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A general approach for predicting the behavior of the Supreme Court of the United States

PloS one, 2017-04, Vol.12 (4), p.e0174698-e0174698

2017

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Neuronal Ceroid Lipofuscinosis in a Mixed-Breed Dog with a Splice Site Variant in CLN6

Genes, 2024-06, Vol.15 (6), p.661

2024

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Lysosomal storage disease associated with a CNP sequence variant in Dalmatian dogs

Gene, 2022-07, Vol.830, p.146513-146513, Article 146513

2022

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Enzyme replacement therapy attenuates disease progression in a canine model of late-infantile neuronal ceroid lipofuscinosis (CLN2 disease)

Journal of neuroscience research, 2014-11, Vol.92 (11), p.1591-1598

2014

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Canine neuronal ceroid lipofuscinoses: Promising models for preclinical testing of therapeutic interventions

Neurobiology of disease, 2017-12, Vol.108, p.277-287

2017

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Beta-mannosidosis in a domestic cat associated with a missense variant in MANBA

Gene, 2024-01, Vol.893, p.147941-147941, Article 147941

2024

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AAV gene transfer delays disease onset in a TPP1-deficient canine model of the late infantile form of Batten disease

Science translational medicine, 2015-11, Vol.7 (313), p.313ra180

2015

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ATP13A2 missense variant in Australian Cattle Dogs with late onset neuronal ceroid lipofuscinosis

Molecular genetics and metabolism, 2019-05, Vol.127 (1), p.95-106

2019

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Characterization of neurological disease progression in a canine model of CLN5 neuronal ceroid lipofuscinosis

Developmental neurobiology (Hoboken, N.J.), 2022-05, Vol.82 (4), p.326-344

2022

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Harnessing legal complexity

Science (American Association for the Advancement of Science), 2017-03, Vol.355 (6332), p.1377-1378

2017

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A Homozygous MAN2B1 Missense Mutation in a Doberman Pinscher Dog with Neurodegeneration, Cytoplasmic Vacuoles, Autofluorescent Storage Granules, and an α-Mannosidase Deficiency

Genes, 2023-08, Vol.14 (9), p.1746

2023

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Variants within the SP110 nuclear body protein modify risk of canine degenerative myelopathy

Proceedings of the National Academy of Sciences - PNAS, 2016-05, Vol.113 (22), p.E3091-E3100

2016

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Mikhail N. Katkov: A political biography. 1818-1887

Katz, Martin

Reprint 2017 edition., 2017

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Homozygous CNP Mutation and Neurodegeneration in Weimaraners: Myelin Abnormalities and Accumulation of Lipofuscin-like Inclusions

Genes, 2024-02, Vol.15 (2), p.246

2024

Volltextzugriff (PDF)

Intravitreal gene therapy preserves retinal function in a canine model of CLN2 neuronal ceroid lipofuscinosis

Experimental eye research, 2023-01, Vol.226, p.109344-109344, Article 109344

2023

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A truncating mutation in ATP13A2 is responsible for adult-onset neuronal ceroid lipofuscinosis in Tibetan terriers

Neurobiology of disease, 2011-06, Vol.42 (3), p.468-474

2011

Volltextzugriff (PDF)

Intravitreal enzyme replacement preserves retinal structure and function in canine CLN2 neuronal ceroid lipofuscinosis

Experimental eye research, 2020-08, Vol.197, p.108130-108130, Article 108130

2020

Volltextzugriff (PDF)

Intravitreal enzyme replacement inhibits progression of retinal degeneration in canine CLN2 neuronal ceroid lipofuscinosis

Experimental eye research, 2020-09, Vol.198, p.108135-108135, Article 108135

2020

Volltextzugriff (PDF)

A mixed breed dog with neuronal ceroid lipofuscinosis is homozygous for a CLN5 nonsense mutation previously identified in Border Collies and Australian Cattle Dogs

Molecular genetics and metabolism, 2019-05, Vol.127 (1), p.107-115

2019

Volltextzugriff (PDF)

