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A Positive Control for Detection of Functional CD4 T Cells in PBMC: The CPI Pool

Cells (Basel, Switzerland), 2017-12, Vol.6 (4), p.47

2017

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High-Throughput GLP-Capable Target Cell Visualization Assay for Measuring Cell-Mediated Cytotoxicity

Cells (Basel, Switzerland), 2018-04, Vol.7 (5), p.35

2018

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Aberrant metal binding by prion protein in human prion disease

Journal of neurochemistry, 2001-09, Vol.78 (6), p.1400-1408

2001

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Protease-Resistant Human Prion Protein and Ferritin Are Cotransported across Caco-2 Epithelial Cells: Implications for Species Barrier in Prion Uptake from the Intestine

The Journal of neuroscience, 2004-12, Vol.24 (50), p.11280-11290

2004

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Oxidative impairment in scrapie‐infected mice is associated with brain metals perturbations and altered antioxidant activities

Journal of neurochemistry, 2001-11, Vol.79 (3), p.689-698

2001

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Intercellular Transfer of the Cellular Prion Protein

The Journal of biological chemistry, 2002-12, Vol.277 (49), p.47671-47678

2002

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Anti-prion antibodies for prophylaxis following prion exposure in mice

Neuroscience letters, 2003-01, Vol.336 (3), p.185-187

2003

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Increased levels of oxidative stress markers detected in the brains of mice devoid of prion protein

Journal of neurochemistry, 2001-01, Vol.76 (2), p.565-572

2001

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Aggresome formation by mutant prion proteins: the unfolding role of proteasomes in familial prion disorders

Journal of Alzheimer's disease, 2003-02, Vol.5 (1), p.15-23

2003

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Heterogeneity of normal prion protein in two‐dimensional immunoblot: presence of various glycosylated and truncated forms

Journal of neurochemistry, 2002-06, Vol.81 (5), p.1092-1101

2002

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An Aggregation-Specific Enzyme-Linked Immunosorbent Assay: Detection of Conformational Differences between Recombinant PrP Protein Dimers and PrPSc Aggregates

Journal of Virology, 2005-10, Vol.79 (19), p.12355-12364

2005

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Prion protein is ubiquitinated after developing protease resistance in the brains of scrapie-infected mice

The Journal of pathology, 2004-05, Vol.203 (1), p.603-608

2004

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Prion Disease: A Loss of Antioxidant Function?

Biochemical and biophysical research communications, 2000-08, Vol.275 (2), p.249-252

2000

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Biochemical Fingerprints of Prion Infection: Accumulations of Aberrant Full-Length and N-Terminally Truncated PrP Species Are Common Features in Mouse Prion Disease

Journal of Virology, 2005-01, Vol.79 (2), p.934-943

2005

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Natural T cell autoreactivity to melanoma antigens: clonally expanded melanoma-antigen specific CD8 + memory T cells can be detected in healthy humans

Cancer Immunology, Immunotherapy, 2019-05, Vol.68 (5), p.709-720

2019

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Novel Differences between Two Human Prion Strains Revealed by Two-dimensional Gel Electrophoresis

The Journal of biological chemistry, 2001-10, Vol.276 (40), p.37284-37288

2001

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Differential expression of cellular prion protein in mouse brain as detected with multiple anti-PrP monoclonal antibodies

Brain research, 2001-03, Vol.896 (1), p.118-129

2001

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Epitope scanning reveals gain and loss of strain specific antibody binding epitopes associated with the conversion of normal cellular prion to scrapie prion

Journal of neurochemistry, 2004-09, Vol.90 (5), p.1205-1217

2004

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The Expression and Potential Function of Cellular Prion Protein in Human Lymphocytes

Cellular immunology, 2001-01, Vol.207 (1), p.49-58

2001

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Normal Cellular Prior Protein Is Preferentially Expressed on Subpopulations of Murine Hemopoietic Cells

