Histone deacetylase inhibitors: possible implications for neurodegenerative disorders
暂无分享,去创建一个
B. Wirth | I. Blümcke | E. Hahnen | I. Eyüpoglu | C. Tränkle | J. Hauke
[1] P. Marks,et al. Histone deacetylase inhibitors: molecular mechanisms of action , 2007, Oncogene.
[2] J. Wong,et al. HDAC3: taking the SMRT-N-CoRrect road to repression , 2007, Oncogene.
[3] C. DiDonato,et al. Animal Models of Spinal Muscular Atrophy , 2007, Journal of child neurology.
[4] Ruben Abagyan,et al. Sirtuin 2 Inhibitors Rescue α-Synuclein-Mediated Toxicity in Models of Parkinson's Disease , 2007, Science.
[5] H. Zoghbi,et al. Trinucleotide repeat disorders. , 2007, Annual review of neuroscience.
[6] Dan Garza,et al. HDAC6 rescues neurodegeneration and provides an essential link between autophagy and the UPS , 2007, Nature.
[7] B. Stockwell,et al. Identification of Potential Therapeutic Drugs for Huntington's Disease using Caenorhabditis elegans , 2007, PloS one.
[8] Joel M Stein,et al. Histone Deacetylase Inhibitors Enhance Memory and Synaptic Plasticity via CREB: CBP-Dependent Transcriptional Activation , 2007, The Journal of Neuroscience.
[9] D. Chuang,et al. Histone Deacetylase Inhibitors Exhibit Anti-Inflammatory and Neuroprotective Effects in a Rat Permanent Ischemic Model of Stroke: Multiple Mechanisms of Action , 2007, Journal of Pharmacology and Experimental Therapeutics.
[10] S. Hersch,et al. Histones associated with downregulated genes are hypo-acetylated in Huntington's disease models. , 2007, Human molecular genetics.
[11] Bin Chen,et al. Functional differences in epigenetic modulators-superiority of mercaptoacetamide-based histone deacetylase inhibitors relative to hydroxamates in cortical neuron neuroprotection studies. , 2007, Journal of medicinal chemistry.
[12] A. Echaniz-Laguna,et al. Sodium Valproate Exerts Neuroprotective Effects In Vivo through CREB-Binding Protein-Dependent Mechanisms But Does Not Improve Survival in an Amyotrophic Lateral Sclerosis Mouse Model , 2007, The Journal of Neuroscience.
[13] David Sinclair,et al. Sirtuins in mammals: insights into their biological function. , 2007, The Biochemical journal.
[14] Li-Huei Tsai,et al. Recovery of learning and memory is associated with chromatin remodelling , 2007, Nature.
[15] Fabrice P Cordelières,et al. Histone Deacetylase 6 Inhibition Compensates for the Transport Deficit in Huntington's Disease by Increasing Tubulin Acetylation , 2007, The Journal of Neuroscience.
[16] A. Guidotti,et al. Histone hyperacetylation induces demethylation of reelin and 67-kDa glutamic acid decarboxylase promoters , 2007, Proceedings of the National Academy of Sciences.
[17] K. Fischbeck,et al. Trichostatin A increases SMN expression and survival in a mouse model of spinal muscular atrophy. , 2007, The Journal of clinical investigation.
[18] M. Szyf,et al. Valproate induces widespread epigenetic reprogramming which involves demethylation of specific genes. , 2007, Carcinogenesis.
[19] A. Chiarugi,et al. Pharmacological Inhibition of Histone Deacetylases by Suberoylanilide Hydroxamic Acid Specifically Alters Gene Expression and Reduces Ischemic Injury in the Mouse Brain , 2006, Molecular Pharmacology.
[20] W. Hwu,et al. Establishing a standardized therapeutic testing protocol for spinal muscular atrophy , 2006, Neurobiology of Disease.
[21] T. Klockgether,et al. Ataxin-3 Represses Transcription via Chromatin Binding, Interaction with Histone Deacetylase 3, and Histone Deacetylation , 2006, The Journal of Neuroscience.
[22] J. Parvin,et al. Alpha-synuclein acts in the nucleus to inhibit histone acetylation and promote neurotoxicity. , 2006, Human molecular genetics.
