Compounds > phenylalanine

phenylalanine and von Willebrand Diseases

phenylalanine has been researched along with von Willebrand Diseases in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (33.33)18.2507
2000's1 (33.33)29.6817
2010's1 (33.33)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Barbon, G; Casonato, A; Cattini, GM; Daidone, V; Gallinaro, L; Pizzo, P; Pontara, E; Zampese, E1
Battiston, M; Casonato, A; De Marco, L; Gallinaro, L; Mazzuccato, M; Pagnan, A; Ruggeri, ZM; Sztukowska, M1
Dechavanne, M; Gaucher, C; Hanss, M; Mazurier, C1

Other Studies

3 other study(ies) available for phenylalanine and von Willebrand Diseases

ArticleYear
Loss of cysteine 584 impairs the storage and release, but not the synthesis of von Willebrand factor.
    Thrombosis and haemostasis, 2014, Volume: 112, Issue:6

    Topics: Adult; Aged; Amino Acid Substitution; Culture Media, Conditioned; Cysteine; DNA Mutational Analysis; Endoplasmic Reticulum; Female; Genetic Predisposition to Disease; Golgi Apparatus; HEK293 Cells; Hemostasis; Humans; Male; Mutation, Missense; Phenotype; Phenylalanine; Protein Multimerization; Protein Transport; Transfection; von Willebrand Diseases; von Willebrand Factor; Weibel-Palade Bodies

2014
Altered von Willebrand factor subunit proteolysis and multimer processing associated with the Cys2362Phe mutation in the B2 domain.
    Thrombosis and haemostasis, 2007, Volume: 97, Issue:4

    Topics: ADAM Proteins; ADAMTS13 Protein; Adult; Blood Coagulation Tests; Cysteine; Female; Heterozygote; Homozygote; Humans; Molecular Weight; Mutation, Missense; Pedigree; Phenotype; Phenylalanine; Protein Conformation; Protein Processing, Post-Translational; Protein Structure, Tertiary; Protein Subunits; Severity of Illness Index; von Willebrand Diseases; von Willebrand Factor

2007
Substitution of cysteine for phenylalanine 751 in mature von Willebrand factor is a novel candidate mutation in a family with type IIA von Willebrand disease.
    British journal of haematology, 1993, Volume: 83, Issue:1

    Topics: Cysteine; Exons; Genotype; Humans; Mutation; Pedigree; Phenotype; Phenylalanine; Polymerase Chain Reaction; Polymorphism, Genetic; von Willebrand Diseases; von Willebrand Factor

1993