Hereditary dentine disorders: dentinogenesis imperfecta and dentine dysplasia
Barron, Martin J, McDonnell, Sinead T, Mackie, Iain, Dixon, Michael J
Published in Orphanet journal of rare diseases (20.11.2008)
Published in Orphanet journal of rare diseases (20.11.2008)
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Journal Article
Mast cell activation test in the diagnosis of allergic disease and anaphylaxis
Bahri, Rajia, Custovic, Adnan, Korosec, Peter, Tsoumani, Marina, Barron, Martin, Wu, Jiakai, Sayers, Rebekah, Weimann, Alf, Ruiz-Garcia, Monica, Patel, Nandinee, Robb, Abigail, Shamji, Mohamed H., Fontanella, Sara, Silar, Mira, Mills, E.N.Clare, Simpson, Angela, Turner, Paul J., Bulfone-Paus, Silvia
Published in Journal of allergy and clinical immunology (01.08.2018)
Published in Journal of allergy and clinical immunology (01.08.2018)
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Journal Article
Whole-Exome Sequencing Identifies FAM20A Mutations as a Cause of Amelogenesis Imperfecta and Gingival Hyperplasia Syndrome
O'Sullivan, James, Bitu, Carolina C., Daly, Sarah B., Urquhart, Jill E., Barron, Martin J., Bhaskar, Sanjeev S., Martelli-Júnior, Hercilio, dos Santos Neto, Pedro Eleuterio, Mansilla, Maria A., Murray, Jeffrey C., Coletta, Ricardo D., Black, Graeme C.M., Dixon, Michael J.
Published in American journal of human genetics (13.05.2011)
Published in American journal of human genetics (13.05.2011)
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Journal Article
A transcriptomic survey of the impact of environmental stress on response to dengue virus in the mosquito, Aedes aegypti
Kang, David S, Barron, Martin S, Lovin, Diane D, Cunningham, Joanne M, Eng, Matthew W, Chadee, Dave D, Li, Jun, Severson, David W
Published in PLoS neglected tropical diseases (01.06.2018)
Published in PLoS neglected tropical diseases (01.06.2018)
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Journal Article
Mitochondrial DNA mutations in human colonic crypt stem cells
Taylor, Robert W, Barron, Martin J, Borthwick, Gillian M, Gospel, Amy, Chinnery, Patrick F, Samuels, David C, Taylor, Geoffrey A, Plusa, Stefan M, Needham, Stephanie J, Greaves, Laura C, Kirkwood, Thomas B L, Turnbull, Douglass M
Published in The Journal of clinical investigation (01.11.2003)
Published in The Journal of clinical investigation (01.11.2003)
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Journal Article
Entry mechanisms of herpes simplex virus 1 into murine epidermis: involvement of nectin-1 and herpesvirus entry mediator as cellular receptors
Petermann, Philipp, Thier, Katharina, Rahn, Elena, Rixon, Frazer J, Bloch, Wilhelm, Özcelik, Semra, Krummenacher, Claude, Barron, Martin J, Dixon, Michael J, Scheu, Stefanie, Pfeffer, Klaus, Knebel-Mörsdorf, Dagmar
Published in Journal of virology (01.01.2015)
Published in Journal of virology (01.01.2015)
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Journal Article
Amelogenesis imperfecta caused by N-terminal enamelin point mutations in mice and men is driven by endoplasmic reticulum stress
Brookes, Steven J, Barron, Martin J, Smith, Claire E L, Poulter, James A, Mighell, Alan J, Inglehearn, Chris F, Brown, Catriona J, Rodd, Helen, Kirkham, Jennifer, Dixon, Michael J
Published in Human molecular genetics (15.05.2017)
Published in Human molecular genetics (15.05.2017)
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Journal Article
The Unfolded Protein Response in Amelogenesis and Enamel Pathologies
Brookes, Steven J, Barron, Martin J, Dixon, Michael J, Kirkham, Jennifer
Published in Frontiers in physiology (08.09.2017)
Published in Frontiers in physiology (08.09.2017)
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Journal Article
Mitochondrial DNA Mutations Are Established in Human Colonic Stem Cells, and Mutated Clones Expand by Crypt Fission
Greaves, Laura C., Preston, Sean L., Tadrous, Paul J., Taylor, Robert W., Barron, Martin J., Oukrif, Dahmane, Leedham, Simon J., Deheragoda, Maesha, Sasieni, Peter, Novelli, Marco R., Jankowski, Janusz A. Z., Turnbull, Douglass M., Wright, Nicholas A., McDonald, Stuart A. C.
