Peripheral nerve injury elicits microstructural and neurochemical changes in the striatum and substantia nigra of a DYT-TOR1A mouse model with dystonia-like movements

[1]  Aya Takeoka,et al.  Neurotransmitter phenotype switching by spinal excitatory interneurons regulates locomotor recovery after spinal cord injury , 2022, Nature neuroscience.

[2]  C. Takayama,et al.  Slow progression of sciatic nerve degeneration and regeneration after loose ligation through microglial activation and decreased KCC2 levels in the mouse spinal cord ventral horn , 2021, Neuroscience Research.

[3]  D. Ladle,et al.  Calcium Homeostasis in Parvalbumin DRG Neurons is Altered After Sciatic Nerve Crush and Sciatic Nerve Transection Injuries. , 2021, Journal of neurophysiology.

[4]  M. Hallett,et al.  Second hit hypothesis in dystonia: Dysfunctional cross talk between neuroplasticity and environment? , 2021, Neurobiology of Disease.

[5]  J. Volkmann,et al.  Multifactorial Assessment of Motor Behavior in Rats after Unilateral Sciatic Nerve Crush Injury. , 2021, Journal of visualized experiments : JoVE.

[6]  J. Volkmann,et al.  The evolution of dystonia-like movements in TOR1A rats after transient nerve injury is accompanied by dopaminergic dysregulation and abnormal oscillatory activity of a central motor network , 2021, Neurobiology of Disease.

[7]  M. Miyata,et al.  Brainstem local microglia induce whisker map plasticity in the thalamus after peripheral nerve injury. , 2021, Cell reports.

[8]  W. Dauer,et al.  TorsinA restoration in a mouse model identifies a critical therapeutic window for DYT1 dystonia. , 2021, The Journal of clinical investigation.

[9]  I. König,et al.  Genotype–Phenotype Relations for Isolated Dystonia Genes: MDSGene Systematic Review , 2021, Movement disorders : official journal of the Movement Disorder Society.

[10]  Eric S. Kuebler,et al.  Neuronal hypertrophy dampens neuronal intrinsic excitability and stress responsiveness during chronic stress , 2020, The Journal of physiology.

[11]  J. Volkmann,et al.  Striatal dopaminergic dysregulation and dystonia-like movements induced by sensorimotor stress in a pharmacological mouse model of rapid-onset dystonia-parkinsonism , 2019, Experimental Neurology.

[12]  M. Edwards,et al.  Peripheral trauma and risk of dystonia: What are the evidences and potential co-risk factors from a population insurance database? , 2019, PloS one.

[13]  K. Bhatia,et al.  Pseudodystonia: A new perspective on an old phenomenon. , 2019, Parkinsonism & related disorders.

[14]  N. Spitzer,et al.  Exercise enhances motor skill learning by neurotransmitter switching in the adult midbrain , 2019, bioRxiv.

[15]  E. Bézard,et al.  RGS9‐2 rescues dopamine D2 receptor levels and signaling in DYT1 dystonia mouse models , 2018, EMBO molecular medicine.

[16]  Marcie L. Rabin,et al.  Hypertrophy of nigral neurons in Torsin1A deletion (DYT1) carriers manifesting dystonia. , 2019, Parkinsonism & related disorders.

[17]  Kevin M. Cury,et al.  DeepLabCut: markerless pose estimation of user-defined body parts with deep learning , 2018, Nature Neuroscience.

[18]  K. Deisseroth,et al.  Neuronal activity regulates neurotransmitter switching in the adult brain following light-induced stress , 2018, Proceedings of the National Academy of Sciences.

[19]  A. Pisani,et al.  Early structural and functional plasticity alterations in a susceptibility period of DYT1 dystonia mouse striatum , 2018, eLife.

[20]  W. Dauer,et al.  TorsinA dysfunction causes persistent neuronal nuclear pore defects , 2018, Human molecular genetics.

[21]  J. Rothwell,et al.  Dystonia , 1996, Nature Reviews Disease Primers.

