Resultados de procura - 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 por Martin Barron

    Publicado 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 por Martin Barron, Jun Li

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

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

    Publicado 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 por Suzanne M. Pilkington, Martin Barron, Rachel Watson, C.E.M. Griffiths, Silvia Bulfone‐Paus

    Publicado 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 por Martin Barron, Steven J. Brookes, Clare E. Draper, David R. Garrod, Jennifer Kirkham, Richard F. Shore, Michael J. Dixon

    Publicado 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 por Laura C. Greaves, Martin Barron, Stefan M. Plusa, Thomas B. L. Kirkwood, John C. Mathers, Robert W. Taylor, Douglass M. Turnbull

    Publicado 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 por Tanja Taivassalo, Justin L. Gardner, Robert W. Taylor, Andrew M. Schaefer, Jane Newman, Martin Barron, Ronald G. Haller, Douglass M. Turnbull

    Publicado 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 por 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

    Publicado 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 por 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

    Publicado 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 por 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

    Publicado 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 por 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

    Publicado 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 por 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

    Publicado 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 por 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

    Publicado 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 por 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

    Publicado 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 por 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

    Publicado 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 por 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

    Publicado 2012
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