Published in Proceedings of the National Academy of Sciences - PNAS (17.01.2006)
Published in Proceedings of the National Academy of Sciences - PNAS (17.01.2006)
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Journal Article
Endurance training and detraining in mitochondrial myopathies due to single large-scale mtDNA deletions
Taivassalo, Tanja, Gardner, Julie L., Taylor, Robert W., Schaefer, Andrew M., Newman, Jane, Barron, Martin J., Haller, Ronald G., Turnbull, Douglass M.
Published in Brain (London, England : 1878) (01.12.2006)
Published in Brain (London, England : 1878) (01.12.2006)
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Journal Article
Mitochondrial DNA defects and selective extraocular muscle involvement in CPEO
Greaves, Laura C, Yu-Wai-Man, Patrick, Blakely, Emma L, Krishnan, Kim J, Beadle, Nina E, Kerin, Jamie, Barron, Martin J, Griffiths, Philip G, Dickinson, Alison J, Turnbull, Douglass M, Taylor, Robert W
Published in Investigative ophthalmology & visual science (01.07.2010)
Published in Investigative ophthalmology & visual science (01.07.2010)
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Journal Article
Defects in multiple complexes of the respiratory chain are present in ageing human colonic crypts
Greaves, Laura C., Barron, Martin J., Plusa, Stefan, Kirkwood, Thomas B., Mathers, John C., Taylor, Robert W., Turnbull, Doug M.
Published in Experimental gerontology (01.08.2010)
Published in Experimental gerontology (01.08.2010)
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Journal Article
A mutation in the mouse Amelx tri-tyrosyl domain results in impaired secretion of amelogenin and phenocopies human X-linked amelogenesis imperfecta
Barron, Martin J., Brookes, Steven J., Kirkham, Jennifer, Shore, Roger C., Hunt, Charlotte, Mironov, Aleksandr, Kingswell, Nicola J., Maycock, Joanne, Shuttleworth, C. Adrian, Dixon, Michael J.
Published in Human molecular genetics (01.04.2010)
Published in Human molecular genetics (01.04.2010)
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Journal Article
A homoplasmic mitochondrial transfer Ribonucleic Acid mutation as a cause of maternally inherited hypertrophic cardiomyopathy
Taylor, Robert W, Giordano, Carla, Davidson, Mercy M, d’Amati, Giulia, Bain, Hugh, Hayes, Christine M, Leonard, Helen, Barron, Martin J, Casali, Carlo, Santorelli, Filippo M, Hirano, Michio, Lightowlers, Robert N, DiMauro, Salvatore, Turnbull, Douglass M
Published in Journal of the American College of Cardiology (21.05.2003)
Published in Journal of the American College of Cardiology (21.05.2003)
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Journal Article
The diagnosis of mitochondrial muscle disease
Taylor, Robert W., Schaefer, Andrew M., Barron, Martin J., McFarland, Robert, Turnbull, Douglass M.
Published in Neuromuscular Disorders (01.04.2004)
Published in Neuromuscular Disorders (01.04.2004)
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Book Review
Journal Article
Is the 32-kDa fragment the functional enamelin unit in all species?
Brookes, Steven J., Kingswell, Nicola J., Barron, Martin J., Dixon, Michael J., Kirkham, Jennifer
Published in European journal of oral sciences (01.12.2011)
Published in European journal of oral sciences (01.12.2011)
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Journal Article