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Items: 1 to 20 of 64

1.
Parkinson’s disease-associated ATP13A2/PARK9 functions as a lysosomal H+,K+-ATPase
Takuto Fujii, Shushi Nagamori, Pattama Wiriyasermkul, Shizhou Zheng, Asaka Yago, Takahiro Shimizu, Yoshiaki Tabuchi, Tomoyuki Okumura, Tsutomu Fujii, Hiroshi Takeshima, Hideki Sakai
Nat Commun. 2023; 14: 2174. Published online 2023 Apr 20. doi: 10.1038/s41467-023-37815-z
PMCID:
PMC10119128
AbstractArticlePDF–1.6M
2.
Structural basis of polyamine transport by human ATP13A2 (PARK9)
Sue Im Sim, Sören von Bülow, Gerhard Hummer, Eunyong Park
Mol Cell. Author manuscript; available in PMC 2022 Nov 18.
Published in final edited form as: Mol Cell. 2021 Nov 18; 81(22): 4635–4649.e8. Published online 2021 Oct 28. doi: 10.1016/j.molcel.2021.08.017
PMCID:
PMC8604775
AbstractArticlePDF–4.2M
3.
ATP13A2 Gene Variants in Patients with Parkinson's Disease in Xinjiang
Dan Wang, Hua Gao, Yanxia Li, Sen Jiang, Xinling Yang
Biomed Res Int. 2020; 2020: 6954820. Published online 2020 Nov 30. doi: 10.1155/2020/6954820
PMCID:
PMC7723492
AbstractArticlePDF–351K
4.
Cryo-EM reveals mechanistic insights into lipid-facilitated polyamine export by human ATP13A2
Atsuhiro Tomita, Takashi Daiho, Tsukasa Kusakizako, Keitaro Yamashita, Satoshi Ogasawara, Takeshi Murata, Tomohiro Nishizawa, Osamu Nureki
Mol Cell. Author manuscript; available in PMC 2022 Feb 28.
Published in final edited form as: Mol Cell. 2021 Dec 2; 81(23): 4799–4809.e5. Published online 2021 Nov 18. doi: 10.1016/j.molcel.2021.11.001
PMCID:
PMC7612442
AbstractArticlePDF–3.8M
5.
Clinical and genetic analysis of ATP13A2 in hereditary spastic paraplegia expands the phenotype
Mehrdad A. Estiar, Etienne Leveille, Dan Spiegelman, Nicolas Dupre, Jean-François Trempe, Guy A. Rouleau, Ziv Gan‐Or
Mol Genet Genomic Med. 2020 Mar; 8(3): e1052. Published online 2020 Jan 15. doi: 10.1002/mgg3.1052
PMCID:
PMC7057081
AbstractArticlePDF–764K
6.
Targeted next-generation sequencing identifies novel variants in candidate genes for Parkinson’s disease in Black South African and Nigerian patients
Oluwafemi G. Oluwole, Helena Kuivaniemi, Shameemah Abrahams, William L. Haylett, Alvera A. Vorster, Carel J. van Heerden, Colin P. Kenyon, David L. Tabb, Michael B. Fawale, Taofiki A. Sunmonu, Abiodun Ajose, Matthew O. Olaogun, Anastasia C. Rossouw, Ludo S. van Hillegondsberg, Jonathan Carr, Owen A. Ross, Morenikeji A. Komolafe, Gerard Tromp, Soraya Bardien
BMC Med Genet. 2020; 21: 23. Published online 2020 Feb 4. doi: 10.1186/s12881-020-0953-1
PMCID:
PMC7001245
AbstractArticlePDF–1.2M
7.
ATP13A2 Knockout Does not Affect the Infarct Size in Mice with Acute Ischemic Stroke
Jian‐Guang Yu, Mei‐Jian Cui, Wei Wang, Kai‐Bing Hu, Guo‐Jun Cai
CNS Neurosci Ther. 2012 Dec; 18(12): 1027–1029. Published online 2012 Nov 3. doi: 10.1111/cns.12023
PMCID:
PMC6493604
ArticlePDF–153K
8.
Loss-of-function mutations in the ATP13A2/PARK9 gene cause complicated hereditary spastic paraplegia (SPG78)
Alejandro Estrada-Cuzcano, Shaun Martin, Teodora Chamova, Matthis Synofzik, Dagmar Timmann, Tine Holemans, Albena Andreeva, Jennifer Reichbauer, Riet De Rycke, Dae-In Chang, Sarah van Veen, Jean Samuel, Ludger Schöls, Thorsten Pöppel, Danny Mollerup Sørensen, Bob Asselbergh, Christine Klein, Stephan Zuchner, Albena Jordanova, Peter Vangheluwe, Ivailo Tournev, Rebecca Schüle
Brain. 2017 Feb; 140(2): 287–305. Published online 2017 Jan 30. doi: 10.1093/brain/aww307
PMCID:
PMC5278306
AbstractArticlePDF–1.8M
9.
Unlocking ATP13A2/PARK9 activity
Shaun Martin, Tine Holemans, Peter Vangheluwe
Cell Cycle. 2015; 14(21): 3341–3342. Published online 2015 Sep 22. doi: 10.1080/15384101.2015.1093420
PMCID:
PMC4825597
ArticlePDF–175K
10.
Characterization of Cellular Protective Effects of ATP13A2/PARK9 Expression and Alterations Resulting From Pathogenic Mutants
Jason P. Covy, Elisa A. Waxman, Benoit I. Giasson
J Neurosci Res. Author manuscript; available in PMC 2015 Jun 29.
