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Items: 1 to 20 of 97

1.

SLC41A1 is essential for magnesium homeostasis in vivo.

Arjona FJ, Latta F, Mohammed SG, Thomassen M, van Wijk E, Bindels RJM, Hoenderop JGJ, de Baaij JHF.

Pflugers Arch. 2019 Jun;471(6):845-860. doi: 10.1007/s00424-018-2234-9. Epub 2018 Nov 12.

2.

Mutation of the Mg2+ transporter SLC41A1 results in a nephronophthisis-like phenotype.

Hurd TW, Otto EA, Mishima E, Gee HY, Inoue H, Inazu M, Yamada H, Halbritter J, Seki G, Konishi M, Zhou W, Yamane T, Murakami S, Caridi G, Ghiggeri G, Abe T, Hildebrandt F.

J Am Soc Nephrol. 2013 May;24(6):967-77. doi: 10.1681/ASN.2012101034. Epub 2013 May 9.

3.

Functional characterization of human SLC41A1, a Mg2+ transporter with similarity to prokaryotic MgtE Mg2+ transporters.

Goytain A, Quamme GA.

Physiol Genomics. 2005 May 11;21(3):337-42. Epub 2005 Feb 15.

PMID:
15713785
4.

Insulin Modulates the Na+/Mg2+ Exchanger SLC41A1 and Influences Mg2+ Efflux from Intracellular Stores in Transgenic HEK293 Cells.

Mastrototaro L, Tietjen U, Sponder G, Vormann J, Aschenbach JR, Kolisek M.

J Nutr. 2015 Nov;145(11):2440-7. doi: 10.3945/jn.115.213918. Epub 2015 Sep 9.

PMID:
26355001
5.

Knockdown of SLC41A1 magnesium transporter promotes mineralization and attenuates magnesium inhibition during osteogenesis of mesenchymal stromal cells.

Tsao YT, Shih YY, Liu YA, Liu YS, Lee OK.

Stem Cell Res Ther. 2017 Feb 21;8(1):39. doi: 10.1186/s13287-017-0497-2.

6.

SLC41A1 is a novel mammalian Mg2+ carrier.

Kolisek M, Launay P, Beck A, Sponder G, Serafini N, Brenkus M, Froschauer EM, Martens H, Fleig A, Schweigel M.

J Biol Chem. 2008 Jun 6;283(23):16235-47. doi: 10.1074/jbc.M707276200. Epub 2008 Mar 25.

7.

Identification of the putative goldfish (Carassius auratus) magnesium transporter SLC41a1 and functional regulation in the gill, kidney, and intestine in response to dietary and environmental manipulations.

Kodzhahinchev V, Kovacevic D, Bucking C.

Comp Biochem Physiol A Mol Integr Physiol. 2017 Apr;206:69-81. doi: 10.1016/j.cbpa.2017.01.016. Epub 2017 Jan 24.

PMID:
28130070
8.

SLC41A1 knockdown inhibits angiotensin II-induced cardiac fibrosis by preventing Mg(2+) efflux and Ca(2+) signaling in cardiac fibroblasts.

Yu N, Jiang J, Yu Y, Li H, Huang X, Ma Y, Zhang L, Zou J, Zhang B, Chen S, Liu P.

Arch Biochem Biophys. 2014 Dec 15;564:74-82. doi: 10.1016/j.abb.2014.09.013. Epub 2014 Sep 27.

PMID:
25263961
9.

SLC41A1 Mg(2+) transport is regulated via Mg(2+)-dependent endosomal recycling through its N-terminal cytoplasmic domain.

Mandt T, Song Y, Scharenberg AM, Sahni J.

Biochem J. 2011 Oct 1;439(1):129-39. doi: 10.1042/BJ20110807.

PMID:
21696366
10.

Variant R244H in Na+/Mg2+ exchanger SLC41A1 in Taiwanese Parkinson's disease is associated with loss of Mg2+ efflux function.

