiratory System; Tyrosine	2006
Hepatic Disorders. Clinics in gastroenterology, 1982, Volume: 11, Issue:1 Topics: Adolescent; Adult; alpha 1-Antitrypsin Deficiency; Amino Acid Metabolism, Inborn Errors; Ammonia; Child; Child, Preschool; Cystic Fibrosis; Female; Fructose Intolerance; Fructose-1,6-Diphosphatase Deficiency; Galactosemias; Glycogen Storage Disease; Humans; Infant; Infant, Newborn; Liver Diseases; Male; Polycystic Kidney Diseases; Porphyrias; Tyrosine; Urea	1982
[Hereditary liver diseases. Recent molecular genetic aspects]. Deutsche medizinische Wochenschrift (1946), 1998, Apr-09, Volume: 123, Issue:15 Topics: alpha 1-Antitrypsin; Animals; Bilirubin; Cholestasis, Intrahepatic; Cystic Fibrosis; Disease Models, Animal; Genetic Therapy; Hepatolenticular Degeneration; Humans; Jaundice, Chronic Idiopathic; Liver Diseases; Metabolism, Inborn Errors; Molecular Biology; Tyrosine	1998
Nitric oxide, peroxynitrite, and lower respiratory tract inflammation. Immunopharmacology, 2000, Jul-25, Volume: 48, Issue:3 Topics: Animals; Asthma; Bronchoalveolar Lavage Fluid; Cystic Fibrosis; Eosinophils; Humans; Nitrates; Nitric Oxide; Pneumonia; Tyrosine	2000
Alpha fetoprotein. La Nouvelle presse medicale, 1976, Mar-06, Volume: 5, Issue:10 Topics: alpha-Fetoproteins; Amino Acid Metabolism, Inborn Errors; Amniotic Fluid; Anencephaly; Animals; Antibody Formation; Ataxia Telangiectasia; Carcinoma, Hepatocellular; Cystic Fibrosis; Depression, Chemical; Estrogens; Female; Fetal Blood; Fetal Proteins; Gestational Age; Hepatitis; Humans; Infant, Newborn; Lectins; Liver Neoplasms; Lymphocyte Activation; Placenta Diseases; Pregnancy; Tyrosine	1976
Metabolic cirrhoses of infancy and early childhood. Perspectives in pediatric pathology, 1976, Volume: 3 Topics: Amino Acid Metabolism, Inborn Errors; Cystic Fibrosis; Cystinosis; Fructose Intolerance; Galactosemias; Genetics, Medical; Glycogen Storage Disease Type IV; Hepatolenticular Degeneration; Humans; Iatrogenic Disease; Infant; Infant, Newborn; Lipid Metabolism, Inborn Errors; Liver; Liver Cirrhosis; Metabolism, Inborn Errors; Mucopolysaccharidoses; Niemann-Pick Diseases; Polycystic Kidney Diseases; Tyrosine	1976

Other Studies

30 other study(ies) available for tyrosine and Cystic Fibrosis

Article	Year
Self-complementary and tyrosine-mutant rAAV vectors enhance transduction in cystic fibrosis bronchial epithelial cells. Experimental cell research, 2018, 11-15, Volume: 372, Issue:2 Topics: Amino Acid Substitution; Bronchi; Cystic Fibrosis; Dependovirus; Epithelial Cells; Genetic Therapy; Genetic Vectors; Humans; Mutation; Phenylalanine; Serogroup; Transduction, Genetic; Tyrosine	2018
Reduced GM1 ganglioside in CFTR-deficient human airway cells results in decreased β1-integrin signaling and delayed wound repair. American journal of physiology. Cell physiology, 2014, May-01, Volume: 306, Issue:9 Topics: Cell Line; Cell Movement; Crk-Associated Substrate Protein; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Down-Regulation; Electric Impedance; Epithelial Cells; Focal Adhesion Kinase 1; G(M1) Ganglioside; Humans; Integrin beta1; Lung; Phosphorylation; RNA Interference; Time Factors; Transfection; Tyrosine; Wound Healing	2014
A "SYDE" effect of hierarchical phosphorylation: possible relevance to the cystic fibrosis basic defect. Cellular and molecular life sciences : CMLS, 2014, Volume: 71, Issue:12 Topics: Amino Acid Sequence; Aspartic Acid; Casein Kinase II; Consensus Sequence; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Dictyostelium; Glutamic Acid; Humans; Molecular Sequence Data; Phosphorylation; Protein Interaction Domains and Motifs; Serine; Tyrosine	2014
