Henthorn PS - Search Results

1

Hereditary β-mannosidosis in a dog: Clinicopathological and molecular genetic characterization.

Bolfa P, Wang P, Nair R, Rajeev S, Armien AG, Henthorn PS, Wood T, Thrall MA, Giger U. Bolfa P, et al. Among authors: henthorn ps. Mol Genet Metab. 2019 Sep-Oct;128(1-2):137-143. doi: 10.1016/j.ymgme.2019.08.002. Epub 2019 Aug 10. Mol Genet Metab. 2019. PMID: 31439511 Free PMC article.

2

A complex rearrangement in GBE1 causes both perinatal hypoglycemic collapse and late-juvenile-onset neuromuscular degeneration in glycogen storage disease type IV of Norwegian forest cats.

Fyfe JC, Kurzhals RL, Hawkins MG, Wang P, Yuhki N, Giger U, Van Winkle TJ, Haskins ME, Patterson DF, Henthorn PS. Fyfe JC, et al. Among authors: henthorn ps. Mol Genet Metab. 2007 Apr;90(4):383-92. doi: 10.1016/j.ymgme.2006.12.003. Epub 2007 Jan 25. Mol Genet Metab. 2007. PMID: 17257876 Free PMC article.

3

A Defect in NIPAL4 Is Associated with Autosomal Recessive Congenital Ichthyosis in American Bulldogs.

Casal ML, Wang P, Mauldin EA, Lin G, Henthorn PS. Casal ML, et al. Among authors: henthorn ps. PLoS One. 2017 Jan 25;12(1):e0170708. doi: 10.1371/journal.pone.0170708. eCollection 2017. PLoS One. 2017. PMID: 28122049 Free PMC article.

4

Molecular basis of canine muscle type phosphofructokinase deficiency.

Smith BF, Stedman H, Rajpurohit Y, Henthorn PS, Wolfe JH, Patterson DF, Giger U. Smith BF, et al. Among authors: henthorn ps. J Biol Chem. 1996 Aug 16;271(33):20070-4. doi: 10.1074/jbc.271.33.20070. J Biol Chem. 1996. PMID: 8702726 Free article.

5

Canine cystinuria: polymorphism in the canine SLC3A1 gene and identification of a nonsense mutation in cystinuric Newfoundland dogs.

Henthorn PS, Liu J, Gidalevich T, Fang J, Casal ML, Patterson DF, Giger U. Henthorn PS, et al. Hum Genet. 2000 Oct;107(4):295-303. doi: 10.1007/s004390000392. Hum Genet. 2000. PMID: 11129328

6

SLC3A1 and SLC7A9 mutations in autosomal recessive or dominant canine cystinuria: a new classification system.

Brons AK, Henthorn PS, Raj K, Fitzgerald CA, Liu J, Sewell AC, Giger U. Brons AK, et al. Among authors: henthorn ps. J Vet Intern Med. 2013 Nov-Dec;27(6):1400-8. doi: 10.1111/jvim.12176. Epub 2013 Sep 3. J Vet Intern Med. 2013. PMID: 24001348 Free PMC article.

7

Epidermolysis bullosa simplex in sibling Eurasier dogs is caused by a PLEC non-sense variant.

Mauldin EA, Wang P, Olivry T, Henthorn PS, Casal ML. Mauldin EA, et al. Among authors: henthorn ps. Vet Dermatol. 2017 Feb;28(1):10-e3. doi: 10.1111/vde.12394. Epub 2016 Nov 7. Vet Dermatol. 2017. PMID: 27878870 Free PMC article.

8

Canine GM2-Gangliosidosis Sandhoff Disease Associated with a 3-Base Pair Deletion in the HEXB Gene.

Wang P, Henthorn PS, Galban E, Lin G, Takedai T, Casal M. Wang P, et al. Among authors: henthorn ps. J Vet Intern Med. 2018 Jan;32(1):340-347. doi: 10.1111/jvim.14862. Epub 2017 Nov 6. J Vet Intern Med. 2018. PMID: 29106755 Free PMC article.

9

Sry-negative XX sex reversal in a family of Norwegian Elkhounds.

Melniczek JR, Dambach D, Prociuk U, Jezyk PF, Henthorn PS, Patterson DF, Giger U. Melniczek JR, et al. Among authors: henthorn ps. J Vet Intern Med. 1999 Nov-Dec;13(6):564-9. doi: 10.1892/0891-6640(1999)013<0564:snxsri>2.3.co;2. J Vet Intern Med. 1999. PMID: 10587257 Free article. Review.

10

A cDNA encoding canine muscle-type phosphofructokinase.

Smith BF, Henthorn PS, Rajpurohit Y, Stedman H, Wolfe JH, Patterson DF, Giger U. Smith BF, et al. Among authors: henthorn ps. Gene. 1996 Feb 12;168(2):275-6. doi: 10.1016/0378-1119(95)00761-x. Gene. 1996. PMID: 8654960 Free article.

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