Browsing by Author Hughes, James

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Issue DateTitleAuthor(s)Citation
2018Abnormal Cell Sorting Underlies the Unique X-Linked Inheritance of PCDH19 EpilepsyDale, Russell; Gecz, Jozef; Hughes, James; Kumar, Raman; Mandelstam, Simone; Mincheva-Tasheva, Stefka; Pederick, Daniel; Petrou, Steven; Piltz, Sandra; Richards, Kay; Scheffer, Ingrid; Thomas, Paul; Childrens Hospital Westmead: Paediatrics & Child HealthAbnormal Cell Sorting Underlies the Unique X-Linked Inheritance of PCDH19 Epilepsy, Neuron, vol.97, 1, 2018,pp 59-66
2016Comparison of KP1019 and NAMI-A in tumour-mimetic environmentsLay, Peter; Levina, Aviva; Glover, Christopher; Gransbury, Gemma K.; Harris, Hugh H; Hughes, James; Kappen, Peter; Musgrave, Ian; Chemistry; ChemistryComparison of KP1019 and NAMI-A in tumour-mimetic environments, Metallomics, vol.8, 8, 2016,pp 762-773
2012Congenital Hydrocephalus and Abnormal Subcommissural Organ Development in Sox3 Transgenic MiceMorris, Michael; Cheah, Pike See; Felquer, Fernando; Hughes, James; Lee, Kristie; Liu, Xuan; Lovell-Badge, Robin; Piltz, Sandra; Rizzoti, Karine; Tan, Jacqueline; Thomas, Paul; School of Medical Sciences: PhysiologyCongenital Hydrocephalus and Abnormal Subcommissural Organ Development in Sox3 Transgenic Mice, PLoS One, vol.7, 1, 2012,pp e29041 - 1-e29041 - 12
2017NAD deficiency, congenital malformations, and niacin supplementationCollins, Felicity; Enriquez, Annabelle; Sillence, David; Smith, Janine Margo; Winlaw, David; et al, Various; Hughes, James; Ip, Eddie; Lim, Chai K; Martin, Ella; Moreau, Julie; Rapadas, M; Shi, Hongjun; Sugimoto, Kotaro; Szot, Justin O.; Wang, Roni; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Genetic Medicine; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Medical Research Ins; Childrens Hospital Westmead: Paediatrics & Child HealthNAD deficiency, congenital malformations, and niacin supplementation, New England Journal of Medicine, vol.377, 6, 2017,pp 544-552