Search Results - "Franková, Věra"

New methodology of TMB assessment from tissue and liquid biopsy in NSCLC by Křížová, Ľudmila, Šafaříková, Markéta, Kalousová, Marta, Pfeiferová, Lucie, Kuběna, Aleš Antonín, Vočka, Michal, Ulrych, Jan, Franková, Věra, Petruželka, Luboš, Zima, Tomáš, Feltl, David

“…Immunotherapy has dramatically influenced and changed therapeutical approach in non-small cell lung cancer (NSCLC) in recent five years. Even though we can…”
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HNF1B, EZH2 and ECI2 in prostate carcinoma. Molecular, immunohistochemical and clinico-pathological study by Dundr, Pavel, Bártů, Michaela, Hojný, Jan, Michálková, Romana, Hájková, Nikola, Stružinská, Ivana, Krkavcová, Eva, Hadravský, Ladislav, Kleissnerová, Lenka, Kopejsková, Jana, Hiep, Bui Quang, Němejcová, Kristýna, Jakša, Radek, Čapoun, Otakar, Řezáč, Jakub, Jirsová, Kateřina, Franková, Věra

“…Hepatocyte nuclear factor 1 beta (HNF1B) is a tissue specific transcription factor, which seems to play an important role in the carcinogenesis of several…”
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Co-designing models for the communication of genomic results for rare diseases: a comparative study in the Czech Republic and the United Kingdom by Costa, Alessia, Franková, Věra, Robert, Glenn, Macek, Milan, Patch, Christine, Alexander, Elizabeth, Arellanesova, Anna, Clayton-Smith, Jill, Hunter, Amy, Havlovicová, Markéta, Pourová, Radka, Pritchard, Marie, Roberts, Lauren, Zoubková, Veronika, Metcalfe, Alison

“…The communication of genomic results to patients and families with rare diseases raise distinctive challenges. However, there is little evidence about optimal…”
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Regulatory landscape of providing information on newborn screening to parents across Europe by Franková, Věra, Driscoll, Riona O, Jansen, Marleen E, Loeber, J Gerard, Kožich, Viktor, Bonham, James, Borde, Patricia, Brincat, Ian, Cheillan, David, Dekkers, Eugenie, Fingerhut, Ralph, Kuš, Iva Bilandžija, Girginoudis, Panagiotis, Groselj, Urh, Hougaard, David, Knapková, Mária, la Marca, Giancarlo, Malniece, Ieva, Nanu, Michaela Iuliana, Nennstiel, Uta, Olkhovych, Nataliia, Oltarzewski, Mariusz, Pettersen, Rolf D, Racz, Gabor, Reinson, Karit, Salimbayeva, Damilya, Songailiene, Jurgita, Vilarinho, Laura, Vogazianos, Marios, Zetterström, Rolf H, Zeyda, Maximilian

“…Newborn screening (NBS) is an important part of public healthcare systems in many countries. The provision of information to parents about NBS is now…”
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Correction to: Co‑designing models for the communication of genomic results for rare diseases: a comparative study in the Czech Republic and the United Kingdom by Costa, Alessia, Franková, Věra, Robert, Glenn, Macek, Milan, Patch, Christine, Alexander, Elizabeth, Arellanesova, Anna, Clayton‑Smith, Jill, Hunter, Amy, Havlovicová, Markéta, Pourová, Radka, Pritchard, Marie, Roberts, Lauren, Zoubková, Veronika, Metcalfe, Alison

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Ethical principles for the usage and sharing of genomic data from researc by Franková, Věra, Svozilová, Hana, Stránecký, Viktor, Kozubík, Kateřina Staňo, Srovnal, Josef, Benešová, Lucie, Uvírová, Magdalena, Macek, Milan, Pospíšilová, Šárka

“…The current significant development of human genome/exome sequencing in biomedical research is one of the important paths leading to personalized medicine…”
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Informing Parents about Newborn Screening: A European Comparison Study by IJzebrink, Amber, van Dijk, Tessa, Franková, Věra, Loeber, Gerard, Kožich, Viktor, Henneman, Lidewij, Jansen, Marleen

“…Knowledge about newborn screening (NBS) is an important factor for parents to make an informed decision about participation. In Europe, countries inform…”
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New methodology of TMB assessment from tissue and liquid biopsy in NSCLC by Ľudmila Křížová, Markéta Šafaříková, Marta Kalousová, Lucie Pfeiferová, Aleš Antonín Kuběna, Michal Vočka, Jan Ulrych, Věra Franková, Luboš Petruželka, Tomáš Zima, David Feltl

“…Immunotherapy has dramatically influenced and changed therapeutical approach in non-small cell lung cancer (NSCLC) in recent five years. Even though we can…”
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Patient preferences in genetic newborn screening for rare diseases: study protocol by MARTIN, Sylvia, Angolini, Emanuele, Audi, Jennifer, Bertini, Dr. Enrico, Bruno, Lucia Pia, Coulter, Joshua, Ferlini, Alessandra, Fortunato, Fernanda, Frankova, Vera, Garnier, Nicolas, Grauman, Åsa, Gross, Edith, Hauber, Brett, Hansson, Mats, Kirschner, Janbernd, Knieling, Ferdinand, Kyosovksa, Gergana, Ottombrino, Silvia, Novelli, Antonio, Raming, Roman, Sansen, Stefaan, Saier, Christina, Veldwijk, Jorien

“…IntroductionRare diseases (RDs) collectively impact over 30 million people in Europe. Most individual conditions have a low prevalence which has resulted in a…”
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Factors Influencing Parental Awareness about Newborn Screening by Franková, Věra, Dohnalová, Alena, Pešková, Karolína, Hermánková, Renata, O’Driscoll, Riona, Ješina, Pavel, Kožich, Viktor

“…Appropriate and timely education about newborn screening (NBS) helps to foster benefits such as prompt follow up, to promote parents’ autonomy via informed…”
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Comparison of DNA isolation using salting-out procedure and automated isolation (MagNA system) by Kalousová, Marta, Levová, Kateřina, Kuběna, Aleš A., Jáchymová, Marie, Franková, Věra, Zima, Tomáš

“…Isolation of genomic DNA is a key step in genetic analysis. The aim of the study was to evaluate the suitability of isolation of DNA from peripheral blood with…”
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The Bank of Biological Material (BBM) of the First Faculty of Medicine of Charles University in Prague, Czech Republic by Franková, Věra, Jirsová, Kateřina, Zima, Tomáš

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National Database of Genotypes--ethical and legal issues by Franková, Vera, Tesínová, Jolana, Brdicka, Radim

“…National Database of Genotypes--ethical and legal issues The aim of the project National Database of Genotypes is to outline structure and rules for the…”
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Type A influenza: Postmortem virus isolations from different organs in human lethal cases by Fraňková, Věra, Jirásek, A., Tůmová, Běla

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Quality of life in patients with autosomal dominant tubulointerstitial kidney disease by Bleyer, Anthony J, Kidd, Kendrah, Johnson, Emily, Robins, Victoria, Martin, Lauren, Taylor, Abbigail, Pinder, Alexander J, Bowline, Isai, Frankova, Vera, Živná, Martina, Taylor, Kate B, Kim, Nathan, Baek, Janet J, Hartmannová, Hana, Hodaňová, Kateřina, Vyleťal, Petr, Votruba, Miroslav, Kmoch, Stanislav

“…The reaction to diagnosis and quality of life (QOL) in autosomal dominant tubulointerstitial kidney disease (ADTKD) due to and mutations from the time of…”
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