Sample Drift Correction Following 4D Confocal Time-lapse Imaging

por Parslow, Adam, Cardona, Albert, Bryson-Richardson, Robert J.
Publicado 2014

In Vivo Wall Shear Measurements within the Developing Zebrafish Heart

por Jamison, R. Aidan, Samarage, Chaminda R., Bryson-Richardson, Robert J., Fouras, Andreas
Publicado 2013

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

por Sztal, Tamar E., Ruparelia, Avnika A., Williams, Caitlin, Bryson-Richardson, Robert J.
Publicado en J Vis Exp (2016)

Recent advances in understanding congenital myopathies

por Ravenscroft, Gianina, Bryson-Richardson, Robert J., Nowak, Kristen J., Laing, Nigel G.
Publicado en F1000Res (2018)

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

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

Functional validation of CHMP7 as an ADHD risk gene

por Dark, Callum, Williams, Caitlin, Bellgrove, Mark A., Hawi, Ziarih, Bryson-Richardson, Robert J.
Publicado en Transl Psychiatry (2020)

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

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

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

por Sztal, Tamar E., McKaige, Emily A., Williams, Caitlin, Ruparelia, Avnika A., Bryson-Richardson, Robert J.
Publicado en PLoS Genet (2018)

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

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

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

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

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

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

The quail anatomy portal

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

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

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

FishNet: an online database of zebrafish anatomy

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

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

por 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.
Publicado 2009

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

por 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.
Publicado en Sci Rep (2018)

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

por 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.
Publicado en Acta Neuropathol (2015)

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

por 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.
Publicado en Am J Hum Genet (2016)

KBTBD13 is an actin-binding protein that modulates muscle kinetics

por 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.
Publicado en J Clin Invest (2020)

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

por 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.
Publicado 2013