Resultats de la cerca - Martin Barron

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  1. 1
    The distributions of mitochondria and sodium channels reflect the specific energy requirements and conduction properties of the human optic nerve head

    The distributions of mitochondria and sodium channels reflect the specific energy requirements and conduction properties of the human optic nerve head per Martin Barron

    Publicat 2004
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  2. 2
    Identifying and removing the cell-cycle effect from single-cell RNA-Sequencing data

    Identifying and removing the cell-cycle effect from single-cell RNA-Sequencing data per Martin Barron, Jun Li

    Publicat 2016
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  3. 3
    Hereditary dentine disorders: dentinogenesis imperfecta and dentine dysplasia

    Hereditary dentine disorders: dentinogenesis imperfecta and dentine dysplasia per Martin Barron, Sinéad McDonnell, I C Mackie, Michael J. Dixon

    Publicat 2008
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  4. 4
    Aged human skin accumulates mast cells with altered functionality that localize to macrophages and vasoactive intestinal peptide‐positive nerve fibres

    Aged human skin accumulates mast cells with altered functionality that localize to macrophages and vasoactive intestinal peptide‐positive nerve fibres per Suzanne M. Pilkington, Martin Barron, Rachel Watson, C.E.M. Griffiths, Silvia Bulfone‐Paus

    Publicat 2018
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  5. 5
    The cell adhesion molecule nectin-1 is critical for normal enamel formation in mice

    The cell adhesion molecule nectin-1 is critical for normal enamel formation in mice per Martin Barron, Steven J. Brookes, Clare E. Draper, David R. Garrod, Jennifer Kirkham, Richard F. Shore, Michael J. Dixon

    Publicat 2008
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  6. 6
    Defects in multiple complexes of the respiratory chain are present in ageing human colonic crypts

    Defects in multiple complexes of the respiratory chain are present in ageing human colonic crypts per Laura C. Greaves, Martin Barron, Stefan M. Plusa, Thomas B. L. Kirkwood, John C. Mathers, Robert W. Taylor, Douglass M. Turnbull

    Publicat 2010
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  7. 7
    Endurance training and detraining in mitochondrial myopathies due to single large-scale mtDNA deletions

    Endurance training and detraining in mitochondrial myopathies due to single large-scale mtDNA deletions per Tanja Taivassalo, Justin L. Gardner, Robert W. Taylor, Andrew M. Schaefer, Jane Newman, Martin Barron, Ronald G. Haller, Douglass M. Turnbull

    Publicat 2006
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  8. 8
    Entry Mechanisms of Herpes Simplex Virus 1 into Murine Epidermis: Involvement of Nectin-1 and Herpesvirus Entry Mediator as Cellular Receptors

    Entry Mechanisms of Herpes Simplex Virus 1 into Murine Epidermis: Involvement of Nectin-1 and Herpesvirus Entry Mediator as Cellular Receptors per Philipp Petermann, Katharina Thier, Elena Rahn, Frazer J. Rixon, Wilhelm Bloch, Semra Özçelik, Claude Krummenacher, Martin Barron, Michael J. Dixon, Stefanie Scheu, Klaus Pfeffer, Dagmar Knebel-Mörsdorf

    Publicat 2014
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  9. 9
    Mitochondrial DNA Defects and Selective Extraocular Muscle Involvement in CPEO

    Mitochondrial DNA Defects and Selective Extraocular Muscle Involvement in CPEO per Laura C. Greaves, Patrick Yu‐Wai‐Man, Emma L. Blakely, Kim J. Krishnan, Nina E. Beadle, Jamie Kerin, Martin Barron, Philip G. Griffiths, Alison Dickinson, Douglass M. Turnbull, Robert W. Taylor

    Publicat 2010
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  10. 10
    Mitochondrial DNA mutations in human colonic crypt stem cells

    Mitochondrial DNA mutations in human colonic crypt stem cells per Robert W. Taylor, Martin Barron, Gillian M. Borthwick, Amy Gospel, Patrick F. Chinnery, David C. Samuels, Geoffrey A. Taylor, Stefan M. Plusa, Stephanie Needham, Laura C. Greaves, Thomas B. L. Kirkwood, Douglass M. Turnbull

