histidine has been researched along with Cystic Fibrosis in 8 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (25.00) | 18.7374 |
| 1990's | 2 (25.00) | 18.2507 |
| 2000's | 4 (50.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| al Habasch, O; Baron, O; Despins, P; Duveau, D; Fabre, S; Haloun, A; Michaud, JL; Treilhaud, M | 1 |
| Crawford, RM; Mehta, A; Treharne, KJ | 1 |
| Adams, KN; Ernst, RK; Kawasaki, K; Kraig, GM; Miller, SI; Moskowitz, SM; Stead, CM; Trent, MS | 1 |
| Comeau, AM; Dorkin, HL; O'Sullivan, BP; Parad, R; Zwerdling, RG | 1 |
| Riordan, JR; Seger, E; Tümmler, B | 1 |
| Bartholomew, DW; Fujita, J; Hojo, S; Miyawaki, H; Obayashi, Y; Takahara, J | 1 |
| Cainarca, S; Cremonesi, L; Ferrari, M; Firpo, S; Gelfi, C; Perego, M; Righetti, PG | 1 |
| Clayton, BE | 1 |
1 review(s) available for histidine and Cystic Fibrosis
| Article | Year |
|---|---|
CFTR, chloride concentration and cell volume: could mammalian protein histidine phosphorylation play a latent role?
Topics: AMP-Activated Protein Kinases; Animals; Cell Membrane; Cell Polarity; Cell Size; Chlorides; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Epithelial Cells; Histidine; Humans; Ion Channel Gating; Multienzyme Complexes; Nucleoside-Diphosphate Kinase; Phosphorylation; Protein Serine-Threonine Kinases; Respiratory Mucosa; Signal Transduction | 2006 |
7 other study(ies) available for histidine and Cystic Fibrosis
| Article | Year |
|---|---|
Retrospective clinical comparison of Celsior solution to modified blood Wallwork solution in lung transplantation for cystic fibrosis.
Topics: Albumins; Chlorides; Cystic Fibrosis; Disaccharides; Electrolytes; Female; Glutamates; Glutathione; Histidine; Humans; Lung; Lung Transplantation; Male; Mannitol; Organ Preservation Solutions; Phosphoprotein Phosphatases; Propionates; Protein Tyrosine Phosphatases; Retrospective Studies | 2002 |
The Pseudomonas aeruginosa lipid A deacylase: selection for expression and loss within the cystic fibrosis airway.
Topics: Acylation; Bacterial Proteins; Carboxylic Ester Hydrolases; Child; Cystic Fibrosis; Gene Expression Regulation, Bacterial; Histidine; Humans; Lipid A; Magnesium; Pseudomonas aeruginosa; Respiratory System; Temperature | 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 |
Systematic study of the hydrolysis of 4-methylumbelliferylguanidinobenzoate in plasma from patients with cystic fibrosis and controls.
Topics: Adolescent; Adult; Child; Child, Preschool; Cystic Fibrosis; Drug Stability; Enzyme Activation; Female; Histidine; Humans; Hydrolysis; Hymecromone; Kinetics; Male; Methods; Peptide Hydrolases; Umbelliferones | 1982 |
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 |
Rapid capillary zone electrophoresis in isoelectric histidine buffer: high resolution of the poly-T tract allelic variants in intron 8 of the CFTR gene.
Topics: Alleles; Buffers; Child; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Electrophoresis, Capillary; Fluorescence; Histidine; Humans; Introns; Lasers; Male; Poly T; Polymerase Chain Reaction; Vas Deferens | 1998 |
Problems affecting the community. Population screening.
Topics: Cystic Fibrosis; Galactosemias; Genetic Testing; Histidine; Humans; Infant; Infant, Newborn; Metabolism, Inborn Errors; Phenylketonurias; Tay-Sachs Disease; United Kingdom | 1974 |