[22]  D. Standaert,et al.  Strength of cholinergic tone dictates the polarity of dopamine D2 receptor modulation of striatal cholinergic interneuron excitability in DYT1 dystonia , 2017, Experimental Neurology.

[23]  A. Richter,et al.  Altered postnatal maturation of striatal GABAergic interneurons in a phenotypic animal model of dystonia , 2017, Experimental Neurology.

[24]  M. Ehrlich,et al.  Disruption of Protein Processing in the Endoplasmic Reticulum of DYT1 Knock-in Mice Implicates Novel Pathways in Dystonia Pathogenesis , 2016, The Journal of Neuroscience.

[25]  J. Volkmann,et al.  Tor1a+/- mice develop dystonia-like movements via a striatal dopaminergic dysregulation triggered by peripheral nerve injury , 2016, Acta neuropathologica communications.

[26]  Philippe Collas,et al.  The Nuclear Envelope , 2016, Methods in Molecular Biology.

[27]  P. Shortland,et al.  Effects of peripheral nerve injury on parvalbumin expression in adult rat dorsal root ganglion neurons , 2015, BMC Neuroscience.

[28]  D. Inta,et al.  New neurons in the adult striatum: from rodents to humans , 2015, Trends in Neurosciences.

[29]  G. Foffani,et al.  Increased cortical responses to forepaw stimuli immediately after peripheral deafferentation of hindpaw inputs , 2014, Scientific Reports.

[30]  A. Pisani,et al.  Anticholinergic drugs rescue synaptic plasticity in DYT1 dystonia: Role of M1 muscarinic receptors , 2014, Movement disorders : official journal of the Movement Disorder Society.

[31]  Samuel Bernard,et al.  Neurogenesis in the Striatum of the Adult Human Brain , 2014, Cell.

[32]  M. Hallett,et al.  Phenomenology and classification of dystonia: A consensus update , 2013, Movement disorders : official journal of the Movement Disorder Society.

[33]  Y. Smith,et al.  Subtle microstructural changes of the striatum in a DYT1 knock-in mouse model of dystonia , 2013, Neurobiology of Disease.

[34]  M. Edwards,et al.  Extragenetic factors and clinical penetrance of DYT1 dystonia: an exploratory study , 2013, Journal of Neurology.

[35]  H. Jinnah,et al.  Functional analysis of dopaminergic systems in a DYT1 knock-in mouse model of dystonia , 2012, Neurobiology of Disease.

[36]  A. Pisani,et al.  Cholinergic dysregulation produced by selective inactivation of the dystonia-associated protein torsinA , 2012, Neurobiology of Disease.

[37]  A. Pisani,et al.  Generation of a novel rodent model for DYT1 dystonia , 2012, Neurobiology of Disease.

[38]  D. Lovinger,et al.  An anticholinergic reverses motor control and corticostriatal LTD deficits in Dyt1 ΔGAG knock-in mice , 2012, Behavioural Brain Research.

[39]  C. Lansink,et al.  Role for mTOR Signaling and Neuronal Activity in Morphine-Induced Adaptations in Ventral Tegmental Area Dopamine Neurons , 2011, Neuron.

[40]  Anatol C. Kreitzer,et al.  Selective Inhibition of Striatal Fast-Spiking Interneurons Causes Dyskinesias , 2011, The Journal of Neuroscience.

[41]  D. Standaert,et al.  Motor Deficits and Decreased Striatal Dopamine Receptor 2 Binding Activity in the Striatum-Specific Dyt1 Conditional Knockout Mice , 2011, PloS one.

[42]  A. Pisani,et al.  Developmental Profile of the Aberrant Dopamine D2 Receptor Response in Striatal Cholinergic Interneurons in DYT1 Dystonia , 2011, PloS one.

[43]  S. Lehéricy,et al.  The functional neuroanatomy of dystonia , 2011, Neurobiology of Disease.

