Corpus 1,276 assessed · 1,177 scored · 644 reproduced ≥75 · 170 flagged ·∅ 74/100

Publications 2 Datasets 392.5k Experiments 4.7k

Explore

Filters: Life & Brain (Germany) ✕ 3 ✕ clear all

2 matching publication(s)

Publication	Journal	Year	Score	Verdict
Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase. PMID 16964263	Nature genetics	2006	—	L1 No data access
The focal adhesion protein β-parvin controls cardiomyocyte shape and sarcomere assembly in response to mechanical load. PMID 35688156	—	2022	—	L1 No computation

Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase.

PMID 16964263 · Nature genetics · 2006

L1 No data access

The focal adhesion protein β-parvin controls cardiomyocyte shape and sarcomere assembly in response to mechanical load.

PMID 35688156 · · 2022

L1 No computation