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Showing results (31-40 of 73) with videos related to

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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 Journal of Biological Chemistry|October 3, 2002
Intercellular transfer of the cellular prion proteinTong Liu, Ruliang Li, Tao Pan, et al.
The FEBS Journal|October 31, 2008
Ligand binding promotes prion protein aggregation--role of the octapeptide repeatsShuiliang Yu, Shaoman Yin, Nancy Pham, 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.
The Biochemical Journal|October 13, 2007
The stability and aggregation of ovine prion protein associated with classical and atypical scrapie correlates with the ease of unwinding of helix-2Tim J Fitzmaurice, David F Burke, Lee Hopkins, et al.
Journal of Neurochemistry|August 30, 2008
Effects of gamma-secretase cleavage-region mutations on APP processing and Abeta formation: interpretation with sequential cleavage and alpha-helical modelJianxin Tan, Guozhang Mao, Mei-Zhen Cui, et al.
Plos One|December 22, 2006
Prion protein in milkNicola Franscini, Ahmed El Gedaily, Ulrich Matthey, et al.
The Journal of Pathology|March 14, 2003
Guanidine hydrochloride extraction and detection of prion proteins in mouse and hamster prion diseases by ELISAShin-Chung Kang, Ruliang Li, Chuanping Wang, et al.
The Journal of Pathology|April 20, 2004
Prion protein is ubiquitinated after developing protease resistance in the brains of scrapie-infected miceShin-Chung Kang, David R Brown, Matthew Whiteman, et al.
Plos One|July 14, 2010
Paradoxical role of prion protein aggregates in redox-iron induced toxicityDola Das, Xiu Luo, Ajay Singh, et al.
Pageof 8

Showing results (31-40 of 73) with videos related to

Sort By:
Pageof 8
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 Journal of Biological Chemistry|October 3, 2002
Intercellular transfer of the cellular prion proteinTong Liu, Ruliang Li, Tao Pan, et al.
The FEBS Journal|October 31, 2008
Ligand binding promotes prion protein aggregation--role of the octapeptide repeatsShuiliang Yu, Shaoman Yin, Nancy Pham, 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.
The Biochemical Journal|October 13, 2007
The stability and aggregation of ovine prion protein associated with classical and atypical scrapie correlates with the ease of unwinding of helix-2Tim J Fitzmaurice, David F Burke, Lee Hopkins, et al.
Journal of Neurochemistry|August 30, 2008
Effects of gamma-secretase cleavage-region mutations on APP processing and Abeta formation: interpretation with sequential cleavage and alpha-helical modelJianxin Tan, Guozhang Mao, Mei-Zhen Cui, et al.
Plos One|December 22, 2006
Prion protein in milkNicola Franscini, Ahmed El Gedaily, Ulrich Matthey, et al.
The Journal of Pathology|March 14, 2003
Guanidine hydrochloride extraction and detection of prion proteins in mouse and hamster prion diseases by ELISAShin-Chung Kang, Ruliang Li, Chuanping Wang, et al.
The Journal of Pathology|April 20, 2004
Prion protein is ubiquitinated after developing protease resistance in the brains of scrapie-infected miceShin-Chung Kang, David R Brown, Matthew Whiteman, et al.
Plos One|July 14, 2010
Paradoxical role of prion protein aggregates in redox-iron induced toxicityDola Das, Xiu Luo, Ajay Singh, et al.
Pageof 8