[23] S. Perlman,et al. Histone deacetylase inhibitors reverse gene silencing in Friedreich's ataxia , 2006, Nature chemical biology.
[24] G. Bates,et al. Histone deacetylase inhibitors as therapeutics for polyglutamine disorders , 2006, Nature Reviews Neuroscience.
[25] L. Tora,et al. Transcriptional alterations and chromatin remodeling in polyglutamine diseases. , 2006, Trends in genetics : TIG.
[26] A. Pestronk,et al. Valproate may improve strength and function in patients with type III/IV spinal muscle atrophy , 2006, Neurology.
[27] A. Hart,et al. Differential Contributions of Caenorhabditis elegans Histone Deacetylases to Huntingtin Polyglutamine Toxicity , 2006, The Journal of Neuroscience.
[28] L. Laimins,et al. Histone deacetylase 3 localizes to the plasma membrane and is a substrate of Src , 2006, Oncogene.
[29] Peter Claus,et al. In vitro and ex vivo evaluation of second‐generation histone deacetylase inhibitors for the treatment of spinal muscular atrophy , 2006, Journal of neurochemistry.
[30] B. Wirth,et al. In vivo activation of SMN in spinal muscular atrophy carriers and patients treated with valproate , 2006, Annals of neurology.
[31] J. Cha,et al. Mechanisms of Disease: histone modifications in Huntington's disease , 2006, Nature Clinical Practice Neurology.
[32] B. Wirth,et al. The benzamide M344, a novel histone deacetylase inhibitor, significantly increases SMN2 RNA/protein levels in spinal muscular atrophy cells , 2006, Human Genetics.
[33] Min Han,et al. Sodium Butyrate Ameliorates Histone Hypoacetylation and Neurodegenerative Phenotypes in a Mouse Model for DRPLA* , 2006, Journal of Biological Chemistry.
[34] M. Beal,et al. Additive neuroprotective effects of a histone deacetylase inhibitor and a catalytic antioxidant in a transgenic mouse model of amyotrophic lateral sclerosis , 2006, Neurobiology of Disease.
[35] J. Olson,et al. Regional and cellular gene expression changes in human Huntington's disease brain. , 2006, Human molecular genetics.
[36] H. Zoghbi,et al. Glutamine-Expanded Ataxin-7 Alters TFTC/STAGA Recruitment and Chromatin Structure Leading to Photoreceptor Dysfunction , 2006, PLoS biology.
[37] H. Przuntek,et al. Dose-dependent improvement of myoclonic hyperkinesia due to Valproic acid in eight Huntington's Disease patients: a case series , 2006, BMC neurology.
[38] R. Kopito,et al. HDAC6 and Microtubules Are Required for Autophagic Degradation of Aggregated Huntingtin* , 2005, Journal of Biological Chemistry.
[39] Elena Cattaneo,et al. Normal huntingtin function: an alternative approach to Huntington's disease , 2005, Nature Reviews Neuroscience.
[40] A. Hannan,et al. GENE–ENVIRONMENT INTERACTIONS, NEURONAL DYSFUNCTION AND PATHOLOGICAL PLASTICITY IN HUNTINGTON'S DISEASE , 2005, Clinical and experimental pharmacology & physiology.
[41] Josephine C. Dorsman,et al. Mutant huntingtin represses CBP, but not p300, by binding and protein degradation , 2005, Molecular and Cellular Neuroscience.
[42] G. Stephanopoulos,et al. Transcriptional therapy with the histone deacetylase inhibitor trichostatin A ameliorates experimental autoimmune encephalomyelitis , 2005, Journal of Neuroimmunology.
[43] J. Yates,et al. Polyglutamine-expanded spinocerebellar ataxia-7 protein disrupts normal SAGA and SLIK histone acetyltransferase activity. , 2005, Proceedings of the National Academy of Sciences of the United States of America.
[44] B. Chait,et al. Polyglutamine-expanded ataxin-7 inhibits STAGA histone acetyltransferase activity to produce retinal degeneration. , 2005, Proceedings of the National Academy of Sciences of the United States of America.
[45] R. Ferrante,et al. Sodium phenylbutyrate prolongs survival and regulates expression of anti‐apoptotic genes in transgenic amyotrophic lateral sclerosis mice , 2005, Journal of neurochemistry.
