The relationship between sonic Hedgehog signaling, cilia, and neural tube defects von Murdoch, Jennifer N., Copp, Andrew J.

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Epidermal Wound Repair Is Regulated by the Planar Cell Polarity Signaling Pathway von Caddy, Jacinta, Wilanowski, Tomasz, Darido, Charbel, Dworkin, Sebastian, Ting, Stephen B., Zhao, Quan, Rank, Gerhard, Auden, Alana, Srivastava, Seema, Papenfuss, Tony A., Murdoch, Jennifer N., Humbert, Patrick O., Boulos, Nidal, Weber, Thomas, Zuo, Jian, Cunningham, John M., Jane, Stephen M.

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Genetic interactions between planar cell polarity genes cause diverse neural tube defects in mice von Murdoch, Jennifer N, Damrau, Christine, Paudyal, Anju, Bogani, Debora, Wells, Sara, Greene, Nicholas D E, Stanier, Philip, Copp, Andrew J

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Scribble is required for normal epithelial cell–cell contacts and lumen morphogenesis in the mammalian lung von Yates, Laura L., Schnatwinkel, Carsten, Hazelwood, Lee, Chessum, Lauren, Paudyal, Anju, Hilton, Helen, Romero, M. Rosario, Wilde, Jonathan, Bogani, Debora, Sanderson, Jeremy, Formstone, Caroline, Murdoch, Jennifer N., Niswander, Lee A., Greenfield, Andy, Dean, Charlotte H.

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Mutation of Celsr1 Disrupts Planar Polarity of Inner Ear Hair Cells and Causes Severe Neural Tube Defects in the Mouse von Curtin, John A., Quint, Elizabeth, Tsipouri, Vicky, Arkell, Ruth M., Cattanach, Bruce, Copp, Andrew J., Henderson, Deborah J., Spurr, Nigel, Stanier, Philip, Fisher, Elizabeth M., Nolan, Patrick M., Steel, Karen P., Brown, Steve D.M., Gray, Ian C., Murdoch, Jennifer N.

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Alpha-synuclein aggresomes inhibit ciliogenesis and multiple functions of the centrosome von Iqbal, Anila, Baldrighi, Marta, Murdoch, Jennifer N., Fleming, Angeleen, Wilkinson, Christopher J.

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Mouse hitchhiker mutants have spina bifida, dorso-ventral patterning defects and polydactyly: identification of Tulp3 as a novel negative regulator of the Sonic hedgehog pathway von Patterson, Victoria L., Damrau, Christine, Paudyal, Anju, Reeve, Benjamin, Grimes, Daniel T., Stewart, Michelle E., Williams, Debbie J., Siggers, Pam, Greenfield, Andy, Murdoch, Jennifer N.

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Disruption of Planar Cell Polarity Signaling Results in Congenital Heart Defects and Cardiomyopathy Attributable to Early Cardiomyocyte Disorganization von Phillips, Helen M, Rhee, Hong Jun, Murdoch, Jennifer N, Hildreth, Victoria, Peat, Jonathan D, Anderson, Robert H, Copp, Andrew J, Chaudhry, Bill, Henderson, Deborah J

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The novel mouse mutant, chuzhoi, has disruption of Ptk7 protein and exhibits defects in neural tube, heart and lung development and abnormal planar cell polarity in the ear von Paudyal, Anju, Damrau, Christine, Patterson, Victoria L, Ermakov, Alexander, Formstone, Caroline, Lalanne, Zuzanna, Wells, Sara, Lu, Xiaowei, Norris, Dominic P, Dean, Charlotte H, Henderson, Deborah J, Murdoch, Jennifer N

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Non–Cell-Autonomous Roles for the Planar Cell Polarity Gene Vangl2 in Development of the Coronary Circulation von Phillips, Helen M, Hildreth, Victoria, Peat, Jonathan D, Murdoch, Jennifer N, Kobayashi, Kazuto, Chaudhry, Bill, Henderson, Deborah J

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Brainstem respiratory oscillators develop independently of neuronal migration defects in the Wnt/PCP mouse mutant looptail von Thoby-Brisson, Muriel, Bouvier, Julien, Glasco, Derrick M, Stewart, Michelle E, Dean, Charlotte, Murdoch, Jennifer N, Champagnat, Jean, Fortin, Gilles, Chandrasekhar, Anand

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The PCP genes Celsr1 and Vangl2 are required for normal lung branching morphogenesis von Yates, Laura L., Schnatwinkel, Carsten, Murdoch, Jennifer N., Bogani, Debora, Formstone, Caroline J., Townsend, Stuart, Greenfield, Andy, Niswander, Lee A., Dean, Charlotte H.

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The genetic basis of mammalian neurulation von Copp, Andrew J, Greene, Nicholas D. E, Murdoch, Jennifer N

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BCAP is a centriolar satellite protein and inhibitor of ciliogenesis von de Saram, Paul, Iqbal, Anila, Murdoch, Jennifer N, Wilkinson, Christopher J

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Disruption of Bardet-Biedl syndrome ciliary proteins perturbs planar cell polarity in vertebrates von Phillips, Helen M, Dollfus, Hélène, Leroux, Michel R, Chapple, J Paul, Jagger, Daniel J, Ross, Alison J, Katsanis, Nicholas, Forge, Andrew, Hill, Josephine, Kemp, David T, Eliot, Marie-Madeleine, Lupski, James R, Leitch, Carmen C, Murdoch, Jennifer N, Beales, Philip L, Fisher, Shannon, Tan, Perciliz L, Henderson, Deborah J, Tada, Masazumi, Eichers, Erica R, May-Simera, Helen, Munro, Peter M, Copp, Andrew J, Kai, Masatake

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Atypical cadherins Celsr1-3 differentially regulate migration of facial branchiomotor neurons in mice von Qu, Yibo, Glasco, Derrick M, Zhou, Libing, Sawant, Anagha, Ravni, Aurélia, Fritzsch, Bernd, Damrau, Christine, Murdoch, Jennifer N, Evans, Sylvia, Pfaff, Samuel L, Formstone, Caroline, Goffinet, André M, Chandrasekhar, Anand, Tissir, Fadel

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Disruption of scribble (Scrb1) causes severe neural tube defects in the circletail mouse von Murdoch, Jennifer N., Henderson, Deborah J., Doudney, Kit, Gaston-Massuet, Carles, Phillips, Helen M., Paternotte, Caroline, Arkell, Ruth, Stanier, Philip, Copp, Andrew J.

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Severe neural tube defects in the loop-tail mouse result from mutation of Lpp1, a novel gene involved in floor plate specification von MURDOCH, Jennifer N, DOUDNEY, Kit, PATERNOTTE, Caroline, COPP, Andrew J, STANIER, Philip

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The mouse Wnt/PCP protein Vangl2 is necessary for migration of facial branchiomotor neurons, and functions independently of Dishevelled von Glasco, Derrick M., Sittaramane, Vinoth, Bryant, Whitney, Fritzsch, Bernd, Sawant, Anagha, Paudyal, Anju, Stewart, Michelle, Andre, Philipp, Cadete Vilhais-Neto, Gonçalo, Yang, Yingzi, Song, Mi-Ryoung, Murdoch, Jennifer N., Chandrasekhar, Anand

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Vangl2 Acts via RhoA Signaling to Regulate Polarized Cell Movements During Development of the Proximal Outflow Tract von Phillips, Helen M, Murdoch, Jennifer N, Chaudhry, Bill, Copp, Andrew J, Henderson, Deborah J

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