PuSH - Publication Server of Helmholtz Zentrum München

7 Records found.
Zum Exportieren der Ergebnisse bitte einloggen.
Lay all publications on this page into basket
1.
Götzl, J.K.* et al.: Opposite microglial activation stages upon loss of PGRN or TREM2 result in reduced cerebral glucose metabolism. EMBO Mol. Med. 11, e9711 (2019)
2.
Lehmer, C.* et al.: Poly-GP in cerebrospinal fluid links C9orf72-associated dipeptide repeat expression to the asymptomatic phase of ALS/FTD. EMBO Mol. Med. 9, 859-868 (2017)
3.
Schulte, E.C. et al.: Rare variants in β-Amyloid Precursor Protein (APP) and Parkinson's disease. Eur. J. Hum. Genet. 23, 1328-1333 (2015)
4.
Schulte, E.C. et al.: Excess of rare coding variants in PLD3 in late- but not early-onset Alzheimer’s disease. Hum. Genome Var. 2:14028 (2015)
5.
van der Zee, J.* et al.: Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration. Acta Neuropathol. 128, 397-410 (2014)
6.
Zech, M. et al.: Niemann-pick C disease gene mutations and age-related neurodegenerative disorders. PLoS ONE 8:e82879 (2013)
7.
Riemenschneider, M.* et al.: A functional polymorphism within plasminogen activator urokinase (PLAU) is associated with Alzheimer's disease. Hum. Mol. Genet. 15, 2446-2456 (2006)