arginine has been researched along with Cystic Fibrosis of Pancreas in 77 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 33 (42.86) | 18.7374 |
1990's | 16 (20.78) | 18.2507 |
2000's | 12 (15.58) | 29.6817 |
2010's | 14 (18.18) | 24.3611 |
2020's | 2 (2.60) | 2.80 |
Authors | Studies |
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D'Alessio, DA; De Leon, DD; Doliba, A; Eiel, JN; Flatt, AJ; Gallagher, K; Gallop, R; Hadjiliadis, D; Kelly, A; Nyirjesy, SC; Peleckis, AJ; Rickels, MR; Rubenstein, RC; Sheikh, S; Stefanovski, D; Tami, A | 1 |
Beigverdi, R; Emaneini, M; Halimi, S; Jabalameli, F; Siroosi, M | 1 |
Ahmadi, S; Bartlett, C; Bear, CE; Gonska, T; Ip, W; Jiang, J; Laselva, O; Lew, A; Moraes, TJ; Ouyang, H; Wellhauser, L; Wu, YS; Xia, S | 1 |
De Biase, RV; Gnessi, L; Isidori, AM; Lenzi, A; Lubrano, C; Pascucci, C; Quattrucci, S; Savi, D | 1 |
Ahmadi, S; Bear, CE; Di Paola, M; Khursigara, CM; Lam, JS; Park, AJ; Roach, EJ; Struder-Kypke, M; Wu, YS | 1 |
Cardona, ST; Kumar, B; Sorensen, JL | 1 |
Ahmadi, S; Bear, CE; Bozoky, Z; Di Paola, M; Du, K; Forman-Kay, J; Gonska, T; Ip, W; Lew, A; Li, M; Lloyd-Kuzik, A; Wu, YS; Xia, S | 1 |
Com, G; Deutz, NE; Engelen, MP; Luiking, YC | 1 |
Grasemann, H; Pencharz, PB | 1 |
Elborn, JS; Ferguson, TE; Hamilton, RA; Harvey, BJ; Hendrick, SM; Martin, SL; Reihill, JA; Saint-Criq, V; Stutts, MJ; Walker, B | 1 |
Baraldi, E; Da Dalt, L; Giordano, G; Gucciardi, A; Lucca, F; Naturale, M; Perilongo, G; Pirillo, P; Ros, M | 1 |
Elnazir, B; Greally, P; Kerley, CP; Kilbride, E | 1 |
Bazer, FW; Carey Satterfield, M; Davis, TA; Kim, SW; Li, P; Marc Rhoads, J; Smith, SB; Spencer, TE; Wu, G; Yin, Y | 1 |
Bassas, L; Casals, T; Domingo, C; Farré, A; Giménez, J; Masvidal, L; Ramos, MD | 1 |
Bienvenu, T; Blayau, M; Cabet-Bey, F; Claustres, M; Costa, C; Feldmann, D; Georges, Md; Girodon, E; Guittard, C; Iron, A; Lalau, G; Leclerc, J; Mittre, H; Paulet, D; René, C | 1 |
Al-Saleh, S; Amin, R; Belik, J; Grasemann, H; Mehl, A; Pencharz, P; Rafii, M; Ratjen, F; Scott, JA; Shehnaz, D | 1 |
Grasemann, H; Ratjen, F | 1 |
Grasemann, H; Ratjen, F; Tullis, E | 1 |
Grasemann, C; Grasemann, H; Kurtz, F; Ratjen, F; Tietze-Schillings, G; Vester, U | 1 |
Donnelly, D; Everard, ML | 1 |
Grasemann, H; Kurtz, F; Ratjen, F | 1 |
Comeau, AM; Dorkin, HL; O'Sullivan, BP; Parad, R; Zwerdling, RG | 1 |
Aznarez, I; Blencowe, BJ; Rommens, JM; Tsui, LC; Zielenski, J | 1 |
Maarsingh, H; Meurs, H; Pera, T | 1 |
Applegarth, DA; Bridges, MA; Davidson, AG; Johannson, J; Wong, LT | 1 |
Berry, HK; Hsieh, MC | 1 |
Nadler, HL; Rao, GJ; Walsh, MM | 1 |
Culler, FL; Meacham, LR | 1 |
Bocian, RC; Chao, AC; Dong, YJ; Gardner, P; Hsu, YP; Kouyama, K; Moss, RB | 1 |
Adjiman, M; Beldjord, C; Bienvenu, T; Kaplan, JC | 1 |
Chang, XB; Hanrahan, JW; Hou, YX; Riordan, JR; Rommens, JM; Tabcharani, JA; Tsui, LC | 1 |
Dapena, J; Estivill, X; Ferrer, J; Giménez, J; Llevadot, R; Nunes, V; Ortigosa, L; Peña, L; Pérez-Frias, J | 1 |
