Search Results - J. David Brook

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  1. 1
    The Impact of Mechanical Forces in Heart Morphogenesis

    The Impact of Mechanical Forces in Heart Morphogenesis by Javier T Granados-Riveron, J. David Brook

    Published 2012
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  2. 2
    Myotonic Dystrophy Is Associated with a Reduced Level of RNA from the DMWD Allele Adjacent to the Expanded Repeat

    Myotonic Dystrophy Is Associated with a Reduced Level of RNA from the DMWD Allele Adjacent to the Expanded Repeat by Madawi Alwazzan, Edward M. Newman, Marion Hamshere, J. David Brook

    Published 1999
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  3. 3
    Differential fates of introns in gene expression due to global alternative splicing

    Differential fates of introns in gene expression due to global alternative splicing by Anjani Kumari, Saam Sedehizadeh, J. David Brook, Piotr Kozłowski, Marzena Wojciechowska

    Published 2021
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  4. 4
    Transcriptional abnormality in myotonic dystrophy affects <i>DMPK</i> but not neighboring genes

    Transcriptional abnormality in myotonic dystrophy affects <i>DMPK</i> but not neighboring genes by Marion Hamshere, Emma E. Newman, Madawi Alwazzan, B.S. Athwal, J. David Brook

    Published 1997
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  5. 5
    Defective mRNA in myotonic dystrophy accumulates at the periphery of nuclear splicing speckles

    Defective mRNA in myotonic dystrophy accumulates at the periphery of nuclear splicing speckles by Ian Holt, Saloni Mittal, Denis Furling, Gillian Butler‐Browne, J. David Brook, Glenn E. Morris

    Published 2007
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  6. 6
    Targeted integration of adeno-associated virus (AAV) into human chromosome 19.

    Targeted integration of adeno-associated virus (AAV) into human chromosome 19. by R. Jude Samulski, Xiaodong Zhu, Xiangwei Xiao, J. David Brook, David E. Housman, Nava Epstein, Lynne A. Hunter

    Published 1991
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  7. 7
    Exon amplification: a strategy to isolate mammalian genes based on RNA splicing.

    Exon amplification: a strategy to isolate mammalian genes based on RNA splicing. by Alan Buckler, David Chang, Sharon Graw, J. David Brook, Daniel A. Haber, Phillip A. Sharp, David E. Housman

    Published 1991
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  8. 8
    Muscleblind-Like Proteins

    Muscleblind-Like Proteins by Ian Holt, Virginie Jacquemin, Majid Fardaei, Caroline A. Sewry, Gillian Butler‐Browne, Denis Furling, J. David Brook, Glenn E. Morris

    Published 2008
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  9. 9
    Expanded CUG Repeats Dysregulate RNA Splicing by Altering the Stoichiometry of the Muscleblind 1 Complex

    Expanded CUG Repeats Dysregulate RNA Splicing by Altering the Stoichiometry of the Muscleblind 1 Complex by Sharan Paul, Warunee Dansithong, Sonali P. Jog, Ian Holt, Saloni Mittal, J. David Brook, Glenn E. Morris, Lucio Comai, Sita Reddy

    Published 2011
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  10. 10
    Physical Interaction between TBX5 and MEF2C Is Required for Early Heart Development

    Physical Interaction between TBX5 and MEF2C Is Required for Early Heart Development by Tushar K. Ghosh, Fei Song, Elizabeth A. Packham, Sarah Buxton, Thelma Robinson, Jonathan Ronksley, Tim Self, Andrew J. Bonser, J. David Brook

    Published 2009
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  11. 11
    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 Javier T Granados-Riveron, Mark Pope, Frances Bu’Lock, Christopher Thornborough, Jacqueline Eason, Kerry Setchfield, Ami Ketley, Edwin P. Kirk, Diane Fatkin, Michael P. Feneley, Richard P. Harvey, J. David Brook

    Published 2011
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  12. 12
    α-Cardiac myosin heavy chain (MYH6) mutations affecting myofibril formation are associated with congenital heart defects

    α-Cardiac myosin heavy chain (MYH6) mutations affecting myofibril formation are associated with congenital heart defects by Javier T Granados-Riveron, Tushar K. Ghosh, Mark Pope, Frances Bu’Lock, Christopher Thornborough, Jacqueline Eason, Edwin P. Kirk, Diane Fatkin, Michael P. Feneley, Richard P. Harvey, John A.L. Armour, J. David Brook

    Published 2010
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  13. 13
    Tropomyosin 1: Multiple roles in the developing heart and in the formation of congenital heart defects

    Tropomyosin 1: Multiple roles in the developing heart and in the formation of congenital heart defects by Jennifer England, Javier T Granados-Riveron, Luis Polo‐Parada, Diji Kuriakose, Chris Moore, J. David Brook, Catrin S. Rutland, Kerry Setchfield, Chris Gell, Tushar K. Ghosh, Frances Bu’Lock, Christopher Thornborough, Elisabeth Ehler, Siobhan Loughna

