A. Taraboulos

发表

A Deleterious Mutation in DNAJC6 Encoding the Neuronal-Specific Clathrin-Uncoating Co-Chaperone Auxilin, Is Associated with Juvenile Parkinsonism

K. Kaestner, A. Brice, S. Lesage, 2012, PloS one.

Immunologic and molecular biologic studies of prion proteins in bovine spongiform encephalopathy.

H Serban, S. Prusiner, J. Gabriel, 1993, The Journal of infectious diseases.

Participation of fresh water in chert diagenesis: evidence from oxygen isotopes and boron alpha-track mapping

Y. Kolodny, A. Taraboulos, U. Frieslander, 1980 .

An SNX10 mutation causes malignant osteopetrosis of infancy

S. Zenvirt, A. Shaag, O. Elpeleg, 2012, Journal of Medical Genetics.

Of mice and (mad) cows--transgenic mice help to understand prions.

R. Gabizon, A. Taraboulos, 1997, Trends in genetics : TIG.

RAPID DETECTION OF CREUTZFELDT-JAKOB DISEASE AND SCRAPIE PRION PROTEINS: 88

S. Prusiner, S. DeArmond, D. Serban, 1990 .

Rapid detection of Creutzfeldt‐Jakob disease and scrapie prion proteins

S. Prusiner, S. DeArmond, D. Serban, 1990, Neurology.

Both raft- and non-raft proteins associate with CHAPS-insoluble complexes: some APP in large complexes.

H. Atlan, A. Taraboulos, A. Rouvinski, 2003, Biochemical and biophysical research communications.

Structural changes in human cytomegalovirus cytoplasmic assembly sites in the absence of UL97 kinase activity.

D. Wolf, A. Honigman, A. Taraboulos, 2006, Virology.

Transgenic over-expression of mammalian heparanase delays prion disease onset and progression.

Y. Tal, A. Taraboulos, I. Vlodavsky, 2015, Biochemical and biophysical research communications.

Methylphenidate prolongs symptom-free period of experimental prion disease in mice

Y. Tal, Kirill Makedonski, A. Taraboulos, 2015, Journal of the Neurological Sciences.

Synthesis andTrafficking ofPrion Proteins inCultured Cells

A. Taraboulos, 1992 .

Protease-sensitive scrapie prion protein in aggregates of heterogeneous sizes.

G. Friedlander, R. Gabizon, Y. Yedidia, 2002, Biochemistry.

Prion adsorption to stainless steel is promoted by nickel and molybdenum.

K. Kristensson, T. Bergman, P. Löw, 2009, The Journal of general virology.

Processing and Degradation of Exogenous Prion Protein by CD11c+ Myeloid Dendritic Cells In Vitro

K. Kristensson, H. Ljunggren, P. Löw, 2002, Journal of Virology.

Biosynthesis of the Scrapie Prion Protein in Scrapie-Infected Cells

S. Prusiner, D. Borchelt, A. Raeber, 1993 .

Live imaging of prions reveals nascent PrPSc in cell-surface, raft-associated amyloid strings and webs

G. Carlson, K. Kristensson, P. Peters, 2014, The Journal of cell biology.

Human Cytomegalovirus UL97 Kinase and Nonkinase Functions Mediate Viral Cytoplasmic Secondary Envelopment

S. Chou, D. Wolf, J. Weinstein, 2011, Journal of Virology.

Scrapie Protein Degradation by Cysteine Proteases in CD11c+ Dendritic Cells and GT1-1 Neuronal Cells

K. Kristensson, H. Ljunggren, P. Löw, 2004, Journal of Virology.

Subcellular colocalization of the cellular and scrapie prion proteins in caveolae-like membranous domains.

S. Prusiner, S. DeArmond, H. Wille, 1996, Proceedings of the National Academy of Sciences of the United States of America.

Evidence for synthesis of scrapie prion proteins in the endocytic pathway.

S. Prusiner, D. Borchelt, A. Taraboulos, 1992, The Journal of biological chemistry.

Cholesterol Depletion and Modification of COOH-Terminal Targeting Sequence of the Priori Protein Inhibit Formation of the Scrapie Isoform

S. Prusiner, A. Taraboulos, M. Scott, 2002 .

Acquisition of protease resistance by prion proteins in scrapie-infected cells does not require asparagine-linked glycosylation.

S. Prusiner, D. Borchelt, M. Scott, 1990, Proceedings of the National Academy of Sciences of the United States of America.

Three scrapie prion isolates exhibit different accumulation patterns of the prion protein scrapie isoform.

R. Bowler, S. Prusiner, S. DeArmond, 1993, Proceedings of the National Academy of Sciences of the United States of America.

Regional mapping of prion proteins in brain.

S. Prusiner, S. DeArmond, D. Serban, 1992, Proceedings of the National Academy of Sciences of the United States of America.

Replication of distinct scrapie prion isolates is region specific in brains of transgenic mice and hamsters.

