proline 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 |
| Bruin, T; Brunzell, JD; Hayden, MR; Henderson, HE; Kastelein, JJ; Ma, Y; Stalenhoef, AF; Sturk, A; Stuyt, PM; Van Diermen, DE | 1 |
3 other study(ies) available for proline 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 |
A missense mutation Pro157 Arg in lipoprotein lipase (LPLNijmegen) resulting in loss of catalytic activity.
Topics: Adult; Amino Acid Sequence; Arginine; Base Sequence; Blotting, Southern; Catalysis; Cell Line; Deoxyribonucleases, Type II Site-Specific; Female; Humans; Hyperlipoproteinemia Type I; Lipoprotein Lipase; Molecular Sequence Data; Mutagenesis, Site-Directed; Mutation; Pedigree; Polymerase Chain Reaction; Proline; Structure-Activity Relationship; Transfection | 1992 |