    Published 2017
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  14. 14
    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 Ami Ketley, Catherine Z. Chen, Xin Li, Sukrat Arya, Thelma Robinson, Javier T Granados-Riveron, I. Udosen, Glenn E. Morris, Ian Holt, Denis Furling, Soraya Chaouch, Ben Haworth, Noel Southall, Paul Shinn, Wei Zheng, Christopher P. Austin, Christopher J. Hayes, J. David Brook

    Published 2013
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  15. 15
    Transcriptome alterations in myotonic dystrophy skeletal muscle and heart

    Transcriptome alterations in myotonic dystrophy skeletal muscle and heart by Eric T. Wang, Daniel J. Treacy, Katy Eichinger, Adam J. Struck, Joseph Estabrook, Hailey Olafson, Thomas T. Wang, Kirti Bhatt, Tony Westbrook, Sam Sedehizadeh, Amanda J. Ward, John Day, J. David Brook, J. Andrew Berglund, Thomas A. Cooper, David E. Housman, Charles A. Thornton, Christopher B. Burge

    Published 2018
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  16. 16
    Mutation in myosin heavy chain 6 causes atrial septal defect

    Mutation in myosin heavy chain 6 causes atrial septal defect by Yung‐Hao Ching, Tushar K. Ghosh, Steve J. Cross, Elizabeth A. Packham, Louise Honeyman, Siobhan Loughna, Thelma Robinson, Andrew Dearlove, Glòria Ribas, Andrew J. Bonser, Neil R. Thomas, Andrew J. Scotter, Leo S. D. Caves, Graham P. Tyrrell, Ruth Newbury‐Ecob, Arnold Münnich, Damien Bonnet, J. David Brook

    Published 2005
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  17. 17
    Alpha-cardiac actin mutations produce atrial septal defects

    Alpha-cardiac actin mutations produce atrial septal defects by Hans Matsson, Jacqueline Eason, Carol S. Bookwalter, Joakim Klar, Peter Gustavsson, Jan Sunnegårdh, Henrik Enell, Anders Jonzon, Miikka Vikkula, Ilse Gutierrez, Javier T Granados-Riveron, Mark Pope, Frances Bu’Lock, I. Jane Cox, Thelma Robinson, Feifei Song, J. David Brook, Steven B. Marston, Kathleen M. Trybus, Niklas Dahl

    Published 2007
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  18. 18
    Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls

    Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls by Rachel Soemedi, Ana Töpf, Ian Wilson, Rebecca Darlay, Thahira Rahman, Elise Glen, Darroch Hall, Ni Huang, Jamie Bentham, Shoumo Bhattacharya, Catherine Cosgrove, J. David Brook, Javier T Granados-Riveron, Kerry Setchfield, Frances Bu’Lock, Chris Thornborough, Koenraad Devriendt, Jeroen Breckpot, Michael Hofbeck, Mark Lathrop, Anita Rauch, Gillian M. Blue, David S. Winlaw, Matthew E. Hurles, Mauro Santibanez‐Koref, Heather J. Cordell, Judith A. Goodship, Bernard Keavney

    Published 2011
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  19. 19
    Contribution of Global Rare Copy-Number Variants to the Risk of Sporadic Congenital Heart Disease

    Contribution of Global Rare Copy-Number Variants to the Risk of Sporadic Congenital Heart Disease by Rachel Soemedi, Ian Wilson, Jamie Bentham, Rebecca Darlay, Ana Töpf, Diana Zélénika, Catherine Cosgrove, Kerry Setchfield, Chris Thornborough, Javier T Granados-Riveron, Gillian M. Blue, Jeroen Breckpot, Stephen Hellens, Simon Zwolinkski, Elise Glen, Chrysovalanto Mamasoula, Thahira Rahman, Darroch Hall, Anita Rauch, Koenraad Devriendt, Marc Gewillig, John O’ Sullivan, David S. Winlaw, Frances Bu’Lock, J. David Brook, Shoumo Bhattacharya, Mark Lathrop, Mauro Santibanez‐Koref, Heather J. Cordell, Judith A. Goodship, Bernard Keavney

    Published 2012
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  20. 20
    Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot

    Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot by Donna J. Page, Matthieu J. Miossec, Simon G. Williams, Richard M. Monaghan, Elisavet Fotiou, Heather J. Cordell, Louise Sutcliffe, Ana Töpf, Mathieu Bourgey, Guillaume Bourque, Robert Eveleigh, Sally L. Dunwoodie, David S. Winlaw, Shoumo Bhattacharya, Jeroen Breckpot, Koenraad Devriendt, Marc Gewillig, J. David Brook, Kerry Setchfield, Frances Bu’Lock, John O’Sullivan, Graham Stuart, Connie R. Bezzina, Barbara J.M. Mulder, Alex V. Postma, James R. Bentham, Martín Baron, Sanjeev S. Bhaskar, Graeme Black, William G. Newman, Kathryn E. Hentges, G.M. Lathrop, Mauro Santibanez‐Koref, Bernard Keavney

    Published 2019
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