Compounds > arginine

arginine and Apolipoprotein C-II Deficiency

arginine has been researched along with Apolipoprotein C-II Deficiency 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
Beisiegel, U; Benlian, P; Bruin, T; Chitayat, D; De Gennes, JL; Forsythe, I; Foubert, L; Funke, H; Liu, MS; Ma, Y1
Benlian, P; Bruin, T; De Gennes, JL; Ehrenborg, E; Foubert, L; Furioli, J; Hayden, M; Kastelein, J1
Bruin, T; Brunzell, JD; Hayden, MR; Henderson, HE; Kastelein, JJ; Ma, Y; Stalenhoef, AF; Sturk, A; Stuyt, PM; Van Diermen, DE1
Chan, L; Faustinella, F; Ishimura-Oka, K; Kihara, S; Oka, K; Smith, LC1

Other Studies

4 other study(ies) available for arginine and Apolipoprotein C-II Deficiency

ArticleYear
Recurrent missense mutations at the first and second base of codon Arg243 in human lipoprotein lipase in patients of different ancestries.
    Human mutation, 1994, Volume: 3, Issue:1

    Topics: Adult; Amino Acid Sequence; Arginine; Base Sequence; Cell Line; Child, Preschool; China; Europe; Exons; Gene Expression Regulation; Haplotypes; Humans; Hyperlipoproteinemia Type I; Lipoprotein Lipase; Middle Aged; Molecular Sequence Data; Mutagenesis; Point Mutation; Polymorphism, Restriction Fragment Length; Sequence Analysis, DNA

1994
A single Ser259Arg mutation in the gene for lipoprotein lipase causes chylomicronemia in Moroccans of Berber ancestry.
    Human mutation, 1997, Volume: 10, Issue:3

    Topics: Adolescent; Adult; Arginine; Child; Chylomicrons; Female; Founder Effect; Humans; Hyperlipoproteinemia Type I; Lipoprotein Lipase; Male; Middle Aged; Morocco; Pedigree; Point Mutation; Serine

1997
A missense mutation Pro157 Arg in lipoprotein lipase (LPLNijmegen) resulting in loss of catalytic activity.
    European journal of biochemistry, 1992, Sep-01, Volume: 208, Issue:2

    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
A missense mutation (Trp86----Arg) in exon 3 of the lipoprotein lipase gene: a cause of familial chylomicronemia.
    American journal of human genetics, 1992, Volume: 50, Issue:6

    Topics: Amino Acid Sequence; Arginine; Base Sequence; Chylomicrons; Cloning, Molecular; Codon; DNA; Exons; Female; Humans; Hyperlipoproteinemia Type I; Introns; Lipoprotein Lipase; Male; Molecular Sequence Data; Mutation; Pedigree; Restriction Mapping; Tryptophan

1992