Martina E Daly

Martina E Daly

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Martina E Daly

Martina E Daly

Publications by authors named "Martina E Daly"

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23Publications

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Gene of the issue: RUNX1 mutations and inherited bleeding.

Platelets 2017 03 17;28(2):208-210. Epub 2017 Feb 17.

b Department of Infection , Immunity and Cardiovascular Disease, University of Sheffield , Sheffield , UK.

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http://dx.doi.org/10.1080/09537104.2017.1280151DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5359732PMC
March 2017

Transient inherited antithrombin deficiency: a real phenomenon?

Thromb Haemost 2017 02 15;117(3):642-643. Epub 2016 Dec 15.

Dr. Martina E. Daly, Department of Infection, Immunity and Cardiovascular Disease, University of Sheffield Medical School, Beech Hill Road, Sheffield, S10 2RX, UK, Tel.: +44 114 2713213, Fax: +44 114 2711863, E-mail:

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http://dx.doi.org/10.1160/TH16-10-0791DOI Listing
February 2017

Transcription factor defects causing platelet disorders.

Authors:
Martina E Daly

Blood Rev 2017 01 16;31(1):1-10. Epub 2016 Jul 16.

Department of Infection, Immunity and Cardiovascular Disease, University of Sheffield Medical School, Beech Hill Road, Sheffield, S10 2RX, UK. Electronic address:

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http://dx.doi.org/10.1016/j.blre.2016.07.002DOI Listing
January 2017

ISTH Advanced Training Course on platelet bleeding disorders: How should they be investigated?.

Platelets 2016 12 14;27(8):719-721. Epub 2016 Nov 14.

a Institute of Cardiovascular Sciences, College of Medical and Dental Sciences, University of Birmingham , Birmingham , UK.

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http://dx.doi.org/10.1080/09537104.2016.1256726DOI Listing
December 2016

Diversity and impact of rare variants in genes encoding the platelet G protein-coupled receptors.

Thromb Haemost 2015 Apr 8;113(4):826-37. Epub 2015 Jan 8.

Dr. A. D. Mumford, University of Bristol, Level 7 Bristol Royal Infirmary, Bristol, BS2 8HW, United Kingdom, Tel.: +44 117 3423152, Fax: +44 117 3424036, E-mail

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http://dx.doi.org/10.1160/TH14-08-0679DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4510585PMC
April 2015

What is the role of genetic testing in the investigation of patients with suspected platelet function disorders?

Br J Haematol 2014 Apr 30;165(2):193-203. Epub 2014 Jan 30.

Department of Cardiovascular Science, University of Sheffield Medical School, University of Sheffield, Sheffield, UK.

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http://dx.doi.org/10.1111/bjh.12751DOI Listing
April 2014

Lack of association between polymorphisms in the interleukin-1 gene cluster and familial thrombophilia.

Thromb Res 2012 May 11;129(5):629-34. Epub 2011 Aug 11.

Department of Cardiovascular Science, University of Sheffield Medical School, Beech Hill Road, Sheffield S10 2RX, UK.

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http://dx.doi.org/10.1016/j.thromres.2011.07.002DOI Listing
May 2012

An intact PDZ motif is essential for correct P2Y12 purinoceptor traffic in human platelets.

Blood 2011 Nov 21;118(20):5641-51. Epub 2011 Sep 21.

School of Physiology and Pharmacology, University of Bristol, Bristol, United Kingdom.

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http://dx.doi.org/10.1182/blood-2011-02-336826DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3217363PMC
November 2011

Common sequence variations in the P2Y12 and CYP3A5 genes do not explain the variability in the inhibitory effects of clopidogrel therapy.

Platelets 2006 Jun;17(4):250-8

Cardiovascular Research Unit, University of Sheffield, Division of Clinical Sciences (North), Northern General Hospital, Sheffield, UK.

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http://www.tandfonline.com/doi/full/10.1080/0953710050047584
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http://dx.doi.org/10.1080/09537100500475844DOI Listing
June 2006

The prevalence of, and molecular defects underlying, inherited protein S deficiency in the general population.

Br J Haematol 2004 Jun;125(5):647-54

Division of Genomic Medicine, University of Sheffield, Royal Hallamshire Hospital, Sheffield, UK.

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http://dx.doi.org/10.1111/j.1365-2141.2004.04961.xDOI Listing
June 2004

Hemostatic regulators of tumor angiogenesis: a source of antiangiogenic agents for cancer treatment?

J Natl Cancer Inst 2003 Nov;95(22):1660-73

Academic Unit of Hematology, School of Medicine and Biomedical Sciences, Sheffield, United Kingdom.

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http://dx.doi.org/10.1093/jnci/djg101DOI Listing
November 2003

Analysis of intracellular storage and regulated secretion of 3 von Willebrand disease-causing variants of von Willebrand factor.

Blood 2003 Oct 5;102(7):2452-8. Epub 2003 Jun 5.

Medical Research Council, Laboratory for Molecular Cell Biology, University College London, United Kingdom.

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http://dx.doi.org/10.1182/blood-2003-02-0599DOI Listing
October 2003

Inherited protein S deficiency: from genotype to phenotype.

Haematologica 2003 Apr;88(4):363-7

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April 2003