Skip to top bar
Skip to header
Skip to content
Skip to footer
CS
>
Publications
>
Publication Records - Search
Publication Records - Search
Advanced search
Repository
Selected publication/outcome records
Brief Report: Inhibition of miR-145 Enhances Reprogramming of Human Dermal Fibroblasts to Induced Pluripotent Stem Cells (2016)
Integration-free reprogramming of primary human fibroblasts into neural stem cells using brief exposure to pluripotency factors (2016)
Generation and Testing of MicroRNA Sponge Constructs (2016)
An inactivating mutation in intestinal cell kinase, ICK, impairs hedgehog signalling and causes short rib-polydactyly syndrome (2016)
miRNAsong: a web-based tool for generation and testing of miRNA sponge constructs in silico (2016)
Properties of Human Embryonic Stem Cells and Their Differentiated Derivatives Depend on Nonhistone DNA-Binding HMGB1 and HMGB2 Proteins (2017)
miRNAsong: microRNA SpONge Generator and tester - high-throughput approach for miRNA sponge design and testing (2016)
The role of microRNA molecules in cell plasticity regulation (2017)
Pluripotent Stem Cell-Derived Hematopoietic Progenitors Are Unable to Downregulate Key Epithelial-Mesenchymal Transition-Associated miRNAs (2018)
Cripto-1 Induces Multicentrosomal Mitoses in Human Embryonic Stem Cells (2017)
microRNA molecules in cell fate specification (2018)
The role of microRNA molecules in cell plasticity induction (2018)
Cripto – 1 is associated with centrosomal amplifications in human embryonic stem cells (2018)
Soluble Cripto-1 Induces Accumulation of Supernumerary Centrosomes and Formation of Aberrant Mitoses in Human Embryonic Stem Cells (2018)
Inactivation of PLK4-STIL Module Prevents Self-Renewal and Triggers p53-Dependent Differentiation in Human Pluripotent Stem Cells (2018)
The PTH/PTHrP-SIK3 pathway affects skeletogenesis through altered mTOR signaling (2018)
Fibroblast growth factor receptor influences primary cilium length through an interaction with intestinal cell kinase (2019)
Human Embryonic Stem Cells Acquire Responsiveness to TRAIL upon Exposure to Cisplatin (2019)
Differentiation of neural rosettes from human pluripotent stem cells in vitro is sequentially regulated on a molecular level and accomplished by the mechanism reminiscent of secondary neurulation (2019)
Oct4-mediated reprogramming induces embryonic-like microRNA expression signatures in human fibroblasts (2019)
Ligase 3-mediated end-joining maintains genome stability of human embryonic stem cells (2019)
Human retinal organoids as a tool for investigation of circadian rhythms. (2019)
miR-183/96/182 cluster is an important morphogenetic factor targetingPAX6expression in differentiating human retinal organoids (2020)
Mutations in GRK2 cause Jeune syndrome by impairing Hedgehog and canonical Wnt signaling (2020)
Conducting composite films based on chitosan or sodium hyaluronate. Properties and cytocompatibility with human induced pluripotent stem cells (2021)
Loss of Sprouty Produces a Ciliopathic Skeletal Phenotype in Mice Through Upregulation of Hedgehog Signaling (2021)
Generation of six human iPSC lines from patients with a familial Alzheimer's disease (n=3) and sex- and age-matched healthy controls (n=3) (2021)
RNF43 inhibits WNT5A-driven signaling and suppresses melanoma invasion and resistance to the targeted therapy (2021)
Název: The role of microRNA and protein-coding genes in the biology of neural stem cells. (2021)
Self-renewal in induced pluripotent stem cells (2021)
Loss of Sprouty produces a ciliopathic skeletal phenotype in mice through elongation of primary cilia and upregulation of Hedgehog signaling (2021)
The Role of Ciliophaty Protein Tmem107 in the Vertebrate Eye Development (2021)
The Role of Ciliophaty Protein Tmem107 in the Vertebrate Eye Development (2021)
Fate of mesenchymal LGR5-positive cells during craniofacial development (2021)
Ztráta Sprouty2/4 u myší vede k ciliopatickému fenotypu (2021)
LuminoCell: a versatile and affordable platform for real-time monitoring of luciferase-based reporters (2022)
