leucine and Hemophilia B

leucine has been researched along with Hemophilia B in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (50.00)	29.6817
2010's	1 (50.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Bartholomae, CC; Gui, T; Hu, G; Kafri, T; Kutschera, I; Monahan, PE; Schmidt, M; Suwanmanee, T; von Kalle, C	1
Chandy, M; Jayandharan, G; Nair, SC; Shaji, RV; Srivastava, A	1

Other Studies

2 other study(ies) available for leucine and Hemophilia B

Article	Year
Integration-deficient lentiviral vectors expressing codon-optimized R338L human FIX restore normal hemostasis in Hemophilia B mice. Molecular therapy : the journal of the American Society of Gene Therapy, 2014, Volume: 22, Issue:3 Topics: Animals; Arginine; Codon; Disease Models, Animal; Factor IX; Genetic Therapy; Genetic Vectors; Hemophilia B; Hep G2 Cells; Humans; Lentivirus; Leucine; Liver; Mice; Mice, Inbred C57BL; Mice, Knockout	2014
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

Article

Year

Integration-deficient lentiviral vectors expressing codon-optimized R338L human FIX restore normal hemostasis in Hemophilia B mice.

Molecular therapy : the journal of the American Society of Gene Therapy, 2014, Volume: 22, Issue:3

Topics: Animals; Arginine; Codon; Disease Models, Animal; Factor IX; Genetic Therapy; Genetic Vectors; Hemophilia B; Hep G2 Cells; Humans; Lentivirus; Leucine; Liver; Mice; Mice, Inbred C57BL; Mice, Knockout

2014

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