ライフサイエンスコーパス: sympathetic ganglion

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1 own regarding the cellular complexity in the sympathetic ganglion.

2 rabies virus, was injected into the stellate sympathetic ganglion.

3 F to intact neurons in the superior cervical sympathetic ganglion.

4 orsal root ganglia and the superior cervical sympathetic ganglion.

5 Sympathetic ganglion and adrenal medulla volume and the

6 Measurements on sympathetic ganglion cells in these mice showed that who

7 be mediated, in part, by a greater number of sympathetic ganglion cells innervating BAT in cold-reare

8 e interscapular BAT (IBAT) and the number of sympathetic ganglion cells projecting to interscapular B

9 d-patch recordings from dissociated bullfrog sympathetic ganglion cells.

10 ot ganglion cultures was only 20% of that in sympathetic ganglion cultures.

11 can promote and attract axonal growth of the sympathetic ganglion in vitro.

12 udies suggests that the increases in DRG and sympathetic ganglion neuronal cell number are due wholly

13 ced oscillations of cytosolic [Ca2+] in frog sympathetic ganglion neurones in 2.0 mM K+ Ringer soluti

14 a indicate that P2X receptors on sensory and sympathetic ganglion neurones involve almost exclusively

15 stem within sensory dorsal root ganglion and sympathetic ganglion neurons and their small diameter pe

16 ly expressed within dorsal root ganglion and sympathetic ganglion neurons and their small-diameter pe

17 enous REEP1 was confirmed in cultured murine sympathetic ganglion neurons by RT-PCR and immunofluores

18 esting that differentiation of noradrenergic sympathetic ganglion neurons depends upon both canonical

19 Frog sympathetic ganglion neurons exhibit a novel Ca2+ uptake

20 , close to impulse trigger zones) and within sympathetic ganglion neurons explains why patients exper

21 on or expression of G beta gamma subunits in sympathetic ganglion neurons induces facilitation and oc

22 el activity evoked by muscarinic agonists in sympathetic ganglion neurons is completely lost in m1 mu

23 ved for the two forms of DMT1 in cultures of sympathetic ganglion neurons isolated from perinatal rat

24 nsion may be due primarily to involvement of sympathetic ganglion neurons rather than ventrolateral m

25 rite outgrowth from dorsal root ganglion and sympathetic ganglion neurons, but it was not effective f

26 Similar results were obtained with chick sympathetic ganglion neurons, though regulation of recep

27 syndrome, erythermalgia, within sensory and sympathetic ganglion neurons, two cell types where Nav1.

28 duce detectable changes in the properties of sympathetic ganglion neurons, while I739V, from patients

29 ressed within dorsal root ganglion (DRG) and sympathetic ganglion neurons.

30 ession in neural crest-derived noradrenergic sympathetic ganglion neurons.

31 he heart, cardiac cushion, and noradrenergic sympathetic ganglion neurons.

32 t nociceptive dorsal root ganglia (DRGs) and sympathetic ganglion neurons.

33 expressed in dorsal root ganglion (DRG) and sympathetic ganglion neurons.

34 (ER) contributes to Ca2+ transients in frog sympathetic ganglion neurons.

35 Ca2+ signals by single action potentials in sympathetic ganglion neurons.

36 on, has a profound effect on excitability of sympathetic ganglion neurons.

37 sed in nocioceptive dorsal root ganglion and sympathetic ganglion neurons.

38 tic precursor cells aggregate to form normal sympathetic ganglion primordia characterized by the expr

39 The timing of dHAND expression in sympathetic ganglion primordia, together with the induct

40 Neurons in the adult rat superior cervical sympathetic ganglion (SCG) dramatically increase their c

41 trkA and p75 mRNAs in the superior cervical sympathetic ganglion (SCG) of NT3-/- mouse embryos incre

42 stem aging using the mouse superior cervical sympathetic ganglion (SCG) which is characterized by the

43 ering at cholinergic synapses in a mammalian sympathetic ganglion, the superior cervical ganglion (SC

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