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Timothy David Maley

  • Lecturer, Physiology - (Educator Series Track)
Contact
  • maleytim@arizona.edu
  • Bio
  • Interests
  • Courses
  • Scholarly Contributions

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Courses

2025-26 Courses

  • Human Anat+Physiology I
    PSIO 201 (Spring 2026)
  • Human Anat+Physiology II
    PSIO 202 (Spring 2026)
  • Independent Study
    PSIO 499 (Spring 2026)
  • Independent Study
    PSIO 699 (Spring 2026)
  • Human Anat+Physiology I
    PSIO 201 (Fall 2025)
  • Human Anat+Physiology II
    PSIO 202 (Fall 2025)
  • Independent Study
    PSIO 499 (Fall 2025)
  • Independent Study
    PSIO 599 (Fall 2025)

2024-25 Courses

  • Human Anat+Physiology I
    PSIO 201 (Summer I 2025)
  • Human Anat+Physiology I
    PSIO 201 (Spring 2025)
  • Human Anat+Physiology II
    PSIO 202 (Spring 2025)

2017-18 Courses

  • Human Anat+Physiology II
    PSIO 202 (Spring 2018)

Related Links

UA Course Catalog

Scholarly Contributions

Journals/Publications

  • Corenblum, M. J., McRobbie-Johnson, A., Carruth, E., Bernard, K., Luo, M., Mandarino, L. J., Peterson, S., Sans-Fuentes, M. A., Billheimer, D., Maley, T., Eggers, E. D., & Madhavan, L. (2023). Parallel neurodegenerative phenotypes in sporadic Parkinson's disease fibroblasts and midbrain dopamine neurons. Progress in neurobiology, 229, 102501.
    More info
    Understanding the mechanisms causing Parkinson's disease (PD) is vital to the development of much needed early diagnostics and therapeutics for this debilitating condition. Here, we report cellular and molecular alterations in skin fibroblasts of late-onset sporadic PD subjects, that were recapitulated in matched induced pluripotent stem cell (iPSC)-derived midbrain dopamine (DA) neurons, reprogrammed from the same fibroblasts. Specific changes in growth, morphology, reactive oxygen species levels, mitochondrial function, and autophagy, were seen in both the PD fibroblasts and DA neurons, as compared to their respective controls. Additionally, significant alterations in alpha synuclein expression and electrical activity were also noted in the PD DA neurons. Interestingly, although the fibroblast and neuronal phenotypes were similar to each other, they differed in their nature and scale. Furthermore, statistical analysis revealed potential novel associations between various clinical measures of the PD subjects and the different fibroblast and neuronal data. In essence, these findings encapsulate spontaneous, in-tandem, disease-related phenotypes in both sporadic PD fibroblasts and iPSC-based DA neurons, from the same patient, and generates an innovative model to investigate PD mechanisms with a view towards rational disease stratification and precision treatments.

Presentations

  • Stanescu, C. I., Klass, M. M., Maley, T. D., McRobbie-Johnson, A. C., Agosttini, J. A., Lease, H. M., Roof, A. K., & Mcnabney, D. R. (2025).

    Creation and Implementation of Low-Cost, Inclusive Course Materials in a Two-Semester Human Anatomy & Physiology Course Sequence.

    . Physiology Majors Interest Group (P-MIG) Conference. Gonzaga University.

Profiles With Related Publications

  • Allyson K Roof
  • Dan McNabney
  • Hilary M. Lease
  • Claudia I Stanescu
  • Mattie Michael Klass

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