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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2012 | 3 |
2013 | 1 |
2014 | 1 |
2024 | 0 |
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4 results
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Page 1
EPHA4 is a disease modifier of amyotrophic lateral sclerosis in animal models and in humans.
Nat Med. 2012 Sep;18(9):1418-22. doi: 10.1038/nm.2901.
Nat Med. 2012.
PMID: 22922411
dSarm/Sarm1 is required for activation of an injury-induced axon death pathway.
Osterloh JM, Yang J, Rooney TM, Fox AN, Adalbert R, Powell EH, Sheehan AE, Avery MA, Hackett R, Logan MA, MacDonald JM, Ziegenfuss JS, Milde S, Hou YJ, Nathan C, Ding A, Brown RH Jr, Conforti L, Coleman M, Tessier-Lavigne M, Züchner S, Freeman MR.
Osterloh JM, et al.
Science. 2012 Jul 27;337(6093):481-4. doi: 10.1126/science.1223899. Epub 2012 Jun 7.
Science. 2012.
PMID: 22678360
Free PMC article.
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Novel mutation in VCP gene causes atypical amyotrophic lateral sclerosis.
González-Pérez P, Cirulli ET, Drory VE, Dabby R, Nisipeanu P, Carasso RL, Sadeh M, Fox A, Festoff BW, Sapp PC, McKenna-Yasek D, Goldstein DB, Brown RH Jr, Blumen SC.
González-Pérez P, et al.
Neurology. 2012 Nov 27;79(22):2201-8. doi: 10.1212/WNL.0b013e318275963b. Epub 2012 Nov 14.
Neurology. 2012.
PMID: 23152587
Free PMC article.
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Widespread spinal cord transduction by intrathecal injection of rAAV delivers efficacious RNAi therapy for amyotrophic lateral sclerosis.
Wang H, Yang B, Qiu L, Yang C, Kramer J, Su Q, Guo Y, Brown RH Jr, Gao G, Xu Z.
Wang H, et al.
Hum Mol Genet. 2014 Feb 1;23(3):668-81. doi: 10.1093/hmg/ddt454. Epub 2013 Sep 18.
Hum Mol Genet. 2014.
PMID: 24108104
Free PMC article.
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