All Stories

  1. Transcriptional dysregulation in the cerebellum triggered by oligodendroglial α-synucleinopathy: insights from a transgenic mouse into the early disease mechanisms of MSA
  2. Nigral Neuroinflammation and Dopaminergic Neurons in Parkinson's Disease and Atypical Parkinsonisms
  3. Rapid iPSC inclusionopathy models shed light on formation, consequence, and molecular subtype of α-synuclein inclusions
  4. Transcriptomic insights into multiple system atrophy from a PLP-α-synuclein transgenic mouse model
  5. Genome sequence analyses identify novel risk loci for multiple system atrophy
  6. Gregor K. Wenning: a brilliant mind
  7. Epsin2, a novel target for multiple system atrophy therapy via α-synuclein/FABP7 propagation
  8. Multiple system atrophy: at the crossroads of cellular, molecular and genetic mechanisms
  9. A Mouse Model of Multiple System Atrophy: Bench to Bedside
  10. Microglia in Parkinson’s Disease
  11. Host oligodendrogliopathy and ɑ-synuclein strains dictate disease severity in multiple system atrophy
  12. The Compound ATH434 Prevents Alpha-Synuclein Toxicity in a Murine Model of Multiple System Atrophy
  13. Spreading of Aggregated α-Synuclein in Sagittal Organotypic Mouse Brain Slices
  14. Therapeutic potential of iron modulating drugs in a mouse model of multiple system atrophy
  15. The Concept of α-Synuclein Strains and How Different Conformations May Explain Distinct Neurodegenerative Disorders
  16. Toll-like receptor 4 deficiency facilitates α-synuclein propagation and neurodegeneration in a mouse model of prodromal Parkinson's disease
  17. Is Multiple System Atrophy a Prion-like Disorder?
  18. Current experimental disease-modifying therapeutics for multiple system atrophy
  19. Neuropathology of multiple system atrophy: Kurt Jellinger`s legacy
  20. ATH434 Reduces α‐Synuclein‐Related Neurodegeneration in a Murine Model of Multiple System Atrophy
  21. Phenotypic Characterization and Brain Structure Analysis of Calcium Channel Subunit α2δ-2 Mutant (Ducky) and α2δ Double Knockout Mice
  22. Shared Genetics of Multiple System Atrophy and Inflammatory Bowel Disease
  23. Targeting α-synuclein by PD03 AFFITOPE® and Anle138b rescues neurodegenerative pathology in a model of multiple system atrophy: clinical relevance
  24. From Synaptic Protein to Prion: The Long and Controversial Journey of α-Synuclein
  25. Signs of early cellular dysfunction in multiple system atrophy
  26. Histone Deacetylase 6 and the Disease Mechanisms of α-Synucleinopathies
  27. Signs of Chronic Hypoxia Suggest a Novel Pathophysiological Event in α‐Synucleinopathies
  28. Shock waves promote spinal cord repair via TLR3
  29. Assessment of the Retina of Plp-α-Syn Mice as a Model for Studying Synuclein-Dependent Diseases
  30. Transcriptional profiling of multiple system atrophy cerebellar tissue highlights differences between the parkinsonian and cerebellar sub-types of the disease
  31. MSA: From basic mechanisms to experimental therapeutics
  32. Genes to treat excitotoxicity ameliorate the symptoms of the disease in mice models of multiple system atrophy
  33. High-salt diet does not boost neuroinflammation and neurodegeneration in a model of α-synucleinopathy
  34. The molecular tweezer CLR01 reduces aggregated, pathologic, and seeding-competent α-synuclein in experimental multiple system atrophy
  35. Neuroinflammation and Glial Phenotypic Changes in Alpha-Synucleinopathies
  36. Induced pluripotent stem cells in multiple system atrophy: recent developments and scientific challenges
  37. L-dopa response pattern in a rat model of mild striatonigral degeneration
  38. Increased anxiety-like behavior following circuit-specific catecholamine denervation in mice
  39. Anle138b modulates α‐synuclein oligomerization and prevents motor decline and neurodegeneration in a mouse model of multiple system atrophy
  40. Region-Specific Effects of Immunotherapy With Antibodies Targeting α-synuclein in a Transgenic Model of Synucleinopathy
  41. Limited effects of dysfunctional macroautophagy on the accumulation of extracellularly derived α-synuclein in oligodendroglia: implications for MSA pathogenesis
  42. Translational therapies for multiple system atrophy: Bottlenecks and future directions
  43. The Relevance of Iron in the Pathogenesis of Multiple System Atrophy: A Viewpoint
  44. Progressive striatonigral degeneration in a transgenic mouse model of multiple system atrophy: translational implications for interventional therapies
