isoleucine has been researched along with Apolipoprotein B-100, Familial Defective in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Emi, M; Ezura, Y; Hopkins, PN; Hunt, SC; Iino, Y; Katayama, Y; Larringa-Shum, S; Ono, S; Stephenson, SH; Takada, D; Wu, LL; Xin, Y | 1 |
| Cariolou, MA; Elisaf, M; Manoli, P; Miltiadous, G; Xenophontos, S | 1 |
2 other study(ies) available for isoleucine and Apolipoprotein B-100, Familial Defective
| Article | Year |
|---|---|
Growth hormone receptor variant (L526I) modifies plasma HDL cholesterol phenotype in familial hypercholesterolemia: intra-familial association study in an eight-generation hyperlipidemic kindred.
Topics: Adult; Amino Acid Substitution; Cholesterol, HDL; Codon; Female; Genetic Variation; Heterozygote; Humans; Hyperlipoproteinemia Type II; Isoleucine; Leucine; Lipoproteins; Male; Middle Aged; Pedigree; Phenotype; Plasma; Polymorphism, Single Nucleotide; Receptors, LDL; Receptors, Somatotropin | 2003 |
Segregation of a novel LDLR gene mutation (I430T) with familial hypercholesterolaemia in a Greek pedigree.
Topics: Amino Acid Substitution; Chromosome Segregation; Greece; Humans; Hyperlipoproteinemia Type II; Isoleucine; Mutation; Pedigree; Receptors, LDL; Threonine | 2000 |