Synapse
⌘+K
Synapse
PulseExploreClubsResearchersJournals
Instagram
HomeClubsExplore
August 21, 2008Human Molecular GeneticsOpen Access

Common variation in the miR-659 binding-site of GRN is a major risk factor for TDP43-positive frontotemporal dementia

View Full Paper
Ask AI
Bookmark
Share

Authors

Rosa Rademakers
Rosa RademakersBoston University
JEJason L. EriksenUniversity of HoustonMBMatt BakerMayo Clinic

Discussion

Loading...

Member takes

Overview

Key Points

Key points are not available for this paper at this time.

Cite This Study

Rademakers et al. (2008) studied this question.

synapsesocial.com/papers/6a6ffef426a7f98052dc88e8https://doi.org/10.1093/hmg/ddn257
View Full Paper
Ask AI
Bookmark
Share

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Neuropathologic Features of Frontotemporal Lobar Degeneration With Ubiquitin-Positive Inclusions With Progranulin Gene (PGRN) Mutations2007 · 185 citations
  2. 2Cerebellar neurodegeneration in the absence of microRNAs2007 · 491 citations
  3. 3Frontotemporal lobar degeneration and ubiquitin immunohistochemistry2004 · 155 citations
  4. 4The law of mass action applied to neurodegenerative disease: a hypothesis concerning the etiology and pathogenesis of complex diseases2004 · 95 citations
  5. 5High-density SNP haplotyping suggests altered regulation of tau gene expression in progressive supranuclear palsy2005 · 167 citations