Patricia Rodriguez-Martin

Las Palmas De Gran Canaria, CN, Spain

Last Updated: 09/26/2026

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Found 12 publications

Endogenous LXR signaling controls pulmonary surfactant homeostasis and prevents lung inflammation.

Endogenous LXR signaling controls pulmonary surfactant homeostasis and prevents lung inflammation.

Journal: Cellular and molecular life sciences : CMLS

Published: February 23, 2024

Reprogramming of the LXRα Transcriptome Sustains Macrophage Secondary Inflammatory Responses.

Reprogramming of the LXRα Transcriptome Sustains Macrophage Secondary Inflammatory Responses.

Journal: Advanced science (Weinheim, Baden-Wurttemberg, Germany)

Published: September 28, 2023

Crosstalk Between LXR and Caveolin-1 Signaling Supports Cholesterol Efflux and Anti-Inflammatory Pathways in Macrophages.

Crosstalk Between LXR and Caveolin-1 Signaling Supports Cholesterol Efflux and Anti-Inflammatory Pathways in Macrophages.

Journal: Frontiers in endocrinology

Published: November 30, 2020

Synthesis and Antiplasmodial Activity of 1,2,3-Triazole-Naphthoquinone Conjugates.

Synthesis and Antiplasmodial Activity of 1,2,3-Triazole-Naphthoquinone Conjugates.

Journal: Molecules (Basel, Switzerland)

Published: October 08, 2019

Signal transducer and activator of transcription (STAT)-5: an opportunity for drug development in oncohematology.

Signal transducer and activator of transcription (STAT)-5: an opportunity for drug development in oncohematology.

Journal: Oncogene

Published: November 09, 2018

Correction: CM363, a novel naphthoquinone derivative which acts as multikinase modulator and overcomes imatinib resistance in chronic myelogenous leukemia.

Correction: CM363, a novel naphthoquinone derivative which acts as multikinase modulator and overcomes imatinib resistance in chronic myelogenous leukemia.

Journal: Oncotarget

Published: September 06, 2018

Lawsone, Juglone, and β-Lapachone Derivatives with Enhanced Mitochondrial-Based Toxicity.

Lawsone, Juglone, and β-Lapachone Derivatives with Enhanced Mitochondrial-Based Toxicity.

Journal: ACS chemical biology

Published: June 08, 2018

A Novel Naphthoquinone-Coumarin Hybrid That Inhibits BCR-ABL1-STAT5 Oncogenic Pathway and Reduces Survival in Imatinib-Resistant Chronic Myelogenous Leukemia Cells.

A Novel Naphthoquinone-Coumarin Hybrid That Inhibits BCR-ABL1-STAT5 Oncogenic Pathway and Reduces Survival in Imatinib-Resistant Chronic Myelogenous Leukemia Cells.

Journal: Frontiers in pharmacology

Published: April 20, 2018

In vitro activity of 1H-phenalen-1-one derivatives against Acanthamoeba castellanii Neff and their mechanisms of cell death.

In vitro activity of 1H-phenalen-1-one derivatives against Acanthamoeba castellanii Neff and their mechanisms of cell death.

Journal: Experimental parasitology

Published: July 14, 2017

5-Ethynylarylnaphthalimides as antitumor agents: Synthesis and biological evaluation.

5-Ethynylarylnaphthalimides as antitumor agents: Synthesis and biological evaluation.

Journal: Bioorganic & medicinal chemistry

Published: January 10, 2017

CM363, a novel naphthoquinone derivative which acts as multikinase modulator and overcomes imatinib resistance in chronic myelogenous leukemia.

CM363, a novel naphthoquinone derivative which acts as multikinase modulator and overcomes imatinib resistance in chronic myelogenous leukemia.

Journal: Oncotarget

Published: April 23, 2016

Synthesis and study of antiproliferative, antitopoisomerase II, DNA-intercalating and DNA-damaging activities of arylnaphthalimides.

Synthesis and study of antiproliferative, antitopoisomerase II, DNA-intercalating and DNA-damaging activities of arylnaphthalimides.

Journal: Bioorganic & medicinal chemistry

Published: July 01, 2013

Showing 1-12 of 12

Last Updated: 09/26/2026