ライフサイエンスコーパス: dura

1 ter trephination of the skull, to the intact dura.

2 r outer segments and the optic nerve pia and dura.

3 al surgical resection including the involved dura.

4 ul culture in scalp (all p<0.05), but not in dura.

5 pplication of retrograde tracer DiI onto the dura.

6 es placed on the surface of the skull or the dura.

7 ures, where they appeared to emerge from the dura.

8 inges differentiate into pia, arachnoid, and dura.

9 V had no visible radiographic crestal lamina dura.

10 nociceptors that innervate the intracranial dura.

11 receptor antagonist RP 67580 (n = 12) in the dura (1.04 +/- 0.11, P = 0.002) and retina (1.08 +/- 0.0

12 The parietal dura above the middle meningeal artery was stimulated th

13 esponse is mediated by direct actions on the dura and does not develop secondary to events within the

14 roved to received convergent inputs from the dura and facial skin.

15 The structural organization of the dura and leptomeninges is reflected in its magnetic reso

16 1 breeding populations generated by crossing Dura and Pisifera individuals.

17 tiated MAS and large-scale planting of elite dura and pisifera parents to generate the new commercial

18 ated side) in vehicle-treated animals in the dura and retina was 1.60 +/- 0.11 and 1.76 +/- 0.18, res

19 e knowledge that the roots are surrounded by dura and root level blocks are done just outside the dur

20 t result from neurogenic inflammation of the dura and subsequent sensitization of dural afferents.

21 horn, which responded to stimulation of the dura and the GON.

22 ive convergent input from the supratentorial dura and the GON.

23 the spinal cord and hindbrain, localized to dura and/or cartilage primordia.

24 iano, Maturana tinta, Schioppettino, Shiraz, Duras and Gamay.

25 at receive peripheral input from the cranial dura, and found a selective inhibition of high-threshold

26 depth to 2 mm, reestablishment of the lamina dura, and radiographical evidence of bone growth.

27 including those encased by cranial bones and dura, and those located in the subarachnoid space.

28 ing in patients, and multi-unit recording of dura- and light-sensitive thalamic neurons in rats to sh

29 higher osteoclast number, and greater lamina dura apposition width.

30 inct enhancement patterns are characterized: dura-arachnoid enhancement and pia-subarachnoid space en

31 The dura-arachnoid pattern consists of curvilinear enhanceme

32 of neurones show convergent input from both dura as well as cervical cutaneous and muscle territorie

33 er detail the axonal trajectories within the dura, as well as the axonal size distribution of the dur

34 atically for oil palm and is recommended for dura breeding programs.

35 ility and leakage of albumin not only in the dura but also in the retina.

36 ed to their activation from the intracranial dura but not facial skin or cornea.

37 Axons traversed large distances across the dura, but the majority of the branching and arborization

38 p2 and Bmp4 in preosteoblasts and periosteal dura causes skull and CV malformations, similar to human

39 proliferated more and grew more rapidly than dura cells [F (1, 46) = 12.94, p<0.008], both tissues co

40 that distribute peripherally, including the dura, cornea, and the sciatic nerve.

41 ses, we found that both postmortem scalp and dura could be successfully reprogrammed into iPSC lines.

42 a family derived from a Deli dura x Nigerian dura (Deli x Nigerian) with 112 individuals.

43 Inadvertent puncture of the dura did not occur.

44 The silicone-based implant e-dura embeds interconnects, electrodes, and chemotrodes t

45 The electronic dura mater, which we call e-dura, embeds interconnects, electrodes, and chemotrodes

46 uggesting that morphogens from the skull and dura establish optimal venous networks independent from

47 thods for implementing GS in an introgressed dura family derived from a Deli dura x Nigerian dura (De

48 acrine BMP signaling from preosteoblasts and dura, highlighting unique cellular interactions that inf

49 Results from preclinical applications of e-dura implants and clinical evidence.

50 s, and that brief noxious stimulation of the dura in conscious rats produced a transient suppression

