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juan880929

1、The miR 302-367 cluster drastically affects self-renewal and infiltration properties of glioma-initiating cells through CXCR4 repression and consequent disruption of the SHH-GLI-NANOG network
0 s# A" O7 ?, W/ }9 y: ]) khttp://www.ncbi.nlm.nih.gov/pubmed/217203844 B$ u' F7 b5 }' q2 B! V' M
2、The Nodal inhibitor Lefty is negatively modulated by the microRNA miR-302 in human embryonic stem cells
* a; `- ^6 s9 {) o- Q) ahttp://www.ncbi.nlm.nih.gov/pubmed/21266536: n0 d4 ?; U5 H
3、Oct4 regulates the miR-302 cluster in P19 mouse embryonic carcinoma cells.' f- l0 U. P9 R- H+ D9 q, Y
http://www.ncbi.nlm.nih.gov/pubmed/20857206! l( a- L' n- T; [
4、miR-290 Cluster Modulates Pluripotency by Repressing Canonical NF-κB Signaling., [' O; Y, k0 `- X
http://www.ncbi.nlm.nih.gov/pubmed/222320845 X" d* m% G: |9 G* b4 `) v; j
5、Immortalized mouse embryo fibroblasts are resistant to miR-290-induced senescence regardless of p53 status.
( u6 ?' B2 x* A# ghttp://www.ncbi.nlm.nih.gov/pubmed/21846807
, d0 M% ~* l5 _6、Genome-wide impact of a recently expanded microRNA cluster in mouse.
" ^" I& I: f1 @" nhttp://www.ncbi.nlm.nih.gov/pubmed/21911408

fufengzhiwang

有两篇没找到