Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Christina S. Pichot"'
Autor:
Seth J. Corey, Jeffrey A. Frost, Jindan Yu, Saad Marzouk, John Bechill, Samuel A. Jensen, Sean M. Hartig, Constadina Arvanitis, Christina S. Pichot
Supplementary Figure 2 from Cdc42-Interacting Protein 4 Promotes Breast Cancer Cell Invasion and Formation of Invadopodia through Activation of N-WASp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c91ab98e482ba03b16e39a90ee8be91a
https://doi.org/10.1158/0008-5472.22384044.v1
https://doi.org/10.1158/0008-5472.22384044.v1
Autor:
Seth J. Corey, Jeffrey A. Frost, Jindan Yu, Saad Marzouk, John Bechill, Samuel A. Jensen, Sean M. Hartig, Constadina Arvanitis, Christina S. Pichot
In the earliest stages of metastasis, breast cancer cells must reorganize the cytoskeleton to affect cell shape change and promote cell invasion and motility. These events require the cytoskeletal regulators Cdc42 and Rho, their effectors such as N-W
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3e95ff1eef6dcd0be38532ab7c709efe
https://doi.org/10.1158/0008-5472.c.6500751
https://doi.org/10.1158/0008-5472.c.6500751
Autor:
Seth J. Corey, Jeffrey A. Frost, Jindan Yu, Saad Marzouk, John Bechill, Samuel A. Jensen, Sean M. Hartig, Constadina Arvanitis, Christina S. Pichot
Supplementary Figure 3 from Cdc42-Interacting Protein 4 Promotes Breast Cancer Cell Invasion and Formation of Invadopodia through Activation of N-WASp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc06788c56f7f417d8a33d759214618f
https://doi.org/10.1158/0008-5472.22384041
https://doi.org/10.1158/0008-5472.22384041
Autor:
Seth J. Corey, Jeffrey A. Frost, Jindan Yu, Saad Marzouk, John Bechill, Samuel A. Jensen, Sean M. Hartig, Constadina Arvanitis, Christina S. Pichot
Supplementary Figure 4 from Cdc42-Interacting Protein 4 Promotes Breast Cancer Cell Invasion and Formation of Invadopodia through Activation of N-WASp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00ff83d0e4e2b449fbfad53bafa9597b
https://doi.org/10.1158/0008-5472.22384038
https://doi.org/10.1158/0008-5472.22384038
Autor:
Seth J. Corey, Jeffrey A. Frost, Jindan Yu, Saad Marzouk, John Bechill, Samuel A. Jensen, Sean M. Hartig, Constadina Arvanitis, Christina S. Pichot
Supplementary Figure 1 from Cdc42-Interacting Protein 4 Promotes Breast Cancer Cell Invasion and Formation of Invadopodia through Activation of N-WASp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5bf0c0b56b084d390f5fb38d39694329
https://doi.org/10.1158/0008-5472.22384047.v1
https://doi.org/10.1158/0008-5472.22384047.v1
Autor:
Christina S. Pichot, John Bechill, Jeffrey A. Frost, Seth J. Corey, Samuel A. Jensen, Jindan Yu, Sean M. Hartig, Constadina Arvanitis, Saad Marzouk
Publikováno v:
Cancer research. 70(21)
In the earliest stages of metastasis, breast cancer cells must reorganize the cytoskeleton to affect cell shape change and promote cell invasion and motility. These events require the cytoskeletal regulators Cdc42 and Rho, their effectors such as N-W
Autor:
Christina S. Pichot
The focus of this project is the contribution of the Cdc42-interacting protein CIP4 to the invasive phenotype of MDA-MB-231 cancer cells. CIP4 is a member of the F-BAR family of proteins, which interact with or induce plasma membrane curvature throug
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::faee7d26c35ddcd48158b79f2ac57eb2
https://doi.org/10.21236/ada517228
https://doi.org/10.21236/ada517228
Autor:
Christina S. Pichot, Seth J. Corey, Yanming Feng, Robert W. Grange, Shuhei Ishikura, Robert M. Raphael, Rachel S Hicklen, Sean M. Hartig, Amira Klip, Elisabeth G. Blanchard, Kevin A. Voelker
Publikováno v:
Journal of cell science. 122(Pt 13)
F-BAR proteins are a newly described family of proteins with unknown physiological significance. Because F-BAR proteins, including Cdc42 interacting protein-4 (CIP4), drive membrane deformation and affect endocytosis, we investigated the role of CIP4