ライフサイエンスコーパス: anterior lobe

1 birth date and are dispersed throughout the anterior lobe.

2 enchymal transition, is absent in the dorsal anterior lobe.

3 yed recall also showed associations with the anterior lobe.

4 Rathke's pouch to cell specification in the anterior lobe.

5 s highly expressed in the rostral tip of the anterior lobe.

6 er projection pattern in lobule VIII and the anterior lobe.

7 al granular layer of the mature meander tail anterior lobe.

8 round the portal venous branch supplying the anterior lobe.

9 erably lower amounts of staining observed in anterior lobes.

10 nal granular layer between the posterior and anterior lobes.

11 E-LPV) and/or the concentration of DA in the anterior lobe (AL) are inversely related to the secretio

12 asia of the intermediate lobe (IL) while the anterior lobe (AL) is not overtly affected.

13 The secretion of prolactin (PRL) from the anterior lobe (AL) of the pituitary gland is tonically i

14 r of the population, and most arise from the anterior lobe (AL).

15 remained unchanged in the inner zone of the anterior lobe (AL-IZ).

16 nce (ME), decreased in the outer zone of the anterior lobe (AL-OZ), as well as the intermediate (IL)

17 eously from Purkinje cells in the paravermal anterior lobe and from muscles of the hand and arm in th

18 ells revealed widespread degeneration in the anterior lobe and in limited areas of the posterior lobe

19 The cerebellar anterior lobe and pars triangularis made significant con

20 ysfunctions were chiefly associated with the anterior lobe and posterior lobule HVI.

21 pe, corticotrope and lactotrope cells in the anterior lobe and the intermediate lobe melanotropes.

22 Measures of the right cerebellar anterior lobe and the left and right pars triangularis c

23 of the paravermal C1 zone in lobule V of the anterior lobe and the rostral folia of the paramedian lo

24 In the cerebellum, the anterior lobe and the superior posterior lobe were profo

25 motor cortex, bilateral putamen and insula, anterior lobe and vermis of the cerebellum and superior

26 s they transition from Rathke's pouch to the anterior lobe appears to be essential for their movement

27 All cells in the anterior lobe are specified and differentiate, but an ea

28 llum is greater than the number of PC in the anterior lobe, as classically defined by the primary fis

29 , and 3) the defect is not restricted to the anterior lobe but involves a portion of the posterior lo

30 tact in Rathke's pouch, the precursor to the anterior lobe, but the anterior lobe was hypoplastic.

31 expressed by folliculo-stellate cells in the anterior lobe, by a group of astrocyte-like cells and by

32 We find that all of the anterior lobe cell types initiate differentiation concur

33 ate lobe melanotropes is delayed relative to anterior lobe cell types.

34 minant caudal pons projections to cerebellar anterior lobe, contrasted with associative-predominant r

35 ss the pro-opiomelanocortin (POMC) gene, the anterior lobe corticotropes, producing adrenocorticotrop

36 s inactivated the cerebellar nuclei, lateral anterior lobe, crus I, rostral crus II, and lobule HVI i

37 ound, in addition to the marked depletion of anterior lobe granule cells ( > 90%), there were also si

38 the neural ectoderm was sufficient to impair anterior lobe growth, but not the differentiation of hor

39 e pouch of conditional embryos led to severe anterior lobe hypoplasia with drastically reduced expres

40 Pituitaries of Hes1 deficient mice have anterior lobe hypoplasia.

41 while the reduction of granule cells in the anterior lobes is substantial, there is an almost comple

42 had chronic hyperprolactinemia and developed anterior lobe lactotroph hyperplasia without evidence of

43 g from pairs of C1 zone sites located in the anterior lobe (lobule V) and C1 or C3 zone sites in rost

44 bjects had greater activity in the bilateral anterior lobe of cerebellum, premotor area, parietal cor

45 with, the caudal extent of the disorganized anterior lobe of meander tail and the rostral extent of

46 genitors transplanted into the granuloprival anterior lobe of neonatal mea mutants differentiated int

47 the paraventricular hypothalamic nuclei, the anterior lobe of pituitary, and the thyroid gland.

48 We show that lesions of the anterior lobe of rabbit cerebellar cortex disrupt the ti

49 eral hypothalamus, Rathke's pouch and in the anterior lobe of the adult pituitary.

50 nditioning results in plasticity in both the anterior lobe of the cerebellar cortex and in the anteri

51 logical analysis suggests that damage to the anterior lobe of the cerebellar cortex is necessary and

52 The volume of the right anterior lobe of the cerebellum distinguished dyslexic f

53 Lesions of the anterior lobe of the cerebellum produced only minor chan

54 near-total depletion of granule cells in the anterior lobe of the cerebellum, as well as aberrantly l

55 he virtual depletion of granule cells in the anterior lobe of the cerebellum.

56 The anterior lobe of the pituitary gland is composed of five

57 1 causes a morphological defect in which the anterior lobe of the pituitary gland protrudes through t

58 I revealed a solid-cystic mass involving the anterior lobe of the pituitary gland.

59 ground develop high-penetrance tumors of the anterior lobe of the pituitary, a class of tumors estima

60 In cells of the anterior lobe of the pituitary, D2 dopamine receptors (b

61 Luteinizing hormone (LH), produced in the anterior lobe of the pituitary, is a member of the hypot

62 progressive, dose-dependent loss of the most anterior lobe of the vermis in mice lacking Fgf17 and in

63 ranule cells that predominantly populate the anterior lobes of the adult cerebellum and later, those

64 lexics exhibited significantly smaller right anterior lobes of the cerebellum, pars triangularis bila

65 The intermediate and anterior lobes of the pituitary gland are derived from a

66 ells were identified in the intermediate and anterior lobes of the pituitary, the thyroid and parathy

67 lly mea/mea granule cells are present in the anterior lobe or, unexpectedly, in the posterior lobe.

68 te mouse gestation and the postnatal period, anterior lobe progenitors re-enter the cell cycle and ex

69 se having lesionectomies, no difference from anterior lobe resection was recorded.

70 , loose the majority of granule cells in the anterior lobe resulting in few axons and atypical Purkin

71 ypoplastic with an abnormal branching of the anterior lobe, revealing a role for microRNAs in pituita

72 from the central vermis, and analysis of the anterior lobe reveals several missing zebrin II- bands.

73 f granule cells to develop in the cerebellar anterior lobe; the mechanism is unknown.

74 lmost always accompanied by dispersal of the anterior lobes themselves.

75 ults in accelerated progression of pituitary anterior lobe tumors and medullary thyroid carcinomas.

76 e transgene was expressed transiently in the anterior lobe vermis.

77 e territory providing climbing fibres to the anterior lobe was centred more laterally than the territ

78 the precursor to the anterior lobe, but the anterior lobe was hypoplastic.

79 ellar vermis and left lobule V of cerebellar anterior lobe were additionally activated for dual-task

80 Cystic cavities observed in pituitary anterior lobes were lined by cuboidal, ciliated epitheli

81 diate lobe and over a subset of cells in the anterior lobe, whereas CRF-R2 transcripts were expressed

82 ngs developed accelerated enlargement of the anterior lobe with predominantly TSH cell hyperplasia.