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J C Lloyd

Showing results (21-30 of 42) with videos related to

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Journal of Experimental Botany|August 25, 2001
Small decreases in SBPase cause a linear decline in the apparent RuBP regeneration rate, but do not affect Rubisco carboxylation capacityE P Harrison, H Olcer, J C Lloyd, et al.
Human Mutation|January 1, 1995
Efficient strategy for the detection of mutations in acrogeric Ehlers-Danlos syndrome type IVP H Johnson, A J Richards, J C Lloyd, et al.
Journal of Hepatology|January 1, 1986
Influence of sexual preference and chronic hepatitis B virus infection on T lymphocyte subsets, natural killer activity, and suppressor cell activityD M Novick, D J Brown, A S Lok, et al.
Vaccine|August 7, 1999
An overview of the vaccine adverse event reporting system (VAERS) as a surveillance system. VAERS Working GroupJ A Singleton, J C Lloyd, G T Mootrey, et al.
Plant Molecular Biology|June 1, 1993
A light- and developmentally-regulated DNA-binding interaction is common to the upstream sequences of the wheat Calvin cycle bisphosphatase genesA J Miles, S C Potts, N M Willingham, et al.
Protein Expression and Purification|October 6, 1998
Purification of active chloroplast sedoheptulose-1,7-bisphosphatase expressed in Escherichia coliR P Dunford, M A Catley, C A Raines, et al.
Plant Molecular Biology|April 1, 1991
A novel proline-rich protein from wheatC A Raines, J C Lloyd, S M Chao, et al.
The Western Journal of Medicine|November 1, 1988
Anti-HIV seroprevalence in California blood and plasma donorsC I Perkins, K W Kizer, M J Hughes, et al.
Human Genetics|June 1, 1992
A single base mutation in the gene for type III collagen (COL3A1) converts glycine 847 to glutamic acid in a family with Ehlers-Danlos syndrome type IV. An unaffected family member is mosaic for the mutationA J Richards, P N Ward, P Narcisi, et al.
Journal of Medical Genetics|July 1, 1991
Characterisation of a glycine to valine substitution at amino acid position 910 of the triple helical region of type III collagen in a patient with Ehlers-Danlos syndrome type IVA J Richards, J C Lloyd, P N Ward, et al.
Pageof 5

Showing results (21-30 of 42) with videos related to

Sort By:
Pageof 5
Journal of Experimental Botany|August 25, 2001
Small decreases in SBPase cause a linear decline in the apparent RuBP regeneration rate, but do not affect Rubisco carboxylation capacityE P Harrison, H Olcer, J C Lloyd, et al.
Human Mutation|January 1, 1995
Efficient strategy for the detection of mutations in acrogeric Ehlers-Danlos syndrome type IVP H Johnson, A J Richards, J C Lloyd, et al.
Journal of Hepatology|January 1, 1986
Influence of sexual preference and chronic hepatitis B virus infection on T lymphocyte subsets, natural killer activity, and suppressor cell activityD M Novick, D J Brown, A S Lok, et al.
Vaccine|August 7, 1999
An overview of the vaccine adverse event reporting system (VAERS) as a surveillance system. VAERS Working GroupJ A Singleton, J C Lloyd, G T Mootrey, et al.
Plant Molecular Biology|June 1, 1993
A light- and developmentally-regulated DNA-binding interaction is common to the upstream sequences of the wheat Calvin cycle bisphosphatase genesA J Miles, S C Potts, N M Willingham, et al.
Protein Expression and Purification|October 6, 1998
Purification of active chloroplast sedoheptulose-1,7-bisphosphatase expressed in Escherichia coliR P Dunford, M A Catley, C A Raines, et al.
Plant Molecular Biology|April 1, 1991
A novel proline-rich protein from wheatC A Raines, J C Lloyd, S M Chao, et al.
The Western Journal of Medicine|November 1, 1988
Anti-HIV seroprevalence in California blood and plasma donorsC I Perkins, K W Kizer, M J Hughes, et al.
Human Genetics|June 1, 1992
A single base mutation in the gene for type III collagen (COL3A1) converts glycine 847 to glutamic acid in a family with Ehlers-Danlos syndrome type IV. An unaffected family member is mosaic for the mutationA J Richards, P N Ward, P Narcisi, et al.
Journal of Medical Genetics|July 1, 1991
Characterisation of a glycine to valine substitution at amino acid position 910 of the triple helical region of type III collagen in a patient with Ehlers-Danlos syndrome type IVA J Richards, J C Lloyd, P N Ward, et al.
Pageof 5