Search Results - "EPANCHINTSEV, Alexey"
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Inactivation of miR-34a by aberrant CpG methylation in multiple types of cancer
Published in Cell cycle (Georgetown, Tex.) (15-08-2008)“…Recently, we and others identified the microRNA miR-34a as a target of the tumor suppressor gene product p53. Ectopic miR-34a induces a G1 cell cycle arrest,…”
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Cockayne’s Syndrome A and B Proteins Regulate Transcription Arrest after Genotoxic Stress by Promoting ATF3 Degradation
Published in Molecular cell (21-12-2017)“…Cockayne syndrome (CS) is caused by mutations in CSA and CSB. The CSA and CSB proteins have been linked to both promoting transcription-coupled repair and…”
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3
Defective transcription of ATF3 responsive genes, a marker for Cockayne Syndrome
Published in Scientific reports (24-01-2020)“…Cockayne syndrome (CS) is a rare genetic disorder caused by mutations (dysfunction) in CSA and CSB . CS patients exhibit mild photosensitivity and severe…”
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4
Comparative performance analysis of human iPSC-derived and primary neural progenitor cells (NPC) grown as neurospheres in vitro
Published in Stem cell research (01-12-2017)“…Developmental neurotoxicity (DNT) testing performed in rats is resource-intensive (costs, time, animals) and bears the issue of species extrapolation. Thus,…”
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5
Functional epigenomics identifies genes frequently silenced in prostate cancer
Published in Cancer research (Chicago, Ill.) (15-05-2005)“…In many cases, silencing of gene expression by CpG methylation is causally involved in carcinogenesis. Furthermore, cancer-specific CpG methylation may serve…”
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Regulatory interplay of Cockayne syndrome B ATPase and stress-response gene ATF3 following genotoxic stress
Published in Proceedings of the National Academy of Sciences - PNAS (18-06-2013)“…Cockayne syndrome type B ATPase (CSB) belongs to the SwItch/Sucrose nonfermentable family. Its mutations are linked to Cockayne syndrome phenotypes and…”
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c-MYC Delays Prometaphase by Direct Transactivation of MAD2 and BubR1: Identification of Mechanisms Underlying c-MYC-Induced DNA Damage and Chromosomal Instability
Published in Cell cycle (Georgetown, Tex.) (01-02-2007)“…Here we show that the human BubR1 and MAD2 genes, which encode inhibitors of the anaphase promoting complex (APC/C), are directly activated by the oncogenic…”
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Digital Karyotyping Reveals Frequent Inactivation of the dystrophin/DMD Gene in Malignant Melanoma
Published in Cell cycle (Georgetown, Tex.) (15-01-2007)“…Malignant melanoma is still poorly understood at the genomic level. Recently, a new technique for the high-resolution analysis of copy number changes named…”
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Differential Regulation of microRNAs by p53 Revealed by Massively Parallel Sequencing: miR-34a is a p53 Target That Induces Apoptosis and G1-arrest
Published in Cell cycle (Georgetown, Tex.) (01-07-2007)“…In a genome-wide screen for microRNAs regulated by the transcription factor encoded by the p53 tumor suppressor gene we found that after p53-activation the…”
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10
AMPKβ1 and AMPKβ2 define an isoform-specific gene signature in human pluripotent stem cells, differentially mediating cardiac lineage specification
Published in The Journal of biological chemistry (18-12-2020)“…AMP-activated protein kinase (AMPK) is a key regulator of energy metabolism that phosphorylates a wide range of proteins to maintain cellular homeostasis. AMPK…”
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11
AMPKβ1 and AMPKβ2 define an isoform-specific gene signature in human pluripotent stem cells, differentially mediating cardiac lineage specification
Published in The Journal of biological chemistry (16-10-2020)“…AMP-activated protein kinase (AMPK) is a key regulator of energy metabolism that phosphorylates a wide range of proteins to maintain cellular homeostasis. AMPK…”
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12
IL‐6, IL‐8, MMP‐2, MMP‐9 are overexpressed in Fanconi anemia cells through a NF‐κB/TNF‐α dependent mechanism
Published in Molecular carcinogenesis (01-12-2015)“…Fanconi anemia (FA) is a rare autosomal recessive genetic disorder associated with a bone‐marrow failure, genome instability, hypersensitivity to DNA…”
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13
IL-6, IL-8, MMP-2, MMP-9 are overexpressed in Fanconi anemia cells through a NF-[kappa]B/TNF-[alpha] dependent mechanism
Published in Molecular carcinogenesis (01-12-2015)“…Fanconi anemia (FA) is a rare autosomal recessive genetic disorder associated with a bone-marrow failure, genome instability, hypersensitivity to DNA…”
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14
MED12-related XLID disorders are dose-dependent of immediate early genes (IEGs) expression
Published in Human molecular genetics (01-06-2017)“…Mediator occupies a key role in protein coding genes expression in mediating the contacts between gene specific factors and the basal transcription machinery…”
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15
AMPKβ1 and AMPKβ2 define an isoform-specific gene signature in human pluripotent stem cells, differentially mediating cardiac lineage specification
Published in The Journal of biological chemistry (18-12-2020)“…AMP-activated protein kinase (AMPK) is a key regulator of energy metabolism that phosphorylates a wide range of proteins to maintain cellular homeostasis. AMPK…”
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Journal Article -
16
Regulatory interplay of Cockayne syndrome B ATPase and stress-response gene ATF3 following genotoxic stress
Published in Proceedings of the National Academy of Sciences - PNAS (18-06-2013)Get full text
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17
Inducible microRNA expression by an all-in-one episomal vector system
Published in Nucleic acids research (01-10-2006)“…Here we describe an episomal, one-vector system which allows the generation of cell populations displaying homogenous, inducible gene inactivation by RNA…”
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