Glucose-related protein 78 (GRP78) is a chaperone protein localized primarily in the endoplasmic reticulum (ER) lumen, where it helps in proper protein folding by targeting misfolded proteins and facilitating protein assembly. In stressed cells, GRP78 is translocated to the cell surface (csGRP78) where it binds to various ligands and triggers different intracellular pathways. Thus, csGRP78 expression is associated with cancer, involved in the maintenance and progression of the disease. Extracellular exposition of csGRP78 leads to the production of autoantibodies as observed in patients with prostate or ovarian cancer, in which the ability to target csGRP78 affects the tumor development. Present on the surface of cancer cells and not normal ...
AbstractMetastasis is the cause of more than 90% of all cancer deaths. Despite this fact, most antic...
Restricted until 17 Apr. 2010.Glucose-regulated protein 78 (GRP78), a molecular chaperone at the end...
Copyright © 2015 Xiao Ma et al.This is an open access article distributed under the Creative Commons...
The 78 kDa glucose-regulated protein (GRP78) is considered an endoplasmic reticulum (ER)-resident mo...
<p>The chaperone protein GRP78 is primarily expressed in the endoplasmic reticulum, but it is also a...
2019-07-12GRP78 is an essential chaperone traditionally known to reside in the endoplasmic reticulum...
Glucose-regulated protein of 78 kD (GRP78) is a chaperone protein mainly located in the endoplasmic ...
Glucose-regulated protein of 78 kD (GRP78) is a chaperone protein mainly located in the endoplasmic ...
AbstractWe have recently identified glucose-regulated protein-78 (GRP78) as a relevant molecular tar...
The 78 kDa glucose-regulated protein (GRP78), a member of the 70 kDa heat-shock family of molecular ...
Traditionally, GRP78 has been regarded as an endoplasmic reticulum (ER) lumenal protein due to its c...
High levels of cell surface glucose regulated protein 78 (sGRP78) have been implicated in cancer gro...
Objective: To investigate the role of GRP78 in regulating cell growth and apoptosis in human breast ...
Metastasis is the cause of more than 90% of all cancer deaths. Despite this fact, most anticancer th...
Traditionally, GRP78 has been regarded as an endoplasmic reticulum (ER) lumenal protein due to its c...
AbstractMetastasis is the cause of more than 90% of all cancer deaths. Despite this fact, most antic...
Restricted until 17 Apr. 2010.Glucose-regulated protein 78 (GRP78), a molecular chaperone at the end...
Copyright © 2015 Xiao Ma et al.This is an open access article distributed under the Creative Commons...
The 78 kDa glucose-regulated protein (GRP78) is considered an endoplasmic reticulum (ER)-resident mo...
<p>The chaperone protein GRP78 is primarily expressed in the endoplasmic reticulum, but it is also a...
2019-07-12GRP78 is an essential chaperone traditionally known to reside in the endoplasmic reticulum...
Glucose-regulated protein of 78 kD (GRP78) is a chaperone protein mainly located in the endoplasmic ...
Glucose-regulated protein of 78 kD (GRP78) is a chaperone protein mainly located in the endoplasmic ...
AbstractWe have recently identified glucose-regulated protein-78 (GRP78) as a relevant molecular tar...
The 78 kDa glucose-regulated protein (GRP78), a member of the 70 kDa heat-shock family of molecular ...
Traditionally, GRP78 has been regarded as an endoplasmic reticulum (ER) lumenal protein due to its c...
High levels of cell surface glucose regulated protein 78 (sGRP78) have been implicated in cancer gro...
Objective: To investigate the role of GRP78 in regulating cell growth and apoptosis in human breast ...
Metastasis is the cause of more than 90% of all cancer deaths. Despite this fact, most anticancer th...
Traditionally, GRP78 has been regarded as an endoplasmic reticulum (ER) lumenal protein due to its c...
AbstractMetastasis is the cause of more than 90% of all cancer deaths. Despite this fact, most antic...
Restricted until 17 Apr. 2010.Glucose-regulated protein 78 (GRP78), a molecular chaperone at the end...
Copyright © 2015 Xiao Ma et al.This is an open access article distributed under the Creative Commons...