Zobrazeno 1 - 10
of 45
pro vyhledávání: '"Carme Fàbrega"'
Autor:
Luis M. Menéndez-Méndez, Carme Fàbrega, Anna Aviñó, Ramon Eritja, Yoon-Sik Lee, Yogesh S. Sanghvi, Susana Fernández, Miguel Ferrero
Publikováno v:
Results in Chemistry, Vol 12, Iss , Pp 101930- (2024)
A critical step in the manufacturing of oligonucleotides is the selection of ideal solid supports. Herein, we evaluate a hybrid core–shell solid support made of polystyrene and polyethyleneglycol, for the preparation of oligonucleotides using phosp
Externí odkaz:
https://doaj.org/article/5d46ba76923f474c957e8a91dcfa08de
Autor:
Carme Fàbrega, Núria Gallisà-Suñé, Alice Zuin, Juan Sebastián Ruíz, Bernat Coll-Martínez, Gemma Fabriàs, Ramon Eritja, Bernat Crosas
Publikováno v:
Cells, Vol 13, Iss 21, p 1767 (2024)
The development of novel tools to tackle viral processes has become a central focus in global health, during the COVID-19 pandemic. The spike protein is currently one of the main SARS-CoV-2 targets, owing to its key roles in infectivity and virion fo
Externí odkaz:
https://doaj.org/article/00d1b154c83841d2a3310f94588a1da2
Autor:
Virginia Martín-Nieves, Luis Miguel Menéndez-Méndez, Carme Fàbrega, Susana Fernández, Yogesh S. Sanghvi, Miguel Ferrero, Ramon Eritja
Publikováno v:
ACS Omega, Vol 8, Iss 47, Pp 44893-44904 (2023)
Externí odkaz:
https://doaj.org/article/b7a56be495fe4d44af169a1bde2d8f4c
Autor:
Carme Fàbrega, Anna Aviñó, Natalia Navarro, Andreia F. Jorge, Santiago Grijalvo, Ramon Eritja
Publikováno v:
Pharmaceutics, Vol 15, Iss 2, p 320 (2023)
Antisense and small interfering RNA (siRNA) oligonucleotides have been recognized as powerful therapeutic compounds for targeting mRNAs and inducing their degradation. However, a major obstacle is that unmodified oligonucleotides are not readily take
Externí odkaz:
https://doaj.org/article/1c74d3f8abe840a29b0c5a7bb3845dec
Publikováno v:
Molecules, Vol 26, Iss 6, p 1741 (2021)
Fluoropyrimidines, such as 5-fluorouracil (5-FU) and related prodrugs have been considered first-line chemotherapy agents for the treatment of colorectal cancer. However, poor specificity and tumor cell resistance remain major limiting bottlenecks. G
Externí odkaz:
https://doaj.org/article/961e53e408164cf6b10be2d14af57cc6
Publikováno v:
Molecules, Vol 19, Iss 7, Pp 10495-10523 (2014)
Oligonucleotide gold nanoparticle conjugates are being used as diagnostic tools and gene silencing experiments. Thiol-chemistry is mostly used to functionalize gold nanoparticles with oligonucleotides and to incorporate DNA or RNA molecules onto gold
Externí odkaz:
https://doaj.org/article/925c8a1dd6e34fd5acb0444306d64566
Publikováno v:
Journal of Nucleic Acids, Vol 2010 (2010)
Human O6-alkylguanine-DNA alkyltransferase (hAGT) is a DNA repair protein that reverses the effects of alkylating agents by removing DNA adducts from the O6 position of guanine. Here, we developed a real-time fluorescence hAGT activity assay that is
Externí odkaz:
https://doaj.org/article/03b526e5b7f548e6974686e91bf09380
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
instname
Background: Nucleoside and nucleobase antimetabolites are an important class of chemotherapeutic agents for the treatment of cancer as well as other diseases. Introduction: In order to avoid undesirable side effects, several prodrug strategies have b
Evaluation of Floxuridine Oligonucleotide Conjugates Carrying Potential Enhancers of Cellular Uptake
Publikováno v:
International Journal of Molecular Sciences
Volume 22
Issue 11
Digital.CSIC: Repositorio Institucional del CSIC
Consejo Superior de Investigaciones Científicas (CSIC)
Digital.CSIC. Repositorio Institucional del CSIC
instname
International Journal of Molecular Sciences, Vol 22, Iss 5678, p 5678 (2021)
Volume 22
Issue 11
Digital.CSIC: Repositorio Institucional del CSIC
Consejo Superior de Investigaciones Científicas (CSIC)
Digital.CSIC. Repositorio Institucional del CSIC
instname
International Journal of Molecular Sciences, Vol 22, Iss 5678, p 5678 (2021)
Conjugation of small molecules such as lipids or receptor ligands to anti-cancer drugs has been used to improve their pharmacological properties. In this work, we studied the biological effects of several small-molecule enhancers into a short oligonu
Publikováno v:
Molecules, Vol 26, Iss 1741, p 1741 (2021)
Digital.CSIC. Repositorio Institucional del CSIC
instname
Molecules
Volume 26
Issue 6
Digital.CSIC. Repositorio Institucional del CSIC
instname
Molecules
Volume 26
Issue 6
luoropyrimidines, such as 5-fluorouracil (5-FU) and related prodrugs have been considered first-line chemotherapy agents for the treatment of colorectal cancer. However, poor specificity and tumor cell resistance remain major limiting bottlenecks. G-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a90d48a3710bbdd2546bf4293a27cbe
http://hdl.handle.net/10261/235359
http://hdl.handle.net/10261/235359