ライフサイエンスコーパス: adrenal medulla

1 n the ovary; and (j) adrenal cortex (but not adrenal medulla).

2 pathetic and enteric nervous systems and the adrenal medulla.

3 tory effect of epinephrine secreted from the adrenal medulla.

4 ats, we surgically removed or denervated the adrenal medulla.

5 , and in presumptive chromaffin cells of the adrenal medulla.

6 and in the cytosol in chromaffin cells from adrenal medulla.

7 ia provokes catecholamine secretion from the adrenal medulla.

8 RH-like immunopositive neurons innervate the adrenal medulla.

9 traversed the adrenal cortex and reached the adrenal medulla.

10 ivity after fluorogold injection to the left adrenal medulla.

11 e hypothalamus, the median eminence, and the adrenal medulla.

12 f the sympathetic nervous system, brain, and adrenal medulla.

13 ent proteins of anterior pituitary gland and adrenal medulla.

14 e coexpressed in all chromaffin cells of the adrenal medulla.

15 inducing the release of epinephrine from the adrenal medulla.

16 creted with catecholamines from cells of the adrenal medulla.

17 ivity is clearly present in the adult bovine adrenal medulla.

18 pardized by physiologic uptake by the normal adrenal medulla.

19 leading to the production of dopamine in the adrenal medulla.

20 parasympathetic ganglia, as well as from the adrenal medulla.

21 f dorsal root or sympathetic ganglia, or the adrenal medulla.

22 ed in neurosecretory chromaffin cells of the adrenal medulla.

23 evated sympathetic activity to stimulate the adrenal medulla.

24 e (TH) protein and enzymatic activity in the adrenal medulla.

25 cognition, and affect to the function of the adrenal medulla.

26 tioxidants reversed the effect of CIH on the adrenal medulla.

27 f clock gene expression in heart, spleen, or adrenal medulla.

28 ks in the cerebral cortex have access to the adrenal medulla.

29 correlated with the amount of CgA present in adrenal medulla.

30 and decreased AT(2) receptor binding in the adrenal medulla.

31 tions with a major sympathetic effector, the adrenal medulla.

32 ns involving the carotid chemoreflex and the adrenal medulla.

33 r mediating catecholamine secretion from the adrenal medulla.

34 sias of neural crest origin arising from the adrenal medulla.

35 transmitter release from SPN innervating the adrenal medulla.

36 uced or abolished in the PVH, but not in the adrenal medulla.

37 aventricular nucleus of the hypothalamus and adrenal medulla.

38 a childhood tumor in sympathetic ganglia and adrenal medulla.

39 he normal development and functioning of the adrenal medulla.

40 y that is found in the brain, platelets, and adrenal medulla.

41 hed in chromaffin granule membranes from the adrenal medulla.

42 e retrograde tracer Fluorogold into the left adrenal medulla 3 days prior to sacrifice resulted in th

43 avioral and cellular experiments that bovine adrenal medulla 8-22 peptide (BAM8-22), a proteolyticall

44 on PC12 cells, which were obtained from the adrenal medulla, a neural crest derivative.

45 kidney, spleen, heart, skeletal muscle, and adrenal medulla after 3 d or 11 weeks of exposure to con

46 ained period of time (at least 1 day) in the adrenal medulla after chronic nicotine administration.

47 Chromaffin cells of the adrenal medulla (AM) represent the main neuroendocrine a

48 tral ventrolateral medulla as well as in the adrenal medulla (AM), a major end organ of the sympathet

49 ve oxygen species (ROS) levels in the CB and adrenal medulla (AM).

50 ulation of neuroblasts that migrate into the adrenal medulla analog following organogenesis.

51 Fos immunoreactivity (ir) in adrenal medulla and brain sites involved in these respon

52 t severe form also have abnormalities of the adrenal medulla and epinephrine deficiency.

