Identification of Transcribed Sequences

von Brook, J David
Veröffentlicht 1995

Formation, Contraction, and Mechanotransduction of Myofribrils in Cardiac Development: Clues from Genetics

von Granados-Riveron, Javier T., Brook, J. David
Veröffentlicht 2012

In vivo co-localisation of MBNL protein with DMPK expanded-repeat transcripts

von Fardaei, Majid, Larkin, Ken, Brook, J. David, Hamshere, Marion G.
Veröffentlicht 2001

Recent advances in congenital heart disease genomics

von Wilsdon, Anna, Sifrim, Alejandro, Hitz, Marc-Phillip, Hurles, Matthew, Brook, J. David
Veröffentlicht in F1000Res (2017)

HDAC4 and 5 repression of TBX5 is relieved by protein kinase D1

von Ghosh, Tushar K., Aparicio-Sánchez, José J., Buxton, Sarah, Brook, J. David
Veröffentlicht in Sci Rep (2019)

Transcriptional abnormality in myotonic dystrophy affects DMPK but not neighboring genes

von Hamshere, Marion G., Newman, Emma E., Alwazzan, Madawi, Athwal, Balwinder S., Brook, J. David
Veröffentlicht 1997

The miR-30 MicroRNA Family Targets smoothened to Regulate Hedgehog Signalling in Zebrafish Early Muscle Development

von Ketley, Ami, Warren, Anne, Holmes, Emily, Gering, Martin, Aboobaker, A. Aziz, Brook, J. David
Veröffentlicht 2013

Correction: The miR-30 MicroRNA Family Targets smoothened to Regulate Hedgehog Signalling in Zebrafish Early Muscle Development

von Ketley, Ami, Warren, Anne, Holmes, Emily, Gering, Martin, Aboobaker, A. Aziz, Brook, J. David
Veröffentlicht 2013

Knockdown of alpha myosin heavy chain disrupts the cytoskeleton and leads to multiple defects during chick cardiogenesis

von Rutland, Catrin, Warner, Louise, Thorpe, Aaran, Alibhai, Aziza, Robinson, Thelma, Shaw, Barry, Layfield, Robert, Brook, J David, Loughna, Siobhan
Veröffentlicht 2009

Zebrafish deficient for Muscleblind-like 2 exhibit features of myotonic dystrophy

von Machuca-Tzili, Laura E., Buxton, Sarah, Thorpe, Aaran, Timson, Cathy M., Wigmore, Peter, Luther, Pradeep K., Brook, J. David
Veröffentlicht 2011

Muscleblind-Like Proteins : Similarities and Differences in Normal and Myotonic Dystrophy Muscle

von Holt, Ian, Jacquemin, Virginie, Fardaei, Majid, Sewry, Caroline A., Butler-Browne, Gillian S., Furling, Denis, Brook, J. David, Morris, Glenn E.
Veröffentlicht 2009

Expanded CUG Repeats Dysregulate RNA Splicing by Altering the Stoichiometry of the Muscleblind 1 Complex

von Paul, Sharan, Dansithong, Warunee, Jog, Sonali P., Holt, Ian, Mittal, Saloni, Brook, J. David, Morris, Glenn E., Comai, Lucio, Reddy, Sita
Veröffentlicht 2011

Global Increase in Circular RNA Levels in Myotonic Dystrophy

von Czubak, Karol, Taylor, Katarzyna, Piasecka, Agnieszka, Sobczak, Krzysztof, Kozlowska, Katarzyna, Philips, Anna, Sedehizadeh, Saam, Brook, J. David, Wojciechowska, Marzena, Kozlowski, Piotr
Veröffentlicht in Front Genet (2019)

Quantitative Methods to Monitor RNA Biomarkers in Myotonic Dystrophy

von Wojciechowska, Marzena, Sobczak, Krzysztof, Kozlowski, Piotr, Sedehizadeh, Saam, Wojtkowiak-Szlachcic, Agnieszka, Czubak, Karol, Markus, Robert, Lusakowska, Anna, Kaminska, Anna, Brook, J. David
Veröffentlicht in Sci Rep (2018)

Physical Interaction between TBX5 and MEF2C Is Required for Early Heart Development

von Ghosh, Tushar K., Song, Fei Fei, Packham, Elizabeth A., Buxton, Sarah, Robinson, Thelma E., Ronksley, Jonathan, Self, Tim, Bonser, Andrew J., Brook, J. David
Veröffentlicht 2009

Combined Mutation Screening of NKX2-5, GATA4, and TBX5 in Congenital Heart Disease: Multiple Heterozygosity and Novel Mutations

von 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, J David
Veröffentlicht 2012

Mutations in SOX9, the Gene Responsible for Campomelic Dysplasia and Autosomal Sex Reversal

von Kwok, Cheni, Weller, Polly A., Guioli, Silvana, Foster, Jamie W., Mansour, Sahar, Zuffardi, Orsetta, Punnett, Hope H., Dominguez-Steglich, Marina A., Brook, J. David, Young, Ian D., Goodfellow, Peter N., Schafer, Alan J.
Veröffentlicht 1995

Tropomyosin 1: Multiple roles in the developing heart and in the formation of congenital heart defects

von England, Jennifer, Granados-Riveron, Javier, Polo-Parada, Luis, Kuriakose, Diji, Moore, Christopher, Brook, J. David, Rutland, Catrin S., Setchfield, Kerry, Gell, Christopher, Ghosh, Tushar K., Bu'Lock, Frances, Thornborough, Christopher, Ehler, Elisabeth, Loughna, Siobhan
Veröffentlicht in J Mol Cell Cardiol (2017)

Low-frequency intermediate penetrance variants in the ROCK1 gene predispose to Tetralogy of Fallot

von Palomino Doza, Julian, Topf, Ana, Bentham, Jamie, Bhattacharya, Shoumo, Cosgrove, Catherine, Brook, J David, Granados-Riveron, Javier, Bu’Lock, Frances A, O’Sullivan, John, Stuart, A Graham, Parsons, Jonathan, Relton, Caroline, Goodship, Judith, Henderson, Deborah J, Keavney, Bernard
Veröffentlicht 2013

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...

von Ketley, Ami, Chen, Catherine Z., Li, Xin, Arya, Sukrat, Robinson, Thelma E., Granados-Riveron, Javier, Udosen, Inyang, Morris, Glenn E., Holt, Ian, Furling, Denis, Chaouch, Soraya, Haworth, Ben, Southall, Noel, Shinn, Paul, Zheng, Wei, Austin, Christopher P., Hayes, Christopher J., Brook, J. David
Veröffentlicht 2014