[44]  Miklos Argyelan,et al.  Impaired sequence learning in dystonia mutation carriers: a genotypic effect. , 2011, Brain : a journal of neurology.

[45]  G. Bernardi,et al.  Dopamine D2 receptor dysfunction is rescued by adenosine A2A receptor antagonism in a model of DYT1 dystonia , 2010, Neurobiology of Disease.

[46]  E. Altenmüller,et al.  Focal dystonia in musicians: phenomenology, pathophysiology, triggering factors, and treatment. , 2010, Medical problems of performing artists.

[47]  P. Lockhart,et al.  Mutant torsinA interacts with tyrosine hydroxylase in cultured cells , 2009, Neuroscience.

[48]  G. Bernardi,et al.  Impairment of bidirectional synaptic plasticity in the striatum of a mouse model of DYT1 dystonia: role of endogenous acetylcholine. , 2009, Brain : a journal of neurology.

[49]  Richard J Smeyne,et al.  A comparison of model-based (2D) and design-based (3D) stereological methods for estimating cell number in the substantia nigra pars compacta (SNpc) of the C57BL/6J mouse , 2009, Neuroscience.

[50]  V. Dhawan,et al.  Abnormal striatal and thalamic dopamine neurotransmission , 2009, Neurology.

[51]  I. König,et al.  THE D216H VARIANT IN THE DYT1 GENE: A SUSCEPTIBILITY FACTOR FOR DYSTONIA IN FAMILIAL CASES? , 2009, Neurology.

[52]  G. Bernardi,et al.  Impaired striatal D2 receptor function leads to enhanced GABA transmission in a mouse model of DYT1 dystonia , 2009, Neurobiology of Disease.

[53]  M. Vidailhet,et al.  Case-control study of writer's cramp. , 2009, Brain : a journal of neurology.

[54]  M. LeDoux,et al.  Abnormal motor function and dopamine neurotransmission in DYT1 ΔGAG transgenic mice , 2008, Experimental Neurology.

[55]  M. Hallett,et al.  The pathophysiological basis of dystonias , 2008, Nature Reviews Neuroscience.

[56]  Jon H. Kaas,et al.  Cortical and subcortical plasticity in the brains of humans, primates, and rats after damage to sensory afferents in the dorsal columns of the spinal cord , 2008, Experimental Neurology.

[57]  G. Vanhoutte,et al.  Overexpression of human wildtype torsinA and human ΔGAG torsinA in a transgenic mouse model causes phenotypic abnormalities , 2007, Neurobiology of Disease.

[58]  N. Risch,et al.  Intragenic Cis and Trans modification of genetic susceptibility in DYT1 torsion dystonia. , 2007, American journal of human genetics.

[59]  J. Jankovic,et al.  Runner's dystonia , 2006, Journal of the Neurological Sciences.

[60]  Fumiaki Yokoi,et al.  Motor deficits and hyperactivity in Dyt1 knockdown mice , 2006, Neuroscience Research.

[61]  T. Illig,et al.  Strong genetic evidence for association of TOR1A/TOR1B with idiopathic dystonia , 2006, Neurology.

[62]  G. Bernardi,et al.  Altered responses to dopaminergic D2 receptor activation and N-type calcium currents in striatal cholinergic interneurons in a mouse model of DYT1 dystonia , 2006, Neurobiology of Disease.

[63]  A. Lees,et al.  Case of DYT1 dystonia triggered by bite from a moray , 2006, Movement disorders : official journal of the Movement Disorder Society.

[64]  A. Richter,et al.  Striatal microinjections of nitric oxide synthase inhibitors and l-arginine fail to exert effects on paroxysmal dystonia in the dt sz mutant , 2006, Neuroscience Letters.

[65]  M. Hamann,et al.  Age‐related changes in striatal nitric oxide synthase‐immunoreactive interneurones in the dystonic dt sz mutant hamster , 2006 .

[66]  W. Dauer,et al.  Loss of the Dystonia-Associated Protein TorsinA Selectively Disrupts the Neuronal Nuclear Envelope , 2005, Neuron.

