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Items: 1 to 20 of 27

1.
The Effect of Manganese Exposure in Atp13a2-deficient Mice
Sheila M. Fleming, Nicholas A. Santiago, Elizabeth J. Mullin, Shanta Pamphile, Swagata Karkare, Andrew Lemkuhl, Osunde R. Ekhator, Stephen C. Linn, John G. Holden, Diana S. Aga, Jerome A. Roth, Benjamin Liou, Ying Sun, Gary E. Shull, Patrick J. Schultheis
Neurotoxicology. Author manuscript; available in PMC 2023 May 12.
Published in final edited form as: Neurotoxicology. 2018 Jan; 64: 256–266. Published online 2017 Jun 6. doi: 10.1016/j.neuro.2017.06.005
PMCID:
PMC10178982
AbstractArticlePDF–958K
2.
ATP13A2 Declines Zinc-Induced Accumulation of α-Synuclein in a Parkinson’s Disease Model
Huiling Gao, Hehong Sun, Nan Yan, Pu Zhao, He Xu, Wei Zheng, Xiaoyu Zhang, Tao Wang, Chuang Guo, Manli Zhong
Int J Mol Sci. 2022 Jul; 23(14): 8035. Published online 2022 Jul 21. doi: 10.3390/ijms23148035
PMCID:
PMC9318580
AbstractArticlePDF–5.1M
3.
Endolysosomal Dysfunction in Parkinson Disease: Recent Developments and Future Challenges
Lauren R. Kett, William T. Dauer
Mov Disord. Author manuscript; available in PMC 2017 Oct 1.
Published in final edited form as: Mov Disord. 2016 Oct; 31(10): 1433–1443. doi: 10.1002/mds.26797
PMCID:
PMC5061051
AbstractArticlePDF–1.0M
4.
ATP13A2 activates the pentose phosphate pathway to promote colorectal cancer growth though TFEB‐PGD axis
Fan Zhang, Zhiwei Wu, Bowen Yu, Zhengping Ning, Zhixing Lu, Liang Li, Fei Long, Qionggui Hu, Chonglei Zhong, Yi Zhang, Changwei Lin
Clin Transl Med. 2023 May; 13(5): e1272. Published online 2023 May 26. doi: 10.1002/ctm2.1272
PMCID:
PMC10220388
AbstractArticlePDF–8.4M
5.
Atp13a2 Deficiency Aggravates Astrocyte‐Mediated Neuroinflammation via NLRP3 Inflammasome Activation
Chen Qiao, Nuo Yin, Huan‐Yu Gu, Jia‐Lei Zhu, Jian‐Hua Ding, Ming Lu, Gang Hu
CNS Neurosci Ther. 2016 Jun; 22(6): 451–460. Published online 2016 Feb 5. doi: 10.1111/cns.12514
PMCID:
PMC6492810
AbstractArticlePDF–851K
6.
Atp13a2-deficient mice exhibit neuronal ceroid lipofuscinosis, limited α-synuclein accumulation and age-dependent sensorimotor deficits
Patrick J. Schultheis, Sheila M. Fleming, Amy K. Clippinger, Jada Lewis, Taiji Tsunemi, Benoit Giasson, Dennis W. Dickson, Joseph R. Mazzulli, Mark E. Bardgett, Kristi L. Haik, Osunde Ekhator, Anil Kumar Chava, John Howard, Matt Gannon, Elizabeth Hoffman, Yinhuai Chen, Vikram Prasad, Stephen C. Linn, Rafael J. Tamargo, Wendy Westbroek, Ellen Sidransky, Dimitri Krainc, Gary E. Shull
Hum Mol Genet. 2013 May 15; 22(10): 2067–2082. Published online 2013 Feb 7. doi: 10.1093/hmg/ddt057
PMCID:
PMC3633373
AbstractArticlePDF–620K
7.
Deficiency of ATP13A2 Leads to Lysosomal Dysfunction, α-Synuclein Accumulation, and Neurotoxicity
Marija Usenovic, Emilie Tresse, Joseph R. Mazzulli, J. Paul Taylor, Dimitri Krainc
J Neurosci. 2012 Mar 21; 32(12): 4240–4246. doi: 10.1523/JNEUROSCI.5575-11.2012
PMCID:
PMC3462811
AbstractArticlePDF–1.5M
8.
Exacerbation of sensorimotor dysfunction in mice deficient in Atp13a2 and overexpressing human wildtype alpha-synuclein
Emily R. Dirr, Osunde R. Ekhator, Rachel Blackwood, John G. Holden, Eliezer Masliah, Patrick J. Schultheis, Sheila M. Fleming
Behav Brain Res. Author manuscript; available in PMC 2019 May 2.
Published in final edited form as: Behav Brain Res. 2018 May 2; 343: 41–49. Published online 2018 Feb 3. doi: 10.1016/j.bbr.2018.01.029
PMCID:
PMC5829010
AbstractArticlePDF–802K
9.
α-Synuclein-Independent Histopathological and Motor Deficits in Mice Lacking the Endolysosomal Parkinsonism Protein Atp13a2
Lauren R. Kett, Barbara Stiller, Megan M. Bernath, Inmaculada Tasset, Javier Blesa, Vernice Jackson-Lewis, Robin B. Chan, Bowen Zhou, Gilbert Di Paolo, Serge Przedborski, Ana Maria Cuervo, William T. Dauer
J Neurosci. 2015 Apr 8; 35(14): 5724–5742. doi: 10.1523/JNEUROSCI.0632-14.2015
PMCID:
PMC4388928
AbstractArticlePDF–8.0M
10.
PARK9-associated ATP13A2 localizes to intracellular acidic vesicles and regulates cation homeostasis and neuronal integrity
David Ramonet, Agata Podhajska, Klodjan Stafa, Sarah Sonnay, Alzbeta Trancikova, Elpida Tsika, Olga Pletnikova, Juan C. Troncoso, Liliane Glauser, Darren J. Moore
Hum Mol Genet. 2012 Apr 15; 21(8): 1725–1743. Published online 2011 Dec 20. doi: 10.1093/hmg/ddr606
PMCID:
PMC3465694
AbstractArticlePDF–904K
11.
ATP13A2 regulates mitochondrial bioenergetics through macroautophagy
Aaron M. Gusdon, Jianhui Zhu, Bennett Van Houten, Charleen T. Chu
Neurobiol Dis. Author manuscript; available in PMC 2013 Mar 1.
Published in final edited form as: Neurobiol Dis. 2012 Mar; 45(3): 962–972. Published online 2011 Dec 13. doi: 10.1016/j.nbd.2011.12.015
PMCID:
PMC3291101
AbstractArticlePDF–4.2M
12.
Zn2+ dyshomeostasis caused by loss of ATP13A2/PARK9 leads to lysosomal dysfunction and alpha-synuclein accumulation
Taiji Tsunemi, Dimitri Krainc
Hum Mol Genet. 2014 Jun 1; 23(11): 2791–2801. Published online 2013 Dec 13. doi: 10.1093/hmg/ddt572
PMCID:
PMC4014186
AbstractArticlePDF–757K
13.
ATP13A2/PARK9 Regulates Secretion of Exosomes and α-Synuclein
Taiji Tsunemi, Kana Hamada, Dimitri Krainc
J Neurosci. 2014 Nov 12; 34(46): 15281–15287. doi: 10.1523/JNEUROSCI.1629-14.2014
PMCID:
PMC4228131
AbstractArticlePDF–1.2M
14.
ATP13A2 facilitates HDAC6 recruitment to lysosome to promote autophagosome–lysosome fusion
Ruoxi Wang, Jieqiong Tan, Tingting Chen, Hailong Han, Runyi Tian, Ya Tan, Yiming Wu, Jingyi Cui, Fang Chen, Jie Li, Lu Lv, Xinjie Guan, Shuai Shang, Jiahong Lu, Zhuohua Zhang
J Cell Biol. 2019 Jan 7; 218(1): 267–284. doi: 10.1083/jcb.201804165
PMCID:
PMC6314552
AbstractArticlePDF–5.0M
15.
The Parkinson's disease-associated genes ATP13A2 and SYT11 regulate autophagy via a common pathway
Carla F. Bento, Avraham Ashkenazi, Maria Jimenez-Sanchez, David C. Rubinsztein
Nat Commun. 2016; 7: 11803. Published online 2016 Jun 9. doi: 10.1038/ncomms11803
PMCID:
PMC4906231
AbstractArticlePDF–3.5M
16.
