Browsing by Author Davis, Ryan

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Issue DateTitleAuthor(s)Citation
2007Adult-only exposure of male rats to a diet of high phytoestrogen content increases apoptosis of meiotic and post-meiotic germ cells.Assinder, Stephen; Davis, Ryan; Fenwick, Mark; Glover, Amy; School of Medical Sciences: PhysiologyAdult-only exposure of male rats to a diet of high phytoestrogen content increases apoptosis of meiotic and post-meiotic germ cells., Reproduction, Fertility and Development, vol.133,(1),2007,pp 11-19
2016A comparison of current serum biomarkers as diagnostic indicators of mitochondrial diseasesDavis, Ryan; Sue, Carolyn; Liang, Christina; Northern Clinical School: Kolling Institute; Northern Clinical School: MedicineA comparison of current serum biomarkers as diagnostic indicators of mitochondrial diseases, Neurology, vol.86, 21, 2016,pp 2010-2015
2013Fibroblast growth factor 21 is a sensitive biomarker of mitochondrial diseaseDavis, Ryan; Liang, Christina; Sue, Carolyn; Edema-Hildebrand, Fabienne; Needham, Merrilee; Riley, Catherine; Northern Clinical School: Kolling Institute; Northern Clinical School: Kolling Institute; Northern Clinical School: MedicineFibroblast growth factor 21 is a sensitive biomarker of mitochondrial disease, Neurology, vol.81, 21, 2013,pp 1819-1826
2011The genetics of mitochondrial diseaseDavis, Ryan; Sue, Carolyn; Northern Clinical School: Kolling Institute; Northern Clinical School: MedicineThe genetics of mitochondrial disease, Seminars in Neurology, vol.31, 5, 2011,pp 519-530
2016Loss of ATP13A2 impairs glycolytic function in Kufor-Rakeb syndrome patient-derived cell modelsDavis, Ryan; Koentjoro, Brianada; Park, Jin-Sung; Sue, Carolyn; Northern Clinical School: Kolling Institute; Northern Clinical School: Kolling Institute; Northern Clinical School: Kolling Institute; Northern Clinical School: MedicineLoss of ATP13A2 impairs glycolytic function in Kufor-Rakeb syndrome patient-derived cell models, Parkinsonism and Related Disorders, vol.27, N/A, 2016,pp 67-73
2016Loss of ATP13A2 impairs glycolytic function in Kufor-Rakeb syndrome patient-derived cell modelsDavis, Ryan; Koentjoro, Brianada; Park, Jin-Sung; Sue, Carolyn; Northern Clinical School: Kolling Institute; Northern Clinical School: Kolling Institute; Northern Clinical School: Kolling Institute; Northern Clinical School: MedicineLoss of ATP13A2 impairs glycolytic function in Kufor-Rakeb syndrome patient-derived cell models, Parkinsonism and Related Disorders, vol.27, N/A, 2016,pp 67-73
2018Mitochondrial diseasesDavis, Ryan; Liang, Christina; Sue, Carolyn; Northern Clinical School: Kolling Institute; Northern Clinical School: Kolling Institute; Northern Clinical School: MedicineMitochondrial diseases, Handbook of Clinical Neurology, vol.147, N/A, 2018,pp 125-141
2018Mitochondrial diseasesDavis, Ryan; Liang, Christina; Sue, Carolyn; Northern Clinical School: Kolling Institute; Northern Clinical School: Kolling Institute; Northern Clinical School: MedicineMitochondrial diseases, Handbook of Clinical Neurology, vol.147, N/A, 2018,pp 125-141
2018Mitochondrial diseasesDavis, Ryan; Liang, Christina; Sue, Carolyn; Northern Clinical School: Kolling Institute; Northern Clinical School: Kolling Institute; Northern Clinical School: MedicineMitochondrial diseases, Handbook of Clinical Neurology, vol.147, N/A, 2018,pp 125-141
2018Mitochondrial diseasesDavis, Ryan; Liang, Christina; Sue, Carolyn; Northern Clinical School: Kolling Institute; Northern Clinical School: Kolling Institute; Northern Clinical School: MedicineMitochondrial diseases, Handbook of Clinical Neurology, vol.147, N/A, 2018,pp 125-141
2018Mitochondrial diseasesDavis, Ryan; Liang, Christina; Sue, Carolyn; Northern Clinical School: Kolling Institute; Northern Clinical School: Kolling Institute; Northern Clinical School: MedicineMitochondrial diseases, Handbook of Clinical Neurology, vol.147, N/A, 2018,pp 125-141
2018Mitochondrial diseasesDavis, Ryan; Liang, Christina; Sue, Carolyn; Northern Clinical School: Kolling Institute; Northern Clinical School: Kolling Institute; Northern Clinical School: MedicineMitochondrial diseases, Handbook of Clinical Neurology, vol.147, N/A, 2018,pp 125-141
