ライフサイエンスコーパス: pinealocyte

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1 issue specificity to cone photoreceptors and pinealocytes.

2 rcadian clock and regulates transcription in pinealocytes.

3 /A)-AR-linked ROS-GC1 transduction system in pinealocytes.

4 expressed exclusively by photoreceptors and pinealocytes.

5 may function as a copper transporter in rat pinealocytes.

6 predominantly in retinal photoreceptors and pinealocytes.

7 xpressed predominantly in photoreceptors and pinealocytes.

8 e midbrain and forebrain, including numerous pinealocytes.

9 st increased melatonin synthesis in neonatal pinealocytes.

10 ay are expressed in the majority of neonatal pinealocytes, although the expression levels of many of

11 PINA is expressed in pinealocytes and a subset of photoreceptors in adult rat

12 VPAC(1) receptor-dependent cAMP efflux from pinealocytes but strongly inhibited GHRH-stimulated grow

13 unctions and connexins were observed between pinealocyte cell bodies, stromal cells, astrocytes, and

14 ng the potential for circadian regulation of pinealocyte electrical excitability and Ca(2+) signallin

15 Chick pinealocytes exhibit all the characteristics of a comple

16 Our basic hypothesis is that mammalian pinealocytes have cycling electrical excitability and Ca

17 It inhibits melatonin synthesis by pinealocytes in culture; it acts via predicted binding s

18 gRgr message was sparsely distributed among pinealocytes in follicles, but not within the follicles

19 Culturing rat pinealocytes in noradrenaline for 24 h induced a low-vol

20 photoreceptors of the retina and a subset of pinealocytes in the pineal gland.

21 e EGFP expression to cone photoreceptors and pinealocytes in transgenic Xenopus laevis; however, the

22 al role; however, unlike photoreceptors, the pinealocyte is devoid of the ROS-GC2/GCAP2 signal transd

23 -gated Ca(2+) channels (CaV channels) in rat pinealocytes is changed by culturing them in noradrenali

24 that ROS-GC1, in a separate subpopulation of pinealocytes, is associated with an opposite Ca(2+) sign

25 or block whole-cell currents in dissociated pinealocytes match closely their potencies and efficacie

26 photoreceptor cells of the retina and in the pinealocytes of the pineal gland.

27 the photoreceptors of the retina and in the pinealocytes of the pineal gland.

28 in the photoreceptors of the retina and the pinealocytes of the pineal gland.

29 stromal cells, astrocytes, and astrocyte and pinealocyte processes.

30 expressed specifically in photoreceptors and pinealocytes, regulate photoreceptor gene expression, ar

31 In certain pinealocytes, ROS-GC1 coexisted with its other Ca(2+) mo

32 In these pinealocytes, S100B was not present.

33 Thus, like photoreceptors, pinealocytes sense both positive and negative Ca(2+) sig

34 Cultured without NA, pinealocytes showed only non-inactivating L-type dihydro

35 of approximately 8000 genes within cultured pinealocytes subjected to both LD and DD.

36 observed similar pharmacological effects on pinealocyte synaptic ribbons.

37 stence of functionally different subtypes of pinealocytes that express varying combinations of photot

38 In addition, we observe in neonatal pinealocytes the expression of both rod-specific and con

39 lonRIgamma polypeptides are expressed in the pinealocyte, the melatonin-secreting cell of the pineal

40 pineal stalk, whereas GLT-1 is expressed by pinealocytes throughout the gland.

41 Both components coexist in pinealocytes where the signaling component alpha(2D/A)-A

42 riven expression was restricted to cones and pinealocytes, while the Prph2 promoter drove expression

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