Adkins, S; Gan, KN; La Du, BN; Mody, M | 1 |
Carson, MR; Teem, JL; Welsh, MJ | 1 |
Harris, A; Hill, DF; Tebbutt, SJ | 1 |
Bartholomew, DW; Fujita, J; Hojo, S; Miyawaki, H; Obayashi, Y; Takahara, J | 1 |
Cotten, JF; Welsh, MJ | 1 |
Koch, C; Lanng, S; Laursen, EM; Müller, J; Rasmussen, MH; Skakkebaek, NE | 1 |
Eto, Y; Iizuka, S; Katsube, A; Morokawa, N; Muraji, T; Tanano, A; Yoshimura, K | 1 |
Gärtig, SS; Grasemann, H; Konietzko, N; Ratjen, F; Teschler, H; Wiesemann, HG | 1 |
Jorissen, M; Lefevere, L; Lindberg, S; Willems, T | 1 |
Barbarotto, GM; Desai, TK; Feldman, GL; Manji, S; Monaghan, KG; Snow, K | 1 |
Dreshaj, IA; Ferkol, T; Haxhiu, MA; Kelley, TJ; Martin, RJ; Mhanna, MJ; van Heeckeren, AM | 1 |
Callahan, JW; Leung, A | 1 |
Butterworth, J; Duncan, JJ | 1 |
Nadler, NL; Rao, GJ; Shapira, E; Wessel, HU | 1 |
Blau, K; Dann, LG | 2 |
Blessing-Moore, J; Bossen, A; Cavalli-Sforza, LL; Parsons, M; Romeo, G | 1 |
Dooley, RR; Lippe, BM; Sperling, MA | 1 |
Calvo Manuel, E; Espinos Pérez, D; Rubio Pérez, P; Sánchez Sánchez, ML; Vila Canella, T | 2 |
Nadler, HL; Platt, MW; Rao, GJ | 1 |
Goldsmith, GH; Ratnoff, OD; Saito, H; Stern, RC | 1 |
Buchanan, KD; Redmond, AO; Trimble, ER | 1 |
Dietzsch, HJ; Gottschalk, B; Heyne, K; Leupoid, W; Wunderlich, P | 1 |
Nadler, HL; Rao, GJ | 2 |
Busch-Petersen, D; Güloz, HU; Hein, J | 1 |
Solomons, C | 1 |
Marchi, AG; Nordio, S | 1 |
Hodson, ME; Pitt, TL; Taylor, RF | 1 |
Dallapiccola, B; Murru, S; Novelli, G; Sangiuolo, F | 1 |
Diem, P; Klein, DJ; Levitt, MD; Moran, A; Robertson, RP | 1 |
Coburn, LA; Coburn, MD; Solomons, CC | 1 |
Nadler, HL; Posner, LA; Rao, GJ | 1 |
Girard, J; Ronen, G; Rutishauser, M; Stahl, M | 1 |
Cotton, EK; Dubois, R; Solomons, CC | 2 |
Gács, G; Hervei, C; Kerpel-Fronius, E | 1 |
Lieberman, J | 1 |
Girard, J; Nars, PW; Rutishauser, M; Stahl, M; Zuppinger, K | 1 |
Agus, SG; Di Sant'Agnese, PA; Kattwinkel, J; Laster, L; Taussig, LM | 1 |
Cotton, E; Hathaway, W; Solomons, C | 1 |
Graham, GG; Solomons, CC | 1 |
Mangos, JA; McSherry, NR | 1 |
Gururangan, S; Horner, M; Marina, NM; Rodman, JH | 1 |
4 review(s) available for arginine and Cystic Fibrosis of Pancreas
Article | Year |
---|---|
Arginine metabolism and nutrition in growth, health and disease.
Topics: Animals; Arginine; Cystic Fibrosis; Fetal Development; Humans; Metabolic Syndrome; Muscle, Skeletal; Neoplasms; Nutritional Requirements; Obesity; Reproduction; Wounds and Injuries | 2009 |
Nitric oxide and L-arginine deficiency in cystic fibrosis.
Topics: Animals; Arginine; Cystic Fibrosis; Humans; Nitric Oxide; Nitric Oxide Synthase | 2012 |
Arginase and pulmonary diseases.
Topics: Animals; Arginase; Arginine; Asthma; Cystic Fibrosis; Disease Models, Animal; Humans; Hypertension, Pulmonary; Lung; Lung Diseases; Nitric Oxide; Nitric Oxide Synthase; Ornithine; Pulmonary Disease, Chronic Obstructive; Pulmonary Fibrosis; Urea | 2008 |
Nasal nitric oxide.
