Publications by authors named "Martin Katz"

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Retinal Function Deficits in American Staffordshire Terriers with a Late-Onset Neurodegenerative Disease Associated with an Variant.
Grace R Kick, Samantha L Marzano, Juri Ota-Kuroki, Garrett Bullock, Martin L Katz

Vet Sci· November 2025

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Canine Neuronal Ceroid Lipofuscinosis-like Disorder Associated with Sequence Variants in and .
Alexander Then, Rebecca Welly, Garrett Bullock, Lucie Chevallier, Martin L Katz

Genes (Basel)· November 2025

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Absence of Retrogene Insertion on Chromosome 18 Results in a Tall Phenotype in Grand Basset Griffon Vendéen Dogs.
Tendai Mhlanga-Mutangadura, Liz Hansen, Martin L Katz

Vet Sci· September 2025

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Dermal pathology in a Catahoula Leopard dog with Dermasparaxis Ehlers Danlos syndrome caused by a homozygous ADAMTS2 missense variant.
Jared A Jaffey, Garrett Bullock, Martin L Katz

Top Companion Anim Med· May 2025

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An RB1CC1 Missense Variant in Nova Scotia Duck Tolling Retrievers with Degenerative Encephalopathy.
Juyuan Guo, Garrett Bullock, Dennis P O'Brien, Gary S Johnson, Martin L Katz

Genes (Basel)· February 2025

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Deletion Variant in Basenji Dogs with Fanconi Syndrome.
Fabiana H G Farias, Tendai Mhlanga-Mutangadura, Juyuan Guo, Liz Hansen, Gary S Johnson, Martin L Katz

Genes (Basel)· November 2024

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Canine Multiple System Degeneration Associated with Sequence Variants in .
Rong Zeng, Juyan Guo, Garrett Bullock, Gary S Johnson, Martin L Katz

Genes (Basel)· October 2024

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Novel COL5A1 variants and associated disease phenotypes in dogs with classical Ehlers-Danlos syndrome.
Garrett Bullock, Jared A Jaffey, Leah A Cohn, Erika Sox, Eric T Hostnik, Martin L Katz

J Vet Intern Med· September 2024

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Neuronal Ceroid Lipofuscinosis in a Mixed-Breed Dog with a Splice Site Variant in .
Tendai Mhlanga-Mutangadura, Garrett Bullock, Sofia Cerda-Gonzalez, Martin L Katz

Genes (Basel)· May 2024

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Homozygous Mutation and Neurodegeneration in Weimaraners: Myelin Abnormalities and Accumulation of Lipofuscin-like Inclusions.
Stefan H Keller, Gary S Johnson, Garrett Bullock, Tendai Mhlanga-Mutangadura, Malte Schwartz, Martin L Katz

Genes (Basel)· February 2024

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Beta-mannosidosis in a domestic cat associated with a missense variant in MANBA.
Martin L Katz, James Cook, Charles H Vite, Rebecca S Campbell, Lyndon M Coghill

Gene· January 2024

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A Homozygous Missense Mutation in a Doberman Pinscher Dog with Neurodegeneration, Cytoplasmic Vacuoles, Autofluorescent Storage Granules, and an α-Mannosidase Deficiency.
Garrett Bullock, Gary S Johnson, Savannah G Pattridge, Tendai Mhlanga-Mutangadura, Juyuan Guo, Martin L Katz

Genes (Basel)· August 2023

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Intravitreal gene therapy preserves retinal function in a canine model of CLN2 neuronal ceroid lipofuscinosis.
Grace Robinson Kick, Rebecca E H Whiting, Juri Ota-Kuroki, Leilani J Castaner, Brandie Morgan-Jack, Martin L Katz

Exp Eye Res· January 2023

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Novel Homozygous Variants and Associated Disease Phenotypes in Dogs with Dermatosparactic Ehlers-Danlos Syndrome.
Jared A Jaffey, Garrett Bullock, Juyuan Guo, Tendai Mhlanga-Mutangadura, Dennis P O'Brien, Martin L Katz

Genes (Basel)· November 2022

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Lysosomal storage disease associated with a CNP sequence variant in Dalmatian dogs.
Garrett Bullock, Gary S Johnson, Tendai Mhlanga-Mutangadura, Scott C Petesch, Samantha Thompson, Martin L Katz

Gene· July 2022

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Characterization of neurological disease progression in a canine model of CLN5 neuronal ceroid lipofuscinosis.
Elizabeth J Meiman, Grace Robinson Kick, Cheryl A Jensen, Joan R Coates, Martin L Katz

Dev Neurobiol· May 2022

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Dose selection for intracerebroventricular cerliponase alfa in children with CLN2 disease, translation from animal to human in a rare genetic disease.
Kevin Hammon, Greg de Hart, Brian R Vuillemenot, Derek Kennedy, Don Musson, Martin L Katz

Clin Transl Sci· September 2021

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Visual system pathology in a canine model of CLN5 neuronal ceroid lipofuscinosis.
Grace Robinson Kick, Elizabeth J Meiman, Julianna C Sabol, Rebecca E H Whiting, Juri Ota-Kuroki, Martin L Katz

Exp Eye Res· September 2021

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Intravitreal enzyme replacement inhibits progression of retinal degeneration in canine CLN2 neuronal ceroid lipofuscinosis.
Rebecca E H Whiting, Grace Robinson Kick, Juri Ota-Kuroki, Stefanie Lim, Leilani J Castaner, Martin L Katz

Exp Eye Res· September 2020

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Neuronal Ceroid Lipofuscinosis in a Domestic Cat Associated with a DNA Sequence Variant That Creates a Premature Stop Codon in .
Martin L Katz, Reuben M Buckley, Vanessa Biegen, Dennis P O'Brien, Gayle C Johnson

G3 (Bethesda)· August 2020

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Intravitreal enzyme replacement preserves retinal structure and function in canine CLN2 neuronal ceroid lipofuscinosis.
Rebecca E H Whiting, Jacqueline W Pearce, Daniella P Vansteenkiste, Katherine Bibi, Stefanie Lim, Martin L Katz

Exp Eye Res· August 2020

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Neuronal ceroid lipofuscinosis in a German Shorthaired Pointer associated with a previously reported nonsense variant.
Juyuan Guo, Gary S Johnson, James Cook, Olivia K Harris, Tendai Mhlanga-Mutangadura, Martin L Katz

Mol Genet Metab Rep· December 2019

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Neurofilament light is a treatment-responsive biomarker in CLN2 disease.
Yuanbin Ru, Carley Corado, Russell K Soon, Andrew C Melton, Adam Harris, Martin L Katz

Ann Clin Transl Neurol· December 2019

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ATP13A2 missense variant in Australian Cattle Dogs with late onset neuronal ceroid lipofuscinosis.
Isabelle Schmutz, Vidhya Jagannathan, Florian Bartenschlager, Veronika M Stein, Achim D Gruber, Martin L Katz

Mol Genet Metab· May 2019

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A mixed breed dog with neuronal ceroid lipofuscinosis is homozygous for a CLN5 nonsense mutation previously identified in Border Collies and Australian Cattle Dogs.
Natalie A Villani, Garrett Bullock, Jennifer R Michaels, Osamu Yamato, Dennis P O'Brien, Martin L Katz

Mol Genet Metab· May 2019

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