All Stories

  1. Natural Antioxidants Reduce Oxidative Stress and the Toxic Effects of RNA-CUG(exp) in an Inducible Glial Myotonic Dystrophy Type 1 Cell Model
  2. Enrichment of H3S28p and H3K9me2 Epigenetic Marks on Inflammatory-Associated Gene Promoters in Response to Severe Burn Injury
  3. Development of a Polymeric Pharmacological Nanocarrier System as a Potential Therapy for Spinocerebellar Ataxia Type 7
  4. RNA Foci Formation in a Retinal Glial Model for Spinocerebellar Ataxia Type 7
  5. Dp71 Point Mutations Induce Protein Aggregation, Loss of Nuclear Lamina Integrity and Impaired Braf35 and Ibraf Function in Neuronal Cells
  6. Myotonic dystrophy RNA toxicity alters morphology, adhesion and migration of mouse and human astrocytes
  7. Transcriptome Analysis Reveals Altered Inflammatory Pathway in an Inducible Glial Cell Model of Myotonic Dystrophy Type 1
  8. Chromatin Landscape During Skeletal Muscle Differentiation
  9. Wide Profiling of Circulating MicroRNAs in Spinocerebellar Ataxia Type 7
  10. Effects of Physical Rehabilitation in Patients with Spinocerebellar Ataxia Type 7
  11. Oxidative Stress in Spinocerebellar Ataxia Type 7 Is Associated with Disease Severity
  12. From traditional biochemical signals to molecular markers for detection of sepsis after burn injuries
  13. Origin of the myotonic dystrophy type 1 mutation in Mexican population and influence of Amerindian ancestry on CTG repeat allelic distribution
  14. A Complete Association of an intronic SNP rs6798742 with Origin of Spinocerebellar Ataxia Type 7-CAG Expansion Loci in the Indian and Mexican Population
  15. Voice Alterations in Patients With Spinocerebellar Ataxia Type 7 (SCA7): Clinical-Genetic Correlations
  16. Flow cytometry for dysferlinopathies
  17. Spinocerebellar Ataxia Type 7: A Neurodegenerative Disorder with Peripheral Neuropathy
  18. A comprehensive clinical and genetic study of a large Mexican population with spinocerebellar ataxia type 7
  19. Altered nuclear structure in myotonic dystrophy type 1-derived fibroblasts
  20. Nucleocytoplasmic shuttling of the Duchenne muscular dystrophy gene product dystrophin Dp71d is dependent on the importin α/β and CRM1 nuclear transporters and microtubule motor dynein
  21. Recessive Spinocerebellar Ataxia with Paroxysmal Cough Attacks: A Report of Five Cases
  22. Origin of the Spinocerebellar Ataxia Type 7 Gene Mutation in Mexican Population
  23. Analysis of CAG repeats in five SCA loci in Mexican population: epidemiological evidence of a SCA7 founder effect
  24. Myotonic dystrophy CTG expansion affects synaptic vesicle proteins, neurotransmission and mouse behaviour
  25. Synaptic protein dysregulation in myotonic dystrophy type 1
  26. Identification of a disulfide bridge essential for structure and function of the voltage-gated Ca2+ channel α2δ-1 auxiliary subunit
  27. Myotonic dystrophy type 1-associated CTG repeats disturb the expression and subcellular distribution of microtubule-associated proteins MAP1A, MAP2, and MAP6/STOP in PC12 cells
  28. Recombinant human ZP3-induced sperm acrosome reaction: Evidence for the involvement of T- and L-type voltage-gated calcium channels
  29. Regulation of CaV3.1 Channels by Glucocorticoids
  30. Histamine‐induced Ca2+ entry in human astrocytoma U373 MG cells: Evidence for involvement of store‐operated channels
  31. Myotonic dystrophy CTG repeat expansion alters Ca2+channel functional expression in PC12 cells
  32. Myotonic dystrophy expanded CUG repeats disturb the expression and phosphorylation of τ in PC12 cells