Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Jody Sandler"'
Autor:
Zhengkui Zhou, Xihui Sheng, Zhiwu Zhang, Keyan Zhao, Lan Zhu, Gang Guo, Steve G Friedenberg, Linda S Hunter, Wendy S Vandenberg-Foels, William E Hornbuckle, Ursula Krotscheck, Elizabeth Corey, Nancy S Moise, Nathan L Dykes, Junya Li, Shangzhong Xu, Lixin Du, Yachun Wang, Jody Sandler, Gregory M Acland, George Lust, Rory J Todhunter
Publikováno v:
PLoS ONE, Vol 5, Iss 10, p e13219 (2010)
BackgroundCanine hip dysplasia (HD) is a common polygenic trait characterized by hip malformation that results in osteoarthritis (OA). The condition in dogs is very similar to developmental dysplasia of the human hip which also leads to OA.Methodolog
Externí odkaz:
https://doaj.org/article/04e0a1af91ff4d2394b08fb768037ae7
Autor:
Rory J. Todhunter, Kang Liu, Nathan L. Dykes, Lan Zhu, Zhiwu Zhang, Paul D. Jones, Ling Xu, Steven Harris, Jody Sandler, Daniel Ogden, George Lust, Faping Duan
Publikováno v:
Journal of Applied Statistics. 40:235-251
The aims of this study were to undertake principal component analysis (PCA) of hip dysplasia (HD) and to examine the power of the principal components (PCs) in genome-wide association studies. A cohort of 278 dogs for PCA and that of 369 dogs for gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cf2778b876a3f5ace8dd66c08a0e417d
https://doi.org/10.1080/02664763.2012.740617
https://doi.org/10.1080/02664763.2012.740617
Autor:
Yuan Zhang, Rory J. Todhunter, Zhengkui Zhou, Gang Guo, Yachun Wang, Stephen Harris, Zhiwu Zhang, Jody Sandler, Paul Glyn Jones, Keyan Zhao, L.S. Hunter, Lan Zhu, Steven G. Friedenberg, Junya Li, Ursula Krotscheck, George Lust
Publikováno v:
Osteoarthritis and Cartilage. 19(4):420-429
Summary Objective To establish a predictive method using whole genome genotyping for early intervention in canine hip dysplasia (CHD) risk management, for the prevention of the progression of secondary osteoarthritis (OA), and for selective breeding.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9909b14cfc1448f7ca6e384f78dccf65
Autor:
Gang Guo, Shang-Zhong Xu, Lixin Du, William E. Hornbuckle, Nathan L. Dykes, Yachun Wang, Gregory M. Acland, Elizabeth Corey, Jody Sandler, Zhiwu Zhang, Nancy S. Moise, Steve G. Friedenberg, Wendy S. Vandenberg-Foels, Keyan Zhao, Ursula Krotscheck, George Lust, Lan Zhu, Xihui Sheng, Junya Li, Zhengkui Zhou, L.S. Hunter, Rory J. Todhunter
Publikováno v:
PLoS ONE, Vol 5, Iss 10, p e13219 (2010)
PLoS ONE
PLoS ONE
BackgroundCanine hip dysplasia (HD) is a common polygenic trait characterized by hip malformation that results in osteoarthritis (OA). The condition in dogs is very similar to developmental dysplasia of the human hip which also leads to OA.Methodolog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::333722d6ed73d4b9a5ac7f6d2dcf19c8
https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/20949002/pdf/?tool=EBI
https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/20949002/pdf/?tool=EBI
Autor:
Zhiwu Zhang, Jody Sandler, N. Sydney Moïse, William E. Hornbuckle, Rory J. Todhunter, Nathan L. Dykes, Jill Egelhoff, Alma J. Williams, Lan Zhu, Ursula Krotscheck, George Lust, Steven S Friedenberg
Publikováno v:
American journal of veterinary research. 70(4)
Objective—To estimate heritabilities and genetic correlations among 4 traits of hip joints (distraction index [DI], dorsolateral subluxation [DLS] score, Norberg angle [NA], and extended–hip joint radiograph [EHR] score) and to derive the breedin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::359404df0b4381a2adb563d5e65837d0
https://pubmed.ncbi.nlm.nih.gov/19335104
https://pubmed.ncbi.nlm.nih.gov/19335104
Autor:
Elizabeth Corey, Rory J. Todhunter, Lan Zhu, Zhiwu Zhang, Janjira Phavaphutanon, Steven G. Friedenberg, Nathan L. Dykes, Jody Sandler, Seung Woo Jung, Gregory M. Acland, Raluca G. Mateescu, Margaret Vernier-Singer, George Lust
Hip dysplasia is a common inherited trait of dogs that results in secondary osteoarthritis. In this article the methods used to uncover the mutations contributing to this condition are reviewed, beginning with hip phenotyping. Coarse, genome-wide, mi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eaf26b2fce10c4a21a31bf95b4592ea0
https://europepmc.org/articles/PMC2679856/
https://europepmc.org/articles/PMC2679856/
