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lysine and Factor X Deficiency

lysine has been researched along with Factor X Deficiency in 4 studies

Research

Studies (4)

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

Authors

AuthorsStudies
Baidya, S; Chandy, M; George, B; Jayandharan, G; Nair, SC; Shaji, RV; Srivastava, A; Viswabandya, A1
Abdel-Razeq, H; Al-Gaili, F; Al-Hilali, A; Herrmann, FH; Saud, KA; Wulff, K1
Forberg, E; Höller, W; Krinninger, B; Nöbauer-Huhmann, IM; Richter, G; Scharrer, I; Turecek, PL; Watzke, HH1
Friedman, P; High, KA; Jagadeeswaran, P; Lechner, K; Mahr, G; Monroe, DM; Reddy, SV; Roberts, HR; Watzke, HH; Welsch, DJ1

Other Studies

4 other study(ies) available for lysine and Factor X Deficiency

ArticleYear
Six novel mutations including triple heterozygosity for Phe31Ser, 514delT and 516T-->G factor X gene mutations are responsible for congenital factor X deficiency in patients of Nepali and Indian origin.
    Journal of thrombosis and haemostasis : JTH, 2005, Volume: 3, Issue:7

    Topics: Arginine; Codon, Nonsense; CpG Islands; DNA Mutational Analysis; DNA Primers; Epitopes; Exons; Factor Va; Factor X; Factor X Deficiency; Frameshift Mutation; Heterozygote; Humans; India; Lysine; Models, Genetic; Models, Molecular; Mutation; Mutation, Missense; Nepal; Phenylalanine; Serine

2005
Analysis of the novel factor X gene mutation Glu51Lys in two families with factor X-Riyadh anomaly.
    Thrombosis and haemostasis, 2007, Volume: 97, Issue:4

    Topics: Adolescent; Adult; Aged; Child; DNA Mutational Analysis; Exons; Factor X; Factor X Deficiency; Female; Genotype; Glutamic Acid; Humans; Lysine; Male; Middle Aged; Mutation, Missense; Partial Thromboplastin Time; Pedigree; Phenotype; Prothrombin Time; Saudi Arabia

2007
Factor X Frankfurt I: molecular and functional characterization of a hereditary factor X deficiency (Gla+25 to Lys).
    Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis, 1998, Volume: 9, Issue:2

    Topics: Adult; Amino Acid Substitution; Factor X; Factor X Deficiency; Genes, Recessive; Humans; Lysine; Male; Point Mutation; Protein Structure, Tertiary; Structure-Activity Relationship

1998
Molecular defect (Gla+14----Lys) and its functional consequences in a hereditary factor X deficiency (factor X "Vorarlberg").
    The Journal of biological chemistry, 1990, Jul-15, Volume: 265, Issue:20

    Topics: Amino Acid Sequence; Base Sequence; Calcium; Exons; Factor X; Factor X Deficiency; Female; Glutamates; Glutamic Acid; Humans; Hypoprothrombinemias; Kinetics; Lysine; Male; Molecular Sequence Data; Mutation; Oligonucleotide Probes; Pedigree; Reference Values

1990