Sample Drift Correction Following 4D Confocal Time-lapse Imaging

gan Parslow, Adam, Cardona, Albert, Bryson-Richardson, Robert J.
Cyhoeddwyd 2014

In Vivo Wall Shear Measurements within the Developing Zebrafish Heart

gan Jamison, R. Aidan, Samarage, Chaminda R., Bryson-Richardson, Robert J., Fouras, Andreas
Cyhoeddwyd 2013

Using Touch-evoked Response and Locomotion Assays to Assess Muscle Performance and Function in Zebrafish

gan Sztal, Tamar E., Ruparelia, Avnika A., Williams, Caitlin, Bryson-Richardson, Robert J.
Cyhoeddwyd yn J Vis Exp (2016)

Recent advances in understanding congenital myopathies

gan Ravenscroft, Gianina, Bryson-Richardson, Robert J., Nowak, Kristen J., Laing, Nigel G.
Cyhoeddwyd yn F1000Res (2018)

The eIF4G–homolog p97 can activate translation independent of caspase cleavage

gan Nousch, Marco, Reed, Victoria, Bryson-Richardson, Robert J., Currie, Peter D., Preiss, Thomas
Cyhoeddwyd 2007

Functional validation of CHMP7 as an ADHD risk gene

gan Dark, Callum, Williams, Caitlin, Bellgrove, Mark A., Hawi, Ziarih, Bryson-Richardson, Robert J.
Cyhoeddwyd yn Transl Psychiatry (2020)

Genome-wide identification of conserved intronic non-coding sequences using a Bayesian segmentation approach

gan Algama, Manjula, Tasker, Edward, Williams, Caitlin, Parslow, Adam C., Bryson-Richardson, Robert J., Keith, Jonathan M.
Cyhoeddwyd yn BMC Genomics (2017)

Genetic compensation triggered by actin mutation prevents the muscle damage caused by loss of actin protein

gan Sztal, Tamar E., McKaige, Emily A., Williams, Caitlin, Ruparelia, Avnika A., Bryson-Richardson, Robert J.
Cyhoeddwyd yn PLoS Genet (2018)

Zebrafish prox1b Mutants Develop a Lymphatic Vasculature, and prox1b Does Not Specifically Mark Lymphatic Endothelial Cells

gan Tao, Shijie, Witte, Merlijn, Bryson-Richardson, Robert J., Currie, Peter D., Hogan, Benjamin M., Schulte-Merker, Stefan
Cyhoeddwyd 2011

Testing of therapies in a novel nebulin nemaline myopathy model demonstrate a lack of efficacy

gan Sztal, Tamar E., McKaige, Emily A., Williams, Caitlin, Oorschot, Viola, Ramm, Georg, Bryson-Richardson, Robert J.
Cyhoeddwyd yn Acta Neuropathol Commun (2018)

Analysis of protein sequence and interaction data for candidate disease gene prediction

gan George, Richard A., Liu, Jason Y., Feng, Lina L., Bryson-Richardson, Robert J., Fatkin, Diane, Wouters, Merridee A.
Cyhoeddwyd 2006

The quail anatomy portal

gan Ruparelia, Avnika A., Simkin, Johanna E., Salgado, David, Newgreen, Donald F., Martins, Gabriel G., Bryson-Richardson, Robert J.
Cyhoeddwyd 2014

The zebrafish candyfloss mutant implicates extracellular matrix adhesion failure in laminin α2-deficient congenital muscular dystrophy

gan Hall, Thomas E., Bryson-Richardson, Robert J., Berger, Silke, Jacoby, Arie S., Cole, Nicholas J., Hollway, Georgina E., Berger, Joachim, Currie, Peter D.
Cyhoeddwyd 2007

FishNet: an online database of zebrafish anatomy

gan Bryson-Richardson, Robert J, Berger, Silke, Schilling, Thomas F, Hall, Thomas E, Cole, Nicholas J, Gibson, Abigail J, Sharpe, James, Currie, Peter D
Cyhoeddwyd 2007

The zebrafish dystrophic mutant softy maintains muscle fibre viability despite basement membrane rupture and muscle detachment

gan Jacoby, Arie S., Busch-Nentwich, Elisabeth, Bryson-Richardson, Robert J., Hall, Thomas E., Berger, Joachim, Berger, Silke, Sonntag, Carmen, Sachs, Caroline, Geisler, Robert, Stemple, Derek L., Currie, Peter D.
Cyhoeddwyd 2009

L-tyrosine supplementation does not ameliorate skeletal muscle dysfunction in zebrafish and mouse models of dominant skeletal muscle α-actin nemaline myopathy

gan Messineo, Adriana M., Gineste, Charlotte, Sztal, Tamar E., McNamara, Elyshia L., Vilmen, Christophe, Ogier, Augustin C., Hahne, Dorothee, Bendahan, David, Laing, Nigel G., Bryson-Richardson, Robert J., Gondin, Julien, Nowak, Kristen J.
Cyhoeddwyd yn Sci Rep (2018)

