57 results on '"Cardinale V."'
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2. Setup of multidisciplinary team discussions for patients with cholangiocarcinoma: current practice and recommendations from the European Network for the Study of Cholangiocarcinoma (ENS-CCA)
3. CALIBRAGEM DE MODELOS PARA ESTIMATIVA DA EVAPORAÇÃO EM FUNÇÃO DO NÍVEL DO LENÇOL FREÁTICO
4. Cell Therapy and Bioengineering in Experimental Liver Regenerative Medicine: In Vivo Injury Models and Grafting Strategies.
5. OC.06.2: POTENTIALOFA NATURAL COMPOUNDAS HEDGEHOG PATHWAY INHIBITOR FOR THE TREATMENT OF INTRAHEPATIC CHOLANGIOCARCINOMA.
6. Survey on hepatic sarcoidosis in Italy.
7. The FXR agonist obeticholic acid inhibits the cancerogenic potential of human cholangiocarcinoma.
8. CONUT score predicts early morbidity after liver transplantation: a collaborative study.
9. Fatigue life of AISI 316L stainless steel welded joints, obtained by GMAW.
10. New insights into liver stem cells.
11. Triple therapies plus different probiotics for Helicobacter pylori eradication.
12. Specific human cholangiocarcinoma (CCA) subpopulations of cancer stem cells (CSCs) express DoubleCortin-Like Kinase 1 (DCLK1) and DCLK1 inhibition induces anti-cancer effects.
13. Pre-treatment risk stratification in primary biliary cholangitis: A predictive model to guide first-line combination therapy.
14. The cancerogenic potential of primary human Cholangioracinoma cells is inhibited by Obeticholic Acid, a Farnesoid X Receptor (FXR) agonist.
15. Ductular reaction, intermediate hepatocytes and fibrosis extension correlate with prediction of treatment failure to ursodeoxycholic acid in primary biliary cholangitis.
16. Human duodenal submucosal glands contain stem cells with potential for liver and pancreatic regenerative medicine.
17. OC.04.1 GENERATION OF 3D ORGANOIDS OF HUMAN FETAL BILIARY TREE STEM CELLS (HBTSCS) AS INNOVATIVE TOOL FOR THE REGENERATIVE MEDICINE OF LIVER AND PANCREAS.
18. OC.08.2 THE FXR AGONIST, OBETICHOLIC ACID, INHIBITS THE CANCEROGENIC POTENTIAL OF PRIMARY HUMAN CHOLANGIOCARCINOMA CELLS: A STUDY ON PRIMARY HUMAN CELL CULTURES.
19. OC.08.1 DOUBLECORTIN-LIKE KINASE 1 (DCLK1) IS A MARKER OF SPECIFIC SUBPOPULATIONS OF CANCER STEM CELLS (CSCS) IN HUMAN CHOLANGIOCARCINOMA (CCA) AND ITS INHIBITION EXERTS ANTI-CANCER EFFECTS.
20. P.04.6 PRIMARY HUMAN BILIARY TREE STEM/PROGENITOR CELLS (HBTSCS) EXPOSED TO MICROENVIRONMENTAL FACTORS SHOWED PROLIFERATION, EPITHELIAL-MESENCHYMAL TRANSITION (EMT) AND SENESCENCE, RECAPITULATING THE PATHOLOGICAL FEATURES TYPICAL OF HUMAN CHOLANGIOPATHIES
21. The exposure of primary cultures of human biliary tree stem/progenitor cells (hBTSCs) to different micro-environmental factors induces proliferation, epithelial-mesenchymal transition (EMT) and senescence, which are typical pathological features of...
22. Establishment of expanding 3D-organoids cultures from human fetal biliary tree stem cells (hBTSCs) as a potential tool for regenerative medicine and disease modeling.
23. OC.13.3: Metformin Inhibits Proliferation, Enhances Apoptosis and Down-Regulates Epithelial to Mesenchymal Transition (EMT) in Human Cholangiocarcinoma (CCA): A Study on Human Primary Cell Cultures.
24. P.10.4: The Differentiation and Metabolism of Human Hepatic and Biliary Tree Stem/Progenitor Cells can be Significantly Modulated by Microgravity.
25. P.10.2: Hyaluronic Acid Improves the Engraftment Efficiency of Human Biliary Tree Stem/Progenitor Cells (HBTSCS).
26. A new strategy to improve the liver engraftment efficiency of transplanted human biliary tree stem/progenitor cells (hBTSCs): Cell coating with hyaluronic acid.
27. Microgravity maintains stemness and enhance glycolytic metabolism in human hepatic and biliary tree stem/progenitor cells.
28. Metformin reduces cell migration and down-regulates epithelial to mesenchymal transition (EMT) by AMPK/Foxo3a pathway in human intrahepatic cholangiocarcinoma (CCA).
