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Select item 101191281.

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

Abstract Article PDF–1.6M

Select item 86047752.

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

Abstract Article PDF–4.2M

Select item 77234923.

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

Abstract Article PDF–351K

Select item 76124424.

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

Abstract Article PDF–3.8M

Select item 70570815.

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

Abstract Article PDF–764K

Select item 70012456.

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

Abstract Article PDF–1.2M

Select item 64936047.

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

Article PDF–153K

Select item 52783068.

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

Abstract Article PDF–1.8M

Select item 48255979.

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

Article PDF–175K

Select item 448483010.

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

Abstract Article PDF–1.3M

Select item 430121711.

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

Abstract Article PDF–644K

Select item 420984012.

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

Abstract Article PDF–75K

Select item 414720013.

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

Abstract Article PDF–733K

Select item 404668714.

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

Abstract Article PDF–1.0M

Select item 401418715.

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

Abstract Article PDF–1.8M

Select item 382270216.

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

Abstract Article PDF–763K

Select item 361944517.

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

Abstract Article PDF–425K

Select item 344288718.

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

Abstract Article PDF–915K

Select item 338613219.

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

Abstract Article PDF–930K

Select item 336332920.

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

Abstract Article PDF–171K

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