Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Kathryn Ann Powell"'
Autor:
Per Olav Johnsen, Himanshu Kishnani, David Thomas, Katja E. Hill, Gary Chinga-Carrasco, Lydia C. Powell, Brita Pukstad, Kathryn Ann Powell, Alison A. Jack, Henriette R. Nordli
Chronic wounds pose an increasingly significant worldwide economic burden (over £1 billion per annum in the UK alone). With the escalation in global obesity and diabetes, chronic wounds will increasingly be a significant cause of morbidity and morta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c75e1814ed41a04bc499367b23ad7648
Autor:
Vanessa J. Davies, Stuart James Moat, Philip P. Nichols, Vanessa Hogan, Michael A. Wride, David G. Brownstein, Michael E. Boulton, Wan Fen Yip, Andrew John Hollins, Marcela Votruba, Malgorzata Piechota, Kathryn E. White, Kathryn Ann Powell, Jennifer Rhian Davies
Publikováno v:
Brain. 131:368-380
Opa3 mRNA is expressed in all tissues examined to date, but currently the function of the OPA3 protein is unknown. Intriguingly, various mutations in the OPA3 gene lead to two similar diseases in humans: autosomal dominant inherited optic atrophy and
Publikováno v:
Acta Ophthalmologica. 88
Purpose OPA1 autosomal dominant optic atrophy is a slowly progressive optic neuropathy. A neurological ‘plus’ phenotype has been reported with some OPA1 mutations, prompting further systemic evaluation of our mouse model. Heterozygous Opa1 mutant
Autor:
Jenny Geatrell, Kathryn Ann Powell, Fiona C. Mansergh, Susan MacLean Hunter, Martin J. Evans, Michael A. Wride, Miguel Jarrin
Publikováno v:
The International journal of developmental biology. 52(7)
We investigated the spatio-temporal profile of hemoglobin subunit expression in developing avascular tissues. Significant up-regulation of hemoglobin subunits was identified in microarray experiments comparing blastocyst inner cell masses with undiff
Publikováno v:
Investigative Opthalmology & Visual Science. 52:4369
Purpose. To investigate the developmental and ocular expression of Opa3 in a mouse model of 3-methylglutaconicaciduria type III and the effect of mutation on protein localization and mitochondrial morphology. \ud \ud Methods. The B6 C3-Opa3L122P mous