Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Eliska Ceznerova"'
Autor:
Leona Chrastinová, Ondřej Pastva, Markéta Bocková, Hana Kovářová, Eliška Ceznerová, Roman Kotlín, Pavla Pecherková, Jana Štikarová, Alžběta Hlaváčková, Marek Havlíček, Jan Válka, Jiří Homola, Jiří Suttnar
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-10 (2023)
Abstract Aberrant glycosylation of glycoproteins has been linked with various pathologies. Therefore, understanding the relationship between aberrant glycosylation patterns and the onset and progression of the disease is an important research goal th
Externí odkaz:
https://doaj.org/article/dbd5e50cdcae47bb974b43bfdcfaaccf
Autor:
Tomas Simurda, Rui Vilar, Jana Zolkova, Eliska Ceznerova, Zuzana Kolkova, Dusan Loderer, Marguerite Neerman-Arbez, Alessandro Casini, Monika Brunclikova, Ingrid Skornova, Miroslava Dobrotova, Marian Grendar, Jan Stasko, Peter Kubisz
Publikováno v:
Biomedicines, Vol 8, Iss 12, p 605 (2020)
Congenital hypofibrinogenemia is a rare bleeding disorder characterized by a proportional decrease of functional and antigenic fibrinogen levels. Hypofibrinogenemia can be considered the phenotypic expression of heterozygous loss of function mutation
Externí odkaz:
https://doaj.org/article/ba8b9f1b146c40b690bf7f4ed9c97dc4
Autor:
Jan Louzil, Jana Stikarova, Dana Provaznikova, Ingrid Hrachovinova, Tereza Fenclova, Jan Musil, Martin Radek, Jirina Kaufmanova, Vera Geierova, Eliska Ceznerova, Peter Salaj, Roman Kotlin
Publikováno v:
International Journal of Molecular Sciences; Volume 23; Issue 22; Pages: 14386
A single-center study was conducted on 120 patients with inherited disorders of primary hemostasis followed at our hematological center. These patients presented a variety of bleeding symptoms; however, they had no definitive diagnosis. Establishing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dfaa1e4b14f2cf0a540790843dd9fdb8
https://pubmed.ncbi.nlm.nih.gov/36430862
https://pubmed.ncbi.nlm.nih.gov/36430862
Autor:
Alzbeta Hlavackova, Jan Vydra, Leona Chrastinova, Eliska Ceznerova, Marek Havlicek, Jana Stikarova, Roman Kotlin, Jiri Suttnar
Publikováno v:
Blood. 140:11833-11833
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9f2250b1a18e43672f9228991bf71761
https://doi.org/10.1182/blood-2022-168549
https://doi.org/10.1182/blood-2022-168549
Autor:
Eliska Ceznerova, Jirina Kaufmanova, Marek Havlicek, Ondrej Pastva, Alzbeta Hlavackova, Roman Kotlin, Jiri Suttnar
Publikováno v:
Blood. 140:2719-2719
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e07eed76db14e7bf98bd1d8b16f3549f
https://doi.org/10.1182/blood-2022-169020
https://doi.org/10.1182/blood-2022-169020
Autor:
Eliska Ceznerova, Miroslava Dobrotova, Dusan Loderer, Monika Brunclikova, Tomas Simurda, Alessandro Casini, Peter Kubisz, Zuzana Kolková, Jana Zolkova, Ingrid Skornova, Jan Stasko, Rui Vilar, Marguerite Neerman-Arbez, Marian Grendar
Publikováno v:
Biomedicines
Biomedicines, Vol 8, Iss 605, p 605 (2020)
Biomedicines, Vol. 8, No 12 (2020) P. 605
Biomedicines, Vol 8, Iss 605, p 605 (2020)
Biomedicines, Vol. 8, No 12 (2020) P. 605
Congenital hypofibrinogenemia is a rare bleeding disorder characterized by a proportional decrease of functional and antigenic fibrinogen levels. Hypofibrinogenemia can be considered the phenotypic expression of heterozygous loss of function mutation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b009e34a860fa627a766c73c05ade98
https://doi.org/10.3390/biomedicines8120605
https://doi.org/10.3390/biomedicines8120605
Autor:
Jaromir Novak, Roman Kotlín, Pavla Roselova, Jana Štikarová, Eliska Ceznerova, Martin Hajšl, Pavel Májek, Martin Maly, Jan Louzil, Leona Chrastinova, Ondrej Kucerka, Jan E. Dyr, Jirina Kaufmanova, Alzbeta Hlavackova, Zofie Sovova, Jiri Suttnar
Publikováno v:
Blood. 132:5011-5011
Background Cardiovascular diseases are linked with oxidative stress which is the source of reactive oxidative and nitrative species, contributors of post-translational modification. Fibrinogen due to its high concentration in blood is considered as o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c73e67ec40c4938fff40aea588928c84
https://doi.org/10.1182/blood-2018-99-118260
https://doi.org/10.1182/blood-2018-99-118260
Autor:
Jan Louzil, Eliska Ceznerova, Pavla Roselova, Peter Salaj, Jan E. Dyr, Jiri Suttnar, Jirina Kaufmanova, Jana Štikarová, Roman Kotlín
Publikováno v:
Blood. 132:5046-5046
Fibrinogen is a 340 kDA glycoprotein that plays a vital role in the hemostasis. The three pairs of polypeptide chains (Aα, Bβ and γ) form a heterodimer structure of fibrinogen, each chain is encoded by a distinct gene (FGA, FGB and FGG). Congenita
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f78b7fc488e06ac835bdc23fd1eccfb8
https://doi.org/10.1182/blood-2018-99-118254
https://doi.org/10.1182/blood-2018-99-118254
Autor:
Eliska Ceznerova, Jan E. Dyr, Peter Salaj, Jiri Suttnar, Alzbeta Hlavackova, Ondrej Pastva, Stikarová Jana, Jaroslav Cermak, Roman Kotlín
Publikováno v:
Blood. 126:4697-4697
Introduction Hemostasis in childhood differs from that of adults; and the hemostatic system is still developing during childhood. These differences offer a protective advantage to children with hemorrhagic and thrombotic complications. Plasma levels
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d816f62f45a346be220f87454dde3799
https://doi.org/10.1182/blood.v126.23.4697.4697
https://doi.org/10.1182/blood.v126.23.4697.4697