51 electrode array was surgically placed on the dura (L1-S1 cord segments) in December 2009, to allow fo

52 The cell bodies and dendrites of such dura/light-sensitive neurons were apposed by axons origi

53 restraint stress also resulted in increased dura mast cell activation in C57BL mice, but not in NK-1

54 Acute stress by immobilization led to dura mast cell degranulation which was prevented by pret

55 timulation had been reported to activate rat dura mast cells and increase vascular permeability, effe

56 In this study, dura mast cells were shown to have characteristics of co

57 ted through estrogen receptors identified on dura mast cells.

58 nhibited plasma protein extravasation within dura mater after electrical trigeminal ganglion stimulat

59 Sclera, pericardium, dura mater and cornea are available as a patch graft.

60 lls in the most external connective tissues (dura mater and epineurium) versus electron-lucent cells

61 ating intracranial tissues, for example, the dura mater and large vessels, as well as their downstrea

62 dies that the intracranial blood vessels and dura mater are important pain-producing structures since

63 The large venous sinuses and dura mater are pain-sensitive and are innervated primari

64 involve neurogenic inflammation (NI) of the dura mater associated with the sensation of throbbing pa

65 e detected induction of interleukin 1beta in dura mater at 2 and 6 h and increased interleukin 6 in d

66 [inducible NOS (iNOS)] mRNA upregulation in dura mater beginning at 2 h and an increase in the corre

67 BMS cells, calvarial-derived osteoblasts and dura mater cells to heal critical-size mouse calvarial d

68 vanced Maillard reaction was investigated in dura mater collagen and lens proteins from dogs that wer

69 nerves or plexuses, which are surrounded by dura mater extending from the dura mater surrounding the

70 ation, and plasma protein leakage within the dura mater in part by a neurokinin-1-receptor mechanism.

71 The dura mater is a vascularized membrane surrounding the br

72 tion of nociceptive afferent C-fibres of the dura mater leads to a sensitization of second-order neur

73 cantly increased 99Tc-G extravasation in the dura mater of C57BL mice.

74 f mast cells, SP and its receptor (NK-1R) in dura mater of mice in response to acute stress.

75 finding of a lymphatic vessel network in the dura mater of the mouse brain.

76 ultimodal neural implants, termed electronic dura mater or e-dura, to fulfill this need.

77 We eliminate postulated roles for dura mater or skull base changes in craniosynostosis.

78 hat TGFbeta signaling within the CNC-derived dura mater provides essential inductive instruction for

79 cultures generated from 146 scalp and/or 53 dura mater samples from 146 postmortem human brain donor

80 ediscoveries of lymphatic vessels within the dura mater surrounding the brain, made possible by moder

81 surrounded by dura mater extending from the dura mater surrounding the spinal cord.

82 riggers NI and mast cell activation in mouse dura mater through the activation of NK-1 receptors.

83 or control solution were applied to the rat dura mater to elicit a presumed state of cephalic pain.

84 ceptive signals transmitted from the cranial dura mater to the brain, is uniquely exacerbated by expo

85 Involvement of dura mater was noted in another.

86 Trigeminal afferents of the supratentorial dura mater were activated by mustard oil (MO) and the re

87 Our study demonstrates that postmortem dura mater, and to a lesser extent, scalp, are viable so

88 ding the central retinal vessels, and in the dura mater, arachnoid, and pia mater of the meningeal sh

89 C severely impairs cell proliferation in the dura mater, consequently resulting in calvaria agenesis.

90 presents extracerebral tissue (scalp, skull, dura mater, subarachnoid space, etc.) and the bottom lay

91 al implants with the shape and elasticity of dura mater, the protective membrane of the brain and spi

92 The electronic dura mater, which we call e-dura, embeds interconnects,

93 ssion and delayed inflammation within rodent dura mater.

94 nd the consequences of its inhibition within dura mater.

95 ere observed outside the vasculature was the dura mater.

