All Stories

  1. Development of a Polymeric Pharmacological Nanocarrier System as a Potential Therapy for Spinocerebellar Ataxia Type 7

    Article • Cells, November 2023, MDPI AG

    Dr Oscar Hernández-Hernández

  2. RNA Foci Formation in a Retinal Glial Model for Spinocerebellar Ataxia Type 7

    Article • Life, December 2022, MDPI AG

    Dr Oscar Hernández-Hernández

  3. Dp71 Point Mutations Induce Protein Aggregation, Loss of Nuclear Lamina Integrity and Impaired Braf35 and Ibraf Function in Neuronal Cells

    Article • International Journal of Molecular Sciences, October 2022, MDPI AG

    Dr Oscar Hernández-Hernández

  4. Myotonic dystrophy RNA toxicity alters morphology, adhesion and migration of mouse and human astrocytes

    Article • Nature Communications, July 2022, Springer Science + Business Media

    Dr Oscar Hernández-Hernández

  5. Transcriptome Analysis Reveals Altered Inflammatory Pathway in an Inducible Glial Cell Model of Myotonic Dystrophy Type 1

    Article • Biomolecules, January 2021, MDPI AG

    Dr Oscar Hernández-Hernández

  6. Chromatin Landscape During Skeletal Muscle Differentiation

    Article • Frontiers in Genetics, September 2020, Frontiers

    Dr Oscar Hernández-Hernández

  7. Wide Profiling of Circulating MicroRNAs in Spinocerebellar Ataxia Type 7

    Article • Molecular Neurobiology, February 2019, Springer Science + Business Media

    Dr Oscar Hernández-Hernández

  8. Effects of Physical Rehabilitation in Patients with Spinocerebellar Ataxia Type 7

    Article • The Cerebellum, January 2019, Springer Science + Business Media

    Dr Hernán Cortés, Dr Oscar Hernández-Hernández

  9. Oxidative Stress in Spinocerebellar Ataxia Type 7 Is Associated with Disease Severity

    Article • The Cerebellum, June 2018, Springer Science + Business Media

    Dr Oscar Hernández-Hernández

  10. From traditional biochemical signals to molecular markers for detection of sepsis after burn injuries

    Article • Burns, May 2018, Elsevier

    Dr Hernán Cortés, Dr Oscar Hernández-Hernández

  11. Origin of the myotonic dystrophy type 1 mutation in Mexican population and influence of Amerindian ancestry on CTG repeat allelic distribution

    Article • Neuromuscular Disorders, December 2017, Elsevier

    Dr Hernán Cortés, Dr Oscar Hernández-Hernández

  12. A Complete Association of an intronic SNP rs6798742 with Origin of Spinocerebellar Ataxia Type 7-CAG Expansion Loci in the Indian and Mexican Population

    Article • Annals of Human Genetics, June 2017, Wiley

    Dr Oscar Hernández-Hernández

  13. Voice Alterations in Patients With Spinocerebellar Ataxia Type 7 (SCA7): Clinical-Genetic Correlations

    Article • Journal of Voice, January 2017, Elsevier

    Dr Oscar Hernández-Hernández

  14. Flow cytometry for dysferlinopathies

    Article • Muscle & Nerve, October 2016, Wiley

    Dr Laura Sánchez-Chapul, Dr Oscar Hernández-Hernández

  15. Spinocerebellar Ataxia Type 7: A Neurodegenerative Disorder with Peripheral Neuropathy

    Article • European Neurology, January 2015, Karger Publishers

    Dr Oscar Hernández-Hernández

  16. A comprehensive clinical and genetic study of a large Mexican population with spinocerebellar ataxia type 7

    Article • Neurogenetics, October 2014, Springer Science + Business Media

    Dr Oscar Hernández-Hernández

  17. Altered nuclear structure in myotonic dystrophy type 1-derived fibroblasts

    Article • Molecular Biology Reports, October 2014, Springer Science + Business Media

    Dr Oscar Hernández-Hernández

  18. 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

    Article • Biochimica et Biophysica Acta (BBA) - Molecular Cell Research, May 2014, Elsevier

    Dr Oscar Hernández-Hernández

  19. Recessive Spinocerebellar Ataxia with Paroxysmal Cough Attacks: A Report of Five Cases

    Article • The Cerebellum, October 2013, Springer Science + Business Media

    Dr Oscar Hernández-Hernández

  20. Origin of the Spinocerebellar Ataxia Type 7 Gene Mutation in Mexican Population

    Article • The Cerebellum, July 2013, Springer Science + Business Media

    Dr Hernán Cortés, Dr Oscar Hernández-Hernández

  21. Analysis of CAG repeats in five SCA loci in Mexican population: epidemiological evidence of a SCA7 founder effect

    Article • Clinical Genetics, March 2013, Wiley

    Dr Oscar Hernández-Hernández

  22. Myotonic dystrophy CTG expansion affects synaptic vesicle proteins, neurotransmission and mouse behaviour

    Article • Brain, February 2013, Oxford University Press (OUP)

    Dr Oscar Hernández-Hernández

  23. Synaptic protein dysregulation in myotonic dystrophy type 1

    Article • Rare Diseases, January 2013, Taylor & Francis

    Dr Oscar Hernández-Hernández

  24. Identification of a disulfide bridge essential for structure and function of the voltage-gated Ca2+ channel α2δ-1 auxiliary subunit

    Article • Cell Calcium, January 2012, Elsevier

    Dr Oscar Hernández-Hernández

  25. 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

    Article • Molecular Biology Reports, May 2011, Springer Science + Business Media

    Dr Oscar Hernández-Hernández

  26. Recombinant human ZP3-induced sperm acrosome reaction: Evidence for the involvement of T- and L-type voltage-gated calcium channels

    Article • Biochemical and Biophysical Research Communications, May 2010, Elsevier

    Dr Mayel Chirinos, Dr Oscar Hernández-Hernández

  27. Regulation of CaV3.1 Channels by Glucocorticoids

    Article • Cellular and Molecular Neurobiology, June 2009, Springer Science + Business Media

    Dr Oscar Hernández-Hernández

  28. Histamine‐induced Ca2+ entry in human astrocytoma U373 MG cells: Evidence for involvement of store‐operated channels

    Article • Journal of Neuroscience Research, July 2008, Wiley

    Dr Oscar Hernández-Hernández

  29. Myotonic dystrophy CTG repeat expansion alters Ca2+channel functional expression in PC12 cells

    Article • FEBS Letters, August 2007, Wiley

    Dr Oscar Hernández-Hernández

  30. Myotonic dystrophy expanded CUG repeats disturb the expression and phosphorylation of τ in PC12 cells

    Article • Journal of Neuroscience Research, July 2006, Wiley

    Dr Oscar Hernández-Hernández