Browsing by Author/Contributor "Sanders, Douglas N., 1973-"

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Accumulation of glial fibrillary acidic protein and histone H4 in brain storage bodies of Tibetan terriers with hereditary neuronal ceroid lipofuscinosis

Katz, Martin L.; Sanders, Douglas N., 1973-; Mooney, Brian P.; Johnson, Gary S. (Springer Netherlands, 2007)

The neuronal ceroid lipofuscinoses (NCLs) are inherited neurodegenerative diseases characterized by massive accumulation of autofluorescent storage bodies in neurons and other cells. A late-onset form of NCL occurs in ...
Autologous bone marrow-derived mesenchymal stem cell transplantation as a therapy for neuronal ceroid lipofuscinosis

Sanders, Douglas N., 1973- (University of Missouri--Columbia, 2007)

The Neuronal Ceroid Lipofuscinoses (NCLs) are a group of rare genetic diseases characterized by neurodegeneration and accumulation of autofluorescent lysosomal storage bodies in numerous cell types. There are currently no ...
Characterization of gene and protein marker expression by human dental pulp stem cells

Wilmore, Lauquyta; Spears, Kathleen; Sanders, Douglas N., 1973-; Kirk, Mark D. (University of Missouri--Columbia. Office of Undergraduate Research, 2008)

Neurodegenerative diseases result from deterioration of neurons or their myelin sheath that over time leads to brain dysfunction and premature death. Cells of the brain and spinal cord do not readily regenerate therefore ...