Manganese

solute carrier family 30 member 10 ; Homo sapiens







27 Article(s)
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1 33911374 Inherited Manganese Disorders and the Brain: What Neurologists Need to Know. 2021 Jan-Feb 2
2 33925013 Molecular Targets of Manganese-Induced Neurotoxicity: A Five-Year Update. 2021 Apr 28 1
3 34315874 GWAS of serum ALT and AST reveals an association of SLC30A10 Thr95Ile with hypermanganesemia symptoms. 2021 Jul 27 1
4 34446561 Up-regulation of the manganese transporter SLC30A10 by hypoxia-inducible factors defines a homeostatic response to manganese toxicity. 2021 Aug 31 1
5 34753157 Manganese Toxicity Associated With Total Parenteral Nutrition: A Review. 2021 Oct 1
6 34849276 Treatable Hereditary Manganese Transport Disorder: Novel SLC30A10 Mutation and its Characteristic Neuroimaging Appearance in Two Siblings. 2021 Dec 1
7 34877518 Atypical presentation of SLC30A10 gene mutation with hypermanganesemia, seizures and polycythemia. 2021 1
8 32392784 The Functions of ZIP8, ZIP14, and ZnT10 in the Regulation of Systemic Manganese Homeostasis. 2020 May 7 5
9 30272946 SLC30A10 Mutation Involved in Parkinsonism Results in Manganese Accumulation within Nanovesicles of the Golgi Apparatus. 2019 Jan 16 1
10 30755481 Zinc transporter 10 (ZnT10)-dependent extrusion of cellular Mn2+ is driven by an active Ca2+-coupled exchange. 2019 Apr 12 2
11 31089831 Genetic Disorders of Manganese Metabolism. 2019 May 14 2
12 31288771 A case of dystonia with polycythemia and hypermanganesemia caused by SLC30A10 mutation: a treatable inborn error of manganese metabolism. 2019 Jul 9 2
13 28789954 Familial manganese-induced neurotoxicity due to mutations in SLC30A10 or SLC39A14. 2018 Jan 1
14 29382362 Hypermanganesemia due to mutations in SLC39A14: further insights into Mn deposition in the central nervous system. 2018 Jan 30 1
15 29429640 Neurotoxicity of manganese: Indications for future research and public health intervention from the Manganese 2016 conference. 2018 Jan 1
16 29989630 Putative metal binding site in the transmembrane domain of the manganese transporter SLC30A10 is different from that of related zinc transporters. 2018 Aug 15 3
17 30619481 Polymorphisms in Manganese Transporters SLC30A10 and SLC39A8 Are Associated With Children's Neurodevelopment by Influencing Manganese Homeostasis. 2018 1
18 28860195 Hypothyroidism induced by loss of the manganese efflux transporter SLC30A10 may be explained by reduced thyroxine production. 2017 Oct 6 5
19 26628504 Common Polymorphisms in the Solute Carrier SLC30A10 are Associated With Blood Manganese and Neurological Function. 2016 Feb 1
20 27107558 Vitamin D3 transactivates the zinc and manganese transporter SLC30A10 via the Vitamin D receptor. 2016 Oct 4
21 27226609 Direct Comparison of Manganese Detoxification/Efflux Proteins and Molecular Characterization of ZnT10 Protein as a Manganese Transporter. 2016 Jul 8 5
22 27307044 Structural Elements in the Transmembrane and Cytoplasmic Domains of the Metal Transporter SLC30A10 Are Required for Its Manganese Efflux Activity. 2016 Jul 29 5
23 25778823 Manganese transport disorder: novel SLC30A10 mutations and early phenotypes. 2015 Jun 1
24 24576911 Interleukin-6 enhances manganese accumulation in SH-SY5Y cells: implications of the up-regulation of ZIP14 and the down-regulation of ZnT10. 2014 Apr 4
25 23357421 Manganese efflux in Parkinsonism: insights from newly characterized SLC30A10 mutations. 2013 Mar 1 1
26 22341971 Mutations in SLC30A10 cause parkinsonism and dystonia with hypermanganesemia, polycythemia, and chronic liver disease. 2012 Mar 9 3
27 22926781 Dystonia with brain manganese accumulation resulting from SLC30A10 mutations: a new treatable disorder. 2012 Sep 1 1