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Showing results (171-180 of 213) with videos related to

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Biochemistry|September 20, 2011
Independent interactions of ubiquitin-binding domains in a ubiquitin-mediated ternary complexThomas P Garner, Joanna Strachan, Elizabeth C Shedden, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 1, 1988
Dynamics of trimethoprim bound to dihydrofolate reductaseM S Searle, M J Forster, B Birdsall, et al.
Journal of Elder Abuse & Neglect|October 20, 2006
The key elements of elder neglect:a survey of adult protective service workersCarmel Bitondo Dyer, Christine Toronjo, Michelle Cunningham, et al.
Nucleic Acids Research|December 12, 2018
DNA replication initiation in Bacillus subtilis: structural and functional characterization of the essential DnaA-DnaD interactionEleyna Martin, Huw E L Williams, Matthaios Pitoulias, et al.
Biospectroscopy|April 27, 1999
Structure/activity studies of the anti-MUC1 monoclonal antibody C595 and synthetic MUC1 mucin-core-related peptides and glycopeptidesD I Spencer, S Missailidis, G Denton, et al.
Calcified Tissue International|May 13, 2006
Loss of ubiquitin binding is a unifying mechanism by which mutations of SQSTM1 cause Paget's disease of boneJ R Cavey, S H Ralston, P W Sheppard, et al.
Nucleic Acids Research|October 11, 1988
Construction of a NotI linking library and isolation of new markers close to the Huntington's disease geneT M Pohl, M Zimmer, M E MacDonald, et al.
Journal of Molecular Biology|November 26, 2009
Dimerisation of the UBA domain of p62 inhibits ubiquitin binding and regulates NF-kappaB signallingJed Long, Thomas P Garner, Maya J Pandya, et al.
FEBS Letters|March 17, 2010
Mutant p62/SQSTM1 UBA domains linked to Paget's disease of bone differ in their abilities to function as stabilization signalsChristian Heinen, Thomas P Garner, Jed Long, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1989
CpG island clones from a deletion encompassing the gene for adenomatous polyposis coliL Varesco, H J Thomas, S Cottrell, et al.
Pageof 22

Showing results (171-180 of 213) with videos related to

Sort By:
Pageof 22
Biochemistry|September 20, 2011
Independent interactions of ubiquitin-binding domains in a ubiquitin-mediated ternary complexThomas P Garner, Joanna Strachan, Elizabeth C Shedden, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 1, 1988
Dynamics of trimethoprim bound to dihydrofolate reductaseM S Searle, M J Forster, B Birdsall, et al.
Journal of Elder Abuse & Neglect|October 20, 2006
The key elements of elder neglect:a survey of adult protective service workersCarmel Bitondo Dyer, Christine Toronjo, Michelle Cunningham, et al.
Nucleic Acids Research|December 12, 2018
DNA replication initiation in Bacillus subtilis: structural and functional characterization of the essential DnaA-DnaD interactionEleyna Martin, Huw E L Williams, Matthaios Pitoulias, et al.
Biospectroscopy|April 27, 1999
Structure/activity studies of the anti-MUC1 monoclonal antibody C595 and synthetic MUC1 mucin-core-related peptides and glycopeptidesD I Spencer, S Missailidis, G Denton, et al.
Calcified Tissue International|May 13, 2006
Loss of ubiquitin binding is a unifying mechanism by which mutations of SQSTM1 cause Paget's disease of boneJ R Cavey, S H Ralston, P W Sheppard, et al.
Nucleic Acids Research|October 11, 1988
Construction of a NotI linking library and isolation of new markers close to the Huntington's disease geneT M Pohl, M Zimmer, M E MacDonald, et al.
Journal of Molecular Biology|November 26, 2009
Dimerisation of the UBA domain of p62 inhibits ubiquitin binding and regulates NF-kappaB signallingJed Long, Thomas P Garner, Maya J Pandya, et al.
FEBS Letters|March 17, 2010
Mutant p62/SQSTM1 UBA domains linked to Paget's disease of bone differ in their abilities to function as stabilization signalsChristian Heinen, Thomas P Garner, Jed Long, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1989
CpG island clones from a deletion encompassing the gene for adenomatous polyposis coliL Varesco, H J Thomas, S Cottrell, et al.
Pageof 22