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Items: 8

1.

Ordered recruitment of dynactin to the microtubule plus-end is required for efficient initiation of retrograde axonal transport.

Moughamian AJ, Osborn GE, Lazarus JE, Maday S, Holzbaur EL.

J Neurosci. 2013 Aug 7;33(32):13190-203. doi: 10.1523/JNEUROSCI.0935-13.2013.

2.

Mutations in rare ataxia genes are uncommon causes of sporadic cerebellar ataxia.

Fogel BL, Lee JY, Lane J, Wahnich A, Chan S, Huang A, Osborn GE, Klein E, Mamah C, Perlman S, Geschwind DH, Coppola G.

Mov Disord. 2012 Mar;27(3):442-6. doi: 10.1002/mds.24064. Epub 2012 Jan 27.

3.

Genome-wide analysis of a Wnt1-regulated transcriptional network implicates neurodegenerative pathways.

Wexler EM, Rosen E, Lu D, Osborn GE, Martin E, Raybould H, Geschwind DH.

Sci Signal. 2011 Oct 4;4(193):ra65. doi: 10.1126/scisignal.2002282.

4.

Regulation of MET by FOXP2, genes implicated in higher cognitive dysfunction and autism risk.

Mukamel Z, Konopka G, Wexler E, Osborn GE, Dong H, Bergman MY, Levitt P, Geschwind DH.

J Neurosci. 2011 Aug 10;31(32):11437-42. doi: 10.1523/JNEUROSCI.0181-11.2011.

5.

Modeling the functional genomics of autism using human neurons.

Konopka G, Wexler E, Rosen E, Mukamel Z, Osborn GE, Chen L, Lu D, Gao F, Gao K, Lowe JK, Geschwind DH.

Mol Psychiatry. 2012 Feb;17(2):202-14. doi: 10.1038/mp.2011.60. Epub 2011 Jun 7.

6.

Wash functions downstream of Rho and links linear and branched actin nucleation factors.

Liu R, Abreu-Blanco MT, Barry KC, Linardopoulou EV, Osborn GE, Parkhurst SM.

Development. 2009 Aug;136(16):2849-60. doi: 10.1242/dev.035246.

7.

Formins in development: orchestrating body plan origami.

Liu R, Linardopoulou EV, Osborn GE, Parkhurst SM.

Biochim Biophys Acta. 2010 Feb;1803(2):207-25. doi: 10.1016/j.bbamcr.2008.09.016. Epub 2008 Oct 14. Review.

8.

Human subtelomeric WASH genes encode a new subclass of the WASP family.

Linardopoulou EV, Parghi SS, Friedman C, Osborn GE, Parkhurst SM, Trask BJ.

PLoS Genet. 2007 Dec;3(12):e237.

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