Rogaeva E - Search Results

1

MTHFSD and DDX58 are novel RNA-binding proteins abnormally regulated in amyotrophic lateral sclerosis.

MacNair L, Xiao S, Miletic D, Ghani M, Julien JP, Keith J, Zinman L, Rogaeva E, Robertson J. MacNair L, et al. Among authors: rogaeva e. Brain. 2016 Jan;139(Pt 1):86-100. doi: 10.1093/brain/awv308. Epub 2015 Nov 2. Brain. 2016. PMID: 26525917

2

Novel splicing mutation in the progranulin gene causing familial corticobasal syndrome.

Masellis M, Momeni P, Meschino W, Heffner R Jr, Elder J, Sato C, Liang Y, St George-Hyslop P, Hardy J, Bilbao J, Black S, Rogaeva E. Masellis M, et al. Among authors: rogaeva e. Brain. 2006 Nov;129(Pt 11):3115-23. doi: 10.1093/brain/awl276. Epub 2006 Oct 9. Brain. 2006. PMID: 17030534

3

Genetic studies of GRN and IFT74 in amyotrophic lateral sclerosis.

Xiao S, Sato C, Kawarai T, Goodall EF, Pall HS, Zinman LH, Robertson J, Morrison K, Rogaeva E. Xiao S, et al. Among authors: rogaeva e. Neurobiol Aging. 2008 Aug;29(8):1279-82. doi: 10.1016/j.neurobiolaging.2007.02.022. Epub 2007 Mar 23. Neurobiol Aging. 2008. PMID: 17383054

4

A mechanism for low penetrance in an ALS family with a novel SOD1 deletion.

Zinman L, Liu HN, Sato C, Wakutani Y, Marvelle AF, Moreno D, Morrison KE, Mohlke KL, Bilbao J, Robertson J, Rogaeva E. Zinman L, et al. Among authors: rogaeva e. Neurology. 2009 Mar 31;72(13):1153-9. doi: 10.1212/01.wnl.0000345363.65799.35. Neurology. 2009. PMID: 19332692 Free PMC article.

5

Lack of evidence of monomer/misfolded superoxide dismutase-1 in sporadic amyotrophic lateral sclerosis.

Liu HN, Sanelli T, Horne P, Pioro EP, Strong MJ, Rogaeva E, Bilbao J, Zinman L, Robertson J. Liu HN, et al. Among authors: rogaeva e. Ann Neurol. 2009 Jul;66(1):75-80. doi: 10.1002/ana.21704. Ann Neurol. 2009. PMID: 19670443

6

SPATACSIN mutations cause autosomal recessive juvenile amyotrophic lateral sclerosis.

Orlacchio A, Babalini C, Borreca A, Patrono C, Massa R, Basaran S, Munhoz RP, Rogaeva EA, St George-Hyslop PH, Bernardi G, Kawarai T. Orlacchio A, et al. Brain. 2010 Feb;133(Pt 2):591-8. doi: 10.1093/brain/awp325. Epub 2010 Jan 28. Brain. 2010. PMID: 20110243 Free PMC article.

7

Amyotrophic lateral sclerosis is a non-amyloid disease in which extensive misfolding of SOD1 is unique to the familial form.

Kerman A, Liu HN, Croul S, Bilbao J, Rogaeva E, Zinman L, Robertson J, Chakrabartty A. Kerman A, et al. Among authors: rogaeva e. Acta Neuropathol. 2010 Mar;119(3):335-44. doi: 10.1007/s00401-010-0646-5. Epub 2010 Jan 29. Acta Neuropathol. 2010. PMID: 20111867

8

Distinct biochemical signatures characterize peripherin isoform expression in both traumatic neuronal injury and motor neuron disease.

McLean J, Liu HN, Miletic D, Weng YC, Rogaeva E, Zinman L, Kriz J, Robertson J. McLean J, et al. Among authors: rogaeva e. J Neurochem. 2010 Aug;114(4):1177-92. doi: 10.1111/j.1471-4159.2010.06846.x. Epub 2010 Jun 1. J Neurochem. 2010. PMID: 20533992 Free article.

9

A novel double mutation in FUS gene causing sporadic ALS.

Robertson J, Bilbao J, Zinman L, Hazrati LN, Tokuhiro S, Sato C, Moreno D, Strome R, Mackenzie IR, Rogaeva E. Robertson J, et al. Among authors: rogaeva e. Neurobiol Aging. 2011 Mar;32(3):553.e27-30. doi: 10.1016/j.neurobiolaging.2010.05.015. Epub 2010 Jun 18. Neurobiol Aging. 2011. PMID: 20561714

10

RNA targets of TDP-43 identified by UV-CLIP are deregulated in ALS.

Xiao S, Sanelli T, Dib S, Sheps D, Findlater J, Bilbao J, Keith J, Zinman L, Rogaeva E, Robertson J. Xiao S, et al. Among authors: rogaeva e. Mol Cell Neurosci. 2011 Jul;47(3):167-80. doi: 10.1016/j.mcn.2011.02.013. Epub 2011 Mar 21. Mol Cell Neurosci. 2011. PMID: 21421050

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