Kaposi's sarcoma-associated herpesvirus protein LANA2 disrupts PML oncogenic domains and inhibits PML-mediated transcriptional repression of the survivin gene
In Cell Death & Disease, 2008
... or WT mice, and the cell lines MCF-7, HEK-293, BSC-40, U251MG, and PC3 were maintained in DMEM supplemented with 10% heat-inactivated-fetal calf serum (Gibco, Life Technologies SA, Madrid, Spain), 5 mmol/l ... Novel particulate spin probe for targeted determination of oxygen in cells and tissuesmore suppliers
In Cell Death & Disease, 2002
... HepG2, UOS2, RKO, Saos-2, H1299, PC3, HeLa, DU145, WRO, Lncap, and T47D, MCF-7 and HCT cells lines were obtained from National Centre for Cell Sciences (Pune, India) ...
Role of calcium in polycystic kidney disease: From signaling to pathology.
Ferrara, Italy. In World J Nephrol, Feb 2016
The PKD1 gene encodes for polycystin-1 (PC1), a large multi-functional membrane receptor protein able to regulate ion channel complexes, whereas polycystin-2 (PC2), encoded by the PKD2 gene, is an integral membrane protein that functions as a calcium-permeable cation channel, located mainly in the endoplasmic reticulum (ER).
Autosomal Dominant Polycystic Kidney Disease: A Path Forward.
Sydney, Australia. In Semin Nephrol, Nov 2015
Autosomal dominant polycystic kidney disease (ADPKD) is the commonest inherited cause of renal failure in adults, and is due to loss-of-function mutations in either the PKD1 or PKD2 genes, which encode polycystin-1 and polycystin-2, respectively.
Direct recording and molecular identification of the calcium channel of primary cilia.
Boston, United States. In Nature, 2014
The polycystin proteins (PC and PKD), identified in linkage studies of polycystic kidney disease, are candidate channels divided into two structural classes: 11-transmembrane proteins (PKD1, PKD1L1 and PKD1L2) remarkable for a large extracellular amino terminus of putative cell adhesion domains and a G-protein-coupled receptor proteolytic site, and the 6-transmembrane channel proteins (PKD2, PKD2L1 and PKD2L2; TRPPs).
The biology and therapeutic targeting of the proprotein convertases.
More papers using
Montréal, Canada. In Nat Rev Drug Discov, 2012
Seven of these (proprotein convertase 1 (PC1), PC2, furin, PC4, PC5, paired basic amino acid cleaving enzyme 4 (PACE4) and PC7) activate cellular and pathogenic precursor proteins by cleavage at single or paired basic residues, whereas subtilisin kexin isozyme 1 (SKI-1) and proprotein convertase subtilisin kexin 9 (PCSK9) regulate cholesterol and/or lipid homeostasis via cleavage at non-basic residues or through induced degradation of receptors.