ライフサイエンスコーパス: cistern

1 other neoplasm of the cerebellopontine angle cistern.

2 al fluid-filled cerebellopontine angle (CPA) cistern.

3 by injection of blood into the prechiasmatic cistern.

4 d involving bilateral cerebellopontine angle cisterns.

5 in surface into sulci and outlines the basal cisterns.

6 Pases most likely present in nearby synaptic cisterns.

7 the skull - 0.086-0.150; index of prepontine cistern - 0.034-0.067; index of interhemispheric fissure

8 m a recreational lake, a groundwater well, a cistern, a farm pond, and drinking water.

9 tion of FH(R127H) provoked enlargement of ER cisterns after treatment with IFN-gamma.

10 cerebrospinal fluid (CSF) cerebellomedullary cistern allows the withdrawal of sufficient volumes of C

11 Targeting both the CPA cistern and CM in sheep, we employed a lumbar spine-inse

12 light reflex, CT findings (compressed basal cistern and midline shift >=5 mm), presence of hypoxia,

13 an that of the cytoplasmic space between the cistern and the plasma membrane.

14 on of neutrophils associated with the venous cisterns and collecting venules.

15 cluding a basal lamina, caveolae, subsurface cisterns and dense bodies.

16 nce" of 350 nm around the ribbon, with fewer cisterns and many more synaptic vesicles.

17 phosphate-gated calcium stores of subsurface cisterns and mitochondria.

18 nt increase in surface area of intracellular cisterns and plasmalemmal infoldings.

19 i.e., terminals associated with postsynaptic cisterns and rough endoplasmic reticulum) were smaller a

20 ort through cerebrospinal fluid to the basal cisterns and subsequent invasion of the basilar arteries

21 reased CSF signal intensity within the basal cisterns and sulci over the cerebral convexities.

22 ium sequestration into, and release from, ER cisterns and the role that this plays in the generation

23 differ in their regulation by intracellular cisterns and/or organelles, suggesting the existence of

24 tion of these two Ca(2+) sources by synaptic cisterns and/or organelles, which could result crucial f

25 he ER membrane system, including the nuclear cistern, and following addition of the chromophore coele

26 nd P-selectin; this class of vessels (venous cisterns) appears to be a unique feature in heart.

27 ) synapses with a near membrane postsynaptic cistern are found on motor neurons and other central neu

28 fissures overly the retinal vessels; and (3) cisterns are continuous with prevascular fissures.

29 the midline or in the cerebellopontine angle cistern area.

30 we analyzed the distribution of vesicles and cisterns around ribbons from serial sections of inner ha

31 Cisterns became more prevalent over the course of the fi

32 sed a long, narrow cleft, with a subsynaptic cistern comparable to previous descriptions of C-type bo

33 ing protocol included high spatial and nerve-cistern contrast resolution imaging acquisitions of the

34 e hypothesized that drug delivery to the CPA cistern could yield widespread CNS distribution.

35 s the ratio of the maximum diameter sum of 3 cisterns divided by the maximum diameter of the skull at

36 he postsynaptic cistern, the distance of the cistern from the plasma membrane, and the average width

37 er stimulation an active subpopulation of ER cisterns had accumulated more Ca than had mitochondria d

38 A near-membrane postsynaptic cistern has been proposed to serve as a store from which

39 s show that the stored water in polyethylene cisterns in the Brazilian semiarid region does not prese

40 stimulation the Ca content of responsive ER cisterns increased as much as 20-fold.

41 odistribution of scAAV9-CB-GFP following CPA cistern infusion with previously reported cisterna magna

42 In vivo, a prechiasmatic cistern injection model was established in rats and mice

43 Hydrocephalus was induced by a single basal cistern injection of kaolin in 3-week-old rats, immediat

44 Animals underwent a basilar cistern inoculation of group B Streptococci to induce me

45 to the sum of the maximum diameter of three cisterns (insular cistern, longitudinal cerebral fissure

46 labeled efferent axons included subsynaptic cisterns, irregularly sized vesicles, and synaptic bodie

47 that formation of new synaptic vesicles from cisterns is rate limiting in the vesicle cycle.

