phenylalanine has been researched along with Hemophilia A in 3 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (33.33) | 29.6817 |
2010's | 2 (66.67) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Ivanciu, L; Margaritis, P; Pavani, G; Small, JC; Stafford, KA; Szeto, JH; Zintner, SM | 1 |
Alvárez-Román, MT; Baena, M; Butta, N; Fernandez, I; Fuentes-Prior, P; Jiménez-Yuste, V; Martín-Salces, M; Rivas, I; Tizzano, EF; Venceslá, A | 1 |
Bayry, J; Christophe, O; Dasgupta, S; Delignat, S; Friboulet, A; Hoebeke, J; Kaveri, SV; Kazatchkine, MD; Lacroix-Desmazes, S; Nagaraja, V; Reinbolt, J; Saenko, E; Wootla, B | 1 |
3 other study(ies) available for phenylalanine and Hemophilia A
Article | Year |
---|---|
One amino acid in mouse activated factor VII defines its endothelial protein C receptor (EPCR) binding and modulates its EPCR-dependent hemostatic activity in vivo.
Topics: Animals; CHO Cells; Cricetinae; Cricetulus; DNA, Complementary; Endothelial Protein C Receptor; Factor VII; Factor VIIa; HEK293 Cells; Hemophilia A; Hemostasis; Humans; Leucine; Mice; Phenylalanine; Plasmids; Protein Binding; Protein Domains; Receptors, Cell Surface; Thrombin | 2017 |
Clinical and genetic findings in five female patients with haemophilia A: Identification of a novel missense mutation, p.Phe2127Ser.
Topics: Adolescent; Androgen-Insensitivity Syndrome; Child; Chromosomes, Human, X; Consanguinity; DNA Mutational Analysis; Factor VIII; Female; Hemarthrosis; Hemophilia A; Humans; Male; Mutation, Missense; Phenylalanine; Serine; Sex; Siblings; Spain; Young Adult | 2010 |
Catalytic IgG from patients with hemophilia A inactivate therapeutic factor VIII.
Topics: Adolescent; Adult; Aged; Antibodies, Catalytic; Arginine; Binding Sites, Antibody; Blood Coagulation; Child; Coumarins; Factor VIII; Hemophilia A; Humans; Hydrolysis; Immunoglobulin G; Middle Aged; Oligopeptides; Phenylalanine; Proline | 2006 |