Topics: Arginine; Asthma; Child; Child, Preschool; Ciliary Motility Disorders; Cystic Fibrosis; Female; Humans; Infant; Luminescent Measurements; Male; Nasal Polyps; Nitric Oxide; Paranasal Sinuses; Respiratory Mucosa; Respiratory Tract Infections; Rhinitis, Allergic, Perennial; Sinusitis; Smoking | 2000 |
4 trial(s) available for arginine and Cystic Fibrosis of Pancreas
Article | Year |
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Effects of GLP-1 and GIP on Islet Function in Glucose-Intolerant, Pancreatic-Insufficient Cystic Fibrosis.
Topics: Adult; Arginine; Blood Glucose; Cystic Fibrosis; Gastric Inhibitory Polypeptide; Glucagon; Glucagon-Like Peptide 1; Glucose; Humans; Incretins; Insulin; Proinsulin | 2022 |
A randomized controlled trial of inhaled L-arginine in patients with cystic fibrosis.
Topics: Administration, Inhalation; Adolescent; Adult; Arginine; Cross-Over Studies; Cystic Fibrosis; Double-Blind Method; Female; Humans; Male; Middle Aged; Nitric Oxide; Respiratory Function Tests; Young Adult | 2013 |
Oral L-arginine supplementation in cystic fibrosis patients: a placebo-controlled study.
Topics: Adolescent; Adult; Arginine; Cross-Over Studies; Cystic Fibrosis; Dose-Response Relationship, Drug; Double-Blind Method; Drug Administration Schedule; Female; Follow-Up Studies; Humans; Male; Nitric Oxide; Pilot Projects; Probability; Reference Values; Respiratory Function Tests; Severity of Illness Index; Treatment Outcome | 2005 |
Normal spontaneous and stimulated GH levels despite decreased IGF-I concentrations in cystic fibrosis patients.
Topics: Adolescent; Adult; Arginine; Body Mass Index; Cystic Fibrosis; Diabetes Mellitus; Female; Glucose Tolerance Test; Human Growth Hormone; Humans; Insulin-Like Growth Factor Binding Protein 3; Insulin-Like Growth Factor I; Male; Middle Aged | 1999 |
69 other study(ies) available for arginine and Cystic Fibrosis of Pancreas
Article | Year |
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Determining effects of nitrate, arginine, and ferrous on antibiotic recalcitrance of clinical strains of Pseudomonas aeruginosa in biofilm-inspired alginate encapsulates.
Topics: Alginates; Amikacin; Anti-Bacterial Agents; Arginine; Biofilms; Ciprofloxacin; Cystic Fibrosis; Humans; Microbial Sensitivity Tests; Nitrates; Pseudomonas aeruginosa; Pseudomonas Infections; Tobramycin | 2023 |
ORKAMBI-Mediated Rescue of Mucociliary Clearance in Cystic Fibrosis Primary Respiratory Cultures Is Enhanced by Arginine Uptake, Arginase Inhibition, and Promotion of Nitric Oxide Signaling to the Cystic Fibrosis Transmembrane Conductance Regulator Channe
Topics: Aminophenols; Aminopyridines; Animals; Arginase; Arginine; Benzodioxoles; Bronchi; Cells, Cultured; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Cytosol; Drug Combinations; Humans; Intestinal Mucosa; Mice; Mutation; Nitric Oxide; Nose; Quinolones | 2019 |
Deregulation of the growth hormone/insulin-like growth factor-1 axis in adults with cystic fibrosis.
Topics: Adolescent; Adult; Arginine; Biomarkers; Cystic Fibrosis; Female; Follow-Up Studies; Growth Disorders; Human Growth Hormone; Humans; Insulin-Like Growth Factor I; Male; Middle Aged; Prognosis; Young Adult | 2018 |
Topics: Amino Acid Transport Systems; Amino Acid Transport Systems, Neutral; Animals; Arginine; Bacterial Adhesion; Cystic Fibrosis; Epithelial Cells; Humans; Mice, Knockout; Plasma Membrane Neurotransmitter Transport Proteins; Pseudomonas aeruginosa; Pseudomonas Infections | 2017 |
A c-di-GMP-Modulating Protein Regulates Swimming Motility of
Topics: Amino Acid Sequence; Amino Acids; Arginine; Bacterial Proteins; Biofilms; Burkholderia cenocepacia; Burkholderia Infections; Cloning, Molecular; Cyclic GMP; Cystic Fibrosis; Escherichia coli Proteins; Flagellin; Gene Expression Regulation, Bacterial; Glutamic Acid; Locomotion; Lung; Mutagenesis, Insertional; Peptide Hydrolases; Phosphoric Diester Hydrolases; Phosphorus-Oxygen Lyases; Sequence Alignment; Sputum | 2018 |
Augmentation of Cystic Fibrosis Transmembrane Conductance Regulator Function in Human Bronchial Epithelial Cells via SLC6A14-Dependent Amino Acid Uptake. Implications for Treatment of Cystic Fibrosis.
