Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Radek Vrtěl"'
Autor:
Petr Vrtel, Ludek Slavik, Radek Vodicka, Julia Stellmachova, Martin Prochazka, Jana Prochazkova, Jana Ulehlova, Peter Rohon, Tomas Simurda, Jan Stasko, Ivana Martinkova, Radek Vrtel
Publikováno v:
Diagnostics, Vol 12, Iss 5, p 1060 (2022)
The deficiency of natural anticoagulants—antithrombin (AT), protein C (PC), and protein S (PS)—is a highly predisposing factor for thrombosis, which is still underdiagnosed at the genetic level. We aimed to establish and evaluate an optimal diagn
Externí odkaz:
https://doaj.org/article/003c59edd04342368e96e880a89cfc57
Autor:
Kristyna Kolarikova, Radek Vodicka, Radek Vrtel, Julia Stellmachova, Martin Prochazka, Katerina Mensikova, Tereza Bartonikova, Tomas Furst, Petr Kanovsky, Jan Geryk
Publikováno v:
Life, Vol 12, Iss 1, p 121 (2022)
Parkinson’s disease and parkinsonism are relatively common neurodegenerative disorders. This study aimed to assess potential genetic risk factors of haplotypes in genes associated with parkinsonism in a population in which endemic parkinsonism and
Externí odkaz:
https://doaj.org/article/b5971695dbe7497280991f88cd222b47
Autor:
Marek Godava, Hana Filipova, Lubomir Dubrava, Radek Vrtel, Kamila Michalkova, Maria Janikova, Lenka Bakaj-Zbrozkova, Jiri Navratil
Publikováno v:
Biomedical Papers, Vol 161, Iss 3, Pp 326-329 (2017)
Background: Presence of multiple cardiac rhabdomyomas is one of the major features of Tuberous sclerosis (TSC), but isolated progressing single giant rhabdomyoma is very rare and not typical of TSC. Case report: This report presents family without ob
Externí odkaz:
https://doaj.org/article/733249aef9eb459fb98bd9f44eb2ce36
Publikováno v:
Diagnostics, Vol 11, Iss 5, p 803 (2021)
The molecular pathology of hemolytic disease of the fetus and newborn (HDFN) is determined by different RHD, RHCE, and KEL genotypes and by blood group incompatibility between the mother and fetus that is caused by erythrocyte antigen presence/absenc
Externí odkaz:
https://doaj.org/article/05d362594be14feb86bf92203e135411
Autor:
Kateřina Menšíková, Radoslav Matěj, Carlo Colosimo, Raymond Rosales, Lucie Tučková, Jiří Ehrmann, Dominik Hraboš, Kristýna Kolaříková, Radek Vodička, Radek Vrtěl, Martin Procházka, Martin Nevrlý, Michaela Kaiserová, Sandra Kurčová, Pavel Otruba, Petr Kaňovský
Publikováno v:
npj Parkinson's Disease, Vol 8, Iss 1, Pp 1-11 (2022)
Abstract The current nosological concept of α-synucleinopathies characterized by the presence of Lewy bodies (LBs) includes Parkinson’s disease (PD), Parkinson’s disease dementia (PDD), and dementia with Lewy bodies (DLB), for which the term “
Externí odkaz:
https://doaj.org/article/f25879c97eaa49cc8111beacfaaaa2b3
Autor:
Kateřina Menšíková, Radoslav Matěj, Carlo Colosimo, Raymond Rosales, Lucie Tučková, Jiří Ehrmann, Dominik Hraboš, Kristýna Kolaříková, Radek Vodička, Radek Vrtěl, Martin Procházka, Martin Nevrlý, Michaela Kaiserová, Sandra Kurčová, Pavel Otruba, Petr Kaňovský
Publikováno v:
npj Parkinson's Disease, Vol 8, Iss 1, Pp 1-2 (2022)
Externí odkaz:
https://doaj.org/article/d2e53caf186d4c66b1f6af550a5df824
Autor:
Zuzana Kahounová, Eva Slabáková, Lucia Binó, Ján Remšík, Radek Fedr, Jan Bouchal, Daniela Kurfűrstová, Radek Vrtěl, Vladimír Študent, Lucie Jurečková, Volodymyr Porokh, Aleš Hampl, Karel Souček
Publikováno v:
Stem Cell Research, Vol 33, Iss , Pp 255-259 (2018)
A human induced pluripotent stem cell line was generated from cancer-associated fibroblasts of a 68-years old patient with diagnosed prostate adenocarcinoma (PCa). The fibroblast cell line was reprogrammed with Epi5™ Episomal iPSC Reprogramming Kit
Externí odkaz:
https://doaj.org/article/ff7f398ed78e4e059a1dbe047213f717
Autor:
Zuzana Kahounová, Eva Slabáková, Lucia Binó, Ján Remšík, Radek Fedr, Jan Bouchal, Radek Vrtěl, Lucie Jurečková, Volodymyr Porokh, Darja Páralová, Aleš Hampl, Karel Souček
Publikováno v:
Stem Cell Research, Vol 35, Iss , Pp - (2019)
Human induced pluripotent stem cell line was generated from commercially available primary human prostate fibroblasts HPrF derived from a fetus, aged 18–24 weeks of gestation. The fibroblast cell line was reprogrammed with Yamanaka factors (OCT4, S
Externí odkaz:
https://doaj.org/article/f112efb59bb94fadb1795db7605ea344
Autor:
Júlia, Štellmachová, Petr, Vrtěl, Radek, Vrtěl, Mária, Janíková, Kristýna, Kolaříková, Martin, Procházka, Radek, Vodička
Publikováno v:
Česká gynekologie. 87:211-216
Objective: Summary of knowledge in the field of ovarian cancer and genetic predisposition. Results: Ovarian tumors are usually diagnosed at advanced stages of the disease and the prognosis for these patients is generally poor. The 5-year overall surv
Autor:
Michaela, Maděrková Tozzi, Vladimír, Dvořák Jr., Eva, Klásková, Soňa, Šuláková, Martin, Wita, Jan, Hálek, Radek, Vrtěl, Václava, Curtisová, Radovan, Pilka, Ladislav, Dušek, Marek, Ľubušký
Publikováno v:
Česká gynekologie. 87:162-172
Objective: The aim of the study was to analyze the results of the screening for congenital defects (CD) and genetic diseases (GD) of the fetus in the Fetal Medicine Centre at the Department of Obstetrics and Gynecology, University Hospital in Olomouc