Fyfe JC - Search Results

1

A novel mitofusin 2 mutation causes canine fetal-onset neuroaxonal dystrophy.

Fyfe JC, Al-Tamimi RA, Liu J, Schäffer AA, Agarwala R, Henthorn PS. Fyfe JC, et al. Neurogenetics. 2011 Aug;12(3):223-32. doi: 10.1007/s10048-011-0285-6. Epub 2011 Jun 4. Neurogenetics. 2011. PMID: 21643798 Free PMC article.

2

Canine Imerslund-Gräsbeck syndrome maps to a region orthologous to HSA14q.

He Q, Fyfe JC, Schäffer AA, Kilkenney A, Werner P, Kirkness EF, Henthorn PS. He Q, et al. Among authors: fyfe jc. Mamm Genome. 2003 Nov;14(11):758-64. doi: 10.1007/s00335-003-2280-1. Mamm Genome. 2003. PMID: 14722725

3

Inherited neuroaxonal dystrophy in dogs causing lethal, fetal-onset motor system dysfunction and cerebellar hypoplasia.

Fyfe JC, Al-Tamimi RA, Castellani RJ, Rosenstein D, Goldowitz D, Henthorn PS. Fyfe JC, et al. J Comp Neurol. 2010 Sep 15;518(18):3771-84. doi: 10.1002/cne.22423. J Comp Neurol. 2010. PMID: 20653033 Free PMC article.

4

An approximately 140-kb deletion associated with feline spinal muscular atrophy implies an essential LIX1 function for motor neuron survival.

Fyfe JC, Menotti-Raymond M, David VA, Brichta L, Schäffer AA, Agarwala R, Murphy WJ, Wedemeyer WJ, Gregory BL, Buzzell BG, Drummond MC, Wirth B, O'Brien SJ. Fyfe JC, et al. Genome Res. 2006 Sep;16(9):1084-90. doi: 10.1101/gr.5268806. Epub 2006 Aug 9. Genome Res. 2006. PMID: 16899656 Free PMC article.

5

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. 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.

6

Amnionless function is required for cubilin brush-border expression and intrinsic factor-cobalamin (vitamin B12) absorption in vivo.

He Q, Madsen M, Kilkenney A, Gregory B, Christensen EI, Vorum H, Højrup P, Schäffer AA, Kirkness EF, Tanner SM, de la Chapelle A, Giger U, Moestrup SK, Fyfe JC. He Q, et al. Among authors: fyfe jc. Blood. 2005 Aug 15;106(4):1447-53. doi: 10.1182/blood-2005-03-1197. Epub 2005 Apr 21. Blood. 2005. PMID: 15845892 Free PMC article.

7

Molecular basis of feline beta-glucuronidase deficiency: an animal model of mucopolysaccharidosis VII.

Fyfe JC, Kurzhals RL, Lassaline ME, Henthorn PS, Alur PR, Wang P, Wolfe JH, Giger U, Haskins ME, Patterson DF, Sun H, Jain S, Yuhki N. Fyfe JC, et al. Genomics. 1999 Jun 1;58(2):121-8. doi: 10.1006/geno.1999.5825. Genomics. 1999. PMID: 10366443

8

Cloning of the canine beta-glucuronidase cDNA, mutation identification in canine MPS VII, and retroviral vector-mediated correction of MPS VII cells.

Ray J, Bouvet A, DeSanto C, Fyfe JC, Xu D, Wolfe JH, Aguirre GD, Patterson DF, Haskins ME, Henthorn PS. Ray J, et al. Among authors: fyfe jc. Genomics. 1998 Mar 1;48(2):248-53. doi: 10.1006/geno.1997.5189. Genomics. 1998. PMID: 9521879 Free article.

9

Congenital hypothyroidism with goiter in Tenterfield terriers.

Dodgson SE, Day R, Fyfe JC. Dodgson SE, et al. Among authors: fyfe jc. J Vet Intern Med. 2012 Nov-Dec;26(6):1350-7. doi: 10.1111/j.1939-1676.2012.01015.x. Epub 2012 Nov 1. J Vet Intern Med. 2012. PMID: 23113744 Free article.

10

Glycogen storage disease type IIIa in curly-coated retrievers.

Gregory BL, Shelton GD, Bali DS, Chen YT, Fyfe JC. Gregory BL, et al. Among authors: fyfe jc. J Vet Intern Med. 2007 Jan-Feb;21(1):40-6. doi: 10.1892/0891-6640(2007)21[40:gsdtii]2.0.co;2. J Vet Intern Med. 2007. PMID: 17338148 Free article.

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