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Results: 1 to 20 of 177

PubMed for Gene (Select 7846)

1.

Mutations in tubulin genes are frequent causes of various foetal malformations of cortical development including microlissencephaly.

Fallet-Bianco C, Laquerrière A, Poirier K, Razavi F, Guimiot F, Dias P, Loeuillet L, Lascelles K, Beldjord C, Carion N, Toussaint A, Revencu N, Addor MC, Lhermitte B, Gonzales M, Martinovich J, Bessieres B, Marcy-Bonnière M, Jossic F, Marcorelles P, Loget P, Chelly J, Bahi-Buisson N.

Acta Neuropathol Commun. 2014 Jul 25;2:69. doi: 10.1186/2051-5960-2-69.

2.

A case of TUBA1A mutation presenting with lissencephaly and Hirschsprung disease.

Hikita N, Hattori H, Kato M, Sakuma S, Morotomi Y, Ishida H, Seto T, Tanaka K, Shimono T, Shintaku H, Tokuhara D.

Brain Dev. 2014 Feb;36(2):159-62. doi: 10.1016/j.braindev.2013.02.006. Epub 2013 Mar 23.

PMID:
23528852
3.

Expanding the spectrum of TUBA1A-related cortical dysgenesis to Polymicrogyria.

Poirier K, Saillour Y, Fourniol F, Francis F, Souville I, Valence S, Desguerre I, Marie Lepage J, Boddaert N, Line Jacquemont M, Beldjord C, Chelly J, Bahi-Buisson N.

Eur J Hum Genet. 2013 Apr;21(4):381-5. doi: 10.1038/ejhg.2012.195. Epub 2012 Sep 5.

4.

Lissencephaly with marked ventricular dilation, agenesis of corpus callosum, and cerebellar hypoplasia caused by TUBA1A mutation.

Okumura A, Hayashi M, Tsurui H, Yamakawa Y, Abe S, Kudo T, Suzuki R, Shimizu T, Shimojima K, Yamamoto T.

Brain Dev. 2013 Mar;35(3):274-9. doi: 10.1016/j.braindev.2012.05.006. Epub 2012 May 26.

PMID:
22633752
5.

TUBA1A mutation-associated lissencephaly: case report and review of the literature.

Sohal AP, Montgomery T, Mitra D, Ramesh V.

Pediatr Neurol. 2012 Feb;46(2):127-31. doi: 10.1016/j.pediatrneurol.2011.11.017. Review.

PMID:
22264709
6.

TUBA1A mutations: from isolated lissencephaly to familial polymicrogyria.

Jansen AC, Oostra A, Desprechins B, De Vlaeminck Y, Verhelst H, Régal L, Verloo P, Bockaert N, Keymolen K, Seneca S, De Meirleir L, Lissens W.

Neurology. 2011 Mar 15;76(11):988-92. doi: 10.1212/WNL.0b013e31821043f5.

PMID:
21403111
7.

Enhanced acetylation of alpha-tubulin in influenza A virus infected epithelial cells.

Husain M, Harrod KS.

FEBS Lett. 2011 Jan 3;585(1):128-32. doi: 10.1016/j.febslet.2010.11.023. Epub 2010 Nov 19.

8.

TUBA1A mutations cause wide spectrum lissencephaly (smooth brain) and suggest that multiple neuronal migration pathways converge on alpha tubulins.

Kumar RA, Pilz DT, Babatz TD, Cushion TD, Harvey K, Topf M, Yates L, Robb S, Uyanik G, Mancini GM, Rees MI, Harvey RJ, Dobyns WB.

Hum Mol Genet. 2010 Jul 15;19(14):2817-27. doi: 10.1093/hmg/ddq182. Epub 2010 May 12.

9.

Refining the phenotype of alpha-1a Tubulin (TUBA1A) mutation in patients with classical lissencephaly.

Morris-Rosendahl DJ, Najm J, Lachmeijer AM, Sztriha L, Martins M, Kuechler A, Haug V, Zeschnigk C, Martin P, Santos M, Vasconcelos C, Omran H, Kraus U, Van der Knaap MS, Schuierer G, Kutsche K, Uyanik G.

Clin Genet. 2008 Nov;74(5):425-33. doi: 10.1111/j.1399-0004.2008.01093.x.

PMID:
18954413
10.

Refinement of cortical dysgeneses spectrum associated with TUBA1A mutations.

