Fecto F - Search Results

1

Differential involvement of optineurin in amyotrophic lateral sclerosis with or without SOD1 mutations.

Deng HX, Bigio EH, Zhai H, Fecto F, Ajroud K, Shi Y, Yan J, Mishra M, Ajroud-Driss S, Heller S, Sufit R, Siddique N, Mugnaini E, Siddique T. Deng HX, et al. Among authors: fecto f. Arch Neurol. 2011 Aug;68(8):1057-61. doi: 10.1001/archneurol.2011.178. Arch Neurol. 2011. PMID: 21825243 Free PMC article.

2

FUS-immunoreactive inclusions are a common feature in sporadic and non-SOD1 familial amyotrophic lateral sclerosis.

Deng HX, Zhai H, Bigio EH, Yan J, Fecto F, Ajroud K, Mishra M, Ajroud-Driss S, Heller S, Sufit R, Siddique N, Mugnaini E, Siddique T. Deng HX, et al. Among authors: fecto f. Ann Neurol. 2010 Jun;67(6):739-48. doi: 10.1002/ana.22051. Ann Neurol. 2010. PMID: 20517935 Free PMC article.

3

Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia.

Deng HX, Chen W, Hong ST, Boycott KM, Gorrie GH, Siddique N, Yang Y, Fecto F, Shi Y, Zhai H, Jiang H, Hirano M, Rampersaud E, Jansen GH, Donkervoort S, Bigio EH, Brooks BR, Ajroud K, Sufit RL, Haines JL, Mugnaini E, Pericak-Vance MA, Siddique T. Deng HX, et al. Among authors: fecto f. Nature. 2011 Aug 21;477(7363):211-5. doi: 10.1038/nature10353. Nature. 2011. PMID: 21857683 Free PMC article.

4

Making connections: pathology and genetics link amyotrophic lateral sclerosis with frontotemporal lobe dementia.

Fecto F, Siddique T. Fecto F, et al. J Mol Neurosci. 2011 Nov;45(3):663-75. doi: 10.1007/s12031-011-9637-9. Epub 2011 Sep 7. J Mol Neurosci. 2011. PMID: 21901496 Review.

5

SQSTM1 mutations in familial and sporadic amyotrophic lateral sclerosis.

Fecto F, Yan J, Vemula SP, Liu E, Yang Y, Chen W, Zheng JG, Shi Y, Siddique N, Arrat H, Donkervoort S, Ajroud-Driss S, Sufit RL, Heller SL, Deng HX, Siddique T. Fecto F, et al. Arch Neurol. 2011 Nov;68(11):1440-6. doi: 10.1001/archneurol.2011.250. Arch Neurol. 2011. PMID: 22084127

6

What is repeated in ALS and FTLD.

Fecto F, Siddique T. Fecto F, et al. Lancet Neurol. 2012 Jan;11(1):25-7. doi: 10.1016/S1474-4422(11)70275-7. Epub 2011 Dec 7. Lancet Neurol. 2012. PMID: 22154784 No abstract available.

7

UBQLN2/P62 cellular recycling pathways in amyotrophic lateral sclerosis and frontotemporal dementia.

Fecto F, Siddique T. Fecto F, et al. Muscle Nerve. 2012 Feb;45(2):157-62. doi: 10.1002/mus.23278. Muscle Nerve. 2012. PMID: 22246868

8

Frameshift and novel mutations in FUS in familial amyotrophic lateral sclerosis and ALS/dementia.

Yan J, Deng HX, Siddique N, Fecto F, Chen W, Yang Y, Liu E, Donkervoort S, Zheng JG, Shi Y, Ahmeti KB, Brooks B, Engel WK, Siddique T. Yan J, et al. Among authors: fecto f. Neurology. 2010 Aug 31;75(9):807-14. doi: 10.1212/WNL.0b013e3181f07e0c. Epub 2010 Jul 28. Neurology. 2010. PMID: 20668259 Free PMC article.

9

Scapuloperoneal spinal muscular atrophy and CMT2C are allelic disorders caused by alterations in TRPV4.

Deng HX, Klein CJ, Yan J, Shi Y, Wu Y, Fecto F, Yau HJ, Yang Y, Zhai H, Siddique N, Hedley-Whyte ET, Delong R, Martina M, Dyck PJ, Siddique T. Deng HX, et al. Among authors: fecto f. Nat Genet. 2010 Feb;42(2):165-9. doi: 10.1038/ng.509. Epub 2009 Dec 27. Nat Genet. 2010. PMID: 20037587 Free PMC article.

10

Mutant TRPV4-mediated toxicity is linked to increased constitutive function in axonal neuropathies.

Fecto F, Shi Y, Huda R, Martina M, Siddique T, Deng HX. Fecto F, et al. J Biol Chem. 2011 May 13;286(19):17281-91. doi: 10.1074/jbc.M111.237685. Epub 2011 Mar 21. J Biol Chem. 2011. PMID: 21454511 Free PMC article.

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