Identification of Transcribed Sequences

Autor Brook, J David
Vydáno 1995

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

Autor Granados-Riveron, Javier T., Brook, J. David
Vydáno 2012

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

Autor Fardaei, Majid, Larkin, Ken, Brook, J. David, Hamshere, Marion G.
Vydáno 2001

Recent advances in congenital heart disease genomics

Autor Wilsdon, Anna, Sifrim, Alejandro, Hitz, Marc-Phillip, Hurles, Matthew, Brook, J. David
Vydáno v F1000Res (2017)

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

Autor Ghosh, Tushar K., Aparicio-Sánchez, José J., Buxton, Sarah, Brook, J. David
Vydáno v Sci Rep (2019)

Transcriptional abnormality in myotonic dystrophy affects DMPK but not neighboring genes

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

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

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

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

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

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

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

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

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

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

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

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

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

Global Increase in Circular RNA Levels in Myotonic Dystrophy

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

Quantitative Methods to Monitor RNA Biomarkers in Myotonic Dystrophy

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

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

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

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

Autor 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
Vydáno 2012

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

Autor 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.
Vydáno 1995

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

Autor 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
Vydáno v J Mol Cell Cardiol (2017)

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

Autor 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
Vydáno 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...

Autor 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
Vydáno 2014