Publications
Journal Article (13)
2018
Journal Article
8, 5858 (2018)
Proteomic profiling of human cancer pseudopodia for the identification of anti-metastatic drug candidates. SCIENTIFIC REPORTS
Journal Article
84 (CN3), pp. 1 - 10 (2018)
multipanelfigure: Simple Assembly of Multiple Plots and Images into a Compound Figure. JOURNAL OF STATISTICAL SOFTWARE
Journal Article
4 (9), eaau1935 (2018)
The CCT chaperonin is a novel regulator of Ca2+ signaling through modulation of Orai1 trafficking. SCIENCE ADVANCES
Journal Article
9, 4600 (2018)
Myh10 deficiency leads to defective extracellular matrix remodeling and pulmonary disease. NATURE COMMUNICATIONS
Journal Article
7, e42209 (2018)
Screening for insulin-independent pathways that modulate glucose homeostasis identifies androgen receptor antagonists. ELIFE
Journal Article
9, 5331 (2018)
Transcriptome 3 ' end organization by PCF11 links alternative polyadenylation to formation and neuronal differentiation of neuroblastoma. NATURE COMMUNICATIONS
Journal Article
50 (7), pp. 990 - + (2018)
MiCEE is a ncRNA-protein complex that mediates epigenetic silencing and nucleolar organization. NATURE GENETICS
Journal Article
14 (11), e1007743 (2018)
Loss of the Mia40a oxidoreductase leads to hepato-pancreatic insufficiency in zebrafish. PLOS GENETICS
Journal Article
9, 4077 (2018)
Loss of pyruvate kinase M2 limits growth and triggers innate immune signaling in endothelial cells. NATURE COMMUNICATIONS
Journal Article
17 (2), pp. 270 - 289 (2018)
Proteotranscriptomics Reveal Signaling Networks in the Ovarian Cancer Microenvironment. MOLECULAR & CELLULAR PROTEOMICS
Journal Article
9, 3853 (2018)
Genome-wide mapping of plasma protein QTLs identifies putatively causal genes and pathways for cardiovascular disease (vol 9, 3268, 2018). NATURE COMMUNICATIONS
Journal Article
9, 3268 (2018)
Genome-wide mapping of plasma protein QTLs identifies putatively causal genes and pathways for cardiovascular disease. NATURE COMMUNICATIONS
Journal Article
27 (6), pp. 1106 - 1121 (2018)
Deep molecular phenotypes link complex disorders and physiological insult to CpG methylation. HUMAN MOLECULAR GENETICS