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18篇 您的检索式:作者名="Wellendorph"
    题名 作者 年代 出处 被引量
1Molecular phar- macology of promiscuous seven transmembranc receptors sensing organic nutrients显示文摘Wellendorph P Johansen LD Brauncr-Osbome H 2009Mol Pharmacol2009,75,3:1
2Structure,phar-macology and therapeutic prospects of family C G-protein coupled re-ceptors显示文摘Brauner-Osborne H Wellendorph P Jensen AA 2007Curr Drug Targets2007,8,1:1
3The emerging role of promiscuous 7TM receptors as chemosensors for food intake 显示文摘WELLENDORPH P JOHANSEN L D BRAUNER- OSBORNE H 2010Vitam Horm2010,84,:1
4The rat GPRC6A: cloning and character- ization 显示文摘WELLENDORPH P BURHENNE N CHRISTIANS- EN B 2007Gene2007,396,:1
5The GPCR , class C , group 6, subtype A ( GPRC6A ) receptor: from cloning to physiological function显示文摘C Clemmensen S Smajilovic P Wellendorph H Br?uner‐Osborne 2014Br J Pharmacol2014,,5:1
6Molecular cloning and pharmacology of functionally distinct isoforms of the human histamine H(3) receptor 显示文摘Wellendorph P Goodman M W Burstein E S 2002Neuropharmacolo- gy2002,42,7:1
7Structure, pharmacology and therapeutic prospects of family C O-protein coupled roceptors显示文摘Brauner O I-I Wellendorph P Jensen A A 2007Curt Drug Targets2007,,:1
8Structure, pharmacology and therapeutic prospects of family C G-protein coupled receptors显示文摘Brauner-Osbome H Wellendorph P Jensen AA 2007Curr Drug Targets2007,1,8:1
9Deorphanization of GPRC6A: a promiscuous L-alpha-amino acid recep- tor with preference for basic amino acids显示文摘WELLENDORPH P HANSEN K B BALSGAARD A 2005Mol Pharmacol2005,67,:1
10Structure, pharmacology and therapeutic prospects of family C G-protein coupled receptors显示文摘Brauner-Osbome H Wellendorph P Jensen AA 2007Curr Drug Targets2007,8,1:1
11The G protein?coupled receptor, class C, group 6, subtype A (GPRC6A) receptor: From cloning to physiological function显示文摘Clemmensen C Smajilovic S Wellendorph P 2014BrJ Pharmacol2014,171,5:1
12The emerging role of proriscuous 7TM receptors as chemosensors for food intake显示文摘Wellendorph P Johansen L D Brǎuner-Osborne H 0,,:1
13Deorphanization of GPRC6A: a promiscuous Lvalpha-amino acid receptor with preference for basic amino acids显示文摘Wellendorph P Hansen KB Balsgaard A 2005Mol Pharmacol2005,67,3:1
14Pharmacological characterization of mouse GPRC6A, an L-alpha-amino-acid receptor modulated by divalent cations显示文摘Christiansen B Hansen KB Wellendorph P 2007BrJ Pharmacol2007,150,6:1
15Structure, pharmacology and therapeutic prospects of family C G-protein coupled receptors显示文摘Brauner-Osborne H Wellendorph P Jensen A A 2007Curr Drug Targets2007,8,1:1
16Molecular cloning,expression,and sequence analysis of GPRC6A,a novel family C G-protein-coupled receptor显示文摘Wellendorph P Br(a)uner-Osborne H 0,,:1
17Deorphanization of GPRC6A:a promiscuous L-alpha-amino acid receptor with preference for basic amino acids显示文摘Wellendorph P Hansen KB Balsgaard A 0,,03:1
18Molecular pharmacology of promiscuous 7 TM receptors sensing organic nutrients 显示文摘Wellendorph P Johansen L D Brauner-Osborne H 2009Mol Phannacol2009,76,3:1
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