Ganokon Urkasemsin

Urkasemsin, G., Nielsen, D. M., Singleton, A., Arepalli, S., Hernandez, D., Agler, C., & Olby, N. J. (2017). Genetics of Hereditary Ataxia in Scottish Terriers. Journal of Veterinary Internal Medicine, 31(4), 1132–1139. https://doi.org/10.1111/jvim.14738

Urkasemsin, G., & Olby, N. J. (2015). Clinical characteristics of Scottie Cramp in 31 cases. Journal of Small Animal Practice, 56(4), 276–280. https://doi.org/10.1111/jsap.12317

Agler, C., Nielsen, D. M., Urkasemsin, G., Singleton, A., Tonomura, N., Sigurdsson, S., … Harris, T. (2014). Canine hereditary ataxia in Old English Sheepdogs and Gordon Setters is associated with a defect in the autophagy gene encoding RAB24. PLoS Genetics, 10(2).

Ferreira, J. R., Padilla, R., Urkasemsin, G., Yoon, K., Goeckner, K., Hu, W. S., & Ko, C. C. (2013). Titanium-enriched hydroxyapatite-gelatin scaffolds with osteogenically differentiated progenitor cell aggregates for calvaria bone regeneration. Tissue Engineering. Part A, 19(15-16), 1803–1816.

Urkasemsin, G., Linder, K. E., Bell, J. S., Lahunta, A., & Olby, N. J. (2012). Mapping of Purkinje Neuron Loss and Polyglucosan Body Accumulation in Hereditary Cerebellar Degeneration in Scottish Terriers. VETERINARY PATHOLOGY, 49(5), 852–859. https://doi.org/10.1177/0300985811412622

Urkasemsin, G., Linder, K. E., Bell, J. S., Lahunta, A., & Olby, N. J. (2010). Hereditary Cerebellar Degeneration in Scottish Terriers. JOURNAL OF VETERINARY INTERNAL MEDICINE, 24(3), 565–570. https://doi.org/10.1111/j.1939-1676.2010.0499.x