Showing 1 - 7 results of 7 for search 'Shoumo Bhattacharya', query time: 0.02s Refine Results
  1. 1
    A comparison of exogenous promoter activity at the ROSA26 locus using a ΦiC31 integrase mediated cassette exchange approach in mouse ES cells.

    A comparison of exogenous promoter activity at the ROSA26 locus using a ΦiC31 integrase mediated cassette exchange approach in mouse ES cells. by Chiann-mun Chen, Jon Krohn, Shoumo Bhattacharya, Benjamin Davies

    Published 2011-01-01
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  2. 2
    Site specific mutation of the Zic2 locus by microinjection of TALEN mRNA in mouse CD1, C3H and C57BL/6J oocytes.

    Site specific mutation of the Zic2 locus by microinjection of TALEN mRNA in mouse CD1, C3H and C57BL/6J oocytes. by Benjamin Davies, Graham Davies, Christopher Preece, Rathi Puliyadi, Dorota Szumska, Shoumo Bhattacharya

    Published 2013-01-01
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  3. 3
    Development of chemokine network inhibitors using combinatorial saturation mutagenesis

    Development of chemokine network inhibitors using combinatorial saturation mutagenesis by Jhanna Kryukova, Serena Vales, Megan Payne, Gintare Smagurauskaite, Soumyanetra Chandra, Charlie J. Clark, Graham Davies, Shoumo Bhattacharya

    Published 2025-04-01
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  4. 4
    Functional significance of SRJ domain mutations in CITED2.

    Functional significance of SRJ domain mutations in CITED2. by Chiann-mun Chen, Jamie Bentham, Catherine Cosgrove, Jose Braganca, Ana Cuenda, Simon D Bamforth, Jürgen E Schneider, Hugh Watkins, Bernard Keavney, Benjamin Davies, Shoumo Bhattacharya

    Published 2012-01-01
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  5. 5
    Mice carrying a hypomorphic Evi1 allele are embryonic viable but exhibit severe congenital heart defects.

    Mice carrying a hypomorphic Evi1 allele are embryonic viable but exhibit severe congenital heart defects. by Emilie A Bard-Chapeau, Dorota Szumska, Bindya Jacob, Belinda Q L Chua, Gouri C Chatterjee, Yi Zhang, Jerrold M Ward, Fatma Urun, Emi Kinameri, Stéphane D Vincent, Sayadi Ahmed, Shoumo Bhattacharya, Motomi Osato, Archibald S Perkins, Adrian W Moore, Nancy A Jenkins, Neal G Copeland

    Published 2014-01-01
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  6. 6
    A mutation in the mitochondrial fission gene Dnm1l leads to cardiomyopathy.

    A mutation in the mitochondrial fission gene Dnm1l leads to cardiomyopathy. by Houman Ashrafian, Louise Docherty, Vincenzo Leo, Christopher Towlson, Monica Neilan, Violetta Steeples, Craig A Lygate, Tertius Hough, Stuart Townsend, Debbie Williams, Sara Wells, Dominic Norris, Sarah Glyn-Jones, John Land, Ivana Barbaric, Zuzanne Lalanne, Paul Denny, Dorota Szumska, Shoumo Bhattacharya, Julian L Griffin, Iain Hargreaves, Narcis Fernandez-Fuentes, Michael Cheeseman, Hugh Watkins, T Neil Dear

    Published 2010-06-01
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  7. 7
    Genetic variation in VEGF does not contribute significantly to the risk of congenital cardiovascular malformation.

    Genetic variation in VEGF does not contribute significantly to the risk of congenital cardiovascular malformation. by Helen R Griffin, Darroch H Hall, Ana Topf, James Eden, A Graham Stuart, Jonathan Parsons, Ian Peart, John E Deanfield, John O'Sullivan, Sonya V Babu-Narayan, Michael A Gatzoulis, Frances A Bu'lock, Shoumo Bhattacharya, Jamie Bentham, Martin Farrall, Javier Granados Riveron, J David Brook, John Burn, Heather J Cordell, Judith A Goodship, Bernard Keavney

    Published 2009-01-01
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