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1 HOD6 cells, which constitutively express the PRL receptor.
2 referentially binds to the short form of the PRL receptor.
3 determined that PLP-J does not interact with PRL receptors.
4 r biological effects by interacting with the PRL receptor, a Janus kinase (JAK)2-coupled cytokine rec
12 ons, one of which is a paucity of functional PRL receptors, and that murine Stat5 overexpression is a
13 hether interruption of this growth loop by a PRL receptor antagonist, an S179D mutant PRL, could inhi
15 a rat ovarian-specific phosphoprotein, PRAP (PRL Receptor Associated Protein), which has no significa
17 d genes, we now report that costimulation of PRL receptors did not interfere with IFN alpha/beta sign
19 ith either the long or the short form of the PRL receptor, fusion proteins with glutathione S-transfe
21 We show dramatically increased expression of PRL receptor in ovarian and endometrial tumors as well a
25 ifying DAergic neuron populations expressing PRL receptor (PRL-R); (2) to describe the effect of ovar
27 novel fusion protein was able to bind to the PRL receptor (PRLR) on T-47D human breast cancer cells a
29 eport that in prolactin (PRL)-treated cells, PRL receptor (PRLR) undergoes cytoplasmic loop dimerizat
31 logous expression system and TG neurons from PRL receptor (PRLR)-null mutant mice by expressing rat P
33 The intracellular domain of the prolactin (PRL) receptor (PRLr) is required for PRL-induced signali
34 ed in hyperosmotic media, the expressions of Prl receptors, prlr1 and prlr2, and the stretch-activate
36 stimulates hypothalamic dopamine neurons via PRL receptors (PRLRs) in a short-loop feedback circuit.
38 the PRL family (e.g., PLP-A does not use the PRL receptor) produced by trophoblast cells of the chori
42 ment with S179D PRL, expression of the short PRL receptor was doubled, and signaling showed a greater
43 smic domain of the long or short form of the PRL receptor were produced, purified, and incubated with
44 y and is preferentially bound by the lamprey PRL receptor, whereas lamprey GH is preferentially bound
45 of transcription 5a (STAT5a) and prolactin (PRL) receptor, which is essential for PRL-provoked STAT5