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recent work on adenosine-producing ectonucleotidases and adenosine signaling and discuss unexpected links University of Montréal Québec Cancer Consortium The University of Montreal Hospital Research Centre Pubmed LinkedIn

have developed antibody-drug conjugates (ADCs) targeting CD97, by screening a synthetic human antibody library We initially tested the ADC using in vitro WST-8 viability assays in human GBM cell lines and cell types Dimitris Placantonakis on the web Placantonakis Lab Google Scholar LinkedIn Adhesion G protein-coupled Nicole Perry-Hauser on the web LinkedIn Research Gate Pubmed Dr.

Scott Leiser on the web University of Michigan Pubmed ResearchGate LinkedIn Dr.

Since starting my laboratory in 2011, I has focused on G protein coupled receptors, in particular, the ligand Our first main research aspect is the identification of endogenous ligand of GPCRs. We also identified DHEA, DHEAS and DOC are endogenous ligands of GPR64 etc (Nature, 2021a, Nat Chem Biol Our fourth main research aspect is ligand coding mechanisms and structural aided drug discovery of GPCR Jin-Peng Sun on the web Google Scholar LinkedIn < Previous Session Next Session >

Brunos Giros on the web The Douglas Research Centre McGill University Pubmed Google Scholar LinkedIn

GPCR Podcast << Back to podcast list Re-cap of Endocrine Metabolic GPCR 2024 with the Organizers About Aylin Hanyaloglu on the web LinkedIn Endocrine Metabolic GPCRs Researchgate Twitter Imperial College Alejandra Tomas on the web Imperial College London Endocrine Metabolic GPCRs ResearchGate Google Scholar LinkedIn : The pHSense Revolution How a Failed Med School Dream Sparked a GPCR Biotech Revolution Thanks for listening

Louis Gendron on the web Université de Sherbrooke Neurosciences Sherbrooke RQRD Pubmed Google Scholar LinkedIn

Signaling Profile of Adhesion GPCR ADGRL1 / Latrophilin-1 Sheila Ribalta-Mena GPR110 modulates anxiety-like Notably, our pilot data from luminal-type breast cancer cell lines representative of breast carcinomas To test this hypothesis, we created WNT-like MB cell lines stably expressing tet-on wild-type BAI3 or Ligand binding and mechanical force applied on the ECR regulate receptor function. Mariam Melkumyan on the web LinkedIn Google Scholar < Previous Session Next Session >

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