Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Claire R. Weston"'
Autor:
Cristina Cellurale, Claire R Weston, Judith Reilly, David S Garlick, D Joseph Jerry, Hayla K Sluss, Roger J Davis
Publikováno v:
PLoS ONE, Vol 5, Iss 8, p e12469 (2010)
The cJun NH2-terminal kinase (JNK) signal transduction pathway has been implicated in mammary carcinogenesis. To test the role of JNK, we examined the effect of ablation of the Jnk1 and Jnk2 genes in a Trp53-dependent model of breast cancer using BAL
Externí odkaz:
https://doaj.org/article/e3edcc8710984e838f206fbeb95f0e60
Autor:
Daniel E Todd, Kathryn Balmanno, Catherine Newson, Sarah A. Molton, Claire R. Weston, Simon J. Cook, Andrew Garner
Publikováno v:
Cellular Signalling. 17:1412-1422
The conditional protein kinase DeltaMEKK3:ER* allows activation of the mitogen-activated and stress-activated protein kinases (MAPKs and SAPKs) without imposing a primary cellular stress or damage. Such separation of stress from stress-induced signal
Autor:
Anthony Wong, Richard A. Flavell, Mary E.P. Goad, Claire R. Weston, J. Perry Hall, Roger J. Davis
Publikováno v:
Proceedings of the National Academy of Sciences. 101:14114-14119
The c-Jun NH 2 -terminal kinase (JNK) group of mitogen-activated protein kinases is activated in response to a wide array of cellular stresses and proinflammatory cytokines. Roles for JNK in the developing nervous system and T-cell-mediated immunity
Autor:
Tamera Barrett, Claire R. Weston, Richard A. Flavell, Marie Helene Delmotte, Nyaya Kelkar, Roger J. Davis, Barbara J. Sheppard
Publikováno v:
Proceedings of the National Academy of Sciences. 100:9843-9848
The murine JNK-interacting protein 3 (JIP3) protein (also known as JSAP1) is expressed exclusively in neurons and has been identified as a scaffold protein for the c-Jun NH 2 -terminal kinase (JNK) signaling pathway and as an adapter protein for carg
Autor:
J. Perry Hall, Richard A. Flavell, Roger J. Davis, Anthony C. Wong, Claire R. Weston, Mary E.P. Goad
Publikováno v:
Genes & Development. 17:1271-1280
The c-Jun NH2-terminal kinase (JNK) group of mitogen-activated protein kinases is stimulated in response to a wide array of cellular stresses and proinflammatory cytokines. Mice lacking individual members of theJnkfamily (Jnk1,Jnk2, andJnk3) are viab
Publikováno v:
Journal of Biological Chemistry. 278:18811-18816
Both the ERK and phosphatidylinositol 3'-kinase (PI3K) signaling pathways can protect cells from apoptosis following withdrawal of survival factors. We have previously shown that the ERK1/2 pathway acts independently of PI3K to block expression of th
Publikováno v:
Science. 296:2345-2347
Mitogen activated protein kinases (MAPKs) are components of signaling pathways that control how cells respond to their environment. There are many different MAPKs and to keep pathways distinct, particular MAPKs must bind their ligands with high speci
Autor:
Claire R. Weston, Roger J. Davis
Publikováno v:
Current opinion in cell biology. 19(2)
The c-Jun NH(2)-terminal kinase (JNK) is a member of an evolutionarily conserved sub-family of mitogen-activated protein (MAP) kinases. Recent studies have led to progress towards understanding the physiological function of the JNK signaling pathway,
Autor:
Yasu-Taka Azuma, Richard A. Flavell, Manchuan Chen, Elise H. Tran, Claire R. Weston, Roger J. Davis
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America. 103(36)
Environmental insults such as microbial pathogens can contribute to the activation of autoreactive T cells, leading to inflammation of target organs and, ultimately, autoimmune disease. Various infections have been linked to multiple sclerosis and it
Autor:
Andrew P. Garner, Claire R. Weston, Catherine Newson, Kathryn Balmanno, Ruth M Densham, Sarah A Molton, Linda Scott, Daniel E Todd, Simon J. Cook
Publikováno v:
Oncogene. 23(19)
To study the mechanisms by which mitogen- and stress-activated protein kinases regulate cell cycle re-entry, we have used a panel of conditional kinases that stimulate defined MAPK or SAPK cascades. Activation of DeltaMEKK3:ER* during serum restimula