[46] C. Monneret. Histone deacetylase inhibitors. , 2005, European journal of medicinal chemistry.
[47] K. Fischbeck,et al. The role of histone acetylation in SMN gene expression. , 2005, Human molecular genetics.
[48] C. Lorson,et al. A non-sequence-specific requirement for SMN protein activity: the role of aminoglycosides in inducing elevated SMN protein levels. , 2005, Human molecular genetics.
[49] Pascal G. P. Martin,et al. Phenylbutyrate up-regulates the adrenoleukodystrophy-related gene as a nonclassical peroxisome proliferator , 2005, The Journal of cell biology.
[50] Johan T den Dunnen,et al. Genetic heterogeneity in Rubinstein-Taybi syndrome: mutations in both the CBP and EP300 genes cause disease. , 2005, American journal of human genetics.
[51] U. Monani,et al. SMNDelta7, the major product of the centromeric survival motor neuron (SMN2) gene, extends survival in mice with spinal muscular atrophy and associates with full-length SMN. , 2005, Human molecular genetics.
[52] E. Bertini,et al. Phenylbutyrate increases SMN gene expression in spinal muscular atrophy patients , 2005, European Journal of Human Genetics.
[53] M. Beal,et al. Neuroprotective Effects of Phenylbutyrate in the N171-82Q Transgenic Mouse Model of Huntington's Disease* , 2005, Journal of Biological Chemistry.
[54] J. Mandel,et al. Functional overlap between ABCD1 (ALD) and ABCD2 (ALDR) transporters: a therapeutic target for X-adrenoleukodystrophy. , 2004, Human molecular genetics.
[55] S. Sakoda,et al. Benefit of valproic acid in suppressing disease progression of ALS model mice , 2004, The European journal of neuroscience.
[56] D. Molfese,et al. Regulation of Histone Acetylation during Memory Formation in the Hippocampus* , 2004, Journal of Biological Chemistry.
[57] Michael J Meaney,et al. Epigenetic programming by maternal behavior , 2004, Nature Neuroscience.
[58] E. Kandel,et al. Chromatin Acetylation, Memory, and LTP Are Impaired in CBP+/− Mice A Model for the Cognitive Deficit in Rubinstein-Taybi Syndrome and Its Amelioration , 2004, Neuron.
[59] M. Mayford,et al. CBP Histone Acetyltransferase Activity Is a Critical Component of Memory Consolidation , 2004, Neuron.
[60] Làszlò Tora,et al. Ataxin-7 is a subunit of GCN5 histone acetyltransferase-containing complexes. , 2004, Human molecular genetics.
[61] D. Chuang,et al. Valproic acid reduces brain damage induced by transient focal cerebral ischemia in rats: potential roles of histone deacetylase inhibition and heat shock protein induction , 2004, Journal of neurochemistry.
[62] Fumiaki Tanaka,et al. Sodium butyrate ameliorates phenotypic expression in a transgenic mouse model of spinal and bulbar muscular atrophy. , 2004, Human molecular genetics.
[63] E. Bertini,et al. Pilot trial of phenylbutyrate in spinal muscular atrophy , 2004, Neuromuscular Disorders.
[64] J. Meinkoth,et al. Histone Deacetylase Is a Target of Valproic Acid-Mediated Cellular Differentiation , 2004, Cancer Research.
[65] J. Loeffler,et al. Critical loss of CBP/p300 histone acetylase activity by caspase‐6 during neurodegeneration , 2003, The EMBO journal.
[66] J. Vance,et al. The Deacetylase HDAC6 Regulates Aggresome Formation and Cell Viability in Response to Misfolded Protein Stress , 2003, Cell.
[67] K. Fischbeck,et al. Valproic acid increases SMN levels in spinal muscular atrophy patient cells , 2003, Annals of neurology.
[68] Ruth Luthi-Carter,et al. Histone Deacetylase Inhibition by Sodium Butyrate Chemotherapy Ameliorates the Neurodegenerative Phenotype in Huntington's Disease Mice , 2003, The Journal of Neuroscience.
[69] Minh N. H. Nguyen,et al. Wild-Type Nonneuronal Cells Extend Survival of SOD1 Mutant Motor Neurons in ALS Mice , 2003, Science.