48 maximum diameter of three cisterns (insular cistern, longitudinal cerebral fissure and cerebral sulc

49 The postsynaptic cistern may play an essential role in calcium homeostasi

50 ic reticulum of muscle, the "synaptoplasmic" cistern of the hair cell efficiently couples synaptic in

51 lectron micrographs showed that postsynaptic cisterns of BKalpha(-/-) OHCs were smaller than those of

52 of lipid droplets (LD), distance between the cisterns of rough endoplasmic reticulum (RER), mitochond

53 Calcium sequestration by cisterns of this subset of ER was graded, reversible, an

54 The synaptic cisterns of wild-type OHCs were closely aligned (14-nm s

55 tion of the lesions composed of fluid-filled cisterns or channels.

56 lly or completely disappeared in the basilar cisterns (P <.001) and cerebral sulcal subarachnoid spac

57 nted with significantly more effaced basilar cisterns (p = 0.0008).

58 zation that specific subsets of dendritic ER cisterns provide spatial and temporal microheterogeneity

59 en somatic plasma membrane and hypolemmal ER cisterns provides a unique mechanism for rapid control o

60 cisternal organelle, a peculiar stack of ER cisterns resembling the spine apparatus and found at axo

61 l cells is sufficient to generate stacked ER cisterns resembling the spine apparatus.

62 Active ER cisterns retained their Ca load much longer (>3 min) tha

63 e of the skull - 0.173-0.255; index of basal cistern sagittal dimension to the size of the skull - 0.

64 Taken together, these data suggest that the cistern serves as a sink or buffer to isolate synaptic c

65 supporting the hypothesis that the synaptic cistern serves primarily as a calcium barrier and sink d

66 hannels may transit through the postsynaptic cistern, since ryanodine and sarcoendoplasmic reticulum

67 rcentage (2-8%) of synapses had a subsurface cistern situated below the axon terminal (C type).

68 m and maximum for all groups: index of basal cistern size to the size of the skull - 0.129-0.197; ind

69 Hypolemmal cisterns such as that at the efferent synapse of the hai

70 There were 16 subjects with SANCC (basilar cistern, sylvian fissure, and/or spinal involvement) dur

71 Animals underwent a basilar cistern tap receiving either sterile saline as a placebo

72 lling is constrained by a thin near-membrane cistern that is co-extensive with the efferent terminal

73 It consists of stacks of ER cisterns that are interconnected by an unknown dense mat

74 -walled (approximately 5 micrometers) venous cisterns that average 200 micrometers in length and vary

75 reticulum (cER) is a network of tubules and cisterns that lie in close apposition to the plasma memb

76 e subarachnoid space (particularly the basal cisterns) that mediate CSF-parenchymal interactions invo

77 s, the appositional area of the postsynaptic cistern, the distance of the cistern from the plasma mem

78 pically apposed by well-defined postsynaptic cisterns, thus acquiring distinctive profiles.

79 raphic relationship of vitreous fissures and cisterns to the underlying vasculature of the posterior

80 e of the skull - 0.129-0.197; index of basal cistern transverse dimension to the size of the skull -

81 The optimal threshold of basal cistern volume for predicting high ICP ([Formula: see te

82 Basal cistern volume was found to correlate significantly with

83 Radiological biomarkers of TBI (basal cistern volume, ventricular volume, volume of extra-axia

84 Synaptic cisterns were present, but smaller than those of wild-ty

85 e regions adjacent to the basal subarachnoid cisterns where blood and oxyhemoglobin concentrations we

86 vian fissure - 0.036-0.085; index of insular cistern width - 0.020-0.074; index of subarachnoid space

87 Cisterns within these stacks are molecularly distinct fr