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Multiple system atrophy/progressive supranuclear palsy: alpha-Synuclein, synphilin, tau, and APOE

Neurology, 2000-12, Vol.55 (12), p.1918-1920

2000

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The precursor protein of non-Aβ component of Alzheimer's disease amyloid is a presynaptic protein of the central nervous system

Neuron (Cambridge, Mass.), 1995-02, Vol.14 (2), p.467-475

1995

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Genetic studies in Alzheimer's disease with an NACP/α-synuclein polymorphism

Annals of neurology, 1996-08, Vol.40 (2), p.207-215

1996

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β-Amyloid-mediated inhibition of redox activity (MTT reduction) is not an indicator of astroglial degeneration

Neuroreport, 1996-08, Vol.7 (12), p.2026-2030

1996

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Cell-specific expression of β-amyloid precursor protein isoform mRNAs and proteins in neurons and astrocytes

Brain research. Molecular brain research., 1997-07, Vol.47 (1), p.147-156

1997

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Presenilins and early-onset familial Alzheimer's disease

Neuroreport, 1997-05, Vol.8 (8), p.i-xii

1997

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Polymorphism and chromosomal localization of the GI-form of human glutathione peroxidase (GPX2) on 14q24.1 by in situ hybridization

Genomics (San Diego, Calif.), 1996-03, Vol.32 (2), p.272-276

1996

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The genetics of Parkinson's disease

Current Opinion in Genetics & Development, 2000-06, Vol.10 (3), p.292-298

2000

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The human NACP/α-synuclein gene: chromosome assignment to 4q21.3–q22 and TaqI RFLP analysis

Genomics (San Diego, Calif.), 1995-03, Vol.26 (2), p.425-427

1995

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Protocol: Preparation and purification of antisera against different regions or isoforms of beta -amyloid precursor protein

Brain research. Brain research protocols, 1997-12, Vol.2 (1), p.23-30

1997

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Preparation and purification of antisera against different regions or isoforms of β-amyloid precursor protein

Brain research. Brain research protocols, 1997-12, Vol.2 (1), p.23-30

1997

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Human endopeptidase (THOP1) is localized on chromosome 19 within the linkage region for the late-onset Alzheimer disease AD2 locus

Genomics (San Diego, Calif.), 1996-01, Vol.31 (2), p.246-249

1996

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A G super(+1) arrow right A transversion at the 5' splice site of intron 69 of the dystrophin gene causing the absence of peripheral nerve Dp116 and severe clinical involvement in a DMD patient

Human molecular genetics, 1995-01, Vol.4 (11), p.2171-2174

1995

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A G+1→A transversion at the 5' splice site of intron 69 of the dystrophin gene causing the absence of peripheral nerve Dp116 and severe clinical involvement in a DMD patient

Human molecular genetics, 1995-11, Vol.4 (11), p.2171-2174

1995

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A STUDY OF THE EXPRESSION OF A PROTEIN PROTEINASE INHIBITOR FROM SWEET CORN (TRYPSIN, BLOOD COAGULATION)

ROHAN DE SILVA, H A

1991

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A Methodological Approach to Identify Natural Compounds with Antifibrotic Activity and the Potential to Treat Pulmonary Fibrosis Using Single-Cell Sequencing and Primary Human Lung Macrophages

International journal of molecular sciences, 2023-10, Vol.24 (20), p.15104

2023

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Characteristics of two distinct clinical phenotypes in pathologically proven progressive supranuclear palsy: Richardson's syndrome and PSP-parkinsonism

Brain (London, England : 1878), 2005-06, Vol.128 (6), p.1247-1258

2005

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The MAPT H1c risk haplotype is associated with increased expression of tau and especially of 4 repeat containing transcripts

Neurobiology of disease, 2007-03, Vol.25 (3), p.561-570

2007

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Rational therapeutic approaches to progressive supranuclear palsy

Brain (London, England : 1878), 2010-06, Vol.133 (6), p.1578-1590

2010

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The tau H2 haplotype is almost exclusively Caucasian in origin

