ライフサイエンスコーパス: truncus

1 are incorporated into both the conus and the truncus.

2 iameter ratio between the pulmonary arterial truncus and the ascending aorta).

3 osition of the great arteries and persistent truncus arteriosis.

4 nic atresia or stenosis (7 patients, 11.5%), truncus arteriosus (6 patients, 10%), TGA (10 patients,

5 of the great arteries (n=14), and persistent truncus arteriosus (n=3).

6 hese cardiac anomalies present as persistent truncus arteriosus (PTA) and interrupted aortic arch (IA

7 nct cardiovascular malformations--persistent truncus arteriosus (PTA) and interrupted aortic arch (IA

8 Persistent truncus arteriosus (PTA) is a failure of septation of th

9 ial arch development and leads to persistent truncus arteriosus (PTA), indicative of neural crest dys

10 t mice lacking Smad4 in NCCs have persistent truncus arteriosus (PTA), severe OFT cushion hypoplasia,

11 enocopying the human heart defect persistent truncus arteriosus (PTA), which trunk neural crest fails

12 defects such as cleft palate and persistent truncus arteriosus (PTA).

13 ed aortic arch (IAA), 34.5% of patients with truncus arteriosus (TA), and 15.9% with tetralogy of Fal

14 ansposition of the great arteries (TGA), and truncus arteriosus (TA).

15 h, a phenotype known in humans as persistent truncus arteriosus (type A4).

16 The embryos displayed persistent truncus arteriosus and abnormalities of the great vessel

17 ular septal defects), aortic sac (persistent truncus arteriosus and aorticopulmonary window), and aor

18 A third mutation causing persistent truncus arteriosus and craniofacial defects, phenotypes

19 neural crest ablation results in persistent truncus arteriosus and failure of addition of myocardium

20 derstand the embryonic defects of persistent truncus arteriosus and impaired semilunar valve formatio

21 ular disease, including tetralogy of Fallot, truncus arteriosus and interruption of the aortic arch.

22 nts were a recipient neonate with persistent truncus arteriosus and irreparable truncal valve dysfunc

23 a, double-outlet right ventricle, persistent truncus arteriosus and right-sided aortic arches.

24 ess penetrant phenotypes included persistent truncus arteriosus and thickened valve leaflets.

25 Congenital heart defects (persistent truncus arteriosus and ventricular septal defect), hypop

26 ow tract remodeling, resulting in persistent truncus arteriosus in the majority of mutant embryos.

27 cells resulted in fully penetrant persistent truncus arteriosus malformations.

28 atrioventricular septal defect, Fallot, and truncus arteriosus operations were 1.1%, 0.6%, 3.6%, 2.3

29 --Sema3CL605P was associated with persistent truncus arteriosus with interrupted aortic arch, and the

30 tion of a common arterial trunk ('persistent truncus arteriosus' or PTA).

31 nificantly increased incidence of persistent truncus arteriosus, a phenotypic change characteristic o

32 embryos die at mid-gestation with persistent truncus arteriosus, a severe cardiac outflow tract defec

33 (mean 7.2+/-4.9); group B, 14 patients with truncus arteriosus, aged 27 to 50 years (mean 33.7+/-7.3

34 cardiovascular defects, including persistent truncus arteriosus, and abnormal maturation of the aorti

35 have a cardiovascular malformation, one had truncus arteriosus, and another had a bicuspid aortic va

36 tricle, transposition of the great arteries, truncus arteriosus, and interrupted aortic arch.

37 from ascending aorta, paracoarctation aorta, truncus arteriosus, and pulmonary trunk in 86 patients w

38 s in ascending aorta, paracoarctation aorta, truncus arteriosus, and pulmonary trunk were prevalent i

39 coarctation, atrioventricular septal defect, truncus arteriosus, aortopulmonary septal defect, and to

40 f 71 (4%) with a secundum ASD, one each with truncus arteriosus, double-outlet right ventricle, L-tra

41 developmental defects, including persistent truncus arteriosus, hypomorphic pulmonary arteries, inte

42 work together to perturb the rotation of the truncus arteriosus, leading to OFT malalignment defects

43 ricle, ventricular septal defect, persistent truncus arteriosus, reduced myocardial proliferation, an

44 vere CHD was defined as tetralogy of Fallot, truncus arteriosus, transposition complexes, endocardial

45 embryonic neural crest results in persistent truncus arteriosus, ventricular dilation, and impaired v

46 atresia, pulmonary stenosis, and persistent truncus arteriosus.

47 x1, whose inactivation results in persistent truncus arteriosus.

48 , valvular disease, tetralogy of Fallot, and truncus arteriosus.

49 uding interrupted aortic arch and persistent truncus arteriosus.

50 notruncal heart defects including persistent truncus arteriosus.

51 cle, aorticopulmonary window, and persistent truncus arteriosus.

52 ral crest ingress, with resultant persistent truncus arteriosus.

53 right renal artery (RRA), orifice of celiac truncus (CT), orifice of superior mesenteric artery (SMA

54 cardiac outlet, consisting of the conus and truncus, does not derive from the paired heart-forming f

55 t give rise to the right ventricle and conus/truncus in the outlet of the looped heart.

56 ere, as well as in the lateral aspect of the truncus of the corpus callosum, due to greater increase

57 The future right ventricle and conus/truncus of the single heart tube fail to form and the en

58 l cushions in the atrioventricular and conus/truncus regions are absent.

59 ending aorta and pulmonary trunk, the distal truncus that was patterned into the two semilunar valves