[70] Y. Hofmann,et al. Valproic acid increases the SMN2 protein level: a well-known drug as a potential therapy for spinal muscular atrophy. , 2003, Human molecular genetics.
[71] T. Tully,et al. A mouse model of Rubinstein-Taybi syndrome: Defective long-term memory is ameliorated by inhibitors of phosphodiesterase 4 , 2003, Proceedings of the National Academy of Sciences of the United States of America.
[72] M. Szyf,et al. Valproate Induces Replication-independent Active DNA Demethylation* , 2003, Journal of Biological Chemistry.
[73] B. Groner,et al. The histone deacetylase inhibitor valproic acid selectively induces proteasomal degradation of HDAC2 , 2003, The EMBO journal.
[74] Eng H. Lo,et al. Neurological diseases: Mechanisms, challenges and opportunities in stroke , 2003, Nature Reviews Neuroscience.
[75] D. Rubinsztein,et al. Transcriptional abnormalities in Huntington disease. , 2003, Trends in genetics : TIG.
[76] Stuart L Schreiber,et al. Domain-selective small-molecule inhibitor of histone deacetylase 6 (HDAC6)-mediated tubulin deacetylation , 2003, Proceedings of the National Academy of Sciences of the United States of America.
[77] Leslie M Thompson,et al. Suberoylanilide hydroxamic acid, a histone deacetylase inhibitor, ameliorates motor deficits in a mouse model of Huntington's disease , 2003, Proceedings of the National Academy of Sciences of the United States of America.
[78] D. Chakravarti,et al. Ataxin-3 Is a Histone-binding Protein with Two Independent Transcriptional Corepressor Activities* , 2002, The Journal of Biological Chemistry.
[79] J. Olson,et al. Polyglutamine and transcription: gene expression changes shared by DRPLA and Huntington's disease mouse models reveal context-independent effects. , 2002, Human molecular genetics.
[80] Charles Kooperberg,et al. Dysregulation of gene expression in the R6/2 model of polyglutamine disease: parallel changes in muscle and brain. , 2002, Human molecular genetics.
[81] Fred Asselbergs,et al. Cloning and Functional Characterization of HDAC11, a Novel Member of the Human Histone Deacetylase Family* , 2002, The Journal of Biological Chemistry.
[82] Xiao-Fan Wang,et al. HDAC6 is a microtubule-associated deacetylase , 2002, Nature.
[83] Dimitri Krainc,et al. Sp1 and TAFII130 Transcriptional Activity Disrupted in Early Huntington's Disease , 2002, Science.
[84] M. Jung,et al. A microplate reader-based nonisotopic histone deacetylase activity assay. , 2002, Analytical biochemistry.
[85] He Li,et al. Interaction of Huntington Disease Protein with Transcriptional Activator Sp1 , 2002, Molecular and Cellular Biology.
[86] Ping Zhu,et al. Valproic acid defines a novel class of HDAC inhibitors inducing differentiation of transformed cells , 2001, The EMBO journal.
[87] K. Fischbeck,et al. Histone deacetylase inhibitors reduce polyglutamine toxicity , 2001, Proceedings of the National Academy of Sciences of the United States of America.
[88] M. Szyf,et al. Demethylase Activity Is Directed by Histone Acetylation* , 2001, The Journal of Biological Chemistry.
[89] D. Housman,et al. Histone deacetylase inhibitors arrest polyglutamine-dependent neurodegeneration in Drosophila , 2001, Nature.
[90] M. Guenther,et al. Histone Deacetylase Is a Direct Target of Valproic Acid, a Potent Anticonvulsant, Mood Stabilizer, and Teratogen* , 2001, The Journal of Biological Chemistry.
[91] C. Ware,et al. Polyglutamine-Expanded Ataxin-7 Antagonizes CRX Function and Induces Cone-Rod Dystrophy in a Mouse Model of SCA7 , 2001, Neuron.
[92] K. Smith,et al. Evaluation of pharmacological induction of fatty acid beta-oxidation in X-linked adrenoleukodystrophy. , 2001, Molecular genetics and metabolism.
[93] Y. Jong,et al. Treatment of spinal muscular atrophy by sodium butyrate , 2001, Proceedings of the National Academy of Sciences of the United States of America.
