Ngā hua rapu - Mark W Neff

Partial deletion of the sulfate transporter SLC13A1 is associated with an osteochondrodysplasia in the Miniature Poodle breed. mā Mark W Neff, John S Beck, Julie M Koeman, Elissa Boguslawski, Lisa Kefene, Andrew Borgman, Alison L Ruhe

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Variation in genes related to cochlear biology is strongly associated with adult-onset deafness in border collies. mā Jennifer S Yokoyama, Ernest T Lam, Alison L Ruhe, Carolyn A Erdman, Kathryn R Robertson, Aubrey A Webb, D Colette Williams, Melanie L Chang, Marjo K Hytönen, Hannes Lohi, Steven P Hamilton, Mark W Neff

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An ADAMTSL2 founder mutation causes Musladin-Lueke Syndrome, a heritable disorder of beagle dogs, featuring stiff skin and joint contractures. mā Hannah L Bader, Alison L Ruhe, Lauren W Wang, Aaron K Wong, Kari F Walsh, Rebecca A Packer, Jonathan Mitelman, Kathryn R Robertson, Dennis P O'Brien, Karl W Broman, G Diane Shelton, Suneel S Apte, Mark W Neff

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Somatic inactivating PTPRJ mutations and dysregulated pathways identified in canine malignant melanoma by integrated comparative genomic analysis. mā William P D Hendricks, Victoria Zismann, Karthigayini Sivaprakasam, Christophe Legendre, Kelsey Poorman, Waibhav Tembe, Nieves Perdigones, Jeffrey Kiefer, Winnie Liang, Valerie DeLuca, Mitchell Stark, Alison Ruhe, Roe Froman, Nicholas S Duesbery, Nicholas S Duesbery, Megan Washington, Jessica Aldrich, Mark W Neff, Matthew J Huentelman, Nicholas Hayward, Kevin Brown, Douglas Thamm, Gerald Post, Chand Khanna, Barbara Davis, Matthew Breen, Alexander Sekulic, Jeffrey M Trent

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