Zobrazeno 1 - 10
of 47
pro vyhledávání: '"De La Mota-Peynado A"'
Autor:
Van Nest, Kortnee, Swistek, Sabrina E, Olmstead, Morgan L, De La Mota-Peynado, Alina, Ewing, Robert D, Brabec, Daniel, Mitzel, Dana, Oppert, Brenda, Cohnstaedt, Lee W, Shults, Phillip
Publikováno v:
Journal of Economic Entomology; August 2024, Vol. 117 Issue: 4 p1280-1288, 9p
Autor:
De La Mota-Peynado, Alina ‡, 1, Lee, Stella Yu-Chien ‡, Pierce, Brianne Marie ‡, Wani, Prashant §, Singh, Chingakham Ranjit ‡, Roelofs, Jeroen ‡, §, 2
Publikováno v:
In Journal of Biological Chemistry 11 October 2013 288(41):29467-29481
Autor:
Montalvo-Ortiz, Brenda L. ‡, 1, Castillo-Pichardo, Linette ‡, §, 1, Hernández, Eliud ¶, Humphries-Bickley, Tessa ‡, De La Mota-Peynado, Alina §, Cubano, Luis A. §, Vlaar, Cornelis P. ¶, 2, Dharmawardhane, Suranganie ‡, 3
Publikováno v:
In Journal of Biological Chemistry 13 April 2012 287(16):13228-13238
Publikováno v:
In Journal of Biological Chemistry 21 October 2011 286(42):36641-36651
Publikováno v:
In Journal of Biological Chemistry 15 April 2011 286(15):13603-13611
Autor:
De La Mota-Peynado, Alina M.
Doctor of Philosophy
Division of Biology
Jeroen Roelofs
The ubiquitin-proteasome pathway is the major pathway of selective protein degradation in the cell. Disruption of this pathway affects cellular protein homeostasis and contributes
Division of Biology
Jeroen Roelofs
The ubiquitin-proteasome pathway is the major pathway of selective protein degradation in the cell. Disruption of this pathway affects cellular protein homeostasis and contributes
Externí odkaz:
http://hdl.handle.net/2097/18200
Publikováno v:
The Journal of Biological Chemistry
The proteasome is responsible for the degradation of many cellular proteins. If and how this abundant and normally stable complex is degraded by cells is largely unknown. Here we show that in yeast, upon nitrogen starvation, proteasomes are targeted
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93f120b59d021759e0443c8b239439d4
http://europepmc.org/articles/PMC4751371
http://europepmc.org/articles/PMC4751371
Autor:
Brianne Marie Pierce, Alina De La Mota-Peynado, Jeroen Roelofs, Chingakham Ranjit Singh, Prashant S. Wani, Stella Y. Lee
Publikováno v:
Journal of Biological Chemistry. 288:29467-29481
Several proteasome-associated proteins regulate degradation by the 26 S proteasome using the ubiquitin chains that mark most substrates for degradation. The proteasome-associated protein Ecm29, however, has no ubiquitin-binding or modifying activity,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::829c0607e53d9a37c4636811e036f0c4
https://doi.org/10.1074/jbc.m113.491662
https://doi.org/10.1074/jbc.m113.491662
Autor:
Brenda L. Montalvo-Ortiz, Cornelis P. Vlaar, Alina De La Mota-Peynado, Tessa Humphries-Bickley, Suranganie Dharmawardhane, Luis A. Cubano, Linette Castillo-Pichardo, Eliud Hernandez
Publikováno v:
Journal of Biological Chemistry. 287:13228-13238
The Rho GTPase Rac regulates actin cytoskeleton reorganization to form cell surface extensions (lamellipodia) required for cell migration/invasion during cancer metastasis. Rac hyperactivation and overexpression are associated with aggressive cancers
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b053776e713e75d6b2fe6a74649542af
https://doi.org/10.1074/jbc.m111.334524
https://doi.org/10.1074/jbc.m111.334524
Autor:
Michelle M. Martínez-Montemayor, Alina De La Mota-Peynado, Suranganie Dharmawardhane, Joel E. Martinez, Luis A. Cubano, Elisa Otero-Franqui
Publikováno v:
Clinical & Experimental Metastasis
To investigate the effects soy isoflavones in established cancers, the role of genistein, daidzein, and combined soy isoflavones was studied on progression of subcutaneous tumors in nude mice created from green fluorescent protein (GFP) tagged-MDA-MB
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3629d74c5092b602abbc4d88573dbb9
https://doi.org/10.1007/s10585-010-9336-x
https://doi.org/10.1007/s10585-010-9336-x