戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1  birth date and are dispersed throughout the anterior lobe.
2 enchymal transition, is absent in the dorsal anterior lobe.
3  Rathke's pouch to cell specification in the anterior lobe.
4 yed recall also showed associations with 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 e folliculostellate cells of the pituitary's anterior lobe.
10 erably lower amounts of staining observed in anterior lobes.
11 nal granular layer between the posterior and anterior lobes.
12 E-LPV) and/or the concentration of DA in the anterior lobe (AL) are inversely related to the secretio
13 asia of the intermediate lobe (IL) while the anterior lobe (AL) is not overtly affected.
14    The secretion of prolactin (PRL) from the anterior lobe (AL) of the pituitary gland is tonically i
15 r of the population, and most arise from the anterior lobe (AL).
16  remained unchanged in the inner zone of the anterior lobe (AL-IZ).
17 nce (ME), decreased in the outer zone of the anterior lobe (AL-OZ), as well as the intermediate (IL)
18 eously from Purkinje cells in the paravermal anterior lobe and from muscles of the hand and arm in th
19 ells revealed widespread degeneration in the anterior lobe and in limited areas of the posterior lobe
20                               The cerebellar anterior lobe and pars triangularis made significant con
21 ysfunctions were chiefly associated with the anterior lobe and posterior lobule HVI.
22 pe, corticotrope and lactotrope cells in the anterior lobe and the intermediate lobe melanotropes.
23             Measures of the right cerebellar anterior lobe and the left and right pars triangularis c
24 of the paravermal C1 zone in lobule V of the anterior lobe and the rostral folia of the paramedian lo
25                       In the cerebellum, the anterior lobe and the superior posterior lobe were profo
26  motor cortex, bilateral putamen and insula, anterior lobe and vermis of the cerebellum and superior
27 gin, with the oral ectoderm contributing the anterior lobe, and the neural ectoderm generating the po
28 s they transition from Rathke's pouch to the anterior lobe appears to be essential for their movement
29                             All cells in the anterior lobe are specified and differentiate, but an ea
30 llum is greater than the number of PC in the anterior lobe, as classically defined by the primary fis
31 , and 3) the defect is not restricted to the anterior lobe but involves a portion of the posterior lo
32 tact in Rathke's pouch, the precursor to the anterior lobe, but the anterior lobe was hypoplastic.
33 expressed by folliculo-stellate cells in the anterior lobe, by a group of astrocyte-like cells and by
34                      We find that all of the anterior lobe cell types initiate differentiation concur
35 ate lobe melanotropes is delayed relative to anterior lobe cell types.
36 minant caudal pons projections to cerebellar anterior lobe, contrasted with associative-predominant r
37 ss the pro-opiomelanocortin (POMC) gene, the anterior lobe corticotropes, producing adrenocorticotrop
38 s inactivated the cerebellar nuclei, lateral anterior lobe, crus I, rostral crus II, and lobule HVI i
39 ound, in addition to the marked depletion of anterior lobe granule cells ( > 90%), there were also si
40 the neural ectoderm was sufficient to impair anterior lobe growth, but not the differentiation of hor
41 e pouch of conditional embryos led to severe anterior lobe hypoplasia with drastically reduced expres
42      Pituitaries of Hes1 deficient mice have anterior lobe hypoplasia.
43 pathology was confined to lobules I-V of the anterior lobe in patients with sporadic ALS in contrast
44  while the reduction of granule cells in the anterior lobes is substantial, there is an almost comple
45 had chronic hyperprolactinemia and developed anterior lobe lactotroph hyperplasia without evidence of
46 g from pairs of C1 zone sites located in the anterior lobe (lobule V) and C1 or C3 zone sites in rost
47 bjects had greater activity in the bilateral anterior lobe of cerebellum, premotor area, parietal cor
48  with, the caudal extent of the disorganized anterior lobe of meander tail and the rostral extent of
49 genitors transplanted into the granuloprival anterior lobe of neonatal mea mutants differentiated int
50 the paraventricular hypothalamic nuclei, the anterior lobe of pituitary, and the thyroid gland.
51                  We show that lesions of the anterior lobe of rabbit cerebellar cortex disrupt the ti
52 eral hypothalamus, Rathke's pouch and in the anterior lobe of the adult pituitary.
53 nditioning results in plasticity in both the anterior lobe of the cerebellar cortex and in the anteri
54 logical analysis suggests that damage to the anterior lobe of the cerebellar cortex is necessary and
55                      The volume of the right anterior lobe of the cerebellum distinguished dyslexic f
56                               Lesions of the anterior lobe of the cerebellum produced only minor chan
57 near-total depletion of granule cells in the anterior lobe of the cerebellum, as well as aberrantly l
58 he virtual depletion of granule cells in the anterior lobe of the cerebellum.
59                                          The anterior lobe of the pituitary gland is composed of five
60 1 causes a morphological defect in which the anterior lobe of the pituitary gland protrudes through t
61 I revealed a solid-cystic mass involving the anterior lobe of the pituitary gland.
62 ground develop high-penetrance tumors of the anterior lobe of the pituitary, a class of tumors estima
63                              In cells of the anterior lobe of the pituitary, D2 dopamine receptors (b
64    Luteinizing hormone (LH), produced in the anterior lobe of the pituitary, is a member of the hypot
65 progressive, dose-dependent loss of the most anterior lobe of the vermis in mice lacking Fgf17 and in
66 ranule cells that predominantly populate the anterior lobes of the adult cerebellum and later, those
67 right superior temporal gyrus, posterior and anterior lobes of the cerebellum, and bilateral parahipp
68 right superior temporal gyrus, posterior and anterior lobes of the cerebellum, bilateral parahippocam
69 lexics exhibited significantly smaller right anterior lobes of the cerebellum, pars triangularis bila
70                         The intermediate and anterior lobes of the pituitary gland are derived from a
71 ells were identified in the intermediate and anterior lobes of the pituitary, the thyroid and parathy
72 lly mea/mea granule cells are present in the anterior lobe or, unexpectedly, in the posterior lobe.
73                               Lesions of the anterior lobe primary sensorimotor representations produ
74 However in-depth analysis has focused on the anterior lobe progenitors (AP), ignoring the posterior p
75 te mouse gestation and the postnatal period, anterior lobe progenitors re-enter the cell cycle and ex
76 se having lesionectomies, no difference from anterior lobe resection was recorded.
77 , loose the majority of granule cells in the anterior lobe resulting in few axons and atypical Purkin
78 ypoplastic with an abnormal branching of the anterior lobe, revealing a role for microRNAs in pituita
79 from the central vermis, and analysis of the anterior lobe reveals several missing zebrin II- bands.
80 f granule cells to develop in the cerebellar anterior lobe; the mechanism is unknown.
81 lmost always accompanied by dispersal of the anterior lobes themselves.
82 ults in accelerated progression of pituitary anterior lobe tumors and medullary thyroid carcinomas.
83 e transgene was expressed transiently in the anterior lobe vermis.
84 e territory providing climbing fibres to the anterior lobe was centred more laterally than the territ
85  the precursor to the anterior lobe, but the anterior lobe was hypoplastic.
86 ellar vermis and left lobule V of cerebellar anterior lobe were additionally activated for dual-task
87        Cystic cavities observed in pituitary anterior lobes were lined by cuboidal, ciliated epitheli
88 diate lobe and over a subset of cells in the anterior lobe, whereas CRF-R2 transcripts were expressed
89 ngs developed accelerated enlargement of the anterior lobe with predominantly TSH cell hyperplasia.