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P W Sheppard

Showing results (1-10 of 7) with videos related to

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The British Journal of Radiology|October 1, 1987
Demonstration of a matrix calculus using computed tomographyP W Sheppard, F E White
Developments in Biological Standardization|January 1, 1990
The production and characterisation of monoclonal antibodies to myc, c-erbB-2 and EFG-receptor using a synthetic peptide approachK M Price, A S Cuthbertson, I M Varndell, et al.
British Journal of Cancer|June 1, 1989
N-myc gene expression and oncoprotein characterisation in medulloblastomaJ A Garson, L F Pemberton, P W Sheppard, et al.
Biochemical Society Transactions|October 21, 2006
p62 mutations, ubiquitin recognition and Paget's disease of boneR Layfield, J R Cavey, D Najat, et al.
Biochemical Society Transactions|October 21, 2004
Structural and functional studies of mutations affecting the UBA domain of SQSTM1 (p62) which cause Paget's disease of boneR Layfield, B Ciani, S H Ralston, 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.
The Journal of Biological Chemistry|October 19, 2001
Presenilin 1 independently regulates beta-catenin stability and transcriptional activityR Killick, C C Pollard, A A Asuni, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
The British Journal of Radiology|October 1, 1987
Demonstration of a matrix calculus using computed tomographyP W Sheppard, F E White
Developments in Biological Standardization|January 1, 1990
The production and characterisation of monoclonal antibodies to myc, c-erbB-2 and EFG-receptor using a synthetic peptide approachK M Price, A S Cuthbertson, I M Varndell, et al.
British Journal of Cancer|June 1, 1989
N-myc gene expression and oncoprotein characterisation in medulloblastomaJ A Garson, L F Pemberton, P W Sheppard, et al.
Biochemical Society Transactions|October 21, 2006
p62 mutations, ubiquitin recognition and Paget's disease of boneR Layfield, J R Cavey, D Najat, et al.
Biochemical Society Transactions|October 21, 2004
Structural and functional studies of mutations affecting the UBA domain of SQSTM1 (p62) which cause Paget's disease of boneR Layfield, B Ciani, S H Ralston, 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.
The Journal of Biological Chemistry|October 19, 2001
Presenilin 1 independently regulates beta-catenin stability and transcriptional activityR Killick, C C Pollard, A A Asuni, et al.
Pageof 1