2018Mitochondrial diseasesDavis, Ryan; Liang, Christina; Sue, Carolyn; Northern Clinical School: Kolling Institute; Northern Clinical School: Kolling Institute; Northern Clinical School: MedicineMitochondrial diseases, Handbook of Clinical Neurology, vol.147, N/A, 2018,pp 125-141
2018Mitochondrial diseasesDavis, Ryan; Liang, Christina; Sue, Carolyn; Northern Clinical School: Kolling Institute; Northern Clinical School: Kolling Institute; Northern Clinical School: MedicineMitochondrial diseases, Handbook of Clinical Neurology, vol.147, N/A, 2018,pp 125-141
2018Mitochondrial diseasesDavis, Ryan; Liang, Christina; Sue, Carolyn; Northern Clinical School: Kolling Institute; Northern Clinical School: Kolling Institute; Northern Clinical School: MedicineMitochondrial diseases, Handbook of Clinical Neurology, vol.147, N/A, 2018,pp 125-141
2018Mitochondrial diseasesDavis, Ryan; Liang, Christina; Sue, Carolyn; Northern Clinical School: Kolling Institute; Northern Clinical School: Kolling Institute; Northern Clinical School: MedicineMitochondrial diseases, Handbook of Clinical Neurology, vol.147, N/A, 2018,pp 125-141
2015Mutation in mitochondrial ribosomal protein S7 (MRPS7) causes congenital sensorineural deafness, progressive hepatic and renal failure and lactic acidemiaAlexander, Stephen; Christodoulou, John; Cooper, Sandra; Davis, Ryan; Menezes, Minal; Riley, Lisa; Sue, Carolyn; Arbuckle, Susan; Dong, Daoyuan; Glessner, Joseph; Guo, Yiran; Hakonarson, Haron; Keating, Brendan; Kirwan, Paul; Li, Jiankang; Li, Zhijun; Thorburn, David; Xu, Xun; Zhang, Jianguo; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Paediatrics & Child Health; Northern Clinical School: Kolling Institute; Childrens Hospital Westmead: Paediatrics & Child Health; Vet Science Faculty; Northern Clinical School: MedicineMutation in mitochondrial ribosomal protein S7 (MRPS7) causes congenital sensorineural deafness, progressive hepatic and renal failure and lactic acidemia, Human Molecular Genetics, vol.24, 8, 2015,pp 2297-2307
2016Mutations in HSPB8 causing a new phenotype of distal myopathy and motor neuropathyClarke, Nigel; Davis, Ryan; Ghaoui, Roula; Kaur, Simranpreet; Sue, Carolyn; Waddell, Leigh Brook; Yiannikas, Konstantinos; Brewer, Janice M.; Evilä, Anni; Hackman, Peter; Huovinen, Sanna; Jonson, Per Harald; Lek, Monkol; Lindfors, Mikaela; MacArthur, Daniel; Needham, Merrilee; North, Kathryn N.; Palmio, J; Penttilä, Sini; Udd, Bjarne; Vihola, Anna K.; Childrens Hospital Westmead: Paediatrics & Child Health; Northern Clinical School: Kolling Institute; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Paediatrics & Child Health; Northern Clinical School: Medicine; Childrens Hospital Westmead: Paediatrics & Child Health; Northern Clinical School: MedicineMutations in HSPB8 causing a new phenotype of distal myopathy and motor neuropathy, Neurology, vol.86, 4, 2016,pp 391-398
2015A novel OPA1 mutation causing variable age of onset autosomal dominant optic atrophy plus in an Australian family.Davis, Ryan; Sue, Carolyn; Ahmad, Kate; Northern Clinical School: Kolling Institute; Northern Clinical School: MedicineA novel OPA1 mutation causing variable age of onset autosomal dominant optic atrophy plus in an Australian family., Australian Family Physician, vol.262, 10, 2015,pp 2323-2328
2015A novel quantitative assay of mitophagy: Combining high content fluorescence microscopy and mitochondrial DNA load to quantify mitophagy and identify novel pharmacological tools against pathogenic heteroplasmic mtDNADavis, Ryan; Sue, Carolyn; Brady, Stefen; Carver, Janet; Diot, Alan; Dombi, Eszter; et al, Various; Fratter, Carl; Hinks-Roberts, Alex; Liao, Chunyan; Lodge, Tiffany; Morten, Karl; Muir, Rebecca; Northern Clinical School: Kolling Institute; Northern Clinical School: MedicineA novel quantitative assay of mitophagy: Combining high content fluorescence microscopy and mitochondrial DNA load to quantify mitophagy and identify novel pharmacological tools against pathogenic heteroplasmic mtDNA, Pharmacological Research, vol.100, N/A, 2015,pp 24-35