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pro vyhledávání: '"Samantha L, Van Buren"'
Publikováno v:
Vet Rec
BACKGROUND The features of juvenile-onset calcium oxalate urolithiasis in dogs have not been previously reported. METHODS Calcium oxalate urolith submissions to the Minnesota Urolith Center between 2012 and 2016 were analyzed to identify those origin
Publikováno v:
Animal geneticsReferences. 52(2)
Autor:
Samantha L, Van Buren, Katie M, Minor, Robert A, Grahn, James R, Mickelson, Jennifer C, Grahn, Julia, Malvick, Jennifer R, Colangelo, Elisabeth, Mueller, Petra, Kuehnlein, Alexandra, Kehl
Publikováno v:
Genes
Altered melanosome transport in melanocytes, resulting from variants in the melanophilin (MLPH) gene, are associated with inherited forms of coat color dilution in many species. In dogs, the MLPH gene corresponds to the D locus and two variants, c.
Autor:
G. Diane Shelton, Rupleen Kaur, Carsten G. Bönnemann, Samantha L. Van Buren, Véronique Bolduc, James R. Mickelson, Joseph C. Glennon, Katia Marioni-Henry, Katie M. Minor, Ying Hu, Ling T. Guo, Steven G. Friedenberg
Publikováno v:
Bolduc, V, Minor, K M, Hu, Y, Kaur, R, Friedenberg, S G, Van Buren, S, Guo, L T, Glennon, J C, Marioni-Henry, K, Mickelson, J R, Bönnemann, C G & Shelton, G D 2020, ' Pathogenic variants in COL6A3 cause Ullrich-like congenital muscular dystrophy in young Labrador Retriever dogs ', Neuromuscular Disorders . https://doi.org/10.1016/j.nmd.2020.03.005
Neuromuscul Disord
Neuromuscular disorders : NMD, vol 30, iss 5
Neuromuscul Disord
Neuromuscular disorders : NMD, vol 30, iss 5
The collagen VI-related muscular dystrophies in people include a broad spectrum of diseases ranging from the severe Ullrich congenital muscular dystrophy to the mild Bethlem myopathy. Clinical features are attributable to both muscle and connective t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7748580a3e84ca0d7e584f31528344ea
https://hdl.handle.net/20.500.11820/88a17405-d60d-467d-a0d5-a5893725a50f
https://hdl.handle.net/20.500.11820/88a17405-d60d-467d-a0d5-a5893725a50f
Publikováno v:
Anim Genet