HDAC6 is a therapeutic target in mutant GARS-induced Charcot-Marie-Tooth disease
暂无分享,去创建一个
M. Z. Cader | W. Robberecht | P. van Damme | K. Talbot | A. Kozikowski | P. Vanden Berghe | L. Van Den Bosch | C. d’Ydewalle | V. Benoy | W. Haeck | R. Prior | Lawrence Van Helleputte | Natasja Geens | W. Scheveneels | Begga Schevenels | Robert Prior
[1] W. Robberecht,et al. HDAC6 inhibition reverses axonal transport defects in motor neurons derived from FUS-ALS patients , 2017, Nature Communications.
[2] L. Bosch,et al. Defective axonal transport: A common pathological mechanism in inherited and acquired peripheral neuropathies , 2017, Neurobiology of Disease.
[3] B. Kalmar,et al. Mitochondrial deficits and abnormal mitochondrial retrograde axonal transport play a role in the pathogenesis of mutant Hsp27-induced Charcot Marie Tooth Disease , 2017, Human molecular genetics.
[4] Fang Yang,et al. Acetylation of lysine ϵ-amino groups regulates aminoacyl-tRNA synthetase activity in Escherichia coli , 2017, The Journal of Biological Chemistry.
[5] M. Z. Cader,et al. PN07 Trk receptor signalling and sensory neuron fate are perturbed in human neuropathy caused by Gars mutations , 2017, Neuromuscular Disorders.
[6] Hyunjung Choi,et al. HDAC6 Inhibitors Rescued the Defective Axonal Mitochondrial Movement in Motor Neurons Derived from the Induced Pluripotent Stem Cells of Peripheral Neuropathy Patients with HSPB1 Mutation , 2016, Stem cells international.
[7] W. Robberecht,et al. Development of Improved HDAC6 Inhibitors as Pharmacological Therapy for Axonal Charcot–Marie–Tooth Disease , 2016, Neurotherapeutics.
[8] V. Baekelandt,et al. Protection against Mitochondrial and Metal Toxicity Depends on Functional Lipid Binding Sites in ATP13A2 , 2016, Parkinson's disease.
[9] R. Burgess,et al. Synaptic Deficits at Neuromuscular Junctions in Two Mouse Models of Charcot–Marie–Tooth Type 2d , 2016, The Journal of Neuroscience.
[10] G. Vistoli,et al. Bicyclic-Capped Histone Deacetylase 6 Inhibitors with Improved Activity in a Model of Axonal Charcot-Marie-Tooth Disease. , 2016, ACS chemical neuroscience.
[11] L. Van Den Bosch,et al. Synthesis and SAR assessment of novel Tubathian analogs in the pursuit of potent and selective HDAC6 inhibitors. , 2016, Organic & biomolecular chemistry.
[12] D. Chuang,et al. Tubastatin A, an HDAC6 inhibitor, alleviates stroke-induced brain infarction and functional deficits: potential roles of α-tubulin acetylation and FGF-21 up-regulation , 2016, Scientific Reports.
[13] L. Greensmith,et al. Regulation of Axonal Transport by Protein Kinases. , 2015, Trends in biochemical sciences.
[14] R. Burgess,et al. CMT2D neuropathy is linked to the neomorphic binding activity of glycyl-tRNA synthetase , 2015, Nature.
[15] Greg W. Clark,et al. Panorama of ancient metazoan macromolecular complexes , 2015, Nature.
[16] R. Burgess,et al. Impaired protein translation in Drosophila models for Charcot–Marie–Tooth neuropathy caused by mutant tRNA synthetases , 2015, Nature Communications.
[17] D. Pareyson,et al. Mitochondrial dynamics and inherited peripheral nerve diseases , 2015, Neuroscience Letters.
[18] K. De Bosscher,et al. Synthesis of benzothiophene-based hydroxamic acids as potent and selective HDAC6 inhibitors. , 2015, Chemical communications.
[19] S. Züchner,et al. Impaired Function is a Common Feature of Neuropathy‐Associated Glycyl‐tRNA Synthetase Mutations , 2014, Human mutation.
[20] A. Whitworth,et al. Increasing microtubule acetylation rescues axonal transport and locomotor deficits caused by LRRK2 Roc-COR domain mutations , 2014, Nature Communications.
[21] L. Bosch,et al. The role of histone deacetylase 6 (HDAC6) in neurodegeneration , 2014 .
[22] K. Fischbeck,et al. CMT-associated mutations in glycyl- and tyrosyl-tRNA synthetases exhibit similar pattern of toxicity and share common genetic modifiers in Drosophila , 2014, Neurobiology of Disease.
[23] P. Verstreken,et al. HDAC6 is a Bruchpilot deacetylase that facilitates neurotransmitter release. , 2014, Cell reports.
[24] M. Z. Cader,et al. Neuromuscular junction maturation defects precede impaired lower motor neuron connectivity in Charcot-Marie-Tooth type 2D mice. , 2014, Human molecular genetics.
[25] Hua Zhu,et al. Tubastatin A/ACY-1215 improves cognition in Alzheimer's disease transgenic mice. , 2014, Journal of Alzheimer's disease : JAD.
[26] S. Züchner,et al. Exome sequencing identifies a significant variant in methionyl-tRNA synthetase (MARS) in a family with late-onset CMT2 , 2013, Journal of Neurology, Neurosurgery & Psychiatry.
