Compounds > threonine

threonine and Hemorrhagic Disorders

threonine has been researched along with Hemorrhagic Disorders in 2 studies

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19901 (50.00)18.7374
1990's0 (0.00)18.2507
2000's1 (50.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Aranda, E; Goycoolea, M; Hendriks, D; Matus, V; Mezzano, D; Panes, O; Pereira, J; Quiroga, T; Willemse, J1
Matsuda, M; Shimura, K; Takahashi, N; Terukina, S; Yamazumi, K1

Other Studies

2 other study(ies) available for threonine and Hemorrhagic Disorders

ArticleYear
Procarboxypeptidase U (TAFI) and the Thr325Ile proCPU polymorphism in patients with hereditary mucocutaneous hemorrhages.
    Clinica chimica acta; international journal of clinical chemistry, 2009, Volume: 401, Issue:1-2

    Topics: Adolescent; Adult; Alleles; Amino Acid Substitution; Carboxypeptidase B2; Child; Child, Preschool; Female; Gene Frequency; Genotype; Hemorrhage; Hemorrhagic Disorders; Humans; Isoleucine; Male; Middle Aged; Polymorphism, Genetic; Threonine; Young Adult

2009
A gamma methionine-310 to threonine substitution and consequent N-glycosylation at gamma asparagine-308 identified in a congenital dysfibrinogenemia associated with posttraumatic bleeding, fibrinogen Asahi.
    The Journal of clinical investigation, 1989, Volume: 83, Issue:5

    Topics: Adult; Amino Acid Sequence; Asparagine; Binding Sites; Carbohydrate Conformation; Carbohydrate Sequence; Chromatography, High Pressure Liquid; Fibrinogens, Abnormal; Glycosylation; Hemorrhagic Disorders; Humans; Male; Methionine; Molecular Sequence Data; Mutation; Oligosaccharides; Peptide Fragments; Threonine; Thrombin

1989