29. PC.01.4 PERIBILIARY GLANDS AS A NICHE OF EXTRA-PANCREATIC INSULIN-PRODUCING AND GLUCOSE-SENSITIVE CELLS.
30. P1145 : Activation and epithelial-to-mesenchymal transition of biliary tree stem cells within peribiliary glands are involved in the pathogenesis of primary sclerosing cholangitis.
31. P0239 : Tumorigenic potential of Cancer Stem Cells (CSCs) isolated from human cholangiocarcinoma (CCA) subtypes in cirrhotic microenvironment.
32. P106 ADULT HUMAN BILIARY TREE STEM/PROGENITOR CELLS (hbTSCS) ARE EFFICIENTLY REPROGRAMMED TO FUNCTIONAL INSULIN-SECRETING β-PANCREATIC ISLET CELLS BY A NEWLY SYNTHESIZED HUMAN Pdx1 PEPTIDE.
33. P103 SUCCESSFUL CRYOPRESERVATION OF HUMAN BILIARY TREE STEM/PROGENITOR CELLS (hbTSCS) ISOLATED FROM ADULT LIVER BASED ON GOOD MANUFACTURING PRACTICE.
34. OC.19.5 TUMORIGENIC POTENTIAL OF CANCER STEM CELLS (CSCS) ISOLATED FROM HUMAN CHOLANGIOCARCINOMA (CCA) SUBTYPES.
35. OC.19.3 HUMAN CHOLANGIOCARCINOMA (CCA) AND CCA CANCER STEM CELLS (CSCS) ARE HIGHLY SENSITIVE TO THE ANTIPROLIFERATIVE EFFECTS OF PI3-KINASE INHIBITORS.
36. OC.09.6 HUMAN ADULT LIVER STEM CELLS ARE EFFICIENTLY REPROGRAMMED TO FUNCTIONAL B-PANCREATIC ISLET CELLS, SECRETING INSULIN, BY A NEWLY SYNTHESIZED HUMAN PDX1 PEPTIDE.
37. OC.16.5 HUMAN BILIARY TREE STEM/PROGENITOR CELLS (HBTSCS) FROM ADULT LIVER POSSESS IMMUNOMODULATORY PROPERTIES THROUGH FAS/FAS LIGAND INDUCED T-CELL APOPTOSIS.
38. P.01.9 SUCCESSFUL CRYOPRESERVATION OF HUMAN BILIARY TREE STEM/PROGENITOR CELLS (HBTSCS) ISOLATED FROM ADULT LIVER BASED ON GOOD MANUFACTURING PRACTICE (GMP).
39. Tumorigenic potential of cancer stem cells (CSCs) isolated from human cholangiocarcinoma (CCA) subtypes.
40. Human biliary tree stem/progenitor cells (hBTSCs) from peribiliary glands (PBGs) of adult liver display immunomodulatory properties through Fas/Fas ligand induced T-cell lymphocyte apoptosis.
41. Adult human biliary tree stem cells (hBTSCs) are efficiently reprogrammed to functional insulin-secreting β-pancreatic islet cells by a newly synthesized human Pdx1 peptide.
42. Human cholangiocarcinoma (CCA) and CCA cancer stem cells (CSCs) are highly sensitive to the antiproliferative effects of PI3-kinase inhibitors.
43. OC.05.2 HUMAN GALLBLADDER IS A HIGHLY AVAILABLE SOURCE OF STEM CELLS WITH MULTIPLE ENDODERMIC MATURE FATES POTENTIALITY.
44. OC-22 Human gallbladder is a highly available source of stem cells with multiple endodermic mature fates potentiality.
45. OC12 Candidate stem cell niches in the peribiliary glands (PBGs) of human extra hepatic bile ducts (hEHBDs).
46. OC9 Isolation, culturing and differentiation of multipotent stem cells from human foetal biliary tree.
47. OC6 In vitro and in vivo demonstration of multipotent cells isolated from human extrahepatic bile ducts (hEHBDs).
48. OC4 Successful isolation, culturing and in vivo differentiation of hepatic progenitor cells isolated from human foetal liver.
49. CS.3.2 MULTIPOTENT STEM CELLS RESIDE IN HUMAN EXTRAHEPATIC BILE DUCTS AND CAN GIVE RISE TO HEPATOCYTES, CHOLANGIOCYTES AND PANCREATIC ISLET CELLS.
50. F.N.1 MULTIPOTENT STEM CELLS RESIDE IN HUMAN EXTRAHEPATIC BILE DUCTS (hEHBDs) AND CAN GIVE RISE TO HEPATOCYTES, CHOLANGIOCYTES AND PANCREATIC ISLET CELLS.
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