Compounds > proline

proline and leucinal

proline has been researched along with leucinal in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19901 (25.00)18.7374
1990's0 (0.00)18.2507
2000's2 (50.00)29.6817
2010's1 (25.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Frick, L; Wolfenden, R1
Brismar, K; Ding, B; Efendic, S; Gu, HF; Kärvestedt, L; Nordman, S; Ostenson, CG1
Kaipio, K; Pesonen, U1
An, SSA; Bagyinszky, E; Giau, VV; Kim, S; Park, J; Shim, K; Youn, YC1

Other Studies

4 other study(ies) available for proline and leucinal

ArticleYear
Mechanistic implications of the inhibition of peptidases by amino aldehydes and bestatin.
    Biochimica et biophysica acta, 1985, Jul-01, Volume: 829, Issue:3

    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.
    Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association, 2005, Volume: 113, Issue:5

    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.
    Neuroscience letters, 2009, Jan-30, Volume: 450, Issue:2

    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.
    Neurobiology of aging, 2017, Volume: 56

    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