Douglas N. Sanders, Ph.D.
Affiliations: | 2007 | University of Missouri - Columbia, Columbia, MO, United States |
Area:
Neuroscience Biology, Ophthalmology, Pathology, Cell BiologyGoogle:
"Douglas Sanders"Mean distance: 53433
Parents
Sign in to add mentor| Martin L. Katz | grad student | 2007 | University of Missouri - Columbia | |
| (Autologous bone marrow-derived mesenchymal stem cell transplantation as a therapy for neuronal ceroid lipofuscinosis.) | ||||
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Publications
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| Tracy CJ, Sanders DN, Bryan JN, et al. (2016) Intravitreal Implantation of Genetically Modified Autologous Bone Marrow-Derived Stem Cells for Treating Retinal Disorders. Advances in Experimental Medicine and Biology. 854: 571-7 |
| Sanders DN, Zeng R, Wenger DA, et al. (2013) GM2 gangliosidosis associated with a HEXA missense mutation in Japanese Chin dogs: a potential model for Tay Sachs disease. Molecular Genetics and Metabolism. 108: 70-5 |
| Sanders DN, Kanazono S, Wininger FA, et al. (2011) A reversal learning task detects cognitive deficits in a Dachshund model of late-infantile neuronal ceroid lipofuscinosis. Genes, Brain, and Behavior. 10: 798-804 |
| Farias FH, Zeng R, Johnson GS, et al. (2011) A truncating mutation in ATP13A2 is responsible for adult-onset neuronal ceroid lipofuscinosis in Tibetan terriers. Neurobiology of Disease. 42: 468-74 |
| Katz ML, Farias FH, Sanders DN, et al. (2011) A missense mutation in canine CLN6 in an Australian shepherd with neuronal ceroid lipofuscinosis. Journal of Biomedicine & Biotechnology. 2011: 198042 |
| Sanders DN, Kanazono S, Coates JR, et al. (2010) COGNITIVE DECLINE IN A DOG MODEL FOR AN INHERITED NEURODEGENERATIVE DISEASE USING T-MAZE PERFORMANCE. Journal of Veterinary Behavior : Clinical Applications and Research : Official Journal of : Australian Veterinary Behaviour Interest Group, International Working Dog Breeding Association. 5: 154 |
| Sanders DN, Farias FH, Johnson GS, et al. (2010) A mutation in canine PPT1 causes early onset neuronal ceroid lipofuscinosis in a Dachshund. Molecular Genetics and Metabolism. 100: 349-56 |
| Farias FH, Johnson GS, Taylor JF, et al. (2010) An ADAMTS17 splice donor site mutation in dogs with primary lens luxation. Investigative Ophthalmology & Visual Science. 51: 4716-21 |
| Katz ML, Sanders DN, Mooney BP, et al. (2007) Accumulation of glial fibrillary acidic protein and histone H4 in brain storage bodies of Tibetan terriers with hereditary neuronal ceroid lipofuscinosis. Journal of Inherited Metabolic Disease. 30: 952-63 |
| Katz ML, Wendt KD, Sanders DN. (2005) RPE65 gene mutation prevents development of autofluorescence in retinal pigment epithelial phagosomes. Mechanisms of Ageing and Development. 126: 513-21 |