Search Results - "Lloyd, Sarah E."

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  1. 1

    New Jobs, New Workers, and New Inequalities: Explaining Employers' Roles in Occupational Segregation by Nativity and Race by HARRISON, Jill Lindsey, LLOYD, Sarah E

    Published in Social problems (Berkeley, Calif.) (01-08-2013)
    “…While sociologists have shown how employers contribute to occupational segregation along lines of race, gender, and nativity, little attention has been paid to…”
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  2. 2

    In vitro screen of prion disease susceptibility genes using the scrapie cell assay by Brown, Craig A, Schmidt, Christian, Poulter, Mark, Hummerich, Holger, Klöhn, Peter-C, Jat, Parmjit, Mead, Simon, Collinge, John, Lloyd, Sarah E

    Published in Human molecular genetics (01-10-2014)
    “…Prion diseases (transmissible spongiform encephalopathies) are fatal neurodegenerative diseases, including Creutzfeldt-Jakob disease in humans, scrapie in…”
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  3. 3

    Sex effects in mouse prion disease incubation time by Akhtar, Shaheen, Wenborn, Adam, Brandner, Sebastian, Collinge, John, Lloyd, Sarah E

    Published in PloS one (13-12-2011)
    “…Prion disease incubation time in mice is determined by many factors including PrP expression level, Prnp alleles, genetic background, prion strain and route of…”
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  4. 4

    HECTD2 is associated with susceptibility to mouse and human prion disease by Lloyd, Sarah E, Maytham, Emma G, Pota, Hirva, Grizenkova, Julia, Molou, Eleni, Uphill, James, Hummerich, Holger, Whitfield, Jerome, Alpers, Michael P, Mead, Simon, Collinge, John

    Published in PLoS genetics (01-02-2009)
    “…Prion diseases are fatal transmissible neurodegenerative disorders, which include Scrapie, Bovine Spongiform Encephalopathy (BSE), Creutzfeldt-Jakob Disease…”
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  5. 5

    Sod1 deficiency reduces incubation time in mouse models of prion disease by Akhtar, Shaheen, Grizenkova, Julia, Wenborn, Adam, Hummerich, Holger, Fernandez de Marco, Mar, Brandner, Sebastian, Collinge, John, Lloyd, Sarah E

    Published in PloS one (22-01-2013)
    “…Prion infections, causing neurodegenerative conditions such as Creutzfeldt-Jakob disease and kuru in humans, scrapie in sheep and BSE in cattle are…”
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  6. 6

    The retinoic acid receptor beta (Rarb) region of Mmu14 is associated with prion disease incubation time in mouse by Grizenkova, Julia, Akhtar, Shaheen, Collinge, John, Lloyd, Sarah E

    Published in PloS one (06-12-2010)
    “…In neurodegenerative conditions such as Alzheimer's and prion disease it has been shown that host genetic background can have a significant effect on…”
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  8. 8

    Genetics of prion diseases by Lloyd, Sarah E, Mead, Simon, Collinge, John

    Published in Current opinion in genetics & development (01-06-2013)
    “…Prion diseases are transmissible, fatal neurodegenerative diseases that include scrapie and bovine spongiform encephalopathy (BSE) in animals and…”
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  9. 9

    Identification of Multiple Quantitative Trait Loci Linked to Prion Disease Incubation Period in Mice by Lloyd, Sarah E., Onwuazor, Obia N., Beck, Jonathan A., Mallinson, Gary, Farrall, Martin, Targonski, Paul, Collinge, John, Elizabeth M. C. Fisher

    “…Polymorphisms in the prion protein gene are known to affect prion disease incubation times and susceptibility in humans and mice. However, studies with inbred…”
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  10. 10

    Illegality at Work: Deportability and the Productive New Era of Immigration Enforcement by Harrison, Jill Lindsey, Lloyd, Sarah E.

    Published in Antipode (01-03-2012)
    “…:  Our goal in this paper is to identify how recent escalations in immigration enforcement and changes in migration practices affect the ability of the state…”
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  11. 11

    A common molecular basis for three inherited kidney stone diseases by Lloyd, Sarah E, Pearce, Simon H. S, Fisher, Simon E, Steinmeyer, Klaus, Schwappach, Blanche, Scheinman, Steven J, Harding, Brian, Bolino, Alessandra, Devoto, Marcella, Goodyer, Paul, Rigden, Susan P. A, Wrong, Oliver, Jentsch, Thomas J, Craig, Ian W, Thakker, Rajesh V