Database resources of the National Center for Biotechnology Information
David L. Wheeler, Deanna M. Church, Alex E. Lash, Detlef D. Leipe, Thomas L. Madden, Joan U. Pontius, Gregory D. Schuler, Lynn M. Schriml, Tatiana A. Tatusova, Lukas Wagner, Barbara A. Rapp
Nucleic Acids Res. 2001 Jan 1; 29(1): 11–16. doi: 10.1093/nar/29.1.11
PMCID:
PMC29800
AbstractArticlePDF–101K
17.
BioID screening of biotinylation sites using the avidin-like protein Tamavidin 2-REV identifies global interactors of stimulator of interferon genes (STING)
Kou Motani, Hidetaka Kosako
J Biol Chem. 2020 Aug 7; 295(32): 11174–11183. Published online 2020 Jun 17. doi: 10.1074/jbc.RA120.014323
PMCID:
PMC7415991
AbstractArticlePDF–2.0M
18.
The International Mouse Phenotyping Consortium Web Portal, a unified point of access for knockout mice and related phenotyping data
Gautier Koscielny, Gagarine Yaikhom, Vivek Iyer, Terrence F. Meehan, Hugh Morgan, Julian Atienza-Herrero, Andrew Blake, Chao-Kung Chen, Richard Easty, Armida Di Fenza, Tanja Fiegel, Mark Grifiths, Alan Horne, Natasha A. Karp, Natalja Kurbatova, Jeremy C. Mason, Peter Matthews, Darren J. Oakley, Asfand Qazi, Jack Regnart, Ahmad Retha, Luis A. Santos, Duncan J. Sneddon, Jonathan Warren, Henrik Westerberg, Robert J. Wilson, David G. Melvin, Damian Smedley, Steve D. M. Brown, Paul Flicek, William C. Skarnes, Ann-Marie Mallon, Helen Parkinson
Nucleic Acids Res. 2014 Jan 1; 42(Database issue): D802–D809. Published online 2013 Nov 3. doi: 10.1093/nar/gkt977
PMCID:
PMC3964955
AbstractArticlePDF–5.7M
19.
Genetic determinants of micronucleus formation in vivo
D. J. Adams, B. Barlas, R. E. McIntyre, I. Salguero, L. van der Weyden, A. Barros, J. R. Vicente, N. Karimpour, A. Haider, M. Ranzani, G. Turner, N. A. Thompson, V. Harle, R. Olvera-León, C. D. Robles-Espinoza, A. O. Speak, N. Geisler, W. J. Weninger, S. H. Geyer, J. Hewinson, N. A. Karp, The Sanger Mouse Genetics Project, B. Fu, F. Yang, Z. Kozik, J. Choudhary, L. Yu, M. S. van Ruiten, B. D. Rowland, C. J. Lelliott, M. del Castillo Velasco-Herrera, R. Verstraten, L. Bruckner, A. G. Henssen, M. A. Rooimans, J. de Lange, T. J. Mohun, M. J. Arends, K. A. Kentistou, P. A. Coelho, Y. Zhao, H. Zecchini, J. R. B. Perry, S. P. Jackson, G. Balmus
Nature. 2024; 627(8002): 130–136. Published online 2024 Feb 14. doi: 10.1038/s41586-023-07009-0
PMCID:
PMC10917660
AbstractArticlePDF–4.8M
20.
A conditional knockout resource for the genome–wide study of mouse gene function
William C. Skarnes, Barry Rosen, Anthony P. West, Manousos Koutsourakis, Wendy Bushell, Vivek Iyer, Alejandro O. Mujica, Mark Thomas, Jennifer Harrow, Tony Cox, David Jackson, Jessica Severin, Patrick Biggs, Jun Fu, Michael Nefedov, Pieter J. de Jong, A. Francis Stewart, Allan Bradley
Nature. Author manuscript; available in PMC 2013 Feb 14.
Published in final edited form as: Nature. 2011 Jun 15; 474(7351): 337–342. Published online 2011 Jun 15. doi: 10.1038/nature10163
PMCID:
PMC3572410
AbstractArticlePDF–1.1M

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