Publications by authors named "Filip Lhota"

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The Cause of Hereditary Hearing Loss in Heterozygotes-A Comprehensive Study of the /DFNB1 Region.
Dana Safka Brozkova, Anna Uhrova Meszarosova, Petra Lassuthova, Lukáš Varga, David Staněk, Filip Lhota

Genes (Basel)· May 2021

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Multigene Panel Germline Testing of 1333 Czech Patients with Ovarian Cancer.
Klara Lhotova, Lenka Stolarova, Petra Zemankova, Michal Vocka, Marketa Janatova, Filip Lhota

Cancers (Basel)· April 2020

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Germline CHEK2 Gene Mutations in Hereditary Breast Cancer Predisposition - Mutation Types and their Biological and Clinical Relevance.
Petra Kleiblová, Lenka Stolařová, Křížová Křížová, Filip Lhota, Jan Hojný

Klin Onkol· January 2020

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Contribution of Massive Parallel Sequencing to Diagnosis of Hereditary Ovarian Cancer in the Czech Republic.
Jana Soukupová, Klára Lhotová, Petra Zemánková, Michal Vočka, Markéta Janatová, Filip Lhota

Klin Onkol· January 2020

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Identification of deleterious germline CHEK2 mutations and their association with breast and ovarian cancer.
Petra Kleiblova, Lenka Stolarova, Katerina Krizova, Filip Lhota, Jan Hojny

Int J Cancer· October 2019

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Validation of CZECANCA (CZEch CAncer paNel for Clinical Application) for targeted NGS-based analysis of hereditary cancer syndromes.
Jana Soukupova, Petra Zemankova, Klara Lhotova, Marketa Janatova, Marianna Borecka, Filip Lhota

PLoS One· July 2018

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Multiplex PCR and NGS-based identification of mRNA splicing variants: Analysis of BRCA1 splicing pattern as a model.
Jan Hojny, Petra Zemankova, Filip Lhota, Jan Sevcik, Viktor Stranecky

Gene· December 2017

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The c.657del5 variant in the NBN gene predisposes to pancreatic cancer.
Marianna Borecka, Petra Zemankova, Filip Lhota, Jana Soukupova, Petra Kleiblova

Gene· August 2016

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Identification and Functional Testing of ERCC2 Mutations in a Multi-national Cohort of Patients with Familial Breast- and Ovarian Cancer.
Andreas Rump, Anna Benet-Pages, Steffen Schubert, Jan Dominik Kuhlmann, Ramūnas Janavičius, Filip Lhota

PLoS Genet· August 2016

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Association of Germline CHEK2 Gene Variants with Risk and Prognosis of Non-Hodgkin Lymphoma.
Ondrej Havranek, Petra Kleiblova, Jan Hojny, Filip Lhota, Pavel Soucek

PLoS One· June 2016

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Expression of human BRCA1Δ17-19 alternative splicing variant with a truncated BRCT domain in MCF-7 cells results in impaired assembly of DNA repair complexes and aberrant DNA damage response.
Jan Sevcik, Martin Falk, Libor Macurek, Petra Kleiblova, Filip Lhota

Cell Signal· May 2013

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The BRCA1 alternative splicing variant Δ14-15 with an in-frame deletion of part of the regulatory serine-containing domain (SCD) impairs the DNA repair capacity in MCF-7 cells.
Jan Sevcik, Martin Falk, Petra Kleiblova, Filip Lhota, Lenka Stefancikova

Cell Signal· May 2012

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Independent regulation of short and long forms of latent TGF-beta binding protein (LTBP)-4 in cultured fibroblasts and human tissues.
Anna K Kantola, Merja J Ryynänen, Filip Lhota, Jorma Keski-Oja, Katri Koli

J Cell Physiol· June 2010

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