Topics: Amino Acid Transport Systems; Arginine; Biological Transport; Bronchi; Cells, Cultured; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Epithelial Cells; Genes, Reporter; Humans; Nitric Oxide; Nitric Oxide Synthase Type II; Recombinant Proteins; Surface Properties; Transduction, Genetic; Tryptophan | 2019 |
Stimulated nitric oxide production and arginine deficiency in children with cystic fibrosis with nutritional failure.
Topics: Adolescent; Arginine; Child; Child Nutrition Disorders; Cystic Fibrosis; Female; Humans; Male; Nitric Oxide; Young Adult | 2013 |
Arginine metabolism in patients with cystic fibrosis.
Topics: Arginine; Child Nutrition Disorders; Cystic Fibrosis; Female; Humans; Male; Nitric Oxide | 2013 |
Inhibition of Protease-Epithelial Sodium Channel Signaling Improves Mucociliary Function in Cystic Fibrosis Airways.
Topics: Arginine; Cells, Cultured; Cystic Fibrosis; Humans; Mucociliary Clearance; Organophosphonates; Respiratory Mucosa; Serine Endopeptidases; Sodium Channel Blockers; Sodium Channels | 2016 |
Asymmetric dimethylarginine and related metabolites in exhaled breath condensate of children with cystic fibrosis.
Topics: Adolescent; Arginine; Biomarkers; Breath Tests; Child; Chromatography, High Pressure Liquid; Cystic Fibrosis; Disease Progression; Exhalation; Female; Follow-Up Studies; Forced Expiratory Volume; Humans; Male; Mass Spectrometry; Prospective Studies | 2018 |
Dietary Nitrate Acutely and Markedly Increased Exhaled Nitric Oxide in a Cystic Fibrosis Case.
Topics: Arginine; Child; Cystic Fibrosis; Diet; Exhalation; Humans; Inflammation; Iron; Male; Nitrates; Nitric Oxide; Nitrites; Placebos; Respiratory Function Tests; Treatment Outcome | 2016 |
The p.Arg258Gly mutation in intracellular loop 2 of CFTR is associated with CFTR-related disorders.
Topics: Adult; Aged; Amino Acid Sequence; Amino Acid Substitution; Arginine; Cohort Studies; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Female; Glycine; Humans; Male; Middle Aged; Molecular Sequence Data; Mutation, Missense | 2009 |
p.Ser1235Arg should no longer be considered as a cystic fibrosis mutation: results from a large collaborative study.
Topics: Amino Acid Sequence; Arginine; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Female; Heterozygote; Humans; Male; Male Urogenital Diseases; Models, Molecular; Molecular Epidemiology; Molecular Sequence Data; Mutation, Missense; Pregnancy; Prenatal Diagnosis; Serine; Urogenital Abnormalities; Vas Deferens | 2011 |
Asymmetric dimethylarginine contributes to airway nitric oxide deficiency in patients with cystic fibrosis.
Topics: Adolescent; Airway Obstruction; Arginine; Child; Chromatography, Liquid; Cystic Fibrosis; Female; Humans; Lung; Male; Nitric Oxide; Respiratory System; Sputum; Tandem Mass Spectrometry | 2011 |
A pilot study of oral L-arginine in cystic fibrosis.
Topics: Administration, Oral; Adolescent; Arginine; Breath Tests; Child; Cystic Fibrosis; Female; Follow-Up Studies; Forced Expiratory Volume; Humans; Male; Nerve Tissue Proteins; Nitric Oxide; Nitric Oxide Synthase; Nitric Oxide Synthase Type I; Nitric Oxide Synthase Type III; Pilot Projects; Treatment Outcome; Vital Capacity | 2005 |
Inhaled L-arginine improves exhaled nitric oxide and pulmonary function in patients with cystic fibrosis.
Topics: Administration, Inhalation; Adolescent; Adult; Arginine; Breath Tests; Citrulline; Cystic Fibrosis; Female; Forced Expiratory Volume; Humans; Lung; Male; Middle Aged; Nitric Oxide; Ornithine; Pilot Projects; Respiratory System Agents | 2006 |
Early pulmonary manifestation of cystic fibrosis in children with the DeltaF508/R117H-7T genotype.
