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Rebecca E Saunders

Showing results (1-10 of 23) with videos related to

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Human Mutation|December 7, 2007
CoagMDB: a database analysis of missense mutations within four conserved domains in five vitamin K-dependent coagulation serine proteases using a text-mining toolRebecca E Saunders, Stephen J Perkins
Seminars in Thrombosis and Hemostasis|April 1, 2006
A user's guide to the interactive Web database of factor H-associated hemolytic uremic syndromeRebecca E Saunders, Stephen J Perkins
BMC Structural Biology|March 28, 2008
Charge environments around phosphorylation sites in proteinsJames Kitchen, Rebecca E Saunders, Jim Warwicker
Database : the Journal of Biological Databases and Curation|October 15, 2013
HTS-DB: an online resource to publish and query data from functional genomics high-throughput siRNA screening projectsRebecca E Saunders, Rachael Instrell, Rossella Rispoli, et al.
Human Mutation|November 11, 2005
An interactive web database of factor H-associated hemolytic uremic syndrome mutations: insights into the structural consequences of disease-associated mutationsRebecca E Saunders, Timothy H J Goodship, Peter F Zipfel, et al.
Human Mutation|August 9, 2005
Factor XI deficiency database: an interactive web database of mutations, phenotypes, and structural analysis toolsRebecca E Saunders, Niamh M O'Connell, Christine A Lee, et al.
Thrombosis and Haemostasis|August 5, 2009
Structural analysis of eight novel and 112 previously reported missense mutations in the interactive FXI mutation database reveals new insight on FXI deficiencyRebecca E Saunders, Nuha Shiltagh, Keith Gomez, et al.
The EMBO Journal|February 23, 2012
Genome-wide siRNA screen reveals amino acid starvation-induced autophagy requires SCOC and WACNicole C McKnight, Harold B J Jefferies, Endalkachew A Alemu, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|February 26, 2008
Association of a factor H mutation with hemolytic uremic syndrome following a diarrheal illnessMatthew M Edey, Paul A Mead, Rebecca E Saunders, et al.
Cell Reports|November 15, 2018
The Dynamics of TGF-β Signaling Are Dictated by Receptor Trafficking via the ESCRT MachineryDaniel S J Miller, Robert D Bloxham, Ming Jiang, et al.
Pageof 3

Showing results (1-10 of 23) with videos related to

Sort By:
Pageof 3
Human Mutation|December 7, 2007
CoagMDB: a database analysis of missense mutations within four conserved domains in five vitamin K-dependent coagulation serine proteases using a text-mining toolRebecca E Saunders, Stephen J Perkins
Seminars in Thrombosis and Hemostasis|April 1, 2006
A user's guide to the interactive Web database of factor H-associated hemolytic uremic syndromeRebecca E Saunders, Stephen J Perkins
BMC Structural Biology|March 28, 2008
Charge environments around phosphorylation sites in proteinsJames Kitchen, Rebecca E Saunders, Jim Warwicker
Database : the Journal of Biological Databases and Curation|October 15, 2013
HTS-DB: an online resource to publish and query data from functional genomics high-throughput siRNA screening projectsRebecca E Saunders, Rachael Instrell, Rossella Rispoli, et al.
Human Mutation|November 11, 2005
An interactive web database of factor H-associated hemolytic uremic syndrome mutations: insights into the structural consequences of disease-associated mutationsRebecca E Saunders, Timothy H J Goodship, Peter F Zipfel, et al.
Human Mutation|August 9, 2005
Factor XI deficiency database: an interactive web database of mutations, phenotypes, and structural analysis toolsRebecca E Saunders, Niamh M O'Connell, Christine A Lee, et al.
Thrombosis and Haemostasis|August 5, 2009
Structural analysis of eight novel and 112 previously reported missense mutations in the interactive FXI mutation database reveals new insight on FXI deficiencyRebecca E Saunders, Nuha Shiltagh, Keith Gomez, et al.
The EMBO Journal|February 23, 2012
Genome-wide siRNA screen reveals amino acid starvation-induced autophagy requires SCOC and WACNicole C McKnight, Harold B J Jefferies, Endalkachew A Alemu, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|February 26, 2008
Association of a factor H mutation with hemolytic uremic syndrome following a diarrheal illnessMatthew M Edey, Paul A Mead, Rebecca E Saunders, et al.
Cell Reports|November 15, 2018
The Dynamics of TGF-β Signaling Are Dictated by Receptor Trafficking via the ESCRT MachineryDaniel S J Miller, Robert D Bloxham, Ming Jiang, et al.
Pageof 3