phenylalanine has been researched along with Hemophilia B in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (33.33) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (66.67) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Baikeev, RF; Gilbert, GE; Grant, MA; Rigby, AC | 1 |
| Chandy, M; Jayandharan, G; Nair, SC; Shaji, RV; Srivastava, A | 1 |
| Fujimura, Y; Fukui, H; Iwanaga, S; Miyata, T; Niinomi, K; Sakai, T; Yamamoto, K; Yoshioka, A | 1 |
3 other study(ies) available for phenylalanine and Hemophilia B
| Article | Year |
|---|---|
Lysine 5 and phenylalanine 9 of the factor IX omega-loop interact with phosphatidylserine in a membrane-mimetic environment.
Topics: Calcium; Cations, Divalent; Circular Dichroism; Factor IX; Hemophilia B; Humans; Lipid Bilayers; Lysine; Models, Molecular; Molecular Mimicry; Nuclear Magnetic Resonance, Biomolecular; Peptides, Cyclic; Phenylalanine; Phosphatidylserines; Protein Binding; Protein Structure, Secondary; Protein Structure, Tertiary | 2004 |
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).
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 |
Blood clotting factor IX Kashihara: amino acid substitution of valine-182 by phenylalanine.
Topics: Amino Acids; Chromatography, High Pressure Liquid; Factor IX; Hemophilia B; Humans; Hydrolysis; Mutation; Peptide Mapping; Phenylalanine; Trypsin; Valine | 1989 |