Topics: Age of Onset; Arginine; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; DNA Mutational Analysis; Female; Genotype; Histidine; Humans; Infant, Newborn; Lung Diseases; Male; Mutation, Missense; Neonatal Screening; Point Mutation; Pseudomonas aeruginosa; Pseudomonas Infections | 2006 |
Exon skipping through the creation of a putative exonic splicing silencer as a consequence of the cystic fibrosis mutation R553X.
Topics: Alternative Splicing; Arginine; Base Sequence; Cell Line; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; DNA Mutational Analysis; Exons; Humans; Molecular Sequence Data; Mutation; RNA Splice Sites; RNA, Messenger | 2007 |
Protease binding by alpha 2 macroglobulin in cystic fibrosis.
Topics: Adolescent; alpha-Macroglobulins; Anthraquinones; Arginine; Child; Coloring Agents; Cystic Fibrosis; Female; Humans; Kinetics; Macromolecular Substances; Male; Peptide Hydrolases; Trypsin; Trypsin Inhibitor, Kunitz Soybean | 1982 |
Measurement of trypsin-like activity of saliva, serum and meconium by a synthetic substrate carbobenzoxy-L-arginine-7-amino-4-methylcoumarin amide (CAMCA).
Topics: Adult; Arginine; Child; Coumarins; Cystic Fibrosis; Humans; Infant, Newborn; Meconium; Saliva; Trypsin | 1984 |
Reaction of 4-methylumbelliferylguanidinobenzoate with proteases in human amniotic fluid.
Topics: Amniotic Fluid; Arginine; Chloroform; Cystic Fibrosis; Ellagic Acid; Female; Guanidines; Humans; Hydrolysis; Hymecromone; Peptide Hydrolases; Pregnancy; Pregnancy Trimester, Second; Pregnancy Trimester, Third; Prenatal Diagnosis; Umbelliferones | 1980 |
Effect of hypersomatostatinemia on growth hormone secretion in cystic fibrosis patients with diabetes.
Topics: Adult; Arginine; Body Mass Index; Carrier Proteins; Cystic Fibrosis; Diabetes Complications; Diabetes Mellitus; Growth Hormone; Humans; Insulin-Like Growth Factor Binding Proteins; Insulin-Like Growth Factor I; Male; Reference Values; Somatomedins; Somatostatin | 1993 |
Activation of CFTR chloride current by nitric oxide in human T lymphocytes.
Topics: Aminoquinolines; Arginine; CD4-Positive T-Lymphocytes; Chloride Channels; Clone Cells; Cyclic GMP; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Guanylate Cyclase; Humans; Membrane Proteins; Nitric Oxide; Patch-Clamp Techniques; Penicillamine; S-Nitroso-N-Acetylpenicillamine; Signal Transduction | 1995 |
Male infertility as the only presenting sign of cystic fibrosis when homozygous for the mild mutation R117H.
Topics: Adult; Arginine; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Homozygote; Humans; Infertility, Male; Male; Membrane Proteins; Point Mutation; Vas Deferens | 1993 |
Multi-ion pore behaviour in the CFTR chloride channel.
Topics: Amino Acid Sequence; Animals; Anions; Arginine; Chloride Channels; Chlorides; CHO Cells; Cricetinae; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Ion Channels; Membrane Potentials; Membrane Proteins; Molecular Sequence Data; Mutagenesis, Site-Directed; Thiocyanates | 1993 |
Clinical characteristics of 16 cystic fibrosis patients with the missense mutation R334W, a pancreatic insufficiency mutation with variable age of onset and interfamilial clinical differences.
Topics: Age of Onset; Arginine; Child; Child, Preschool; Cystic Fibrosis; Exocrine Pancreatic Insufficiency; Female; Forced Expiratory Volume; Genotype; Humans; Intestinal Obstruction; Lung; Male; Phenotype; Point Mutation; Tryptophan; Vital Capacity | 1995 |
Molecular basis for the polymorphic forms of human serum paraoxonase/arylesterase: glutamine or arginine at position 191, for the respective A or B allozymes.
Topics: Amino Acid Sequence; Arginine; Aryldialkylphosphatase; Base Sequence; Chromosomes, Human, Pair 7; Cloning, Molecular; Cystic Fibrosis; DNA; Female; Gene Library; Glutamine; Humans; Isoenzymes; Liver; Male; Molecular Sequence Data; Pedigree; Phosphoric Monoester Hydrolases; Polymerase Chain Reaction; Polymorphism, Genetic | 1993 |
Mutation of R555 in CFTR-delta F508 enhances function and partially corrects defective processing.
Topics: Amino Acid Sequence; Arginine; ATP-Binding Cassette Transporters; Cyclic AMP; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Electric Conductivity; Fungal Proteins; Humans; Ion Channel Gating; Lysine; Molecular Sequence Data; Mutagenesis, Site-Directed; Protein Processing, Post-Translational; Recombinant Fusion Proteins; Suppression, Genetic; Yeasts | 1996 |
An ovine CFTR variant as a putative cystic fibrosis causing mutation.
