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1 sed to assemble disulfide cross-linked human choriogonadotropin analogs that contain an additional al
4 ults are presented for bovine serum albumin, choriogonadotropin, glyceraldehyde-3-phosphate dehydroge
5 ated in regulating specificity between human choriogonadotropin (hCG) and human follicle-stimulating
9 amino acid residues of rat LH/CG-R in human choriogonadotropin (hCG) binding and hCG-mediated cAMP p
11 fforts to identify the manner in which human choriogonadotropin (hCG) contacts lutropin receptors (LH
13 in-coupled receptor which binds either human choriogonadotropin (hCG) or lutropin (luteinizing hormon
14 the region interacts with the hormone, human choriogonadotropin (hCG) was photoaffinity-labeled with
17 n receptor (rLHR) internalize agonist (human choriogonadotropin, hCG) at a rate that is about 1 order
18 expected finding that most assembly of human choriogonadotropin, human follitropin, and human thyrotr
20 n desensitization of the luteinizing hormone/choriogonadotropin (LH/CG) receptor, independent of rece
23 ive but unphosphorylated luteinizing hormone/choriogonadotropin receptor (LH/CG R) in ovarian follicl
24 t desensitization of the luteinizing hormone/choriogonadotropin receptor (LH/CG R) is GTP-dependent,
28 partial agonist for the luteinizing hormone/choriogonadotropin receptor (LHCGR) and the closely rela
29 teinizing hormone (LH) acting through the LH/choriogonadotropin receptor (LHCGR) to stimulate androge
30 the same active conformation of the lutropin/choriogonadotropin receptor (LHR) is involved in the sti
32 sing the C-terminal tail of the rat lutropin/choriogonadotropin receptor (rLHR) as "bait" in a yeast
33 293 cells transfected with the rat lutropin/choriogonadotropin receptor (rLHR) internalize agonist (
36 -induced phosphorylation of the rat lutropin/choriogonadotropin receptor (rLHR) to a locus of four se
37 me 2p21, adjacent to the luteinizing hormone/choriogonadotropin receptor gene (LHCGR; 2p21), telomeri
42 he roles of the five TM Pros of the lutropin/choriogonadotropin receptor, these residues were individ
43 uences of the human (h) and rat (r) lutropin/choriogonadotropin receptors (LHR) are 87% identical, bu
45 on SDS gels, is increased further upon human choriogonadotropin treatment of the stably transfected c
46 rease in cAMP accumulation elicited by human choriogonadotropin was reduced in cells transfected with
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