Petr Vojta
Olomouc, 78371, Czech Republic
Last Updated: 09/26/2026
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Found 20 publications
Correction of aberrant splicing of ELP1 pre-mRNA by kinetin derivatives - A structure activity relationship study.
Journal: European journal of medicinal chemistry
Published: July 06, 2024
Missense mutation in RPS7 causes Diamond-Blackfan anemia via alteration of erythrocyte metabolism, protein translation and induction of ribosomal stress.
Journal: Blood cells, molecules & diseases
Published: December 29, 2021
Development and extensive analytical validation of deep amplicon sequencing for detecting KRAS and NRAS mutations in metastatic colorectal cancer samples.
Journal: Neoplasma
Published: September 07, 2021
Prognostic value of tumor-infiltrating lymphocytes (TILs) and their association with PD-L1 expression and DNA repair protein RAD51 in patients with resected non-small cell lung carcinoma.
Journal: Lung cancer (Amsterdam, Netherlands)
Published: December 25, 2019
Heterogenous mutation spectrum and deregulated cellular pathways in aberrant plasma cells underline molecular pathology of light-chain amyloidosis.
Journal: Haematologica
Published: October 08, 2019
Czech and Slovak Diamond-Blackfan Anemia (DBA) Registry update: Clinical data and novel causative genetic lesions.
Journal: Blood cells, molecules & diseases
Published: August 30, 2019
Establishing community reference samples, data and call sets for benchmarking cancer mutation detection using whole-genome sequencing.
Journal: Nature biotechnology
Published: May 02, 2019
Corrigendum: Modification of Barley Plant Productivity Through Regulation of Cytokinin Content by Reverse-Genetics Approaches.
Journal: Frontiers in plant science
Published: December 16, 2018
Toward best practice in cancer mutation detection with whole-genome and whole-exome sequencing.
Journal: Nature biotechnology
Published: September 26, 2018
Modification of Barley Plant Productivity Through Regulation of Cytokinin Content by Reverse-Genetics Approaches.
Journal: Frontiers in plant science
Published: June 30, 2018
Newly designed 11-gene panel reveals first case of hereditary amyloidosis captured by massive parallel sequencing.
Journal: Journal of clinical pathology
Published: December 21, 2017
Last Updated: 09/26/2026