Topics: Animals; Arginine; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; DNA Primers; Glutamine; Lymphocytes; Mutation; Pedigree; Polymerase Chain Reaction; Polymorphism, Single-Stranded Conformational; Sequence Analysis; Sheep | 1996 |
Severe cystic fibrosis associated with a deltaF508/R347H + D979A compound heterozygous genotype.
Topics: Adult; Alanine; Arginine; Asparagine; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Female; Genotype; Heterozygote; Histidine; Humans; Male; Point Mutation; Severity of Illness Index | 1998 |
Cystic fibrosis-associated mutations at arginine 347 alter the pore architecture of CFTR. Evidence for disruption of a salt bridge.
Topics: Amino Acid Substitution; Arginine; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Hydrogen-Ion Concentration; Membrane Potentials; Mutagenesis, Site-Directed; Patch-Clamp Techniques; Phenotype; Protein Conformation; Salts; Static Electricity | 1999 |
Severe cystic fibrosis in a Japanese girl caused by two novel CFTR (ABCC7) gene mutations: M152R and 1540del10.
Topics: Amino Acid Substitution; Arginine; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Female; Frameshift Mutation; Gene Deletion; Humans; Methionine; Mutation, Missense | 2000 |
Effect of L-arginine infusion on airway NO in cystic fibrosis and primary ciliary dyskinesia syndrome.
Topics: Adolescent; Adult; Arginine; Breath Tests; Child; Ciliary Motility Disorders; Cystic Fibrosis; Female; Humans; Infusions, Intravenous; Male; Nitric Oxide; Syndrome | 1999 |
Frequency and clinical significance of the S1235R mutation in the cystic fibrosis transmembrane conductance regulator gene: results from a collaborative study.
Topics: Adolescent; Adult; Aged; Amino Acid Substitution; Arginine; Child; Child, Preschool; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Female; Gene Frequency; Humans; Infant; Infant, Newborn; Male; Middle Aged; Mutation, Missense; Pregnancy; Serine | 2000 |
Nitric oxide deficiency contributes to impairment of airway relaxation in cystic fibrosis mice.
Topics: Animals; Arginine; Bronchoconstriction; Cystic Fibrosis; Dinoprostone; Disease Models, Animal; Electric Stimulation; Enzyme Inhibitors; Female; In Vitro Techniques; Male; Mice; Mice, Inbred CFTR; Muscle Relaxation; Nitric Oxide; Nitric Oxide Synthase; Nitroarginine; Substance P; Trachea | 2001 |
Arginine esterase and lysosomal hydrolases in liver from cystic fibrosis subjects.
Topics: Adolescent; Adult; Arginine; Cathepsins; Child; Child, Preschool; Cystic Fibrosis; Esterases; Female; Humans; Hydrogen-Ion Concentration; Hydrolases; Isoelectric Focusing; Liver; Lysosomes; Male | 1977 |
Carboxypeptidase B activity of cultured skin fibroblasts and relationship to cystic fibrosis.
Topics: Arginine; Carboxypeptidases; Cells, Cultured; Cystic Fibrosis; Dithiothreitol; Fibroblasts; Hippurates; Humans; Hydrogen-Ion Concentration; Subcellular Fractions | 1979 |
Absence of an alpha two-macroglobulin-protease complex in cystic fibrosis.
Topics: alpha-Macroglobulins; Animals; Arginine; Cystic Fibrosis; Esterases; Humans; Hydrolysis; Immune Sera; Immunoelectrophoresis; Immunologic Techniques; Rabbits | 1976 |
Exocrine-gland function and the basic biochemical defect in cystic fibrosis.
Topics: Absorption; Arginine; Calcium; Cell Membrane; Chlorine; Cystic Fibrosis; Esterases; Humans; Kinins; Models, Biological; Salivary Glands; Sodium | 1978 |
Arginine esterase in amniotic fluid: possible marker for cystic fibrosis.
Topics: Amniotic Fluid; Arginine; Benzoates; Carboxylic Ester Hydrolases; Coumarins; Cystic Fibrosis; Esterases; Female; Genetic Markers; Humans; Methods; Pregnancy | 1979 |
Binding of 125I-labeled proteinases to plasma proteins in cystic fibrosis.
Topics: alpha-Macroglobulins; Arginine; Blood Proteins; Cystic Fibrosis; Electrophoresis, Polyacrylamide Gel; Endopeptidases; Esterases; Humans; Immunoelectrophoresis; Immunoglobulin G; Iodine Radioisotopes; Protein Binding; Trypsin | 1979 |
Pancreatic alpha and beta cell functions in cystic fibrosis.
