Clinical-genetic analysis of selected genes involved in the development of the human skeleton in 128 Czech patients with suspected congenital skeletal abnormalities
Spurná, Z, Čapková, P, Punová, L, DuchoslavovÁ, J, Aleksijevic, D, Venháčová, P, Srovnal, J, Štellmachová, J, Curtisová, V, Bitnerová, V, Petřková, J, Kolaříková, K, Janíková, M, Kratochvílová, R, Vrtěl, P, Vodička, R, Vrtěl, R, Zapletalová, J
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Published in Gene (20.01.2024)
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Tumors overexpressing RNF168 show altered DNA repair and responses to genotoxic treatments, genomic instability and resistance to proteotoxic stress
Chroma, K, Mistrik, M, Moudry, P, Gursky, J, Liptay, M, Strauss, R, Skrott, Z, Vrtel, R, Bartkova, J, Kramara, J, Bartek, J
Published in Oncogene (27.04.2017)
Published in Oncogene (27.04.2017)
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Familial, autosomal-dominant neurodegenerative parkinsonism with cognitive deterioration spanning five generations in a genetically isolated population of South-Eastern Moravia, Czech Republic
Mensikova, K, Godava, M, Kanovsky, P, Otruba, P, Kaiserova, M, Vastik, M, Mikulicova, L, Bartonikova, T, Vrtel, R, Vodicka, R, Kurcova, S, Jugas, P, Ovecka, J, Sachova, L, Dvorsky, F
Published in Journal of the neurological sciences (15.10.2015)
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The contribution of X-chromosome genomic imprinting to the bicuspid aortic valve and aortic coarctation prevalence in women with Turner syndrome
Klaskova, E, Vrtel, P, Vrtel, R, Adamova, K, Vrbicka, D.I.T.A, Zapletalova, J, Prochazka, M, Pavlicek, J, Lebl, J, Stara, V, Soucek, O, Snajderova, M, Hana, V
Published in European heart journal (01.11.2020)
Published in European heart journal (01.11.2020)
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Analysis of cell free fetal DNA fragmentation rate in pregnant women during the course of gravidit
Vodicka, R, Böhmová, J, Dhaifalah, I, Blumenthalová, J, Kratochvílová, R, Santavý, J, Procházka, M, Vrtĕl, R
Published in Ceská gynekologie (01.08.2010)
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Published in Ceská gynekologie (01.08.2010)
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Endemic parkinsonism: clusters, biology and clinical features
Menšíková, Katerina, Steele, John C, Rosales, Raymond, Colosimo, Carlo, Spencer, Peter, Lannuzel, Annie, Ugawa, Yoshikazu, Sasaki, Ryogen, Giménez-Roldán, Santiago, Matej, Radoslav, Tuckova, Lucie, Hrabos, Dominik, Kolarikova, Kristyna, Vodicka, Radek, Vrtel, Radek, Strnad, Miroslav, Hlustik, Petr, Otruba, Pavel, Prochazka, Martin, Bares, Martin, Boluda, Susana, Buee, Luc, Ransmayr, Gerhard, Kaňovský, Petr
Published in Nature reviews. Neurology (01.10.2023)
Published in Nature reviews. Neurology (01.10.2023)
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Reply to: Questioning the cycad theory of Kii ALS-PDC causation
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Published in Nature reviews. Neurology (01.03.2024)
Published in Nature reviews. Neurology (01.03.2024)
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The identification of molecular-genetic background of familial atypical parkinsonism in "Hornacko", a specific region of the South-Eastern Moravia, Czech Republic
Mensikova, K., Vodicka, R., Vrtel, R., Kolarikova, K., Otruba, P., Kaiserova, M., Vastik, M., Bartonikova, T., Kanovsky, P.
