Search Results - Ketley, Ami

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  1. 1
    The miR-30 microRNA family targets smoothened to regulate hedgehog signalling in zebrafish early muscle development

    The miR-30 microRNA family targets smoothened to regulate hedgehog signalling in zebrafish early muscle development by Ketley, Ami, Warren, Anne, Holmes, Emily, Gering, Martin, Aboobaker, A. Aziz, Brook, J. David

    Published 2013
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  2. 2
    Acetylation of TBX5 by KAT2B and KAT2A regulates heart and limb development

    Acetylation of TBX5 by KAT2B and KAT2A regulates heart and limb development by Ghosh, Tushar K., Aparicio-Sánchez, José J., Buxton, Sarah, Ketley, Ami, Mohamed, Tasabeeh, Rutland, Catrin S., Loughna, Siobhan, Brook, J. David

    Published 2018
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  3. 3
    Combined mutation screening of NKX2-5, GATA4, and TBX5 in congenital heart disease: multiple heterozygosity and novel mutations

    Combined mutation screening of NKX2-5, GATA4, and TBX5 in congenital heart disease: multiple heterozygosity and novel mutations by Granados-Riveron, Javier T., Pope, Mark, Bu'Lock, Frances A., Thornborough, Christopher, Eason, Jacqueline, Setchfield, Kerry, Ketley, Ami, Kirk, Edwin P., Fatkin, Diane, Feneley, Michael P., Harvey, Richard P., Brook, David

    Published 2012
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  4. 4
    High-content screening identifies small molecules that remove nuclear foci, affect MBNL distribution and CELF1 protein levels via a PKC-independent pathway in myotonic dystrophy cell lines

    High-content screening identifies small molecules that remove nuclear foci, affect MBNL distribution and CELF1 protein levels via a PKC-independent pathway in myotonic dystrophy ce... by Ketley, Ami, Chen, Catherine Z., Li, Xin, Arya, Sukrat, Robinson, Thelma E., Granados-Riveron, Javier T., Udosen, Inyang, Morris, Glenn E., Holt, Ian, Furling, Dennis, Chaouch, Soraya, Haworth, Ben, Southall, Noel, Shinn, Paul, Zheng, Wei, Austin, Christopher P., Hayes, Christopher J., Brook, J. David

    Published 2014
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  5. 5
    Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing

    Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing by Sifrim, Alejandro, Hitz, Marc-Phillip, Wilsdon, Anna, Breckpot, Jeroen, Turki, Saeed H Al, Thienpont, Bernard, McRae, Jeremy, Fitzgerald, Tomas W, Singh, Tarjinder, Swaminathan, Ganesh Jawahar, Prigmore, Elena, Rajan, Diana, Abdul-Khaliq, Hashim, Banka, Siddharth, Bauer, Ulrike M.M., Bentham, Jamie, Berger, Felix, Bhattacharya, Shoumo, Bu'Lock, Frances A., Canham, Natalie, Colgiu, Irina-Gabriela, Cosgrove, Catherine, Cox, Helen, Daehnert, Ingo, Daly, Allan, Danesh, John, Fryer, Alan, Gewillig, Marc, Hobson, Emma, Hoff, Kirstin, Homfray, Tessa, Kahlert, Anne-Karin, Ketley, Ami, Kramer, Hans-Heiner, Lachlan, Katherine, Lampe, Anne Katrin, Louw, Jacoba J., Manickara, Ashok Kumar, Manase, Dorin, McCarthy, Karen P., Metcalfe, Kay, Moore, Carmel, Newbury-Ecob, Ruth, Omer, Seham Osman, Ouwehand, Willem H., Park, Soo-Mi, Parker, Michael J., Pickardt, Thomas, Pollard, Martin O., Robert, Leema, Roberts, David J., Sambrook, Jennifer, Setchfield, Kerry, Stiller, Brigitte, Thornborough, Christopher, Toka, Okan, Watkins, Hugh, Williams, Denise, Wright, Michael, Mital, Seema, Daubeney, Piers E.F., Keavney, Bernard, Goodship, Judith, Abu-Sulaiman, Riyadh Mahdi, Klaassen, Sabine, Wright, Caroline F., Firth, Helen V., Barrett, Jeffrey C., Devriendt, Koenraad, FitzPatrick, David R., Brook, J. David, Hurles, Matthew E.

    Published 2016
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