leucine has been researched along with Apolipoprotein C-II Deficiency in 3 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 3 (100.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Deshaies, Y; Julien, P; Lévesque, G; Lupien, PJ; Ven Murthy, MR | 1 |
Anwar, R; Markham, AF; Puntis, JW | 1 |
Halliday, D; Mitropoulos, KA; Pacy, PJ; Venkatesan, S; Watts, GF | 1 |
3 other study(ies) available for leucine and Apolipoprotein C-II Deficiency
Article | Year |
---|---|
A rapid restriction site screening method for the Pro207-->Leu mutation in the lipoprotein lipase gene.
Topics: Base Sequence; DNA Mutational Analysis; DNA Primers; DNA Restriction Enzymes; France; Genetic Testing; Humans; Hyperlipoproteinemia Type I; Leucine; Lipoprotein Lipase; Molecular Epidemiology; Molecular Sequence Data; Point Mutation; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Proline; Quebec | 1994 |
A new mutation in the human lipoprotein lipase gene causing familial hyperchylomicronaemia.
Topics: Child; Exons; Female; Humans; Hyperlipoproteinemia Type I; Infant, Newborn; Leucine; Lipoprotein Lipase; Male; Point Mutation; Polymerase Chain Reaction; Proline | 1997 |
Fractional and absolute synthetic rate of very low density lipoprotein apo B-100 in lipoprotein lipase deficient patients.
Topics: Adult; Apolipoprotein B-100; Apolipoproteins B; Carbon Isotopes; Female; Humans; Hyperlipoproteinemia Type I; Isotope Labeling; Leucine; Lipoproteins, VLDL; Male; Middle Aged; Reference Values | 1992 |