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1 r progenitor cells and the developing murine cerebella.
2 lla are less than half the size of wild-type cerebella.
3 emodeling process occurring in all agranular cerebella.
4 in certain areas of the transplanted animals cerebella.
5 (A)-enriched RNA isolated from postnatal rat cerebella.
6 s of AD brains compared to the corresponding cerebella.
7 howing a much smaller increase in the larger cerebella.
8 an medulloblastoma tumors relative to normal cerebella.
9 croscopy volumes and immunostaining of mouse cerebella.
10 lls to neuronal lineages in developing fetal cerebella.
11 ., the Math1-null and Pax6-null (Sey) mutant cerebella.
12 n and cerebellar foliation in Shp2-deficient cerebella.
13 oth of which were elevated over 1.52-fold in cerebella.
14 evelopment in ATXN1[30Q]-D776 and ATXN1[82Q] cerebella.
15 human MB and negligible expression in normal cerebella.
16 l hemisphere foliation patterns in mammalian cerebella.
17  activated and ACC inhibited in Cu deficient cerebella.
18 ine peptide levels remained unchanged in Cu- cerebella.
19  was studied in young rats in rapidly frozen cerebella.
20 imaging experiments in acute slices from rat cerebella.
21 tween PC death and zonal organization in NBD cerebella.
22 ion is altered in adult leaner and tottering cerebella.
23 33A, were compared with subjects with normal cerebella.
24  12 in tottering but not leaner or wild type cerebella.
25 n of nNOS in developing leaner and tottering cerebella.
26 e cells of the posterior lobe of Barhl1(-)/- cerebella.
27 uman cerebella were closest to mouse P30-P60 cerebella.
28 croarrays to assess the trisomic and euploid cerebella.
29 ies, and "cyclin D3-only" mice lacked normal cerebella.
30 slatability of this approach in adult rhesus cerebella.
31                   Previous analyses of mouse cerebella(3-5) have not fully defined the compositional
32 bra distinct from the clustering of 33 of 34 cerebella, 7 of 7 pons, and all 3 livers.
33 nd tottering cerebella compared to wild type cerebella and compared to each other.
34  and neurological defects including enlarged cerebella and dentate gyri with increased size of neuron
35 ntegrated single-cell atlases of human fetal cerebella and MBs show potential cell populations predis
36  for p16 was negative in all examined normal cerebella and medulloblastomas.
37 ties in protruding and proportionately large cerebella and relatively narrow, flattened orbital surfa
38 solution view of A-to-I RNA editing in human cerebella and suggest that A-to-I editing of synaptic ge
39  neocortices, right and left hippocampi, the cerebella, and brainstems) of 21-day-old rats.
40 edulloblastomas were closest to mouse P1-P10 cerebella, and normal human cerebella were closest to mo
41  receptors, immunoaffinity purified from rat cerebella, and resolve their structures using cryo-elect
42 d a greater attrition of neurons, with their cerebella appearing to be particularly reduced (approxim
43  nNOS expression in the leaner and tottering cerebella are compensatory in nature with NO most likely
44 s to ionizing radiation at a time when their cerebella are developing.
45 s species, and showed in addition that large cerebella are disproportionately more folded than smalle
46 ella of similar size; however, mature mutant cerebella are less than half the size of wild-type cereb
47 filing of age-matched control and FXTAS mice cerebella at 16-20 weeks and 55 weeks.
48 ng pathways was also investigated in the rat cerebella by real-time RT-PCR after CO exposure.
49                                   In control cerebella, CB(1) receptors produced less than additive i
50                                Compared with cerebella (CBs) of non-Tg littermates, those of Tg mice
51 y analyses of the NEPs from injured neonatal cerebella compared to controls show a temporary increase
52 erentially expressed in leaner and tottering cerebella compared to wild type cerebella and compared t
53 oblasts and is upregulated in cyclin A2 null cerebella, cyclin E1 expression was unable to compensate
54    Analyses of rare human del chr 6p25 fetal cerebella demonstrate extensive phenotypic overlap with
55                         In vivo, Nr-CAM-null cerebella did not exhibit obvious histological defects,
56  that the axonal remodeling in granuloprival cerebella does not affect the noradrenergic afferent sys
57 s a useful model, since over 90% of autistic cerebella examined at autopsy have shown well-defined ce
58           Interestingly, ASC-deficient SmoA1 cerebella exhibited disrupted expression of genes in the
59 iddle occipital/fusiform gyri, and bilateral cerebella for both the rhyming and meaning tasks.
