Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Audrey Hobson"'
Autor:
Paul A. Sieving, Paul F. Kenna, Niamh McNally, Noheed W. Khan, G. Jane Farrar, Marian M. Humphries, Ron A. Bush, Audrey Hobson, Peter Humphries
Publikováno v:
Human Molecular Genetics. 8:1309-1312
Mice carrying a targeted disruption of the rhodopsin gene develop a severe degenerative retinopathy, failing to elaborate rod photoreceptor outer segments (ROS), having no recordable rod electroretinogram (ERG) and losing all of their rod cells over
Autor:
David J. McConnell, Børge Diderichsen, Steen Troels Jørgensen, Catherine M. Buckley, Audrey Hobson
Publikováno v:
The Journal of Biochemistry. 118:575-581
The lipA gene of Pseudomonas cepacia DSM3959 requires a downstream gene, limA, in oder to express lipase activity. The product of the lim gene, LimA, is a molecular chaperone required during the folding of lipase in oder for the lipase to adopt an ac
Autor:
Børge Diderichsen, Steen Troels Jørgensen, Catherine M. Buckley, Jesper L. Aamand, David J. McConnell, Audrey Hobson
Publikováno v:
Molecular and General Genetics MGG. 245:556-564
An extracellular Pseudomonas cepacia lipase, LipA, is inactive when expressed in the absence of the product of the limA gene. Evidence has been presented that LimA is a molecular chaperone. The lipA and limA genes have been cloned in separate and ind
Autor:
Maryanne Donovan, Paul F. Kenna, Shigeki Machida, Thomas G. Cotter, Audrey Hobson, Sophie Kiang, Peter Humphries, Niamh McNally, Paul A. Sieving, Ronald A. Bush, Marian M. Humphries, Jane Farrar
Publikováno v:
Visual neuroscience. 18(3)
To explore the possible influence of defined genetic backgrounds on photoreceptor viability and function in mice carrying a targeted disruption of the rhodopsin gene, the severities of retinopathies in Rho-/- mice on C57BL/6J and 129Sv congenic backg
Autor:
John Jackson, Audrey Hobson, Christine C. McCormack, Sean Doyle, Cormac G. Kilty, Alexander S. Whitehead
Publikováno v:
Journal of immunological methods. 198(1)
Human acute phase serum amyloid A (the A-SAA2 isoform) was expressed at high levels using the pGEX bacterial expression system. A-SAA2 protein was expressed in E. coli NM544 as part of a fusion protein facilitating rapid purification. A-SAA2 was clea