Neuroscience letters, 2004-10, Vol.369 (3), p.183-185

2004

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Variation at the TRIM11 locus modifies progressive supranuclear palsy phenotype

Annals of neurology, 2018-10, Vol.84 (4), p.485-496

2018

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Argyrophilic Grain Disease Is a Sporadic 4-Repeat Tauopathy

Journal of neuropathology and experimental neurology, 2002-06, Vol.61 (6), p.547-556

2002

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Association of Dyslipidemia and Glucose Abnormalities With Antiretroviral Treatment in a Cohort of HIV-Infected Latin American Children

Journal of acquired immune deficiency syndromes (1999), 2017-01, Vol.74 (1), p.e1-e8

2017

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The expression of DJ‐1 (PARK7) in normal human CNS and idiopathic Parkinson’s disease

Brain (London, England : 1878), 2004-02, Vol.127 (2), p.420-430

2004

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Nonalcoholic fatty liver disease among potential live liver donors—A preliminary experience from Sri Lanka

Indian journal of gastroenterology, 2014-11, Vol.33 (6), p.573-574

2014

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Multiple system atrophy/progressive supranuclear palsy: alpha-Synuclein, synphilin, tau, and APOE

The precursor protein of non-Aβ component of Alzheimer's disease amyloid is a presynaptic protein of the central nervous system

Genetic studies in Alzheimer's disease with an NACP/α-synuclein polymorphism

β-Amyloid-mediated inhibition of redox activity (MTT reduction) is not an indicator of astroglial degeneration

Cell-specific expression of β-amyloid precursor protein isoform mRNAs and proteins in neurons and astrocytes

Presenilins and early-onset familial Alzheimer's disease

Polymorphism and chromosomal localization of the GI-form of human glutathione peroxidase (GPX2) on 14q24.1 by in situ hybridization

The genetics of Parkinson's disease

The human NACP/α-synuclein gene: chromosome assignment to 4q21.3–q22 and TaqI RFLP analysis

Protocol: Preparation and purification of antisera against different regions or isoforms of beta -amyloid precursor protein

Preparation and purification of antisera against different regions or isoforms of β-amyloid precursor protein

Human endopeptidase (THOP1) is localized on chromosome 19 within the linkage region for the late-onset Alzheimer disease AD2 locus

A G super(+1) arrow right A transversion at the 5' splice site of intron 69 of the dystrophin gene causing the absence of peripheral nerve Dp116 and severe clinical involvement in a DMD patient

A G+1→A transversion at the 5' splice site of intron 69 of the dystrophin gene causing the absence of peripheral nerve Dp116 and severe clinical involvement in a DMD patient

A STUDY OF THE EXPRESSION OF A PROTEIN PROTEINASE INHIBITOR FROM SWEET CORN (TRYPSIN, BLOOD COAGULATION)

A Methodological Approach to Identify Natural Compounds with Antifibrotic Activity and the Potential to Treat Pulmonary Fibrosis Using Single-Cell Sequencing and Primary Human Lung Macrophages

Characteristics of two distinct clinical phenotypes in pathologically proven progressive supranuclear palsy: Richardson's syndrome and PSP-parkinsonism

The MAPT H1c risk haplotype is associated with increased expression of tau and especially of 4 repeat containing transcripts

Rational therapeutic approaches to progressive supranuclear palsy

The tau H2 haplotype is almost exclusively Caucasian in origin

Variation at the TRIM11 locus modifies progressive supranuclear palsy phenotype

Argyrophilic Grain Disease Is a Sporadic 4-Repeat Tauopathy

Association of Dyslipidemia and Glucose Abnormalities With Antiretroviral Treatment in a Cohort of HIV-Infected Latin American Children

The expression of DJ‐1 (PARK7) in normal human CNS and idiopathic Parkinson’s disease

Nonalcoholic fatty liver disease among potential live liver donors—A preliminary experience from Sri Lanka

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