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Search for publications relevant for "mutation testing"
mutation testing
Publication
Class
Person
Publication
Programmes
publication
Consensus for EGFR Mutation Testing in Non-small Cell Lung Cancer: Results from a European Workshop
2010 |
First Faculty of Medicine
publication
Informing patients about their mutation tests: CDKN2A c.256G>A in melanoma as an example
2020 |
Faculty of Medicine in Pilsen
publication
Detection of EGFR Variants in Plasma A Multilaboratory Comparison of a Real-Time PCR EGFR Mutation Test in Europe
2018 |
Publication without faculty affiliation
publication
KRAS mutation testing in therapeutic algorithm for treatment of metastatic colorectal carcinoma
2011 |
First Faculty of Medicine, Faculty of Medicine in Hradec Králové
publication
KRAS mutation testing in therapeutic algorithm for treatment of metastatic colorectal carcinoma
2011 |
First Faculty of Medicine
publication
Fault-based test generation for regular expressions by mutation
2019 |
Faculty of Mathematics and Physics
publication
European consensus-based interdisciplinary guideline for melanoma. Part 1: Diagnostics - Update 2019
2020 |
Third Faculty of Medicine
publication
European consensus-based interdisciplinary guideline for melanoma. Part 1: Diagnostics: Update 2022
2022 |
Third Faculty of Medicine
publication
Population-based study of BRCA1/2 mutations: family history based criteria identify minority of mutation carriers.
2010 |
First Faculty of Medicine
publication
Identification of five new families strengthens the link between childhood choroid plexus carcinoma and germline TP53 mutations
2005 |
First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
publication
Detection of DNA variations in the polymorphic hydroxymethylbilane synthase gene by high-resolution melting analysis
2009 |
First Faculty of Medicine
publication
Detection of DNA variations in the polymorphic hydroxymethylbilane synthase gene by high-resolution melting analysis
2009 |
Publication without faculty affiliation
publication
Practical diagnostics of Lynch syndrome: pathologists perspective
2014 |
Faculty of Medicine in Pilsen
publication
Targeting amino acid metabolism in cancer
2022 |
Second Faculty of Medicine, Central Library of Charles University
publication
Somatic TP53 Mutation Mosaicism in a Patient With Li-Fraumeni Syndrome
2009 |
Second Faculty of Medicine
publication
Expanding the phenotypic spectrum of lipomatosis of the sciatic nerve: Early-onset colonic diverticular disease
2020 |
Faculty of Physical Education and Sport
publication
The PALB2 Gene Is a Strong Candidate for Clinical Testing in BRCA1- and BRCA2-Negative Hereditary Breast Cancer
2013 |
First Faculty of Medicine
publication
Carrier rates of the ancestral Indian W24X mutation in GJB2 in the general gypsy population and individual subisolates
2007 |
Second Faculty of Medicine
publication
Open-label, multicentre safety study of vemurafenib in 3219 patients with BRAF(V600) mutation-positive metastatic melanoma: 2-year follow-up data and long-term responders' analysis
2017 |
Publication without faculty affiliation
publication
Detection of EGFR Mutations in Circulating Tumor DNA (ctDNA) Retrieved from Plasma - Interlaboratory Quality Assessment in the Czech Republic
2018 |
First Faculty of Medicine, Faculty of Medicine in Hradec Králové, Second Faculty of Medicine, Central Library of Charles University
publication
Detection and Quantification of ctDNA for Longitudinal Monitoring of Treatment in Non-Small Cell Lung Cancer Patients Using a Universal Mutant Detection Assay by Denaturing Capillary Electrophoresis
2022 |
Faculty of Medicine in Pilsen, Central Library of Charles University, Faculty of Science