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Items: 1 to 20 of 26

1.
Manganese efflux transporter SLC30A10 missense polymorphism T95I associated with liver injury retains manganese efflux activity
Kerem C. Gurol, Danyang Li, Karin Broberg, Somshuvra Mukhopadhyay
Am J Physiol Gastrointest Liver Physiol. 2023 Jan 1; 324(1): G78–G88. Published online 2022 Nov 22. doi: 10.1152/ajpgi.00213.2022
PMCID:
PMC9829465
AbstractArticle
2.
Characterization of in vitro models of SLC30A10 deficiency
Milankumar Prajapati, Michael A. Pettiglio, Heather L. Conboy, Courtney J. Mercadante, Shintaro Hojyo, Toshiyuki Fukada, Thomas B. Bartnikas
Biometals. Author manuscript; available in PMC 2022 Jun 1.
Published in final edited form as: Biometals. 2021 Jun; 34(3): 573–588. Published online 2021 Mar 13. doi: 10.1007/s10534-021-00296-y
PMCID:
PMC8204349
AbstractArticlePDF–1.3M
3.
A case of dystonia with polycythemia and hypermanganesemia caused by SLC30A10 mutation: a treatable inborn error of manganese metabolism
Azita Tavasoli, Khadije Arjmandi Rafsanjani, Saba Hemmati, Marziyeh Mojbafan, Elham Zarei, Soudabeh Hosseini
BMC Pediatr. 2019; 19: 229. Published online 2019 Jul 9. doi: 10.1186/s12887-019-1611-7
PMCID:
PMC6615235
AbstractArticlePDF–1.5M
4.
SLC30A10 mutation involved in parkinsonism results in manganese accumulation within nano-vesicles of the Golgi apparatus
Asuncion Carmona, Charles E. Zogzas, Stéphane Roudeau, Francesco Porcaro, Jan Garrevoet, Kathryn M. Spiers, Murielle Salomé, Peter Cloetens, Somshuvra Mukhopadhyay, Richard Ortega
ACS Chem Neurosci. Author manuscript; available in PMC 2020 Jan 16.
Published in final edited form as: ACS Chem Neurosci. 2019 Jan 16; 10(1): 599–609. Published online 2018 Oct 15. doi: 10.1021/acschemneuro.8b00451
PMCID:
PMC6465179
AbstractArticlePDF–1.5M
5.
Zinc transporter 10 (ZnT10)-dependent extrusion of cellular Mn2+ is driven by an active Ca2+-coupled exchange
Moshe Levy, Nadav Elkoshi, Shiran Barber-Zucker, Eitan Hoch, Raz Zarivach, Michal Hershfinkel, Israel Sekler
J Biol Chem. 2019 Apr 12; 294(15): 5879–5889. Published online 2019 Feb 12. doi: 10.1074/jbc.RA118.006816
PMCID:
PMC6463715
AbstractArticlePDF–2.3M
6.
Disease-Homologous Mutation in the Cation Diffusion Facilitator Protein MamM Causes Single-Domain Structural Loss and Signifies Its Importance
Shiran Barber-Zucker, René Uebe, Geula Davidov, Yotam Navon, Dror Sherf, Jordan H. Chill, Itamar Kass, Ronit Bitton, Dirk Schüler, Raz Zarivach
Sci Rep. 2016; 6: 31933. Published online 2016 Aug 23. doi: 10.1038/srep31933
PMCID:
PMC4994047
AbstractArticlePDF–1.3M
7.
Structural Elements in the Transmembrane and Cytoplasmic Domains of the Metal Transporter SLC30A10 Are Required for Its Manganese Efflux Activity
Charles E. Zogzas, Michael Aschner, Somshuvra Mukhopadhyay
J Biol Chem. 2016 Jul 29; 291(31): 15940–15957. Published online 2016 Jun 15. doi: 10.1074/jbc.M116.726935
PMCID:
PMC4965547
AbstractArticlePDF–3.7M
8.
