Buckling without Bending: A New Paradigm in Morphogenesis von Engstrom, T A, Zhang, Teng, Lawton, A K, Joyner, A L, Schwarz, J M

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Embryonic origins of ZebrinII parasagittal stripes and establishment of topographic Purkinje cell projections von Sillitoe, R.V, Gopal, N, Joyner, A.L

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Early anterior/posterior patterning of the midbrain and cerebellum von AIMIN LIU, JOYNER, Alexandra L

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Mouse Gli1 mutants are viable but have defects in SHH signaling in combination with a Gli2 mutation von Park, H L, Bai, C, Platt, K A, Matise, M P, Beeghly, A, Hui, C C, Nakashima, M, Joyner, A L

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Engrailed, Wnt and Pax genes regulate midbrain-hindbrain development von Joyner, Alexandra L.

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A role for Gbx2 in repression of Otx2 and positioning the mid/hindbrain organizer von Joyner, Alexandra L, Millet, Sandrine, Campbell, Kenneth, Epstein, Douglas J, Losos, Kasia, Harris, Esther

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The mouse Engrailed-1 gene and ventral limb patterning von Loomis, Cynthia A, Harris, Esther, Michaud, Jacques, Wurst, Wolfgang, Hanks, Mark, Joyner, Alexandra L

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EN and GBX2 play essential roles downstream of FGF8 in patterning the mouse mid/hindbrain region von Liu, A, Joyner, A L

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Establishment and Chimera Analysis of 129/SvEv- and C57BL/6-Derived Mouse Embryonic Stem Cell Lines von Auerbach, W, Dunmore, J.H, Fairchild-Huntress, V, Fang, Q, Auerbach, A.B, Huszar, D, Joyner, A.L

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Glucose intolerance but normal satiety in mice with a null mutation in the glucagon-like peptide 1 receptor gene von Scrocchi, L.A, Brown, T.J, Maclusky, N, Brubaker, P.L, Auerbach, A.B, Joyner, A.L, Drucker, D.J

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Huntingtin is required for neurogenesis and is not impaired by the Huntington's disease CAG expansion von White, Jacqueline K, Auerbach, Wojtek, Duyao, Mabel P, Vonsattel, Jean-Paul, Gusella, James F, Joyner, Alexandra L, MacDonald, Marcy E

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Essential role of Mash-2 in extraembryonic development von Guillemot, François, Nagy, Andras, Auerbach, Anna, Rossant, Janet, Joyner, Alexandra L

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Length-Dependent Gametic CAG Repeat Instability in the Huntington's Disease Knock-in Mouse von Wheeler, Vanessa C., Auerbach, Wojtek, White, Jacqueline K., Srinidhi, Jayalakshmi, Auerbach, Anna, Ryan, Angela, Duyao, Mabel P., Vrbanac, Vladimir, Weaver, Meredith, Gusella, James F., Joyner, Alexandra L., MacDonald, Marcy E.

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Mammalian achaete-scute homolog 1 is required for the early development of olfactory and autonomic neurons von Guillemot, François, Lo, Li-Ching, Johnson, Jane E., Auerbach, Anna, Anderson, David J., Joyner, Alexandra L.

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Rescue of the En-1 Mutant Phenotype by Replacement of En-1 with En-2 von Hanks, Mark, Wurst, Wolfgang, Anson-Cartwright, Lynn, Auerbach, Anna B., Joyner, Alexandra L.

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Multiple developmental defects in Engrailed-1 mutant mice: an early mid-hindbrain deletion and patterning defects in forelimbs and sternum von WURST, W, AUERBACH, A. B, JOYNER, A. L

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Inactivation of the Mouse Huntington's Disease Gene Homolog Hdh von Duyao, Mabel P., Auerbach, Anna B., Ryan, Angela, Persichetti, Francesca, Barnes, Glenn T., McNeil, Sandra M., Ge, Pei, Vonsattel, Jean-Paul, Gusella, James F., Joyner, Alexandra L., MacDonald, Marcy E.

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Expression of Three Mouse Homologs of the Drosophila Segment Polarity Gene cubitus interruptus, Gli, Gli-2, and Gli-3, in Ectoderm- and Mesoderm-Derived Tissues Suggests Multiple R... von Hui, Chi-Chung, Slusarski, Diane, Platt, Kenneth A., Holmgren, Robert, Joyner, Alexandra L.

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Targeted disruption of the trkB neurotrophin receptor gene results in nervous system lesions and neonatal death von KLEIN, R, SMEYNE, R. J, WURST, W, LONG, L. K, AUERBACH, B. A, JOYNER, A. L, BARBACID, M

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Subtle Cerebellar Phenotype in Mice Homozygous for a Targeted Deletion of the En-2 Homeobox von Joyner, A. L., Herrup, K., Auerbach, B. A., Davis, C. A., Rossant, J.

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