- Genetic variation screening of TNNT2 and MYH7 genes in a cohort of patients with hypertrophic and dilated cardiomyopathyPublikace bez příslušnosti k fakultě
- Genetic variation screening of TNNT2 Gene in a cohort of patients with hypertrophic and dilated cardiomyopathy2012 | 1. lékařská fakulta
- The prevalence of genetic variations in patients with hypertrophic and dilated cardiomyopathyPublikace bez příslušnosti k fakultě
- Deletion of the PDR16 gene influences the plasma membrane properties of the yeast Kluyveromyces lactis2015 | Matematicko-fyzikální fakulta
- Vliv benzo[a]pyrenu na expresi jaterního cytochrromu P450 a NADPH: cytochrrom P450 reductasy v myších s deletovanou jaterní NADPH:cytochrom P450 reduktasou2007 | Přírodovědecká fakulta
- Genomic landscape of pediatric B-other acute lymphoblastic leukemia in a consecutive European cohort2019 | 2. lékařská fakulta
- IKZF1(plus) Defines a New Minimal Residual Disease-Dependent Very-Poor Prognostic Profile in Pediatric B-Cell Precursor Acute Lymphoblastic Leukemia2018 | 2. lékařská fakulta
- Contiguous X-chromosome deletion syndrome Encompassing the BTK, TIMM8A, TAF7L and DRP2 genes2007 | 1. lékařská fakulta
- Leishmania infantum nicotinamidase is required for late-stage development in its natural sand fly vector, Phlebotomus perniciosus2012 | Přírodovědecká fakulta
- Screening of transcription factors regulating ATO gene expression within yeast colonies2013 | Přírodovědecká fakulta
- NBN 657del5 heterozygous mutations and colorectal cancer risk in the Czech Republic2009 | 1. lékařská fakulta, 2. lékařská fakulta, 3. lékařská fakulta
- Use of In Vitro Transcription System for Analysis of Corynebacterium glutamicum Promoters Recognized by Two Sigma Factors2016 | Ústřední knihovna
- Systematic functional analysis of Leishmania protein kinases identifies regulators of differentiation or survival2021 | Přírodovědecká fakulta
- Evidence for a new contiguous gene syndrome, the chromosome 16p13.3 deletion syndrome alias severe Rubinstein-Taybi syndrome2006 | 2. lékařská fakulta
- Prognostic significance of 1p36 locus deletion in adenoid cystic carcinoma of the salivary glands2018 | Lékařská fakulta v Plzni
- Frequency of CYP21 gene mutations in Czech patients with steroid 21-hydroxylase deficiency and statistical comparison with other populations2003 | 2. lékařská fakulta
- Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects2020 | 2. lékařská fakulta