Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Hannah Y.‐Y. Lee"'
Publikováno v:
Meat science. 143
High pressure processing (HPP) of pre-rigor longissimus thoracis (strip loin) from prime and bull animals substantially decreased the shear force and improved consumer eating attributes of the final meat product. The improved tenderness in both prime
Autor:
R. Grant Pearson, Roy Bickerstaffe, Hannah Y.-Y. Lee, Susan L. Mason, James D. Morton, Stephanie Smithson
Publikováno v:
Meat science. 133
Strip loins from different grades of cattle were subjected to two levels of high pressure processing (HPP) within 1h of slaughter at a commercial meat processing plant and chilled for 1day before freezing. The physical and eating quality characterist
Publikováno v:
Food Chemistry. 117:318-325
Various physicochemical and biochemical properties were compared between raw mature and immature chinook salmon (Oncorhynchus tshawytscha) roe. The pH, osmolality and moisture content were lower for mature salmon roe but egg size, viscosity, protein,
Autor:
Andrew D. Abell, Matthew A. Jones, James M. Coxon, James D. Morton, Steven G. Aitken, Stephen B. McNabb, Hannah Y.‐Y. Lee, Janna M. Mehrtens, Nathan A. Alexander, Blair G. Stuart, Axel T. Neffe, Roy Bickerstaffe
Publikováno v:
Angewandte Chemie. 121:1483-1486
Autor:
Joshua D McDermott, James M. Coxon, Matthew A. Jones, Janna M. Mehrtens, Andrew D. Abell, Lucinda J. G. Robertson, James D. Morton, Roy Bickerstaffe, Hannah Y.-Y. Lee
Publikováno v:
Clinical & Experimental Ophthalmology. 36:852-860
The aim of this study is to evaluate the therapeutic potential of a newly synthesized calpain inhibitor, CAT0059, using a naturally occurring in vivo sheep cataract model.The selectivity of CAT0059 was investigated by an in vitro protease assay. The
Autor:
Roy Bickerstaffe, Hannah Y.-Y. Lee, Matthew A. Jones, Lucinda J. G. Robertson, Andrew D. Abell, James D. Morton, Josh D. McDermott, James M. Coxon
Publikováno v:
Investigative ophthalmologyvisual science. 54(1)
We used sheep with an autosomal dominant gene for cortical cataract as an animal model to evaluate novel macrocyclic calpain inhibitors with potential for the medical treatment of human cataract.The macrocyclic aldehyde, CAT811, identified previously
Autor:
Axel T. Neffe, Blair G. Stuart, James D. Morton, Janna M. Mehrtens, James M. Coxon, Andrew D. Abell, Roy Bickerstaffe, Hannah Y.-Y. Lee, Matthew A. Jones, Steven G. Aitken, Stephen B. McNabb, Nathan A. Alexander
Publikováno v:
Angewandte Chemie (International ed. in English). 48(8)
The design and elaboration of a series of macrocyclic templates that exhibit a propensity to adopt a beta-strand-like peptide-backbone conformation led to potent and selective inhibitors of calpain 2. Macrocycle 1 retarded calcium-induced opacificati
Autor:
Lucinda J. G. Robertson, Roy Bickerstaffe, Hannah Y.-Y. Lee, James D. Morton, Julie Sanderson
Publikováno v:
Veterinary ophthalmology. 11(6)
Objective To investigate biochemical changes accompanying Ca2+-induced lens opacification and the possible role of calpain activation in opacification within an ovine lens culture system. Methods Sheep lenses were cultured in minimal media. Lens opac
Autor:
Janna M. Mehrtens, James D. Morton, Andrew D. Abell, James M. Coxon, Steven G. Aitken, Matthew A. Jones, Stephen B. McNabb, Axel T. Neffe, Roy Bickerstaffe, Shigeru Miyamoto, Hannah Y.-Y. Lee, Lucinda J. G. Robertson, Karl Gately, Jacqueline M. Wood
Publikováno v:
Bioorganicmedicinal chemistry. 16(14)
A series of N-heterocyclic dipeptide aldehydes 4-13 have been synthesised and evaluated as inhibitors of ovine calpain 1 (o-CAPN1) and ovine calpain 2 (o-CAPN2). 5-Formyl-pyrrole 9 (IC(50) values of 290 and 25nM against o-CAPN1 and o-CAPN2, respectiv
Autor:
James M. Coxon, Stephen B. McNabb, Hannah Y.-Y. Lee, Thomas P. Cain, Axel T. Neffe, Blair G. Stuart, James D. Morton, Richard J. Payne, Andrew D. Abell, David Pearson, Matthew A. Jones, Steven G. Aitken
Publikováno v:
Journal of medicinal chemistry. 50(12)
The photoswitchable N-terminal diazo and triazene-dipeptide aldehydes 8a−d, 10a,b, and 17a,b present predominantly as the (E)-isomer, which purportedly binds deep in the S3 pocket of calpain. All compounds are potent inhibitors of m-calpain, with 8