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Results: 1 to 20 of 124

Similar articles for PubMed (Select 18996916)

1.

Disruption of neural progenitors along the ventricular and subventricular zones in periventricular heterotopia.

Ferland RJ, Batiz LF, Neal J, Lian G, Bundock E, Lu J, Hsiao YC, Diamond R, Mei D, Banham AH, Brown PJ, Vanderburg CR, Joseph J, Hecht JL, Folkerth R, Guerrini R, Walsh CA, Rodriguez EM, Sheen VL.

Hum Mol Genet. 2009 Feb 1;18(3):497-516. doi: 10.1093/hmg/ddn377. Epub 2008 Nov 7.

2.
3.

A glial origin for periventricular nodular heterotopia caused by impaired expression of Filamin-A.

Carabalona A, Beguin S, Pallesi-Pocachard E, Buhler E, Pellegrino C, Arnaud K, Hubert P, Oualha M, Siffroi JP, Khantane S, Coupry I, Goizet C, Gelot AB, Represa A, Cardoso C.

Hum Mol Genet. 2012 Mar 1;21(5):1004-17. doi: 10.1093/hmg/ddr531. Epub 2011 Nov 10.

4.

Filamin A regulates neuronal migration through brefeldin A-inhibited guanine exchange factor 2-dependent Arf1 activation.

Zhang J, Neal J, Lian G, Hu J, Lu J, Sheen V.

J Neurosci. 2013 Oct 2;33(40):15735-46. doi: 10.1523/JNEUROSCI.1939-13.2013.

5.

Filamin A mediated Big2 dependent endocytosis: From apical abscission to periventricular heterotopia.

Sheen VL.

Tissue Barriers. 2014 Jun 16;2:e29431. doi: 10.4161/tisb.29431. eCollection 2014.

6.

Filamin a regulates neural progenitor proliferation and cortical size through Wee1-dependent Cdk1 phosphorylation.

Lian G, Lu J, Hu J, Zhang J, Cross SH, Ferland RJ, Sheen VL.

J Neurosci. 2012 May 30;32(22):7672-84. doi: 10.1523/JNEUROSCI.0894-12.2012.

7.

Brefeldin A-inhibited guanine exchange factor 2 regulates filamin A phosphorylation and neuronal migration.

Zhang J, Neal J, Lian G, Shi B, Ferland RJ, Sheen V.

J Neurosci. 2012 Sep 5;32(36):12619-29. doi: 10.1523/JNEUROSCI.1063-12.2012.

8.

Mutations in ARFGEF2 implicate vesicle trafficking in neural progenitor proliferation and migration in the human cerebral cortex.

Sheen VL, Ganesh VS, Topcu M, Sebire G, Bodell A, Hill RS, Grant PE, Shugart YY, Imitola J, Khoury SJ, Guerrini R, Walsh CA.

Nat Genet. 2004 Jan;36(1):69-76. Epub 2003 Nov 30.

PMID:
14647276
9.

Periventricular heterotopia: phenotypic heterogeneity and correlation with Filamin A mutations.

Parrini E, Ramazzotti A, Dobyns WB, Mei D, Moro F, Veggiotti P, Marini C, Brilstra EH, Dalla Bernardina B, Goodwin L, Bodell A, Jones MC, Nangeroni M, Palmeri S, Said E, Sander JW, Striano P, Takahashi Y, Van Maldergem L, Leonardi G, Wright M, Walsh CA, Guerrini R.

Brain. 2006 Jul;129(Pt 7):1892-906. Epub 2006 May 9.

10.

Trouble making the first move: interpreting arrested neuronal migration in the cerebral cortex.

Sarkisian MR, Bartley CM, Rakic P.

Trends Neurosci. 2008 Feb;31(2):54-61. doi: 10.1016/j.tins.2007.11.009. Epub 2008 Jan 16. Review.

PMID:
18201775
11.

Filamin A and Filamin B are co-expressed within neurons during periods of neuronal migration and can physically interact.

Sheen VL, Feng Y, Graham D, Takafuta T, Shapiro SS, Walsh CA.