Bahi-Buisson N, Poirier K, Boddaert N, Saillour Y, Castelnau L, Philip N, Buyse G, Villard L, Joriot S, Marret S, Bourgeois M, Van Esch H, Lagae L, Amiel J, Hertz-Pannier L, Roubertie A, Rivier F, Pinard JM, Beldjord C, Chelly J.

J Med Genet. 2008 Oct;45(10):647-53. doi: 10.1136/jmg.2008.058073. Epub 2008 Aug 26.

PMID:
18728072
11.

Neuropathological phenotype of a distinct form of lissencephaly associated with mutations in TUBA1A.

Fallet-Bianco C, Loeuillet L, Poirier K, Loget P, Chapon F, Pasquier L, Saillour Y, Beldjord C, Chelly J, Francis F.

Brain. 2008 Sep;131(Pt 9):2304-20. doi: 10.1093/brain/awn155. Epub 2008 Jul 18.

12.

A pachygyria-causing alpha-tubulin mutation results in inefficient cycling with CCT and a deficient interaction with TBCB.

Tian G, Kong XP, Jaglin XH, Chelly J, Keays D, Cowan NJ.

Mol Biol Cell. 2008 Mar;19(3):1152-61. doi: 10.1091/mbc.E07-09-0861. Epub 2008 Jan 16.

13.

Structural basis of cofactor-mediated stabilization and substrate recognition of the α-tubulin acetyltransferase αTAT1.

Yuzawa S, Kamakura S, Hayase J, Sumimoto H.

Biochem J. 2015 Apr 1;467(1):103-13. doi: 10.1042/BJ20141193.

PMID:
25602620
14.

Direct interaction between selenoprotein P and tubulin.

Du X, Qiu S, Wang Z, Wang R, Wang C, Tian J, Liu Q.

Int J Mol Sci. 2014 Jun 6;15(6):10199-214. doi: 10.3390/ijms150610199.

15.

MCL-1 degradation mediated by JNK activation via MEKK1/TAK1-MKK4 contributes to anticancer activity of new tubulin inhibitor MT189.

Wang W, Wang YQ, Meng T, Yi JM, Huan XJ, Ma LP, Tong LJ, Chen Y, Ding J, Shen JK, Miao ZH.

Mol Cancer Ther. 2014 Jun;13(6):1480-91. doi: 10.1158/1535-7163.MCT-13-0629. Epub 2014 Mar 31.

16.

Phosphorylation of α-tubulin by protein kinase C stimulates microtubule dynamics in human breast cells.

De S, Tsimounis A, Chen X, Rotenberg SA.

Cytoskeleton (Hoboken). 2014 Apr;71(4):257-72. doi: 10.1002/cm.21167. Epub 2014 Feb 26.

17.

Brain malformations and mutations in α- and β-tubulin genes: a review of the literature and description of two new cases.

Romaniello R, Arrigoni F, Cavallini A, Tenderini E, Baschirotto C, Triulzi F, Bassi MT, Borgatti R.

Dev Med Child Neurol. 2014 Apr;56(4):354-60. doi: 10.1111/dmcn.12370. Epub 2014 Jan 7. Review.

PMID:
24392928
18.

Tubulin-interactive stilbene derivatives as anticancer agents.

Mikstacka R, Stefański T, Różański J.

Cell Mol Biol Lett. 2013 Sep;18(3):368-97. doi: 10.2478/s11658-013-0094-z. Epub 2013 Jul 1. Review.

PMID:
23818224
19.

Overlapping cortical malformations and mutations in TUBB2B and TUBA1A.

Cushion TD, Dobyns WB, Mullins JG, Stoodley N, Chung SK, Fry AE, Hehr U, Gunny R, Aylsworth AS, Prabhakar P, Uyanik G, Rankin J, Rees MI, Pilz DT.

Brain. 2013 Feb;136(Pt 2):536-48. doi: 10.1093/brain/aws338. Epub 2013 Jan 29.

20.

The human Ino80 binds to microtubule via the E-hook of tubulin: implications for the role in spindle assembly.

Park EJ, Hur SK, Lee HS, Lee SA, Kwon J.

Biochem Biophys Res Commun. 2011 Dec 16;416(3-4):416-20. doi: 10.1016/j.bbrc.2011.11.069. Epub 2011 Nov 19.

PMID:
22133677
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