ライフサイエンスコーパス: posterior lobe

1 s in development of the infundibulum and the posterior lobe.

2 the pituitary, irBC was noted mainly in the posterior lobe.

3 -R2 transcripts were expressed mainly in the posterior lobe.

4 he anterior lobe and in limited areas of the posterior lobe.

5 f strong directional selection acting on the posterior lobe.

6 sed primarily in Purkinje cells (PCs) of the posterior lobe.

7 ut to the hindlimb C1 zone in the cerebellar posterior lobe.

8 n the anterior lobe or, unexpectedly, in the posterior lobe.

9 ts a history of directional selection on the posterior lobe.

10 anterior lobe but involves a portion of the posterior lobe.

11 ociated with pediatric TBI, localized to the posterior lobe.

12 lobe, and the neural ectoderm generating the posterior lobe.

13 ccurred mostly in the inferior aspect of the posterior lobes.

14 elopment and in the prospective anterior and posterior lobes.

15 nd preferential loss of granule cells in the posterior lobes.

16 he primary fissure, between the anterior and posterior lobes.

17 ring the posterior progenitors (PP) from the posterior lobes.

18 lso significantly fewer granule cells in the posterior lobe (20-30%) without a concomitant loss of Pu

19 ritiana differ markedly in morphology of the posterior lobe, a male-specific genitalic structure.

20 Here, we investigated the evolution of the posterior lobe, a novel structure in the male genitalia

21 The origins of the posterior lobe, a recently evolved structure in some spe

22 (The ostensibly 'normal' meander tail posterior lobe also benefited from repletion of a more s

23 re independent from those that contribute to posterior lobe and anal plate divergence.

24 ant intrinsically for the development of the posterior lobe and pituitary stalk, and it has significa

25 sporadic ALS in contrast to the considerable posterior lobe and vermis disease burden identified in C

26 complex, with staining observed primarily in posterior lobes and considerably lower amounts of staini

27 be may be more severe than that of the three posterior lobes and may account for the prominence of pr

28 The morphology of the claspers, posterior lobes, and anal plates exhibit striking differ

29 ivation of climbing fibres projecting to the posterior lobe cerebellar cortex by focal stimulation of

30 s and Purkinje cells in Crus I and II of the posterior lobe cerebellar hemisphere to activation of pe

31 Lesions of the posterior lobe cognitive-emotional cerebellum produce dy

32 e necessary for cell height increases during posterior lobe development.

33 nd confirmed that changes in Sox21b underlie posterior lobe evolution between these species.

34 tial expression of BETA2/NeuroD1 and TrkC in posterior lobes explains the earlier start of cell apopt

35 Volumes of the vermis, inferior posterior lobe, fourth ventricle, and total cerebellum a

36 l sample of Purkinje cells recorded from the posterior lobe hemisphere in awake cats.

37 leg in one patient, and on the left inferior posterior lobe in another patient to stimulation of left

38 The posterior lobe is derived from the infundibulum, which i

39 inant rostral pons projections to cerebellar posterior lobe, is consistent with new hypotheses regard

40 )(11)(,)(12)(,)(14)(,)(15)(,)(16)(,)(17) The posterior lobes likely evolved from co-option of a Hox-r

41 ed volume in subregions primarily within the posterior lobe (lobule VIIB, crus II), vermis (VI, VIII)

42 gests a mechanism whereby development of the posterior lobe may affect the development of the anterio

43 al introgressions that have large effects on posterior lobe morphology and that posterior lobe size a

44 Here, we dissect the genetic basis of posterior lobe morphology between D. mauritiana and D. s

45 c inputs to establish differences in overall posterior lobe morphology between D. mauritiana and D. s

46 ically downregulated in granule cells of the posterior lobe of Barhl1(-)/- cerebella.

47 e-supplementary motor area and the bilateral posterior lobe of cerebellum, compared to young subjects

48 recently evolved morphological novelty, the posterior lobe of D. melanogaster.

49 inent in patients with lesions involving the posterior lobe of the cerebellum and the vermis, and in

50 d simultaneously from two or more PCs in the posterior lobe of the ketamine/xylazine-anaesthetized ra

51 The size and shape of the posterior lobe of the male genital arch differs dramatic

52 The posterior lobe of the male genital arch shows striking d

53 itiana, differ markedly in morphology of the posterior lobe of the male genital arch.

54 cephalon, including the infundibulum and the posterior lobe of the pituitary.

55 ex to the cerebellar cortical C1 zone in the posterior lobe of the rat cerebellum was investigated us

56 /z 2000 were detected and sequenced from the posterior lobe of the rat pituitary gland.

57 The epandrial posterior lobes of male genitalia are a novelty of parti

58 their respective impact on the anterior and posterior lobes of the PG (APG and PPG) remains unclear,

59 atrix, which also became integrated into the posterior lobe program.

60 midsagittal area and volume of the inferior posterior lobe remained significantly smaller in the sch

61 morphology and that posterior lobe size and posterior lobe shape can be separated genetically for so

62 rge effects on either posterior lobe size or posterior lobe shape.

63 Unexpectedly, we found that the posterior lobe signaling center emerged from a preexisti

64 ffects on posterior lobe morphology and that posterior lobe size and posterior lobe shape can be sepa

65 Furthermore, we found that posterior lobe size differences caused by the species-sp

66 types that each have large effects on either posterior lobe size or posterior lobe shape.

67 re, we show that Sox21b negatively regulates posterior lobe size.

68 ion in D. mauritiana, which develops smaller posterior lobes than D. simulans.

69 nded in lobe-forming species, connecting the posterior lobe to the ancestrally derived aECM network.

70 found that Purkinje cells recorded from the posterior lobe vermis and hemisphere have high simple sp

71 folia of the paramedian lobule (PML) in the posterior lobe were investigated in cats by using a comb

72 rebellum, the anterior lobe and the superior posterior lobe were profoundly reduced in both vermis an

73 expression appeared mostly restricted to the posterior lobe, where it followed a caudal-to-rostral gr

74 intermediate lobe, and by pituicytes in the posterior lobe, whereas GLT-1 is expressed only by the a

75 on of three cognitive representations in the posterior lobe, which are interconnected with cerebral a