Emma Deas

Emma Deas

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Emma Deas

Emma Deas

Publications by authors named "Emma Deas"

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PINK1 deficiency in β-cells increases basal insulin secretion and improves glucose tolerance in mice.

Open Biol 2014 May 7;4:140051. Epub 2014 May 7.

Department of Molecular Neuroscience, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK.

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http://dx.doi.org/10.1098/rsob.140051DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4042854PMC
May 2014

The role of the mitochondrial NCX in the mechanism of neurodegeneration in Parkinson's disease.

Adv Exp Med Biol 2013 ;961:241-9

Department of Molecular Neuroscience, UCL Institute of Neurology, London, UK.

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http://dx.doi.org/10.1007/978-1-4614-4756-6_20DOI Listing
March 2013

Mitophagy and Parkinson's disease: the PINK1-parkin link.

Biochim Biophys Acta 2011 Apr 21;1813(4):623-33. Epub 2010 Aug 21.

Department of Molecular Neuroscience, UCL Institute of Neurology, Queen Square, London, UK.

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http://dx.doi.org/10.1016/j.bbamcr.2010.08.007DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3925795PMC
April 2011

PINK1 cleavage at position A103 by the mitochondrial protease PARL.

Hum Mol Genet 2011 Mar 6;20(5):867-79. Epub 2010 Dec 6.

Department of Molecular Neuroscience, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK.

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http://dx.doi.org/10.1093/hmg/ddq526DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3033179PMC
March 2011

Targeting mitochondrial dysfunction in neurodegenerative disease: Part II.

Expert Opin Ther Targets 2010 May;14(5):497-511

UCL Institute of Neurology, Department of Molecular Neuroscience, Queen Square, London WC1N 3BG, UK.

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http://dx.doi.org/10.1517/14728221003730434DOI Listing
May 2010

Targeting mitochondrial dysfunction in neurodegenerative disease: Part I.

Expert Opin Ther Targets 2010 Apr;14(4):369-85

UCL Institute of Neurology, Department of Molecular Neuroscience, Queen Square, London WC1N 3BG, UK.

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http://dx.doi.org/10.1517/14728221003652489DOI Listing
April 2010

Unraveling LRRK2 pathogenesis: common pathways for complex genes?

J Neurosci 2010 Feb;30(5):1577-9

Department of Molecular Neuroscience, UCL Institute of Neurology, University College London, London WC1N 3BG, United Kingdom.

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http://dx.doi.org/10.1523/JNEUROSCI.5531-09.2010DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6633995PMC
February 2010

PINK1 function in health and disease.

EMBO Mol Med 2009 Jun;1(3):152-65

Department of Molecular Neuroscience, UCL Institute of Neurology, Queen Square, London WC1N3BG, UK.

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http://embomolmed.embopress.org/cgi/doi/10.1002/emmm.2009000
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http://dx.doi.org/10.1002/emmm.200900024DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3378127PMC
June 2009

What have PINK1 and HtrA2 genes told us about the role of mitochondria in Parkinson's disease?

Ann N Y Acad Sci 2008 Dec;1147:30-6

Department of Molecular Neuroscience, Institute of Neurology, Queen Square, London, UK.

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http://dx.doi.org/10.1196/annals.1427.032DOI Listing
December 2008

The mitochondrial protease HtrA2 is regulated by Parkinson's disease-associated kinase PINK1.

Nat Cell Biol 2007 Nov 30;9(11):1243-52. Epub 2007 Sep 30.

Signal Transduction, Cancer Research UK London Research Institute, 44 Lincoln's Inn Fields, London WC2A 3PX, UK.

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http://dx.doi.org/10.1038/ncb1644DOI Listing
November 2007

Degradation of DIAP1 by the N-end rule pathway is essential for regulating apoptosis.

Nat Cell Biol 2003 May;5(5):467-73

The Breakthrough Toby Robins Breast Cancer Research Centre, Institute of Cancer Research, Mary-Jean Mitchell Green Building, Chester Beatty Laboratories, Fulham Road, London SW3 6JB, UK.

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http://dx.doi.org/10.1038/ncb984DOI Listing
May 2003