Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Wan-Chin Liaw"'
Autor:
Wan-Chin Liaw, 廖婉淳
102
The top 10 leading global retailers are exemplary as far as operations and management practices are concerned and are often imitated. Other retailers can uplift their performance levels if they learn from the key successful factors (KSF) of
The top 10 leading global retailers are exemplary as far as operations and management practices are concerned and are often imitated. Other retailers can uplift their performance levels if they learn from the key successful factors (KSF) of
Externí odkaz:
http://ndltd.ncl.edu.tw/handle/00186237463237647828
Autor:
Wan Chin Liaw, Janice M. Fletcher, Peter Sharp, Matilda R. Jackson, Xiaodan Ding, Chun Ong, Xenia Kaidonis, Enzo Ranieri, Sharon Byers, Ainslie L.K. Derrick-Roberts
Publikováno v:
Molecular Genetics and Metabolism. 131:197-205
The cause of neurodegeneration in MPS mouse models is the focus of much debate and what the underlying cause of disease pathology in MPS mice is. The timing of development of pathology and when this can be reversed or impacted is the key to developin
Autor:
Ainslie Derrick-Roberts, Xenia Kaidonis, Matilda R. Jackson, Wan Chin Liaw, XiaoDan Ding, Chun Ong, Enzo Ranieri, Peter Sharp, Janice Fletcher, Sharon Byers
Publikováno v:
Molecular Genetics and Metabolism. 135:114
Autor:
Kaidonis, Xenia1,2, Wan Chin Liaw1, Roberts, Ainslie Derrick1,3, Ly, Marleesa1,3, Anson, Donald1,3, Byers, Sharon1,2,3 sharon.byers@adelaide.edu.au
Publikováno v:
European Journal of Human Genetics. Feb2010, Vol. 18 Issue 2, p194-199. 6p. 1 Chart, 5 Graphs.
Autor:
Ainslie Derrick Roberts, Marleesa Ly, Sharon Byers, Donald S. Anson, Xenia Kaidonis, Wan Chin Liaw
Publikováno v:
European Journal of Human Genetics. 18:194-199
Neurological pathology is characteristic of the mucopolysaccharidoses (MPSs) that store heparan sulphate (HS) glycosaminoglycan (gag) and has been proven to be refractory to systemic therapies. Substrate deprivation therapy (SDT) using general inhibi
Autor:
Kerry A. Lymn, Ainslie L.K. Roberts, Cuong D. Tran, Gordon S. Howarth, Ross N. Butler, Roger Yazbeck, Wan Chin Liaw, Janice M. Fletcher, Sharon Byers, Simon Moretta, Stamatiki Kritas
Mucopolysaccharidosis type IIIA (MPS IIIA) is a lysosomal storage disorder caused by a deficiency in sulphamidase (NS), a lysosomal enzyme required for the degradation of heparan sulphate glycosaminoglycans (gags). The MPS IIIA mouse is a naturally o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15f42cfd13de329683dd44ba48f2e9ed
https://hdl.handle.net/1959.8/132763
https://hdl.handle.net/1959.8/132763
Autor:
ROBERTS, AINSLIE L. K. DERRICK, HOWARTH, GORDON S., WAN CHIN LIAW, MORETTA, SIMON, KRITAS, STAMATIKI, LYMN, KERRY A., YAZBECK, ROGER, TRAN, CUONG, FLETCHER, JANICE M., BUTLER, ROSS N., BYERS, SHARON
Publikováno v:
Journal of Cellular Physiology; May2009, Vol. 219 Issue 2, p259-264, 6p, 1 Diagram, 2 Charts, 3 Graphs