Browsing by Author Watson, Catherine

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Issue DateTitleAuthor(s)Citation
2013Alternative lengthening of telomeres in normal mammalian somatic cellsNeumann, Axel; Pickett, Hilda; Reddel, Roger; Tam, Patrick; Watson, Catherine; Noble, Jane R; Children's Hospital Westmead: Childrens Medical Research Ins; Children's Hospital Westmead: Childrens Medical Research Ins; Children's Hospital Westmead: Childrens Medical Research Ins; Children's Hospital Westmead: Childrens Medical Research Ins; Children's Hospital Westmead: Childrens Medical Research InsAlternative lengthening of telomeres in normal mammalian somatic cells, Genes and Devleopment, vol.27, 1, 2013,pp 18-23
2005Distinct expression profiles of Mecp2 transcripts with different lengths of 3'UTR in the brain and visceral organs during mouse development.Christodoulou, John; Pelka, G; Tam, Patrick; Watson, Catherine; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Childrens Medical Research Ins; Children's Hospital Westmead: Childrens Medical Research Ins; Children's Hospital Westmead: Childrens Medical Research InsDistinct expression profiles of Mecp2 transcripts with different lengths of 3'UTR in the brain and visceral organs during mouse development., Genomics, vol.85,(4),2005,pp 441-452
2006Mecp2 deficiency is associated with learning and cognitive deficits and altered gene activity in the hippocampal region of mice.Christodoulou, John; Hayward, Melinda; Lahooti, Hooshang; Pelka, G; Radziewic, T; Tam, Patrick; Watson, Catherine; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Childrens Medical Research Ins; Nepean Clinical School: Medicine; Children's Hospital Westmead: Childrens Medical Research Ins; Children's Hospital Westmead: Childrens Medical Research Ins; Children's Hospital Westmead: Childrens Medical Research Ins; Children's Hospital Westmead: Childrens Medical Research InsMecp2 deficiency is associated with learning and cognitive deficits and altered gene activity in the hippocampal region of mice., Brain (2005), vol.129,(Pt 4),2006,pp 887-898
2004Mutations Of Cdkl5 Cause A Severe Neurodevelopmental Disorder With Infantile Spasms And Mental Retardation.Bennetts, Bruce; Christodoulou, John; Ellaway, Carolyn; Lahooti, Hooshang; Pelka, G; Tam, Patrick; Watson, Catherine; Weaving, Linda; Williamson, Susan; Archer, Hayley; Clarke, Angus; Evans, Julie; Friend, Kathie L; Gecz, Jozef; Leonard, Helen; McKenzie, Olivia L D; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Paediatrics & Child Health; Nepean Clinical School: Medicine; Children's Hospital Westmead: Childrens Medical Research Ins; Children's Hospital Westmead: Childrens Medical Research Ins; Children's Hospital Westmead: Childrens Medical Research Ins; Children's Hospital Westmead: Paediatrics & Child Health; Medicine Faculty OfficeMutations Of Cdkl5 Cause A Severe Neurodevelopmental Disorder With Infantile Spasms And Mental Retardation., American Journal of Human Genetics, vol.75,(N/A),2004,pp 1079-1093
2005Reduced proportion of Purkinje cells expressing paternally derived mutant Mecp2 308 allele in female mouse cerebellum is not due to a skewed primary pattern of X-chromosome inactivationChristodoulou, John; Pelka, G; Radziewic, T; Tam, Patrick; Watson, Catherine; Williamson, Susan; Shahbazian, Mona D.; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Childrens Medical Research Ins; Children's Hospital Westmead: Childrens Medical Research Ins; Children's Hospital Westmead: Childrens Medical Research Ins; Children's Hospital Westmead: Childrens Medical Research Ins; Medicine Faculty OfficeReduced proportion of Purkinje cells expressing paternally derived mutant Mecp2 308 allele in female mouse cerebellum is not due to a skewed primary pattern of X-chromosome inactivation, Human Molecular Genetics, 2005, vol.14,(13),2005,pp 1851-1861