Topics: Adolescent; Adult; Arginine; Child; Cystic Fibrosis; Female; Glucagon; Glucose Tolerance Test; Humans; Insulin; Insulin Secretion; Islets of Langerhans; Male; Prediabetic State | 1977 |
[Blood insulin levels and incidence of diabetes mellitus in patients with cystic fibrosis].
Topics: Adolescent; Adult; Arginine; Child; Cystic Fibrosis; Diabetes Complications; Diabetes Mellitus; Female; Glucose Tolerance Test; Humans; Insulin; Islets of Langerhans; Male | 1978 |
[Levels of somatotropic hormone in plasma and growth changes in patients with cystic fibrosis].
Topics: Adolescent; Adult; Arginine; Body Height; Body Weight; Child; Cystic Fibrosis; Female; Growth Disorders; Growth Hormone; Humans; Male; Pituitary Gland; Stimulation, Chemical | 1978 |
Reaction of 4-methylumbelliferylguanidinobenzoate with proteases in plasma of patients with cystic fibrosis.
Topics: Adolescent; Arginine; Binding Sites; Child; Child, Preschool; Cystic Fibrosis; Guanidines; Humans; Hymecromone; In Vitro Techniques; Isoelectric Focusing; Molecular Weight; Peptide Hydrolases; Umbelliferones | 1978 |
Normal plasma arginine esterase and the Hageman factor (factor XII) -prekallikrein-kininogen system in cystic fibrosis.
Topics: Adolescent; Adult; Arginine; Child; Cystic Fibrosis; Esterases; Factor XII; Humans; Kallikreins; Kininogens; Prekallikrein; Tosylarginine Methyl Ester | 1977 |
Insulin and glucagon response to arginine infusion in cystic fibrosis.
Topics: Arginine; Blood Glucose; Body Height; Body Weight; Child; Child, Preschool; Cystic Fibrosis; Fasting; Female; Glucagon; Humans; Injections, Intravenous; Insulin; Insulin Secretion; Male | 1977 |
Cystic fibrosis: comparison of two mucolytic drugs for inhalation treatment (acetylcysteine and arginine hydrochloride).
Topics: Acetylcysteine; Aerosols; Arginine; Bronchoscopy; Carbon Dioxide; Child; Child, Preschool; Cough; Cystic Fibrosis; Drug Evaluation; Expectorants; Female; Humans; Male; Mucus; Oxygen; Radionuclide Imaging; Respiration; Respiratory Function Tests; Spirometry; Sputum | 1975 |
Deficiency of arginine esterase in cystic fibrosis of the pancreas: demonstration of the proteolytic nature of the activity.
Topics: Adolescent; Arginine; Carboxylic Ester Hydrolases; Child; Child, Preschool; Cystic Fibrosis; Enzyme Inhibitors; Esterases; Heterozygote; Humans; Hydrolysis; Hydroxymercuribenzoates; Lung Diseases; Pancreatic Diseases; Peptides; Protamines; Tosyllysine Chloromethyl Ketone; Trypsin Inhibitors | 1975 |
[Inhalations with L-arginine in the treatment of cystic fibrosis (author's transl)].
Topics: Adolescent; Aerosols; Alanine Transaminase; Arginine; Aspartate Aminotransferases; Blood Glucose; Child; Child, Preschool; Creatinine; Cystic Fibrosis; Female; Follow-Up Studies; Humans; Male; Radiography; Viscosity | 1975 |
Letter: Questions regarding arginine hydrochloride inhalation.
Topics: Arginine; Cystic Fibrosis; Humans | 1976 |
[Therapy of cystic fibrosis].
Topics: Anti-Bacterial Agents; Arginine; Bicarbonates; Cysteine; Cystic Fibrosis; Humans; Infant | 1976 |
Auxotrophy of Pseudomonas aeruginosa in cystic fibrosis.
Topics: Amino Acids; Arginine; Bronchiectasis; Cystic Fibrosis; Humans; Methionine; Proline; Pseudomonas aeruginosa; Sputum; Thiamine | 1992 |
A serine-to-arginine (AGT-to-CGT) mutation in codon 549 of the CFTR gene in an Italian patient with severe cystic fibrosis.
Topics: Arginine; Base Sequence; Codon; Cystic Fibrosis; DNA; Exons; Female; Humans; Male; Molecular Sequence Data; Mutation; Serine | 1991 |
Pancreatic endocrine function in cystic fibrosis.
Topics: Adult; Arginine; C-Peptide; Cystic Fibrosis; Fasting; Glucagon; Glucose Tolerance Test; Humans; Hyperglycemia; Hypoglycemia; Insulin; Pancreas; Pancreatic Polypeptide; Time Factors | 1991 |
Letter: Plasma arginine esterase activity in cystic fibrosis.
