Zhu PP - Search Results

1

Characterization of a novel SPG3A deletion in a French-Canadian family.

Meijer IA, Dion P, Laurent S, Dupré N, Brais B, Levert A, Puymirat J, Rioux MF, Sylvain M, Zhu PP, Soderblom C, Stadler J, Blackstone C, Rouleau GA. Meijer IA, et al. Among authors: zhu pp. Ann Neurol. 2007 Jun;61(6):599-603. doi: 10.1002/ana.21114. Ann Neurol. 2007. PMID: 17427918

2

SPG3A protein atlastin-1 is enriched in growth cones and promotes axon elongation during neuronal development.

Zhu PP, Soderblom C, Tao-Cheng JH, Stadler J, Blackstone C. Zhu PP, et al. Hum Mol Genet. 2006 Apr 15;15(8):1343-53. doi: 10.1093/hmg/ddl054. Epub 2006 Mar 14. Hum Mol Genet. 2006. PMID: 16537571

3

Cellular localization, oligomerization, and membrane association of the hereditary spastic paraplegia 3A (SPG3A) protein atlastin.

Zhu PP, Patterson A, Lavoie B, Stadler J, Shoeb M, Patel R, Blackstone C. Zhu PP, et al. J Biol Chem. 2003 Dec 5;278(49):49063-71. doi: 10.1074/jbc.M306702200. Epub 2003 Sep 23. J Biol Chem. 2003. PMID: 14506257 Free article.

4

Pharmacologic rescue of axon growth defects in a human iPSC model of hereditary spastic paraplegia SPG3A.

Zhu PP, Denton KR, Pierson TM, Li XJ, Blackstone C. Zhu PP, et al. Hum Mol Genet. 2014 Nov 1;23(21):5638-48. doi: 10.1093/hmg/ddu280. Epub 2014 Jun 6. Hum Mol Genet. 2014. PMID: 24908668 Free PMC article.

5

Atlastin GTPases are required for Golgi apparatus and ER morphogenesis.

Rismanchi N, Soderblom C, Stadler J, Zhu PP, Blackstone C. Rismanchi N, et al. Among authors: zhu pp. Hum Mol Genet. 2008 Jun 1;17(11):1591-604. doi: 10.1093/hmg/ddn046. Epub 2008 Feb 12. Hum Mol Genet. 2008. PMID: 18270207 Free PMC article.

6

Hereditary spastic paraplegia proteins REEP1, spastin, and atlastin-1 coordinate microtubule interactions with the tubular ER network.

Park SH, Zhu PP, Parker RL, Blackstone C. Park SH, et al. Among authors: zhu pp. J Clin Invest. 2010 Apr;120(4):1097-110. doi: 10.1172/JCI40979. J Clin Invest. 2010. PMID: 20200447 Free PMC article.

7

Intra- and intermolecular domain interactions of the C-terminal GTPase effector domain of the multimeric dynamin-like GTPase Drp1.

Zhu PP, Patterson A, Stadler J, Seeburg DP, Sheng M, Blackstone C. Zhu PP, et al. J Biol Chem. 2004 Aug 20;279(34):35967-74. doi: 10.1074/jbc.M404105200. Epub 2004 Jun 18. J Biol Chem. 2004. PMID: 15208300 Free article.

8

Hereditary spastic paraplegia SPG8 mutations impair CAV1-dependent, integrin-mediated cell adhesion.

Lee S, Park H, Zhu PP, Jung SY, Blackstone C, Chang J. Lee S, et al. Among authors: zhu pp. Sci Signal. 2020 Jan 7;13(613):eaau7500. doi: 10.1126/scisignal.aau7500. Sci Signal. 2020. PMID: 31911435 Free PMC article.

9

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. Zhao G, et al. Among authors: zhu pp. Exp Cell Res. 2016 Nov 15;349(1):32-44. doi: 10.1016/j.yexcr.2016.09.015. Epub 2016 Sep 23. Exp Cell Res. 2016. PMID: 27669642

10

L166P mutant DJ-1, causative for recessive Parkinson's disease, is degraded through the ubiquitin-proteasome system.

Miller DW, Ahmad R, Hague S, Baptista MJ, Canet-Aviles R, McLendon C, Carter DM, Zhu PP, Stadler J, Chandran J, Klinefelter GR, Blackstone C, Cookson MR. Miller DW, et al. Among authors: zhu pp. J Biol Chem. 2003 Sep 19;278(38):36588-95. doi: 10.1074/jbc.M304272200. Epub 2003 Jul 8. J Biol Chem. 2003. PMID: 12851414 Free article.

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