  45. Recommendations of the Global Multiple System Atrophy Research Roadmap Meeting
  46. Multiple system atrophy: experimental models and reality
  47. Toll-like receptor 4 stimulation with monophosphoryl lipid A ameliorates motor deficits and nigral neurodegeneration triggered by extraneuronal α-synucleinopathy
  48. Lower Affinity of Isradipine for L-Type Ca2+ Channels during Substantia Nigra Dopamine Neuron-Like Activity: Implications for Neuroprotection in Parkinson's Disease
  49. Very late-onset pure autonomic failure
  50. Distinct Parameters in the EEG of the PLP α-SYN Mouse Model for Multiple System Atrophy Reinforce Face Validity
  51. Neuroprotection by Epigenetic Modulation in a Transgenic Model of Multiple System Atrophy
  52. Anle138b Partly Ameliorates Motor Deficits Despite Failure of Neuroprotection in a Model of Advanced Multiple System Atrophy
  53. Changes in the miRNA-mRNA Regulatory Network Precede Motor Symptoms in a Mouse Model of Multiple System Atrophy: Clinical Implications
  54. Microglia activation as a therapeutic target in multiple system atrophy: the timing, the good and the bad
  55. Preface
  56. Review: Multiple system atrophy: emerging targets for interventional therapies
  57. Toward disease modification in multiple system atrophy: Pitfalls, bottlenecks, and possible remedies
  58. Glia and alpha-synuclein in neurodegeneration: A complex interaction
  59. Overexpression of α-synuclein in oligodendrocytes does not increase susceptibility to focal striatal excitotoxicity
  60. Shock Wave Treatment Protects From Neuronal Degeneration via a Toll‐Like Receptor 3 Dependent Mechanism: Implications of a First‐Ever Causal Treatment for Ischemic Spinal Cord Injury
  61. Involvement of Peripheral Nerves in the Transgenic PLP-α-Syn Model of Multiple System Atrophy: Extending the Phenotype
  62. Enteric nervous system α-synuclein immunoreactivity in idiopathic REM sleep behavior disorder
  63. Alpha-synuclein immunoreactivity patterns in the enteric nervous system
  64. Failure of Neuroprotection Despite Microglial Suppression by Delayed-Start Myeloperoxidase Inhibition in a Model of Advanced Multiple System Atrophy: Clinical Implications
  65. Animal models of multiple system atrophy
  66. Multiple System Atrophy: Genetic or Epigenetic?
  67. Multiple system atrophy as emerging template for accelerated drug discovery in α-synucleinopathies
  68. Towards translational therapies for multiple system atrophy
  69. CaV1.2 Calcium Channel Expression in Reactive Astrocytes is associated with the Formation of Amyloid-β Plaques in an Alzheimer's Disease Mouse Model
  70. Oligodendroglial alpha-synucleinopathy and MSA-like cardiovascular autonomic failure: Experimental evidence
  71. Intact Olfaction in a Mouse Model of Multiple System Atrophy
  72. Bladder dysfunction in a transgenic mouse model of multiple system atrophy
  73. Models of Multiple System Atrophy
  74. Cell Fate Analysis of Embryonic Ventral Mesencephalic Grafts in the 6-OHDA Model of Parkinson's Disease
  75. Toll‐like receptor 4 is required for α‐synuclein dependent activation of microglia and astroglia
  76. The Role of Glia in Alpha-Synucleinopathies
  77. Systemic proteasome inhibition triggers neurodegeneration in a transgenic mouse model expressing human α-synuclein under oligodendrocyte promoter: implications for multiple system atrophy
  78. Myeloperoxidase Inhibition Ameliorates Multiple System Atrophy-Like Degeneration in a Transgenic Mouse Model
  79. Toll-Like Receptor 4 Promotes α-Synuclein Clearance and Survival of Nigral Dopaminergic Neurons
  80. Mesenchymal Stem Cells in a Transgenic Mouse Model of Multiple System Atrophy: Immunomodulation and Neuroprotection
  81. Glial dysfunction in the pathogenesis of α-synucleinopathies: emerging concepts
  82. Nogo-B is associated with cytoskeletal structures in human monocyte-derived macrophages
  83. Erythropoietin is neuroprotective in a transgenic mouse model of multiple system atrophy
  84. Targeted overexpression of human α-synuclein in oligodendroglia induces lesions linked to MSA -like progressive autonomic failure
  85. Kappa opioid receptor activation blocks progressive neurodegeneration after kainic acid injection
  86. Multiple system atrophy: an update
  87. Mitochondrial inhibitor 3-nitroproprionic acid enhances oxidative modification of alpha-synuclein in a transgenic mouse model of multiple system atrophy