S. Prusiner, S. DeArmond, M. Scott, 1992, Genes & development.

Scrapie and cellular prion proteins differ in their kinetics of synthesis and topology in cultured cells

S. Prusiner, D. Borchelt, N. Stahl, 1990, The Journal of cell biology.

Scrapie‐like prion protein accumulates in aggresomes of cyclosporin A‐treated cells

E. Cohen, A. Taraboulos, 2003, The EMBO journal.

Proteasomes and ubiquitin are involved in the turnover of the wild‐type prion protein

Albert Taraboulos, Y. Yedidia, A. Taraboulos, 2001, The EMBO journal.

Subcellular trafficking abnormalities of a prion protein with a disrupted disulfide loop

Z. Meiner, R. Gabizon, A. Taraboulos, 1999, FEBS letters.

Cholesterol depletion and modification of COOH-terminal targeting sequence of the prion protein inhibit formation of the scrapie isoform [published erratum appears in J Cell Biol 1995 Jul;130(2):501]

S. Prusiner, M. Scott, D. Avrahami, 1995, The Journal of cell biology.

Scrapie prion proteins accumulate in the cytoplasm of persistently infected cultured cells

S. Prusiner, D. Serban, A. Taraboulos, 1990, The Journal of cell biology.

Synthesis and trafficking of prion proteins in cultured cells.

S. Prusiner, D. Borchelt, A. Raeber, 1992, Molecular biology of the cell.

Scrapie-infected murine neuroblastoma cells produce protease-resistant prion proteins

S. Prusiner, D. Borchelt, D. Kingsbury, 1988, Journal of virology.

The Priority position paper: Protecting Europe's food chain from prions

A. Aguzzi, K. Kristensson, J. D. del Río, 2016, Prion.

Protease-resistant and Detergent-insoluble Prion Protein Is Not Necessarily Associated with Prion Infectivity*

Z. Meiner, R. Gabizon, G. Shaked, 1999, The Journal of Biological Chemistry.

Complete Freund's adjuvant immunization prolongs survival in experimental prion disease in mice

I. Cohen, Z. Meiner, Y. Tal, 2003, Journal of neuroscience research.

Characterization of Detergent-insoluble Complexes Containing the Cellular Prion Protein and Its Scrapie Isoform*

G. Friedlander, N. Naslavsky, A. Taraboulos, 1997, The Journal of Biological Chemistry.

The Anti-prion Activity of Congo Red

R. Gabizon, A. Taraboulos, A. Yanai, 1998, The Journal of Biological Chemistry.

Cellular Heparan Sulfate Participates in the Metabolism of Prions*

J. Esko, Y. Tal, A. Taraboulos, 2003, Journal of Biological Chemistry.

Modulation of proteinase‐K resistant prion protein by prion peptide immunization

I. Cohen, Y. Tal, A. Taraboulos, 2001, European journal of immunology.

Scrapie‐Infected Mice and PrP Knockout Mice Share Abnormal Localization and Activity of Neuronal Nitric Oxide Synthase

R. Gabizon, H. Ovadia, G. Keshet, 1999, Journal of neurochemistry.

Heparan Sulfate Is a Cellular Receptor for Purified Infectious Prions*

Y. Yedidia, D. Papy-Garcia, A. Taraboulos, 2005, Journal of Biological Chemistry.

Scrapie prions alter receptor‐mediated calcium responses in cultured cells

S. Prusiner, S. DeArmond, K. Kristensson, 1993, Neurology.

Novel heparan mimetics potently inhibit the scrapie prion protein and its endocytosis.

R. Gabizon, D. Papy-Garcia, A. Taraboulos, 2003, Biochemical and biophysical research communications.

Ultrastructural localization of scrapie prion proteins in cytoplasmic vesicles of infected cultured cells.

S. Prusiner, S. DeArmond, N. Gonatas, 1991, Laboratory investigation; a journal of technical methods and pathology.

Cationic polysaccharides as antiprion agents.

A. Domb, T. Azzam, A. Taraboulos, 2005, Journal of medicinal chemistry.

Intracellular accumulation of the cellular prion protein after mutagenesis of its Asn-linked glycosylation sites.

S. Prusiner, M. Rogers, A. Taraboulos, 1990, Glycobiology.

Sphingolipid Depletion Increases Formation of the Scrapie Prion Protein in Neuroblastoma Cells Infected with Prions*

G. Friedlander, Y. Barenholz, H. Shmeeda, 1999, The Journal of Biological Chemistry.

Reconstitution of Prion Infectivity from Solubilized Protease-resistant PrP and Nonprotein Components of Prion Rods*

Z. Meiner, R. Gabizon, G. Shaked, 2001, The Journal of Biological Chemistry.

Cholesterol depletion and modification of COOH-terminal targeting sequence of the prion protein inhibit formation of the scrapie isoform [published erratum appears in J Cell Biol 1995 Jul;130(2):501]

S. Prusiner, M. Scott, A. Taraboulos, 1995, The Journal of cell biology.

Protein and Its Scrapie Isoform Complexes Containing the Cellular Prion Characterization of Detergent-insoluble Cell Biology and Metabolism:

G. Friedlander, A. Taraboulos, A. Yanai, 2013 .

Prion adsorption to stainless steel is promoted by nickel and molybdenum.

K. Kristensson, T. Bergman, P. Löw, 2009, The Journal of general virology.

Biosynthesis of the prion proteins in scrapie-infected cells in culture.

A. Taraboulos, M. Scott, A. Semenov, 1994, Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas.