Sample Drift Correction Following 4D Confocal Time-lapse Imaging

著者: Parslow, Adam, Cardona, Albert, Bryson-Richardson, Robert J.
出版事項 2014

In Vivo Wall Shear Measurements within the Developing Zebrafish Heart

著者: Jamison, R. Aidan, Samarage, Chaminda R., Bryson-Richardson, Robert J., Fouras, Andreas
出版事項 2013

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

著者: Sztal, Tamar E., Ruparelia, Avnika A., Williams, Caitlin, Bryson-Richardson, Robert J.
出版年 J Vis Exp (2016)

Recent advances in understanding congenital myopathies

著者: Ravenscroft, Gianina, Bryson-Richardson, Robert J., Nowak, Kristen J., Laing, Nigel G.
出版年 F1000Res (2018)

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

著者: Nousch, Marco, Reed, Victoria, Bryson-Richardson, Robert J., Currie, Peter D., Preiss, Thomas
出版事項 2007

Functional validation of CHMP7 as an ADHD risk gene

著者: Dark, Callum, Williams, Caitlin, Bellgrove, Mark A., Hawi, Ziarih, Bryson-Richardson, Robert J.
出版年 Transl Psychiatry (2020)

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

著者: Algama, Manjula, Tasker, Edward, Williams, Caitlin, Parslow, Adam C., Bryson-Richardson, Robert J., Keith, Jonathan M.
出版年 BMC Genomics (2017)

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

著者: Sztal, Tamar E., McKaige, Emily A., Williams, Caitlin, Ruparelia, Avnika A., Bryson-Richardson, Robert J.
出版年 PLoS Genet (2018)

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

著者: Tao, Shijie, Witte, Merlijn, Bryson-Richardson, Robert J., Currie, Peter D., Hogan, Benjamin M., Schulte-Merker, Stefan
出版事項 2011

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

著者: Sztal, Tamar E., McKaige, Emily A., Williams, Caitlin, Oorschot, Viola, Ramm, Georg, Bryson-Richardson, Robert J.
出版年 Acta Neuropathol Commun (2018)

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

著者: George, Richard A., Liu, Jason Y., Feng, Lina L., Bryson-Richardson, Robert J., Fatkin, Diane, Wouters, Merridee A.
出版事項 2006

The quail anatomy portal

著者: Ruparelia, Avnika A., Simkin, Johanna E., Salgado, David, Newgreen, Donald F., Martins, Gabriel G., Bryson-Richardson, Robert J.
出版事項 2014

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

著者: Hall, Thomas E., Bryson-Richardson, Robert J., Berger, Silke, Jacoby, Arie S., Cole, Nicholas J., Hollway, Georgina E., Berger, Joachim, Currie, Peter D.
出版事項 2007

FishNet: an online database of zebrafish anatomy

著者: Bryson-Richardson, Robert J, Berger, Silke, Schilling, Thomas F, Hall, Thomas E, Cole, Nicholas J, Gibson, Abigail J, Sharpe, James, Currie, Peter D
出版事項 2007

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

著者: 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.
出版事項 2009

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

著者: 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.
出版年 Sci Rep (2018)

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

著者: 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.
出版年 Acta Neuropathol (2015)

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

著者: 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.
出版年 Am J Hum Genet (2016)

KBTBD13 is an actin-binding protein that modulates muscle kinetics

著者: 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.
出版年 J Clin Invest (2020)

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

著者: 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.
出版事項 2013