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Journal of Neurochemistry|December 21, 2004
Biochemical fingerprints of prion diseases: scrapie prion protein in human prion diseases that share prion genotype and typeTao Pan, Ruliang Li, Shin-Chung Kang, et al.
The Biochemical Journal|May 15, 2007
Normal cellular prion protein is a ligand of selectins: binding requires Le(X) but is inhibited by sLe(X)Chaoyang Li, Poki Wong, Tao Pan, et al.
Muscle & Nerve|June 24, 2011
Sodium and chloride channelopathies with myositis: coincidence or connection?Emma Matthews, James A L Miller, Malcolm R MacLeod, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 9, 2004
Motif-grafted antibodies containing the replicative interface of cellular PrP are specific for PrPScGianluca Moroncini, Nnennaya Kanu, Laura Solforosi, et al.
Ultrastructural Pathology|November 13, 2010
Ultrastructural characteristics (or evaluation) of Creutzfeldt-Jakob disease and other human transmissible spongiform encephalopathies or prion diseasesPaweł P Liberski, Beata Sikorska, Jean-Jacques Hauw, et al.
European Journal of Cancer (Oxford, England : 1990)|March 15, 2005
Outcome for patients with metastatic (M2-3) medulloblastoma treated with SIOP/UKCCSG PNET-3 chemotherapyRoger E Taylor, Clifford C Bailey, Kathryn J Robinson, et al.
Radiotherapy and Oncology : Journal of the European Society for Therapeutic Radiology and Oncology|March 31, 2009
Impact of radiotherapy parameters on outcome for patients with supratentorial primitive neuro-ectodermal tumours entered into the SIOP/UKCCSG PNET 3 studyRoger E Taylor, Paul H J Donachie, Claire L Weston, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 10, 2003
Abbreviated incubation times for human prions in mice expressing a chimeric mouse-human prion protein transgeneCarsten Korth, Kiyotoshi Kaneko, Darlene Groth, et al.
FEBS Letters|January 27, 2005
Pre-symptomatic detection of prions by cyclic amplification of protein misfoldingClaudio Soto, Laurence Anderes, Silvia Suardi, et al.
The New England Journal of Medicine|August 8, 2014
Prions in the urine of patients with variant Creutzfeldt-Jakob diseaseFabio Moda, Pierluigi Gambetti, Silvio Notari, et al.
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