Publications by authors named "Alison T Merryweather-Clarke"

19Publications

Does osteogenic potential of clonal human bone marrow mesenchymal stem/stromal cells correlate with their vascular supportive ability?

Stem Cell Res Ther 2018 12 19;9(1):351. Epub 2018 Dec 19.

Stem Cell Research, Nuffield Division of Clinical Laboratory Medicine, Radcliffe Department of Medicine, University of Oxford, John Radcliffe Hospital, Oxford, OX3 9BQ, UK.

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http://dx.doi.org/10.1186/s13287-018-1095-7DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6300038PMC
December 2018

Distinct mechanisms of inadequate erythropoiesis induced by tumor necrosis factor alpha or malarial pigment.

PLoS One 2015 17;10(3):e0119836. Epub 2015 Mar 17.

Nuffield Division of Clinical Laboratory Sciences, University of Oxford, Oxford OX3 9BQ, United Kingdom; National Health Service Blood and Transplant, John Radcliffe Hospital, Headington, Oxford OX3 9BQ, United Kingdom.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0119836PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4363658PMC
March 2016

Global gene expression analysis of human erythroid progenitors.

Blood 2011 Mar 26;117(13):e96-108. Epub 2011 Jan 26.

Medical Research Council Molecular Hematology Unit, Weatherall Institute of Molecular Medicine, Oxford, UK.

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http://dx.doi.org/10.1182/blood-2010-07-290825DOI Listing
March 2011

A novel HFE mutation (c.del478) results in nonsense-mediated decay of the mutant transcript in a hemochromatosis patient.

Blood Cells Mol Dis 2009 Sep-Oct;43(2):194-8. Epub 2009 May 24.

Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, Headington, Oxford, UK.

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http://dx.doi.org/10.1016/j.bcmd.2009.04.007DOI Listing
October 2009

Gene symbol: DCYTB/CYBRD1. Disease: primary iron overload.

Hum Genet 2005 Dec;118(3-4):549

Department of Genetics, University of Stellenbosch, South Africa.

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December 2005

Gene symbol: DCYTB/CYBRD1. Disease: primary iron overload.

Hum Genet 2005 Dec;118(3-4):548-9

Department of Genetics, University of Stellenbosch, South Africa.

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December 2005

Gene symbol: SLC40A1. Disease: primary iron overload.

Hum Genet 2005 Dec;118(3-4):547

Department of Genetics, University of Stellenbosch, South Africa.

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December 2005

Gene symbol: DCYTB/CYBRD1. Disease: primary iron overload.

Hum Genet 2005 Dec;118(3-4):546

Department of Genetics, University of Stellenbosch, South Africa.

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December 2005

In vitro functional analysis of human ferroportin (FPN) and hemochromatosis-associated FPN mutations.

Blood 2005 May 3;105(10):4096-102. Epub 2005 Feb 3.

Molecular Immunology Group, Weatherall Institute of Molecular Medicine, Headley Way, Oxford, OX3 9DS, United Kingdom.

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http://dx.doi.org/10.1182/blood-2004-11-4502DOI Listing
May 2005

Analysis of genes implicated in iron regulation in individuals presenting with primary iron overload.

Hum Genet 2004 Oct 24;115(5):409-17. Epub 2004 Aug 24.

MRC Molecular Haematology Unit, Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, Oxford, United Kingdom.

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http://dx.doi.org/10.1007/s00439-004-1166-yDOI Listing
October 2004

Prevalence of HFE mutations among the Thai population and correlation with iron loading in haemoglobin E disorder.

Eur J Haematol 2004 Jul;73(1):43-9

Department of Pediatrics, Siriraj-Thalassaemia Research Program and WHO Collaborating Centre for the Control of Haemoglobinopathies, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.

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http://dx.doi.org/10.1111/j.1600-0609.2004.00246.xDOI Listing
July 2004

Hemochromatosis gene (HFE) mutations in South East Asia: a potential for iron overload.

Blood Cells Mol Dis 2003 May-Jun;30(3):302-6

MRC Molecular Haematology Unit, Weatherall Institute of Molecular Medicine, Headley Way, Headington, Oxford OX3 9DS, United Kingdom.

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http://dx.doi.org/10.1016/s1079-9796(03)00041-xDOI Listing
March 2004