60 I editing of 10 synaptic genes in postmortem cerebella from 14 neurotypical and 11 autistic individua
61         This issue is addressed by examining cerebella from adult chimeras in which both the genotype
62 mporal appearance of c-fos expression in rat cerebella from birth to postnatal day 21 (P21) and follo
63 RNA B1 was found more commonly in postmortem cerebella from individuals with autism.
64  as revealed by phosphoproteomic analysis of cerebella from mice expressing a human SCA14-associated
65   Examination of postmortem samples of human cerebella from neurologically typical individuals suppor
66               Targeted analysis performed on cerebella from transgenic mice expressing a dominant act
67        We show that in early postnatal mouse cerebella, granule cell migration accelerates during lig
68 lular examinations indicate that Gas1 mutant cerebella have a reduced number of granule cells and BG
69         Granule neurons purified from weaver cerebella have greatly reduced G protein-activated inwar
70     Transcriptome profiling of Tmem67 mutant cerebella identified ectopic increased expression of hom
71 S/MS-based proteomic analysis of Mecr mutant cerebella identified loss of subunits of complex I of ox
72                                              Cerebella in 137 (47.1%), 71 (24.4%), and 83 (28.5%) of
73                                     In vivo, cerebella in Mef2d knock-out mice manifest increased sus
74 tilized primary cultures from neonatal mouse cerebella in order to determine (i) whether Shh initiate
75 ge tracing experiments in Foxc1 mutant mouse cerebella indicate that aberrant migration of granule ce
76                Consequently, IP6K3 knock-out cerebella manifest abnormalities in Purkinje cell struct
77                              In mutant mouse cerebella, NaCh were absent from axon initial segments o
78         Glycolipid catabolism in primary rat cerebella neurons was probed by incubation with tetramet
79 o cultured cells and primary hippocampal and cerebella neurons.
80                   Therefore, we screened the cerebella of 12 patients with alpha-synucleinopathies fo
81 neuron density in the Purkinje cell layer of cerebella of 13 SZ and 17 BP disorder patients from the
82 -driven neurodegeneration, we examined aging cerebella of adult astrocyte-specific Yin Yang1 (Yy1) co
83               qPCR analysis of cDNA from the cerebella of affected and unaffected horses suggested th
84 a are greater in granule cells obtained from cerebella of animals in the first postnatal week, coinci
85                                          The cerebella of astrotactin null mice are approximately 10%
86 gene expression changes were observed in the cerebella of At-65Q and N171-82Q mice.
87                                          The cerebella of ATM-/- mice appear normal by histologic exa
88 he same CpG island is hypermethylated in the cerebella of cases in whom aberrant histone methylation
89 d in the cerebral cortices, brain stems, and cerebella of caspase 3(-/-) mice.
90                                       In the cerebella of cdf/cdf homozygous mice, approximately 40%
91 recapitulates known clinical features in the cerebella of CHARGE patients.
92 ial cells exhibit normal morphologies in the cerebella of chimeric mice indicating that the mea gene
93 A is cerebellar specific, is not seen in the cerebella of exercised or stressed animals, and is disti
94 present in protein lysates prepared from the cerebella of female and male Sprague-Dawley rat pups.
95 oach, we counted Purkinje cells in the right cerebella of four human male control specimens, aged 41,
96                   A comparative study in the cerebella of heterozygous reeler mice (HRM), in which re
97 ogressively in granule neurons isolated from cerebella of increasing age.
98                                              Cerebella of IP6K2-deleted mice (IP6K2-knockout [KO]) pr
99 enesis markers (PGC1-alpha and NRF-1) in the cerebella of IP6K2-deleted mice (IP6K2-knockout), point
100 tified miRNAs whose expression is altered in cerebella of Mecp2-null mice before and after the onset
101 genes in Nestin(+) neural progenitors in the cerebella of mice by retroviral transfer in combination
102 1), adenosine A(1), and GABA(B) receptors in cerebella of mice undergoing prolonged treatment with ve
103 -1 transgenic mice were also observed in the cerebella of mouse models expressing full-length mutant
104                                              Cerebella of neuroD2-null mice expressed reduced levels
105  nestin-expressing neural progenitors in the cerebella of newborn mice.
