Výsledky vyhledávání - "Markéta, Urbanová"

Two Czech patients with familial adenomatous polyposis presenting mosaicism in APC gene

Autor: B Janosikova, J Kotlas, Stekrová J, L Obeidova, Markéta Urbanová, J Lastuvkova, Katerina Hirschfeldova, M Lukas

Publikováno v: Neoplasma. 66:294-300

During standard molecular diagnostic procedure, two Czech families with APC (Adenomatous polyposis coli gene) mosaicism have been detected. A woman with attenuated familial adenomatous polyposis (AFAP, OMIM #175100) was recently inspected by next gen

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::decb9d2942610fb7e7e661e84fd6a52d
https://doi.org/10.4149/neo_2018_180731n559

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Re: ERCC3, a new ovarian cancer susceptibility gene?

Publikováno v: European journal of cancer (Oxford, England : 1990). 150

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9678ba11eedd02517caa56bb036fbae3
https://pubmed.ncbi.nlm.nih.gov/33888390

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Oxidative Damage in Sporadic Colorectal Cancer: Molecular Mapping of Base Excision Repair Glycosylases in Colorectal Cancer Patients

Autor: Alena Opattova, Veronika Vymetalkova, Michaela Schneiderova, Markéta Urbanová, Kristyna Tomasova, Ludmila Vodickova, Pavol Makovicky, Rudolf Stetina, Klara Kostovcikova, Anna Siskova, Pavel Vodicka, Michal Kroupa

Publikováno v: International Journal of Molecular Sciences, Vol 21, Iss 2473, p 2473 (2020)
International Journal of Molecular Sciences

Oxidative stress with subsequent premutagenic oxidative DNA damage has been implicated in colorectal carcinogenesis. The repair of oxidative DNA damage is initiated by lesion-specific DNA glycosylases (hOGG1, NTH1, MUTYH). The direct evidence of the

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dcaf75f444f076edb0f17c3b77903119
https://www.mdpi.com/1422-0067/21/7/2473

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Bleomycin‐induced chromosomal damage and shortening of telomeres in peripheral blood lymphocytes of incident cancer patients

Autor: Sivaramakrishna Rachakonda, Michal Kroupa, Ludmila Vodickova, Markéta Urbanová, Zdenka Polivkova, Tomas Buchler, Katerina Jiraskova, Pavel Vodicka, Sona Vodenkova, Kari Hemminki, Michaela Schneiderova, Rajesh Kumar

Publikováno v: Genes, Chromosomes and Cancer. 57:61-69

Disruption of genomic integrity due to deficient DNA repair capacity and telomere shortening constitute hallmarks of malignant diseases. Incomplete or deficient repair of DNA double-strand breaks (DSB) is manifested by chromosomal aberrations and the

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d58fa4ea667d337ee17876c8f8bbc5d
https://doi.org/10.1002/gcc.22508

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Relationship of telomere length in colorectal cancer patients with cancer phenotype and patient prognosis

Autor: Ludmila Vodickova, Katerina Jiraskova, Vaclav Liska, Ondrej Vycital, Markéta Urbanová, Michal Kroupa, Nalini Srinivas, Veronika Vymetalkova, Pavel Vodicka, Sivarama Krishna Rachakonda, Michaela Schneiderova, Rajesh Kumar

Publikováno v: British Journal of Cancer

BACKGROUND Telomeres, repetitive DNA capping ends of eukaryotic chromosomes, are important in the maintenance of genomic integrity. Perturbed telomeres are common features of many human malignancies, including colorectal cancer. METHODS Telomere leng

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bffe319645e4ea12476ee95446b41103
https://pubmed.ncbi.nlm.nih.gov/31312029

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Detection of SHOX gene aberrations in routine diagnostic practice and evaluation of phenotype scoring form effectiveness

Autor: Martina Florianova, Vera Kebrdlova, Katerina Hirschfeldova, Stekrová J, Markéta Urbanová

Publikováno v: Journal of Human Genetics. 62:253-257

Heterozygous aberrations of SHOX gene have been reported to be responsible for Leri-Weill dyschondrosteosis (LWD) and small portion of idiopathic short stature. The study was established to assess effectiveness of using phenotype 'scoring form' in pa

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::707a52e64c282a40ba897078c2526cef
https://doi.org/10.1038/jhg.2016.117

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Formation of TiO/Al2O3/C composite in thermal co-decomposition of aluminium(III) acetylacetonate and titanium(IV) oxyacetylacetonate

Autor: Michal Pola, Tomáš Křenek, Lucie Kullová, Tomáš Kovářík, Josef Pola, Dana Pokorná, Petr Bezdička, Zdeněk Bastl, Jaroslav Kupčík, Markéta Urbanová

Publikováno v: Journal of Analytical and Applied Pyrolysis. 117:182-190

Thermal co-decomposition of Al(III) acetylacetonate-Ti(IV) oxyacetylacetonate mixture has been examined by using thermal gravimetry, differential scanning calorimetry and complementary analyses of evaporated products and solid residues by Fourier Tra

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::21b41b6d6ce3bf8981c1e734e5d51df8
https://doi.org/10.1016/j.jaap.2015.12.002

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Abstract A35: Cell-free tumor DNA profiling of colon cancer patients: Searching for mechanisms of chemoresistance

Autor: Veronika Vymetalkova, Klara Cervena, Barbara Pardini, Pavel Vodicka, Markéta Urbanová, Alessio Naccarati

Publikováno v: Clinical Cancer Research. 26:A35-A35

Colorectal cancer (CRC) is a worldwide health burden, with nearly 1.2 million new cases expected each year. Significant efforts are currently being employed to find patients who will benefit from chemotherapy. In fact, drug resistance is a limiting f

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https://doi.org/10.1158/1557-3265.liqbiop20-a35

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Base excision repair capacity as a determinant of prognosis and therapy response in colon cancer patients

Autor: Vaclav Liska, Markéta Urbanová, Alena Opattova, Veronika Vymetalkova, Ludmila Vodickova, Michal Kroupa, Sona Vodenkova, Tomas Buchler, Andrew Collins, Miroslav Levy, Pavel Vodicka, Michaela Schneiderova, Jana Slyskova, Katerina Jiraskova

Publikováno v: DNA repair. 72

The DNA-damaging agent 5-fluorouracil represents the most commonly used chemotherapeutic drug for colorectal cancer patients. DNA lesions associated with 5-fluorouracil therapy are primarily repaired by base excision repair (BER) and mismatch repair

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https://pubmed.ncbi.nlm.nih.gov/30314738

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[Gitelman´s syndrome as common cause of hypokalemia and hypomagnesemia]

Autor: Romana, Ryšavá, Jana, Reiterová, Markéta, Urbanová, Jitka, Štekrová, Petr, Lněnička, Vladimír, Tesař

Publikováno v: Vnitrni lekarstvi. 62

The Gitelman syndrome (GS) is an autosomal recessive disorder characterized by hypokalemic metabolic alkalosis and presence of hypocalciuria and hypomagnesemia. It is one of the most common congenital "salt-wasting" tubulo-pathies, where the impairme

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https://pubmed.ncbi.nlm.nih.gov/28124936

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