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Year | Number of Results |
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1992 | 1 |
2011 | 1 |
2012 | 1 |
2019 | 1 |
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MpzR98C arrests Schwann cell development in a mouse model of early-onset Charcot-Marie-Tooth disease type 1B.
Brain. 2012 Jul;135(Pt 7):2032-47. doi: 10.1093/brain/aws140. Epub 2012 Jun 10.
Brain. 2012.
PMID: 22689911
Free PMC article.
Mouse P0 gene disruption leads to hypomyelination, abnormal expression of recognition molecules, and degeneration of myelin and axons.
Giese KP, Martini R, Lemke G, Soriano P, Schachner M.
Giese KP, et al.
Cell. 1992 Nov 13;71(4):565-76. doi: 10.1016/0092-8674(92)90591-y.
Cell. 1992.
PMID: 1384988
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P0S63del impedes the arrival of wild-type P0 glycoprotein to myelin in CMT1B mice.
Fratta P, Saveri P, Zambroni D, Ferri C, Tinelli E, Messing A, D'Antonio M, Feltri ML, Wrabetz L.
Fratta P, et al.
Hum Mol Genet. 2011 Jun 1;20(11):2081-90. doi: 10.1093/hmg/ddr081. Epub 2011 Mar 1.
Hum Mol Genet. 2011.
PMID: 21363884
Free PMC article.
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A nonsense mutation in myelin protein zero causes congenital hypomyelination neuropathy through altered P0 membrane targeting and gain of abnormal function.
Fratta P, Ornaghi F, Dati G, Zambroni D, Saveri P, Belin S, D'Adamo P, Shy M, Quattrini A, Laura Feltri M, Wrabetz L.
Fratta P, et al.
Hum Mol Genet. 2019 Jan 1;28(1):124-132. doi: 10.1093/hmg/ddy336.
Hum Mol Genet. 2019.
PMID: 30239779
Free PMC article.
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