Published in Journal of the neurological sciences (15.10.2017)
Published in Journal of the neurological sciences (15.10.2017)
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Noninvasive fetal sex detection from maternal plasma in pregnant women
Vodicka, R, Vrtĕl, R, Schneiderová, E, Vrbická, D, Procházka, M, Dhaifalah, I, Santavá, A, Santavý, J
Published in Ceská gynekologie (01.06.2008)
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Published in Ceská gynekologie (01.06.2008)
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Prenatal detection of copy number variants in fetuses with detected congenital devolpmental disordes, from 2015 to 2020 by Multiplex Ligation-Dependent Probe Amplification and microarray analysis
Štefeková, Andrea, Čapková, Pavlína, Curtisová, Václava, Mracká, Enghjargalan, Filipová, Hana, Spurná, Zuzana, Procházka, Martin, Ľubušký, Marek, Pilka, Radovan, Vrtěl, Radek
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Published in Ceská gynekologie (01.01.2023)
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DNA damage signalling barrier, oxidative stress and treatment-relevant DNA repair factor alterations during progression of human prostate cancer
Kurfurstova, Daniela, Bartkova, Jirina, Vrtel, Radek, Mickova, Alena, Burdova, Alena, Majera, Dusana, Mistrik, Martin, Kral, Milan, Santer, Frederic R., Bouchal, Jan, Bartek, Jiri
Published in Molecular oncology (01.06.2016)
Published in Molecular oncology (01.06.2016)
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The identification of molecular-genetic background of familial atypical parkinsonism in “Hornacko”, a specific region of the South-Eastern Moravia, Czech Republic
Mensikova, K., Vodicka, R., Kolarikova, K., Bartonikova, T., Mikulicova, L., Kaiserova, M., Vastik, M., Vrtel, R., Otruba, P., Bares, M., Janout, V., Kanovsky, P.
Published in Parkinsonism & related disorders (01.01.2018)
Published in Parkinsonism & related disorders (01.01.2018)
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Identification of a nonsense mutation at the 5' end of the TSC2 gene in a family with a presumptive diagnosis of tuberous sclerosis complex
Vrtel, R, Verhoef, S, Bouman, K, Maheshwar, M M, Nellist, M, van Essen, A J, Bakker, P L, Hermans, C J, Bink-Boelkens, M T, van Elburg, R M, Hoff, M, Lindhout, D, Sampson, J, Halley, D J, van den Ouweland, A M
Published in Journal of medical genetics (01.01.1996)
Published in Journal of medical genetics (01.01.1996)
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Recurrent mutation 4882delTT in the GAP-related domain of the tuberous sclerosis TSC2 gene
Verhoef, S., Vrtel, R., Bakker, L., Stolte-Dijkstra, I., Nellist, M., Begeer, J.H., Zaremba, J., Jozwiak, S., Tempelaars, A.M.P., Lindhout, D., Halley, D.J.J., van den Ouweland, A.M.W.
Published in Human mutation (1998)
Published in Human mutation (1998)
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Identification of a large insertion and two novel point mutations (3671del8 and S1221X) in tuberous sclerosis complex (TSC) patients. Mutations in brief no. 119. Online
Wang, Q, Verhoef, S, Tempelaars, A M, Bakker, P L, Vrtel, R, Hesseling-Janssen, A L, Nellist, M, Oranje, A P, Stroink, H, Lindhout, D, Halley, D J, van den Ouweland, A M
Published in Human mutation (1998)
Published in Human mutation (1998)
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Angiomyolipoma--its role in prenatal diagnosis of tuberous sclerosis
Vrtĕl, R, Vodicka, R, Santavá, A, Santavý, J, Krejciríková, E
Published in Časopis lékařů českých (2004)
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Published in Časopis lékařů českých (2004)
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Modulation of the E2F1-Driven Cancer Cell Fate by the DNA Damage Response Machinery and Potential Novel E2F1 Targets in Osteosarcomas
Liontos, Michalis, Niforou, Katerina, Velimezi, Georgia, Vougas, Konstantinos, Evangelou, Konstantinos, Apostolopoulou, Kalliopi, Vrtel, Radek, Damalas, Alexandros, Kontovazenitis, Panayiotis, Kotsinas, Athanassios, Zoumpourlis, Vassilis, Tsangaris, George Th, Kittas, Christos, Ginsberg, Doron, Halazonetis, Thanos D, Bartek, Jiri, Gorgoulis, Vassilis G
Published in The American journal of pathology (01.07.2009)
Published in The American journal of pathology (01.07.2009)
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Molecular genetic study of causes of the Prader-Willi and Angelman syndrome
Capková, C P, Vrtĕl, R, Santavá, A, Zapletalová, J, Krsiaková, J, Hyjánek, J, Santavý, J
Published in Časopis lékařů českých (2005)
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Published in Časopis lékařů českých (2005)
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