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 ially overlap with those of Reelin-deficient reeler mice.
2 elin, and radial glial fibers in control and reeler mice.
3 oth control (wild-type and heterozygous) and reeler mice.
4 and GAD67 mRNAs in both WT and heterozygous reeler mice.
5 transplanted HNSCs in wild-type, but not in reeler mice.
6 rent from both wild-type mice and homozygous reeler mice.
7 ruption of cell positioning in the retina of reeler mice.
8 a developmental event that fails to occur in reeler mice.
9 lacement of neurons and associated ataxia in reeler mice.
10 ssed in normal mouse brain that is absent in reeler mice.
11 basal forebrain markers Dlx1/2 in normal and reeler mice.
12 ese interneurons is not generally altered in reeler mice.
13 e disrupted cortical lamination phenotype in reeler mice and subsequent identification of the Reelin
18 ative study in the cerebella of heterozygous reeler mice (HRM), in which reelin expression is down-re
22 ding that the brains of developing and adult reeler mice of both sexes contained a markedly reduced n
23 the extracellular matrix protein missing in reeler mice, plays an important role in neuronal migrati
26 reelin and GAD67 in both WT and heterozygous reeler mice, suggesting an epigenetic action through the
30 rons migrated and differentiated normally in reeler mice, the migrations of both sympathetic (SPNs) a
31 r initial migration, SPN in both control and reeler mice were closely apposed to radial glial fibers
32 This callosal phenotype is not detected in reeler mice, which also exhibit defects in cortical lami
WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。