methionine has been researched along with Hyperlipoproteinemia Type II in 7 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 3 (42.86) | 18.7374 |
| 1990's | 3 (42.86) | 18.2507 |
| 2000's | 1 (14.29) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Alias, L; Baiget, M; Ferrer, I; Gallano, P; Martínez-Matos, JA; Moreno, D; Olivé, M; Pujol, R | 1 |
| Bilheimer, DW; Brown, MS; Goldstein, JL; Grundy, SM; Starzl, TE | 1 |
| Fischer, J; Keller, C; Manke, C; Schuster, H; Wolfram, G; Zöllner, N | 1 |
| Defesche, JC; Hayden, MR; Kastelein, JJ; Lamping, RJ; Lansberg, PJ; Reymer, PW; van Diermen, DE | 1 |
| Fischer, HJ; Keller, C; Schuster, H; Wolfram, G; Zöllner, N | 1 |
| Funahashi, T; Miyake, Y; Yamamoto, A | 1 |
| Knight, BL; Patel, DD; Soutar, AK | 1 |
7 other study(ies) available for methionine and Hyperlipoproteinemia Type II
| Article | Year |
|---|---|
A novel mutation in the caveolin-3 gene causing familial isolated hyperCKaemia.
Topics: Adolescent; Adult; Biopsy; Blotting, Western; Caveolin 3; Caveolins; DNA Mutational Analysis; Dystrophin; Exons; Female; Humans; Hyperlipoproteinemia Type II; Immunohistochemistry; Male; Methionine; Molecular Sequence Data; Muscles; Mutation; NAD; Pedigree; Polymorphism, Single-Stranded Conformational; Sarcolemma; Staining and Labeling; Valine | 2004 |
Liver transplantation to provide low-density-lipoprotein receptors and lower plasma cholesterol in a child with homozygous familial hypercholesterolemia.
Topics: Cells, Cultured; Child; Cholesterol, LDL; Female; Fibroblasts; Heart Transplantation; Homozygote; Humans; Hyperlipoproteinemia Type II; Lipoproteins, LDL; Liver; Liver Transplantation; Methionine; Receptors, LDL; Sulfur Radioisotopes | 1984 |
Identification of the valine 408 to methionine mutation in the LDL receptor in a Greek patient with homozygous familial hypercholesterolemia.
Topics: Base Sequence; Child; Germany; Greece; Haplotypes; Humans; Hyperlipoproteinemia Type II; Male; Methionine; Molecular Sequence Data; Mutation; Receptors, LDL; Valine | 1995 |
South African founder mutations in the low-density lipoprotein receptor gene causing familial hypercholesterolemia in the Dutch population.
Topics: Alleles; DNA; Exons; Haplotypes; Humans; Hyperlipoproteinemia Type II; Methionine; Netherlands; Point Mutation; Polymorphism, Restriction Fragment Length; Receptors, LDL; South Africa; Valine | 1993 |
Identification of the 408 valine to methionine mutation in the low density lipoprotein receptor in a German family with familial hypercholesterolemia.
Topics: Adolescent; Adult; Aged; DNA Mutational Analysis; Female; Germany; Humans; Hyperlipoproteinemia Type II; Lipoproteins; Male; Methionine; Middle Aged; Mutation; Pedigree; Polymerase Chain Reaction; Receptors, LDL; Valine | 1993 |
Cells of an internalization-defective familial hypercholesterolemia mutant secrete low density lipoprotein receptors.
Topics: Antibodies, Monoclonal; Cells, Cultured; Female; Fibroblasts; Humans; Hyperlipoproteinemia Type II; Immunologic Techniques; Kinetics; Male; Methionine; Molecular Weight; Mutation; Protein Processing, Post-Translational; Receptors, LDL | 1987 |
Regulation of synthesis and cell content of the low-density-lipoprotein receptor protein in cultured fibroblasts from normal and familial hypercholesterolaemic subjects.
Topics: Acetates; Cell Membrane; Cells, Cultured; Cholesterol; Fibroblasts; Humans; Hyperlipoproteinemia Type II; Immunochemistry; Lipoproteins; Lovastatin; Methionine; Naphthalenes; Radioimmunoassay; Receptors, LDL | 1987 |