Zhu PP - Search Results

1

Transverse endoplasmic reticulum expansion in hereditary spastic paraplegia corticospinal axons.

Zhu PP, Hung HF, Batchenkova N, Nixon-Abell J, Henderson J, Zheng P, Renvoisé B, Pang S, Xu CS, Saalfeld S, Funke J, Xie Y, Svara F, Hess HF, Blackstone C. Zhu PP, et al. Hum Mol Genet. 2022 Aug 23;31(16):2779-2795. doi: 10.1093/hmg/ddac072. Hum Mol Genet. 2022. PMID: 35348668 Free PMC article.

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

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.

4

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.

5

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.

6

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

7

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.

8

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.

9

A class of dynamin-like GTPases involved in the generation of the tubular ER network.

Hu J, Shibata Y, Zhu PP, Voss C, Rismanchi N, Prinz WA, Rapoport TA, Blackstone C. Hu J, et al. Among authors: zhu pp. Cell. 2009 Aug 7;138(3):549-61. doi: 10.1016/j.cell.2009.05.025. Cell. 2009. PMID: 19665976 Free PMC article.

10

Hereditary spastic paraplegia type 43 (SPG43) is caused by mutation in C19orf12.

Landouré G, Zhu PP, Lourenço CM, Johnson JO, Toro C, Bricceno KV, Rinaldi C, Meilleur KG, Sangaré M, Diallo O, Pierson TM, Ishiura H, Tsuji S, Hein N, Fink JK, Stoll M, Nicholson G, Gonzalez MA, Speziani F, Dürr A, Stevanin G, Biesecker LG; NIH Intramural Sequencing Center; Accardi J, Landis DM, Gahl WA, Traynor BJ, Marques W Jr, Züchner S, Blackstone C, Fischbeck KH, Burnett BG. Landouré G, et al. Among authors: zhu pp. Hum Mutat. 2013 Oct;34(10):1357-60. doi: 10.1002/humu.22378. Epub 2013 Aug 12. Hum Mutat. 2013. PMID: 23857908 Free PMC article.

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