ライフサイエンスコーパス: cerebella

1 emodeling process occurring in all agranular cerebella.

2 in certain areas of the transplanted animals cerebella.

3 (A)-enriched RNA isolated from postnatal rat cerebella.

4 s of AD brains compared to the corresponding cerebella.

5 ., the Math1-null and Pax6-null (Sey) mutant cerebella.

6 n and cerebellar foliation in Shp2-deficient cerebella.

7 oth of which were elevated over 1.52-fold in cerebella.

8 evelopment in ATXN1[30Q]-D776 and ATXN1[82Q] cerebella.

9 human MB and negligible expression in normal cerebella.

10 l hemisphere foliation patterns in mammalian cerebella.

11 activated and ACC inhibited in Cu deficient cerebella.

12 ine peptide levels remained unchanged in Cu- cerebella.

13 was studied in young rats in rapidly frozen cerebella.

14 slatability of this approach in adult rhesus cerebella.

15 imaging experiments in acute slices from rat cerebella.

16 tween PC death and zonal organization in NBD cerebella.

17 ion is altered in adult leaner and tottering cerebella.

18 33A, were compared with subjects with normal cerebella.

19 12 in tottering but not leaner or wild type cerebella.

20 n of nNOS in developing leaner and tottering cerebella.

21 e cells of the posterior lobe of Barhl1(-)/- cerebella.

22 uman cerebella were closest to mouse P30-P60 cerebella.

23 croarrays to assess the trisomic and euploid cerebella.

24 ies, and "cyclin D3-only" mice lacked normal cerebella.

25 lla are less than half the size of wild-type cerebella.

26 bra distinct from the clustering of 33 of 34 cerebella, 7 of 7 pons, and all 3 livers.

27 nd tottering cerebella compared to wild type cerebella and compared to each other.

28 and neurological defects including enlarged cerebella and dentate gyri with increased size of neuron

29 for p16 was negative in all examined normal cerebella and medulloblastomas.

30 ties in protruding and proportionately large cerebella and relatively narrow, flattened orbital surfa

31 solution view of A-to-I RNA editing in human cerebella and suggest that A-to-I editing of synaptic ge

32 neocortices, right and left hippocampi, the cerebella, and brainstems) of 21-day-old rats.

33 edulloblastomas were closest to mouse P1-P10 cerebella, and normal human cerebella were closest to mo

34 d a greater attrition of neurons, with their cerebella appearing to be particularly reduced (approxim

35 nNOS expression in the leaner and tottering cerebella are compensatory in nature with NO most likely

36 s to ionizing radiation at a time when their cerebella are developing.

37 ella of similar size; however, mature mutant cerebella are less than half the size of wild-type cereb

38 ng pathways was also investigated in the rat cerebella by real-time RT-PCR after CO exposure.

39 In control cerebella, CB(1) receptors produced less than additive i

40 Compared with cerebella (CBs) of non-Tg littermates, those of Tg mice

41 erentially expressed in leaner and tottering cerebella compared to wild type cerebella and compared t

42 oblasts and is upregulated in cyclin A2 null cerebella, cyclin E1 expression was unable to compensate

43 Analyses of rare human del chr 6p25 fetal cerebella demonstrate extensive phenotypic overlap with

44 In vivo, Nr-CAM-null cerebella did not exhibit obvious histological defects,

45 that the axonal remodeling in granuloprival cerebella does not affect the noradrenergic afferent sys

46 s a useful model, since over 90% of autistic cerebella examined at autopsy have shown well-defined ce

47 Interestingly, ASC-deficient SmoA1 cerebella exhibited disrupted expression of genes in the

48 iddle occipital/fusiform gyri, and bilateral cerebella for both the rhyming and meaning tasks.

49 I editing of 10 synaptic genes in postmortem cerebella from 14 neurotypical and 11 autistic individua

50 This issue is addressed by examining cerebella from adult chimeras in which both the genotype

51 mporal appearance of c-fos expression in rat cerebella from birth to postnatal day 21 (P21) and follo

52 RNA B1 was found more commonly in postmortem cerebella from individuals with autism.

53 Targeted analysis performed on cerebella from transgenic mice expressing a dominant act

54 We show that in early postnatal mouse cerebella, granule cell migration accelerates during lig

55 lular examinations indicate that Gas1 mutant cerebella have a reduced number of granule cells and BG

56 Granule neurons purified from weaver cerebella have greatly reduced G protein-activated inwar

57 Cerebella in 137 (47.1%), 71 (24.4%), and 83 (28.5%) of

58 In vivo, cerebella in Mef2d knock-out mice manifest increased sus

59 tilized primary cultures from neonatal mouse cerebella in order to determine (i) whether Shh initiate

60 ge tracing experiments in Foxc1 mutant mouse cerebella indicate that aberrant migration of granule ce

61 Consequently, IP6K3 knock-out cerebella manifest abnormalities in Purkinje cell struct

62 In mutant mouse cerebella, NaCh were absent from axon initial segments o

63 Glycolipid catabolism in primary rat cerebella neurons was probed by incubation with tetramet

64 o cultured cells and primary hippocampal and cerebella neurons.

