Browsing by Author Mercer, Julian

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Issue DateTitleAuthor(s)Citation
2012Altered intracellular localization and valosin-containing protein (p97 VCP) interaction underlie ATP7A-related distal motor neuropathyKennerson, Marina; Donsante, Anthony; Garbern, James; Kaler, Stephen; Mercer, Julian; Yi, Ling; Concord Clinical School: ANZAC Research InstituteAltered intracellular localization and valosin-containing protein (p97 VCP) interaction underlie ATP7A-related distal motor neuropathy, Human Molecular Genetics, vol.21, 8, 2012,pp 1794-1807
2016Copper dyshomoeostasis in Parkinson's disease: Implications for pathogenesis and indications for novel therapeuticsDouble, Kay; Chen, Nicholas; Davies, Katherine; Mercer, Julian; School of Medical Sciences: Biomedical SciencesCopper dyshomoeostasis in Parkinson's disease: Implications for pathogenesis and indications for novel therapeutics, Clinical Science, vol.130, 8, 2016,pp 565-574
2016Copper dyshomoeostasis in Parkinson's disease: Implications for pathogenesis and indications for novel therapeuticsDouble, Kay; Chen, Nicholas; Davies, Katherine; Mercer, Julian; School of Medical Sciences: Biomedical SciencesCopper dyshomoeostasis in Parkinson's disease: Implications for pathogenesis and indications for novel therapeutics, Clinical Science, vol.130, 8, 2016,pp 565-574
2014Copper pathology in vulnerable brain regions in Parkinson's diseaseDouble, Kay; Bohic, Sylvain; Carmona, Asuncion; Cottam, V; Davies, Katherine; Finberg, John; Halliday, Glenda; Hare, Dominic; Mercer, Julian; Ortega, Richard; Reyes, S; School of Medical Sciences: Biomedical SciencesCopper pathology in vulnerable brain regions in Parkinson's disease, Neurobiology of Aging, vol.35, 4, 2014,pp 858-866
2010Missense Mutations in the Copper Transporter Gene ATP7A Cause X-Linked Distal Hereditary Motor NeuropathyChu, Shannon; Kennerson, Marina; Kowlaski, Bartosz; Nicholson, Garth; Almeida-Souza, Leonardo; Baets, Jonathan; et al, various; Fischer, Dirk; Kaler, Stephen; Llanos, Roxana; Mercer, Julian; Speck-Martins, Carlos; Takata, Reinaldo; Tang, Jingrong; Concord Clinical School: ANZAC Research Institute; Concord Clinical School: ANZAC Research Institute; Concord Clinical School: ANZAC Research Institute; Concord Clinical School: ANZAC Research InstituteMissense Mutations in the Copper Transporter Gene ATP7A Cause X-Linked Distal Hereditary Motor Neuropathy, American Journal of Human Genetics, vol.86, 3,pp 343-352
2010Role of Glutaredoxin1 and Glutathione in Regulating the Activity of the Copper-transporting P-type ATPases, ATP7A and ATP7BRichardson, Desi; Yu, Yu; Cater, Michael; Ke, Bi-Xia; La Fontaine, Sharon; McInnes, Kelly; McKirdy, Ross; Mercer, Julian; Singleton, William; Taylor, Philip; Winnall, Wendy; School of Medical Sciences: Pathology; School of Medical Sciences: PathologyRole of Glutaredoxin1 and Glutathione in Regulating the Activity of the Copper-transporting P-type ATPases, ATP7A and ATP7B, Journal of Biological Chemistry, vol.285, N/A,pp 27111-27121