Browsing by Author Gayevskiy, Velimir

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Issue DateTitleAuthor(s)Citation
2015Dataset from the global phosphoproteomic mapping of early mitotic exit in human cellsChaudhuri, Rima; Hoffman, Nolan; James, David; Parker, Benjamin Leo; Burgess, Andrew J; Daly, Roger; Gayevskiy, Velimir; McCloy, Rachael; Rogers, Samuel; Watkins, D Neil; Molecular Bioscience; Molecular Bioscience; Molecular Bioscience; Molecular BioscienceDataset from the global phosphoproteomic mapping of early mitotic exit in human cells, Data in Brief, vol.5, N/A, 2015,pp 45-52
2016Defining the genetic basis of early onset hereditary spastic paraplegia using whole genome sequencingKumar, Kishore Raj; Roscioli, Tony; Sue, Carolyn; Wali, Gautam; Cowley, Mark; Dinger, Marcel; Gayevskiy, Velimir; Kamate, Mahesh; Minoche, Andre; Pinese, Mark; Puttick, Clare; Wali, G. M.; Northern Clinical School: Kolling Institute; Central Clinical School: Medicine; Northern Clinical School: Medicine; Northern Clinical School: Kolling InstituteDefining the genetic basis of early onset hereditary spastic paraplegia using whole genome sequencing, Neurogenetics, vol.17, 4, 2016,pp 265-270
2017Germline variants in familial pituitary tumour syndrome genes are common in young patients and families with additional endocrine tumoursGill, Anthony; Wu, Kathy; Brook, Katelyn; Cowley, M; De Sousa, S; Dinger, M; Earls, Peter; Gayevskiy, Velimir; McCabe, M; McCormack, A; Rawlings, Lesley H; Roscioli, T; Scott, H; Thompson, T; Northern Clinical School: Pathology; Central Clinical School: Save Sight & Eye Health Inst.Germline variants in familial pituitary tumour syndrome genes are common in young patients and families with additional endocrine tumours, European Journal of Endocrinology, vol.176, 5, 2017,pp 635-644
2015Global Phosphoproteomic Mapping of Early Mitotic Exit in Human Cells Identifies Novel Substrate Dephosphorylation MotifsChaudhuri, Rima; Hoffman, Nolan; James, David; Parker, Benjamin Leo; Ali, Naveid; Burgess, Andrew; Castro, Anna; Daly, Roger; Gayevskiy, Velimir; Lorca, Thierry; McCloy, Rachael; Rogers, Samuel; Watkins, Neil; Molecular Bioscience; Molecular Bioscience; Molecular Bioscience; Molecular BioscienceGlobal Phosphoproteomic Mapping of Early Mitotic Exit in Human Cells Identifies Novel Substrate Dephosphorylation Motifs, Molecular and Cellular Proteomics, vol.14, 8, 2015,pp 2194-2212
2017A SLC39A8 variant causes manganese deficiency, and glycosylation and mitochondrial disordersBalasubramaniam, Shanti; Christodoulou, John; Riley, Lisa; Sue, Carolyn; Bahlo, Melanie; Cowley, Mark; Gayevskiy, Velimir; Prelog, Kristina; Roscioli, T; Thorburn, David; Childrens Hospital Westmead: Medicine; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Paediatrics & Child Health; Northern Clinical School: MedicineA SLC39A8 variant causes manganese deficiency, and glycosylation and mitochondrial disorders, Journal of Inherited Metabolic Disease, vol.40, 2, 2017,pp 261-269
2017Unique presentation of cutis laxa with Leigh-like syndrome due to ECHS1 deficiencyBalasubramaniam, Shanti; Christodoulou, John; Riley, Lisa; Bratkovic, D; Cowley, Mark; Gardeitchik, T; Gayevskiy, Velimir; Ketteridge, D; Manton, N; Mohamed, M; Morava, E; Roscioli, Tony; Childrens Hospital Westmead: Medicine; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Paediatrics & Child HealthUnique presentation of cutis laxa with Leigh-like syndrome due to ECHS1 deficiency, Journal of Inherited Metabolic Disease, vol.40, 5, 2017,pp 745-747