Rocío Isabel
Rodríguez Macías
Catedrática de Universidad
Marta
Rodríguez Romero
Profesora Titular de Universidad
Marta Rodríguez Romero-rekin lankidetzan egindako argitalpenak (19)
2024
2022
2020
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Cellular mechanisms accounting for the refractoriness of colorectal carcinoma to pharmacological treatment
Cancers, Vol. 12, Núm. 9, pp. 1-34
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Clinical relevance of the relationship between changes in gut microbiota and bile acid metabolism in patients with intrahepatic cholangiocarcinoma
HEPATOBILIARY SURGERY AND NUTRITION
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Liver and gastrointestinal cancers
DRUG EFFLUX PUMPS IN CANCER RESISTANCE PATHWAYS: FROM MOLECULAR RECOGNITION AND CHARACTERIZATION TO POSSIBLE INHIBITION STRATEGIES IN CHEMOTHERAPY (ACADEMIC PRESS LTD-ELSEVIER SCIENCE LTD), pp. 197-250
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Molecular bases of drug resistance in hepatocellular carcinoma
Cancers, Vol. 12, Núm. 6, pp. 1-26
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Pilot multi-omic analysis of human bile from benign and malignant biliary strictures: A machine-learning approach
Cancers, Vol. 12, Núm. 6, pp. 1-30
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Relationship between changes in the exon-recognition machinery and SLC22A1 alternative splicing in hepatocellular carcinoma
Biochimica et Biophysica Acta - Molecular Basis of Disease, Vol. 1866, Núm. 5
2018
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Chemoresistance and chemosensitization in cholangiocarcinoma
Biochimica et Biophysica Acta - Molecular Basis of Disease, Vol. 1864, Núm. 4, pp. 1444-1453
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Molecular bases of the poor response of liver cancer to chemotherapy
Clinics and Research in Hepatology and Gastroenterology
2012
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Characterization of the role of ABCG2 as a bile acid transporter in liver and placenta
Molecular Pharmacology, Vol. 81, Núm. 2, pp. 273-283
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No correlation between the expression of FXR and genes involved in multidrug resistance phenotype of primary liver tumors
Molecular Pharmaceutics, Vol. 9, Núm. 6, pp. 1693-1704
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Up-regulation of FXR isoforms is not required for stimulation of the expression of genes involved in the lack of response of colon cancer to chemotherapy
Pharmacological Research, Vol. 66, Núm. 5, pp. 419-427
2011
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Further characterization of the electrogenicity and ph sensitivity of the human organic anion-transporting polypeptides OATP1B1 and OATP1B3
Molecular Pharmacology, Vol. 79, Núm. 3, pp. 596-607
2008
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Cytosol-nucleus traffic and colocalization with FXR of conjugated bile acids in rat hepatocytes
American Journal of Physiology - Gastrointestinal and Liver Physiology, Vol. 295, Núm. 1
2007
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Novel bile acid derivatives (BANBs) with cytostatic activity obtained by conjugation of their side chain with nitrogenated bases
Biochemical Pharmacology, Vol. 73, Núm. 9, pp. 1394-1404
2006
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OATP8/1B3-mediated cotransport of bile acids and glutathione: An export pathway for organic anions from hepatocytes?
Journal of Biological Chemistry, Vol. 281, Núm. 41, pp. 30326-30335
2005
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Effect of artemisinin/artesunate as inhibitors of hepatitis B virus production in an "in vitro" replicative system
Antiviral Research, Vol. 68, Núm. 2, pp. 75-83
2002
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Evidence for dual effects of DNA-reactive bile acid derivatives (Bamets) on hepatitis B virus life cycle in an in vitro replicative system
Antiviral Chemistry and Chemotherapy, Vol. 13, Núm. 6, pp. 371-380