tyrosine and Hemophilia B

tyrosine has been researched along with Hemophilia B 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
Herzog, RW; Markusic, DM; Marsic, D; Merricks, EP; Nichols, TC; Palaschak, B; Srivastava, A; Zolotukhin, I; Zolotukhin, S1
Aslanidi, GV; Herzog, RW; Hoffman, BE; Jayandharan, GR; Li, B; Li, M; Ling, C; Ma, W; Markusic, DM; Srivastava, A; Zhong, L; Zolotukhin, I; Zolotukhin, S1
Chandy, M; Jayandharan, G; Nair, SC; Shaji, RV; Srivastava, A1

Other Studies

3 other study(ies) available for tyrosine and Hemophilia B

ArticleYear
Evaluation of engineered AAV capsids for hepatic factor IX gene transfer in murine and canine models.
    Journal of translational medicine, 2017, 05-01, Volume: 15, Issue:1

    Topics: Animals; Capsid; Dependovirus; Dogs; Factor IX; Gene Transfer Techniques; Genetic Engineering; Genetic Vectors; Hemophilia B; Hepatocytes; Liver; Lysine; Male; Mice, Inbred BALB C; Mice, Inbred C57BL; Models, Animal; Mutation; Transduction, Genetic; Tyrosine

2017
High-efficiency transduction and correction of murine hemophilia B using AAV2 vectors devoid of multiple surface-exposed tyrosines.
    Molecular therapy : the journal of the American Society of Gene Therapy, 2010, Volume: 18, Issue:12

    Topics: Animals; Dependovirus; Genetic Therapy; Genetic Vectors; HeLa Cells; Hemophilia B; Hepatocytes; Humans; Mice; Mice, Inbred C57BL; Plasmids; Recombinant Proteins; Transduction, Genetic; Tyrosine

2010
Novel missense mutations in two patients with factor XI deficiency (Val271Leu and Tyr351Ser) and one patient with combined factor XI and factor IX deficiency (Phe349Val).
    Journal of thrombosis and haemostasis : JTH, 2005, Volume: 3, Issue:4

    Topics: Child; Codon; DNA Primers; Exons; Factor IX; Factor XI; Factor XI Deficiency; Female; Genotype; Hemophilia B; Hemorrhage; Humans; Introns; Leucine; Male; Mutation; Mutation, Missense; Phenotype; Phenylalanine; Polymerase Chain Reaction; Serine; Tyrosine; Valine

2005