Structural and Functional Characterization of Four Novel Fibrinogen Mutations in FGB Causing Congenital Fibrinogen Disorder

por Ceznerová, Eliška, Kaufmanová, Jiřina, Sovová, Žofie, Štikarová, Jana, Loužil, Jan, Kotlín, Roman, Suttnar, Jiří
Publicado 2022

Diagnosing Czech Patients with Inherited Platelet Disorders

por Louzil, Jan, Stikarova, Jana, Provaznikova, Dana, Hrachovinova, Ingrid, Fenclova, Tereza, Musil, Jan, Radek, Martin, Kaufmanova, Jirina, Geierova, Vera, Ceznerova, Eliska, Salaj, Peter, Kotlin, Roman
Publicado 2022

Linking aberrant glycosylation of plasma glycoproteins with progression of myelodysplastic syndromes: a study based on plasmonic biosensor and lectin array

por Chrastinová, Leona, Pastva, Ondřej, Bocková, Markéta, Kovářová, Hana, Ceznerová, Eliška, Kotlín, Roman, Pecherková, Pavla, Štikarová, Jana, Hlaváčková, Alžběta, Havlíček, Marek, Válka, Jan, Homola, Jiří, Suttnar, Jiří
Publicado 2023

A Novel Nonsense Mutation in FGB (c.1421G>A; p.Trp474Ter) in the Beta Chain of Fibrinogen Causing Hypofibrinogenemia with Bleeding Phenotype

por Simurda, Tomas, Vilar, Rui, Zolkova, Jana, Ceznerova, Eliska, Kolkova, Zuzana, Loderer, Dusan, Neerman-Arbez, Marguerite, Casini, Alessandro, Brunclikova, Monika, Skornova, Ingrid, Dobrotova, Miroslava, Grendar, Marian, Stasko, Jan, Kubisz, Peter
Publicado 2020