Differentiation of pluripotent stem cells using odontoblasts-specific transcription factors (2021)
Inherited arrhythmias: from gene variants to ionic channel dysfunctions (2022)
Idiopathic ventricular fibrillation as an inherited channelopathy? (2022)
Změny v elektrické aktivitě varianty Y4734C-RYR2 asociované s idiopatickou fibrilací komor. (2022)
Action potential characteristics in derived cardiomyocytes of a patient carrying RYR2 variant (2022)
Translational research in the field of inherited arrhythmias (2022)
Epigenetic Regulations of Perineural Invasion in Head and Neck Squamous Cell Carcinoma (2022)
Differentiation of pluripotent stem cells using odontoblast-specific transcription factors (2022)
MicroRNA Profiling of Self-Renewing Human Neural Stem Cells Reveals Novel Sets of Differentially Expressed microRNAs During Neural Differentiation In Vitro (2023)
Skeletal diseases caused by mutations in PTH1R show aberrant differentiation of skeletal progenitors due to dysregulation of DEPTOR (2023)
Light-responsive microRNA molecules in human retinal organoids are differentially regulated by distinct wavelengths of light (2023)
Modelling genetically linked arrhythmias in vitro (2023)
Kardiomyocyty diferencované z lidských indukovaných pluripotentních buněk: Výhody a úskalí jejich využití při studiu dědičných arytmií (2023)
Změny spontánní aktivity derivovaných kardiomyocytů s variantou Y4734C-RYR2 za vybraných arytmogenních podmínek (2023)
Nástrahy hodnocení křivky elektrické aktivity u pacient-specifických kardiomyocytů diferencovaných z lidských indukovaných pluripotentních buněk (2023)
Spontaneous electrical activity of cardiomyocytes derived from hiPSCs of a patient with idiopathic ventricular fibrillation and RYR2 variant: impact of isoprenaline and varying concentrations of Ca2+ (2023)
Role of ciliopathy protein TMEM107 in eye development: insights from a mouse model and retinal organoid (2023)
Possible proarrhythmic stimuli in Y4734C-RYR2 variant associated with idiopathic ventricular fibrillation (2023)
Illuminating the mechanism and allosteric behavior of NanoLuc luciferase (2023)
MIR204 n.37C>T variant as a cause of chorioretinal dystrophy variably associated with iris coloboma, early-onset cataracts and congenital glaucoma (2023)
DEVELOPMENT TOWARDS THERAPY OF MACULAR DEGENERATION OF RETINA BY DERIVATIVES OF HUMAN PLURIPOTENT STEM CELLS (2024)
DEVELOPMENT TOWARDS THERAPY OF MACULAR DEGENERATION OF RETINA BY DERIVATIVES OF HUMAN PLURIPOTENT STEM CELLS (2024)
Analysis of calcium transients in cardiomyocytes derived from hiPSCs: the variant p. Y4734C in RYR2 vs. unrelated healthy controls (2024)
Effect of isoprenaline and arrhythmogenic conditions on the spontaneous electrical activity of hiPSC-CM with Y4734C-RYR2 variant (2024)
2. Offsite Meeting of the Department of Histology and Embryology (ÚHE): Advancing Science and Collaboration (2024)
Armed with PRICKLE(3)s: PCP complexes protection against RNF43 (2024)
Generation of human induced pluripotent stem cell lines from patients with a RYR2 gene variant c.14201A>G (p.Y4734C): Implications for idiopathic ventricular fibrillation and catecholaminergic polymorphic ventricular tachycardia (2024)
Pacient-specifické kardiomyocyty s variantou Y4734C-RYR2: Ca2+ přechody v kontrole a po aplikaci kofeinu (2024)
Analýza variability délky cyklu u pacient-specifických hiPSC kardiomyocytů (2024)
Spontaneous electrical activity of hiPSC-CM from a patient with idiopathic ventricular fibrillation under possibly arrhythmogenic conditions (2024)
Spontaneous electrical activity of patient-specific cardiomyocytes with a variant in the RYR2 gene recorded by multielectrode array technique (2024)
Genetické pozadí pacientů s idiopatickou fibrilací komor (2024)
Remove all the items
Operations on the selected outcomes
Export and print
List of selected records
Other applications
Publications
Information System
Skip to top barSkip to headerSkip to contentSkip to footer
