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Animal medical genetics: a historical perspective on more than 50 years of research into genetic disorders of animals at Massey University

New Zealand veterinary journal, 2021-07, Vol.69 (5), p.255-266

2021

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Glial activation spreads from specific cerebral foci and precedes neurodegeneration in presymptomatic ovine neuronal ceroid lipofuscinosis (CLN6)

Neurobiology of disease, 2005-10, Vol.20 (1), p.49-63

2005

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Defective Endoplasmic Reticulum-resident Membrane Protein CLN6 Affects Lysosomal Degradation of Endocytosed Arylsulfatase A

The Journal of biological chemistry, 2004-05, Vol.279 (21), p.22347-22352

2004

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Lysine 43 Is Trimethylated in Subunit c from Bovine Mitochondrial ATP Synthase and in Storage Bodies Associated with Batten Disease

The Journal of biological chemistry, 2004-05, Vol.279 (21), p.21883-21887

2004

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Mutational Analysis of the Defective Protease in Classic Late-Infantile Neuronal Ceroid Lipofuscinosis, a Neurodegenerative Lysosomal Storage Disorder

American journal of human genetics, 1999-06, Vol.64 (6), p.1511-1523

1999

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Enhanced expression of manganese-dependent superoxide dismutase in human and sheep CLN6 tissues

Biochemical journal, 2003-12, Vol.376 (Pt 2), p.369-376

2003

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Neuronal ceroid-lipofuscinosis in Borderdale sheep

New Zealand veterinary journal, 2002-10, Vol.50 (5), p.199-202

2002

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Neuronal ceroid lipofuscinosis in Merino sheep

Australian veterinary journal, 2002-05, Vol.80 (5), p.292-297

2002

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The origin of fluorescence in the neuronal ceroid lipofuscinoses (Batten disease) and neuron cultures from affected sheep for studies of neurodegeneration

Archives of gerontology and geriatrics, 2002-05, Vol.34 (3), p.343-357

2002

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Ion Pores Made of Mitochondrial ATP Synthase Subunit c in the Neuronal Plasma Membrane and Batten Disease

Molecular genetics and metabolism, 1999-04, Vol.66 (4), p.387-392

1999

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Accumulation of the adenosine triphosphate synthase subunit C in the mnd mutant mouse. A model for neuronal ceroid lipofuscinosis

The American journal of pathology, 1994-04, Vol.144 (4), p.829-835

1994

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Different patterns of hydrophobic protein storage in different forms of neuronal ceroid lipofuscinosis (NCL, Batten disease)

Neuropediatrics, 1997-02, Vol.28 (1), p.45-48

1997

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Ovine ceroid lipofuscinosis. The major lipopigment protein and the lipid-binding subunit of mitochondrial ATP synthase have the same NH2-terminal sequence

The Journal of biological chemistry, 1989-04, Vol.264 (10), p.5736-5740

1989

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The sequence of the major protein stored in ovine ceroid lipofuscinosis is identical with that of the dicyclohexylcarbodiimide-reactive proteolipid of mitochondrial ATP synthase

Biochemical journal, 1990-06, Vol.268 (3), p.751-758

1990

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The neuronal ceroid-lipofuscinoses (Batten diseases): comparative aspects

Neuropathology and applied neurobiology, 1995-02, Vol.21 (1), p.50-60

1995

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Mitochondrial ATP synthase subunit c storage in the ceroid-lipofuscinoses (Batten disease)

American journal of medical genetics, 1992-02, Vol.42 (4), p.561-567

1992

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In vitro culture of neurons from sheep with Batten disease

Molecular genetics and metabolism, 1999-05, Vol.67 (1), p.83-88

1999

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Canine ceroid-lipofuscinoses: A review and classification

Journal of small animal practice, 1994-06, Vol.35 (6), p.299-306

1994

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Splicing Variants in Sheep CLN3, the Gene Underlying Juvenile Neuronal Ceroid Lipofuscinosis

Molecular genetics and metabolism, 1999-06, Vol.67 (2), p.169-175

1999

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Accumulation of sphingolipid activator proteins (SAPs) A and D in granular osmiophilic deposits in miniature Schnauzer dogs with ceroid‐lipofuscinosis

