Výsledky vyhledávání - Howard R. Slater

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  1. 1
    Rapid, high throughput prenatal detection of aneuploidy using a novel quantitative method (MLPA)

    Rapid, high throughput prenatal detection of aneuploidy using a novel quantitative method (MLPA) Autor Howard R. Slater

    Vydáno 2003
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    Carta
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  2. 2
    Effects of cholestyramine on receptor-mediated plasma clearance and tissue uptake of human low density lipoproteins in the rabbit.

    Effects of cholestyramine on receptor-mediated plasma clearance and tissue uptake of human low density lipoproteins in the rabbit. Autor Howard R. Slater, C.J. Packard, S Bicker, J. Shepherd

    Vydáno 1980
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    Artigo
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  3. 3
    Transforming growth factor beta 1 and interleukin 4 induced alpha smooth muscle actin expression and myofibroblast-like differentiation in human synovial fibroblasts in vitro: modulation by basic fibroblast growth factor

    Transforming growth factor beta 1 and interleukin 4 induced alpha smooth muscle actin expression and myofibroblast-like differentiation in human synovial fibroblasts in vitro: modu... Autor Derek L. Mattey, P. T. Dawes, Nicola B Nixon, Howard R. Slater

    Vydáno 1997
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    Artigo
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  4. 4
    Diagnostic application of kidney allograft-derived absolute cell-free DNA levels during transplant dysfunction

    Diagnostic application of kidney allograft-derived absolute cell-free DNA levels during transplant dysfunction Autor John Whitlam, Ling Ling, Alison Skene, John Kanellis, F. Ierino, Howard R. Slater, Damien L. Bruno, David A. Power

    Vydáno 2018
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  5. 5
    High-Resolution Identification of Chromosomal Abnormalities Using Oligonucleotide Arrays Containing 116,204 SNPs

    High-Resolution Identification of Chromosomal Abnormalities Using Oligonucleotide Arrays Containing 116,204 SNPs Autor Howard R. Slater, Dione K. Bailey, Hua Ren, Manqiu Cao, Katrina M. Bell, Steven Nasioulas, Robert Henke, K. H. Andy Choo, Giulia C. Kennedy

    Vydáno 2005
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    Artigo
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  6. 6
    Methylation of novel markers of fragile X alleles is inversely correlated with FMRP expression and FMR1 activation ratio

    Methylation of novel markers of fragile X alleles is inversely correlated with FMRP expression and FMR1 activation ratio Autor David E. Godler, Flora Tassone, Danuta Z. Loesch, Annette Kimball Taylor, Freya Gehling, Randi J. Hagerman, Trent Burgess, Devika Ganesamoorthy, Debbie Hennerich, Lavinia Gordon, Andrew Evans, K.H. Andy Choo, Howard R. Slater

    Vydáno 2010
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  7. 7
    Evidence for the toxicity of bidirectional transcripts and mitochondrial dysfunction in blood associated with small CGG expansions in the FMR1 gene in patients with parkinsonism

    Evidence for the toxicity of bidirectional transcripts and mitochondrial dysfunction in blood associated with small CGG expansions in the FMR1 gene in patients with parkinsonism Autor Danuta Z. Loesch, David E. Godler, Andrew Evans, Minh Bui, Freya Gehling, Katya Kotschet, Nicholas Trost, Elsdon Storey, Paige Stimpson, Glynda Kinsella, David Francis, David R. Thorburn, Alison Venn, Howard R. Slater, Malcolm Horne

    Vydáno 2011
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  8. 8
    Early Detection of Fragile X Syndrome: Applications of a Novel Approach for Improved Quantitative Methylation Analysis in Venous Blood and Newborn Blood Spots

    Early Detection of Fragile X Syndrome: Applications of a Novel Approach for Improved Quantitative Methylation Analysis in Venous Blood and Newborn Blood Spots Autor Yoshimi Inaba, Charles E. Schwartz, Minh Bui, Xin Li, Cindy Skinner, Michael Field, Tiffany Wotton, Randi J. Hagerman, David Francis, David J. Amor, John L. Hopper, Danuta Z. Loesch, Lesley Bretherton, Howard R. Slater, David E. Godler

    Vydáno 2014
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  9. 9
    Molecular and clinical characterization of 25 individuals with exonic deletions of <i>NRXN1</i> and comprehensive review of the literature

    Molecular and clinical characterization of 25 individuals with exonic deletions of <i>NRXN1</i> and comprehensive review of the literature Autor Frédérique Béna, Damien L. Bruno, Mats Eriksson, Conny M.A. van Ravenswaaij‐Arts, Zornitza Stark, Trijnie Dijkhuizen, Erica H. Gerkes, Stefania Gimelli, Devika Ganesamoorthy, Ann‐Charlotte Thuresson, Audrey Labalme, Marianne Till, Frédéric Bilan, Laurent Pasquier, Alain Kitzis, Christele Dubourgm, Massimiliano Rossi, Armand Bottani, Maryline Gagnebin, Damien Sanlaville, Brigitte Gilbert‐Dussardier, Michel Guipponi, Arie van Haeringen, Marjolein Kriek, Claudia Ruivenkamp, Stylianos E. Antonarakis, Britt Marie Anderlid, Howard R. Slater, Jacqueline Schoumans

    Vydáno 2013
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    Revisão
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