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1 ro (P0) and/or fatty acid binding protein 7 (Fabp7).
2 in with characteristics distinct from native FABP7.
3  in strongly reduced expression of Sox10 and Fabp7.
4 gh Sox10 levels and to trigger expression of Fabp7.
5  melanomas by immunohistochemistry with anti-FABP7 Ab showed 73 and 27% positivity, respectively (P<0
6 ic analysis as fatty acid binding protein 7 (FABP7), also known as brain lipid binding protein) which
7 he brain fatty acid-binding protein (B-FABP; FABP7) and glial fibrillary acidic protein (GFAP) genes
8 s, CSDE1 binds fatty acid binding protein 7 (FABP7) and vimentin (VIM) mRNAs, as well as transcripts
9 urther investigated one gene from the group, FABP7, and confirmed its association with survival in tw
10 central nervous system (FABP3, FABP4, FABP5, FABP7, and PMP2).
11                                              FABP7 as a surrogate biomarker for circulating tumor cel
12 stoma cells after overexpression of FABP5 or FABP7, but not FABP3.
13 L cell line proliferation and growth on LTR2-FABP7 chimeric protein expression.
14                                     The LTR2-FABP7 chimeric transcript encodes a novel chimeric isofo
15    Assessment of patients' blood showed that FABP7(+) CTC decreased with disease progression.
16                                              FABP7 detection of metastatic tissues was inversely corr
17                                Expression of FABP7 enhanced the motility of glioma-derived cells in v
18                                   Given that Fabp7 expression is confined to astrocytes and neural pr
19                                   To examine FABP7 expression loss in advanced melanomas, loss of het
20 sing microsatellite markers encompassing the FABP7 gene.
21                Fatty acid-binding protein-7 (FABP7) has been shown to be expressed in cutaneous melan
22  astrocyte brain fatty acid binding protein (Fabp7) has previously been shown to have a coordinated d
23 ng proteins (FABPs), in particular FABP5 and FABP7, have recently been identified by us as intracellu
24 e expression in cancer and suggest that LTR2-FABP7 may contribute to the pathogenesis of DLBCL in a s
25                                              FABP7 may function as a tumor progression gene and can b
26 In this study, we confirmed an enrichment of Fabp7 mRNA and protein in the astrocytic perisynaptic co
27                            Here we show that Fabp7 mRNA coimmunoprecipitated with CPEB1 from primary
28  change in the intracellular distribution of Fabp7 mRNA in molecular layers of hippocampus.
29 lar trafficking and localized translation of Fabp7 mRNA in the tripartite synapse of mammalian brain.
30 e brain, the synchronized cycling pattern of Fabp7 mRNA is a novel discovery among known CPE-regulate
31 ed time-of-day-dependent oscillation for the Fabp7 mRNA poly(A) tail throughout murine brain.
32                                              FABP7 mRNA was highly expressed in 60 of 87 (69%) primar
33 ving a fatty acid-binding protein gene (LTR2-FABP7), normally expressed in brain, that was ectopicall
34 d 12 (Cxcl12), fatty acid binding protein 7 (Fabp7), plasma membrane proteolipid (Pllp), and suppress
35 of-day changes in expression and trafficking Fabp7 to the perisynaptic process are not known.
36                                Expression of FABP7 was assessed during melanoma progression through a
37 observations, we hypothesized that FABP5 and FABP7 would provide excellent pharmacological targets.

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