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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& {- J& g  Q" l; I* i) f
http://www.ncbi.nlm.nih.gov/pubmed/21720384. i2 u/ d% S+ O: o3 i& H) y
2、The Nodal inhibitor Lefty is negatively modulated by the microRNA miR-302 in human embryonic stem cells5 T  b2 t+ y" e0 K: }7 V( D1 x
http://www.ncbi.nlm.nih.gov/pubmed/21266536
: x# f: U" A$ w3、Oct4 regulates the miR-302 cluster in P19 mouse embryonic carcinoma cells.
# c* k) s. E5 Z" h6 p" Chttp://www.ncbi.nlm.nih.gov/pubmed/20857206
$ z3 v7 F3 I6 r# b% Y) ^4、miR-290 Cluster Modulates Pluripotency by Repressing Canonical NF-κB Signaling.- W0 Z$ T3 q% v& G8 o7 i; W4 |0 T
http://www.ncbi.nlm.nih.gov/pubmed/22232084  p2 X, Q. C- u- `  W% A4 D
5、Immortalized mouse embryo fibroblasts are resistant to miR-290-induced senescence regardless of p53 status.( r1 |' ?4 y; T2 m& I
http://www.ncbi.nlm.nih.gov/pubmed/21846807! G& z3 m8 I; i8 R* X/ o9 \- O
6、Genome-wide impact of a recently expanded microRNA cluster in mouse.
, J  w4 g$ J, O5 Q* N+ ehttp://www.ncbi.nlm.nih.gov/pubmed/21911408

fufengzhiwang

有两篇没找到