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A CNTNAP1 Missense Variant Is Associated with Canine Laryngeal Paralysis and Polyneuropathy.
Letko A, Minor KM, Friedenberg SG, Shelton GD, Salvador JP, Mandigers PJJ, Leegwater PAJ, Winkler PA, Petersen-Jones SM, Stanley BJ, Ekenstedt KJ, Johnson GS, Hansen L, Jagannathan V, Mickelson JR, Drögemüller C. Letko A, et al. Among authors: ekenstedt kj. Genes (Basel). 2020 Nov 27;11(12):1426. doi: 10.3390/genes11121426. Genes (Basel). 2020. PMID: 33261176 Free PMC article.
Inheritance of recurrent exertional rhabdomyolysis in thoroughbreds.
Dranchak PK, Valberg SJ, Onan GW, Gallant EM, MacLeay JM, McKenzie EC, De La Corte FD, Ekenstedt K, Mickelson JR. Dranchak PK, et al. J Am Vet Med Assoc. 2005 Sep 1;227(5):762-7. doi: 10.2460/javma.2005.227.762. J Am Vet Med Assoc. 2005. PMID: 16178398 Free article.
Chromosomal assignments for the equine AMPK family genes.
Dranchak PK, Ekenstedt KJ, Valberg SJ, Chowdhary BP, Raudsepp T, Mickelson JR. Dranchak PK, et al. Among authors: ekenstedt kj. Anim Genet. 2006 Jun;37(3):293-4. doi: 10.1111/j.1365-2052.2006.01431.x. Anim Genet. 2006. PMID: 16734697 No abstract available.
Canine epilepsy genetics.
Ekenstedt KJ, Patterson EE, Mickelson JR. Ekenstedt KJ, et al. Mamm Genome. 2012 Feb;23(1-2):28-39. doi: 10.1007/s00335-011-9362-2. Epub 2011 Oct 30. Mamm Genome. 2012. PMID: 22037590 Review.
A large animal model for CNGB1 autosomal recessive retinitis pigmentosa.
Winkler PA, Ekenstedt KJ, Occelli LM, Frattaroli AV, Bartoe JT, Venta PJ, Petersen-Jones SM. Winkler PA, et al. Among authors: ekenstedt kj. PLoS One. 2013 Aug 19;8(8):e72229. doi: 10.1371/journal.pone.0072229. eCollection 2013. PLoS One. 2013. PMID: 23977260 Free PMC article.
33 results