The evolution of human artistic creativity von Morriss‐Kay, Gillian M.

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Growth of the normal skull vault and its alteration in craniosynostosis: insights from human genetics and experimental studies von Morriss‐Kay, Gillian M., Wilkie, Andrew O. M.

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Mechanism of skull suture maintenance and interdigitation von Miura, Takashi, Perlyn, Chad A., Kinboshi, Masato, Ogihara, Naomichi, Kobayashi‐Miura, Mikiko, Morriss‐Kay, Gillian M., Shiota, Kohei

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Mutations of Ephrin-B1 (EFNB1), a Marker of Tissue Boundary Formation, Cause Craniofrontonasal Syndrome von Stephen R. F. Twigg, Kan, Rui, Babbs, Christian, Bochukova, Elena G., Robertson, Stephen P., Wall, Steven A., Morriss-Kay, Gillian M., Andrew O. M. Wilkie, Weatherall, David

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A Gain-of-Function Mutation of Fgfr2c Demonstrates the Roles of This Receptor Variant in Osteogenesis von Eswarakumar, Veraragavan P., Horowitz, Mark C., Locklin, Rachel, Morriss-Kay, Gillian M., Lonai, Peter, Schlessinger, Joseph

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The IIIc alternative of Fgfr2 is a positive regulator of bone formation von Eswarakumar, Vereragavan P, Monsonego-Ornan, Efrat, Pines, Mark, Antonopoulou, Ileana, Morriss-Kay, Gillian M, Lonai, Peter

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Genetics of craniofacial development and malformation von Wilkie, Andrew O. M., Morriss-Kay, Gillian M.

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Alx4 and Msx2 play phenotypically similar and additive roles in skull vault differentiation von Antonopoulou, Ileana, Mavrogiannis, Lampros A., Wilkie, Andrew O. M., Morriss‐Kay, Gillian M.

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Derivation of the mammalian skull vault von MORRISS‐KAY, GILLIAN M.

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Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defects von Mavrogiannis, Lampros A., Antonopoulou, Ileana, Baxová, Alica, Kutílek, Stepán, Kim, Chong A., Sugayama, Sofia M., Salamanca, Alberto, Wall, Steven A., Morriss-Kay, Gillian M., Wilkie, Andrew O.M.

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Tissue Origins and Interactions in the Mammalian Skull Vault von Jiang, Xiaobing, Iseki, Sachiko, Maxson, Robert E., Sucov, Henry M., Morriss-Kay, Gillian M.

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Developmental mechanisms underlying polydactyly in the mouse mutant Doublefoot von Crick, Alexandra P., Babbs, Christian, Brown, Jennifer M., Morriss‐Kay, Gillian M.

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Skeletal analysis of the Fgfr3(P244R) mouse, a genetic model for the Muenke craniosynostosis syndrome von Twigg, Stephen R F, Healy, Chris, Babbs, Christian, Sharpe, Jacqueline A, Wood, William G, Sharpe, Paul T, Morriss-Kay, Gillian M, Wilkie, Andrew O M

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Nprl3 is required for normal development of the cardiovascular system von Kowalczyk, Monika S, Hughes, Jim R, Babbs, Christian, Sanchez-Pulido, Luis, Szumska, Dorota, Sharpe, Jacqueline A, Sloane-Stanley, Jacqueline A, Morriss-Kay, Gillian M, Smoot, Leslie B, Roberts, Amy E, Watkins, Hugh, Bhattacharya, Shoumo, Gibbons, Richard J, Ponting, Chris P, Wood, William G, Higgs, Douglas R

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Functional anatomy of the human brain von Marshall, John C., Morriss‐Kay, Gillian M.

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CD34 expression patterns during early mouse development are related to modes of blood vessel formation and reveal additional sites of hematopoiesis von WOOD, H. B, MAY, G, HEALY, L, ENVER, T, MORRISS-KAY, G. M

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Craniofacial defects in AP-2 null mutant mice von Morriss-Kay, Gillian M.

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Treatment of Mice with Retinoids In Vivo and In Vitro von Morriss-Kay, Gillian M.

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Computational mouse atlases and their application to automatic assessment of craniofacial dysmorphology caused by the Crouzon mutation Fgfr2(C342Y) von Olafsdóttir, Hildur, Darvann, Tron A, Hermann, Nuno V, Oubel, Estanislao, Ersbøll, Bjarne K, Frangi, Alejandro F, Larsen, Per, Perlyn, Chad A, Morriss-Kay, Gillian M, Kreiborg, Sven

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Skeletal analysis of the Fgfr3P244R mouse, a genetic model for the Muenke craniosynostosis syndrome von Twigg, Stephen R. F., Healy, Chris, Babbs, Christian, Sharpe, Jacqueline A., Wood, William G., Sharpe, Paul T., Morriss‐Kay, Gillian M., Wilkie, Andrew O. M.

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