Dr. Christopher Dirk Keene MD, PHD
Neuropathologist | Neuropathology
325 9th Ave Box 359791, Room 2eh Seattle WA, 98104About
Dr. Christopher Keene is a Neuropsychiatrist practicing in Seattle, WA. Dr. Keene studies, evaluates, diagnoses, and treats mental disorders attributable to diseases of the nervous system. Neuropsychiatrists are trained to treat disorders occurring in patients due to irritability, attention deficit disorder, epilepsy, and many other conditions.
Board Certification
PathologyAmerican Board of PathologyABP- Neuropathology
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Human bone marrow stem cells exhibit neural phenotypes and ameliorate neurological deficits after grafting into the ischemic brain of rats.
- Pluripotency of mesenchymal stem cells derived from adult marrow.
- Neural differentiation and incorporation of bone marrow-derived multipotent adult
- Highly resolved in vivo 1H NMR spectroscopy of the mouse brain at 9.4 T.
- Neural induction of adult bone marrow and umbilical cord stem cells.
- Thymidine analogs are transferred from prelabeled donor to host cells in the central nervous system after transplantation: a word of caution.
- Neurochemical changes in Huntington R6/2 mouse striatum detected by in vivo 1H NMR spectroscopy.
- Comparison of analytical mathematical approaches for identifying key nuclear magnetic resonance spectroscopy biomarkers in the diagnosis and assessment of clinical change of diseases.
- Apolipoprotein E isoform-dependent microglia migration.
- Apolipoprotein C-I is an APOE genotype-dependent suppressor of glial activation.
- Gravin is a transitory effector of polo-like kinase 1 during cell division.
- Downregulation of cannabinoid receptor 1 from neuropeptide Y interneurons in the basal ganglia of patients with Huntington's disease and mouse models.
- Ablation of the microglial protein DOCK2 reduces amyloid burden in a mouse model of Alzheimer's disease.
- Perivascular, but not parenchymal, cerebral engraftment of donor cells after non-myeloablative bone marrow transplantation.
- Suppressed retinal degeneration in aged wild type and APPswe/PS1ΔE9 mice by bone marrow transplantation.
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