All Stories

  1. The interplay of aging, genetics and environmental factors in the pathogenesis of Parkinson’s disease
  2. Age-dependent accumulation of oligomeric SNCA/α-synuclein from impaired degradation in mutant LRRK2 knockin mouse model of Parkinson disease: role for therapeutic activation of chaperone-mediated autophagy (CMA)
  3. Role of Nurr1 in the regulation of Synaptogyrin 3 (SYNGR3)
  4. Activation of hypothalamic RIP‐Cre neurons promotes beiging of WAT via sympathetic nervous system
  5. Development of phospho-specific Rab protein antibodies to monitor in vivo activity of the LRRK2 Parkinson's disease kinase
  6. Combined LRRK2 mutation, aging and chronic low dose oral rotenone as a model of Parkinson’s disease
  7. Chronic adiponectin deficiency leads to Alzheimer’s disease-like cognitive impairments and pathologies through AMPK inactivation and cerebral insulin resistance in aged mice
  8. Deficiency of Cks1 Leads to Learning and Long-Term Memory Defects and p27 Dependent Formation of Neuronal Cofilin Aggregates
  9. Phos-tag analysis of Rab10 phosphorylation by LRRK2: a powerful assay for assessing kinase function and inhibitors
  10. Revealing ecological risks of priority endocrine disrupting chemicals in four marine protected areas in Hong Kong through an integrative approach
  11. Efficient attenuation of Friedreich's ataxia (FRDA) cardiomyopathy by modulation of iron homeostasis-human induced pluripotent stem cell (hiPSC) as a drug screening platform for FRDA
  12. PMCA 4 ( ATP 2B4) mutation in familial spastic paraplegia causes delay in intracellular calcium extrusion
  13. PMCA4 (ATP2B4) Mutation in Familial Spastic Paraplegia
  14. LRRK2 R1441G mice are more liable to dopamine depletion and locomotor inactivity
  15. Modeling of Friedreich ataxia-related iron overloading cardiomyopathy using patient-specific-induced pluripotent stem cells
  16. Assessment of Cellular Estrogenic Activity Based on Estrogen Receptor-Mediated Reduction of Soluble-Form Catechol-O-Methyltransferase (COMT) Expression in an ELISA-Based System
  17. Central nervous system inflammatory demyelinating disorders among Hong Kong Chinese
  18. Modeling of Friedreich Ataxia related iron overloading cardiomyopathy using patient-specific induced pluripotent stem cellsCellp
  19. Human Mesenchymal Stem Cells Upregulate CD1dhighCD5+Regulatory B Cells in Experimental Autoimmune Encephalomyelitis
  20. Adiponectin is Protective against Oxidative Stress Induced Cytotoxicity in Amyloid-Beta Neurotoxicity
  21. UCP4 is a target effector of the NF-κB c-Rel prosurvival pathway against oxidative stress
  22. Plasma amyloid-β oligomers level is a biomarker for Alzheimer’s disease diagnosis
  23. Human neuronal uncoupling proteins 4 and 5 (UCP4 and UCP5): structural properties, regulation, and physiological role in protection against oxidative stress and mitochondrial dysfunction
  24. Aquaporin-4 autoantibodies cause asymptomatic aquaporin-4 loss and activate astrocytes in mouse
  25. Detection of endocrine disruptors - from simple assays to whole genome scanning
  26. Uncoupling Protein-4 (UCP4) Increases ATP Supply by Interacting with Mitochondrial Complex II in Neuroblastoma Cells
  27. Mitochondrial neuronal uncoupling proteins: a target for potential disease-modification in Parkinson's disease
  28. Brain Involvement in Neuromyelitis Optica Spectrum Disorders
  29. Clinical outcome of relapsing remitting multiple sclerosis among Hong Kong Chinese
  30. Aquaporin-4 water channel expression by thymoma of patients with and without myasthenia gravis
  31. Mitochondrial UCP5 is neuroprotective by preserving mitochondrial membrane potential, ATP levels, and reducing oxidative stress in MPP+ and dopamine toxicity
  32. Transcriptional regulation of UCP4 by NF-κB and its role in mediating protection against MPP+ toxicity
  33. Aquaporin-4 autoantibodies in neuromyelitis optica spectrum disorders: comparison between tissue-based and cell-based indirect immunofluorescence assays
  34. Mitochondrial Uncoupling Protein-2 (UCP2) Mediates Leptin Protection Against MPP+ Toxicity in Neuronal Cells
  35. Mitochondrial UCP4 attenuates MPP+- and dopamine-induced oxidative stress, mitochondrial depolarization, and ATP deficiency in neurons and is interlinked with UCP2 expression
  36. −459C>T point mutation in 5′ non-coding region of humanGJB1gene is linked to X-linked Charcot-Marie-Tooth neuropathy
  37. Effects of Plasticisers and Related Compounds on the Expression of the Soluble Form of Catechol-O-Methyltransferase in MCF-7 Cells
  38. Estrogenic Phenol and Catechol Metabolites of PCBs Modulate Catechol-Omethyltransferase Expression Via the Estrogen Receptor: Potential Contribution to Cancer Risk
  39. Abnormal diffusion tensor in nonsymptomatic familial amyotrophic lateral sclerosis with a causative superoxide dismutase 1 mutation
  40. Knockdown of uncoupling protein-5 in neuronal SH-SY5Y cells: Effects on MPP+-induced mitochondrial membrane depolarization, ATP deficiency, and oxidative cytotoxicity
  41. Clinical phenotypes of a large Chinese multigenerational kindred with autosomal dominant familial ALS due to Ile149Thr SOD1 gene mutation
  42. Uncoupling proteins: Targets of endocrine disruptors?
  43. Methyl-4-phenylpyridinium ion modulates expression of mitochondrial uncoupling proteins 2, 4, and 5 in catecholaminergic (SK-N-SH) cells
  44. Bis(7)-tacrine, a novel acetylcholinesterase inhibitor, reverses AF64A-induced deficits in navigational memory in rats
  45. Effects of bis(7)-tacrine, a novel anti-Alzheimerʼs agent, on rat brain AChE