Browsing by Author Harvey, Richard P

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Showing results 1 to 17 of 17
Issue DateTitleAuthor(s)Citation
2017Advances in the Genetics of Congenital Heart Disease: A Clinician's GuideBlue, Gillian; Sholler, Gary; Winlaw, David; Dunwoodie, Sally L; Giannoulatou, Eleni; Harvey, Richard P; Kirk, Edwin P.; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Medicine; Childrens Hospital Westmead: Paediatrics & Child HealthAdvances in the Genetics of Congenital Heart Disease: A Clinician's Guide, Journal of the American College of Cardiology, vol.69, 7, 2017,pp 859-870
2017Altered cytokine profile, pain sensitivity, and stress responsivity in mice with co-disruption of the developmental genes Neuregulin-1 x DISC1Lai, Donna; Cox, Rachel; Desbonnet, Lieve; Harvey, Richard P; O'Tuathaigh, Colm M. P.; Tighe, Orna; Waddington, John L.; School of Medical Sciences: School of Medical SciencesAltered cytokine profile, pain sensitivity, and stress responsivity in mice with co-disruption of the developmental genes Neuregulin-1 x DISC1, Behavioural Brain Research, vol.320, N/A, 2017,pp 113-118
2015Bioengineering and Stem Cell Technology in the Treatment of Congenital Heart DiseaseBlue, Gillian; Edel, Michael; Winlaw, David; Bosman, Alexis; Dilley, Rodney J; Harvey, Richard P; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Paediatrics & Child HealthBioengineering and Stem Cell Technology in the Treatment of Congenital Heart Disease, Journal of Clinical Medicine, vol.4, 4, 2015,pp 768-781
2008BMP/SMAD1 signaling sets a threshold for the left/right pathway in lateral plate mesoderm and limits availability of SMAD4Jones, Vanessa; Biben, Christine; Costa, Mauro; Dunwoodie, S. L.; Furtado, Milena B; Harvey, Richard P; Preis, Jost I; Robertson, Elizabeth J.; Saga, Yumiko; Solloway, Mark J; Sparrow, D. B.; Tam, Patrick; Wolstein, Olrit; MedicineBMP/SMAD1 signaling sets a threshold for the left/right pathway in lateral plate mesoderm and limits availability of SMAD4, Genes and Development, vol.22, N/A, 2008,pp 3037-3049
2009Conformational stability and DNA binding specificity of the cardiac T-box transcription factor Tbx20Glockner, Laura; Macindoe, Ingrid; Mackay, Joel; Sunde, Margaret; Vukasin, Paul; Costa, Mauro; Harvey, Richard P; Stennard, Fiona A; School of Molecular Bioscience; School of Molecular Bioscience; School of Molecular Bioscience; School of Molecular Bioscience; School of Molecular BioscienceConformational stability and DNA binding specificity of the cardiac T-box transcription factor Tbx20, Journal of Molecular Biology, vol.389, 3,pp 606-618
2012Congenital heart disease: current knowledge about causes and inheritanceSholler, Gary; Winlaw, David; Blue, Gillian; Harvey, Richard P; Kirk, Edwin; Children's Hospital Westmead: Medicine; Children's Hospital Westmead: Paediatrics & Child HealthCongenital heart disease: current knowledge about causes and inheritance, Medical Journal of Australia, vol.197, 3, 2012,pp 155-159
2014Developmental origins and lineage descendants of endogenous adult cardiac progenitor cellsChong, James; Forte, Elvira; Harvey, Richard P; Western Clinical School: Westmead Millennium InstituteDevelopmental origins and lineage descendants of endogenous adult cardiac progenitor cells, Stem Cell Research, vol.13, 3, 2014,pp 592-614
2014Epicardial Origin of Resident Mesenchymal Stem Cells in the Adult Mammalian HeartAsli, Naisana; Xaymardan, Munira; Harvey, Richard P; Dentistry Faculty; Dentistry FacultyEpicardial Origin of Resident Mesenchymal Stem Cells in the Adult Mammalian Heart, Journal of Developmental Biology, vol.2, 2, 2014,pp 117-137
2010A Gain-of-function TBX20 Mutation Causes Congenital Atrial Septal Defects, Patent Foramen Ovale and Cardiac Valve DefectsSunde, Margaret; Al Khatib, Iman; Berger, Felix; Dietz, Rainer; Gramlich, Michael; Harvey, Richard P; Kersten, Andrea; Lee, Stella; Megarbane, Andre; Nemer, Georges; Ozcelik, Cemil; Panek, Anna; Perrot, Andreas; Posch, Maximilian G; Richter, Silke; Schmitt, Katharina R; Stiller, Brigitte; School of Molecular BioscienceA Gain-of-function TBX20 Mutation Causes Congenital Atrial Septal Defects, Patent Foramen Ovale and Cardiac Valve Defects, Journal of Medical Genetics, vol.47, 4,pp 230-235
