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Role of the 3-mercaptopyruvate sulfurtransferase in colon/colorectal cancers

European journal of cell biology, 2024-06, Vol.103 (2), p.151415, Article 151415

2024

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Endogenous H2S producing enzymes are involved in apoptosis induction in clear cell renal cell carcinoma

BMC cancer, 2018-05, Vol.18 (1), p.591-591, Article 591

2018

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KIT Expression Is Regulated by DNA Methylation in Uveal Melanoma Tumors

International journal of molecular sciences, 2021-10, Vol.22 (19), p.10748

2021

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A novel 3D mesenchymal stem cell model of the multiple myeloma bone marrow niche: biologic and clinical applications

Oncotarget, 2016-11, Vol.7 (47), p.77326-77341

2016

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Monosomy 3 Influences Epithelial-Mesenchymal Transition Gene Expression in Uveal Melanoma Patients; Consequences for Liquid Biopsy

International journal of molecular sciences, 2020-12, Vol.21 (24), p.9651

2020

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Decitabine-induced DNA methylation-mediated transcriptomic reprogramming in human breast cancer cell lines; the impact of DCK overexpression

Frontiers in pharmacology, 2022-10, Vol.13, p.991751-991751

2022

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Variant c.2158-2A>G in MANBA is an important and frequent cause of hereditary hearing loss and beta-mannosidosis among the Czech and Slovak Roma population- evidence for a new ethnic-specific variant

Orphanet journal of rare diseases, 2020-08, Vol.15 (1), p.1-222, Article 222

2020

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High-level expression and purification of recombinant human growth hormone produced in soluble form in Escherichia coli

Protein expression and purification, 2014-08, Vol.100, p.40-47

2014

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Uncovering accurate prognostic markers for high‐risk uveal melanoma through DNA methylation profiling

Clinical and translational medicine, 2023-07, Vol.13 (7), p.e1317-n/a

2023

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Structural and Functional Impact of Seven Missense Variants of Phenylalanine Hydroxylase

Genes, 2019-06, Vol.10 (6), p.459

2019

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Breakpoints characterisation of the genomic deletions identified by MLPA in alkaptonuria patients

European journal of human genetics : EJHG, 2023-04, Vol.31 (4), p.485-489

2023

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Mathematical modeling based on RT-qPCR analysis of SARS-CoV-2 in wastewater as a tool for epidemiology

Scientific reports, 2021-09, Vol.11 (1), p.1-10, Article 19456

2021

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Alkaptonuria in Russia

European journal of human genetics : EJHG, 2022-02, Vol.30 (2), p.237-242

2022

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Genome-wide DNA methylome and transcriptome changes induced by inorganic nanoparticles in human kidney cells after chronic exposure

Cell biology and toxicology, 2023-10, Vol.39 (5), p.1939-1956

2023

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The importance of defining the age-specific TREC/KREC levels for detection of various inborn errors of immunity in pediatric and adult patients

Clinical immunology (Orlando, Fla.), 2022-12, Vol.245, p.109155-109155, Article 109155

2022

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Prognostic Value of Genotype-Phenotype Correlations in X-Linked Myotubular Myopathy and the Use of the Face2Gene Application as an Effective Non-Invasive Diagnostic Tool

Genes, 2023-12, Vol.14 (12), p.2174

2023

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Homogentisate 1,2-dioxygenase (HGD) gene variants, their analysis and genotype-phenotype correlations in the largest cohort of patients with AKU

European journal of human genetics : EJHG, 2019-06, Vol.27 (6), p.888-902

2019

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Severe congenital T-lymphocytopenia may affect the outcome of neonatal intensive care

Biomedical papers of the Medical Faculty of the University Palacký, Olomouc, Czechoslovakia, 2023-07

2023

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Type 3 inositol 1,4,5-trisphosphate receptor has antiapoptotic and proliferative role in cancer cells

Cell death & disease, 2019-02, Vol.10 (3), p.186-186, Article 186

2019

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Clinical manifestation of CDKL5 deficiency disorder and identified mutations in a cohort of Slovak patients

