Zebrafish: a vertebrate tool for studying basal body biogenesis, structure, and function

por Marshall, Ryan A., Osborn, Daniel P. S.
Publicado 2016

A CRISPR/Cas9-generated mutation in the zebrafish orthologue of PPP2R3B causes idiopathic scoliosis

por Seda, Marian, Crespo, Berta, Corcelli, Michelangelo, Osborn, Daniel P., Jenkins, Dagan
Publicado 2023

Basal body stability and ciliogenesis requires the conserved component Poc1

por Pearson, Chad G., Osborn, Daniel P.S., Giddings, Thomas H., Beales, Philip L., Winey, Mark
Publicado 2009

Fgf-driven Tbx protein activities directly induce myf5 and myod to initiate zebrafish myogenesis

por Osborn, Daniel P. S., Li, Kuoyu, Cutty, Stephen J., Nelson, Andrew C., Wardle, Fiona C., Hinits, Yaniv, Hughes, Simon M.
Publicado 2020

Heat shock induces rapid resorption of primary cilia

por Prodromou, Natalia V., Thompson, Clare L., Osborn, Daniel P. S., Cogger, Kathryn F., Ashworth, Rachel, Knight, Martin M., Beales, Philip L., Chapple, J. Paul
Publicado 2012

Loss of FTO Antagonises Wnt Signaling and Leads to Developmental Defects Associated with Ciliopathies

por Osborn, Daniel P. S., Roccasecca, Rosa Maria, McMurray, Fiona, Hernandez-Hernandez, Victor, Mukherjee, Sriparna, Barroso, Inês, Stemple, Derek, Cox, Roger, Beales, Philip L., Christou-Savina, Sonia
Publicado 2014

Mutations in the lectin complement pathway genes COLEC11 and MASP1 cause 3MC syndrome

por Rooryck, Caroline, Diaz-Font, Anna, Osborn, Daniel P.S., Chabchoub, Elyes, Hernandez-Hernandez, Victor, Shamseldin, Hanan, Kenny, Joanna, Waters, Aoife, Jenkins, Dagan, Kaissi, Ali Al, Leal, Gabriela F., Dallapiccola, Bruno, Carnevale, Franco, Bitner-Glindzicz, Maria, Lees, Melissa, Hennekam, Raoul, Stanier, Philip, Burns, Alan J., Peeters, Hilde, Alkuraya, Fowzan S, Beales, Philip L.
Publicado 2011

Cardiomyopathy with lethal arrhythmias associated with inactivation of KLHL24

por Hedberg-Oldfors, Carola, Abramsson, Alexandra, Osborn, Daniel P S, Danielsson, Olof, Fazlinezhad, Afsoon, Nilipour, Yalda, Hübbert, Laila, Nennesmo, Inger, Visuttijai, Kittichate, Bharj, Jaipreet, Petropoulou, Evmorfia, Shoreim, Azza, Vona, Barbara, Ahangari, Najmeh, López, Marcela Dávila, Doosti, Mohammad, Banote, Rakesh Kumar, Maroofian, Reza, Edling, Malin, Taherpour, Mehdi, Zetterberg, Henrik, Karimiani, Ehsan Ghayoor, Oldfors, Anders, Jamshidi, Yalda
Publicado 2019

Mutations in INPP5K Cause a Form of Congenital Muscular Dystrophy Overlapping Marinesco-Sjögren Syndrome and Dystroglycanopathy

por Osborn, Daniel P.S., Pond, Heather L., Mazaheri, Neda, Dejardin, Jeremy, Munn, Christopher J., Mushref, Khaloob, Cauley, Edmund S., Moroni, Isabella, Pasanisi, Maria Barbara, Sellars, Elizabeth A., Hill, R. Sean, Partlow, Jennifer N., Willaert, Rebecca K., Bharj, Jaipreet, Malamiri, Reza Azizi, Galehdari, Hamid, Shariati, Gholamreza, Maroofian, Reza, Mora, Marina, Swan, Laura E., Voit, Thomas, Conti, Francesco J., Jamshidi, Yalda, Manzini, M. Chiara
Publicado 2017

Bi-allelic variants in RNF170 are associated with hereditary spastic paraplegia

por Wagner, Matias, Osborn, Daniel P. S., Gehweiler, Ina, Nagel, Maike, Ulmer, Ulrike, Bakhtiari, Somayeh, Amouri, Rim, Boostani, Reza, Hentati, Faycal, Hockley, Maryam M., Hölbling, Benedikt, Schwarzmayr, Thomas, Karimiani, Ehsan Ghayoor, Kernstock, Christoph, Maroofian, Reza, Müller-Felber, Wolfgang, Ozkan, Ege, Padilla-Lopez, Sergio, Reich, Selina, Reichbauer, Jennifer, Darvish, Hossein, Shahmohammadibeni, Neda, Tafakhori, Abbas, Vill, Katharina, Zuchner, Stephan, Kruer, Michael C., Winkelmann, Juliane, Jamshidi, Yalda, Schüle, Rebecca
Publicado 2019