65 Therefore, we screened the cerebella of 12 patients with alpha-synucleinopathies fo

66 neuron density in the Purkinje cell layer of cerebella of 13 SZ and 17 BP disorder patients from the

67 qPCR analysis of cDNA from the cerebella of affected and unaffected horses suggested th

68 a are greater in granule cells obtained from cerebella of animals in the first postnatal week, coinci

69 The cerebella of astrotactin null mice are approximately 10%

70 gene expression changes were observed in the cerebella of At-65Q and N171-82Q mice.

71 The cerebella of ATM-/- mice appear normal by histologic exa

72 he same CpG island is hypermethylated in the cerebella of cases in whom aberrant histone methylation

73 d in the cerebral cortices, brain stems, and cerebella of caspase 3(-/-) mice.

74 In the cerebella of cdf/cdf homozygous mice, approximately 40%

75 recapitulates known clinical features in the cerebella of CHARGE patients.

76 ial cells exhibit normal morphologies in the cerebella of chimeric mice indicating that the mea gene

77 A is cerebellar specific, is not seen in the cerebella of exercised or stressed animals, and is disti

78 present in protein lysates prepared from the cerebella of female and male Sprague-Dawley rat pups.

79 oach, we counted Purkinje cells in the right cerebella of four human male control specimens, aged 41,

80 A comparative study in the cerebella of heterozygous reeler mice (HRM), in which re

81 ogressively in granule neurons isolated from cerebella of increasing age.

82 tified miRNAs whose expression is altered in cerebella of Mecp2-null mice before and after the onset

83 genes in Nestin(+) neural progenitors in the cerebella of mice by retroviral transfer in combination

84 1), adenosine A(1), and GABA(B) receptors in cerebella of mice undergoing prolonged treatment with ve

85 -1 transgenic mice were also observed in the cerebella of mouse models expressing full-length mutant

86 Cerebella of neuroD2-null mice expressed reduced levels

87 nestin-expressing neural progenitors in the cerebella of newborn mice.

88 Between the ages of 3 and 23 months, the cerebella of NIH Fischer 344 rats lose 30% of the thickn

89 yl-indocarbocyanine perchlorate (DiI) in the cerebella of normal and staggerer mutant mice at a serie

90 e have investigated amino acid metabolism in cerebella of NPC1-deficient mice at different stages of

91 ession of these miRNAs in GNPs isolated from cerebella of postnatal (P) day P6 Ink4c-/-; Ptch1+/- mic

92 Postmortem analysis of cerebella of PS1-E280A carrier revealed greater Purkinje

93 als to NMDA in granule neurons cultured from cerebella of rat neonates exposed to alcohol (ethanol) d

94 AMPK activation, was robustly higher in Cu- cerebella of rat pups at two ages and in two separate ex

95 's area 22), hippocampi, caudate nuclei, and cerebella of schizophrenia patients and their matched no

96 At birth, wild-type and mutant mice have cerebella of similar size; however, mature mutant cerebe

97 enesis by targeting MYCN (and luciferase) to cerebella of transgenic mice.

98 n engineered microRNA targeting ATXN1 to the cerebella of well-established mouse models improved moto

99 we used CGC cultures prepared from immature cerebella of wild-type mice (MT1/MT2 CGC) and MT1- and M

100 Compared to Cu+ cerebella, pACC content was significantly higher in all

101 on of the Kip1 and Ink4c genes in N-Myc-null cerebella partially rescues GNP cell proliferation and c

102 The transcriptomes of developing and adult cerebella presented in this study emphasize the importan

103 hange in tandem, having significantly larger cerebella relative to neocortex size than other anthropo

104 is in PND21, PND28, PND42, and PND84 NBD rat cerebella revealed a complex pattern of PC degeneration.

105 Morphological analyses of A-T [M] cerebella revealed no substantial cellular defects, simi

106 tailed analysis of both adult and developing cerebella reveals a pattern of selectivity to the loss o

107 m the rostral region of perinatal Gpr56(-/-) cerebella show loss of adhesion to extracellular matrix

108 Moreover, Fbw7-deficient cerebella showed supranumeral fissures and aberrant prog

109 ng, histological, and functional analyses of cerebella showed that deletion of Dicer in cerebellar as

110 of Purkinje cells in the mammalian and avian cerebella such that there is a characteristic parasagitt

111 tic MBs were highly associated with mouse P5 cerebella, suggesting that a clinically distinct subset

112 ng defects are observed resulting in smaller cerebella that are devoid of foliation.

113 geted granular layers (GL) of rat and turtle cerebella that are populated with large and geometricall

114 tal Purkinje cell number for the four entire cerebella to be 27.03, 19.74, 20.44 and 22.03 million ce

115 odulus (lobule X) from postnatal day 8 mouse cerebella to identify the neurotransmitter and receptors

116 tates (epigenomes) for developing, and adult cerebella using integrative massive-parallel sequencing

117 On hard-copy US images, cerebella were assigned three grades of appearance.

118 to mouse P1-P10 cerebella, and normal human cerebella were closest to mouse P30-P60 cerebella.

119 Cerebella were evaluated in 10-microm-thick, formaldehyd

120 Isolated cerebella were immersed in normal, oxygenated physiologi

121 s of Purkinje cells in developing and mature cerebella were much reduced in size but increased in num

122 In whole cerebella, Western blotting revealed a significant incre

123 The caudal pattern was retained in postnatal cerebella, where, by postnatal day 0 (P0), transgene-pos

124 ses demonstrate reduced levels of S4 in SCA7 cerebella without evident alterations in the levels of o