Lin CH, Wu YR, Chen WL, Wang HC, Lee CM, Lee-Chen GJ, Chen CM.

Parkinsonism Relat Disord. 2014 Jun;20(6):600-3. doi: 10.1016/j.parkreldis.2014.02.027. Epub 2014 Mar 12.

PMID:
24661466
11.

Magnesium transporter protein solute carrier family 41 member 1 suppresses human pancreatic ductal adenocarcinoma through magnesium-dependent Akt/mTOR inhibition and bax-associated mitochondrial apoptosis.

Xie J, Cheng CS, Zhu XY, Shen YH, Song LB, Chen H, Chen Z, Liu LM, Meng ZQ.

Aging (Albany NY). 2019 May 8;11(9):2681-2698. doi: 10.18632/aging.101940.

12.

SLC41 transporters--molecular identification and functional role.

Schweigel-Röntgen M, Kolisek M.

Curr Top Membr. 2014;73:383-410. doi: 10.1016/B978-0-12-800223-0.00011-6. Review.

PMID:
24745990
13.

CNNM2 mutations cause impaired brain development and seizures in patients with hypomagnesemia.

Arjona FJ, de Baaij JH, Schlingmann KP, Lameris AL, van Wijk E, Flik G, Regele S, Korenke GC, Neophytou B, Rust S, Reintjes N, Konrad M, Bindels RJ, Hoenderop JG.

PLoS Genet. 2014 Apr 3;10(4):e1004267. doi: 10.1371/journal.pgen.1004267. eCollection 2014 Apr.

14.

The rise and fall of novel renal magnesium transporters.

Schäffers OJM, Hoenderop JGJ, Bindels RJM, de Baaij JHF.

Am J Physiol Renal Physiol. 2018 Jun 1;314(6):F1027-F1033. doi: 10.1152/ajprenal.00634.2017. Epub 2018 Feb 7. Review.

15.

Molecular Physiology of an Extra-renal Cl(-) Uptake Mechanism for Body Fluid Cl(-) Homeostasis.

Wang YF, Yan JJ, Tseng YC, Chen RD, Hwang PP.

Int J Biol Sci. 2015 Aug 15;11(10):1190-203. doi: 10.7150/ijbs.11737. eCollection 2015.

16.

Human gene SLC41A1 encodes for the Na+/Mg²+ exchanger.

Kolisek M, Nestler A, Vormann J, Schweigel-Röntgen M.

Am J Physiol Cell Physiol. 2012 Jan 1;302(1):C318-26. doi: 10.1152/ajpcell.00289.2011. Epub 2011 Oct 26.

17.

Substitution p.A350V in Na⁺/Mg²⁺ exchanger SLC41A1, potentially associated with Parkinson's disease, is a gain-of-function mutation.

Kolisek M, Sponder G, Mastrototaro L, Smorodchenko A, Launay P, Vormann J, Schweigel-Röntgen M.

PLoS One. 2013 Aug 15;8(8):e71096. doi: 10.1371/journal.pone.0071096. eCollection 2013.

18.

The art of magnesium transport.

de Baaij JH.

Magnes Res. 2015 Jul-Sep;28(3):85-91. doi: 10.1684/mrh.2015.0388. Review.

19.

Solute Carrier Family SLC41, what do we really know about it?

Fleig A, Schweigel-Röntgen M, Kolisek M.

Wiley Interdiscip Rev Membr Transp Signal. 2013;2(6). doi: 10.1002/wmts.95.

20.

A novel mutant Na+ /HCO3- cotransporter NBCe1 in a case of compound-heterozygous inheritance of proximal renal tubular acidosis.

Myers EJ, Yuan L, Felmlee MA, Lin YY, Jiang Y, Pei Y, Wang O, Li M, Xing XP, Marshall A, Xia WB, Parker MD.

J Physiol. 2016 Nov 1;594(21):6267-6286. doi: 10.1113/JP272252. Epub 2016 Aug 2.

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