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Developmental malformations in Huntington disease: neuropathologic evidence of focal neuronal migration defects in a subset of adult brains

Acta neuropathologica, 2021-03, Vol.141 (3), p.399-413

2021

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Peroxisome biogenesis disorders: The role of peroxisomes and metabolic dysfunction in developing brain

Journal of inherited metabolic disease, 2005-01, Vol.28 (3), p.369-383

2005

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Increased number of Purkinje cell dendritic swellings in essential tremor

European journal of neurology, 2012-04, Vol.19 (4), p.625-630

2012

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Abnormal cerebellar histogenesis in PEX2 Zellweger mice reflects multiple neuronal defects induced by peroxisome deficiency

Journal of comparative neurology (1911), 2003-06, Vol.461 (3), p.394-413

Faust, Phyllis L.

2003

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Neuropathology of lubag (x-linked dystonia parkinsonism)

Movement disorders, 1993, Vol.8 (3), p.387-390

1993

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Cloning and Sequence Analysis of cDNA for Human Cathepsin D

Proceedings of the National Academy of Sciences - PNAS, 1985-08, Vol.82 (15), p.4910-4914

1985

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Generation of a lysosomal enzyme targeting signal in the secretory protein pepsinogen

Cell, 1990-10, Vol.63 (2), p.281-291

1990

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Neuropathological changes in essential tremor: 33 cases compared with 21 controls

Brain (London, England : 1878), 2007-12, Vol.130 (12), p.3297-3307

2007

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Targeted Deletion of the PEX2 Peroxisome Assembly Gene in Mice Provides a Model for Zellweger Syndrome, a Human Neuronal Migration Disorder

The Journal of cell biology, 1997-12, Vol.139 (5), p.1293-1305

1997

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Disturbed Cholesterol Homeostasis in a Peroxisome-Deficient PEX2 Knockout Mouse Model

Molecular and Cellular Biology, 2004-01, Vol.24 (1), p.1-13

2004

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Activation of p47(PHOX), a cytosolic subunit of the leukocyte NADPH oxidase. Phosphorylation of ser-359 or ser-370 precedes phosphorylation at other sites and is required for activity

The Journal of biological chemistry, 1998-12, Vol.273 (52), p.35147-35152

1998

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Renin, a Secretory Glycoprotein, Acquires Phosphomannosyl Residues

The Journal of cell biology, 1987-11, Vol.105 (5), p.1947-1955

1987

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Polyglucosan body disease simulating amyotrophic lateral sclerosis

Neurology, 1993-04, Vol.43 (4), p.785-785

1993

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Increased number of heterotopic Purkinje cells in essential tremor

Journal of neurology, neurosurgery and psychiatry, 2011-09, Vol.82 (9), p.1038-1040

2011

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Overexpression, purification, and some properties of the AdoCbl-dependent ethanolamine ammonia-lyase from Salmonella typhimurium

Archives of biochemistry and biophysics, 1992-04, Vol.294 (1), p.50-54

1992

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New directions for neuronal migration

Current opinion in neurobiology, 1998-02, Vol.8 (1), p.45-54

1998

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Rest tremor in advanced essential tremor: a post-mortem study of nine cases

Journal of neurology, neurosurgery and psychiatry, 2011-03, Vol.82 (3), p.261-265

2011

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Biopsy-proven isolated sarcoid meningitis. Case report

Journal of neurosurgery, 1993-06, Vol.78 (6), p.994-996

1993

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The peroxisome deficient PEX2 Zellweger mouse: pathologic and biochemical correlates of lipid dysfunction

Journal of molecular neuroscience, 2001-04, Vol.16 (2-3), p.289-298

2001

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Expression of the yeast aspartyl protease, proteinase A. Phosphorylation and binding to the mannose 6-phosphate receptor are altered by addition of cathepsin D sequences

The Journal of biological chemistry, 1989-01, Vol.264 (1), p.479-488

1989

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Gonadotroph tumours with a low SF‐1 labelling index are more likely to recur and are associated with enrichment of the PI3K‐AKT pathway

Neuropathology and applied neurobiology, 2021-04, Vol.47 (3), p.415-427

2021

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Expression of Human Cathepsin D in Xenopus Oocytes: Phosphorylation and Intracellular Targeting

The Journal of cell biology, 1987-11, Vol.105 (5), p.1937-1945

1987

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"Hairy Baskets" Associated With Degenerative Purkinje Cell Changes in Essential Tremor

Journal of neuropathology and experimental neurology, 2010-03, Vol.69 (3), p.262-271

2010

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Purification of brain peroxisomes and localization of 3‐hydroxy‐3‐methylglutaryl coenzyme A reductase

European journal of biochemistry, 2001-09, Vol.268 (18), p.4850-4859

2001

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The phosphorylation of the respiratory burst oxidase component p47phox during neutrophil activation. Phosphorylation of sites recognized by protein kinase C and by proline-directed kinases

The Journal of biological chemistry, 1994-09, Vol.269 (38), p.23431-23436

1994

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Developmental malformations in Huntington disease: neuropathologic evidence of focal neuronal migration defects in a subset of adult brains

Peroxisome biogenesis disorders: The role of peroxisomes and metabolic dysfunction in developing brain

Increased number of Purkinje cell dendritic swellings in essential tremor

Abnormal cerebellar histogenesis in PEX2 Zellweger mice reflects multiple neuronal defects induced by peroxisome deficiency

Neuropathology of lubag (x-linked dystonia parkinsonism)

Cloning and Sequence Analysis of cDNA for Human Cathepsin D

Generation of a lysosomal enzyme targeting signal in the secretory protein pepsinogen

Neuropathological changes in essential tremor: 33 cases compared with 21 controls

Targeted Deletion of the PEX2 Peroxisome Assembly Gene in Mice Provides a Model for Zellweger Syndrome, a Human Neuronal Migration Disorder

Disturbed Cholesterol Homeostasis in a Peroxisome-Deficient PEX2 Knockout Mouse Model

Activation of p47(PHOX), a cytosolic subunit of the leukocyte NADPH oxidase. Phosphorylation of ser-359 or ser-370 precedes phosphorylation at other sites and is required for activity

Renin, a Secretory Glycoprotein, Acquires Phosphomannosyl Residues

Polyglucosan body disease simulating amyotrophic lateral sclerosis

Increased number of heterotopic Purkinje cells in essential tremor

Overexpression, purification, and some properties of the AdoCbl-dependent ethanolamine ammonia-lyase from Salmonella typhimurium

New directions for neuronal migration

Rest tremor in advanced essential tremor: a post-mortem study of nine cases

Biopsy-proven isolated sarcoid meningitis. Case report

The peroxisome deficient PEX2 Zellweger mouse: pathologic and biochemical correlates of lipid dysfunction

Expression of the yeast aspartyl protease, proteinase A. Phosphorylation and binding to the mannose 6-phosphate receptor are altered by addition of cathepsin D sequences

Gonadotroph tumours with a low SF‐1 labelling index are more likely to recur and are associated with enrichment of the PI3K‐AKT pathway

Expression of Human Cathepsin D in Xenopus Oocytes: Phosphorylation and Intracellular Targeting

"Hairy Baskets" Associated With Degenerative Purkinje Cell Changes in Essential Tremor

Purification of brain peroxisomes and localization of 3‐hydroxy‐3‐methylglutaryl coenzyme A reductase

The phosphorylation of the respiratory burst oxidase component p47phox during neutrophil activation. Phosphorylation of sites recognized by protein kinase C and by proline-directed kinases

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