Hum Mol Genet. 2002 Nov 1;11(23):2845-54.

12.

Periventricular heterotopia in 6q terminal deletion syndrome: role of the C6orf70 gene.

Conti V, Carabalona A, Pallesi-Pocachard E, Parrini E, Leventer RJ, Buhler E, McGillivray G, Michel FJ, Striano P, Mei D, Watrin F, Lise S, Pagnamenta AT, Taylor JC, Kini U, Clayton-Smith J, Novara F, Zuffardi O, Dobyns WB, Scheffer IE, Robertson SP, Berkovic SF, Represa A, Keays DA, Cardoso C, Guerrini R.

Brain. 2013 Nov;136(Pt 11):3378-94. doi: 10.1093/brain/awt249. Epub 2013 Sep 20.

13.

Mutation in filamin A causes periventricular heterotopia, developmental regression, and West syndrome in males.

Masruha MR, Caboclo LO, Carrete H Jr, Cendes IL, Rodrigues MG, Garzon E, Yacubian EM, Sakamoto AC, Sheen V, Harney M, Neal J, Hill RS, Bodell A, Walsh C, Vilanova LC.

Epilepsia. 2006 Jan;47(1):211-4.

PMID:
16417552
14.

MEKK4 signaling regulates filamin expression and neuronal migration.

Sarkisian MR, Bartley CM, Chi H, Nakamura F, Hashimoto-Torii K, Torii M, Flavell RA, Rakic P.

Neuron. 2006 Dec 7;52(5):789-801.

15.

Atypical male and female presentations of FLNA-related periventricular nodular heterotopia.

Fergelot P, Coupry I, Rooryck C, Deforges J, Maurat E, Solé G, Boute O, Dieux-Coeslier A, David A, Marchal C, Thambo JB, Lacombe D, Arveiler B, Goizet C.

Eur J Med Genet. 2012 May;55(5):313-8. doi: 10.1016/j.ejmg.2012.01.018. Epub 2012 Feb 8.

PMID:
22366253
16.

Vascular and connective tissue anomalies associated with X-linked periventricular heterotopia due to mutations in Filamin A.

Reinstein E, Frentz S, Morgan T, García-Miñaúr S, Leventer RJ, McGillivray G, Pariani M, van der Steen A, Pope M, Holder-Espinasse M, Scott R, Thompson EM, Robertson T, Coppin B, Siegel R, Bret Zurita M, Rodríguez JI, Morales C, Rodrigues Y, Arcas J, Saggar A, Horton M, Zackai E, Graham JM, Rimoin DL, Robertson SP.

Eur J Hum Genet. 2013 May;21(5):494-502. doi: 10.1038/ejhg.2012.209. Epub 2012 Oct 3.

17.

Periventricular heterotopia.

Lu J, Sheen V.

Epilepsy Behav. 2005 Sep;7(2):143-9. Review.

PMID:
15996530
18.

Lung disease associated with periventricular nodular heterotopia and an FLNA mutation.

Masurel-Paulet A, Haan E, Thompson EM, Goizet C, Thauvin-Robinet C, Tai A, Kennedy D, Smith G, Khong TY, Solé G, Guerineau E, Coupry I, Huet F, Robertson S, Faivre L.

Eur J Med Genet. 2011 Jan-Feb;54(1):25-8. doi: 10.1016/j.ejmg.2010.09.010. Epub 2010 Oct 1.

PMID:
20888935
19.

Movement disorder and neuronal migration disorder due to ARFGEF2 mutation.

de Wit MC, de Coo IF, Halley DJ, Lequin MH, Mancini GM.

Neurogenetics. 2009 Oct;10(4):333-6. doi: 10.1007/s10048-009-0192-2. Epub 2009 Apr 22.

20.

Rcan1 deficiency impairs neuronal migration and causes periventricular heterotopia.

Li Y, Wang J, Zhou Y, Li D, Xiong ZQ.

J Neurosci. 2015 Jan 14;35(2):610-20. doi: 10.1523/JNEUROSCI.1003-14.2015.

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