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Genome-wide analysis of two parental human embryonic stem cell (ESC) lines (hESM01 and n5), three n5-derived somatic cell lines (N-neurons, F-fibroblasts, R-retinal pigment epithelium), and three pairs of induced pluripotent stem cell (iPSC) clones (iN, iF, iR) at gene expression level. All lines ar...
ORGANISM(S): Homo sapiens 
Genome wide DNA methylation profiling of two parental human embryonic stem cell (ESC) lines (hESM01 and n5), three n5-derived somatic cell lines (N-neurons, F-fibroblasts, R-retinal pigment epithelium), and three pairs of induced pluripotent stem cell (iPSC) clones (iN, iF, iR). All lines are isogen...
ORGANISM(S): Homo sapiens 
Ovarian cancer is characterized by transcoelomic metastasis into the peritoneal cavity. The peritoneal malignant ascites is enriched with ovarian cancer cells and a small amount of tumor-associated immune cells which create a unique microenvironment actively contributing to progression of the diseas...
ORGANISM(S): Homo sapiens (Human) 
2024-05-29 | PXD019327 | Pride
Exogenous signals from drug-stressed cancer cells accelerate the proliferation of neighboring tumor cells and promote them to acquire a more aggressive phenotype. We have recently found an exciting phenomenon: drug-stressed cancer cells secrete various components of the spliceosome: proteins and a n...
ORGANISM(S): Homo sapiens (Human) 
2024-05-29 | PXD027950 | Pride
Ovarian cancer is characterized by transcoelomic metastasis into the peritoneal cavity. The peritoneal malignant ascites is enriched with ovarian cancer cells and a small amount of tumor-associated immune cells which create a unique microenvironment actively contributing to progression of the diseas...
ORGANISM(S): Homo sapiens (Human) 
2024-05-29 | PXD045647 | Pride
Exogenous signals from drug-stressed cancer cells promote acquisition of a more aggressive phenotype of neighboring tumor cells. Recently, we examined how cancer cell secretome changes in response to chemotherapy. Moreover, therapy-induced secretomes significantly increased resistance of cancer cell...
ORGANISM(S): Homo sapiens (Human) 
2024-05-29 | PXD027794 | Pride
Exogenous signals from drug-stressed cancer cells promote acquisition of a more aggressive phenotype of neighboring tumor cells. To identify extracellular signaling molecules that potentially contribute to the development of therapy resistance, we examined how cancer cell secretome changes in respon...
ORGANISM(S): Homo sapiens (Human) 
2024-05-29 | PXD045663 | Pride
Exogenous signals from drug-stressed cancer cells accelerate the proliferation of neighboring tumor cells and promote them to acquire a more aggressive phenotype. We have recently found an exciting phenomenon: drug-stressed cancer cells secrete various spliceosomal proteins. We have observed this ph...
ORGANISM(S): Homo sapiens (Human) 
2024-05-29 | PXD027948 | Pride
Exogenous signals from drug-stressed cancer cells promote acquisition of a more aggressive phenotype of neighboring tumor cells. To identify extracellular signaling molecules that potentially contribute to the development of therapy resistance, we examined how cancer cell secretome changes in respon...
ORGANISM(S): Homo sapiens (Human) 
2024-05-29 | PXD019096 | Pride
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