Direct Comparison of Manganese Detoxification/Efflux Proteins and Molecular Characterization of ZnT10 Protein as a Manganese Transporter
Yukina Nishito, Natsuko Tsuji, Hitomi Fujishiro, Taka-aki Takeda, Tomohiro Yamazaki, Fumie Teranishi, Fumiko Okazaki, Ayu Matsunaga, Karin Tuschl, Rajini Rao, Satoshi Kono, Hiroaki Miyajima, Hiroshi Narita, Seiichiro Himeno, Taiho Kambe
J Biol Chem. 2016 Jul 8; 291(28): 14773–14787. Published online 2016 May 10. doi: 10.1074/jbc.M116.728014
PMCID:
PMC4938194
AbstractArticlePDF–3.4M
9.
Common Polymorphisms in the Solute Carrier SLC30A10 are Associated With Blood Manganese and Neurological Function
Karin Wahlberg, Maria Kippler, Ayman Alhamdow, Syed Moshfiqur Rahman, Donald R. Smith, Marie Vahter, Roberto G. Lucchini, Karin Broberg
Toxicol Sci. 2016 Feb; 149(2): 473–483. Published online 2015 Dec 1. doi: 10.1093/toxsci/kfv252
PMCID:
PMC4725612
AbstractArticlePDF–489K
10.
Altered Expression of ZnT10 in Alzheimer's Disease Brain
Helen J. Bosomworth, Paul A. Adlard, Dianne Ford, Ruth A. Valentine
PLoS One. 2013; 8(5): e65475. Published online 2013 May 31. doi: 10.1371/journal.pone.0065475
PMCID:
PMC3669266
AbstractArticlePDF–195K
11.
Manganese Efflux in Parkinsonism: Insights from Newly Characterized SLC30A10 Mutations
Margaret R. DeWitt, Pan Chen, Michael Aschner
Biochem Biophys Res Commun. Author manuscript; available in PMC 2014 Mar 1.
Published in final edited form as: Biochem Biophys Res Commun. 2013 Mar 1; 432(1): 1–4. Published online 2013 Jan 26. doi: 10.1016/j.bbrc.2013.01.058
PMCID:
PMC3594538
AbstractArticlePDF–290K
12.
Mutations in SLC30A10 Cause Parkinsonism and Dystonia with Hypermanganesemia, Polycythemia, and Chronic Liver Disease
Marialuisa Quadri, Antonio Federico, Tianna Zhao, Guido J. Breedveld, Carla Battisti, Cathérine Delnooz, Lies-Anne Severijnen, Lara Di Toro Mammarella, Andrea Mignarri, Lucia Monti, Antioco Sanna, Peng Lu, Francesca Punzo, Giovanni Cossu, Rob Willemsen, Fabrizio Rasi, Ben A. Oostra, Bart P. van de Warrenburg, Vincenzo Bonifati
Am J Hum Genet. 2012 Mar 9; 90(3): 467–477. doi: 10.1016/j.ajhg.2012.01.017
PMCID:
PMC3309204
AbstractArticlePDF–1.5M
13.
Genome-wide and Mendelian randomisation studies of liver MRI yield insights into the pathogenesis of steatohepatitis
Constantinos A. Parisinos, Henry R. Wilman, E. Louise Thomas, Matt Kelly, Rowan C. Nicholls, John McGonigle, Stefan Neubauer, Aroon D. Hingorani, Riyaz S. Patel, Harry Hemingway, Jimmy D. Bell, Rajarshi Banerjee, Hanieh Yaghootkar
J Hepatol. 2020 Aug; 73(2): 241–251. doi: 10.1016/j.jhep.2020.03.032
Correction in:
J Hepatol. 2020 Dec; 73(6): 1594–1595.
PMCID:
PMC7372222
AbstractArticlePDF–1.3M
14.
Polymorphisms in manganese transporters show developmental stage and sex specific associations with manganese concentrations in primary teeth
Karin Wahlberg, Manish Arora, Austen Curtin, Paul Curtin, Robert O. Wright, Donald R. Smith, Roberto G. Lucchini, Karin Broberg, Christine Austin
Neurotoxicology. Author manuscript; available in PMC 2018 Jul 20.