53 the follicular cells of the thyroid and the adrenal medulla and expressed at lower levels in brain,

54 a subset of chromaffin cells within the rat adrenal medulla and in a subset of cells coexpressing al

55 ious sympathetic ganglia, enteric plexus and adrenal medulla and in somata of the sensory ganglia imp

56 TSPO expression in the adrenal medulla and increased epinephrine production wer

57 NB develops in sympathetic ganglia and adrenal medulla and is elicited by forced Lin28B express

58 R activation induced c-fos expression in the adrenal medulla and neurons in autonomic control sites i

59 flight response, epinephrine released by the adrenal medulla and norepinephrine released from sympath

60 Chromaffin cells of the adrenal medulla and PC12 cells contained both P2X1- and

61 ndant in chromaffin cells that reside in the adrenal medulla and respond to cholinergic stimulation b

62 ndent on a hormonal signal released from the adrenal medulla and suggest a novel mechanism of sensiti

63 th catecholamines from secretory vesicles in adrenal medulla and sympathetic axons.

64 e adrenal cortex and catecholamines from the adrenal medulla and sympathetic nerves.

65 s from catecholamine storage vesicles of the adrenal medulla and sympathetic neurons.

66 ediated by transcriptional mechanisms in the adrenal medulla and the locus coeruleus.

67 ter function between chromaffin cells in the adrenal medulla and those maintained in primary culture

68 induces hypoxic sensitivity in the adult rat adrenal medulla and, if so, by what mechanism(s).

69 and sympathetic autonomic ganglia and in the adrenal medulla and, therefore, markedly impairs autonom

70 asal and induced Penk gene expression in rat adrenal (medulla) and striatum.

71 but scantily in adult tissues except brain, adrenal medulla, and atretic ovary.

72 l for oxygen sensing by the carotid body and adrenal medulla, and for their control of cardio-respira

73 for hypoxic sensing by the carotid body and adrenal medulla, and is required for maintenance of card

74 ce develop carcinoma in the thymus, stomach, adrenal medulla, and mammary gland but not in other orga

75 us system, autonomic nervous system, retina, adrenal medulla, and PC12 cells.

76 try in several tissues, including the brain, adrenal medulla, and pituitary.

77 Chromaffin cells of the adrenal medulla are a primary neuroendocrine output of t

78 Chromaffin cells of the adrenal medulla are innervated by the sympathetic nervou

79 ibility that PACAP-IR fibers observed in the adrenal medulla are primarily sensory in origin.

80 epleted in CIPA, but chromaffin cells of the adrenal medulla are spared.

81 id body and catecholamine secretion from the adrenal medulla are the principal mechanisms for maintai

82 e more posterior sympathetic ganglia and the adrenal medulla are unaffected.

83 strate that Postn-Cre ablates Hand2 from the adrenal medulla as well as the sphenopalatine ganglia of

84 component for neuroendocrine function in the adrenal medulla, as it may represent an additional lever

85 2DG-induced Fos-ir was abolished in the adrenal medulla but not in the PVH.

86 irway smooth muscle, cardiac Purkinje cells, adrenal medulla cells, peripheral blood leukocytes, and

87 TH promoter activity in TH-expressing bovine adrenal medulla chromaffin (BAMC) cells and inhibits pro

88 and (Met)enkephalin in secretory vesicles of adrenal medulla (chromaffin granules).

89 ggest that hypoxia-evoked CA efflux from the adrenal medulla contributes, in part, to elevated blood

90 n and transcription factors Egr-1 and Sp1 in adrenal medulla-derived PC12 cells.

91 uromas, but displayed ganglioneuromas of the adrenal medulla, enlargement of the associated sympathet

92 Chromaffin cells of the adrenal medulla express NF subunits under culture condit

93 lymerase chain reaction experiments of human adrenal medulla gland and of cultured human adrenal chro

94 es in both the structure and function of the adrenal medulla have been shown in patients with classic

95 the kidney and adrenal medulla in male rats, adrenal medulla in female rats, hematopoietic system in

96 related neoplasms occurred in the kidney and adrenal medulla in male rats, adrenal medulla in female

97 his mechanism intrinsic hypo- or hyperactive adrenal medullas in some individuals may shape opposite

98 n neonates, catecholamine secretion from the adrenal medulla is critical for maintaining homeostasis

99 adrenaline (epinephrine) secretion from the adrenal medulla is markedly reduced with age.

