Katz ML - Search Results

1

Nonclinical evaluation of CNS-administered TPP1 enzyme replacement in canine CLN2 neuronal ceroid lipofuscinosis.

Vuillemenot BR, Kennedy D, Cooper JD, Wong AM, Sri S, Doeleman T, Katz ML, Coates JR, Johnson GC, Reed RP, Adams EL, Butt MT, Musson DG, Henshaw J, Keve S, Cahayag R, Tsuruda LS, O'Neill CA. Vuillemenot BR, et al. Among authors: katz ml. Mol Genet Metab. 2015 Feb;114(2):281-93. doi: 10.1016/j.ymgme.2014.09.004. Epub 2014 Sep 16. Mol Genet Metab. 2015. PMID: 25257657

2

Juvenile ceroid lipofuscinosis. Evidence for methylated lysine in neural storage body protein.

Katz ML, Rodrigues M. Katz ML, et al. Am J Pathol. 1991 Feb;138(2):323-32. Am J Pathol. 1991. PMID: 1899540 Free PMC article.

3

Canine hereditary ceroid-lipofuscinosis: evidence for a defect in the carnitine biosynthetic pathway.

Katz ML, Siakotos AN. Katz ML, et al. Am J Med Genet. 1995 Jun 5;57(2):266-71. doi: 10.1002/ajmg.1320570231. Am J Med Genet. 1995. PMID: 7668343

4

Mouse gene knockout models for the CLN2 and CLN3 forms of ceroid lipofuscinosis.

Katz ML, Johnson GS. Katz ML, et al. Eur J Paediatr Neurol. 2001;5 Suppl A:109-14. doi: 10.1053/ejpn.2000.0445. Eur J Paediatr Neurol. 2001. PMID: 11588979

5

A mutation in the cathepsin D gene (CTSD) in American Bulldogs with neuronal ceroid lipofuscinosis.

Awano T, Katz ML, O'Brien DP, Taylor JF, Evans J, Khan S, Sohar I, Lobel P, Johnson GS. Awano T, et al. Among authors: katz ml. Mol Genet Metab. 2006 Apr;87(4):341-8. doi: 10.1016/j.ymgme.2005.11.005. Epub 2006 Jan 4. Mol Genet Metab. 2006. PMID: 16386934

6

A frame shift mutation in canine TPP1 (the ortholog of human CLN2) in a juvenile Dachshund with neuronal ceroid lipofuscinosis.

Awano T, Katz ML, O'Brien DP, Sohar I, Lobel P, Coates JR, Khan S, Johnson GC, Giger U, Johnson GS. Awano T, et al. Among authors: katz ml. Mol Genet Metab. 2006 Nov;89(3):254-60. doi: 10.1016/j.ymgme.2006.02.016. Epub 2006 Apr 18. Mol Genet Metab. 2006. PMID: 16621647

7

Ocular phenotype in a mouse gene knockout model for infantile neuronal ceroid lipofuscinosis.

Lei B, Tullis GE, Kirk MD, Zhang K, Katz ML. Lei B, et al. Among authors: katz ml. J Neurosci Res. 2006 Oct;84(5):1139-49. doi: 10.1002/jnr.21008. J Neurosci Res. 2006. PMID: 16881055 Free PMC article.

8

Phenotypic characterization of a mouse model of juvenile neuronal ceroid lipofuscinosis.

Katz ML, Johnson GS, Tullis GE, Lei B. Katz ML, et al. Neurobiol Dis. 2008 Feb;29(2):242-53. doi: 10.1016/j.nbd.2007.08.017. Epub 2007 Sep 7. Neurobiol Dis. 2008. PMID: 17962032 Free PMC article.

9

Retinal pathology in a canine model of late infantile neuronal ceroid lipofuscinosis.

Katz ML, Coates JR, Cooper JJ, O'Brien DP, Jeong M, Narfström K. Katz ML, et al. Invest Ophthalmol Vis Sci. 2008 Jun;49(6):2686-95. doi: 10.1167/iovs.08-1712. Epub 2008 Mar 14. Invest Ophthalmol Vis Sci. 2008. PMID: 18344450

10

Genome-wide association analysis reveals a SOD1 mutation in canine degenerative myelopathy that resembles amyotrophic lateral sclerosis.

Awano T, Johnson GS, Wade CM, Katz ML, Johnson GC, Taylor JF, Perloski M, Biagi T, Baranowska I, Long S, March PA, Olby NJ, Shelton GD, Khan S, O'Brien DP, Lindblad-Toh K, Coates JR. Awano T, et al. Among authors: katz ml. Proc Natl Acad Sci U S A. 2009 Feb 24;106(8):2794-9. doi: 10.1073/pnas.0812297106. Epub 2009 Feb 2. Proc Natl Acad Sci U S A. 2009. PMID: 19188595 Free PMC article.

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