Search Results - "Kazantsev, Aleksey G."
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Therapeutic application of histone deacetylase inhibitors for central nervous system disorders
Published in Nature reviews. Drug discovery (01-10-2008)“…Key Points This Review focuses on the family of histone deacetylases (HDACs) and their regulatory roles in cells with specific application to neurons. It…”
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Sirtuins in Alzheimer's Disease: SIRT2-Related GenoPhenotypes and Implications for PharmacoEpiGenetics
Published in International journal of molecular sciences (12-03-2019)“…Sirtuins (SIRT1-7) are NAD⁺-dependent protein deacetylases/ADP ribosyltransferases with important roles in chromatin silencing, cell cycle regulation, cellular…”
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The Sirtuin 2 Inhibitor AK-7 Is Neuroprotective in Huntington’s Disease Mouse Models
Published in Cell reports (Cambridge) (27-12-2012)“…Inhibition of sirtuin 2 (SIRT2) deacetylase mediates protective effects in cell and invertebrate models of Parkinson’s disease and Huntington’s disease (HD)…”
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KEAP1-modifying small molecule reveals muted NRF2 signaling responses in neural stem cells from Huntington’s disease patients
Published in Proceedings of the National Academy of Sciences - PNAS (06-06-2017)“…The activity of the transcription factor nuclear factor-erythroid 2 p45-derived factor 2 (NRF2) is orchestrated and amplified through enhanced transcription of…”
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The sirtuin-2 inhibitor AK7 is neuroprotective in models of Parkinson's disease but not amyotrophic lateral sclerosis and cerebral ischemia
Published in PloS one (21-01-2015)“…Sirtuin deacetylases regulate diverse cellular pathways and influence disease processes. Our previous studies identified the brain-enriched sirtuin-2 (SIRT2)…”
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SIRT2 inhibition achieves neuroprotection by decreasing sterol biosynthesis
Published in Proceedings of the National Academy of Sciences - PNAS (27-04-2010)“…Huntington's disease (HD), an incurable neurodegenerative disorder, has a complex pathogenesis including protein aggregation and the dysregulation of neuronal…”
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SIRT2- and NRF2-Targeting Thiazole-Containing Compound with Therapeutic Activity in Huntington's Disease Models
Published in Cell chemical biology (21-07-2016)“…There are currently no disease-modifying therapies for the neurodegenerative disorder Huntington's disease (HD). This study identified novel…”
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SIRT2 as a Therapeutic Target for Age-Related Disorders
Published in Frontiers in pharmacology (01-01-2012)“…Sirtuin proteins are conserved regulators of aging that have recently emerged as important modifiers of several diseases which commonly occur later in life…”
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A Potent Small Molecule Inhibits Polyglutamine Aggregation in Huntington's Disease Neurons and Suppresses Neurodegeneration in vivo
Published in Proceedings of the National Academy of Sciences - PNAS (18-01-2005)“…Polyglutamine (polyQ) disorders, including Huntington's disease (HD), are caused by expansion of polyQ-encoding repeats within otherwise unrelated gene…”
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Pharmacological Promotion of Inclusion Formation: A Therapeutic Approach for Huntington's and Parkinson's Diseases
Published in Proceedings of the National Academy of Sciences - PNAS (14-03-2006)“…Misfolded proteins accumulate in many neurodegenerative diseases, including huntingtin in Huntington's disease and α-synuclein in Parkinson's disease. The…”
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The role of Nrf2 signaling in counteracting neurodegenerative diseases
Published in The FEBS journal (01-10-2018)“…The transcription factor Nrf2 (nuclear factor‐erythroid 2 p45‐related factor 2) functions at the interface of cellular redox and intermediary metabolism. Nrf2…”
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Inhibition of Sirtuin 2 with Sulfobenzoic Acid Derivative AK1 is Non-Toxic and Potentially Neuroprotective in a Mouse Model of Frontotemporal Dementia
Published in Frontiers in pharmacology (01-01-2012)“…Tauopathies including tau-associated Frontotemporal dementia (FTD) and Alzheimer's disease are characterized pathologically by the formation of tau-containing…”
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Identification of Tri- and Tetracyclic Pyrimidinediones as Sirtuin Inhibitors
Published in ChemMedChem (03-05-2010)“…Sirtuins are deacetylase proteins that regulate transcription, genome maintenance, longevity, and metabolism. Eight compounds were identified as a novel class…”
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Loss of Huntingtin Function Complemented by Small Molecules Acting as Repressor Element 1/Neuron Restrictive Silencer Element Silencer Modulators
Published in The Journal of biological chemistry (24-08-2007)“…Increased levels of the repressor element 1/neuron restrictive silencer element (RE1/NRSE) silencing activity promoter, and a consequent reduction in the…”
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Editorial on special topic: sirtuins in metabolism, aging, and disease
Published in Frontiers in pharmacology (01-01-2012)Get full text
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New Directions for Neurodegenerative Disease Therapy: Using Chemical Compounds to Boost the Formation of Mutant Protein Inclusions
Published in Cell cycle (Georgetown, Tex.) (15-07-2006)“…Neurodegenerative disease such as Huntington's, Parkinson's, and Alzheimer'sdiseases are marked by neuronal accumulation of toxic misfolded protein…”
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Sirtuin 2 Inhibitors Rescue α-Synuclein-Mediated Toxicity in Models of Parkinson's Disease
Published in Science (American Association for the Advancement of Science) (27-07-2007)“…The sirtuins are members of the histone deacetylase family of proteins that participate in a variety of cellular functions and play a role in aging. We…”
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RNA Interference-Mediated Silencing of Mutant Superoxide Dismutase Rescues Cyclosporin A-Induced Death in Cultured Neuroblastoma Cells
Published in Proceedings of the National Academy of Sciences - PNAS (02-03-2004)“…Amyotrophic lateral sclerosis (ALS) is a progressive and fatal neurodegenerative disorder resulting from selective death of motor neurons in the brain and…”
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The Sirtuin 2 microtubule deacetylase is an abundant neuronal protein that accumulates in the aging CNS
Published in Human molecular genetics (15-10-2011)“…Sirtuin 2 (SIRT2) is one of seven known mammalian protein deacetylases homologous to the yeast master lifespan regulator Sir2. In recent years, the sirtuin…”
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Huntington's disease: From molecular basis to therapeutic advances
Published in The international journal of biochemistry & cell biology (2011)“…Huntington's disease is an autosomal dominant genetic neurodegenerative disorder, which is characterized by progressive motor dysfunction, emotional…”
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