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162 related items for PubMed ID: 28033651

  • 1. Axons get ahead: Insights into axon guidance and congenital cranial dysinnervation disorders.
    Chilton JK, Guthrie S.
    Dev Neurobiol; 2017 Jul; 77(7):861-875. PubMed ID: 28033651
    [Abstract] [Full Text] [Related]

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  • 3. The Rac-GAP alpha2-Chimaerin Signals via CRMP2 and Stathmins in the Development of the Ocular Motor System.
    Carretero-Rodriguez L, Guðjónsdóttir R, Poparic I, Reilly ML, Chol M, Bianco IH, Chiapello M, Feret R, Deery MJ, Guthrie S.
    J Neurosci; 2021 Aug 04; 41(31):6652-6672. PubMed ID: 34168008
    [Abstract] [Full Text] [Related]

  • 4. Axonal Growth Abnormalities Underlying Ocular Cranial Nerve Disorders.
    Whitman MC.
    Annu Rev Vis Sci; 2021 Sep 15; 7():827-850. PubMed ID: 34081534
    [Abstract] [Full Text] [Related]

  • 5. The genetic basis of complex strabismus.
    Engle EC.
    Pediatr Res; 2006 Mar 15; 59(3):343-8. PubMed ID: 16492969
    [Abstract] [Full Text] [Related]

  • 6. The ECEL1-related strabismus phenotype is consistent with congenital cranial dysinnervation disorder.
    Khan AO, Shaheen R, Alkuraya FS.
    J AAPOS; 2014 Aug 15; 18(4):362-7. PubMed ID: 25173900
    [Abstract] [Full Text] [Related]

  • 7. Ephexin1 Is Required for Eph-Mediated Limb Trajectory of Spinal Motor Axons.
    Chang CJ, Chang MY, Chou SY, Huang CC, Chuang JY, Hsu TI, Chang HF, Wu YH, Wu CC, Morales D, Kania A, Kao TJ.
    J Neurosci; 2018 Feb 21; 38(8):2043-2056. PubMed ID: 29363583
    [Abstract] [Full Text] [Related]

  • 8. Protocadherin-Mediated Cell Repulsion Controls the Central Topography and Efferent Projections of the Abducens Nucleus.
    Asakawa K, Kawakami K.
    Cell Rep; 2018 Aug 07; 24(6):1562-1572. PubMed ID: 30089266
    [Abstract] [Full Text] [Related]

  • 9. Nck2 is essential for limb trajectory selection by spinal motor axons.
    Chang CJ, Chang MY, Lee YC, Chen KY, Hsu TI, Wu YH, Chuang JY, Kao TJ.
    Dev Dyn; 2018 Sep 07; 247(9):1043-1056. PubMed ID: 30016580
    [Abstract] [Full Text] [Related]

  • 10. Patterning and axon guidance of cranial motor neurons.
    Guthrie S.
    Nat Rev Neurosci; 2007 Nov 07; 8(11):859-71. PubMed ID: 17948031
    [Abstract] [Full Text] [Related]

  • 11. α2-Chimaerin regulates a key axon guidance transition during development of the oculomotor projection.
    Clark C, Austen O, Poparic I, Guthrie S.
    J Neurosci; 2013 Oct 16; 33(42):16540-51. PubMed ID: 24133258
    [Abstract] [Full Text] [Related]

  • 12. The congenital cranial dysinnervation disorders.
    Gutowski NJ, Chilton JK.
    Arch Dis Child; 2015 Jul 16; 100(7):678-81. PubMed ID: 25633065
    [Abstract] [Full Text] [Related]

  • 13. Axon pathfinding for locomotion.
    Bonanomi D.
    Semin Cell Dev Biol; 2019 Jan 16; 85():26-35. PubMed ID: 29141181
    [Abstract] [Full Text] [Related]

  • 14. Axon guidance in the developing ocular motor system and Duane retraction syndrome depends on Semaphorin signaling via alpha2-chimaerin.
    Ferrario JE, Baskaran P, Clark C, Hendry A, Lerner O, Hintze M, Allen J, Chilton JK, Guthrie S.
    Proc Natl Acad Sci U S A; 2012 Sep 04; 109(36):14669-74. PubMed ID: 22912401
    [Abstract] [Full Text] [Related]

  • 15. SNARE proteins play a role in motor axon guidance in vertebrates and invertebrates.
    Barrecheguren PJ, Ros O, Cotrufo T, Kunz B, Soriano E, Ulloa F, Stoeckli ET, Araújo SJ.
    Dev Neurobiol; 2017 Sep 04; 77(8):963-974. PubMed ID: 28033683
    [Abstract] [Full Text] [Related]

  • 16. How does calcium interact with the cytoskeleton to regulate growth cone motility during axon pathfinding?
    Gasperini RJ, Pavez M, Thompson AC, Mitchell CB, Hardy H, Young KM, Chilton JK, Foa L.
    Mol Cell Neurosci; 2017 Oct 04; 84():29-35. PubMed ID: 28765051
    [Abstract] [Full Text] [Related]

  • 17. Imaging findings in congenital cranial dysinnervation disorders.
    Ferreira RM, Amaral LL, Gonçalves MV, Lin K.
    Top Magn Reson Imaging; 2011 Dec 04; 22(6):283-94. PubMed ID: 24132067
    [Abstract] [Full Text] [Related]

  • 18. Congenital cranial dysinnervation disorders.
    Singh A, Pandey PK, Agrawal A, Mittal SK, Rana KM, Bahuguna C.
    Int Ophthalmol; 2017 Dec 04; 37(6):1369-1381. PubMed ID: 27837354
    [Abstract] [Full Text] [Related]

  • 19. CCDD Phenotype Associated with a Small Chromosome 2 Deletion.
    Abu-Amero KK, Bosley TM, Kondkar AA, Oystreck DT, Khan AO.
    Semin Ophthalmol; 2015 Dec 04; 30(5-6):435-42. PubMed ID: 24475916
    [Abstract] [Full Text] [Related]

  • 20. Oculomotility disorders arising from disruptions in brainstem motor neuron development.
    Engle EC.
    Arch Neurol; 2007 May 04; 64(5):633-7. PubMed ID: 17502461
    [Abstract] [Full Text] [Related]

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