[94] C A Ross,et al. Interference by Huntingtin and Atrophin-1 with CBP-Mediated Transcription Leading to Cellular Toxicity , 2001, Science.
[95] I. Kanazawa,et al. Expanded polyglutamine stretches interact with TAFII130, interfering with CREB-dependent transcription , 2000, Nature Genetics.
[96] D. Housman,et al. The Huntington's disease protein interacts with p53 and CREB-binding protein and represses transcription. , 2000, Proceedings of the National Academy of Sciences of the United States of America.
[97] B. Wirth. An update of the mutation spectrum of the survival motor neuron gene (SMN1) in autosomal recessive spinal muscular atrophy (SMA) , 2000, Human mutation.
[98] B. Oostra,et al. Synergistic effect of histone hyperacetylation and DNA demethylation in the reactivation of the FMR1 gene. , 1999, Human molecular genetics.
[99] C. Lorson,et al. A single nucleotide in the SMN gene regulates splicing and is responsible for spinal muscular atrophy. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[100] T. Nabeshima,et al. Truncated CBP protein leads to classical Rubinstein-Taybi syndrome phenotypes in mice: implications for a dominant-negative mechanism. , 1999, Human molecular genetics.
[101] A. Moser,et al. Gene redundancy and pharmacological gene therapy: Implications for X-linked adrenoleukodystrophy , 1998, Nature Medicine.
[102] J. Strouboulis,et al. Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription , 1998, Nature Genetics.
[103] Colin A. Johnson,et al. Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex , 1998, Nature.
[104] C. Lorson,et al. SMN oligomerization defect correlates with spinal muscular atrophy severity , 1998, Nature Genetics.
[105] P. Marks,et al. A class of hybrid polar inducers of transformed cell differentiation inhibits histone deacetylases. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[106] A. Hackam,et al. Length of huntingtin and its polyglutamine tract influences localization and frequency of intracellular aggregates , 1998, Nature Genetics.
[107] H. Masuya,et al. Abnormal skeletal patterning in embryos lacking a single Cbp allele: a partial similarity with Rubinstein-Taybi syndrome. , 1997, Proceedings of the National Academy of Sciences of the United States of America.
[108] H. Selbmann,et al. Learning to recognize objects , 1999, Trends in Cognitive Sciences.
[109] M. Hayden,et al. Cleavage of huntingtin by apopain, a proapoptotic cysteine protease, is modulated by the polyglutamine tract , 1996, Nature Genetics.
[110] J. Weissenbach,et al. Identification and characterization of a spinal muscular atrophy-determining gene , 1995, Cell.
[111] Minoru Yoshida,et al. [Potent and specific inhibition of mammalian histone deacetylase both in vivo and in vitro by trichostatin A]. , 1990, Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme.
[112] V. Ingram,et al. n-Butyrate causes histone modification in HeLa and Friend erythroleukaemia cells , 1977, Nature.
[113] Melges Fj. A NEW ANTIFUNGAL ANTIBIOTIC. , 1964 .
[114] J H RUBINSTEIN,et al. Broad thumbs and toes and facial abnormalities. A possible mental retardation syndrome. , 1963, American journal of diseases of children.
[115] R. Abagyan,et al. Sirtuin 2 inhibitors rescue alpha-synuclein-mediated toxicity in models of Parkinson's disease. , 2007, Science.
[116] L. Maffei,et al. Environmental enrichment delays the onset of memory deficits and reduces neuropathological hallmarks in a mouse model of Alzheimer-like neurodegeneration. , 2007, Journal of Alzheimer's disease : JAD.
[117] A. Sik,et al. Chromogranin-mediated secretion of mutant superoxide dismutase proteins linked to amyotrophic lateral sclerosis , 2006, Nature Neuroscience.
[118] 須貝 文宣. Benefit of valproic acid in suppressing disease progression of ALS model mice , 2005 .
[119] E. Bertini,et al. Phenylbutyrate increases SMN expression in vitro: relevance for treatment of spinal muscular atrophy , 2004, European Journal of Human Genetics.
[120] J. Herman,et al. Synergy of demethylation and histone deacetylase inhibition in the re-expression of genes silenced in cancer , 1999, Nature Genetics.
[121] K. Nagashima,et al. A new antifungal antibiotic, trichostatin. , 1976, The Journal of antibiotics.