spironolactone has been researched along with glycine in 6 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (16.67) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 2 (33.33) | 29.6817 |
2010's | 3 (50.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Barnes, JC; Bradley, P; Day, NC; Fourches, D; Reed, JZ; Tropsha, A | 1 |
Campillo, NE; Guerra, A; Páez, JA | 1 |
Cohen, LA; Farber, L | 1 |
Hur, JK; Kim, JB; Lee, KY | 1 |
Fagart, J; Fay, MR; Huyet, J; Pinon, GM; Rafestin-Oblin, ME | 1 |
Kil, TH; Kim, JB | 1 |
6 other study(ies) available for spironolactone and glycine
Article | Year |
---|---|
Cheminformatics analysis of assertions mined from literature that describe drug-induced liver injury in different species.
Topics: Animals; Chemical and Drug Induced Liver Injury; Cluster Analysis; Databases, Factual; Humans; MEDLINE; Mice; Models, Chemical; Molecular Conformation; Quantitative Structure-Activity Relationship | 2010 |
Neural computational prediction of oral drug absorption based on CODES 2D descriptors.
Topics: Administration, Oral; Humans; Models, Chemical; Neural Networks, Computer; Permeability; Quantitative Structure-Activity Relationship; Technology, Pharmaceutical | 2010 |
The specific cleavage of tyrosyl-peptide bonds by electrolytic oxidation.
Topics: Angiotensin II; Chemical Phenomena; Chemistry; Electrolysis; Glycine; Insulin; Ketones; Peptides; Spironolactone; Tyrosine | 1966 |
A Korean family of hypokalemic periodic paralysis with mutation in a voltage-gated calcium channel (R1239G).
Topics: Acetazolamide; Adolescent; Arginine; Calcium Channels; Calcium Channels, L-Type; Codon; Exons; Family Health; Female; Glycine; Humans; Hypokalemia; Hypokalemic Periodic Paralysis; Korea; Male; Muscle, Skeletal; Mutation; Pedigree; Protein Structure, Tertiary; Sequence Analysis, DNA; Spironolactone | 2005 |
Structural basis of spirolactone recognition by the mineralocorticoid receptor.
Topics: Amino Acid Substitution; Arginine; Asparagine; Binding Sites; Cell Line; Crystallography, X-Ray; Glycine; Humans; Hydrogen Bonding; Kidney; Ligands; Mineralocorticoid Receptor Antagonists; Models, Molecular; Molecular Structure; Protein Binding; Protein Structure, Tertiary; Receptors, Mineralocorticoid; Spironolactone; Structure-Activity Relationship; Time Factors; Transcriptional Activation; Transfection | 2007 |
Severe respiratory phenotype caused by a de novo Arg528Gly mutation in the CACNA1S gene in a patient with hypokalemic periodic paralysis.
Topics: Adolescent; Amiloride; Amino Acid Substitution; Arginine; Calcium Channels; Calcium Channels, L-Type; Cold Temperature; DNA Mutational Analysis; Genotype; Glycine; Humans; Hypokalemic Periodic Paralysis; Male; Mutation; Potassium; Respiratory Insufficiency; Spironolactone | 2010 |