DCTN4 as a modifier of chronic Pseudomonas aeruginosa infection in cystic fibrosis. The clinical respiratory journal, 2016, Volume: 10, Issue:6 Topics: Adolescent; Adult; Child; Child, Preschool; Cysteine; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Dynactin Complex; Female; Genetic Predisposition to Disease; Humans; Incidence; Infant; Male; Middle Aged; Mutation, Missense; Pseudomonas aeruginosa; Pseudomonas Infections; Retrospective Studies; Sex Factors; Tyrosine; Young Adult	2016
Cystic fibrosis transmembrane conductance regulator trafficking modulates the barrier function of airway epithelial cell monolayers. The Journal of physiology, 2010, Apr-15, Volume: 588, Issue:Pt 8 Topics: Bronchi; Cell Line; Cell Membrane Permeability; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Epithelial Cells; Genistein; Green Fluorescent Proteins; Humans; Mannitol; Phosphorylation; Protein Kinase Inhibitors; Temperature; Tight Junctions; Tyrosine	2010
Identifying peroxidases and their oxidants in the early pathology of cystic fibrosis. Free radical biology & medicine, 2010, Nov-15, Volume: 49, Issue:9 Topics: Bronchoalveolar Lavage Fluid; Child; Child, Preschool; Cystic Fibrosis; Disease Progression; Female; Humans; Infant; Inflammation; Male; Neutrophils; Oxidation-Reduction; Peroxidase; Pseudomonas aeruginosa; Respiratory Tract Infections; Tyrosine	2010
When is mass spectrometry combined with affinity approaches essential? A case study of tyrosine nitration in proteins. Journal of the American Society for Mass Spectrometry, 2012, Volume: 23, Issue:11 Topics: Amino Acid Sequence; Animals; Antibodies, Immobilized; Binding Sites; Chromatography, Affinity; Cystic Fibrosis; Eosinophil Granule Proteins; Humans; Mass Spectrometry; Models, Molecular; Molecular Sequence Data; Peptide Fragments; Tyrosine	2012
Nitric oxide and protein nitration in the cystic fibrosis airway. Archives of biochemistry and biophysics, 2002, Oct-01, Volume: 406, Issue:1 Topics: Adult; Aged; Analysis of Variance; Cystic Fibrosis; Female; Humans; Male; Middle Aged; Nitrates; Nitric Oxide; Nitric Oxide Synthase; Nitric Oxide Synthase Type I; Nitric Oxide Synthase Type II; Reference Values; Respiratory Mechanics; Respiratory System; Tyrosine	2002
NMR analysis of neutrophil activation in sputum samples from patients with cystic fibrosis. Magnetic resonance in medicine, 2004, Volume: 52, Issue:4 Topics: Adult; Cell Count; Cystic Fibrosis; Female; Humans; Magnetic Resonance Spectroscopy; Male; Neutrophil Activation; Neutrophils; Regression Analysis; Sputum; Statistics, Nonparametric; Tyrosine	2004
Pseudomonas invasion of type I pneumocytes is dependent on the expression and phosphorylation of caveolin-2. The Journal of biological chemistry, 2005, Feb-11, Volume: 280, Issue:6 Topics: Animals; Caveolin 1; Caveolin 2; Caveolins; Cell Adhesion; Cell Line; Cells, Cultured; Coloring Agents; Cystic Fibrosis; Epithelial Cells; Immunoprecipitation; Lipid Metabolism; Lipids; Lung; Membrane Microdomains; Mice; Microscopy, Confocal; Microscopy, Electron; Phosphorylation; Pseudomonas; Pulmonary Alveoli; Rats; Rats, Sprague-Dawley; RNA Interference; Tetrazolium Salts; Thiazoles; Tyrosine	2005
Free 3-nitrotyrosine in exhaled breath condensates of children fails as a marker for oxidative stress in stable cystic fibrosis and asthma. Nitric oxide : biology and chemistry, 2006, Volume: 15, Issue:3 Topics: Adolescent; Adult; Asthma; Biomarkers; Breath Tests; Child; Child, Preschool; Cystic Fibrosis; Exhalation; Female; Humans; Male; Middle Aged; Oxidative Stress; Tyrosine	2006
