valine has been researched along with Angiohemophilia in 7 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 6 (85.71) | 18.2507 |
| 2000's | 1 (14.29) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Cloutier, S; Duan, Z; Jackson, SC; Poon, MC; Rand, ML; Sinclair, GD | 1 |
| Anbo, H; Furukawa, T; Handa, M; Kawai, Y; Moriki, T; Murata, M; Nikkuni, K; Shibata, A; Takahashi, H; Watanabe, K | 1 |
| Murata, M; Ruggeri, ZM; Russell, SR; Ware, J | 1 |
| Anbo, H; Handa, M; Ikeda, Y; Kitaguchi, T; Moriki, T; Murata, M; Takahashi, H; Watanabe, K | 1 |
| Canciani, MT; Di Rocco, N; Federici, AB; Mannucci, PM; Miyata, S; Ruggeri, ZM; Stabile, F; Ware, J | 1 |
| Giles, AR; Lillicrap, D; Murray, EW | 1 |
| Carty, RP; Dykes, DC; Miller, JL; Pincus, MR | 1 |
7 other study(ies) available for valine and Angiohemophilia
| Article | Year |
|---|---|
The Montreal platelet syndrome kindred has type 2B von Willebrand disease with the VWF V1316M mutation.
Topics: Amino Acid Substitution; Blood Coagulation Tests; Blood Platelet Disorders; Blood Platelets; DNA Mutational Analysis; Family; Female; Humans; Male; Methionine; Mutation, Missense; Pedigree; Platelet Aggregation; Syndrome; Valine; von Willebrand Diseases; von Willebrand Factor | 2009 |
Substitution of Val for Met at residue 239 of platelet glycoprotein Ib alpha in Japanese patients with platelet-type von Willebrand disease.
Topics: Amino Acid Sequence; Base Sequence; Blood Platelets; Codon; DNA Primers; Female; Genetic Carrier Screening; Humans; Japan; Male; Methionine; Molecular Sequence Data; Pedigree; Platelet Aggregation; Platelet Membrane Glycoproteins; Point Mutation; Polymerase Chain Reaction; Valine; von Willebrand Diseases | 1995 |
Expression of the phenotypic abnormality of platelet-type von Willebrand disease in a recombinant glycoprotein Ib alpha fragment.
Topics: Amino Acid Sequence; Animals; Blood Platelets; CHO Cells; Cricetinae; Crotalid Venoms; Genetic Variation; Glycine; Hemagglutinins; Humans; Kinetics; Macromolecular Substances; Phenotype; Platelet Membrane Glycoproteins; Recombinant Proteins; Ristocetin; Transfection; Valine; von Willebrand Diseases; von Willebrand Factor | 1993 |
Expression and functional characterization of an abnormal platelet membrane glycoprotein Ib alpha (Met239 --> Val) reported in patients with platelet-type von Willebrand disease.
Topics: Analysis of Variance; Humans; Methionine; Platelet Aggregation; Platelet Aggregation Inhibitors; Platelet Glycoprotein GPIb-IX Complex; Point Mutation; Recombinant Proteins; Ristocetin; Transfection; Valine; von Willebrand Diseases | 1997 |
A type 2b von Willebrand disease mutation (Ile546-->Val) associated with an unusual phenotype.
Topics: Adult; Anti-Bacterial Agents; Child; Female; Humans; Isoleucine; Male; Middle Aged; Phenotype; Platelet Aggregation; Point Mutation; Restriction Mapping; Ristocetin; Sequence Analysis, DNA; Valine; von Willebrand Diseases; von Willebrand Factor | 1997 |
Germ-line mosaicism for a valine-to-methionine substitution at residue 553 in the glycoprotein Ib-binding domain of von Willebrand factor, causing type IIB von Willebrand disease.
Topics: Autoradiography; Base Sequence; Blood Coagulation Tests; DNA; Electrophoresis, Polyacrylamide Gel; Humans; Leukocytes; Male; Methionine; Molecular Sequence Data; Mosaicism; Mutation; Pedigree; Platelet Membrane Glycoproteins; Polymerase Chain Reaction; Polymorphism, Genetic; Spermatozoa; Valine; von Willebrand Diseases; von Willebrand Factor | 1992 |
Conformational energy analysis of the substitution of Val for Gly 233 in a functional region of platelet GPIb alpha in platelet-type von Willebrand disease.
Topics: Amino Acid Sequence; Blood Platelets; Computer Simulation; Glycine; Humans; Macromolecular Substances; Models, Molecular; Molecular Sequence Data; Mutation; Peptide Fragments; Platelet Aggregation; Platelet Membrane Glycoproteins; Protein Conformation; Valine; von Willebrand Diseases | 1991 |