Martin L. Katz

Affiliations: 
University of Missouri - Columbia, Columbia, MO, United States 
Area:
Neuroscience Biology, Ophthalmology, Pathology, Cell Biology
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"Martin Katz"
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Publications

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Bullock G, Johnson GS, Pattridge SG, et al. (2023) A Homozygous Missense Mutation in a Doberman Pinscher Dog with Neurodegeneration, Cytoplasmic Vacuoles, Autofluorescent Storage Granules, and an α-Mannosidase Deficiency. Genes. 14
Kick GR, Whiting REH, Ota-Kuroki J, et al. (2022) Intravitreal gene therapy preserves retinal function in a canine model of CLN2 neuronal ceroid lipofuscinosis. Experimental Eye Research. 226: 109344
Bullock G, Johnson GS, Mhlanga-Mutangadura T, et al. (2022) Lysosomal Storage Disease Associated with a CNP Sequence Variant in Dalmatian Dogs. Gene. 146513
Meiman EJ, Kick GR, Jensen CA, et al. (2022) Characterization of neurological disease progression in a canine model of CLN5 neuronal ceroid lipofuscinosis. Developmental Neurobiology. 82: 326-344
Kick GR, Meiman EJ, Sabol JC, et al. (2021) Visual system pathology in a canine model of CLN5 neuronal ceroid lipofuscinosis. Experimental Eye Research. 108686
Whiting REH, Robinson GO, Ota-Kuroki J, et al. (2020) Intravitreal enzyme replacement inhibits progression of retinal degeneration in canine CLN2 neuronal ceroid lipofuscinosis. Experimental Eye Research. 108135
Whiting REH, Pearce JW, Vansteenkiste DP, et al. (2020) Intravitreal enzyme replacement preserves retinal structure and function in canine CLN2 neuronal ceroid lipofuscinosis. Experimental Eye Research. 108130
Katz ML, Buckley RM, Biegen V, et al. (2020) Neuronal Ceroid Lipofuscinosis in a Domestic Cat Associated with a DNA Sequence Variant That Creates a Premature Stop Codon in . G3 (Bethesda, Md.)
Ru Y, Corado C, Soon RK, et al. (2019) Neurofilament light is a treatment-responsive biomarker in CLN2 disease. Annals of Clinical and Translational Neurology
Guo J, Johnson GS, Cook J, et al. (2019) Neuronal ceroid lipofuscinosis in a German Shorthaired Pointer associated with a previously reported nonsense variant. Molecular Genetics and Metabolism Reports. 21: 100521
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