Compounds > valine

valine and Hyperlipoproteinemia Type II

valine has been researched along with Hyperlipoproteinemia Type II in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's3 (60.00)18.2507
2000's2 (40.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Alias, L; Baiget, M; Ferrer, I; Gallano, P; Martínez-Matos, JA; Moreno, D; Olivé, M; Pujol, R1
Choumerianou, DM; Dedoussis, GV; Maumus, S; Pitsavos, C; Skoumas, J; Stefanadis, C; Visvikis-Siest, S1
Fischer, J; Keller, C; Manke, C; Schuster, H; Wolfram, G; Zöllner, N1
Defesche, JC; Hayden, MR; Kastelein, JJ; Lamping, RJ; Lansberg, PJ; Reymer, PW; van Diermen, DE1
Fischer, HJ; Keller, C; Schuster, H; Wolfram, G; Zöllner, N1

Other Studies

5 other study(ies) available for valine and Hyperlipoproteinemia Type II

ArticleYear
A novel mutation in the caveolin-3 gene causing familial isolated hyperCKaemia.
    Neuromuscular disorders : NMD, 2004, Volume: 14, Issue:5

    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
Natriuretic peptide Val7Met substitution and risk of coronary artery disease in Greek patients with familial hypercholesterolemia.
    Journal of clinical laboratory analysis, 2006, Volume: 20, Issue:3

    Topics: Adult; Atrial Natriuretic Factor; Comorbidity; Coronary Artery Disease; Female; Genetic Predisposition to Disease; Greece; Humans; Hyperlipoproteinemia Type II; Lipids; Male; Polymorphism, Single Nucleotide; Risk Factors; Valine

2006
Identification of the valine 408 to methionine mutation in the LDL receptor in a Greek patient with homozygous familial hypercholesterolemia.
    Clinical genetics, 1995, Volume: 48, Issue:2

    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.
    Human genetics, 1993, Volume: 92, Issue:6

    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.
    Human genetics, 1993, Volume: 91, Issue:3

    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