2010GATA4 Mutations in 357 Unrelated Patients with Congenital Heart MalformationButler, Tanya; Sholler, Gary; Winlaw, David; Blue, Gillian; Cole, Andrew; Costa, Mauro; Esposito, Giorgia; Feneley, Michael; Harvey, Richard P; Kirk, E. P. E.; Waddell, Leigh; Walizada, Gina; Children's Hospital Westmead: Paediatrics & Child Health; Medical Radiation Sciences; Children's Hospital Westmead: Paediatrics & Child HealthGATA4 Mutations in 357 Unrelated Patients with Congenital Heart Malformation, Genetic Testing and Molecular Biomarkers, vol.14, 6,pp 1-6
2014Gene-environment interaction demonstrates the vulnerability of the embryonic heartChapman, Bogdan; Chapman, Gavin; Grieve, Stuart; Dunwoodie, S. L.; Harvey, Richard P; James, Alexander C; Johnson, Randall S; Lopes Floro, Kylie; OReilly, Victoria C; Preis, Jost I; Shi, Hongjun; Sparrow, D. B.; Molecular Bioscience; Molecular Bioscience; Northern Clinical School: MedicineGene-environment interaction demonstrates the vulnerability of the embryonic heart, Developmental Biology, vol.391, 1, 2014,pp 99-110
2002Hop is an unusual homeobox gene that modulates cardiac developmentMackay, Joel; Biben, Christine; Chen, Fabian; Epstein, Jonathan A; Gitler, Aaron D; Harvey, Richard P; Jen, Kuangyu; Kook, Hyun; Li, Jun; Lu, Min Min; Milewski, Rita; Mullins, Mary C; Nazarian, Ronniel; Novotny, Jiri; Runke, Greg; Schnepp, Robert; Schwartz, Robert J; Molecular & Microbial BioscienHop is an unusual homeobox gene that modulates cardiac development, Cell, vol.110,(6),2002,pp 713-723
2014Phenotypic effects of maternal immune activation and early postnatal milieu in mice mutant for the schizophrenia risk gene neuregulin-1Lai, Donna; Clarke, Niamh; Desbonnet, Lieve; Harvey, Richard P; O'Leary, C.; O'Tuathaigh, Colm M. P.; Petit, Emilie; Tighe, O; Waddington, John L.; School of Medical Sciences: School of Medical SciencesPhenotypic effects of maternal immune activation and early postnatal milieu in mice mutant for the schizophrenia risk gene neuregulin-1, Neuroscience, vol.277, C, 2014,pp 294-305
2006Quantitative Trait Loci Modifying Cardiac Atrial Septal Morphology and Risk of Patent Foramen Ovale in the MouseMartin, Ian; Moran, Christopher; Thomson, Peter; Biben, C; Buckley, M; Castro, M; Harvey, Richard P; Hyun, C; Kirk, Edwin P; Lai, D; Vet Science Faculty; Vet Science Faculty; Vet Science FacultyQuantitative Trait Loci Modifying Cardiac Atrial Septal Morphology and Risk of Patent Foramen Ovale in the Mouse, Circulation Research, vol.98,(5),2006,pp 651-658
2010Schizophrenia-related endophenotypes in heterozygous neuregulin-1 'knockout' mice.Lai, Donna; Blau, C.; Fagan, A.J.; Harte, M.; Harvey, Richard P; Kerskens, C.; O'Leary, C.; O'Sullivan, Gerard J.; O'Tuathaigh, Colm M. P.; Reynolds, G.P.; Tighe, O; Waddington, John L.; School of Medical Sciences: School of Medical SciencesSchizophrenia-related endophenotypes in heterozygous neuregulin-1 'knockout' mice., European Journal of Neuroscience, vol.31, 2,pp 2010-349
2011Somatic Mutations in NKX2-5, GATA4, and HAND1 Are Not a Common Cause of Tetralogy of Fallot or Hypoplastic Left HeartBlue, Gillian; Butler, Tanya; Sholler, Gary; Winlaw, David; Cole, Andrew; Esposito, Giorgia; Grossfeld, Paul; Harvey, Richard P; Kirk, E. P. E.; Perryman, Benjamin; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Medicine; Children's Hospital Westmead: Paediatrics & Child HealthSomatic Mutations in NKX2-5, GATA4, and HAND1 Are Not a Common Cause of Tetralogy of Fallot or Hypoplastic Left Heart, American Journal of Medical Genetics. Part A, vol.155, 10, 2011,pp 2416-2421
2014Targeted next-generation sequencing identifies pathogenic variants in familial congenital heart diseaseBlue, Gillian; Sholler, Gary; Winlaw, David; Dunwoodie, Sally; Giannoulatou, Eleni; Harvey, Richard P; Hilton, Desiree C.K; Ho, Joshua W.K.; Kirk, Edwin; White, Susan M.; Childrens Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Medicine; Childrens Hospital Westmead: Paediatrics & Child HealthTargeted next-generation sequencing identifies pathogenic variants in familial congenital heart disease, Journal of the American College of Cardiology, vol.64, 23, 2014,pp 2498-2506