ライフサイエンスコーパス: microvascular network

1 of the peripapillary retina revealed a dense microvascular network.

2 of transport costs may be prioritized by the microvascular network.

3 ndothelial cell apoptosis within the mucosal microvascular network.

4 cosal injury requires reestablishment of the microvascular network.

5 in an in vivo frog (Rana pipiens) mesenteric microvascular network.

6 that contributes to the stabilization of the microvascular network.

7 formation and controlled 3D organization of microvascular networks.

8 cale blood flow in physiologically realistic microvascular networks.

9 on of neovascular tufts in postnatal retinal microvascular networks.

10 distributions at bifurcations in dichotomous microvascular networks.

11 ess using a ligation strategy for mesenteric microvascular networks.

12 to-cell electrotonic transmission within the microvascular networks.

13 ts) based on induced changes in the detected microvascular networks.

14 alone to generate stable hydraulically tuned microvascular networks.

15 EC) and pericyte interactions to form stable microvascular networks.

16 Reorganization of regenerating microvascular networks accompanies the recovery of blood

17 nsport to tissue is an important part of the microvascular network adaptation to local brain metaboli

18 and functional characteristics of the native microvascular network, allowing efficient recellularizat

19 sing two microfluidic devices, an artificial microvascular network (AMVN) and a multiplexed microcapi

20 Model simulations suggest that microvascular network anatomy can affect the optimal hem

21 ct the degree of organization of the hepatic microvascular network and are correlated to the severity

22 oaded RV to uncover the 3D properties of the microvascular network and determine whether deficient mi

23 patterned ECMs used for engineering perfused microvascular networks and functional epidermis and for

24 ometric details of physiologically realistic microvascular networks, and deformation of every one of

25 Microvascular network architecture defines coupling of f

26 Overly dense microvascular networks are treated by selective reductio

27 n the adult brain, NPCs are found near brain microvascular networks (BMVNs) in specialized microenvir

28 This rapid formation of long-lasting microvascular networks by postnatal progenitor cells obt

29 eserving kidney homeostasis as they maintain microvascular networks by stabilizing the vasculature an

30 ), the 3D construct containing the lymphatic microvascular network can be analyzed by microscopy (sta

31 trated on three in vivo 2PM image volumes of microvascular networks (capillaries, arterioles and venu

32 Scenario), which are compared with realistic microvascular network components (Heterogeneous Scenario

33 muscle-mimicking microenvironments through a microvascular network concentrically wrapped with mural

34 efficacy of signalling between myofibres and microvascular networks controlling their oxygen supply.

35 ight scatter limits the visualization of the microvascular network deep inside the living mammal.

36 technology to fabricate complex, functional microvascular networks directly in vivo.

37 tterning can be used to fabricate functional microvascular networks directly in vivo.

38 in a polymer coating via a three-dimensional microvascular network embedded in the substrate.

39 ence of TGF synchronization across the renal microvascular network enables an understanding of how NV

40 dicine applications based on implantation of microvascular networks expanded ex vivo or the generatio

41 ells can serve to generate highly functional microvascular networks for tissue engineered bone grafts

42 EGF-A and alphaVbeta3 on fibroblast-mediated microvascular network formation.

43 he microdevice features self-organized human microvascular networks formed over 4-5 d, after which th

44 n the integration of the spheroid within the microvascular networks formed.

45 ity-mediated response may expand the mucosal microvascular network, foster immune cell recruitment, a

46 ells (RBCs) are performed in three realistic microvascular networks from the mouse cerebral cortex.

47 employed blood flow simulations in realistic microvascular networks from the mouse cortex to quantify

48 ta provide robust mechanistic information of microvascular network functionality and flexibility duri

49 and is capable of incorporating realistic 3D microvascular network geometries.

50 e computational method to predict cancer and microvascular network growth patterns.

51 -scale tissue engineered vascular grafts and microvascular networks have been well-established, but e

52 od and interventions to repair diseased iBRB microvascular networks have not been developed.

53 reporter protein expression across a dynamic microvascular network in an adult mammal.

54 The bMFA consists of an endothelialized microvascular network in communication with a tissue com

55 of prenatal alcohol exposure on the cortical microvascular network in human controls and fetal alcoho

56 showed the absence of a radial peripapillary microvascular network in these 12 eyes.

57 2D cultures and the formation of a complete microvascular network in vitro in 3D cultures.

58 of prenatal alcohol exposure on the cortical microvascular network in vivo and ex vivo and the action

59 o augment the formation and stabilization of microvascular networks in a previously uncharacterized t

60 and pericytes, and can self-organize to form microvascular networks in an engineered matrix.

61 Remodeling of microvascular networks in mammals is critical for physio

62 ls (RBCs) must navigate through such complex microvascular networks in order to maintain tissue perfu

63 The success of these microvascular networks in recapitulating these phenomena

64 We have engineered living microvascular networks in three-dimensional tissue scaff

65 thelial cells to self-assemble into perfused microvascular networks in vivo.

66 s shown potential to noninvasively visualize microvascular networks in vivo.

67 expansion of the cancer cell population and microvascular network increases, cells undergo prolifera

68 A microvascular network is critical for the survival and f

69 flow and pressure distribution in realistic microvascular networks is needed for improving our under

70 her vascular smooth muscle cells in cultured microvascular networks maintain the ability to constrict

71 lular organisation, extracellular matrix and microvascular network mimic human heart tissue.

72 dentifying signalling components that impact microvascular network morphology as well as endothelial

73 l integration also requires consideration of microvascular network morphology in relation to local co

74 These microvascular networks (muVNs) allow for multiweek cultu

75 letion, substantial disruption of the luteal microvascular network occurred and was associated with a

76 liomas are indistinguishable on imaging, the microvascular network of pilomyxoid astrocytoma, a subty

77 The microvascular network of the left frontal cortex was eva

78 ns confirmed the presence of a peripapillary microvascular network only in MGS cases supports the hyp

79 r signals, and cellular behaviors to predict microvascular network patterning events.

80 ep multi-photon imaging in mice, we examined microvascular networks perfusing myelinated tissues in c

81 counting for the complex architecture of the microvascular network remains a challenge from a modelli

82 simulations in realistic representations of microvascular networks should provide a theoretical fram

83 Sample results in a microvascular network show an enhancement of diffusive s

84 ystems that mimic the vasculature (synthetic microvascular networks) showed that rod-shaped nanoparti

85 nsions (3D) between epithelial tissues and a microvascular network since vascularization is vital for

86 e used to generate physiologically realistic microvascular network structures.

87 tissue and organ applications, incorporating microvascular networks, structures for transport and fil

88 Microvascular networks support metabolic activity and de

89 The microvascular network supported viability and function o

90 The vasa vasorum are a vital microvascular network supporting the outer wall of large

91 Despite rapid advancement in microvascular network systems and organoid technologies,

92 eport transcriptomic data from diabetic iBRB microvascular networks that may reveal drug targets, and

93 Strategies to fabricate microvascular networks that structurally and functionall

94 We study occlusive dynamics within a model microvascular network: the embryonic zebrafish trunk.

95 usly to cellular elements in the neighboring microvascular network through gap junctions, where it re

96 te the fabrication of three-dimensional (3D) microvascular networks through direct-write assembly of

97 propagate over significant distances in the microvascular network, thus dramatically increasing the

98 gnals within the highly interconnected brain microvascular network to increase local CBF.

99 ygen transport from a three-dimensional (3D) microvascular network to the surrounding tissue in the p

100 patially-variable dynamic structure of tumor microvascular networks to simulate blood flow distributi

101 technique to study the responses of cerebral microvascular networks to single and repeated cocaine ad

102 sly undescribed strategy for creating stable microvascular networks to support engineered tissues of

103 cs involved in angiogenesis within an intact microvascular network using time-lapse imaging.

104 In normal discs, a dense microvascular network was visible on OCT angiography.

105 banding PAB surgery and properties of the RV microvascular network were assessed using 3D imaging and

106 At peak disease (postnatal day 18), microvascular networks were analyzed to examine intraret

107 On Day 0 and Day 3 live microvascular networks were visualized with FITC conjuga

108 We envisage that 3D microvascular networks will provide an enabling platform

109 T-synthase-deficient brains formed a chaotic microvascular network with distorted capillary lumens an

110 Examples include 3D microvascular networks with sophisticated layouts, deter

111 e is useful more generally for investigating microvascular networks within 3D engineered tissues with

112 d after implantation reveals highly branched microvascular networks within the implants that connect