106     Between the ages of 3 and 23 months, the cerebella of NIH Fischer 344 rats lose 30% of the thickn
107 yl-indocarbocyanine perchlorate (DiI) in the cerebella of normal and staggerer mutant mice at a serie
108 e have investigated amino acid metabolism in cerebella of NPC1-deficient mice at different stages of
109 served decreased zebrin-II expression in the cerebella of patients with SCA7.
110 ession of these miRNAs in GNPs isolated from cerebella of postnatal (P) day P6 Ink4c-/-; Ptch1+/- mic
111                       Postmortem analysis of cerebella of PS1-E280A carrier revealed greater Purkinje
112 als to NMDA in granule neurons cultured from cerebella of rat neonates exposed to alcohol (ethanol) d
113  AMPK activation, was robustly higher in Cu- cerebella of rat pups at two ages and in two separate ex
114 's area 22), hippocampi, caudate nuclei, and cerebella of schizophrenia patients and their matched no
115     At birth, wild-type and mutant mice have cerebella of similar size; however, mature mutant cerebe
116 enesis by targeting MYCN (and luciferase) to cerebella of transgenic mice.
117 n engineered microRNA targeting ATXN1 to the cerebella of well-established mouse models improved moto
118  we used CGC cultures prepared from immature cerebella of wild-type mice (MT1/MT2 CGC) and MT1- and M
119                              Compared to Cu+ cerebella, pACC content was significantly higher in all
120 on of the Kip1 and Ink4c genes in N-Myc-null cerebella partially rescues GNP cell proliferation and c
121                                  In the same cerebella, PC axons in lobule HV were 2.2-fold thicker t
122   The transcriptomes of developing and adult cerebella presented in this study emphasize the importan
123 hange in tandem, having significantly larger cerebella relative to neocortex size than other anthropo
124 is in PND21, PND28, PND42, and PND84 NBD rat cerebella revealed a complex pattern of PC degeneration.
125            Morphological analyses of A-T [M] cerebella revealed no substantial cellular defects, simi
126 tailed analysis of both adult and developing cerebella reveals a pattern of selectivity to the loss o
127 m the rostral region of perinatal Gpr56(-/-) cerebella show loss of adhesion to extracellular matrix
128                     Moreover, Fbw7-deficient cerebella showed supranumeral fissures and aberrant prog
129 ng, histological, and functional analyses of cerebella showed that deletion of Dicer in cerebellar as
130                                         WHIM cerebella single-cell profiling revealed major transcrip
131 of Purkinje cells in the mammalian and avian cerebella such that there is a characteristic parasagitt
132 tic MBs were highly associated with mouse P5 cerebella, suggesting that a clinically distinct subset
133 ng defects are observed resulting in smaller cerebella that are devoid of foliation.
134 geted granular layers (GL) of rat and turtle cerebella that are populated with large and geometricall
135 tal Purkinje cell number for the four entire cerebella to be 27.03, 19.74, 20.44 and 22.03 million ce
136 ll profiling of freshly isolated human fetal cerebella to establish a reference map delineating hiera
137 odulus (lobule X) from postnatal day 8 mouse cerebella to identify the neurotransmitter and receptors
138 tates (epigenomes) for developing, and adult cerebella using integrative massive-parallel sequencing
139 l morphology of Rac1(+/flox); Rac3(-/-); Cre cerebella was normal.
140                                        In ET cerebella, we identified motor lobule-specific PC axon p
141                      On hard-copy US images, cerebella were assigned three grades of appearance.
142  to mouse P1-P10 cerebella, and normal human cerebella were closest to mouse P30-P60 cerebella.
143                                              Cerebella were evaluated in 10-microm-thick, formaldehyd
144              At mid-gestation, Tmem67 mutant cerebella were hypoplastic and had aberrantly high canon
145                                     Isolated cerebella were immersed in normal, oxygenated physiologi
146 s of Purkinje cells in developing and mature cerebella were much reduced in size but increased in num
147                                     In whole cerebella, Western blotting revealed a significant incre
148 The caudal pattern was retained in postnatal cerebella, where, by postnatal day 0 (P0), transgene-pos
149 ses demonstrate reduced levels of S4 in SCA7 cerebella without evident alterations in the levels of o

 
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