The Journal of immunology (1950), 2001-03, Vol.166 (6), p.3733-3742

2001

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Novel Antibody-Lectin Enzyme-Linked Immunosorbent Assay That Distinguishes Prion Proteins in Sporadic and Variant Cases of Creutzfeldt-Jakob Disease

Journal of Clinical Microbiology, 2005-03, Vol.43 (3), p.1118-1126

2005

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Biochemical fingerprints of prion diseases: scrapie prion protein in human prion diseases that share prion genotype and type

Journal of neurochemistry, 2005-01, Vol.92 (1), p.132-142

2005

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Induction of HO-1 and NOS in Doppel-Expressing Mice Devoid of PrP: Implications for Doppel Function

Molecular and cellular neuroscience, 2001-04, Vol.17 (4), p.768-775

2001

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Absence of protease-resistant prion protein in the cerebrospinal fluid of Creutzfeldt-Jakob disease

The Journal of pathology, 2001-05, Vol.194 (1), p.9-14

2001

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Guanidine hydrochloride extraction and detection of prion proteins in mouse and hamster prion diseases by ELISA

The Journal of pathology, 2003-04, Vol.199 (4), p.534-541

2003

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A Positive Control for Detection of Functional CD4 T Cells in PBMC: The CPI Pool

High-Throughput GLP-Capable Target Cell Visualization Assay for Measuring Cell-Mediated Cytotoxicity

Aberrant metal binding by prion protein in human prion disease

Protease-Resistant Human Prion Protein and Ferritin Are Cotransported across Caco-2 Epithelial Cells: Implications for Species Barrier in Prion Uptake from the Intestine

Oxidative impairment in scrapie‐infected mice is associated with brain metals perturbations and altered antioxidant activities

Intercellular Transfer of the Cellular Prion Protein

Anti-prion antibodies for prophylaxis following prion exposure in mice

Increased levels of oxidative stress markers detected in the brains of mice devoid of prion protein

Aggresome formation by mutant prion proteins: the unfolding role of proteasomes in familial prion disorders

Heterogeneity of normal prion protein in two‐dimensional immunoblot: presence of various glycosylated and truncated forms

An Aggregation-Specific Enzyme-Linked Immunosorbent Assay: Detection of Conformational Differences between Recombinant PrP Protein Dimers and PrPSc Aggregates

Prion protein is ubiquitinated after developing protease resistance in the brains of scrapie-infected mice

Prion Disease: A Loss of Antioxidant Function?

Biochemical Fingerprints of Prion Infection: Accumulations of Aberrant Full-Length and N-Terminally Truncated PrP Species Are Common Features in Mouse Prion Disease

Natural T cell autoreactivity to melanoma antigens: clonally expanded melanoma-antigen specific CD8 + memory T cells can be detected in healthy humans

Novel Differences between Two Human Prion Strains Revealed by Two-dimensional Gel Electrophoresis

Differential expression of cellular prion protein in mouse brain as detected with multiple anti-PrP monoclonal antibodies

Epitope scanning reveals gain and loss of strain specific antibody binding epitopes associated with the conversion of normal cellular prion to scrapie prion

The Expression and Potential Function of Cellular Prion Protein in Human Lymphocytes

Normal Cellular Prior Protein Is Preferentially Expressed on Subpopulations of Murine Hemopoietic Cells

Novel Antibody-Lectin Enzyme-Linked Immunosorbent Assay That Distinguishes Prion Proteins in Sporadic and Variant Cases of Creutzfeldt-Jakob Disease

Biochemical fingerprints of prion diseases: scrapie prion protein in human prion diseases that share prion genotype and type

Induction of HO-1 and NOS in Doppel-Expressing Mice Devoid of PrP: Implications for Doppel Function

Absence of protease-resistant prion protein in the cerebrospinal fluid of Creutzfeldt-Jakob disease

Guanidine hydrochloride extraction and detection of prion proteins in mouse and hamster prion diseases by ELISA

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