Here, we describe new tools, referred to as "SynTAMs" for synaptic targeting molecules, that enable localized

largest family of membrane proteins in eukaryotes and the largest drug target family to date, exhibit diversity

essential in biology and understanding how cells integrate signals from a variety of information-coding molecules

LPAs) are bioactive phospholipids implicated in a wide range of cellular activities that regulate a diverse

However, it is unclear how diverse GPCRs similarly affect Aβ and tau pathogenesis.

Adrenergic receptors on B cells and intracellular β2-ADR downstream molecules (G protein-coupled receptor

is not universally true that kisspeptin/KISS1R stimulate migration or pro-metastatic behaviour, as divergent Whether this divergence is related to the observed differences in β-arrestin complements warrants further

peptide-1 receptor dimerization differentially regulates agonist signaling but does not affect small molecule

Divergence, however, in the amino acid sequences of rodent and human PTH receptors (rat and mouse PTH1Rs

Administration of Exendin-4 to MI rats reduced the infarct size and reversed the aforementioned signaling molecules

operate on the principle of energy transfer between a fluorescent or luminescent donor and acceptor molecules

proteins has been implicated in a range of diseases, and understanding the mechanisms of these complex molecules