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LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00003511naa a2200673 4500
001oai:DiVA.org:uu-238747
003SwePub
008141216s2014 | |||||||||||000 ||eng|
024a https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-2387472 URI
024a https://doi.org/10.1111/nyas.125802 DOI
040 a (SwePub)uu
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Liebscher, Ines4 aut
2451 0a New functions and signaling mechanisms for the class of adhesion G protein-coupled receptors
264 c 2014-11-25
264 1b Wiley,c 2014
338 a print2 rdacarrier
520 a The class of adhesion G protein-coupled receptors (aGPCRs), with 33 human homologs, is the second largest family of GPCRs. In addition to a seven-transmembrane α-helix-a structural feature of all GPCRs-the class of aGPCRs is characterized by the presence of a large N-terminal extracellular region. In addition, all aGPCRs but one (GPR123) contain a GPCR autoproteolysis-inducing (GAIN) domain that mediates autoproteolytic cleavage at the GPCR autoproteolysis site motif to generate N- and a C-terminal fragments (NTF and CTF, respectively) during protein maturation. Subsequently, the NTF and CTF are associated noncovalently as a heterodimer at the plasma membrane. While the biological function of the GAIN domain-mediated autocleavage is not fully understood, mounting evidence suggests that the NTF and CTF possess distinct biological activities in addition to their function as a receptor unit. We discuss recent advances in understanding the biological functions, signaling mechanisms, and disease associations of the aGPCRs.
650 7a MEDICIN OCH HÄLSOVETENSKAPx Medicinska och farmaceutiska grundvetenskaperx Neurovetenskaper0 (SwePub)301052 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Basic Medicinex Neurosciences0 (SwePub)301052 hsv//eng
700a Ackley, Brian4 aut
700a Araç, Demet4 aut
700a Ariestanti, Donna M4 aut
700a Aust, Gabriela4 aut
700a Bae, Byoung-Il4 aut
700a Bista, Bigyan R4 aut
700a Bridges, James P4 aut
700a Duman, Joseph G4 aut
700a Engel, Felix B4 aut
700a Giera, Stefanie4 aut
700a Goffinet, André M4 aut
700a Hall, Randy A4 aut
700a Hamann, Jörg4 aut
700a Hartmann, Nicole4 aut
700a Lin, Hsi-Hsien4 aut
700a Liu, Mingyao4 aut
700a Luo, Rong4 aut
700a Mogha, Amit4 aut
700a Monk, Kelly R4 aut
700a Peeters, Miriam C4 aut
700a Prömel, Simone4 aut
700a Ressl, Susanne4 aut
700a Schiöth, Helgi Bu Uppsala universitet,Funktionell farmakologi4 aut0 (Swepub:uu)helgschi
700a Sigoillot, Séverine M4 aut
700a Song, Helen4 aut
700a Talbot, William S4 aut
700a Tall, Gregory G4 aut
700a White, James P4 aut
700a Wolfrum, Uwe4 aut
700a Xu, Lei4 aut
700a Piao, Xianhua4 aut
710a Uppsala universitetb Funktionell farmakologi4 org
773t Annals of the New York Academy of Sciencesd : Wileyg 1333, s. 43-64q 1333<43-64x 0077-8923x 1749-6632
856u https://europepmc.org/articles/pmc4278406?pdf=render
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-238747
8564 8u https://doi.org/10.1111/nyas.12580

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