Comprehensive repertoire and phylogenetic analysis of the G protein-coupled receptors in human and mouse.
By Thóra K. Bjarnadóttir, David E. Gloriam, Sofia H Hellstrand, H. Kristiansson, Robert Fredriksson, Helgi B. Schiöth. 2006
435 citations recorded by the source corpus.
Subfields: Cellular and Molecular Neuroscience, Molecular Biology
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In Cellular and Molecular Neuroscience
In Molecular Biology
- Lim Heo
- David E. Gloriam
- Michael Feig
- Helgi B. Schiöth
- Robert Fredriksson
- K. Currie
- Collin F Arbour
- Yang Zhang
Citations in the corpus
- Multi-State Modeling of G-protein Coupled Receptors at Experimental Accuracy (2021, background): “2, 10, 11 They are subdivided into several classes according to sequence homology and functional similarity: class A (rhodopsin), B1 (secretin), B2(adhesion), C (glutamate), F (frizzled), T (taste 2).(12) Dysregulation of GPCRs can cause diseases including cardiovascular disease(11) and Parkinson’s ”
- G protein inhibition of CaV2 calcium channels (2010, background): “Almost 800 human genes encode G protein coupled receptors (GPCRs) and over 30% of drugs on the market today target GPCRs.(21,22) GPCRs are characterized by seven transmembrane spanning alpha helices with extracellular N-and intracellular Figure 1.”
- The G protein-coupled receptor subset of the rat genome (2007, methodology): “The mouse Glutamate, Rhodopsin (non-ORs), Adhesion, Frizzled and Secretin GPCRs are not included in these trees since they have been described before in relation to the human repertoires [21], and the exact orthologous and paralogous relationships are viewed in a table listing the receptors in the t”
- PRESTO-TANGO: an open-source resource for interrogation of the druggable human GPCR-ome (2015, neutral): “Approximately one-third of the nonolfactory GPCRs in the human genome are orphan GPCRs, whose endogenous or natural ligands are unknown 2–4 , whereas many more have been inadequately interrogated with respect to their ligands.”