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On the adsorption of human acidic proline-rich proteins (PRP-1 and PRP-3) and statherin at solid/liquid interfacesLINDH, L; GLANTZ, P-O; STRÖMBERG, N et al.Biofouling (Print). 2002, Vol 18, Num 2, pp 87-94, issn 0892-7014Article

Inactivation of Template-Directed Misfolding of Infectious Prion Protein by OzoneNING DING; NEUMANN, Norman F; PRICE, Luke M et al.Applied and environmental microbiology (Print). 2012, Vol 78, Num 3, pp 613-620, issn 0099-2240, 8 p.Article

HEPES inhibits the conversion of prion protein in cell cultureDELMOULY, Karine; BELONDRADE, Maxime; CASANOVA, Danielle et al.Journal of general virology. 2011, Vol 92, pp 1244-1250, issn 0022-1317, 7 p., 5Article

The effects of leukodepletion on the generation and removal of microvesicles and prion protein in blood componentsKRAILADSIRI, Pranee; SEGHATCHIAN, Jerard; TURNER, Marc et al.Transfusion (Philadelphia, PA). 2006, Vol 46, Num 3, pp 407-417, issn 0041-1132, 11 p.Article

Substrate threading through the central pore of the Hsp104 chaperone as a common mechanism for protein disaggregation and prion propagationTESSARZ, Peter; MOGK, Axel; BUKAU, Bernd et al.Molecular microbiology (Print). 2008, Vol 68, Num 1, pp 87-97, issn 0950-382X, 11 p.Article

Crucial Role for Prion Protein Membrane Anchoring in the Neuroinvasion and Neural Spread of Prion InfectionKLINGEBORN, Mikael; RACE, Brent; MEADE-WHITE, Kimberly D et al.Journal of virology. 2011, Vol 85, Num 4, pp 1484-1494, issn 0022-538X, 11 p.Article

Feasibility study of a screening assay that identifies the abnormal prion protein PrPTSE in plasma: initial results with 20,000 samplesGUNTZ, Philippe; WALTER, Christine; SCHOSSELER, Patricia et al.Transfusion (Philadelphia, PA). 2010, Vol 50, Num 5, pp 989-995, issn 0041-1132, 7 p.Article

Sequestration of essential proteins causes prion associated toxicity in yeastVISHVESHWARA, Namitha; BRADLEY, Michael E; LIEBMAN, Susan W et al.Molecular microbiology (Print). 2009, Vol 73, Num 6, pp 1101-1114, issn 0950-382X, 14 p.Article

Divergent expression of cellular prion protein on blood cells of human and nonhuman primatesHOLADA, Karel; SIMAK, Jan; BROWN, Paul et al.Transfusion (Philadelphia, PA). 2007, Vol 47, Num 12, pp 2223-2232, issn 0041-1132, 10 p.Article

Pathogenic prion protein is degraded by a manganese oxide mineral found in soilsRUSSO, Fabio; JOHNSON, Christopher J; JOHNSON, Chad J et al.Journal of general virology. 2009, Vol 90, pp 275-280, issn 0022-1317, 6 p., 1Article

Prion Protein Expression and Release by Mast Cells After ActivationHADDON, D. James; HUGHES, Michael R; ANTIGNANO, Frann et al.The Journal of infectious diseases. 2009, Vol 200, Num 5, pp 827-831, issn 0022-1899, 5 p.Article

Prion Protein Glycosylation Is Not Required for Strain-Specific NeurotropismPIRO, Justin R; HARRIS, Brent T; NISHINA, Koren et al.Journal of virology. 2009, Vol 83, Num 11, pp 5321-5328, issn 0022-538X, 8 p.Article

Physiological role of the cellular prion proteinZOMOSA-SIGNORET, Viviana; ARNAUD, Jacques-Damien; FONTES, Pascaline et al.Veterinary research (Print). 2008, Vol 39, Num 4, pp 57-72, issn 0928-4249, 16 p.Article

Clinical Characterization of a Kindred With a Novel 12-Octapeptide Repeat Insertion in the Prion Protein GeneKUMAR, Neeraj; BOEVE, Bradley F; JACK, Clifford R et al.Archives of neurology (Chicago). 2011, Vol 68, Num 9, pp 1165-1170, issn 0003-9942, 6 p.Article

A novel insertional mutation in the prion protein gene : clinical and bio-molecular findingsMAURO, C; GIACCONE, G; COTRUFO, R et al.Journal of neurology, neurosurgery and psychiatry. 2008, Vol 79, Num 12, pp 1395-1398, issn 0022-3050, 4 p.Article

Polymorphisms within the prion (PrP) and prion-like protein (Doppel) genes in ADGOLANSKA, E; HULAS-BIGOSZEWSKA, K; RUTKIEWICZ, E et al.Neurology. 2004, Vol 62, Num 2, pp 313-315, issn 0028-3878, 3 p.Article

Aptamer-mediated magnetic and gold-coated magnetic nanoparticles as detection assay for prion protein assessmentKOUASSI, Gilles K; PING WANG; SREEVATAN, Srinand et al.Biotechnology progress. 2007, Vol 23, Num 5, pp 1239-1244, issn 8756-7938, 6 p.Article

Novel prion protein gene mutation presenting with subacute PSP-like syndromeROWE, D. B; LEWIS, V; NEEDHAM, M et al.Neurology. 2007, Vol 68, Num 11, pp 868-870, issn 0028-3878, 3 p.Article

Quantitative profiling of the pathological prion protein allotypes in bank voles by liquid chromatography-mass spectrometryCARTONI, C; SCHININA, M. E; POCCHIARI, M et al.Journal of chromatography. B. 2007, Vol 849, Num 1-2, pp 302-306, issn 1570-0232, 5 p.Article

Underestimation of the expression of cellular prion protein on human red blood cellsPANIGAJ, Martin; BROUCKOVA, Adela; GLIEROVA, Hana et al.Transfusion (Philadelphia, PA). 2011, Vol 51, Num 5, pp 1012-1021, issn 0041-1132, 10 p.Article

Amyloid Fibrils of the HET-s(218-289) Prion Form a β Solenoid with a Triangular Hydrophobic CoreWASMER, Christian; LANGE, Adam; VAN MELCKEBEKE, Hélène et al.Science (Washington, D.C.). 2008, Vol 319, Num 5869, pp 1523-1526, issn 0036-8075, 4 p.Article

Scrapie PrP 27-30 is a sialoglycoproteinBOLTON, D. C; MEYER, R. K; PRUSINER, S. B et al.Journal of virology. 1985, Vol 53, Num 2, pp 596-606, issn 0022-538XArticle

Prion Protein with an Insertional Mutation Accumulates on Axonal and Dendritic Plasmalemma and Is Associated with Distinctive Ultrastructural ChangesJEFFREY, Martin; GOODSIR, Caroline; MCGOVERN, Gillian et al.The American journal of pathology. 2009, Vol 175, Num 3, pp 1208-1217, issn 0002-9440, 10 p.Article

Insights into the role of the immune system in prion diseasesBERG, L. J.Proceedings of the National Academy of Sciences of the United States of America. 1994, Vol 91, Num 2, pp 429-432, issn 0027-8424Article

Calreticulin Inhibits Prion Protein PrP-(23-98) Aggregation in VitroSHIRAISHI, Noriyuki; INAI, Yoko; HIRANO, Yoshiaki et al.Bioscience, biotechnology, and biochemistry. 2011, Vol 75, Num 8, pp 1625-1627, issn 0916-8451, 3 p.Article

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