Zobrazeno 1 - 10
of 97
pro vyhledávání: '"Paula S. Henthorn"'
Publikováno v:
Canine Medicine and Genetics, Vol 7, Iss 1, Pp 1-6 (2020)
Abstract Background Evidence for an autoimmune etiology in canine diabetes is inconsistent and could vary based on breed. Previous studies demonstrated that small percentages of diabetic dogs possess autoantibodies to antigens known to be important i
Externí odkaz:
https://doaj.org/article/cf593e70d12f41d99cacc450c2eae419
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 4, Iss C, Pp 62-71 (2017)
Duchenne muscular dystrophy (DMD) is a lethal, X-linked, muscle-wasting disorder caused by mutations in the large, 2.4-Mb dystrophin gene. The majority of DMD-causing mutations are sporadic, multi-exon, frameshifting deletions, with the potential for
Externí odkaz:
https://doaj.org/article/baaed901fbc14b398a47c288c15dcfd1
Publikováno v:
Canine Medicine and Genetics, Vol 7, Iss 1, Pp 1-6 (2020)
Canine Medicine and Genetics
Canine Medicine and Genetics
BackgroundEvidence for an autoimmune etiology in canine diabetes is inconsistent and could vary based on breed. Previous studies demonstrated that small percentages of diabetic dogs possess autoantibodies to antigens known to be important in human ty
Publikováno v:
Journal of Veterinary Internal Medicine
Background GM2-gangliosidosis is a fatal neurodegenerative lysosomal storage disease (LSD) caused by deficiency of either β-hexosaminidase A (Hex-A) and β-hexosaminidase B (Hex-B) together, or the GM2 activator protein. Clinical signs can be variab
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 4, Iss C, Pp 62-71 (2017)
Molecular Therapy. Methods & Clinical Development
Molecular Therapy. Methods & Clinical Development
Duchenne muscular dystrophy (DMD) is a lethal, X-linked, muscle-wasting disorder caused by mutations in the large, 2.4-Mb dystrophin gene. The majority of DMD-causing mutations are sporadic, multi-exon, frameshifting deletions, with the potential for
Autor:
Eileen M. Shore, Paula S. Henthorn, Yael Porat-Mosenco, Meiqi Xu, Maja Zakošek Pipan, Margret L. Casal, Wilfried Mai, Julie B. Engiles, Patricia O'Donnell, Kirsten Wurzburg, Asaf Berkowitz, Keith G. Thompson, Robyn S Allen
Publikováno v:
Veterinary pathology, vol. 56, no. 4, pp. 614-618, 2019.
Two domestic shorthair cats, 1 intact female and 1 intact male, presented with progressive limb lameness and digital deformities at 4 and 6 months of age. Stiffness and swelling of the distal thoracic and pelvic limb joints progressed to involve hip
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d9a7858b2f4c7d40c5335a4bbfec6df
https://repozitorij.uni-lj.si/Dokument.php?id=120092&dn=
https://repozitorij.uni-lj.si/Dokument.php?id=120092&dn=
Autor:
Margret L, Casal, Julie B, Engiles, Maja, Zakošek Pipan, Asaf, Berkowitz, Yael, Porat-Mosenco, Wilfried, Mai, Kirsten, Wurzburg, Mei-Qi, Xu, Robyn, Allen, Patricia A, ODonnell, Paula S, Henthorn, Keith, Thompson, Eileen M, Shore
Publikováno v:
Veterinary pathology. 56(4)
Two domestic shorthair cats, 1 intact female and 1 intact male, presented with progressive limb lameness and digital deformities at 4 and 6 months of age. Stiffness and swelling of the distal thoracic and pelvic limb joints progressed to involve hip
Autor:
Aníbal G. Armién, Paula S. Henthorn, Ping Wang, Tim Wood, Pompei Bolfa, Rajeev Nair, Sreekumari Rajeev, Urs Giger, Mary Anna Thrall
Publikováno v:
Mol Genet Metab
Hereditary β-mannosidosis causing progressive lysosomal neuropathy and other clinical signs, has been previously described in humans, Nubian goats, and Salers cattle. Here we report the clinicopathological, metabolic, and molecular genetic features
Publikováno v:
Journal of Heredity
Samoyeds and Australian Terriers are the 2 dog breeds at highest risk (>10-fold) for diabetes mellitus in the United States. It is unknown if the insulin (INS) gene is involved in the pathophysiology of diabetes in Samoyeds and Australian Terriers. I
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3b2332b26409485b533324517124240
http://hdl.handle.net/11573/1327852
http://hdl.handle.net/11573/1327852