Paper chromatography of some weakly basic urine constituents and the estimation of urinary tyrosine. Clinica chimica acta; international journal of clinical chemistry, 1967, Volume: 17, Issue:3 Topics: Acetates; Amino Acid Metabolism, Inborn Errors; Chromatography, Paper; Cystic Fibrosis; Humans; Hydrogen-Ion Concentration; Imidazoles; Phenylketonurias; Tyrosine	1967
A novel cystic fibrosis mutation, Y109C, in the first transmembrane domain of CFTR. Human molecular genetics, 1994, Volume: 3, Issue:6 Topics: Adolescent; Chloride Channels; Cysteine; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; DNA Primers; Exons; Female; Frameshift Mutation; Humans; Introns; Membrane Proteins; Point Mutation; Polymerase Chain Reaction; Tyrosine	1994
Matrilysin expression and function in airway epithelium. The Journal of clinical investigation, 1998, Oct-01, Volume: 102, Issue:7 Topics: Amides; Animals; Cell Movement; Cystic Fibrosis; Enzyme Induction; Epithelial Cells; Female; Gene Expression Regulation, Enzymologic; Humans; Lung; Lung Diseases; Lung Neoplasms; Matrix Metalloproteinase 7; Metalloendopeptidases; Mice; Mice, Knockout; Protease Inhibitors; Pulmonary Alveoli; Tetradecanoylphorbol Acetate; Trachea; Tumor Cells, Cultured; Tyrosine	1998
The carboxyl terminus of the cystic fibrosis transmembrane conductance regulator binds to AP-2 clathrin adaptors. The Journal of biological chemistry, 2000, Feb-04, Volume: 275, Issue:5 Topics: Adaptor Protein Complex alpha Subunits; Adaptor Proteins, Vesicular Transport; Amino Acid Sequence; Animals; Binding Sites; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Humans; Membrane Proteins; Molecular Sequence Data; Protein Binding; Sequence Alignment; Tyrosine	2000
A novel missense mutation (Y89C) in exon 3 of the CFTR (ABCC7) gene in a young male. Human mutation, 2000, Volume: 15, Issue:5 Topics: Adult; Amino Acid Substitution; Animals; ATP-Binding Cassette Transporters; Cysteine; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Exons; Humans; Male; Mice; Mutation, Missense; Rats; Tyrosine	2000
Elevation of nitrotyrosine and nitrate concentrations in cystic fibrosis sputum. Pediatric pulmonology, 2000, Volume: 30, Issue:2 Topics: Adolescent; Adult; Cystic Fibrosis; Female; Free Radicals; Humans; Inflammation; Male; Nitrates; Nitric Oxide; Sputum; Superoxides; Tyrosine	2000
Myeloperoxidase and protein oxidation in cystic fibrosis. American journal of physiology. Lung cellular and molecular physiology, 2000, Volume: 279, Issue:3 Topics: Adult; Bronchi; Case-Control Studies; Cell Line; Chromatography, High Pressure Liquid; Cystic Fibrosis; Drug Synergism; Humans; Hydrogen Peroxide; Nitrates; Nitrites; Oxidants; Oxidation-Reduction; Peroxidase; Peroxidases; Proteins; Respiratory System; Sputum; Trachea; Tyrosine	2000
Increased nitrotyrosine in exhaled breath condensate in cystic fibrosis. The European respiratory journal, 2001, Volume: 17, Issue:6 Topics: Adult; Breath Tests; Cystic Fibrosis; Female; Humans; Lung Volume Measurements; Male; Oxidative Stress; Reactive Nitrogen Species; Reference Values; Tyrosine	2001
A peroral test of pancreatic insufficiency with 4-(N-acetyl-L-tyrosyl)aminobenzoic acid in children with cystic fibrosis. The Journal of pediatrics, 1979, Volume: 94, Issue:6 Topics: 4-Aminobenzoic Acid; Adolescent; Aminobenzoates; Child; Child, Preschool; Cystic Fibrosis; Female; Humans; Male; Pancreas; para-Aminobenzoates; Tyrosine	1979