[27] J. Auwerx,et al. Hdac6 deletion delays disease progression in the SOD1G93A mouse model of ALS. , 2013, Human molecular genetics.
[28] Peng Yao,et al. Charcot – Marie – Tooth disease : An inheritable human disease caused by mutations in cytoplasmic ARSs , 2013 .
[29] J. Lupski,et al. A Loss‐of‐Function Variant in the Human Histidyl‐tRNA Synthetase (HARS) Gene is Neurotoxic In Vivo , 2013, Human mutation.
[30] O. Schlüter,et al. Reducing HDAC6 ameliorates cognitive deficits in a mouse model for Alzheimer's disease , 2012, EMBO molecular medicine.
[31] M. Cilli,et al. Electrophysiological features of the mouse tail nerves and their changes in chemotherapy induced peripheral neuropathy (CIPN) , 2012, Journal of Neuroscience Methods.
[32] K. Fischbeck,et al. Charcot-Marie-Tooth–Linked Mutant GARS Is Toxic to Peripheral Neurons Independent of Wild-Type GARS Levels , 2011, PLoS genetics.
[33] B. Asselbergh,et al. Small Heat-Shock Protein HSPB1 Mutants Stabilize Microtubules in Charcot-Marie-Tooth Neuropathy , 2011, The Journal of Neuroscience.
[34] W. Robberecht,et al. HDAC6 inhibitors reverse axonal loss in a mouse model of mutant HSPB1–induced Charcot-Marie-Tooth disease , 2011, Nature Medicine.
[35] R. Burgess,et al. An assessment of mechanisms underlying peripheral axonal degeneration caused by aminoacyl-tRNA synthetase mutations , 2011, Molecular and Cellular Neuroscience.
[36] Nancy F. Hansen,et al. Compound heterozygosity for loss-of-function lysyl-tRNA synthetase mutations in a patient with peripheral neuropathy. , 2010, American journal of human genetics.
[37] P. Schimmel,et al. New functions of aminoacyl-tRNA synthetases beyond translation , 2010, Nature Reviews Molecular Cell Biology.
[38] Kyle V. Butler,et al. Rational design and simple chemistry yield a superior, neuroprotective HDAC6 inhibitor, tubastatin A. , 2010, Journal of the American Chemical Society.
[39] R. Durbin,et al. Systematic Analysis of Human Protein Complexes Identifies Chromosome Segregation Proteins , 2010, Science.
[40] E. Broussolle,et al. A major determinant for binding and aminoacylation of tRNA(Ala) in cytoplasmic Alanyl-tRNA synthetase is mutated in dominant axonal Charcot-Marie-Tooth disease. , 2010, American journal of human genetics.
[41] Kyle V. Butler,et al. Rational Design and Simple Chemistry Yield a Superior , Neuroprotective HDAC 6 Inhibitor , Tubastatin A , 2010 .
[42] M. Z. Cader,et al. An ENU-induced mutation in mouse glycyl-tRNA synthetase (GARS) causes peripheral sensory and motor phenotypes creating a model of Charcot-Marie-Tooth type 2D peripheral neuropathy , 2009, Disease Models & Mechanisms.
[43] Hongfang Liu,et al. SpliceCenter: A suite of web-based bioinformatic applications for evaluating the impact of alternative splicing on RT-PCR, RNAi, microarray, and peptide-based studies , 2008, BMC Bioinformatics.
[44] A. Grierson,et al. Role of axonal transport in neurodegenerative diseases. , 2008, Annual review of neuroscience.
[45] Sharon Y. R. Dent,et al. HDAC6 modulates cell motility by altering the acetylation level of cortactin. , 2007, Molecular cell.
[46] Xiang-Lei Yang,et al. Charcot–Marie–Tooth disease-associated mutant tRNA synthetases linked to altered dimer interface and neurite distribution defect , 2007, Proceedings of the National Academy of Sciences.
[47] Xiang-Lei Yang,et al. Long-range structural effects of a Charcot–Marie–Tooth disease-causing mutation in human glycyl-tRNA synthetase , 2007, Proceedings of the National Academy of Sciences.
[48] M. Reilly. Sorting out the inherited neuropathies. , 2007, Practical neurology.
[49] R. Burgess,et al. An Active Dominant Mutation of Glycyl-tRNA Synthetase Causes Neuropathy in a Charcot-Marie-Tooth 2D Mouse Model , 2006, Neuron.
[50] J. Thevelein,et al. Disrupted function and axonal distribution of mutant tyrosyl-tRNA synthetase in dominant intermediate Charcot-Marie-Tooth neuropathy , 2006, Nature Genetics.
[51] G. Hennig,et al. Characteristics of intermittent mitochondrial transport in guinea pig enteric nerve fibers. , 2004, American journal of physiology. Gastrointestinal and liver physiology.
[52] Richard A Lewis,et al. Motor unit number estimate of distal and proximal muscles in Charcot–Marie–Tooth disease , 2003, Muscle & nerve.
[53] K. Fischbeck,et al. Glycyl tRNA synthetase mutations in Charcot-Marie-Tooth disease type 2D and distal spinal muscular atrophy type V. , 2003, American journal of human genetics.
[54] F. Speleman,et al. Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes , 2002, Genome Biology.
[55] B. Sefton,et al. Protein kinases. , 1989, Cancer cells.
[56] H. Skre,et al. Genetic and clinical aspects of Charcot‐Marie‐Tooth's disease , 1974, Clinical genetics.