Elizabeth M Thompson

Elizabeth M Thompson

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Elizabeth M Thompson

Elizabeth M Thompson

Publications by authors named "Elizabeth M Thompson"

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Selective Osmotic Shock for Islet Isolation in the Cadaveric Canine Pancreas.

Cell Transplant 2018 03 5;27(3):542-550. Epub 2018 Jun 5.

1 Department of Clinical Sciences, North Carolina State University, Raleigh, NC, USA.

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http://dx.doi.org/10.1177/0963689717752947DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6038033PMC
March 2018

Disorders of sex development: insights from targeted gene sequencing of a large international patient cohort.

Genome Biol 2016 11 29;17(1):243. Epub 2016 Nov 29.

Murdoch Childrens Research Institute, Melbourne, VIC, Australia.

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http://dx.doi.org/10.1186/s13059-016-1105-yDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5126855PMC
November 2016

Pachyonychia Congenita: A Spectrum of KRT6a Mutations in Australian Patients.

Pediatr Dermatol 2016 May 4;33(3):337-42. Epub 2016 Apr 4.

Flinders Medical Centre, Adelaide, South Australia, Australia.

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http://dx.doi.org/10.1111/pde.12841DOI Listing
May 2016

Modulating DNA methylation in activated CD8+ T cells inhibits regulatory T cell-induced binding of Foxp3 to the CD8+ T Cell IL-2 promoter.

J Immunol 2015 Feb 29;194(3):990-8. Epub 2014 Dec 29.

Department of Population Health and Pathobiology, College of Veterinary Medicine, North Carolina State University, Raleigh, NC 27607

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http://dx.doi.org/10.4049/jimmunol.1401762DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4297683PMC
February 2015

Genetic heterogeneity in Cornelia de Lange syndrome (CdLS) and CdLS-like phenotypes with observed and predicted levels of mosaicism.

J Med Genet 2014 Oct 14;51(10):659-68. Epub 2014 Aug 14.

MRC Human Genetics Unit, MRC Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, UK.

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http://dx.doi.org/10.1136/jmedgenet-2014-102573DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4173748PMC
October 2014

In vitro effect of multiple hydrogen peroxide gas plasma sterilizations on the rate of closure of ameroid constrictors.

Am J Vet Res 2014 Oct;75(10):924-8

Departments of Veterinary Clinical Sciences, College of Veterinary Medicine, Purdue University, West Lafayette, IN 47907.

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http://dx.doi.org/10.2460/ajvr.75.10.924DOI Listing
October 2014

Cognitive deficit and autism spectrum disorders: prospective diagnosis by array CGH.

Pathology 2014 Jan;46(1):41-5

1Cytogenetics, Department of Genetic Medicine, Directorate of Genetics and Molecular Pathology, SA Pathology at Women's and Children's Hospital, North Adelaide 2Molecular Genetics, Department of Genetic Medicine, Directorate of Genetics and Molecular Pathology, SA Pathology at Women's and Children's Hospital, North Adelaide 3School of Molecular and Biomedical Sciences, The University of Adelaide 4School of Paediatrics and Reproductive Health, The University of Adelaide 5South Australian Clinical Genetics Service, SA Pathology at Women's and Children's Hospital, North Adelaide 6Centre for Disability Health, North East Clinic, Modbury Hospital, Adelaide 7Ashford Medical Centre, Ashford, Adelaide 8Flinders Medical Centre, Bedford Park 9Calvary Hospital, North Adelaide 10Women's and Children's Health Network, North Adelaide 11Parks Community Health Service, Angle Park, South Australia, Australia 12see Acknowledgements for all members.

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http://linkinghub.elsevier.com/retrieve/pii/S003130251630641
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http://dx.doi.org/10.1097/PAT.0000000000000043DOI Listing
January 2014

CD8+ clonality is associated with prolonged acute plasma viremia and altered mRNA cytokine profiles during the course of feline immunodeficiency virus infection.

Vet Immunol Immunopathol 2013 Apr 20;152(3-4):200-8. Epub 2012 Dec 20.

Department of Population Health and Pathobiology, North Carolina State University College of Veterinary Medicine, Raleigh, NC 27607, United States.

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http://dx.doi.org/10.1016/j.vetimm.2012.12.005DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3595358PMC
April 2013

Whole exome sequencing in foetal akinesia expands the genotype-phenotype spectrum of GBE1 glycogen storage disease mutations.

Neuromuscul Disord 2013 Feb 3;23(2):165-9. Epub 2012 Dec 3.

Western Australian Institute for Medical Research and the Centre for Medical Research, University of Western Australia, Nedlands, Western Australia, Australia.

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http://dx.doi.org/10.1016/j.nmd.2012.11.005DOI Listing
February 2013

Epilepsy with cognitive deficit and autism spectrum disorders: prospective diagnosis by array CGH.

Am J Med Genet B Neuropsychiatr Genet 2013 Jan 26;162B(1):24-35. Epub 2012 Nov 26.

Department of Genetic Medicine, SA Pathology at Women's and Children's Hospital, North Adelaide, South Australia, Australia.

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http://dx.doi.org/10.1002/ajmg.b.32114DOI Listing
January 2013

Functional performance in young Australian children with achondroplasia.

Dev Med Child Neurol 2011 Oct 12;53(10):944-50. Epub 2011 Aug 12.

School of Health and Rehabilitation Sciences, The University of Queensland, Brisbane, Queensland, Australia.

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http://dx.doi.org/10.1111/j.1469-8749.2011.04050.xDOI Listing
October 2011

Intraspecific polymorphism to interspecific divergence: genetics of pigmentation in Drosophila.

Science 2009 Oct;326(5952):540-4

Department of Ecology and Evolutionary Biology, University of Michigan, Ann Arbor, MI 48109, USA.

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http://dx.doi.org/10.1126/science.1176980DOI Listing
October 2009