The CXCL12/CXCR4 Axis Plays a Critical Role in Coronary Artery Development von Ivins, Sarah, Chappell, Joel, Vernay, Bertrand, Suntharalingham, Jenifer, Martineau, Alexandrine, Mohun, Timothy J., Scambler, Peter J.

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Molecular genetics of 22q11.2 deletion syndrome von Morrow, Bernice E., McDonald‐McGinn, Donna M., Emanuel, Beverly S., Vermeesch, Joris R., Scambler, Peter J.

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Splice-Site Mutations in the Axonemal Outer Dynein Arm Docking Complex Gene CCDC114 Cause Primary Ciliary Dyskinesia von Onoufriadis, Alexandros, Paff, Tamara, Antony, Dinu, Shoemark, Amelia, Micha, Dimitra, Kuyt, Bertus, Schmidts, Miriam, Petridi, Stavroula, Dankert-Roelse, Jeanette E., Haarman, Eric G., Daniels, Johannes M.A., Emes, Richard D., Wilson, Robert, Hogg, Claire, Scambler, Peter J., Chung, Eddie M.K., Pals, Gerard, Mitchison, Hannah M.

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Hyperdynamic Plasticity of Chromatin Proteins in Pluripotent Embryonic Stem Cells von Meshorer, Eran, Yellajoshula, Dhananjay, George, Eric, Scambler, Peter J., Brown, David T., Misteli, Tom

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Mechanisms and cell lineages in lymphatic vascular development von Jafree, Daniyal J., Long, David A., Scambler, Peter J., Ruhrberg, Christiana

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Neural crest-derived SEMA3C activates endothelial NRP1 for cardiac outflow tract septation von Plein, Alice, Calmont, Amélie, Fantin, Alessandro, Denti, Laura, Anderson, Naomi A, Scambler, Peter J, Ruhrberg, Christiana

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Loss of CXCL12/CXCR4 signalling impacts several aspects of cardiovascular development but does not exacerbate Tbx1 haploinsufficiency von Page, Mahalia, Ridge, Liam, Gold Diaz, Diana, Tsogbayar, Tsolmon, Scambler, Peter J, Ivins, Sarah

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Tbx1 regulates the BMP-Smad1 pathway in a transcription independent manner von Fulcoli, F Gabriella, Huynh, Tuong, Scambler, Peter J, Baldini, Antonio

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Dual role for CXCL12 signaling in semilunar valve development von Ridge, Liam A., Kewbank, Dania, Schütz, Dagmar, Stumm, Ralf, Scambler, Peter J., Ivins, Sarah

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CHD7 Maintains Neural Stem Cell Quiescence and Prevents Premature Stem Cell Depletion in the Adult Hippocampus von Jones, Kieran M., Sarić, Nemanja, Russell, John P., Andoniadou, Cynthia L., Scambler, Peter J., Basson, M. Albert

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Short-Rib Polydactyly and Jeune Syndromes Are Caused by Mutations in WDR60 von McInerney-Leo, Aideen M., Schmidts, Miriam, Cortés, Claudio R., Leo, Paul J., Gener, Blanca, Courtney, Andrew D., Gardiner, Brooke, Harris, Jessica A., Lu, Yeping, Marshall, Mhairi, Scambler, Peter J., Beales, Philip L., Brown, Matthew A., Zankl, Andreas, Mitchison, Hannah M., Duncan, Emma L., Wicking, Carol

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Activation of podocyte Notch mediates early Wt1 glomerulopathy von Asfahani, Rowan I., Tahoun, Mona M., Miller-Hodges, Eve V., Bellerby, Jack, Virasami, Alex K., Sampson, Robert D., Moulding, Dale, Sebire, Neil J., Hohenstein, Peter, Scambler, Peter J., Waters, Aoife M.

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Spatiotemporal dynamics and heterogeneity of renal lymphatics in mammalian development and cystic kidney disease von Jafree, Daniyal J, Moulding, Dale, Kolatsi-Joannou, Maria, Perretta Tejedor, Nuria, Price, Karen L, Milmoe, Natalie J, Walsh, Claire L, Correra, Rosa Maria, Winyard, Paul Jd, Harris, Peter C, Ruhrberg, Christiana, Walker-Samuel, Simon, Riley, Paul R, Woolf, Adrian S, Scambler, Peter J, Long, David A

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IFT80 , which encodes a conserved intraflagellar transport protein, is mutated in Jeune asphyxiating thoracic dystrophy von Scambler, Peter J, Beales, Philip L, Bland, Elizabeth, Tobin, Jonathan L, Bacchelli, Chiara, Tuysuz, Beyhan, Hill, Josephine, Rix, Suzanne, Pearson, Chad G, Kai, Masatake, Hartley, Jane, Johnson, Colin, Irving, Melita, Elcioglu, Nursel, Winey, Mark, Tada, Masazumi

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Tbx1 haploinsufficiency in the DiGeorge syndrome region causes aortic arch defects in mice von Lindsay, Elizabeth A, Vitelli, Francesca, Su, Hong, Morishima, Masae, Huynh, Tuong, Pramparo, Tiziano, Jurecic, Vesna, Ogunrinu, George, Sutherland, Helen F, Scambler, Peter J, Bradley, Allan, Baldini, Antonio

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HIRA Is Required for Heart Development and Directly Regulates Tnni2 and Tnnt3 von Dilg, Daniel, Saleh, Rasha Noureldin M, Phelps, Sarah Elizabeth Lee, Rose, Yoann, Dupays, Laurent, Murphy, Cian, Mohun, Timothy, Anderson, Robert H, Scambler, Peter J, Chapgier, Ariane L A

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Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome von Paylor, Richard, Glaser, Beate, Mupo, Annalisa, Ataliotis, Paris, Spencer, Corinne, Sobotka, Angela, Sparks, Chelsey, Choi, Chul-Hee, Oghalai, John, Curran, Sarah, Murphy, Kieran C, Monks, Stephen, Williams, Nigel, O'Donovan, Michael C, Owen, Michael J, Scambler, Peter J, Lindsay, Elizabeth

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A critical role for the chromatin remodeller CHD7 in anterior mesoderm during cardiovascular development von Payne, Sophie, Burney, Matthew J., McCue, Karen, Popal, Nelo, Davidson, Sean M., Anderson, Robert H., Scambler, Peter J.

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Tbx1 controls cardiac neural crest cell migration during arch artery development by regulating Gbx2 expression in the pharyngeal ectoderm von Calmont, Amélie, Ivins, Sarah, Van Bueren, Kelly Lammerts, Papangeli, Irinna, Kyriakopoulou, Vanessa, Andrews, William D, Martin, James F, Moon, Anne M, Illingworth, Elizabeth A, Basson, M Albert, Scambler, Peter J

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Neonatal epileptic encephalopathy caused by mutations in the PNPO gene encoding pyridox(am)ine 5′-phosphate oxidase von Mills, Philippa B., Surtees, Robert A.H., Champion, Michael P., Beesley, Clare E., Dalton, Neil, Scambler, Peter J., Heales, Simon J.R., Briddon, Anthony, Scheimberg, Irene, Hoffmann, Georg F., Zschocke, Johannes, Clayton, Peter T.

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