  88. Striatal transplantation for multiple system atrophy — Are grafts affected by α-synucleinopathy?
  89. Recent developments in multiple system atrophy
  90. Striatal transplantation in a rodent model of multiple system atrophy: Effects on L-Dopa response
  91. Multiple system atrophy: A primary oligodendrogliopathy
  92. Rasagiline is neuroprotective in a transgenic model of multiple system atrophy
  93. Axl and Growth Arrest–Specific Gene 6 Are Frequently Overexpressed in Human Gliomas and Predict Poor Prognosis in Patients with Glioblastoma Multiforme
  94. Microglial activation mediates neurodegeneration related to oligodendroglial α-synucleinopathy: Implications for multiple system atrophy
  95. High dose levodopa therapy is not toxic in multiple system atrophy: Experimental evidence
  96. Loss of dopaminergic responsiveness in a double lesion rat model of the Parkinson variant of multiple system atrophy
  97. Evidence for dopaminergic re-innervation by embryonic allografts in an optimized rat model of the Parkinsonian variant of multiple system atrophy
  98. Animal models of multiple system atrophy
  99. Oxidative Stress in Transgenic Mice with Oligodendroglial α-Synuclein Overexpression Replicates the Characteristic Neuropathology of Multiple System Atrophy
  100. Evaluation of [123I]IBZM pinhole SPECT for the detection of striatal dopamine D2 receptor availability in rats
  101. In vitro models of multiple system atrophy
  102. Riluzole improves motor deficits and attenuates loss of striatal neurons in a sequential double lesion rat model of striatonigral degeneration (parkinson variant of multiple system atrophy)
  103. Failure of caspase inhibition in the double-lesion rat model of striatonigral degeneration (multiple system atrophy)
  104. Effects of pulsatile l-DOPA treatment in the double lesion rat model of striatonigral degeneration (multiple system atrophy)
  105. Neuroprotective agents for clinical trials in Parkinson's disease: A systematic assessment
  106. Failure of neuronal protection by inhibition of glial activation in a rat model of striatonigral degeneration
  107. Neuropathological and behavioral changes induced by various treatment paradigms with MPTP and 3-nitropropionic acid in mice: towards a model of striatonigral degeneration (multiple system atrophy)
  108. Tumor necrosis factor-?-induced cell death in U373 cells overexpressing ?-synuclein
  109. Dystonia is predictive of subsequent altered dopaminergic responsiveness in a chronic 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine+3-nitropropionic acid model of striatonigral degeneration in monkeys
  110. Freezing of gait in postmortem‐confirmed atypical parkinsonism
  111. Ultrastructure of α-synuclein-positive aggregations in U373 astrocytoma and rat primary glial cells
  112. Overstimulation of the α1B-adrenergic receptor causes a “seizure plus” syndrome
  113. Glial cell death induced by overexpression of ?-synuclein
  114. Multiple System Atrophy
  115. Failure of Neuroprotection by Embryonic Striatal Grafts in a Double Lesion Rat Model of Striatonigral Degeneration (Multiple System Atrophy)
  116. γ-Aminobutyric acid-immunoreactive neurons in the amygdala of the rat – sex differences and effect of early postnatal castration
  117. Sex and age differences of neurons expressing gaba‐immunoreactivity in the rat bed nucleus of the stria terminalis