leucinal has been researched along with proline in 4 studies
Studies (leucinal) | Trials (leucinal) | Recent Studies (post-2010) (leucinal) | Studies (proline) | Trials (proline) | Recent Studies (post-2010) (proline) |
---|---|---|---|---|---|
14 | 0 | 3 | 22,134 | 520 | 5,973 |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (25.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 2 (50.00) | 29.6817 |
2010's | 1 (25.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Frick, L; Wolfenden, R | 1 |
Brismar, K; Ding, B; Efendic, S; Gu, HF; Kärvestedt, L; Nordman, S; Ostenson, CG | 1 |
Kaipio, K; Pesonen, U | 1 |
An, SSA; Bagyinszky, E; Giau, VV; Kim, S; Park, J; Shim, K; Youn, YC | 1 |
4 other study(ies) available for leucinal and proline
Article | Year |
---|---|
Mechanistic implications of the inhibition of peptidases by amino aldehydes and bestatin.
Topics: Alanine; Aldehydes; Aminopeptidases; Animals; Aspartic Acid Endopeptidases; Dipeptidyl-Peptidases and Tripeptidyl-Peptidases; Kidney; Kinetics; Leucine; Leucyl Aminopeptidase; Male; Peptide Hydrolases; Proline; Protease Inhibitors; Rats; Testis | 1985 |
Leu7Pro polymorphism in the neuropeptide Y (NPY) gene is associated with impaired glucose tolerance and type 2 diabetes in Swedish men.
Topics: Adult; Alleles; Blood Glucose; Body Mass Index; Diabetes Mellitus, Type 2; Fasting; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glucose Intolerance; Heterozygote; Humans; Insulin; Leucine; Male; Middle Aged; Neuropeptide Y; Odds Ratio; Polymerase Chain Reaction; Polymorphism, Genetic; Proline; Sex Characteristics; Sweden | 2005 |
The intracellular mobility of NPY and a putative mitochondrial form of NPY in neuronal cells.
Topics: Cell Line, Tumor; Green Fluorescent Proteins; Humans; Leucine; Microscopy, Confocal; Mitochondria; Neuroblastoma; Neurons; Neuropeptide Y; Polymorphism, Genetic; Proline; Protein Transport; Transfection | 2009 |
Identification of a novel PSEN1 mutation (Leu232Pro) in a Korean patient with early-onset Alzheimer's disease and a family history of dementia.
Topics: Adult; Alzheimer Disease; Asian People; Atrophy; Codon; Dementia; Exons; Genetic Association Studies; Genetic Predisposition to Disease; Helix-Loop-Helix Motifs; Humans; Leucine; Magnetic Resonance Imaging; Mutation, Missense; Neuroimaging; Parietal Lobe; Presenilin-1; Proline | 2017 |