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Items: 15

1.

Mammalian knock out cells reveal prominent roles for atlastin GTPases in ER network morphology.

Zhao G, Zhu PP, Renvoisé B, Maldonado-Báez L, Park SH, Blackstone C.

Exp Cell Res. 2016 Nov 15;349(1):32-44. doi: 10.1016/j.yexcr.2016.09.015. Epub 2016 Sep 23.

PMID:
27669642
2.

Reep1 null mice reveal a converging role for hereditary spastic paraplegia proteins in lipid droplet regulation.

Renvoisé B, Malone B, Falgairolle M, Munasinghe J, Stadler J, Sibilla C, Park SH, Blackstone C.

Hum Mol Genet. 2016 Dec 1;25(23):5111-5125. doi: 10.1093/hmg/ddw315.

3.

A new glucocerebrosidase-deficient neuronal cell model provides a tool to probe pathophysiology and therapeutics for Gaucher disease.

Westbroek W, Nguyen M, Siebert M, Lindstrom T, Burnett RA, Aflaki E, Jung O, Tamargo R, Rodriguez-Gil JL, Acosta W, Hendrix A, Behre B, Tayebi N, Fujiwara H, Sidhu R, Renvoise B, Ginns EI, Dutra A, Pak E, Cramer C, Ory DS, Pavan WJ, Sidransky E.

Dis Model Mech. 2016 Jul 1;9(7):769-78. doi: 10.1242/dmm.024588. Epub 2016 May 19.

4.

Neuronal Cx3cr1 Deficiency Protects against Amyloid β-Induced Neurotoxicity.

Dworzak J, Renvoisé B, Habchi J, Yates EV, Combadière C, Knowles TP, Dobson CM, Blackstone C, Paulsen O, Murphy PM.

PLoS One. 2015 Jun 3;10(6):e0127730. doi: 10.1371/journal.pone.0127730. eCollection 2015.

5.

Mutation in CPT1C Associated With Pure Autosomal Dominant Spastic Paraplegia.

Rinaldi C, Schmidt T, Situ AJ, Johnson JO, Lee PR, Chen KL, Bott LC, Fadó R, Harmison GH, Parodi S, Grunseich C, Renvoisé B, Biesecker LG, De Michele G, Santorelli FM, Filla A, Stevanin G, Dürr A, Brice A, Casals N, Traynor BJ, Blackstone C, Ulmer TS, Fischbeck KH.

JAMA Neurol. 2015 May;72(5):561-70. doi: 10.1001/jamaneurol.2014.4769. Erratum in: JAMA Neurol. 2015 May;72(5):608.

6.

Spastin-interacting protein NA14/SSNA1 functions in cytokinesis and axon development.

Goyal U, Renvoisé B, Chang J, Blackstone C.

PLoS One. 2014 Nov 12;9(11):e112428. doi: 10.1371/journal.pone.0112428. eCollection 2014.

7.

Lysosomal abnormalities in hereditary spastic paraplegia types SPG15 and SPG11.

Renvoisé B, Chang J, Singh R, Yonekawa S, FitzGibbon EJ, Mankodi A, Vanderver A, Schindler A, Toro C, Gahl WA, Mahuran DJ, Blackstone C, Pierson TM.

Ann Clin Transl Neurol. 2014 Jun 1;1(6):379-389.

8.

MITD1 is recruited to midbodies by ESCRT-III and participates in cytokinesis.

Lee S, Chang J, Renvoisé B, Tipirneni A, Yang S, Blackstone C.

Mol Biol Cell. 2012 Nov;23(22):4347-61. doi: 10.1091/mbc.E12-04-0292. Epub 2012 Sep 26.

9.

Spg20-/- mice reveal multimodal functions for Troyer syndrome protein spartin in lipid droplet maintenance, cytokinesis and BMP signaling.

Renvoisé B, Stadler J, Singh R, Bakowska JC, Blackstone C.

Hum Mol Genet. 2012 Aug 15;21(16):3604-18. doi: 10.1093/hmg/dds191. Epub 2012 May 22.

10.

A role for protein phosphatase PP1γ in SMN complex formation and subnuclear localization to Cajal bodies.

Renvoisé B, Quérol G, Verrier ER, Burlet P, Lefebvre S.

J Cell Sci. 2012 Jun 15;125(Pt 12):2862-74. doi: 10.1242/jcs.096255. Epub 2012 Mar 27.

11.

SPG20 protein spartin is recruited to midbodies by ESCRT-III protein Ist1 and participates in cytokinesis.

Renvoisé B, Parker RL, Yang D, Bakowska JC, Hurley JH, Blackstone C.

Mol Biol Cell. 2010 Oct 1;21(19):3293-303. doi: 10.1091/mbc.E09-10-0879. Epub 2010 Aug 18.

12.

Emerging themes of ER organization in the development and maintenance of axons.

Renvoisé B, Blackstone C.

Curr Opin Neurobiol. 2010 Oct;20(5):531-7. doi: 10.1016/j.conb.2010.07.001. Epub 2010 Aug 2. Review.

13.

The loss of the snoRNP chaperone Nopp140 from Cajal bodies of patient fibroblasts correlates with the severity of spinal muscular atrophy.

Renvoisé B, Colasse S, Burlet P, Viollet L, Meier UT, Lefebvre S.

Hum Mol Genet. 2009 Apr 1;18(7):1181-9. doi: 10.1093/hmg/ddp009. Epub 2009 Jan 7.

14.

Structural basis for midbody targeting of spastin by the ESCRT-III protein CHMP1B.

Yang D, Rismanchi N, Renvoisé B, Lippincott-Schwartz J, Blackstone C, Hurley JH.

Nat Struct Mol Biol. 2008 Dec;15(12):1278-86. doi: 10.1038/nsmb.1512. Epub 2008 Nov 9.

15.

Distinct domains of the spinal muscular atrophy protein SMN are required for targeting to Cajal bodies in mammalian cells.

Renvoisé B, Khoobarry K, Gendron MC, Cibert C, Viollet L, Lefebvre S.

J Cell Sci. 2006 Feb 15;119(Pt 4):680-92. Epub 2006 Jan 31.

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