Pharmacology 514:
Current Topics in Pharmacology
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Current Topics in Pharmacology
Phcol 514
12:30 PM, Wednesday, October 29, 1997
Room T-530/530A HSC

Speaker: Laird Sheldahl
Topic: Who makes up these Journal Club titles? A clearly SMAD person

References:

  1. Imamura, T., Takase, M., Nishihara, A., Oeda, E., Hanai, J., Kawabata, M., Miyazono, K. Smad6 inhibits signalling by the TGF-beta superfamily. Nature 389:622-626, 1997.

  2. Nakao, A., Afrakhte, M., Moren, A., Nakayama, T., Christian, J.L., Heuchel, R., Itoh, S., Kawabata, M., Heldin, N.E., Heldin, C.H., ten Dijke, P. Identification of Smad7, a TGF beta-inducible antagonist of TGF-beta signalling. Nature 389:631-635, 1997.

  3. Nakao, A., Imamura, T., Souchelnytskyi, S., Kawabata, M., Ishisaki, A., Oeda, E., Tamaki, K., Hanai, Ji., Heldin, C.H., Miyazono, K., ten Dijke, P. TGF-beta receptor-mediated signalling through Smad2, Smad3 and Smad4. EMBO J 16:5353-5362, 1997.

  4. Macias-Silva, M., Abdollah, S., Hoodless, P.A., Pirone, R., Attisano, L., Wrana, J.L. MADR2 is a substrate of the TGF beta receptor and its phosphorylation is required for nuclear accumulation and signaling. Cell 87:1215-1224, 1996.

  5. Zhang, Y., Musci, T., Derynck, R. The tumor suppressor Smad4/DPC 4 as a central mediator of Smad function. Curr Biol 7:270-276, 1997.

Reviews:

  1. Massagué, J., Hata, A. and Liu, F. TGF-beta signalling through the Smad pathway. Trends in Cell. Biol. 7:187-192, 1997.

  2. Yingling, J.M., Wang, X.F., Bassing, C.H. Signaling by the transforming growth factor-beta receptors. Biochim Biophys Acta 1242:115-136, 1995.


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