Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Marek Godava"'
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
Autor:
Katerina Mensikova, Marek Godava, Petr Kanovsky, Pavel Otruba, Michaela Kaiserova, Miroslav Vastik, Lenka Mikulicova, Tereza Bartonikova, Radek Vrtel, Radek Vodicka, Sandra Kurcova, Petr Jugas, Josef Ovecka, Ludmila Sachova, Frantisek Dvorsky
Publikováno v:
Biomedical Papers, Vol 160, Iss 1, Pp 158-160 (2016)
Background: An epidemiological study conducted over four years revealed increased prevalence of neurodegenerative parkinsonism in a small, isolated region (10 villages, with a combined population of 8664, with approx. 2927 over 50 years of age) of so
Externí odkaz:
https://doaj.org/article/18bc6b39476c45b2acc8b29d79471ca6
Autor:
Radek Vrtel, Lubomír Dubrava, Kamila Michálková, Hana Filipova, Jiri Navratil, Maria Janikova, Lenka Bakaj-Zbrozkova, Marek Godava
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://explore.openaire.eu/search/publication?articleId=doi_dedup___::a439cdd63c28365861673fcceec04671
https://biomed.papers.upol.cz/artkey/bio-201703-0013_Single_giant_mediastinal_rhabdomyoma_as_a_sole_manifestation_of_TSC_in_foetus.php
https://biomed.papers.upol.cz/artkey/bio-201703-0013_Single_giant_mediastinal_rhabdomyoma_as_a_sole_manifestation_of_TSC_in_foetus.php
Autor:
Miroslav Vastik, Marek Godava, Tereza Bartoníková, J. Ovecka, Radek Vrtel, Pavel Otruba, Radek Vodicka, Katerina Mensikova, Sandra Kurcova, Lenka Mikulicova, F. Dvorsky, Michaela Kaiserová, L. Sachova, P. Jugas, Petr Kanovsky
Publikováno v:
Biomedical Papers, Vol 160, Iss 1, Pp 158-160 (2016)
ResearcherID
ResearcherID
Background: An epidemiological study conducted over four years revealed increased prevalence of neurodegenerative parkinsonism in a small, isolated region (10 villages, with a combined population of 8664, with approx. 2927 over 50 years of age) of so
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82d8849430d0ff49ef7b236776686a80
https://biomed.papers.upol.cz/artkey/bio-201601-0023_Familial_autosomal-dominant_neurodegenerative_parkinsonism_with_cognitive_deterioration_spanning_five_generati.php
https://biomed.papers.upol.cz/artkey/bio-201601-0023_Familial_autosomal-dominant_neurodegenerative_parkinsonism_with_cognitive_deterioration_spanning_five_generati.php
Autor:
Jiri Muzik, Vladimír Mihál, Eva Schneiderova, Radek Vodicka, Frantisek Kopriva, Radek Vrtel, Marek Godava, Marie Markova, Ladislav Dušek
Publikováno v:
Biomedical Papers. 157:367-373
Introduction. ADAM33 is the candidate gene most commonly associated with asthma and airway hyperreactivity (AHR). Aim. The aim of this study was to determine whether level of AHR is associated with certain alleles or haplotypes of the ADAM33 gene in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a7ac66c5f00679540e41d07d5c60074
https://doi.org/10.5507/bp.2013.025
https://doi.org/10.5507/bp.2013.025
Autor:
Petr Dzubak, Josef Srovnal, Frantisek Kopriva, Lenka Radová, Marian Hajduch, Jan Potesil, Marek Godava, Vladimír Mihál
Publikováno v:
Central European Journal of Immunology. 4:518-529
Multidrug resistance protein 1 (MDr1, abCb1 or P-glycoprotein) and multidrug resistance-associated protein 1 (MrP1, abCC1 or ltC4 transporter) are active membrane-associated efflux transporters with broad substrate specificity. the aim of this study
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6a6ea1dd12e66d957b2ea86c3189ea9b
https://doi.org/10.5114/ceji.2013.39770
https://doi.org/10.5114/ceji.2013.39770
Autor:
Josef Zamecnik, Radim Mazanec, Tomas Honzik, Stanislav Voháňka, Vratislav Smolka, Petr Vondráček, Martin Magner, Daniela Skálová, Dana Šišková, Hana Ošlejšková, Vladimir Gregor, Lenka Fajkusová, Jiří Zeman, Jana Zídková, Kristýna Stehlíková, Martina Langová, Jana Haberlová, Lenka Mrázová, Marek Godava
Publikováno v:
Clinical genetics. 91(3)
Inherited neuromuscular disorder (NMD) is a wide term covering different genetic disorders affecting muscles, nerves, and neuromuscular junctions. Genetic and clinical heterogeneity is the main drawback in a routine gene-by-gene diagnostics. We prese
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c03ec742c1eef99ae1e4a744b54a6325
https://pubmed.ncbi.nlm.nih.gov/27447704
https://pubmed.ncbi.nlm.nih.gov/27447704
Autor:
Josef Ovecka, Tereza Bartoníková, Kristýna Kolařiková, František Dvorský, Vladimir Janout, Pavel Otruba, Martin Bareš, Radek Vodicka, Marek Godava, Miroslav Vastik, Petr Kaňovský, Petr Hluštík, Michaela Kaiserová, Lenka Mikulicova, Petr Jugas, Martin Prochazka, Kateřina Menšíková, Radek Vrtěl, Jiří Krša, Ludmila Šáchová
Publikováno v:
Medicine
An increased prevalence of familial neurodegenerative parkinsonism or cognitive deterioration was recently found in a small region of southeastern Moravia. The aim of the study was to assess the genetic background of this familial disease. Variants i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d7068ba96e72dcc2822e36e81417f63
https://doi.org/10.1097/md.0000000000012313
https://doi.org/10.1097/md.0000000000012313
Publikováno v:
Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia. 157(2)
Background. STAT6 has an important role in the IL-4 / IL-13 signalling pathway. Genome - wide association studies have shown that particular polymorphism (SNP) or haplotype variants of STAT6 as well as epigenetic gene modifications are associated wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c5dc578c77260be30098264c6396bbc
https://pubmed.ncbi.nlm.nih.gov/23752766
https://pubmed.ncbi.nlm.nih.gov/23752766
Autor:
Jan Muzik, Michaela Cvanová, Marie Markova, Eva Schneiderova, Marek Godava, Frantisek Kopriva, Ladislav Dušek, Jana Bohmova, Radek Vrtel, Radek Vodicka
Publikováno v:
Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia. 156(3)
Background. ADAM33 and STAT6 belong to the candidate genes that have been commonly associated with asthma, bronchial hyperresponsiveness or IgE levels. Our objective was to assess the association of 11 SNPs of the ADAM33 and 6 of the STAT6 and their
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af6d80792dc35ab7a0c05e45ca2cf11f
https://pubmed.ncbi.nlm.nih.gov/22660217
https://pubmed.ncbi.nlm.nih.gov/22660217