    Published in Nature (London) (01-02-1996)
    “…Kidney stones (nephrolithiasis), which affect 12% of males and 5% of females in the western world, are familial in 45% of patients and are most commonly…”
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  12. 12

    Characterization of two distinct prion strains derived from bovine spongiform encephalopathy transmissions to inbred mice by Lloyd, Sarah E, Linehan, Jacqueline M, Desbruslais, Melanie, Joiner, Susan, Buckell, Jennifer, Brandner, Sebastian, Wadsworth, Jonathan D. F, Collinge, John

    Published in Journal of general virology (01-08-2004)
    “…MRC Prion Unit and Department of Neurodegenerative Disease, Institute of Neurology, University College, London WC1N 3BG, UK Correspondence John Collinge…”
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  13. 13

    HECTD2, a candidate susceptibility gene for Alzheimer's disease on 10q by Lloyd, Sarah E, Rossor, Martin, Fox, Nick, Mead, Simon, Collinge, John

    Published in BMC genetics (15-09-2009)
    “…Late onset Alzheimer's disease (LOAD) is a neurodegenerative disorder characterised by the deposition of amyloid plaques and neurofibrillary tangles in the…”
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  14. 14

    Activating the Countryside: Rural Power, the Power of the Rural and the Making of Rural Politics by Bell, Michael M., Lloyd, Sarah E., Vatovec, Christine

    Published in Sociologia ruralis (01-07-2010)
    “…Against the current moment of rural doubt, we argue that the material, symbolic and relational practices of the rural continue to be articulate aspects of our…”
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  15. 15

    Microglial Cx3cr1 knockout reduces prion disease incubation time in mice by Grizenkova, Julia, Akhtar, Shaheen, Brandner, Sebastian, Collinge, John, Lloyd, Sarah E

    Published in BMC neuroscience (21-03-2014)
    “…Microglia are resident mononuclear phagocytes of the brain that become activated in response to insults including neurodegenerative diseases such as…”
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  16. 16

    Creating and consuming the heartland: Symbolic boundaries in representations of femininity and rurality in U.S. Magazines by Keller, Julie C., Lloyd, Sarah E., Bell, Michael M.

    Published in Journal of rural studies (01-12-2015)
    “…Scholars of rural studies have investigated a range of places and subcultures to identify varieties of rural masculinity—both new and old—and to understand how…”
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  17. 17

    Human Prion Protein with Valine 129 Prevents Expression of Variant CJD Phenotype by Jonathan D. F. Wadsworth, Asante, Emmanuel A., Desbruslais, Melanie, Linehan, Jacqueline M., Joiner, Susan, Gowland, Ian, Welch, Julie, Stone, Lisa, Lloyd, Sarah E., Hill, Andrew F., Brandner, Sebastian, Collinge, John

    “…Variant Creutzfeldt-Jakob disease (vCJD) is a unique and highly distinctive clinicopathological and molecular phenotype of human prion disease associated with…”
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  18. 18

    BSE prions propagate as either variant CJD-like or sporadic CJD-like prion strains in transgenic mice expressing human prion protein by Asante, Emmanuel A., Linehan, Jacqueline M., Desbruslais, Melanie, Joiner, Susan, Gowland, Ian, Wood, Andrew L., Welch, Julie, Hill, Andrew F., Lloyd, Sarah E., Wadsworth, Jonathan D.F., Collinge, John

    Published in The EMBO journal (01-12-2002)
    “…Variant Creutzfeldt–Jakob disease (vCJD) has been recognized to date only in individuals homozygous for methionine at PRNP codon 129. Here we show that…”
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    Rare structural genetic variation in human prion diseases by Lukic, Ana, Uphill, James, Brown, Craig A, Beck, John, Poulter, Mark, Campbell, Tracy, Adamson, Gary, Hummerich, Holger, Whitfield, Jerome, Ponto, Claudia, Zerr, Inga, Lloyd, Sarah E, Collinge, John, Mead, Simon

    Published in Neurobiology of aging (01-05-2015)
    “…Abstract Prion diseases are a diverse group of neurodegenerative conditions, caused by the templated misfolding of prion protein. Aside from the strong genetic…”
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  20. 20

    Identification and characterization of a novel mouse prion gene allele by Lloyd, Sarah E, Thompson, Simon R, Beck, Jonathan A, Linehan, Jacqueline M, Wadsworth, Jonathan D F, Brandner, Sebastian, Collinge, John, Fisher, Elizabeth M C

    Published in Mammalian genome (01-05-2004)
    “…The major determinant of prion disease incubation time in mice is thought to be the amino acid sequence of the prion protein. Two alleles of the mouse prion…”
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