Compounds > asparagine

asparagine and Afibrinogenemia, Congenital

asparagine has been researched along with Afibrinogenemia, Congenital in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (33.33)29.6817
2010's2 (66.67)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Chen, Y; Cheng, Y; Duan, X; Liao, Z; Liu, C; Luo, M; Tan, Y; Tang, H; Wang, D; Xie, Y; Xu, S1
Bowley, SR; Lord, ST; Okumura, N1
Castillo, O; De Sáez Ruiz, A; Marchi, R; Meyer, M; Rojas, H; Weisel, JW1

Other Studies

3 other study(ies) available for asparagine and Afibrinogenemia, Congenital

ArticleYear
Fibrinogen Hangzhou: congenital dysfibrinogenemia caused by the novel missense mutation in FGG (γ308Asn→Thr).
    Clinica chimica acta; international journal of clinical chemistry, 2014, Jan-20, Volume: 428

    Topics: Afibrinogenemia; Asparagine; China; Fibrinogen; Humans; Male; Middle Aged; Mutation, Missense; Threonine

2014
Impaired protofibril formation in fibrinogen gamma N308K is due to altered D:D and "A:a" interactions.
    Biochemistry, 2009, Sep-15, Volume: 48, Issue:36

    Topics: Afibrinogenemia; Asparagine; Crystallography, X-Ray; Fibrinogens, Abnormal; Hemorrhagic Disorders; Humans; Hydrogen Bonding; Lysine; Protein Interaction Mapping; Protein Stability; Protein Structure, Tertiary

2009
A novel missense mutation in the FGB g. 3354 T>A (p. Y41N), fibrinogen Caracas VIII.
    Thrombosis and haemostasis, 2011, Volume: 105, Issue:4

    Topics: Adult; Afibrinogenemia; Asparagine; Cell Line; DNA Mutational Analysis; Endothelium, Vascular; Fibrin; Fibrinogens, Abnormal; Humans; Male; Microscopy, Electron; Mutation, Missense; Protein Binding; Thrombin Time; Tyrosine

2011