96 lbumin from postcapillary venules within the dura mater.

97 1.0mM was delivered through each cup on the dura mater.

98 in response to electrical stimulation of the dura mater.

99 mulation (ES) electrodes were secured to the dura matter at L2.

100 re used: CVX (cardiovascular), PDX (preclude dura membrane), and DLM (dual mesh plus).

101 myelinated axons in the nerves supplying the dura (nervus spinosus and tentorial nerves) could be cla

102 Local application to the dura of dibutyryl adenosine 3',5'-cyclic monophosphate (

103 375 ml) was injected (0.05 ml/min) under the dura of the right parietal cortex.

104 lammatory mediators (IM) were applied to the dura of unanesthetized rats via previously implanted can

105 entials recorded with an electrode placed on dura overlying the hindlimb somatosensory cortex.

106 yielding organs mesocarp and endosperm from Dura, Pisifera and Tenera.

107 isms of hybrids vigor (or heterosis) between Dura, Pisifera and their hybrid progeny Tenera has not y

108 in trigeminal ganglion cells innervating the dura, prominently characterized by increased labelling o

109 al properties and integrated modalities of e-dura provide future opportunities to treat or alleviate

110 er contusive spinal cord injury in which the dura remains intact.

111 Individual dura-sensitive neurons identified and characterized elec

112 ural tract tracing in the rat, we identified dura-sensitive neurons in the posterior thalamus whose a

113 The findings that individual dura-sensitive Po, LP, and LD neurons project to many fu

114 tinal pathway that modulates the activity of dura-sensitive thalamocortical neurons.

115 massive axonal arbors of trigeminovascular (dura-sensitive) thalamic neurons in multiple cortical ar

116 root level blocks are done just outside the dura should afford all paravertebral blocks the same res

117 cation with MO, mechanical thresholds of the dura significantly decreased (P < 0.05) and an enlargeme

118 Dura stimulated by SP and carbachol in situ released his

119 vealed two separate systems of fibers in the dura that could be distinguished by the orientation of t

120 ion in the ratio of extravasation within the dura to 1.10 +/- 0.06 (P = 0.002) and in the retina to 0

121 These unique mechanical properties allow e-dura to conform to the circumvolutions of the brain and

122 brain was labeled by exposure of the intact dura to fluorescein-dextrans (M(r) 4, 70, and 500 kDa).

123 implants, termed electronic dura mater or e-dura, to fulfill this need.

124 ngeal nociceptors that innervate the cranial dura, using single-unit recording in the trigeminal gang

125 se veins lie inside the neurocranium, in the dura ventral to the brain, and return blood from the eye

126 (n = 53), the odds of success for culture in dura was 16-fold as compared to scalp (OR = 16.0, 95% CI

127 ery, holes were drilled in the skull but the dura was not penetrated.

128 application of inflammatory soup (IS) on the dura were determined when the drug was administered eith

129 ponsiveness to mechanical stimulation of the dura were studied after either topical administration or

130 wley rats (n = 16) by compressing the intact dura with a 4-mm-diameter cylinder equipped with a laser

131 tity: 0.3-2.8 m s(-1)) while stimulating the dura with a servo force-controlled stimulator or von Fre

132 Preincubation of dura with estradiol slightly augmented histamine release

133 etwork of fibers extending across the entire dura, with an especially dense plexus running along the

134 introgressed dura family derived from a Deli dura x Nigerian dura (Deli x Nigerian) with 112 individu

135 in-shelled tenera derived from thick-shelled dura x shell-less pisifera generally contain 30% higher

136 The DURA-Z coating achieves a rarely reported long-term biof

137 DURA-Z coating effectively solves several key challenges

138 The fabricated DURA-Z coating retains antifouling property after 90 d o

139 to strongly immobilize the superhydrophilic DURA-Z coating through interpenetration.

140 le and ultrarobust antifouling zwitterionic (DURA-Z) coating is created that can be easily and univer