Zobrazeno 1 - 10
of 23
pro vyhledávání: '"P 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:
PLoS ONE, Vol 15, Iss 9, p e0239542 (2020)
The Australian Terrier breed is the breed at highest risk for naturally-occurring diabetes mellitus in the United States, where it is 32 times more likely to develop diabetes compared to mixed breed dogs. However, the heritability and mode of inherit
Externí odkaz:
https://doaj.org/article/839ee79ef2814bfabd6caa4af7355211
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:
PLoS ONE, Vol 12, Iss 1, p e0170708 (2017)
Autosomal recessive congenital ichthyosis in the American bulldog is characterized by generalized scaling and erythema with adherent scale on the glabrous skin. We had previously linked this disorder to NIPAL4, which encodes the protein ichthyin. Seq
Externí odkaz:
https://doaj.org/article/0ac506e5dd644183b1f66fb208c30cde
Autor:
P. Werner, M. G. Raducha, U. Prociuk, L. A. Lyons, J. S. Kehler, P. S. Henthorn, D. F. Patterson
Publikováno v:
Animal Genetics. 29:220-223
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::776bbeff740caefc9a61dba7bc45f804
https://doi.org/10.1111/j.1365-2052.1998.00328.x
https://doi.org/10.1111/j.1365-2052.1998.00328.x
Autor:
P S Henthorn, M P Whyte
Publikováno v:
Clinical Chemistry. 38:2501-2505
Hypophosphatasia is an inborn error of metabolism that is characterized clinically by defective bone mineralization and biochemically by deficient activity of the tissue-nonspecific isoenzyme of alkaline phosphatase (TNSALP) in serum and in tissues.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac0cbe69712faef89b6e78f47f75718b
https://doi.org/10.1093/clinchem/38.12.2501
https://doi.org/10.1093/clinchem/38.12.2501
Autor:
W. R. McCombie, R. Preston, Vivekanand Balija, Lidia Nascimento, L. Santos, Theresa Zutavern, A. O'Shaughnessy, Lance E. Palmer, P. S. Henthorn, Gregory J. Hannon
Publikováno v:
The Journal of heredity. 94(1)
We have initially sequenced approximately 8,000 canine expressed sequence tags (ESTs) from several complementary DNA (cDNA) libraries: testes, whole brain, and Madin-Darby canine kidney (MDCK) cells. Analysis of these sequences shows that they provid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d5b60ae9b8257c9994ea9adc8294556a
https://pubmed.ncbi.nlm.nih.gov/12692157
https://pubmed.ncbi.nlm.nih.gov/12692157
Publikováno v:
Journal of veterinary internal medicine. 13(6)
Two related female Norwegian Elkhounds were evaluated at 6 and 8 months of age for enlarged clitori. Both had a 78 XX karyotype. Histology of their internal reproductive tracts demonstrated 1 to be an XX true hermaphrodite with bilateral ovotestes an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e8f75dc85d85e834fb67e8559a49a477
https://pubmed.ncbi.nlm.nih.gov/10587257
https://pubmed.ncbi.nlm.nih.gov/10587257
Autor:
C A, Moore, C J, Curry, P S, Henthorn, J A, Smith, J C, Smith, P, O'Lague, S P, Coburn, D D, Weaver, M P, Whyte
Publikováno v:
American journal of medical genetics. 86(5)
We describe four pregnancies in two families in which mild hypophosphatasia, apparently transmitted as an autosomal dominant trait, manifested in utero as severe long bone bowing. Postnatally, there was spontaneous improvement of the skeletal defects
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0d20e944ddbd449534914df6b411f5f8
https://pubmed.ncbi.nlm.nih.gov/10508980
https://pubmed.ncbi.nlm.nih.gov/10508980