|
|
|
|
LEADER |
01351 am a22002293u 4500 |
001 |
97234 |
042 |
|
|
|a dc
|
100 |
1 |
0 |
|a Yamamura, Yasuko
|e author
|
100 |
1 |
0 |
|a Massachusetts Institute of Technology. Department of Biology
|e contributor
|
100 |
1 |
0 |
|a Whitehead Institute for Biomedical Research
|e contributor
|
100 |
1 |
0 |
|a Lodish, Harvey F.
|e contributor
|
700 |
1 |
0 |
|a Hua, Xianxin
|e author
|
700 |
1 |
0 |
|a Bergelson, Svetlana
|e author
|
700 |
1 |
0 |
|a Lodish, Harvey F
|e author
|
245 |
0 |
0 |
|a Critical Role of Smad and AP-1 Complexes in TGF-β-Dependent Apoptosis
|
260 |
|
|
|b Hindawi Publishing Corporation,
|c 2015-06-09T13:37:50Z.
|
856 |
|
|
|z Get fulltext
|u http://hdl.handle.net/1721.1/97234
|
520 |
|
|
|a Transforming growth factor-β1 (TGF-β1) induces not only cell growth inhibition but also apoptosis in hepatocytes, myeloid cells, and epithelial cells. Smad complexes (Smad2-Smad4 and Smad3-Smad4) are identified as key signaling molecules which transmit TGF-β1 signal for growth inhibition from the TGF-β receptors to the nucleus (1, 2). However, their roles are unclear in the induction of apoptosis. Our results show here that both Smad and AP-1 complexes play a critical role in TGF-β1 signaling for apoptosis.
|
520 |
|
|
|a National Institutes of Health (U.S.) (Grant CA63260)
|
546 |
|
|
|a en
|
655 |
7 |
|
|a Article
|
773 |
|
|
|t The Scientific World JOURNAL
|