Zobrazeno 1 - 10
of 48
pro vyhledávání: '"Pavel Vít"'
Autor:
Iva Synková, Markéta Bébarová, Irena Andršová, Larisa Chmelikova, Olga Švecová, Jan Hošek, Michal Pásek, Pavel Vít, Iveta Valášková, Renata Gaillyová, Rostislav Navrátil, Tomáš Novotný
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-13 (2021)
Abstract The variant c.926C > T (p.T309I) in KCNQ1 gene was identified in 10 putatively unrelated Czech families with long QT syndrome (LQTS). Mutation carriers (24 heterozygous individuals) were more symptomatic compared to their non-affected relati
Externí odkaz:
https://doaj.org/article/78136d3d7b394d9da2840cbe7a5654c8
Autor:
Iva Synková, Markéta Bébarová, Irena Andršová, Larisa Chmelikova, Olga Švecová, Jan Hošek, Michal Pásek, Pavel Vít, Iveta Valášková, Renata Gaillyová, Rostislav Navrátil, Tomáš Novotný
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-3 (2021)
An amendment to this paper has been published and can be accessed via a link at the top of the paper.
Externí odkaz:
https://doaj.org/article/7c77c1c50fb8444f9500e1f8d6f47bde
Autor:
Roman Panovský, Martin Pešl, Tomáš Holeček, Jan Máchal, Věra Feitová, Lenka Mrázová, Jana Haberlová, Alžběta Slabá, Pavel Vít, Veronika Stará, Vladimír Kincl
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-10 (2019)
Abstract Background The progressive cardiomyopathy that develops in boys with Duchenne and Becker muscular dystrophy (DMD/BMD) is presumed to be a secondary consequence of the fibrosis within the myocardium. There are only limited data on using param
Externí odkaz:
https://doaj.org/article/e270fad8cbb14404947ba4608b8deb53
Autor:
Kristina Rücklová, Jan David, Karel Koubský, Jan Pavlíček, Eva Klásková, Vojtěch Šedivý, Sylvia Krupičková, Hana Malcová, Jitka Komínová, Pavel Vít, Peter Kubuš
Publikováno v:
Cor et Vasa. 65:82-89
Autor:
Sergey Bespalyy, Gulmira Alnazarova, Vincenzo Nunzio Scalcione, Pavel Vitliemov, Aleksandr Sichinava, Alexandr Petrenko, Andrey Kaptsov
Publikováno v:
Discover Sustainability, Vol 5, Iss 1, Pp 1-18 (2024)
Abstract Education for sustainable development in universities is shaping the agenda in this area, demanding continuous improvement in quality. There is a trend towards integrating sustainability issues and the implementation of sustainable developme
Externí odkaz:
https://doaj.org/article/e9e821bf851c47dd80013757a6cb847c
Autor:
Tereza Nešporová, Pavel Vítámvás, Klára Kosová, Radovan Hynek, Sebastien Planchon, Jenny Renaut
Publikováno v:
Plant Stress, Vol 13, Iss , Pp 100509- (2024)
Drought as water deficit in the soil represents the most commonly occurring and the most variable environmental stress factor worldwide. Plants have evolved various strategies to cope with drought stress in relation to their other needs such as the n
Externí odkaz:
https://doaj.org/article/362b57dd3d2e48ddb34ea65ae0aaca47
Publikováno v:
Pediatrie pro praxi. 21:364-368
Kawasakiho choroba (KCH) je znama vice než 50 roků a v nasich podminkach stale patři mezi onemocněni vzacna. Dosud nebyla objasněna jeji etiopatogeneze. Podobně take chybi specificke nalezy pomocných vysetřeni a diagnoza nemoci se proto stale
Autor:
Jan Janoušek, Petr Jehlička, Reich O, Hana Jičínská, Viktor Tomek, Pavel Balatka, Petr Hecht, Pavel Vít, Eva Klásková
Publikováno v:
Cor et Vasa. 62:60-63
Vrozena srdecni vada je nejcastějsi vrozenou vadou vedouci k umrti v dětskem věku. Jeji prevalence se udava mezi 4–13 na 1 000 živě narozených děti. Strukturalni vay srdce jsou nejcastěji nerozpoznanou vrozenou vadou v prenatalnim screening
Autor:
Miroslav Klíma, Yamen H. Shmeit, Pavel Kopecký, Pavel Vítámvás, Klára Kosová, Ilja T. Prášil, Eloy Fernández-Cusimamani
Publikováno v:
Czech Journal of Genetics and Plant Breeding, Vol 60, Iss 2, Pp 79-85 (2024)
Several antimitotic agents were tested in three embryogenic doubled haploid (DH) lines of swede (Brassica napus ssp. napobrassica). No effect on embryogenesis was observed at the given concentrations of colchicine (5 μmol/L or 50 mg/L) and treatment
Externí odkaz:
https://doaj.org/article/0b726d8bf590463d8d50d25df8b5f536
Autor:
Michal Pásek, Iva Synková, Larisa Chmelikova, Rostislav Navrátil, Renata Gaillyová, Irena Andršová, Olga Švecová, Pavel Vít, Iveta Valášková, Jan Hošek, Markéta Bébarová, Tomáš Novotný
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-3 (2021)
Scientific Reports
Scientific Reports
The variant c.926C T (p.T309I) in KCNQ1 gene was identified in 10 putatively unrelated Czech families with long QT syndrome (LQTS). Mutation carriers (24 heterozygous individuals) were more symptomatic compared to their non-affected relatives (17 ind