Sample Drift Correction Following 4D Confocal Time-lapse Imaging

le Parslow, Adam, Cardona, Albert, Bryson-Richardson, Robert J.
Foilsithe 2014

In Vivo Wall Shear Measurements within the Developing Zebrafish Heart

le Jamison, R. Aidan, Samarage, Chaminda R., Bryson-Richardson, Robert J., Fouras, Andreas
Foilsithe 2013

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

le Sztal, Tamar E., Ruparelia, Avnika A., Williams, Caitlin, Bryson-Richardson, Robert J.
Foilsithe in J Vis Exp (2016)

Recent advances in understanding congenital myopathies

le Ravenscroft, Gianina, Bryson-Richardson, Robert J., Nowak, Kristen J., Laing, Nigel G.
Foilsithe in F1000Res (2018)

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

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

Functional validation of CHMP7 as an ADHD risk gene

le Dark, Callum, Williams, Caitlin, Bellgrove, Mark A., Hawi, Ziarih, Bryson-Richardson, Robert J.
Foilsithe in Transl Psychiatry (2020)

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

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

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

le Sztal, Tamar E., McKaige, Emily A., Williams, Caitlin, Ruparelia, Avnika A., Bryson-Richardson, Robert J.
Foilsithe in PLoS Genet (2018)

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

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

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

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

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

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

The quail anatomy portal

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

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

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

FishNet: an online database of zebrafish anatomy

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

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

le 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.
Foilsithe 2009

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

le 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.
Foilsithe in Sci Rep (2018)

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

le 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.
Foilsithe in Acta Neuropathol (2015)

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

le 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.
Foilsithe in Am J Hum Genet (2016)

KBTBD13 is an actin-binding protein that modulates muscle kinetics

le 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.
Foilsithe in J Clin Invest (2020)

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

le 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.
Foilsithe 2013