Format
Items per page
Sort by

Send to:

Choose Destination

Results: 7

Cited In for PubMed (Select 15622541)

1.

Familial behavioral variant frontotemporal dementia associated with astrocyte-predominant tauopathy.

Ferrer I, Legati A, García-Monco JC, Gomez-Beldarrain M, Carmona M, Blanco R, Seeley WW, Coppola G.

J Neuropathol Exp Neurol. 2015 Apr;74(4):370-9. doi: 10.1097/NEN.0000000000000180.

PMID:
25756587
2.

Familial dementia with frontotemporal features associated with M146V presenilin-1 mutation.

Riudavets MA, Bartoloni L, Troncoso JC, Pletnikova O, St George-Hyslop P, Schultz M, Sevlever G, Allegri RF.

Brain Pathol. 2013 Sep;23(5):595-600. doi: 10.1111/bpa.12051. Epub 2013 Apr 25.

3.

Familial frontotemporal dementia-associated presenilin-1 c.548G>T mutation causes decreased mRNA expression and reduced presenilin function in knock-in mice.

Watanabe H, Xia D, Kanekiyo T, Kelleher RJ 3rd, Shen J.

J Neurosci. 2012 Apr 11;32(15):5085-96. doi: 10.1523/JNEUROSCI.0317-12.2012.

4.

Presenilins function in ER calcium leak and Alzheimer's disease pathogenesis.

Supnet C, Bezprozvanny I.

Cell Calcium. 2011 Sep;50(3):303-9. doi: 10.1016/j.ceca.2011.05.013. Epub 2011 Jun 12. Review.

5.

Pharmacological and genetic reversal of age-dependent cognitive deficits attributable to decreased presenilin function.

McBride SM, Choi CH, Schoenfeld BP, Bell AJ, Liebelt DA, Ferreiro D, Choi RJ, Hinchey P, Kollaros M, Terlizzi AM, Ferrick NJ, Koenigsberg E, Rudominer RL, Sumida A, Chiorean S, Siwicki KK, Nguyen HT, Fortini ME, McDonald TV, Jongens TA.

J Neurosci. 2010 Jul 14;30(28):9510-22. doi: 10.1523/JNEUROSCI.1017-10.2010.

6.

Worldwide distribution of PSEN1 Met146Leu mutation: a large variability for a founder mutation.

Bruni AC, Bernardi L, Colao R, Rubino E, Smirne N, Frangipane F, Terni B, Curcio SA, Mirabelli M, Clodomiro A, Di Lorenzo R, Maletta R, Anfossi M, Gallo M, Geracitano S, Tomaino C, Muraca MG, Leotta A, Lio SG, Pinessi L, Rainero I, Sorbi S, Nee L, Milan G, Pappatà S, Postiglione A, Abbamondi N, Forloni G, St George Hyslop P, Rogaeva E, Bugiani O, Giaccone G, Foncin JF, Spillantini MG, Puccio G.

Neurology. 2010 Mar 9;74(10):798-806. doi: 10.1212/WNL.0b013e3181d52785. Epub 2010 Feb 17.

7.

p25alpha relocalizes in oligodendroglia from myelin to cytoplasmic inclusions in multiple system atrophy.

Song YJ, Lundvig DM, Huang Y, Gai WP, Blumbergs PC, Højrup P, Otzen D, Halliday GM, Jensen PH.

Am J Pathol. 2007 Oct;171(4):1291-303. Epub 2007 Sep 6.

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk