ライフサイエンスコーパス: thoracic duct

1 for visualization of the thoracic duct ( TD thoracic duct ).

2 vessels and large lymphatic trunks like the thoracic duct.

3 formation of the PAC and, subsequently, the thoracic duct.

4 bsequently heal, permitting DCs to enter the thoracic duct.

5 f trunk lymphatic vessels and did not form a thoracic duct.

6 ump in both mesenteric lymphatics and in the thoracic duct.

7 al effusions, ascites, and dilatation of the thoracic duct.

8 muscle myosin heavy chain (SM-MHC), whereas thoracic duct and arterioles expressed both SMA and SMB

9 le activities and MLC(20) phosphorylation of thoracic duct and cervical lymphatics were determined in

10 atic contractions in isolated human vessels (thoracic duct and mesenteric lymphatics) maintained unde

11 and their messages in mesenteric lymphatics, thoracic duct, and arterioles.

12 pment of the lymphatic system, including the thoracic duct, and that alpha9 deficiency could be one c

13 The active pump of the thoracic duct appeared more sensitive to flow than did t

14 ults show lymphatic endothelial cells of the thoracic duct arise from primitive veins through a novel

15 n is transiently expressed in the developing thoracic duct at embryonic day 14, but expression is rap

16 it completely stopped phasic contractions of thoracic duct at that concentration.

17 ting intestinal lymph DCs were collected via thoracic duct cannulation from B27-transgenic and contro

18 Intranodal lymphangiogram and thoracic duct catheterization was successful in all pati

19 ML-7 treatment of the thoracic duct caused a significant decrease in both the

20 of tension were both significantly higher in thoracic duct compared to cervical lymphatics.

21 ing of PKG-Ialpha protein in the wall of rat thoracic duct confirmed its localization inside TD muscl

22 all models used in vivo (3 murine models and thoracic duct development in zebrafish) and in vitro (ly

23 t both Cx37 and Cx43 are required for normal thoracic duct development, including valve formation.

24 igher frequency of LALM (29% vs 9%, P<.001), thoracic duct dilatation (4% vs 0, P=.3), pleural effusi

25 mmon in TSC/LAM, while lymphatic involvement-thoracic duct dilatation, chylous pleural effusion, asci

26 lcified pulmonary nodules, pleural effusion, thoracic duct dilatation, hepatic and renal angiomyolipo

27 letion: batch plasmapheresis (BP; n = 5) and thoracic duct drainage (TD; n = 5).

28 In this study, the thoracic duct exhibited significant functional differenc

29 These data indicate that thoracic duct has an enhanced sensitivity to MLCK inhibi

30 gulatory mechanism that maintains pumping in thoracic duct in an energy-saving/efficient mode: it imp

31 ed ascites in eight (10%), dilatation of the thoracic duct in seven (9%), and hepatic AML in three (4

32 s of the neck or chest wall can be caused by thoracic duct injury.

33 sults from retrograde flow of chyle from the thoracic duct into lymphatic tributaries with defective

34 Although retrograde flow of chyle from the thoracic duct is considered a potential mechanism underl

35 phatic network in the zebrafish, whereas the thoracic duct is initially dispensable for lymphatic fun

36 Less-invasive surgical procedures such as thoracic duct ligation by video-assisted thoracoscopy ar

37 Thoracic duct ligation has been reported as a highly suc

38 se agonists produce lymphopenia in blood and thoracic duct lymph by sequestration of lymphocytes in l

39 ed in the intestinal (afferent) and efferent thoracic duct lymph of rats during the course (0 to 289

40 rough the gut (mesenteric efferent and lower thoracic duct lymph).

41 In thoracic duct lymph, cells that could prevent diabetes w

42 e and was transported to the circulation via thoracic duct lymph.

43 er tone at a given pressure when compared to thoracic duct lymphatics.

44 y analyzed the TCR Vbeta repertoires of CD4+ thoracic duct lymphocytes (TDL) collected during the ini

45 positively selected miHA-specific donor CD8+ thoracic duct lymphocytes (TDL) collected from irradiate

46 y almost 100-fold as measured by enumerating thoracic duct lymphocytes (TDL) obtained early post-tran

47 alloreactive T cell expansion and function, thoracic duct lymphocytes (TDL) were analyzed.

48 To determine how RAPA inhibited GVHD, thoracic duct lymphocytes (TDL) were isolated from recip

49 Fewer CD4+ thoracic duct lymphocytes (TDL) were obtained in mAb-tre

50 perimental data on migration of 51Cr-labeled thoracic duct lymphocytes (TDLs) via major lymphoid and

51 d functional analysis of positively selected thoracic duct lymphocytes 4 days after transplant and by

52 e, systems view of recirculation kinetics of thoracic duct lymphocytes in the whole organism.

53 In thoracic duct MLC(20) di-phosphorylation, but not mono-p

54 luorescent tracer revealed that lymph in the thoracic duct of these mice could enter the thoracic cav

55 ntestinal lymph was collected by cannulating thoracic ducts of mesenteric lymphadenectomized animals.

56 agent through the lymphatic system to the TD thoracic duct outlet was 244 seconds (range, 201-387 sec

57 However, in thoracic duct, predominantly cardiac alpha-actin and vas

58 nsible for the self-regulatory adjustment of thoracic duct pumping to changes in lymph flow pattern.

59 ACNA1C were consistently detected from human thoracic duct samples examined and the CaV1.2 protein wa

60 either lymphatic embolization procedures or thoracic duct stenting with covered stents to exclude re

61 imaging specialist for visualization of the thoracic duct ( TD thoracic duct ).

62 : 2 patients (8%) with traumatic leak from a thoracic duct (TD) branch, 14 patients (56%) with pulmon

63 of the lymphatic network with blood from the thoracic duct (TD) in both neonatal and mature mice.

64 We show that mouse thoracic duct (TD) lymph contains HSPCs that possess sho

65 dependent regulation of contractility in rat thoracic duct (TD).

66 onstrated retrograde lymphatic flow from the thoracic duct toward lung parenchyma.

67 Enhancement was seen in the TD thoracic duct up to 1 hour after injection.

68 In contrast, the TD thoracic duct was visualized in all five of the animals

69 The TD thoracic duct was visualized in three of the five animal

70 Lymphatic segments of the rat thoracic duct were isolated, cannulated and pressurized.

71 Rat mesenteric lymphatics and thoracic ducts were isolated, cannulated and pressurized

72 both the active peak and plateau tensions of thoracic duct, whereas only the active peak tension of c

73 phatic contraction, we hypothesized that the thoracic duct would be more sensitive to the modulation