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Author/Creator Wolfer, David P

1. Loss of all three APP family members during development impairs synaptic function and plasticity, disrupts learning, and causes an autism‐like phenotype. (19th May 2021)

Authors:
Steubler, Vicky; Erdinger, Susanne; Back, Michaela K; Ludewig, Susann; Fässler, Dominique; Richter, Max; Han, Kang; Slomianka, Lutz; Amrein, Irmgard; von Engelhardt, Jakob; Wolfer, David P; Korte, Martin; Müller, Ulrike C
Journal:
EMBO journal
Issue:
Volume 40:Number 12(2021)
Page Start:
n/a
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

3. Distinct in vivo roles of secreted APP ectodomain variants APPsα and APPsβ in regulation of spine density, synaptic plasticity, and cognition. (16th April 2018)

Authors:
Richter, Max C; Ludewig, Susann; Winschel, Alex; Abel, Tobias; Bold, Charlotte; Salzburger, Leonie R; Klein, Susanne; Han, Kang; Weyer, Sascha W; Fritz, Ann‐Kristina; Laube, Bodo; Wolfer, David P; Buchholz, Christian J; Korte, Martin; Müller, Ulrike C
Journal:
EMBO journal
Issue:
Volume 37:Number 11(2018)
Page Start:
n/a
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

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