Zebrafish models for nemaline myopathy reveal a spectrum of nemaline bodies contributing to reduced muscle function

gan Sztal, Tamar E., Zhao, Mo, Williams, Caitlin, Oorschot, Viola, Parslow, Adam C., Giousoh, Aminah, Yuen, Michaela, Hall, Thomas E., Costin, Adam, Ramm, Georg, Bird, Phillip I., Busch-Nentwich, Elisabeth M., Stemple, Derek L., Currie, Peter D., Cooper, Sandra T., Laing, Nigel G., Nowak, Kristen J., Bryson-Richardson, Robert J.
Cyhoeddwyd yn Acta Neuropathol (2015)

Variants in the Oxidoreductase PYROXD1 Cause Early-Onset Myopathy with Internalized Nuclei and Myofibrillar Disorganization

gan O’Grady, Gina L., Best, Heather A., Sztal, Tamar E., Schartner, Vanessa, Sanjuan-Vazquez, Myriam, Donkervoort, Sandra, Abath Neto, Osorio, Sutton, Roger Bryan, Ilkovski, Biljana, Romero, Norma Beatriz, Stojkovic, Tanya, Dastgir, Jahannaz, Waddell, Leigh B., Boland, Anne, Hu, Ying, Williams, Caitlin, Ruparelia, Avnika A., Maisonobe, Thierry, Peduto, Anthony J., Reddel, Stephen W., Lek, Monkol, Tukiainen, Taru, Cummings, Beryl B., Joshi, Himanshu, Nectoux, Juliette, Brammah, Susan, Deleuze, Jean-François, Ing, Viola Oorschot, Ramm, Georg, Ardicli, Didem, Nowak, Kristen J., Talim, Beril, Topaloglu, Haluk, Laing, Nigel G., North, Kathryn N., MacArthur, Daniel G., Friant, Sylvie, Clarke, Nigel F., Bryson-Richardson, Robert J., Bönnemann, Carsten G., Laporte, Jocelyn, Cooper, Sandra T.
Cyhoeddwyd yn Am J Hum Genet (2016)

KBTBD13 is an actin-binding protein that modulates muscle kinetics

gan de Winter, Josine M., Molenaar, Joery P., Yuen, Michaela, van der Pijl, Robbert, Shen, Shengyi, Conijn, Stefan, van de Locht, Martijn, Willigenburg, Menne, Bogaards, Sylvia J.P., van Kleef, Esmee S.B., Lassche, Saskia, Persson, Malin, Rassier, Dilson E., Sztal, Tamar E., Ruparelia, Avnika A., Oorschot, Viola, Ramm, Georg, Hall, Thomas E., Xiong, Zherui, Johnson, Christopher N., Li, Frank, Kiss, Balazs, Lozano-Vidal, Noelia, Boon, Reinier A., Marabita, Manuela, Nogara, Leonardo, Blaauw, Bert, Rodenburg, Richard J., Küsters, Benno, Doorduin, Jonne, Beggs, Alan H., Granzier, Henk, Campbell, Ken, Ma, Weikang, Irving, Thomas, Malfatti, Edoardo, Romero, Norma B., Bryson-Richardson, Robert J., van Engelen, Baziel G.M., Voermans, Nicol C., Ottenheijm, Coen A.C.
Cyhoeddwyd yn J Clin Invest (2020)

Mutations in KLHL40 Are a Frequent Cause of Severe Autosomal-Recessive Nemaline Myopathy

gan Ravenscroft, Gianina, Miyatake, Satoko, Lehtokari, Vilma-Lotta, Todd, Emily J., Vornanen, Pauliina, Yau, Kyle S., Hayashi, Yukiko K., Miyake, Noriko, Tsurusaki, Yoshinori, Doi, Hiroshi, Saitsu, Hirotomo, Osaka, Hitoshi, Yamashita, Sumimasa, Ohya, Takashi, Sakamoto, Yuko, Koshimizu, Eriko, Imamura, Shintaro, Yamashita, Michiaki, Ogata, Kazuhiro, Shiina, Masaaki, Bryson-Richardson, Robert J., Vaz, Raquel, Ceyhan, Ozge, Brownstein, Catherine A., Swanson, Lindsay C., Monnot, Sophie, Romero, Norma B., Amthor, Helge, Kresoje, Nina, Sivadorai, Padma, Kiraly-Borri, Cathy, Haliloglu, Goknur, Talim, Beril, Orhan, Diclehan, Kale, Gulsev, Charles, Adrian K., Fabian, Victoria A., Davis, Mark R., Lammens, Martin, Sewry, Caroline A., Manzur, Adnan, Muntoni, Francesco, Clarke, Nigel F., North, Kathryn N., Bertini, Enrico, Nevo, Yoram, Willichowski, Ekkhard, Silberg, Inger E., Topaloglu, Haluk, Beggs, Alan H., Allcock, Richard J.N., Nishino, Ichizo, Wallgren-Pettersson, Carina, Matsumoto, Naomichi, Laing, Nigel G.
Cyhoeddwyd 2013