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Proteomic analysis reveals co-ordinated alterations in protein synthesis and degradation pathways in LRRK2 knockout mice.
Pellegrini L, Hauser DN, Li Y, Mamais A, Beilina A, Kumaran R, Wetzel A, Nixon-Abell J, Heaton G, Rudenko I, Alkaslasi M, Ivanina N, Melrose HL, Cookson MR, Harvey K. Pellegrini L, et al. Among authors: wetzel a. Hum Mol Genet. 2018 Sep 15;27(18):3257-3271. doi: 10.1093/hmg/ddy232. Hum Mol Genet. 2018. PMID: 29917075 Free PMC article.
Back to the tubule: microtubule dynamics in Parkinson's disease.
Pellegrini L, Wetzel A, Grannó S, Heaton G, Harvey K. Pellegrini L, et al. Among authors: wetzel a. Cell Mol Life Sci. 2017 Feb;74(3):409-434. doi: 10.1007/s00018-016-2351-6. Epub 2016 Sep 6. Cell Mol Life Sci. 2017. PMID: 27600680 Free PMC article. Review.
Loss of the protein-tyrosine phosphatase DEP-1/PTPRJ drives meningioma cell motility.
Petermann A, Haase D, Wetzel A, Balavenkatraman KK, Tenev T, Gührs KH, Friedrich S, Nakamura M, Mawrin C, Böhmer FD. Petermann A, et al. Among authors: wetzel a. Brain Pathol. 2011 Jul;21(4):405-18. doi: 10.1111/j.1750-3639.2010.00464.x. Epub 2010 Dec 27. Brain Pathol. 2011. PMID: 21091576 Free PMC article.
Role of Na(v)1.9 in activity-dependent axon growth in motoneurons.
Subramanian N, Wetzel A, Dombert B, Yadav P, Havlicek S, Jablonka S, Nassar MA, Blum R, Sendtner M. Subramanian N, et al. Among authors: wetzel a. Hum Mol Genet. 2012 Aug 15;21(16):3655-67. doi: 10.1093/hmg/dds195. Epub 2012 May 28. Hum Mol Genet. 2012. PMID: 22641814
A de novo gain-of-function mutation in SCN11A causes loss of pain perception.
Leipold E, Liebmann L, Korenke GC, Heinrich T, Giesselmann S, Baets J, Ebbinghaus M, Goral RO, Stödberg T, Hennings JC, Bergmann M, Altmüller J, Thiele H, Wetzel A, Nürnberg P, Timmerman V, De Jonghe P, Blum R, Schaible HG, Weis J, Heinemann SH, Hübner CA, Kurth I. Leipold E, et al. Among authors: wetzel a. Nat Genet. 2013 Nov;45(11):1399-404. doi: 10.1038/ng.2767. Epub 2013 Sep 15. Nat Genet. 2013. PMID: 24036948
175 results