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Year | Number of Results |
---|---|
2004 | 1 |
2010 | 1 |
2012 | 1 |
2018 | 1 |
2024 | 1 |
PubMed for id: 261599068
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Page 1
Genetic determinants of micronucleus formation in vivo.
Nature. 2024 Mar;627(8002):130-136. doi: 10.1038/s41586-023-07009-0. Epub 2024 Feb 14.
Nature. 2024.
PMID: 38355793
Free PMC article.
Parkinson disease related ATP13A2 evolved early in animal evolution.
Sørensen DM, Holemans T, van Veen S, Martin S, Arslan T, Haagendahl IW, Holen HW, Hamouda NN, Eggermont J, Palmgren M, Vangheluwe P.
Sørensen DM, et al.
PLoS One. 2018 Mar 5;13(3):e0193228. doi: 10.1371/journal.pone.0193228. eCollection 2018.
PLoS One. 2018.
PMID: 29505581
Free PMC article.
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A mutation in the Srrm4 gene causes alternative splicing defects and deafness in the Bronx waltzer mouse.
Nakano Y, Jahan I, Bonde G, Sun X, Hildebrand MS, Engelhardt JF, Smith RJ, Cornell RA, Fritzsch B, Bánfi B.
Nakano Y, et al.
PLoS Genet. 2012;8(10):e1002966. doi: 10.1371/journal.pgen.1002966. Epub 2012 Oct 4.
PLoS Genet. 2012.
PMID: 23055939
Free PMC article.
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The E646D-ATP13A4 mutation associated with autism reveals a defect in calcium regulation.
Vallipuram J, Grenville J, Crawford DA.
Vallipuram J, et al.
Cell Mol Neurobiol. 2010 Mar;30(2):233-46. doi: 10.1007/s10571-009-9445-8.
Cell Mol Neurobiol. 2010.
PMID: 19731010
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Characterization of the P5 subfamily of P-type transport ATPases in mice.
Schultheis PJ, Hagen TT, O'Toole KK, Tachibana A, Burke CR, McGill DL, Okunade GW, Shull GE.
Schultheis PJ, et al.
Biochem Biophys Res Commun. 2004 Oct 22;323(3):731-8. doi: 10.1016/j.bbrc.2004.08.156.
Biochem Biophys Res Commun. 2004.
PMID: 15381061
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