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2011 | 3 |
2012 | 5 |
2013 | 1 |
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Page 1
UBQLN2/ubiquilin 2 mutation and pathology in familial amyotrophic lateral sclerosis.
Neurobiol Aging. 2012 Oct;33(10):2527.e3-10. doi: 10.1016/j.neurobiolaging.2012.05.008. Epub 2012 Jun 19.
Neurobiol Aging. 2012.
PMID: 22717235
Mutation analysis of VCP in familial and sporadic amyotrophic lateral sclerosis.
Williams KL, Solski JA, Nicholson GA, Blair IP.
Williams KL, et al. Among authors: solski ja.
Neurobiol Aging. 2012 Jul;33(7):1488.e15-6. doi: 10.1016/j.neurobiolaging.2011.11.022. Epub 2011 Dec 22.
Neurobiol Aging. 2012.
PMID: 22196955
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Mutation analysis of the optineurin gene in familial amyotrophic lateral sclerosis.
Solski JA, Williams KL, Yang S, Nicholson GA, Blair IP.
Solski JA, et al.
Neurobiol Aging. 2012 Jan;33(1):210.e9-10. doi: 10.1016/j.neurobiolaging.2011.09.023. Epub 2011 Oct 19.
Neurobiol Aging. 2012.
PMID: 22015311
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A yeast functional screen predicts new candidate ALS disease genes.
Couthouis J, Hart MP, Shorter J, DeJesus-Hernandez M, Erion R, Oristano R, Liu AX, Ramos D, Jethava N, Hosangadi D, Epstein J, Chiang A, Diaz Z, Nakaya T, Ibrahim F, Kim HJ, Solski JA, Williams KL, Mojsilovic-Petrovic J, Ingre C, Boylan K, Graff-Radford NR, Dickson DW, Clay-Falcone D, Elman L, McCluskey L, Greene R, Kalb RG, Lee VM, Trojanowski JQ, Ludolph A, Robberecht W, Andersen PM, Nicholson GA, Blair IP, King OD, Bonini NM, Van Deerlin V, Rademakers R, Mourelatos Z, Gitler AD.
Couthouis J, et al. Among authors: solski ja.
Proc Natl Acad Sci U S A. 2011 Dec 27;108(52):20881-90. doi: 10.1073/pnas.1109434108. Epub 2011 Nov 7.
Proc Natl Acad Sci U S A. 2011.
PMID: 22065782
Free PMC article.
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A novel TARDBP insertion/deletion mutation in the flail arm variant of amyotrophic lateral sclerosis.
Solski JA, Yang S, Nicholson GA, Luquin N, Williams KL, Fernando R, Pamphlett R, Blair IP.
Solski JA, et al.
Amyotroph Lateral Scler. 2012 Sep;13(5):465-70. doi: 10.3109/17482968.2012.662690. Epub 2012 Mar 16.
Amyotroph Lateral Scler. 2012.
PMID: 22424122
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Evaluating the role of the FUS/TLS-related gene EWSR1 in amyotrophic lateral sclerosis.
Couthouis J, Hart MP, Erion R, King OD, Diaz Z, Nakaya T, Ibrahim F, Kim HJ, Mojsilovic-Petrovic J, Panossian S, Kim CE, Frackelton EC, Solski JA, Williams KL, Clay-Falcone D, Elman L, McCluskey L, Greene R, Hakonarson H, Kalb RG, Lee VM, Trojanowski JQ, Nicholson GA, Blair IP, Bonini NM, Van Deerlin VM, Mourelatos Z, Shorter J, Gitler AD.
Couthouis J, et al. Among authors: solski ja.
Hum Mol Genet. 2012 Jul 1;21(13):2899-911. doi: 10.1093/hmg/dds116. Epub 2012 Mar 27.
Hum Mol Genet. 2012.
PMID: 22454397
Free PMC article.
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Frontotemporal dementia-amyotrophic lateral sclerosis syndrome locus on chromosome 16p12.1-q12.2: genetic, clinical and neuropathological analysis.
Dobson-Stone C, Luty AA, Thompson EM, Blumbergs P, Brooks WS, Short CL, Field CD, Panegyres PK, Hecker J, Solski JA, Blair IP, Fullerton JM, Halliday GM, Schofield PR, Kwok JB.
Dobson-Stone C, et al. Among authors: solski ja.
Acta Neuropathol. 2013 Apr;125(4):523-33. doi: 10.1007/s00401-013-1078-9. Epub 2013 Jan 22.
Acta Neuropathol. 2013.
PMID: 23338750
Free PMC article.
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