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35 items found for "Enrico Rovati"
Posts (13)
- Hop in the Time Machine with GPCR: Unraveling the Future of Research! ⦿ Nov 24 - Dec 1, 2024
GPCR) pharmacogenomics Miles D Thompson , David Reiner-Link , Alessandro Berghella , Brinda K Rana , G Enrico Rovati , Valerie Capra , Caroline M Gorvin , Alexander S Hauser Calcineurin-fusion facilitates cryo-EM
- Recurrent high-impact mutations at cognate structural positions in class A G protein-coupled ...
We hypothesized that somatic mutations in tumor samples may not be enriched within a single gene but Individual cancer types were enriched for highly impactful, recurrent mutations at selected cognate positions
- High hedgehog signaling is transduced by a multikinase-dependent switch controlling the...
Moreover, in the presence of very high levels of HH, the second effect of FU leads to the local enrichment
Other Pages (22)
- Transcriptomic analysis of human cytomegalovirus to survey the indirect effects on renal transplant recipients
Afterward, Gene Ontology (GO) and pathway enrichment analyses were conducted to determine the enriched KEGG pathway analysis revealed the enrichment of DEGs in IL18 signaling, AGE-RAGE signaling pathway in The expression levels of six genes involved in enriched pathways including F3, PTX3, ADRA2B, GNG11, GP9
- Unbiased multitissue transcriptomic analysis reveals complex neuroendocrine regulatory networks mediated by spinal cord injury-induced immunodeficiency
results showed that the downregulated differentially expressed genes (DEGs) in the T3-SCI group were enriched Traf6, Akap8, Gfer, Cxcl10, Tnfaip3, Icam1, Fcgr2b, Ager, Dusp10, and Mapkapk2) were significantly enriched the downregulated genes (hub genes: Grm4, Nmu, P2ry12, rt1-bb1, Oprm1, Zfhx2, Gpr83, and Chrm2) were enriched The upregulated genes in the adrenal glands (hub genes: Ciart, per2, per3, cry1, and cry2) were enriched IL7r, rt1-bb, rt1-bb1, rt1-da, rt1-ba, cd74, cxcr3, vcam1, ccl5, bin1, and IL8) were significantly enriched
- Investigating isoform switching in RHBDF2 and its role in neoplastic growth in breast cancer
Furthermore, interacting partners were found via correlation and enriched to explain their antagonistic Neither EGFR nor ERAD was found enriched. and the proteasomal degradation pathway and cytoplasmic ribosomal protein pathways were significantly enriched