Intravitreal implantation of TPP1-transduced stem cells delays retinal degeneration in canine CLN2 neuronal ceroid lipofuscinosis

Experimental eye research, 2016-11, Vol.152, p.77-87

2016

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Visual system pathology in a canine model of CLN5 neuronal ceroid lipofuscinosis

Experimental eye research, 2021-09, Vol.210, p.108686-108686, Article 108686

2021

Volltextzugriff (PDF)

Neuronal Ceroid Lipofuscinosis in a Domestic Cat Associated with a DNA Sequence Variant That Creates a Premature Stop Codon in CLN6

G3 : genes - genomes - genetics, 2020-08, Vol.10 (8), p.2741-2751

2020

Volltextzugriff (PDF)

Conflicting perspectives on neurobehavioral theories of the depressive disorders and drug actions

Acta neuropsychiatrica, 2016-12, Vol.28 (6), p.311-314

Katz, Martin M.

2016

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Onset and Early Behavioral Effects of Pharmacologically Different Antidepressants and Placebo in Depression

Neuropsychopharmacology (New York, N.Y.), 2004-03, Vol.29 (3), p.566-579

2004

Volltextzugriff (PDF)

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

Molecular genetics and metabolism, 2015-02, Vol.114 (2), p.281-293

2015

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A general approach for predicting the behavior of the Supreme Court of the United States

Neuronal Ceroid Lipofuscinosis in a Mixed-Breed Dog with a Splice Site Variant in CLN6

Lysosomal storage disease associated with a CNP sequence variant in Dalmatian dogs

Enzyme replacement therapy attenuates disease progression in a canine model of late-infantile neuronal ceroid lipofuscinosis (CLN2 disease)

Canine neuronal ceroid lipofuscinoses: Promising models for preclinical testing of therapeutic interventions

Beta-mannosidosis in a domestic cat associated with a missense variant in MANBA

AAV gene transfer delays disease onset in a TPP1-deficient canine model of the late infantile form of Batten disease

ATP13A2 missense variant in Australian Cattle Dogs with late onset neuronal ceroid lipofuscinosis

Characterization of neurological disease progression in a canine model of CLN5 neuronal ceroid lipofuscinosis

Harnessing legal complexity

A Homozygous MAN2B1 Missense Mutation in a Doberman Pinscher Dog with Neurodegeneration, Cytoplasmic Vacuoles, Autofluorescent Storage Granules, and an α-Mannosidase Deficiency

Variants within the SP110 nuclear body protein modify risk of canine degenerative myelopathy

Mikhail N. Katkov: A political biography. 1818-1887

Homozygous CNP Mutation and Neurodegeneration in Weimaraners: Myelin Abnormalities and Accumulation of Lipofuscin-like Inclusions

Intravitreal gene therapy preserves retinal function in a canine model of CLN2 neuronal ceroid lipofuscinosis

A truncating mutation in ATP13A2 is responsible for adult-onset neuronal ceroid lipofuscinosis in Tibetan terriers

Intravitreal enzyme replacement preserves retinal structure and function in canine CLN2 neuronal ceroid lipofuscinosis

Intravitreal enzyme replacement inhibits progression of retinal degeneration in canine CLN2 neuronal ceroid lipofuscinosis

A mixed breed dog with neuronal ceroid lipofuscinosis is homozygous for a CLN5 nonsense mutation previously identified in Border Collies and Australian Cattle Dogs

Intravitreal implantation of TPP1-transduced stem cells delays retinal degeneration in canine CLN2 neuronal ceroid lipofuscinosis

Visual system pathology in a canine model of CLN5 neuronal ceroid lipofuscinosis

Neuronal Ceroid Lipofuscinosis in a Domestic Cat Associated with a DNA Sequence Variant That Creates a Premature Stop Codon in CLN6

Conflicting perspectives on neurobehavioral theories of the depressive disorders and drug actions

Onset and Early Behavioral Effects of Pharmacologically Different Antidepressants and Placebo in Depression

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

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