glutamine has been researched along with Angiohemophilia in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 3 (75.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (25.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Budde, U; Castaman, G; Eikenboom, J; Federici, AB; Goodeve, A; Goudemand, J; Hampshire, D; Hickson, N; James, P; Peake, I; Rodeghiero, F; Schneppenheim, R; Winship, P | 1 |
| Alessi, MC; Boyer-Neumann, C; Lavergne, JM; Meyer, D; Piao, YC; Schandelong, A | 1 |
| Arnout, J; Briët, E; Eikenboom, JC; Peerlinck, K; Ploos Van Amstel, HK; Reitsma, PH; Sangtawesin, W; Vermylen, J | 1 |
| Fahs, SA; Friedman, KD; Kroner, PA; Montgomery, RR; Scott, JP | 1 |
4 other study(ies) available for glutamine and Angiohemophilia
| Article | Year |
|---|---|
von Willebrand factor variant p.Arg924Gln marks an allele associated with reduced von Willebrand factor and factor VIII levels.
Topics: ABO Blood-Group System; Alleles; Arginine; Case-Control Studies; Factor VIII; Founder Effect; Genetic Variation; Genotype; Glutamine; Heterozygote; Humans; Mutation; Phenotype; Recombinant Proteins; von Willebrand Diseases; von Willebrand Factor | 2010 |
Arg578Gln mutations in the von Willebrand factor gene in three unrelated cases of type IIB von Willebrand disease.
Topics: Adult; Aged; Arginine; Base Sequence; Child, Preschool; DNA, Complementary; Female; Glutamine; Humans; Male; Molecular Sequence Data; Mutation; Polymerase Chain Reaction; von Willebrand Diseases; von Willebrand Factor | 1993 |
A patient with von Willebrand's disease characterized by a compound heterozygosity for a substitution of Arg854 by Gln in the putative factor-VIII-binding domain of von Willebrand factor (vWF) on one allele and very low levels of mRNA from the second vWF
Topics: Adult; Alleles; Arginine; Base Sequence; Factor VIII; Female; Glutamine; Heterozygote; Humans; Molecular Sequence Data; Mutation; Polymerase Chain Reaction; RNA, Messenger; von Willebrand Diseases; von Willebrand Factor | 1992 |
Abnormal binding of factor VIII is linked with the substitution of glutamine for arginine 91 in von Willebrand factor in a variant form of von Willebrand disease.
Topics: Arginine; Autoradiography; Base Sequence; Cell Line; Electrophoresis, Polyacrylamide Gel; Factor VIII; Gene Expression; Glutamine; Humans; Molecular Sequence Data; Mutation; Polymorphism, Genetic; RNA, Messenger; von Willebrand Diseases; von Willebrand Factor | 1991 |