Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 97

1.

Endodomain diversity in the Drosophila Dscam and its roles in neuronal morphogenesis.

Yu HH, Yang JS, Wang J, Huang Y, Lee T.

J Neurosci. 2009 Feb 11;29(6):1904-14. doi: 10.1523/JNEUROSCI.5743-08.2009.

2.

Transmembrane/juxtamembrane domain-dependent Dscam distribution and function during mushroom body neuronal morphogenesis.

Wang J, Ma X, Yang JS, Zheng X, Zugates CT, Lee CH, Lee T.

Neuron. 2004 Sep 2;43(5):663-72.

3.
4.

Molecular diversity of Dscam and self-recognition.

Shi L, Lee T.

Adv Exp Med Biol. 2012;739:262-75. doi: 10.1007/978-1-4614-1704-0_17. Review.

PMID:
22399408
5.

Analysis of Dscam diversity in regulating axon guidance in Drosophila mushroom bodies.

Zhan XL, Clemens JC, Neves G, Hattori D, Flanagan JJ, Hummel T, Vasconcelos ML, Chess A, Zipursky SL.

Neuron. 2004 Sep 2;43(5):673-86.

6.
7.

Human down syndrome cell adhesion molecules (DSCAMs) are functionally conserved with Drosophila Dscam[TM1] isoforms in controlling neurodevelopment.

Huang J, Wang Y, Raghavan S, Feng S, Kiesewetter K, Wang J.

Insect Biochem Mol Biol. 2011 Oct;41(10):778-87. doi: 10.1016/j.ibmb.2011.05.008. Epub 2011 May 27.

PMID:
21645617
8.

Homophilic Dscam interactions control complex dendrite morphogenesis.

Hughes ME, Bortnick R, Tsubouchi A, Bäumer P, Kondo M, Uemura T, Schmucker D.

Neuron. 2007 May 3;54(3):417-27.

9.

Linking cell surface receptors to microtubules: tubulin folding cofactor D mediates Dscam functions during neuronal morphogenesis.

Okumura M, Sakuma C, Miura M, Chihara T.

J Neurosci. 2015 Feb 4;35(5):1979-90. doi: 10.1523/JNEUROSCI.0973-14.2015.

10.

Dscam diversity is essential for neuronal wiring and self-recognition.

Hattori D, Demir E, Kim HW, Viragh E, Zipursky SL, Dickson BJ.

Nature. 2007 Sep 13;449(7159):223-7.

11.

Molecular diversity of Dscam: recognition of molecular identity in neuronal wiring.

Schmucker D.

Nat Rev Neurosci. 2007 Dec;8(12):915-20. Review.

PMID:
18026165
12.

The zebrafish down syndrome cell adhesion molecule is involved in cell movement during embryogenesis.

Yimlamai D, Konnikova L, Moss LG, Jay DG.

Dev Biol. 2005 Mar 1;279(1):44-57.

13.

The molecular diversity of Dscam is functionally required for neuronal wiring specificity in Drosophila.

Chen BE, Kondo M, Garnier A, Watson FL, Püettmann-Holgado R, Lamar DR, Schmucker D.

Cell. 2006 May 5;125(3):607-20.

14.

Ultra-deep profiling of alternatively spliced Drosophila Dscam isoforms by circularization-assisted multi-segment sequencing.

Sun W, You X, Gogol-Döring A, He H, Kise Y, Sohn M, Chen T, Klebes A, Schmucker D, Chen W.

EMBO J. 2013 Jul 17;32(14):2029-38. doi: 10.1038/emboj.2013.144. Epub 2013 Jun 21.

15.

Drosophila Dscam is an axon guidance receptor exhibiting extraordinary molecular diversity.

Schmucker D, Clemens JC, Shu H, Worby CA, Xiao J, Muda M, Dixon JE, Zipursky SL.

Cell. 2000 Jun 9;101(6):671-84.

16.

The evolution of Dscam genes across the arthropods.

Armitage SA, Freiburg RY, Kurtz J, Bravo IG.

BMC Evol Biol. 2012 Apr 13;12:53. doi: 10.1186/1471-2148-12-53.

17.

Competing RNA secondary structures are required for mutually exclusive splicing of the Dscam exon 6 cluster.

May GE, Olson S, McManus CJ, Graveley BR.

RNA. 2011 Feb;17(2):222-9. doi: 10.1261/rna.2521311. Epub 2010 Dec 15.

18.

Drosophila Vap-33 is required for axonal localization of Dscam isoforms.

Yang Z, Huh SU, Drennan JM, Kathuria H, Martinez JS, Tsuda H, Hall MC, Clemens JC.

J Neurosci. 2012 Nov 28;32(48):17241-50. doi: 10.1523/JNEUROSCI.2834-12.2012.

19.

A regulator of Dscam mutually exclusive splicing fidelity.

Olson S, Blanchette M, Park J, Savva Y, Yeo GW, Yeakley JM, Rio DC, Graveley BR.

Nat Struct Mol Biol. 2007 Dec;14(12):1134-40.

20.

Regulation of Dscam exon 17 alternative splicing by steric hindrance in combination with RNA secondary structures.

Yue Y, Li G, Yang Y, Zhang W, Pan H, Chen R, Shi F, Jin Y.

RNA Biol. 2013 Dec;10(12):1822-33. doi: 10.4161/rna.27176. Epub 2013 Nov 21.

Supplemental Content

Support Center