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Andrea Soltysova

Showing results (21-30 of 35) with videos related to

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Orphanet Journal of Rare Diseases|August 28, 2020
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 variantDana Safka Brozkova, Lukas Varga, Anna Uhrova Meszarosova, et al.
Investigative Ophthalmology & Visual Science|March 25, 2025
Clinical Value of MLPA for Prognostic Assessment of Chromosomal Rearrangements and DNA Methylation in Uveal MelanomaAndrea Soltysova, Dana Dvorska, Andrej Ficek, et al.
Cell Death & Disease|February 24, 2019
Type 3 inositol 1,4,5-trisphosphate receptor has antiapoptotic and proliferative role in cancer cellsIngeborg Rezuchova, Sona Hudecova, Andrea Soltysova, et al.
Oncology|March 20, 2014
Augmenting clinical interpretability of thiopurine methyltransferase laboratory evaluationRegina Demlova, Martina Mrkvicova, Jaroslav Sterba, et al.
International Journal of Molecular Sciences|December 22, 2020
Monosomy 3 Influences Epithelial-Mesenchymal Transition Gene Expression in Uveal Melanoma Patients; Consequences for Liquid BiopsyAndrea Soltysova, Tatiana Sedlackova, Dana Dvorska, et al.
Oncotarget|October 21, 2016
A novel 3D mesenchymal stem cell model of the multiple myeloma bone marrow niche: biologic and clinical applicationsJana Jakubikova, Danka Cholujova, Teru Hideshima, et al.
European Journal of Human Genetics : EJHG|February 10, 2019
Homogentisate 1,2-dioxygenase (HGD) gene variants, their analysis and genotype-phenotype correlations in the largest cohort of patients with AKUDavid B Ascher, Ottavia Spiga, Martina Sekelska, et al.
Frontiers in Pharmacology|October 24, 2022
Decitabine-induced DNA methylation-mediated transcriptomic reprogramming in human breast cancer cell lines; the impact of DCK overexpressionVerona Buocikova, Silvia Tyciakova, Eleftherios Pilalis, et al.
Clinical and Translational Medicine|July 21, 2023
Uncovering accurate prognostic markers for high-risk uveal melanoma through DNA methylation profilingAndrea Soltysova, Dana Dvorska, Viera Horvathova Kajabova, et al.
The Journal of Clinical Investigation|November 9, 2023
Biallelic Cys141Tyr variant of SEL1L is associated with neurodevelopmental disorders, agammaglobulinemia, and premature deathDenisa Weis, Liangguang L Lin, Huilun H Wang, et al.
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Showing results (21-30 of 35) with videos related to

Sort By:
Pageof 4
Orphanet Journal of Rare Diseases|August 28, 2020
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 variantDana Safka Brozkova, Lukas Varga, Anna Uhrova Meszarosova, et al.
Investigative Ophthalmology & Visual Science|March 25, 2025
Clinical Value of MLPA for Prognostic Assessment of Chromosomal Rearrangements and DNA Methylation in Uveal MelanomaAndrea Soltysova, Dana Dvorska, Andrej Ficek, et al.
Cell Death & Disease|February 24, 2019
Type 3 inositol 1,4,5-trisphosphate receptor has antiapoptotic and proliferative role in cancer cellsIngeborg Rezuchova, Sona Hudecova, Andrea Soltysova, et al.
Oncology|March 20, 2014
Augmenting clinical interpretability of thiopurine methyltransferase laboratory evaluationRegina Demlova, Martina Mrkvicova, Jaroslav Sterba, et al.
International Journal of Molecular Sciences|December 22, 2020
Monosomy 3 Influences Epithelial-Mesenchymal Transition Gene Expression in Uveal Melanoma Patients; Consequences for Liquid BiopsyAndrea Soltysova, Tatiana Sedlackova, Dana Dvorska, et al.
Oncotarget|October 21, 2016
A novel 3D mesenchymal stem cell model of the multiple myeloma bone marrow niche: biologic and clinical applicationsJana Jakubikova, Danka Cholujova, Teru Hideshima, et al.
European Journal of Human Genetics : EJHG|February 10, 2019
Homogentisate 1,2-dioxygenase (HGD) gene variants, their analysis and genotype-phenotype correlations in the largest cohort of patients with AKUDavid B Ascher, Ottavia Spiga, Martina Sekelska, et al.
Frontiers in Pharmacology|October 24, 2022
Decitabine-induced DNA methylation-mediated transcriptomic reprogramming in human breast cancer cell lines; the impact of DCK overexpressionVerona Buocikova, Silvia Tyciakova, Eleftherios Pilalis, et al.
Clinical and Translational Medicine|July 21, 2023
Uncovering accurate prognostic markers for high-risk uveal melanoma through DNA methylation profilingAndrea Soltysova, Dana Dvorska, Viera Horvathova Kajabova, et al.
The Journal of Clinical Investigation|November 9, 2023
Biallelic Cys141Tyr variant of SEL1L is associated with neurodevelopmental disorders, agammaglobulinemia, and premature deathDenisa Weis, Liangguang L Lin, Huilun H Wang, et al.
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