Published in final edited form as: J Neurosci Res. 2012 Dec; 90(12): 2306–2316. Published online 2012 Jul 30. doi: 10.1002/jnr.23112
PMCID:
PMC4484830
AbstractArticlePDF–1.3M
11.
Analysis of Thr12Met and Ala1144Thr Mutations of the ATP13A2 Gene in Parkinson’s Disease Patients in Xinjiang Uygur and Han Ethnic Groups
Guihua Li, Zhenzhong Zhang, Huan Xia, Xinling Yang
Med Sci Monit. 2014; 20: 2177–2182. Published online 2014 Nov 6. doi: 10.12659/MSM.892821
PMCID:
PMC4301217
AbstractArticlePDF–644K
12.
The role of the Ala746Thr variant in the ATP13A2 gene among Chinese patients with Parkinson’s disease
Anne Y.Y. Chan, Larry Baum, Nelson L.S. Tang, Christine Y.K. Lau, Ping Wing Ng, Kwok Fai Hui, Yoshi Mizuno, Justin Y. Kwan, Vincent C.T. Mok, Sheng-Han Kuo
J Clin Neurosci. Author manuscript; available in PMC 2014 Oct 27.
Published in final edited form as: J Clin Neurosci. 2013 May; 20(5): 761–762. Published online 2013 Mar 20. doi: 10.1016/j.jocn.2012.05.052
PMCID:
PMC4209840
AbstractArticlePDF–75K
13.
Mutations in the ATP13A2 Gene and Parkinsonism: A Preliminary Review
Xinglong Yang, Yanming Xu
Biomed Res Int. 2014; 2014: 371256. Published online 2014 Aug 14. doi: 10.1155/2014/371256
PMCID:
PMC4147200
AbstractArticlePDF–733K
14.
ATP13A2 (PARK9) protein levels are reduced in brain tissue of cases with Lewy bodies
Karen E Murphy, Louise Cottle, Amanda M Gysbers, Antony A Cooper, Glenda M Halliday
Acta Neuropathol Commun. 2013; 1(1): 11. Published online 2013 May 9. doi: 10.1186/2051-5960-1-11
PMCID:
PMC4046687
AbstractArticlePDF–1.0M
15.
Parkinson's disease-associated human ATP13A2 (PARK9) deficiency causes zinc dyshomeostasis and mitochondrial dysfunction
Jin-Sung Park, Brianada Koentjoro, David Veivers, Alan Mackay-Sim, Carolyn M. Sue
Hum Mol Genet. 2014 Jun 1; 23(11): 2802–2815. Published online 2014 Jan 7. doi: 10.1093/hmg/ddt623
PMCID:
PMC4014187
AbstractArticlePDF–1.8M
16.
Altered apoptosis regulation in Kufor–Rakeb syndrome patients with mutations in the ATP13A2 gene
Elena Radi, Patrizia Formichi, Giuseppe Di Maio, Carla Battisti, Antonio Federico
J Cell Mol Med. 2012 Aug; 16(8): 1916–1923. Published online 2012 Jul 29. doi: 10.1111/j.1582-4934.2011.01488.x
PMCID:
PMC3822702
AbstractArticlePDF–763K
17.
Analysis of ATP13A2 in large neurodegeneration with brain iron accumulation (NBIA) and dystonia-parkinsonism cohorts
Michael C. Kruer, Reema Paudel, Wendy Wagoner, Lynn Sanford, Eleanna Kara, Allison Gregory, Tom Foltynie, Andrew Lees, Kailash Bhatia, John Hardy, Susan J. Hayflick, Henry Houlden
Neurosci Lett. Author manuscript; available in PMC 2013 Aug 8.
Published in final edited form as: Neurosci Lett. 2012 Aug 8; 523(1): 35–38. Published online 2012 Jun 25. doi: 10.1016/j.neulet.2012.06.036
PMCID:
PMC3619445
AbstractArticlePDF–425K
18.
Lysosomal dysfunction in Parkinson disease: ATP13A2 gets into the groove
Benjamin Dehay, Marta Martinez-Vicente, Alfredo Ramirez, Celine Perier, Christine Klein, Miquel Vila, Erwan Bezard
Autophagy. 2012 Sep 1; 8(9): 1389–1391. doi: 10.4161/auto.21011
PMCID:
PMC3442887
AbstractArticlePDF–915K
19.
Loss of P-type ATPase ATP13A2/PARK9 function induces general lysosomal deficiency and leads to Parkinson disease neurodegeneration
Benjamin Dehay, Alfredo Ramirez, Marta Martinez-Vicente, Celine Perier, Marie-Hélène Canron, Evelyne Doudnikoff, Anne Vital, Miquel Vila, Christine Klein, Erwan Bezard
Proc Natl Acad Sci U S A. 2012 Jun 12; 109(24): 9611–9616. Published online 2012 May 30. doi: 10.1073/pnas.1112368109
PMCID:
PMC3386132
AbstractArticlePDF–930K
20.
Mutation of the parkinsonism gene ATP13A2 causes neuronal ceroid-lipofuscinosis
Jose Bras, Alain Verloes, Susanne A. Schneider, Sara E. Mole, Rita J. Guerreiro
Hum Mol Genet. 2012 Jun 15; 21(12): 2646–2650. Published online 2012 Mar 2. doi: 10.1093/hmg/dds089
PMCID:
PMC3363329
AbstractArticlePDF–171K

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