ライフサイエンスコーパス: atrioventricular canal

1 ube, and communicate during formation of the atrioventricular canal.

2 al cells derived from the endocardium at the atrioventricular canal.

3 at populated the pulmonary veins, atria, and atrioventricular canal.

4 ssion of versican and bmp4 to the developing atrioventricular canal.

5 gulating the morphogenesis of the RV and the atrioventricular canal.

6 rdium of the developing heart, including the atrioventricular canal.

7 al cells in the outflow tract but not in the atrioventricular canal.

8 ntricle and outflow tract in addition to the atrioventricular canal.

9 , may regulate the expression of RhoU at the atrioventricular canal.

10 We identified atrioventricular canal 1 (avc1), a mouse mutation that c

11 Loss of RhoU function recapitulated the atrioventricular canal and cardiac looping defects obser

12 ions like ventricular septal defects, common atrioventricular canal and double outlet right ventricle

13 is required for the proper remodeling of the atrioventricular canal and for cardiac looping, and that

14 icantly enlarged endocardial cushions in the atrioventricular canal and in the outflow tract.

15 essed in the outflow tract, inner curvature, atrioventricular canal and inflow tract, corresponding t

16 ing pathways resulted in failure to form the atrioventricular canal and loop the linear heart tube.

17 ndocardial-mesenchymal transformation in the atrioventricular canal and outflow tract regions.

18 from E9.5 to E11.5 in endocardium along the atrioventricular canal and outflow tract.

19 e outflow tract, the interatrial groove, the atrioventricular canal and right and left ventricles, as

20 l defects are observed in development of the atrioventricular canal and septation of the outflow trac

21 n the myocardial cells of the outflow tract, atrioventricular canal, and future right ventricle.

22 zed by a thin ventricular myocardium, common atrioventricular canal, and the tetralogy of Fallot malf

23 l-to-mesenchymal transdifferentiation in the atrioventricular canal, and thus play a key role in form

24 highest intensity in the right ventricle and atrioventricular canal, as well as in the sinus venosus.

25 ed to repress chamber differentiation in the atrioventricular canal at 9.5 dpc.

26 marking experiments in ovo suggest that the atrioventricular canal, atria and conotruncus are added

27 chick heart, in the myocardium overlying the atrioventricular canal (AV) and outflow tract (OFT) cush

28 s more cranial in the pSHF contribute to the atrioventricular canal (AVC) and atria, whereas those mo

29 ital malformations involving the non-chamber atrioventricular canal (AVC) and inner curvature (IC) re

30 in the proximal outflow tract (pOFT) but not atrioventricular canal (AVC) cushions.

31 Alk3 CKO embryos also displayed defects in atrioventricular canal (AVC) endocardial cushion formati

32 lls (EMT) at the outflow tract (OFT) but not atrioventricular canal (AVC) endocardial cushions.

33 embryogenesis, the formation of the cardiac atrioventricular canal (AVC) facilitates the transition

34 First, the atrioventricular canal (AVC) is closed by the mechanical

35 Proper patterning of the atrioventricular canal (AVC) is essential for delay of e

36 lium-mesenchymal-transformation (EMT) in the atrioventricular canal (AVC) region; the number of mesen

37 ise from the endocardial cushions within the atrioventricular canal (AVC) through dynamic interaction

38 cardiographic variables of unbalanced common atrioventricular canal (CAVC) that could aid in appropri

39 These embryos had common atrioventricular canal (CAVC), double outlet right ventr

40 tation frozen ventricle (frv) causes ectopic atrioventricular canal characteristics in the ventricula

41 Snai1 overexpression studies in atrioventricular canal collagen I gel explants indicate

42 common human congenital heart abnormalities, atrioventricular canal defect (AVCD).

43 h homologue dachsous1b resulted in a cardiac atrioventricular canal defect that could be rescued by w

44 Atrioventricular canal defects (AVCDs) are most commonly

45 Wnt signaling, which has been implicated in atrioventricular canal development (Verhoeven et al., 20

46 rhgef7b/Pak kinase pathway in order to guide atrioventricular canal development and cardiac looping.

47 a role of frv in the regional restriction of atrioventricular canal differentiation.

48 nd discovered that RhoU was expressed at the atrioventricular canal during the time when it forms.

49 rs of death include the presence of complete atrioventricular canal (hazard ratio 4.76, 95% CI 1.59 t

50 r, conduction is markedly slowed through the atrioventricular canal in the e.d. 10.5 heart, forming t

51 ocardial cells at the ventricular end of the atrioventricular canal, intensifies and extends from E9.

52 In the mutant, the expressions of the atrioventricular canal marker genes, such as tbx2b, hyal

53 dant function in the endocardium to regulate atrioventricular canal morphogenesis and outflow tract f

54 = 433), pulmonary atresia (n = 121), common atrioventricular canal (n = 17), absent pulmonary valve

55 efect (n = 11), tetralogy of Fallot (n = 3), atrioventricular canal (n = 3), and others (n = 8).

56 irectly represses Nmyc1 in outflow tract and atrioventricular canal of the developing heart, resultin

57 lacZ expression in mesenchymal cells of the atrioventricular canal of Tie2-Cre;CAG-CAT-Z double-tran

58 rst intron, was expressed exclusively in the atrioventricular canal region of the heart.

59 lly localized to the dorsal venous valve and atrioventricular canal regions.

60 In the atrioventricular canal, Tbx5 haploinsufficiency caused a

61 is normally restricted to outflow tract and atrioventricular canal, throughout the heart.

62 endocardial endothelial cells that line the atrioventricular canal undergo an EndMT to form the endo