Journal of inherited metabolic disease, 1997-03, Vol.20 (1), p.74-84

1997

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Disease-Specific Pathology in Neurons Cultured from Sheep Affected with Ceroid Lipofuscinosis

Molecular genetics and metabolism, 1999-04, Vol.66 (4), p.381-386

1999

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Use of Electrospray Ionization Mass Spectrometry and Tandem Mass Spectrometry to Study Binding of F 0 Inhibitors to Ceroid Lipofuscinosis Protein, a Model System for Subunit c of Mitochondrial ATP Synthase

Rapid communications in mass spectrometry, 1996, Vol.10 (7), p.790-796

1996

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The neuronal ceroid lipofuscinoses (Batten disease): a group of lysosomal proteinoses

Advances in experimental medicine and biology, 1996, Vol.389, p.129

1996

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The Frequent Occurrence of Thyroid Tumours in Aged Horses

Journal of comparative pathology, 1994, Vol.110 (1), p.57-64

1994

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Ceroid, lipofuscin and the ceroid‐lipofuscinoses (Batten Disease)

Journal of inherited metabolic disease, 1993-03, Vol.16 (2), p.280-283

1993

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Animal medical genetics: a historical perspective on more than 50 years of research into genetic disorders of animals at Massey University

Glial activation spreads from specific cerebral foci and precedes neurodegeneration in presymptomatic ovine neuronal ceroid lipofuscinosis (CLN6)

Defective Endoplasmic Reticulum-resident Membrane Protein CLN6 Affects Lysosomal Degradation of Endocytosed Arylsulfatase A

Lysine 43 Is Trimethylated in Subunit c from Bovine Mitochondrial ATP Synthase and in Storage Bodies Associated with Batten Disease

Mutational Analysis of the Defective Protease in Classic Late-Infantile Neuronal Ceroid Lipofuscinosis, a Neurodegenerative Lysosomal Storage Disorder

Enhanced expression of manganese-dependent superoxide dismutase in human and sheep CLN6 tissues

Neuronal ceroid-lipofuscinosis in Borderdale sheep

Neuronal ceroid lipofuscinosis in Merino sheep

The origin of fluorescence in the neuronal ceroid lipofuscinoses (Batten disease) and neuron cultures from affected sheep for studies of neurodegeneration

Ion Pores Made of Mitochondrial ATP Synthase Subunit c in the Neuronal Plasma Membrane and Batten Disease

Accumulation of the adenosine triphosphate synthase subunit C in the mnd mutant mouse. A model for neuronal ceroid lipofuscinosis

Different patterns of hydrophobic protein storage in different forms of neuronal ceroid lipofuscinosis (NCL, Batten disease)

Ovine ceroid lipofuscinosis. The major lipopigment protein and the lipid-binding subunit of mitochondrial ATP synthase have the same NH2-terminal sequence

The sequence of the major protein stored in ovine ceroid lipofuscinosis is identical with that of the dicyclohexylcarbodiimide-reactive proteolipid of mitochondrial ATP synthase

The neuronal ceroid-lipofuscinoses (Batten diseases): comparative aspects

Mitochondrial ATP synthase subunit c storage in the ceroid-lipofuscinoses (Batten disease)

In vitro culture of neurons from sheep with Batten disease

Canine ceroid-lipofuscinoses: A review and classification

Splicing Variants in Sheep CLN3, the Gene Underlying Juvenile Neuronal Ceroid Lipofuscinosis

Accumulation of sphingolipid activator proteins (SAPs) A and D in granular osmiophilic deposits in miniature Schnauzer dogs with ceroid‐lipofuscinosis

Disease-Specific Pathology in Neurons Cultured from Sheep Affected with Ceroid Lipofuscinosis

Use of Electrospray Ionization Mass Spectrometry and Tandem Mass Spectrometry to Study Binding of F 0 Inhibitors to Ceroid Lipofuscinosis Protein, a Model System for Subunit c of Mitochondrial ATP Synthase

The neuronal ceroid lipofuscinoses (Batten disease): a group of lysosomal proteinoses

The Frequent Occurrence of Thyroid Tumours in Aged Horses

Ceroid, lipofuscin and the ceroid‐lipofuscinoses (Batten Disease)

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