Browsing by Author Quinlan (nee Edwards), Kate Gemma

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Showing results 1 to 11 of 11
Issue DateTitleAuthor(s)Citation
2013ACTN3 genotype infuences muscle performance through the regulation of calcineurin signalingGarton, Fleur; Hogarth, Marshall; Houweling, Peter; Lek, Monkol; MacArthur, Daniel; North, Kathryn; Quinlan (nee Edwards), Kate Gemma; Seto, Jane Tin Chi; Yang, Nan; Zheng, Xi; Cooney, Gregory; Gregorevic, Paul; Turner, Nigel; Western Clinical School: Medicine (Westmead); Children's Hospital Westmead: Medicine; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Paediatrics & Child HealthACTN3 genotype infuences muscle performance through the regulation of calcineurin signaling, Journal of Clinical Investigation, vol.123, 10, 2013,pp 4255-4263
2014alpha-Actinin-3 deficiency alters muscle adaptation in response to denervation and immobilisationGarton, Fleur; Houweling, Peter; North, Kathryn; Quinlan (nee Edwards), Kate Gemma; Seto, Jane Tin Chi; Yang, Nan; Western Clinical School: Medicine (Westmead); Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Paediatrics & Child Healthalpha-Actinin-3 deficiency alters muscle adaptation in response to denervation and immobilisation, Human Molecular Genetics, vol.23, 7, 2014,pp 1879-1893
2015Altered Ca2+ Kinetics Associated with α-Actinin-3 Deficiency May Explain Positive Selection for ACTN3 Null Allele in Human EvolutionQuinlan (nee Edwards), Kate Gemma; Chan, Stephen; Friedrich, Oliver; Head, Nicholas J; Houweling, Peter; Murphy, Robyn; North, Kathryn; Wagner, Soeren; Childrens Hospital Westmead: Paediatrics & Child HealthAltered Ca2+ Kinetics Associated with α-Actinin-3 Deficiency May Explain Positive Selection for ACTN3 Null Allele in Human Evolution, PLoS Genetics, vol.11, 1, 2015,pp 1-18
2016Analysis of the ACTN3 heterozygous genotype suggests that (aplha)-actinin-3 controls sarcomeric composition and muscle function in a dose-dependent fashionGarton, Fleur; Hogarth, Marshall; Houweling, Peter; North, Kathryn; Quinlan (nee Edwards), Kate Gemma; Head, Stewart I; Lek, Monkol; MacArthur, Daniel; Seto, Jane T; Tukiainen, Taru; Yang, Nan; Western Clinical School: Medicine (Westmead); Childrens Hospital Westmead: Medicine; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Paediatrics & Child HealthAnalysis of the ACTN3 heterozygous genotype suggests that (aplha)-actinin-3 controls sarcomeric composition and muscle function in a dose-dependent fashion, Human Molecular Genetics, vol.25, 5, 2016,pp 866-877
2016Analysis of the ACTN3 heterozygous genotype suggests that (aplha)-actinin-3 controls sarcomeric composition and muscle function in a dose-dependent fashionGarton, Fleur; Hogarth, Marshall; Houweling, Peter; North, Kathryn; Quinlan (nee Edwards), Kate Gemma; Head, Stewart I; Lek, Monkol; MacArthur, Daniel; Seto, Jane T; Tukiainen, Taru; Yang, Nan; Western Clinical School: Medicine (Westmead); Childrens Hospital Westmead: Medicine; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Paediatrics & Child HealthAnalysis of the ACTN3 heterozygous genotype suggests that (aplha)-actinin-3 controls sarcomeric composition and muscle function in a dose-dependent fashion, Human Molecular Genetics, vol.25, 5, 2016,pp 866-877
2014Evidence Based Selection of Commonly Used RT-qPCR Reference Genes for the Analysis of Mouse Skeletal MuscleGarces Suarez, Francia; Houweling, Peter; North, Kathryn; Quinlan (nee Edwards), Kate Gemma; Yang, Nan; Zheng, Xi; Raftery, Joanna M; Thomas, Kristen; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Paediatrics & Child HealthEvidence Based Selection of Commonly Used RT-qPCR Reference Genes for the Analysis of Mouse Skeletal Muscle, PloS One, vol.9, 2, 2014,pp 1-11
2016How does ?-actinin-3 deficiency alter muscle function? Mechanistic insights into ACTN3, the 'gene for speed'Lee, Fiona; Quinlan (nee Edwards), Kate Gemma; Houweling, Peter; North, Kathryn N.; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Paediatrics & Child HealthHow does ?-actinin-3 deficiency alter muscle function? Mechanistic insights into ACTN3, the 'gene for speed', BBA: Biochimica et Biophysica Acta - Molecular Cell Research, vol.1863, 4, 2016,pp 686-693
2014The Identification and Structure of an N-Terminal PR Domain Show that FOG1 Is a Member of the PRDM Family of ProteinsClifton, Molly; Crossley, Paul (Merlin); Mackay, Joel; O'Connell, Mitchell; Quinlan (nee Edwards), Kate Gemma; Shepherd, Nicholas; Thong, Sock; Webster, Michael William; Westman, Belinda; Blobel, Gerd; Molecular Bioscience; Molecular Bioscience; Molecular Bioscience; Molecular Bioscience; Children's Hospital Westmead: Paediatrics & Child Health; Molecular Bioscience; Molecular Bioscience; Molecular Bioscience; Molecular BioscienceThe Identification and Structure of an N-Terminal PR Domain Show that FOG1 Is a Member of the PRDM Family of Proteins, PLoS One, vol.9, 8, 2014,pp e106011-N/A
2014Leiomodin-3 dysfunction results in thin filament disorganization and nemaline myopathyClarke, Nigel; Houweling, Peter; Quinlan (nee Edwards), Kate Gemma; Sandaradura, Sarah; Waddell, Leigh Brook; Yuen, Michaela; Ceyhan-Birsoy, Ozge; Dowling, James; et al, Various; Gokhin, David; Kostyukova, Alla; Lehtokari, Vilma-Lotta; Maluenda, Jérome; Moroz, Natalia; Ravenscroft, Gianina; Todd, Emily; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Paediatrics & Child Health; Northern Clinical School: Paediatrics & Child HealthLeiomodin-3 dysfunction results in thin filament disorganization and nemaline myopathy, Journal of Clinical Investigation, vol.124, 11, 2014,pp 4693-4708
2014NF1 is a critical regulator of muscle development and metabolismDeo, Nikita; El-Hoss, Jad; Garton, Fleur; Little, David; North, Kathryn; Quinlan (nee Edwards), Kate Gemma; Schindeler, Aaron; Seto, Jane Tin Chi; Cooney, Gregory; Gdalevitch, Marie; Kolanczyk, Mateusz; Sullivan, K; Turner, Nigel; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Paediatrics & Child Health; Western Clinical School: Medicine (Westmead); Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Paediatrics & Child HealthNF1 is a critical regulator of muscle development and metabolism, Human Molecular Genetics, vol.23, 5, 2014,pp 1250-1259
2015Skeletal muscle and motor deficits in Neurofibromatosis Type 1Little, David; Payne, Jonathan; Quinlan (nee Edwards), Kate Gemma; Schindeler, Aaron; North, Kathryn N; Summers, M A; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Paediatrics & Child HealthSkeletal muscle and motor deficits in Neurofibromatosis Type 1, Journal of Musculoskeletal and Neuronal Interactions, vol.15, 2, 2015,pp 161-170