Published in final edited form as: Neurotoxicology. 2018 Jan; 64: 103–109. Published online 2017 Sep 13. doi: 10.1016/j.neuro.2017.09.003
PMCID:
PMC6053672
AbstractArticlePDF–402K
15.
Familial manganese-induced neurotoxicity due to mutations in SLC30A10 or SLC39A14
Somshuvra Mukhopadhyay
Neurotoxicology. Author manuscript; available in PMC 2019 Jan 1.
Published in final edited form as: Neurotoxicology. 2018 Jan; 64: 278–283. Published online 2017 Aug 5. doi: 10.1016/j.neuro.2017.07.030
PMCID:
PMC5799044
AbstractArticlePDF–282K
16.
SLC30A10 Is a Cell Surface-Localized Manganese Efflux Transporter, and Parkinsonism-Causing Mutations Block Its Intracellular Trafficking and Efflux Activity
Dinorah Leyva-Illades, Pan Chen, Charles E. Zogzas, Steven Hutchens, Jonathan M. Mercado, Caleb D. Swaim, Richard A. Morrisett, Aaron B. Bowman, Michael Aschner, Somshuvra Mukhopadhyay
J Neurosci. 2014 Oct 15; 34(42): 14079–14095. doi: 10.1523/JNEUROSCI.2329-14.2014
PMCID:
PMC4198546
AbstractArticlePDF–3.4M
17.
GWAS of serum ALT and AST reveals an association of SLC30A10 Thr95Ile with hypermanganesemia symptoms
Lucas D. Ward, Ho-Chou Tu, Chelsea B. Quenneville, Shira Tsour, Alexander O. Flynn-Carroll, Margaret M. Parker, Aimee M. Deaton, Patrick A. J. Haslett, Luca A. Lotta, Niek Verweij, Manuel A. R. Ferreira, Regeneron Genetics Center, Geisinger-Regeneron DiscovEHR Collaboration, Aris Baras, Gregory Hinkle, Paul Nioi
Nat Commun. 2021; 12: 4571. Published online 2021 Jul 27. doi: 10.1038/s41467-021-24563-1
PMCID:
PMC8316433
AbstractArticlePDF–4.3M
18.
The Functions of ZIP8, ZIP14, and ZnT10 in the Regulation of Systemic Manganese Homeostasis
James W.W. Winslow, Kirsten H. Limesand, Ningning Zhao
Int J Mol Sci. 2020 May; 21(9): 3304. Published online 2020 May 7. doi: 10.3390/ijms21093304
PMCID:
PMC7246657
AbstractArticlePDF–1.3M
19.
Syndrome of Hepatic Cirrhosis, Dystonia, Polycythemia, and Hypermanganesemia Caused by Mutations in SLC30A10, a Manganese Transporter in Man
Karin Tuschl, Peter T. Clayton, Sidney M. Gospe, Jr., Shamshad Gulab, Shahnaz Ibrahim, Pratibha Singhi, Roosy Aulakh, Reinaldo T. Ribeiro, Orlando G. Barsottini, Maha S. Zaki, Maria Luz Del Rosario, Sarah Dyack, Victoria Price, Andrea Rideout, Kevin Gordon, Ron A. Wevers, W.K. “Kling” Chong, Philippa B. Mills
Am J Hum Genet. 2012 Mar 9; 90(3): 457–466. doi: 10.1016/j.ajhg.2012.01.018
Correction in:
Am J Hum Genet. 2016 Aug 4; 99(2): 521.
PMCID:
PMC3309187
AbstractArticlePDF–1.0M
20.
Angiotensin II Requires Zinc and Downregulation of the Zinc Transporters ZnT3 and ZnT10 to Induce Senescence of Vascular Smooth Muscle Cells
Nikolay Patrushev, Bonnie Seidel-Rogol, Gloria Salazar
PLoS One. 2012; 7(3): e33211. Published online 2012 Mar 12. doi: 10.1371/journal.pone.0033211
PMCID:
PMC3299759
AbstractArticlePDF–1.1M

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