Topics: Adult; Arginine; Child; Cystic Fibrosis; Electrophoresis, Polyacrylamide Gel; Esterases; Humans; Proteins | 1974 |
Deficiency of kallikrein activity in plasma of patients with cystic fibrosis.
Topics: Adult; Aprotinin; Arginine; Child; Cystic Fibrosis; Esterases; Heterozygote; Humans; Kallikreins | 1972 |
[Arginine test for the examination of endocrine pancreatic function in childhood].
Topics: Adolescent; Anorexia Nervosa; Arginine; Blood Glucose; Child; Child, Preschool; Cystic Fibrosis; Fasting; Female; Glucagon; Humans; Injections, Intravenous; Insulin; Islets of Langerhans; Methods; Pancreatic Diseases | 1974 |
L-arginine and cystic fibrosis.
Topics: Adolescent; Amylases; Arginine; Child; Cystic Fibrosis; Humans; Lipase; Pancreas; Trypsin | 1973 |
Growth hormone in marasmus die to cerebral disease.
Topics: Adolescent; Arginine; Astrocytoma; Birth Injuries; Blood Glucose; Brain Diseases; Brain Neoplasms; Celiac Disease; Child; Child, Preschool; Cystic Fibrosis; Dehydration; Depression, Chemical; Fatty Acids, Nonesterified; Female; Glucose; Growth Hormone; Humans; Hydrocephalus; Hypoglycemia; Hypoproteinemia; Infant; Insulin; Male; Nutrition Disorders; Radioimmunoassay; Stimulation, Chemical | 1973 |
Plasma arginine esterase activity in cystic fibrosis.
Topics: Acids; Adolescent; Adult; Arginine; Chloroform; Cystic Fibrosis; Enzyme Activation; Esterases; Humans; Middle Aged; Trypsin Inhibitors | 1974 |
Endocrine function of the pancreas in cystic fibrosis: evidence for an impaired glucagon and insulin response following arginine infusion.
Topics: Adolescent; Antigens; Arginine; Blood Glucose; Child; Child, Preschool; Cystic Fibrosis; Female; Glucagon; Humans; Insulin; Insulin Secretion; Male; Pancreas | 1974 |
Arginine esterase in cystic fibrosis of the pancreas.
Topics: Arginine; Blood; Chromatography, DEAE-Cellulose; Chromatography, Ion Exchange; Cystic Fibrosis; Electrophoresis, Polyacrylamide Gel; Esterases; Humans; Hydrogen-Ion Concentration; Trypsin Inhibitors | 1974 |
The use of L-arginine and sodium bicarbonate in the treatment of malabsorption due to cystic fibrosis.
Topics: Adolescent; Adult; Arginine; Bicarbonates; Body Weight; Carotenoids; Child; Cystic Fibrosis; Duodenum; Fats; Feces; Humans; Intestinal Secretions; Malabsorption Syndromes; Nitrogen; Pancreatic Extracts; Peptide Hydrolases; Sodium | 1972 |
L-arginine, the sickling phenomenon, and cystic fibrosis.
Topics: Aerosols; Anemia, Sickle Cell; Arginine; Cystic Fibrosis; Fever; Humans | 1972 |
Buffered L-arginine as treatment of cystic fibrosis: state of the evidence.
Topics: Adolescent; Aerosols; Arginine; Buffers; Child; Child, Preschool; Cystic Fibrosis; Female; Humans; Infant; Infant, Newborn; Lipid Metabolism; Pregnancy; Sputum; Structure-Activity Relationship | 1972 |
The use of buffered L-arginine in the treatment of cystic fibrosis.
Topics: Adolescent; Arginine; Body Weight; Buffers; Child; Child, Preschool; Cystic Fibrosis; Humans | 1971 |
Studies on the mechanism of inhibition of sodium transport in cystic fibrosis of the pancreas.
Topics: Animals; Arginine; Biological Transport; Cell Membrane Permeability; Cystic Fibrosis; Heparin; Humans; Imines; Lysine; Macromolecular Substances; Male; Parotid Gland; Rats; Saliva; Sodium | 1968 |
Successful treatment of acute lymphoblastic leukemia in a child with cystic fibrosis.
Topics: Antineoplastic Combined Chemotherapy Protocols; Asparaginase; Child, Preschool; Cystic Fibrosis; Cytarabine; Daunorubicin; Female; Humans; Mercaptopurine; Methotrexate; Precursor B-Cell Lymphoblastic Leukemia-Lymphoma; Precursor Cell Lymphoblastic Leukemia-Lymphoma; Prednisone; Remission Induction; Teniposide; Vincristine | 1994 |