100 duced catecholamine secretion in the newborn adrenal medulla is mediated by reversible inhibition of

101 n processing enzyme in secretory vesicles of adrenal medulla (known as chromaffin granules).

102 Catecholamine release from the adrenal medulla likely contributes to this response.

103 novel sites: the neuroendocrine cells of the adrenal medulla, megakaryocytes, and platelets.

104 o AT(1) and AT(2) receptors in rat liver and adrenal medulla membranes, respectively, and competed wi

105 holinergic innervation and morphology of the adrenal medulla, normal adrenal catecholamine and blood

106 hology and the accumulation of PrP(d) in the adrenal medulla of scrapie affected sheep using light an

107 d chromaffin) and fibers was robust in fetal adrenal medulla of sheep while nonexistent in baboons.

108 eports that while NF-L may be lacking in the adrenal medulla of some species, NF-L immunoreactivity i

109 ells derived by enzymatic digestion from the adrenal medulla of the bovine adrenal gland.

110 rine cells and tumors including those of the adrenal medulla, parathyroid, and pancreatic islets.

111 neurons, and epinephrine, released from the adrenal medulla, participate in a number of physiologica

112 15 amino acid C-terminal fragment of bovine adrenal medulla peptide 22), a peptide agonist derived f

113 gesic effect of intrathecally applied bovine adrenal medulla peptide 8-22 (BAM 8-22), an MrgprC11 ago

114 Spinal application of bovine adrenal medulla peptide 8-22 also significantly attenuat

115 ECE-2 processes proenkephalin-derived bovine adrenal medulla peptides, and this processing leads to p

116 shown that catecholamine secretion from the adrenal medulla plays a critical role in chronic intermi

117 dial wall cortical regions projecting to the adrenal medulla, positively correlated with increases in

118 Neuroendocrine chromaffin granules of adrenal medulla represent regulated secretory vesicles t

119 ectors of the sympathetic nervous system and adrenal medulla, respectively, are thought to control ad

120 Analysis of germline VGF-knockout mouse adrenal medulla revealed decreased LDCV size in noradren

121 expression levels of such antigens in normal adrenal medulla samples and in adrenomedullary tumors.

122 fter vagotomy, additional denervation of the adrenal medulla significantly reversed these effects ove

123 ted by single and repeated stress in the rat adrenal medulla, suggesting distinct roles in establishi

124 e of chromaffin granules (CG) present in the adrenal medulla, supporting the biosynthesis of norepine

125 rant in peripheral tissues such as blood and adrenal medulla that can be implicated in Alzheimer's di

126 ands, including the epinephrine cells of the adrenal medulla, the posterior pituitary, and the pineal

127 otine injection; however, in contrast to the adrenal medulla, there is no sustained transcriptional r

128 erentiate into chromaffin cells in the adult adrenal medulla, they no longer express Kuz.

129 s found in cytosolic fractions of the bovine adrenal medulla to bind to an immobilized annexin in a C

130 indicating that the response of the newborn adrenal medulla to hypoxia is an intrinsic property of t

131 Stress stimulates the adrenal medulla to rapidly secrete catecholamines (CAs),

132 ently mutated, and also affected thyroid and adrenal medulla tumors and intestinal polyps.

133 CIH induces hypoxic sensing in the adult rat adrenal medulla via mechanisms involving increased gener

134 of the hypothalamic-pituitary axis with the adrenal medulla via mediators of the unspecific immune s

135 Sympathetic ganglion and adrenal medulla volume and the expression level of Let-7

136 ilateral adrenalectomy, the formation of the adrenal medulla was incomplete, and electron-microscopic

137 ile neuroblastoma is often RD3-positive, the adrenal medulla, where many neuroblastomas originate, is

138 ilities to metastasize to the bone, lung, or adrenal medulla, which suggests that metastases to diffe

139 ve oxygen species (ROS) levels in the CB and adrenal medulla, which were a result of DNA methylation-

140 the thyroid and parathyroid glands, and the adrenal medulla within the first 3 months of postnatal d