Browse by Authors and EditorsJump to: Article Number of items: 4. ArticleEngland, Jennifer, Granados-Riveron, Javier T., Polo-Parada, Luis, Kuriakose, Diji, Moore, Christopher, Brook, J. David, Rutland, Catrin S., Setchfield, Kerry, Gell, Christopher, Ghosh, Tushar K., Bu'Lock, Frances A., Thornborough, Christopher, Ehler, Elisabeth and Loughna, Siobhan (2017) Tropomyosin 1: multiple roles in the developing heart and in the formation of congenital heart defects. Journal of Molecular and Cellular Cardiology, 106 . pp. 1-13. ISSN 1095-8584 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. and Brook, J. David (2014) 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. Human Molecular Genetics, 23 (6). pp. 1551-1562. ISSN 1460-2083 Granados-Riveron, Javier T. and Brook, David (2012) Formation, contraction, and mechanotransduction of myofribrils in cardiac development: clues from genetics. Biochemistry Research International, 2012 (504906). pp. 1-6. ISSN 2090-2247 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. and Brook, David (2012) Combined mutation screening of NKX2-5, GATA4, and TBX5 in congenital heart disease: multiple heterozygosity and novel mutations. Congenital Heart Disease, 7 (2). pp. 151-159. ISSN 1747-079X |