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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
; K6 N8 X" D1 K5 H% Shttp://www.ncbi.nlm.nih.gov/pubmed/21720384
. b! v* s! R0 d" S9 ?9 R3 b2、The Nodal inhibitor Lefty is negatively modulated by the microRNA miR-302 in human embryonic stem cells7 x% k. u% x/ W
http://www.ncbi.nlm.nih.gov/pubmed/21266536! D+ C3 {* j( j0 e2 `1 ?3 V
3、Oct4 regulates the miR-302 cluster in P19 mouse embryonic carcinoma cells.
+ N9 a/ U" D' P) H/ @8 ~! vhttp://www.ncbi.nlm.nih.gov/pubmed/20857206; l3 \2 Q2 J6 d7 f. k: T
4、miR-290 Cluster Modulates Pluripotency by Repressing Canonical NF-κB Signaling.8 [9 i+ r& T8 S; ?8 @! v
http://www.ncbi.nlm.nih.gov/pubmed/222320843 T( E  q& |0 l4 ~1 K
5、Immortalized mouse embryo fibroblasts are resistant to miR-290-induced senescence regardless of p53 status.# f5 S5 b* i5 D$ U
http://www.ncbi.nlm.nih.gov/pubmed/21846807
4 c  b3 [% u0 o; N6 s& R7 n- h) _6、Genome-wide impact of a recently expanded microRNA cluster in mouse.
1 P( P& d4 |6 o. \" N* q% yhttp://www.ncbi.nlm.nih.gov/pubmed/21911408

fufengzhiwang

有两篇没找到