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Keywords: prion protein
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Biochem J (2014) 458 (2): 365–374.
Published: 14 February 2014
...Anita Alvarez-Laviada; Ivan Kadurin; Assunta Senatore; Roberto Chiesa; Annette C. Dolphin It has been shown recently that PrP (prion protein) and the calcium channel auxiliary α 2 δ subunits interact in neurons and expression systems [Senatore, Colleoni, Verderio, Restelli, Morini, Condliffe...
Biochem J (2012) 446 (2): 243–251.
Published: 14 August 2012
...Ivana Biljan; Gabriele Giachin; Gregor Ilc; Igor Zhukov; Janez Plavec; Giuseppe Legname The most common form of prion disease in humans is sCJD (sporadic Creutzfeldt–Jakob disease). The naturally occurring E219K polymorphism in the HuPrP (human prion protein) is considered to protect against sCJD...
Includes: Supplementary data
Biochem J (2010) 428 (2): 169–182.
Published: 13 May 2010
...Catherine A. Tabrett; Christopher F. Harrison; Bryan Schmidt; Shayne A. Bellingham; Tristan Hardy; Yves-Henri Sanejouand; Andrew F. Hill; Philip J. Hogg Prion diseases are fatal transmissible neurodegenerative diseases that result from structural conversion of the prion protein into a disease...
Biochem J (2009) 417 (2): 525–533.
Published: 23 December 2008
... to chelation of cholesterol, maintain outside-out orientation of membrane glycoproteins, have prolonged (18 h) stability at 37 °C, and are vesicles or sheets up to 150–200 nm diameter. DRMs containing GPI (glycosylphosphatidylinositol)-anchored proteins PrP (prion protein) and Thy-1 can be separated...
Includes: Supplementary data
Biochem J (2007) 406 (2): 333–341.
Published: 13 August 2007
...Chaoyang Li; Poki Wong; Tao Pan; Fan Xiao; Shaoman Yin; Binggong Chang; Shin-Chung Kang; James Ironside; Man-Sun Sy The normal PrP C (cellular prion protein) contains sLe X [sialyl-Le X (Lewis X)] and Le X . sLe X is a ligand of selectins. To examine whether PrP C is a ligand of selectins, we...
Biochem J (2007) 401 (2): 475–483.
Published: 21 December 2006
...-detector CDI utilizes N-terminal- and C-terminal-specific anti-PrP monoclonal antibodies that recognize regions of the prion protein differentially buried or exposed depending on the extent of denaturation of the molecule. PrPSc was precipitated from scrapie-infected brain stem and cerebellum tissue...
Biochem J (2005) 387 (1): 247–255.
Published: 22 March 2005
...Noriyuki SHIRAISHI; Yoko INAI; Wenxiang BI; Morimitsu NISHIKIMI Prion protein consists of an N-terminal domain containing a series of octapeptide repeats with the consensus sequence PHGGGWGQ and a C-terminal domain composed of three α-helices and two short β-strands. Several studies have shown that...
Biochem J (2003) 373 (2): 485–494.
Published: 15 July 2003
...Sheena M. WHYTE; Ian D. SYLVESTER; Stephen R. MARTIN; Andrew C. GILL; Franziska WOPFNER; Hermann M. SCHÄTZL; Guy G. DODSON; Peter M. BAYLEY Both prion protein and the structurally homologous protein doppel are associated with neurodegenerative disease by mechanisms which remain elusive. We have...
Biochem J (1999) 344 (1): 23–30.
Published: 08 November 1999
... relative to a variety of DIG marker proteins (alkaline phosphatase, flotillin, F3 protein and prion protein) and non-DIG proteins (alkaline phosphodiesterase I, aminopeptidase A and clathrin) has been examined. Alkaline phosphatase, flotillin, F3 protein and the prion protein were present exclusively in...