Published Data Registry | SyNergy Research Data Platform

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Title	Authors	Journal	Publication year	DOI PMID
The ER under rapid fire.	Schwenk BM, Edbauer D	The EMBO journal	2014	10.1002/embj.201488692 24788411
Overexpression of Q-rich prion-like proteins suppresses polyQ cytotoxicity and alters the polyQ interactome.	Ripaud L, Chumakova V, (...), Hipp MS	Proceedings of the National Academy of Sciences of the United States of America	2014	10.1073/pnas.1421313111 25489109
In vivo targeting of adult neural stem cells in the dentate gyrus by a split-cre approach.	Beckervordersandforth R, Deshpande A, (...), Götz M	Stem cell reports	2014	10.1016/j.stemcr.2014.01.004 24527389
Role of radial glial cells in cerebral cortex folding.	Borrell V, Götz M	Current opinion in neurobiology	2014	10.1016/j.conb.2014.02.007 24632307
Rare sequence variants in ANO3 and GNAL in a primary torsion dystonia series and controls.	Zech M, Gross N, (...), Winkelmann J	Movement disorders : official journal of the Movement Disorder Society	2014	10.1002/mds.25715 24151159
Mutations in GTPBP3 cause a mitochondrial translation defect associated with hypertrophic cardiomyopathy, lactic acidosis, and encephalopathy.	Kopajtich R, Nicholls TJ, (...), Prokisch H	American journal of human genetics	2014	10.1016/j.ajhg.2014.10.017 25434004
Progranulin transcripts with short and long 5' untranslated regions (UTRs) are differentially expressed via posttranscriptional and translational repression.	Capell A, Fellerer K, Haass C	The Journal of biological chemistry	2014	10.1074/jbc.M114.560128 25056957
TREM2 mutations implicated in neurodegeneration impair cell surface transport and phagocytosis.	Kleinberger G, Yamanishi Y, (...), Haass C	Science translational medicine	2014	10.1126/scitranslmed.3009093 24990881
Blood cis-eQTL analysis fails to identify novel association signals among sub-threshold candidates from genome-wide association studies in restless legs syndrome.	Schulte EC, Schramm K, (...), Winkelmann J	PloS one	2014	10.1371/journal.pone.0098092 24875634
Targeted resequencing and systematic in vivo functional testing identifies rare variants in MEIS1 as significant contributors to restless legs syndrome.	Schulte EC, Kousi M, (...), Winkelmann J	American journal of human genetics	2014	10.1016/j.ajhg.2014.06.005 24995868

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