ライフサイエンスコーパス: truncus arteriosus

1 atresia, pulmonary stenosis, and persistent truncus arteriosus.

2 x1, whose inactivation results in persistent truncus arteriosus.

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

4 uding interrupted aortic arch and persistent truncus arteriosus.

5 notruncal heart defects including persistent truncus arteriosus.

6 cle, aorticopulmonary window, and persistent truncus arteriosus.

7 ral crest ingress, with resultant persistent truncus arteriosus.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

32 cells resulted in fully penetrant persistent truncus arteriosus malformations.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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