Marcal Anglada-Pastor
Av. Diagonal 643
Barcelona, CT 08028, Spain
Barcelona, CT 08028, Spain
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 54 publications
Equilibrative nucleoside transporter 1 deficiency protects against diet-induced MASLD and is stage-associated in human liver disease.
Journal: Metabolism: clinical and experimental
Published: January 21, 2026
Building together a "trencadís" of nucleotide metabolism.
Journal: Nucleosides, nucleotides & nucleic acids
Published: December 13, 2025
Leveraging the Aggregated Protein Dye YAT2150 for Malaria Chemotherapy.
Journal: Pharmaceutics
Published: July 01, 2024
RNase H-sensitive multifunctional ASO-based constructs as promising tools for the treatment of multifactorial complex pathologies.
Journal: Bioorganic chemistry
Published: May 08, 2024
Latanoprost-Loaded Nanotransfersomes Designed for Scalp Administration Enhance Keratinocytes Proliferation.
Journal: Molecular pharmaceutics
Published: December 12, 2022
Inborn Errors of Nucleoside Transporter (NT)-Encoding Genes (SLC28 and SLC29).
Journal: International journal of molecular sciences
Published: July 07, 2022
Insights into the Pharmacogenetics of Tacrolimus Pharmacokinetics and Pharmacodynamics.
Journal: Pharmaceutics
Published: July 06, 2022
OncomiRs miR-106a and miR-17 negatively regulate the nucleoside-derived drug transporter hCNT1.
Journal: Cellular and molecular life sciences : CMLS
Published: June 25, 2021
From Inflammation to the Onset of Fibrosis through A2A Receptors in Kidneys from Deceased Donors.
Journal: International journal of molecular sciences
Published: October 15, 2020
Expression of the nucleoside transporters hENT1 (SLC29) and hCNT1 (SLC28) in pediatric acute myeloid leukemia.
Journal: Nucleosides, nucleotides & nucleic acids
Published: April 22, 2020
FMS-like tyrosine kinase 3 (FLT3) modulates key enzymes of nucleotide metabolism implicated in cytarabine responsiveness in pediatric acute leukemia.
Journal: Pharmacological research
Published: August 02, 2019
Deficiency of perforin and hCNT1, a novel inborn error of pyrimidine metabolism, associated with a rapidly developing lethal phenotype due to multi-organ failure.
Journal: Biochimica et biophysica acta. Molecular basis of disease
Published: August 17, 2018
Last Updated: 09/26/2026