ライフサイエンスコーパス: infundibular

1 Scattered NKB neurons were present in the infundibular and paraventricular nuclei, paraolfactory g

2 ngiogenic VEGF-Axxxb from the PT, inhibiting infundibular angiogenesis and diminishing lactotroph (LT

3 In selected cases, the infundibular apex can be separated from the rest of the

4 ration of a portion of the right ventricular infundibular apex into the physiological left ventricle.

5 left ventricular apex and right ventricular infundibular apex.

6 Left ventricular-infundibular apical VSDs constitute a distinct morpholog

7 e P and neurokinin B gene transcripts in the infundibular (arcuate) nucleus, accompanied by increased

8 that a group of neurons in the hypothalamic infundibular/arcuate nucleus form an important component

9 he thoracic neural tube and CNC, resulted in infundibular bulging and coronary anomalies similar to t

10 genitor cells, demonstrates a dual origin of infundibular cells and reveals a crucial role for FGF si

11 neuronal fates and Fgf10(+) anterior-dorsal infundibular cells.

12 unknown, but the observation of necrotizing infundibular crystalline folliculitis in biopsied patien

13 specific pathological pattern of necrotizing infundibular crystalline folliculitis was observed in 4

14 xhibited UVR-induced melanoma and follicular infundibular cyst formation, and tumor-associated melano

15 From the "infundibular cysts", hair germs form centrifugally follo

16 that are sculpted by apoptosis to generate "infundibular cysts".

17 model GATA6-mediated down-regulation of the infundibular differentiation program is mediated by indu

18 ity is due to intrinsic myocardial damage by infundibular distortion, it is chronically furthered by

19 Dopamine (DA), produced by tubero-infundibular dopaminergic (TIDA) neurons of the arcuate

20 ed and compared with sham-operated controls: infundibular dysfunction (INF), PV insufficiency (PI), a

21 ole for FGF signalling in governing extended infundibular growth.

22 ratum cellulare externum, inferior hypo. n., infundibular hypo. n., median eminence, three layers wit

23 the pituitary and arcuate ventro-medial and infundibular hypothalamus of swine and humans was cloned

24 ic paraventricular, supraoptic, dorsomedial, infundibular (IN), lateral hypothalamic, Edinger-Westpha

25 l ventricular septal defect closure, a short infundibular incision with avoidance of muscle resection

26 were also observed in the preoptic area; the infundibular, intermediate, dorsomedial, and ventromedia

27 djacent to basal, suprabasal, and follicular infundibular keratinocytes that when mutated can give ri

28 the infundibulum, and that IL-1alpha acts on infundibular keratinocytes to promote cornification.

29 lar adhesion molecule (ICAM)-1 and HLA-DR by infundibular keratinocytes, as determined by immunohisto

30 Infundibular kisspeptin neurons, which coexpress NKB, re

31 luded malrotation of the aorta and excessive infundibular myocardium.

32 cular outflow tract obstruction ranging from infundibular narrowing to isolated narrowing of right or

33 ods were used to compare the total number of infundibular neurons between groups of young (premenopau

34 ignificant difference in the total number of infundibular neurons between young (520,000 +/- 42,000 n

35 iabetes showed reduced ASB4 abundance in the infundibular nuclei, the human equivalent of the arcuate

36 , lamina terminalis, and periventricular and infundibular nuclei.

37 in the periventricular, paraventricular, and infundibular nuclei.

38 ssing proopiomelanocortin (POMC) mRNA in the infundibular nucleus of older women is decreased.

39 er, expression of DUSP8 was increased in the infundibular nucleus of T2D humans.

40 the PVH, in the SON, in the LHA, in the Arc (infundibular nucleus) and in the DMH.

41 undant in the PVN, supraoptic nucleus (SON), infundibular nucleus, and premammillary nucleus, whereas

42 en is not accompanied by degeneration of the infundibular nucleus.

43 ral preoptic area/anterior hypothalamus, and infundibular nucleus/median eminence.

44 26, main pulmonary arterioplasty in 22, and infundibular patching in 2.

45 The infundibular portion is marked with the organized and pr

46 of ectopic VSM and endothelial cells in the infundibular pouch and in some regions of the right vent

47 sis plays a pivotal role in formation of the infundibular pouches and suggests an essential role for

48 last and vascular smooth muscle cells in the infundibular pouches of the connexin43 knockout mouse he

49 To elucidate the origin of the infundibular pouches, we used microarray analysis to inv

50 rth from outflow obstruction associated with infundibular pouches.

51 ese mice exhibit outflow obstruction, but no infundibular pouches.

52 n (INF), PV insufficiency (PI), and combined infundibular-PV dysfunction (TAP).

53 ithin the basal forebrain and preoptic area, infundibular region, central hypothalamus, basal ganglia

54 found labeled fibers throughout the preoptic-infundibular region.

55 ll treatment groups but most in animals with infundibular scarring (INF and TAP).

56 ined to a population of tanycytes within the infundibular stalk/caudal median eminence, termed here g

57 e, dorsomedial, and ventromedial nuclei; the infundibular stalk; the amygdala; the bed nucleus of str

58 medial mammillary nucleus, median eminence, infundibular stem, periaqueductal gray, area postrema, p

59 tenosis (47.28%) found, followed by isolated infundibular stenosis (34.23%).

60 This study investigates the contribution of infundibular versus pulmonary valve (PV) dysfunction on

61 Infundibular with pulmonary valvular stenosis was the mo