Search

Author/Creator Rading, Sebastian

1. A rare heterozygous TREM2 coding variant identified in familial clustering of dementia affects an intrinsically disordered protein region and function of TREM2. Issue 1 (15th September 2019)

Authors:
Karsak, Meliha; Glebov, Konstantin; Scheffold, Marina; Bajaj, Thomas; Kawalia, Amit; Karaca, Ilker; Rading, Sebastian; Kornhuber, Johannes; Peters, Oliver; Diez‐Fairen, Monica; Frölich, Lutz; Hüll, Michael; Wiltfang, Jens; Scherer, Martin; Riedel‐Heller, Steffi; Schneider, Anja; Heneka, Michael T...
Journal:
Human mutation
Issue:
Volume 41:Issue 1(2020)
Page Start:
169
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

2. P2‐049: Functional characterization of a novel TREM2 coding variant linked to familial Alzheimer's disease. (1st July 2015)

Authors:
Ramirez, Alfredo; Karsak, Meliha; Thelen, Mathias; Glebov, Konstantin; Nagler, Marina; Rading, Sebastian; Thiele, Holger; Lernnarz, Martina; Jessen, Frank; Maier, Wolfgang; Nuernberg, Peter; Pastor, Pau; Walter, Jochen
Journal:
Alzheimer's & dementia
Issue:
Volume 11(2015)Supplement 7:Part 10
Page Start:
P500
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

Limit your search