Mutations in lectin complement pathway genes COLEC11 and MASP1 cause 3MC syndrome von Beales, Philip L, 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

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A CRISPR/Cas9-generated mutation in the zebrafish orthologue of PPP2R3B causes idiopathic scoliosis von Seda, Marian, Crespo, Berta, Corcelli, Michelangelo, Osborn, Daniel P., Jenkins, Dagan

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Heat shock induces rapid resorption of primary cilia von Prodromou, Natalia V, Thompson, Clare L, Osborn, Daniel P S, Cogger, Kathryn F, Ashworth, Rachel, Knight, Martin M, Beales, Philip L, Chapple, J Paul

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Characterization of CCDC28B reveals its role in ciliogenesis and provides insight to understand its modifier effect on Bardet–Biedl syndrome von Cardenas-Rodriguez, Magdalena, Osborn, Daniel P. S., Irigoín, Florencia, Graña, Martín, Romero, Héctor, Beales, Philip L., Badano, Jose L.

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

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

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Differential requirements for myogenic regulatory factors distinguish medial and lateral somitic, cranial and fin muscle fibre populations von Hinits, Yaniv, Osborn, Daniel P S, Hughes, Simon M

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Basal body stability and ciliogenesis requires the conserved component Poc1 von Pearson, Chad G, Osborn, Daniel P.S, Giddings, Thomas H. Jr, Beales, Philip L, Winey, Mark

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Loss of FTO antagonises Wnt signaling and leads to developmental defects associated with ciliopathies von 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

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Bi-allelic mutations in MYL1 cause a severe congenital myopathy von Ravenscroft, Gianina, Zaharieva, Irina T, Bortolotti, Carlo A, Lambrughi, Matteo, Pignataro, Marcello, Borsari, Marco, Sewry, Caroline A, Phadke, Rahul, Haliloglu, Goknur, Ong, Royston, Goullée, Hayley, Whyte, Tamieka, Consortium, UK10K, Manzur, Adnan, Talim, Beril, Kaya, Ulkuhan, Osborn, Daniel P S, Forrest, Alistair R R, Laing, Nigel G, Muntoni, Francesco

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Bbs8, together with the planar cell polarity protein Vangl2, is required to establish left–right asymmetry in zebrafish von May-Simera, Helen L., Kai, Masatake, Hernandez, Victor, Osborn, Daniel P.S., Tada, Masazumi, Beales, Philip L.

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Zebrafish: a vertebrate tool for studying basal body biogenesis, structure, and function von Marshall, Ryan A, Osborn, Daniel P S

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Cdkn1c drives muscle differentiation through a positive feedback loop with Myod von Osborn, Daniel P.S., Li, Kuoyu, Hinits, Yaniv, Hughes, Simon M.

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Fgf-driven Tbx protein activities directly induce myf5 and myod to initiate zebrafish myogenesis von Osborn, Daniel P S, Li, Kuoyu, Cutty, Stephen J, Nelson, Andrew C, Wardle, Fiona C, Hinits, Yaniv, Hughes, Simon M

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Cardiomyopathy with lethal arrhythmias associated with inactivation of KLHL24 von 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

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Evaluation of zebrafish kidney function using a fluorescent clearance assay von Christou-Savina, Sonia, Beales, Philip L, Osborn, Daniel P S

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Signals and myogenic regulatory factors restrict pax3 and pax7 expression to dermomyotome-like tissue in zebrafish von Hammond, Christina L., Hinits, Yaniv, Osborn, Daniel P.S., Minchin, James E.N., Tettamanti, Gianluca, Hughes, Simon M.

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Mrf4 ( myf6) is dynamically expressed in differentiated zebrafish skeletal muscle von Hinits, Yaniv, Osborn, Daniel P.S., Carvajal, Jaime J., Rigby, Peter W.J., Hughes, Simon M.

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WDR11‐mediated Hedgehog signalling defects underlie a new ciliopathy related to Kallmann syndrome von Kim, Yeon‐Joo, Osborn, Daniel PS, Lee, Ji‐Young, Araki, Masatake, Araki, Kimi, Mohun, Timothy, Känsäkoski, Johanna, Brandstack, Nina, Kim, Hyun‐Taek, Miralles, Francesc, Kim, Cheol‐Hee, Brown, Nigel A, Kim, Hyung‐Goo, Martinez‐Barbera, Juan Pedro, Ataliotis, Paris, Raivio, Taneli, Layman, Lawrence C, Kim, Soo‐Hyun

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The Bardet-Biedl syndrome-related protein CCDC28B modulates mTORC2 function and interacts with SIN1 to control cilia length independently of the mTOR complex von Cardenas-Rodriguez, Magdalena, Irigoín, Florencia, Osborn, Daniel P S, Gascue, Cecilia, Katsanis, Nicholas, Beales, Philip L, Badano, Jose L

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