Epilepsy research, 2021-10, Vol.176, p.106699-106699, Article 106699

2021

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A Study among the Genotype, Functional Alternations, and Phenotype of 9 SCN1A Mutations in Epilepsy Patients

Scientific reports, 2020-06, Vol.10 (1), p.10288, Article 10288

2020

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Biallelic Cys141Tyr variant of SEL1L is associated with neurodevelopmental disorders, agammaglobulinemia, and premature death

The Journal of clinical investigation, 2024-01, Vol.134 (2), p.1-14

2024

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Making Waves: Collaboration in the time of SARS-CoV-2 - rapid development of an international co-operation and wastewater surveillance database to support public health decision-making

Water research (Oxford), 2021-07, Vol.199, p.117167-117167, Article 117167

2021

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MARVELD2 (DFNB49) mutations in the hearing impaired Central European Roma population--prevalence, clinical impact and the common origin

PloS one, 2015-04, Vol.10 (4), p.e0124232-e0124232

2015

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Studying the Gene Expression of Penicillium rubens Under the Effect of Eight Essential Oils

Antibiotics (Basel), 2020-06, Vol.9 (6), p.343

2020

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Role of the 3-mercaptopyruvate sulfurtransferase in colon/colorectal cancers

Endogenous H2S producing enzymes are involved in apoptosis induction in clear cell renal cell carcinoma

KIT Expression Is Regulated by DNA Methylation in Uveal Melanoma Tumors

A novel 3D mesenchymal stem cell model of the multiple myeloma bone marrow niche: biologic and clinical applications

Monosomy 3 Influences Epithelial-Mesenchymal Transition Gene Expression in Uveal Melanoma Patients; Consequences for Liquid Biopsy

Decitabine-induced DNA methylation-mediated transcriptomic reprogramming in human breast cancer cell lines; the impact of DCK overexpression

Variant c.2158-2A>G in MANBA is an important and frequent cause of hereditary hearing loss and beta-mannosidosis among the Czech and Slovak Roma population- evidence for a new ethnic-specific variant

High-level expression and purification of recombinant human growth hormone produced in soluble form in Escherichia coli

Uncovering accurate prognostic markers for high‐risk uveal melanoma through DNA methylation profiling

Structural and Functional Impact of Seven Missense Variants of Phenylalanine Hydroxylase

Breakpoints characterisation of the genomic deletions identified by MLPA in alkaptonuria patients

Mathematical modeling based on RT-qPCR analysis of SARS-CoV-2 in wastewater as a tool for epidemiology

Alkaptonuria in Russia

Genome-wide DNA methylome and transcriptome changes induced by inorganic nanoparticles in human kidney cells after chronic exposure

The importance of defining the age-specific TREC/KREC levels for detection of various inborn errors of immunity in pediatric and adult patients

Prognostic Value of Genotype-Phenotype Correlations in X-Linked Myotubular Myopathy and the Use of the Face2Gene Application as an Effective Non-Invasive Diagnostic Tool

Homogentisate 1,2-dioxygenase (HGD) gene variants, their analysis and genotype-phenotype correlations in the largest cohort of patients with AKU

Severe congenital T-lymphocytopenia may affect the outcome of neonatal intensive care

Type 3 inositol 1,4,5-trisphosphate receptor has antiapoptotic and proliferative role in cancer cells

Clinical manifestation of CDKL5 deficiency disorder and identified mutations in a cohort of Slovak patients

A Study among the Genotype, Functional Alternations, and Phenotype of 9 SCN1A Mutations in Epilepsy Patients

Biallelic Cys141Tyr variant of SEL1L is associated with neurodevelopmental disorders, agammaglobulinemia, and premature death

Making Waves: Collaboration in the time of SARS-CoV-2 - rapid development of an international co-operation and wastewater surveillance database to support public health decision-making

MARVELD2 (DFNB49) mutations in the hearing impaired Central European Roma population--prevalence, clinical impact and the common origin

Studying the Gene Expression of Penicillium rubens Under the Effect of Eight Essential Oils

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