Compounds > threonine

threonine and Hypophosphatasia

threonine has been researched along with Hypophosphatasia in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (50.00)18.2507
2000's1 (25.00)29.6817
2010's1 (25.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Ishida, Y; Komaru, K; Oda, K1
Chaidaroglou, A; Kantrowitz, ER1
Fukushi, M; Igarashi, A; Ikehara, Y; Misumi, Y; Oda, K; Ohashi, Y; Shibata, H1
Hu, JC; Mornet, E; Plaetke, R; Simmer, JP; Sun, X; Thomas, HF; Zhang, C1

Other Studies

4 other study(ies) available for threonine and Hypophosphatasia

ArticleYear
Molecular characterization of tissue-nonspecific alkaline phosphatase with an Ala to Thr substitution at position 116 associated with dominantly inherited hypophosphatasia.
    Biochimica et biophysica acta, 2011, Volume: 1812, Issue:3

    Topics: Alanine; Alkaline Phosphatase; Amino Acid Substitution; Animals; Blotting, Western; Chlorocebus aethiops; CHO Cells; COS Cells; Cricetinae; Cricetulus; Disulfides; Gene Expression; Genes, Dominant; Humans; Hypophosphatasia; Immunoprecipitation; Mutation, Missense; Threonine

2011
The Ala-161-->Thr substitution in Escherichia coli alkaline phosphatase does not result in loss of enzymatic activity although the homologous mutation in humans causes hypophosphatasia.
    Biochemical and biophysical research communications, 1993, Jun-30, Volume: 193, Issue:3

    Topics: Alanine; Alkaline Phosphatase; Amino Acid Sequence; Bone and Bones; Electrophoresis, Polyacrylamide Gel; Escherichia coli; Humans; Hypophosphatasia; Isoenzymes; Kidney; Kinetics; Liver; Mutagenesis, Site-Directed; Point Mutation; Recombinant Proteins; Threonine

1993
Defective intracellular transport of tissue-nonspecific alkaline phosphatase with an Ala162-->Thr mutation associated with lethal hypophosphatasia.
    Journal of biochemistry, 1998, Volume: 123, Issue:5

    Topics: Alanine; Alkaline Phosphatase; Amino Acid Substitution; Animals; Biological Transport; COS Cells; Endoplasmic Reticulum; Fluorescent Antibody Technique; Glycosylphosphatidylinositols; Hexosaminidases; Hypophosphatasia; Intracellular Fluid; Isoenzymes; Mannosyl-Glycoprotein Endo-beta-N-Acetylglucosaminidase; Mutation; Threonine

1998
Characterization of a family with dominant hypophosphatasia.
    European journal of oral sciences, 2000, Volume: 108, Issue:3

    Topics: Alanine; Alkaline Phosphatase; Amino Acid Substitution; Child; Dental Cementum; Dental Enamel Hypoplasia; Diseases in Twins; Ethanolamines; Family Health; Female; Genes, Dominant; Genetic Linkage; Humans; Hypophosphatasia; Male; Pedigree; Point Mutation; Threonine; Tooth Exfoliation; Twins, Dizygotic

2000