[67]  M. Hamann,et al.  Age-Dependent Alterations of Striatal Calretinin Interneuron Density in a Genetic Animal Model of Primary Paroxysmal Dystonia , 2005, Journal of neuropathology and experimental neurology.

[68]  M. Baxter,et al.  Impaired Motor Learning in Mice Expressing TorsinA with the DYT1 Dystonia Mutation , 2005, The Journal of Neuroscience.

[69]  V. Dhawan,et al.  Decreased striatal D2 receptor binding in non-manifesting carriers of the DYT1 dystonia mutation , 2005, Neurology.

[70]  D. Truong,et al.  Natural history of posttraumatic cervical dystonia , 2004, Movement disorders : official journal of the Movement Disorder Society.

[71]  B. Ganetzky,et al.  A Drosophila model of early onset torsion dystonia suggests impairment in TGF-beta signaling. , 2004, Human molecular genetics.

[72]  William T Dauer,et al.  Mislocalization to the nuclear envelope: an effect of the dystonia-causing torsinA mutation. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[73]  S. Bressman,et al.  Penetrance and expression of dystonia genes. , 2004, Advances in neurology.

[74]  H. Siebner,et al.  Abnormal associative plasticity of the human motor cortex in writer's cramp. , 2003, Brain : a journal of neurology.

[75]  M. Ghilardi,et al.  Impaired sequence learning in carriers of the DYT1 dystonia mutation , 2003, Annals of neurology.

[76]  M. Edwards,et al.  Unusual phenotypes in DYT1 dystonia: A report of five cases and a review of the literature , 2003, Movement disorders : official journal of the Movement Disorder Society.

[77]  S. Augood,et al.  TorsinA protein and neuropathology in early onset generalized dystonia with GAG deletion , 2003, Neurobiology of Disease.

[78]  S. Augood,et al.  Dopamine transmission in DYT1 dystonia: A biochemical and autoradiographical study , 2002, Neurology.

[79]  Laurie Ozelius,et al.  Intrafamilial phenotypic variability of the DYT1 dystonia: From asymptomatic TOR1A gene carrier status to dystonic storm , 2002, Movement disorders : official journal of the Movement Disorder Society.

[80]  G. Beer,et al.  Standardizing Nerve Crushes with a Non-Serrated Clamp , 2001, Journal of reconstructive microsurgery.

[81]  M. Gernert,et al.  Deficit of Striatal Parvalbumin-Reactive GABAergic Interneurons and Decreased Basal Ganglia Output in a Genetic Rodent Model of Idiopathic Paroxysmal Dystonia , 2000, The Journal of Neuroscience.

[82]  A. A. Reilly,et al.  Habituation of Activity in an Open Field: A Survey of Inbred Strains and F1 Hybrids , 2000, Behavior genetics.

[83]  A. Berardelli,et al.  Possible risk factors for primary adult onset dystonia: a case-control investigation by the Italian Movement Disorders Study Group , 1998, Journal of neurology, neurosurgery, and psychiatry.

[84]  S. Mackinnon,et al.  Nerve Crush Injuries—A Model for Axonotmesis , 1994, Experimental Neurology.

[85]  A. Seaber,et al.  The functional recovery of peripheral nerves following defined acute crush injuries , 1992, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.

[86]  N. Risch,et al.  Segregation analysis of idiopathic torsion dystonia in Ashkenazi Jews suggests autosomal dominant inheritance. , 1990, American journal of human genetics.

[87]  G. Lundborg,et al.  Mechanical effects of compression of peripheral nerves. , 1986, Journal of biomechanical engineering.

[88]  C. Marsden,et al.  TRAUMA AND PAIN IN SPASMODIC TORTICOLLIS , 1980, The Lancet.

[89]  D. Sholl Dendritic organization in the neurons of the visual and motor cortices of the cat. , 1953, Journal of anatomy.

[90]  JoVE Video Dataset , 2022 .