State screening for metabolic disorders in newborns. American family physician, 1988, Volume: 37, Issue:4 Topics: Adrenal Hyperplasia, Congenital; Amidohydrolases; Amino Acid Metabolism, Inborn Errors; Anemia, Sickle Cell; Biotinidase; Congenital Hypothyroidism; Cystic Fibrosis; Galactosemias; Homocystinuria; Humans; Hypothyroidism; Infant, Newborn; Maple Syrup Urine Disease; Mass Screening; Metabolism, Inborn Errors; Phenylketonurias; Tyrosine; United States	1988
Tyrosine metabolism and faecal aminoacids in cystic fibrosis of the pancreas. Lancet (London, England), 1967, Apr-22, Volume: 1, Issue:7495 Topics: Adolescent; Amino Acids; Child; Child, Preschool; Cystic Fibrosis; Feces; Humans; Infant; Liver; Phenylacetates; Tyrosine	1967
Screening for inborn errors of metabolism. Report of a WHO Scientific Group. World Health Organization technical report series, 1968, Volume: 401 Topics: Adrenal Hyperplasia, Congenital; Amino Acid Metabolism, Inborn Errors; Carrier State; Ceruloplasmin; Cholinesterases; Cystic Fibrosis; Diagnostic Services; Female; Galactosemias; Genetic Diseases, Inborn; Hepatolenticular Degeneration; Humans; Infant; Infant, Newborn; Male; Maple Syrup Urine Disease; Metabolism, Inborn Errors; Phenylketonurias; Porphyrias; Tyrosine; World Health Organization	1968
Nutritional requirements of infants and children with liver disease. The American journal of clinical nutrition, 1970, Volume: 23, Issue:5 Topics: Adolescent; Bile; Body Weight; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Cystic Fibrosis; Female; Galactosemias; Glycogen; Hepatitis A; Hepatolenticular Degeneration; Humans; India; Infant; Infant Nutritional Physiological Phenomena; Liver Diseases; Male; Tyrosine	1970
The determination of urinary phenylacetylglutamine as phenylacetic acid. Studies on its origin in normal subjects and children with cystic fibrosis. Clinica chimica acta; international journal of clinical chemistry, 1971, Volume: 35, Issue:1 Topics: Administration, Oral; Capsules; Child; Child, Preschool; Chromatography, Gas; Chromatography, Ion Exchange; Circadian Rhythm; Cystic Fibrosis; Diet; Female; Glutamine; Humans; Hydrolysis; Infant; Infant, Newborn; Lactates; Male; Phenethylamines; Phenylacetates; Phenylalanine; Phenylpyruvic Acids; Time Factors; Tyramine; Tyrosine	1971
Albumin synthesis rates in patients with hypoproteinemia. The Journal of pediatrics, 1971, Volume: 78, Issue:5 Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Anaphylaxis; Anorexia Nervosa; Bile Ducts; Child; Child, Preschool; Chromatography, Gel; Colitis, Ulcerative; Cystic Fibrosis; Female; Glomerulonephritis; Humans; Hypoproteinemia; Infant; Injections, Intravenous; Intellectual Disability; Kinetics; Liver; Liver Cirrhosis; Liver Cirrhosis, Biliary; Liver Diseases; Male; Methionine; Nephrotic Syndrome; Psychomotor Disorders; Purpura; Radioisotopes; Selenium; Serum Albumin; Spectrophotometry; Tyrosine	1971
Tyrosine in fibrocystic disease. The Journal of pediatrics, 1968, Volume: 72, Issue:5 Topics: Cystic Fibrosis; Tyrosine	1968
Plasma tyrosine levels in patients with cystic fibrosis. The Journal of pediatrics, 1968, Volume: 73, Issue:4 Topics: Child; Cystic Fibrosis; Humans; Statistics as Topic; Tyrosine	1968
Plasma tyrosine levels in patients with cystic fibrosis. The Journal of pediatrics, 1968, Volume: 73, Issue:4 Topics: Child; Cystic Fibrosis; Humans; Tyrosine	1968
Tyrosine metabolism in cystic fibrosis. Clinica chimica acta; international journal of clinical chemistry, 1966, Volume: 14, Issue:2 Topics: Ascorbic Acid; Child; Chromatography; Cystic Fibrosis; Humans; Hydro-Lyases; Phenylacetates; Tyrosine	1966