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lysine and Broad Beta Disease

lysine has been researched along with Broad Beta Disease in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's4 (100.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Boomsma, DI; de Knijff, P; Frants, RR; Havekes, LM; Kastelein, JJ; Marais, AD; Smelt, AH; Stalenhoef, AF; van den Maagdenberg, AM1
Brewer, HB; Lohse, P; Rader, DJ1
Arakawa, F; Arakawa, K; Araki, K; Kaneko, S; Matsunaga, A; Moriyama, K; Sasaki, J; Takada, Y1
Brewer, HB; Lohse, P; Mann, WA; Stein, EA1

Other Studies

4 other study(ies) available for lysine and Broad Beta Disease

ArticleYear
Variable expression of familial dysbetalipoproteinemia in apolipoprotein E*2 (Lys146-->Gln) Allele carriers.
    The Journal of clinical investigation, 1994, Volume: 94, Issue:3

    Topics: Adolescent; Adult; Aged; Aged, 80 and over; Alleles; Amino Acid Sequence; Apolipoprotein E2; Apolipoproteins E; Base Sequence; Child; DNA Primers; Female; Gene Expression; Genetic Carrier Screening; Glutamine; Humans; Hyperlipoproteinemia Type III; Lysine; Male; Middle Aged; Molecular Sequence Data; Pedigree; Point Mutation; Polymerase Chain Reaction

1994
Heterozygosity for apolipoprotein E-4Philadelphia(Glu13----Lys, Arg145----Cys) is associated with incomplete dominance of type III hyperlipoproteinemia.
    The Journal of biological chemistry, 1992, Jul-05, Volume: 267, Issue:19

    Topics: Adolescent; Adult; Aged; Apolipoprotein E3; Apolipoprotein E4; Apolipoproteins E; Arginine; Child; Cysteine; DNA; Electrophoresis, Polyacrylamide Gel; Female; Genes, Dominant; Glutamates; Glutamic Acid; Heterozygote; Homozygote; Humans; Hyperlipoproteinemia Type III; Lysine; Male; Middle Aged; Pedigree; Phenotype; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length

1992
Apolipoprotein E1 Lys-146----Glu with type III hyperlipoproteinemia.
    Biochimica et biophysica acta, 1992, Sep-22, Volume: 1128, Issue:1

    Topics: Adult; Amino Acid Sequence; Apolipoprotein E2; Apolipoproteins E; Base Sequence; Child; DNA; Electrophoresis, Gel, Two-Dimensional; Female; Genetic Carrier Screening; Glutamates; Glutamic Acid; Humans; Hyperlipoproteinemia Type III; Lysine; Male; Middle Aged; Molecular Sequence Data; Oligodeoxyribonucleotides; Pedigree; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length

1992
Apolipoprotein E-4Philadelphia (Glu13----Lys,Arg145----Cys). Homozygosity for two rare point mutations in the apolipoprotein E gene combined with severe type III hyperlipoproteinemia.
    The Journal of biological chemistry, 1991, Jun-05, Volume: 266, Issue:16

    Topics: Adult; Amino Acid Sequence; Animals; Apolipoprotein E4; Apolipoproteins E; Arginine; Base Sequence; Cystine; DNA; Electrophoresis, Polyacrylamide Gel; Exons; Female; Glutamine; Humans; Hyperlipoproteinemia Type III; Lysine; Molecular Sequence Data; Mutation; Polymorphism, Restriction Fragment Length; Restriction Mapping

1991