    Publicat 2003
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  11. 11
    A homoplasmic mitochondrial transfer Ribonucleic Acid mutation as a cause of maternally inherited hypertrophic cardiomyopathy

    A homoplasmic mitochondrial transfer Ribonucleic Acid mutation as a cause of maternally inherited hypertrophic cardiomyopathy per Robert W. Taylor, Carla Giordano, Mercy M. Davidson, Giulia d’Amati, H H Bain, Christine Hayes, Helen Leonard, Martin Barron, Carlo Casali, Filippo M. Santorelli, Michio Hirano, Robert N. Lightowlers, Salvatore DiMauro, Douglass M. Turnbull

    Publicat 2003
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  12. 12
    Mitochondrial DNA mutations are established in human colonic stem cells, and mutated clones expand by crypt fission

    Mitochondrial DNA mutations are established in human colonic stem cells, and mutated clones expand by crypt fission per Laura C. Greaves, Sean Preston, Paul Tadrous, Robert W. Taylor, Martin Barron, Dahmane Oukrif, Simon J. Leedham, Maesha Deheragoda, Peter Sasieni, Marco Novelli, Janusz Jankowski, Douglass M. Turnbull, Nicholas A. Wright, Stuart A.C. McDonald

    Publicat 2006
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  13. 13
    Whole-Exome Sequencing Identifies FAM20A Mutations as a Cause of Amelogenesis Imperfecta and Gingival Hyperplasia Syndrome

    Whole-Exome Sequencing Identifies FAM20A Mutations as a Cause of Amelogenesis Imperfecta and Gingival Hyperplasia Syndrome per James O’Sullivan, Carolina Cavalcante Bitu, Sarah B. Daly, Jill Urquhart, Martin Barron, Sanjeev S. Bhaskar, Hercílio Martelli‐Júnior, Pedro Eleutério dos Santos Neto, M. Adela Mansilla, Jeffrey C. Murray, Ricardo D. Coletta, Graeme Black, Michael J. Dixon

    Publicat 2011
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  14. 14
    Mast cell activation test in the diagnosis of allergic disease and anaphylaxis

    Mast cell activation test in the diagnosis of allergic disease and anaphylaxis per Rajia Bahri, Adnan Čustović, Peter Korošec, Marina Tsoumani, Martin Barron, Jiakai Wu, Rebekah Sayers, Alf Weimann, Mónica Ruiz-García, Nandinee Patel, Abigail Robb, Mohamed H. Shamji, Sara Fontanella, Mira Šilar, E. N. Clare Mills, Angela Simpson, Paul Turner, Silvia Bulfone‐Paus

    Publicat 2018
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  15. 15
    CNS-Native Myeloid Cells Drive Immune Suppression in the Brain Metastatic Niche through Cxcl10

    CNS-Native Myeloid Cells Drive Immune Suppression in the Brain Metastatic Niche through Cxcl10 per Ian H. Guldner, Qingfei Wang, Lin Yang, Samantha M. Golomb, Zhuo Zhao, Jacqueline Lopez, Abigail Brunory, Erin N. Howe, Yizhe Zhang, Bhavana Palakurthi, Martin Barron, Hongyu Gao, Xiaoling Xuei, Yunlong Liu, Jun Li, Danny Z. Chen, Gary E. Landreth, Siyuan Zhang

    Publicat 2020
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  16. 16
    Mutations in C4orf26, Encoding a Peptide with In Vitro Hydroxyapatite Crystal Nucleation and Growth Activity, Cause Amelogenesis Imperfecta

    Mutations in C4orf26, Encoding a Peptide with In Vitro Hydroxyapatite Crystal Nucleation and Growth Activity, Cause Amelogenesis Imperfecta per David Parry, Steven J. Brookes, Clare V. Logan, James A. Poulter, Walid El‐Sayed, Suhaila Al‐Bahlani, Sharifa Al-Harasi, Jihad Sayed, El Mostafa Raïf, Richard F. Shore, Mayssoon Dashash, Martin Barron, Joanne Morgan, Ian Carr, Graham R. Taylor, Colin A. Johnson, Michael J. Aldred, Michael J. Dixon, J. Tim Wright, Jennifer Kirkham, Chris F. Inglehearn, Alan J. Mighell

    Publicat 2012
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