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2006 2
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2009 1
2010 2
2020 3
2024 0

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Page 1
Intricacies of aetiology in intrafamilial degenerative disease.
Lowry JL, Ryan ÉB, Esengul YT, Siddique N, Siddique T. Lowry JL, et al. Brain Commun. 2020 Oct 6;2(2):fcaa120. doi: 10.1093/braincomms/fcaa120. eCollection 2020. Brain Commun. 2020. PMID: 33134917 Free PMC article. Review.
Genetics of amyotrophic lateral sclerosis.
Siddique N, Siddique T. Siddique N, et al. Phys Med Rehabil Clin N Am. 2008 Aug;19(3):429-39, vii. doi: 10.1016/j.pmr.2008.05.001. Phys Med Rehabil Clin N Am. 2008. PMID: 18625408 Free PMC article. Review.
ALS/FTD mutations in UBQLN2 impede autophagy by reducing autophagosome acidification through loss of function.
Wu JJ, Cai A, Greenslade JE, Higgins NR, Fan C, Le NTT, Tatman M, Whiteley AM, Prado MA, Dieriks BV, Curtis MA, Shaw CE, Siddique T, Faull RLM, Scotter EL, Finley D, Monteiro MJ. Wu JJ, et al. Proc Natl Acad Sci U S A. 2020 Jun 30;117(26):15230-15241. doi: 10.1073/pnas.1917371117. Epub 2020 Jun 8. Proc Natl Acad Sci U S A. 2020. PMID: 32513711 Free PMC article.
Disease-modifying effects of an SCAF4 structural variant in a predominantly SOD1 ALS cohort.
Pytte J, Flynn LL, Anderton RS, Mastaglia FL, Theunissen F, James I, Pfaff A, Koks S, Saunders AM, Bedlack R, Burns DK, Lutz MW, Siddique N, Siddique T, Roses AD, Akkari PA. Pytte J, et al. Neurol Genet. 2020 Jul 1;6(4):e470. doi: 10.1212/NXG.0000000000000470. eCollection 2020 Aug. Neurol Genet. 2020. PMID: 32754644 Free PMC article.
Conversion to the amyotrophic lateral sclerosis phenotype is associated with intermolecular linked insoluble aggregates of SOD1 in mitochondria.
Deng HX, Shi Y, Furukawa Y, Zhai H, Fu R, Liu E, Gorrie GH, Khan MS, Hung WY, Bigio EH, Lukas T, Dal Canto MC, O'Halloran TV, Siddique T. Deng HX, et al. Proc Natl Acad Sci U S A. 2006 May 2;103(18):7142-7. doi: 10.1073/pnas.0602046103. Epub 2006 Apr 24. Proc Natl Acad Sci U S A. 2006. PMID: 16636275 Free PMC article.