Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2011 | 1 |
2012 | 1 |
2013 | 2 |
2024 | 0 |
Search Results
3 results
Results by year
Filters applied: . Clear all
Page 1
Human gene SLC41A1 encodes for the Na+/Mg²+ exchanger.
Am J Physiol Cell Physiol. 2012 Jan 1;302(1):C318-26. doi: 10.1152/ajpcell.00289.2011. Epub 2011 Oct 26.
Am J Physiol Cell Physiol. 2012.
PMID: 22031603
Free article.
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.
Hurd TW, et al.
J Am Soc Nephrol. 2013 May;24(6):967-77. doi: 10.1681/ASN.2012101034. Epub 2013 May 9.
J Am Soc Nephrol. 2013.
PMID: 23661805
Free PMC article.
Item in Clipboard
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.
Kolisek M, et al.
PLoS One. 2013 Aug 15;8(8):e71096. doi: 10.1371/journal.pone.0071096. eCollection 2013.
PLoS One. 2013.
PMID: 23976986
Free PMC article.
Item in Clipboard
Cite
Cite