En el momento de iniciar esta tesis, trabajos recientes de nuestro laboratorio en colaboración con el Dr. García del Portillo habían descrito que alelos viables del gen esencial igaA activaban el sistema de transducción de señales Rcs, y que dicha activación atenuaba la virulencia de Salmonella. Se trataba, pues, de un fenómeno nuevo,...
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November 27, 2014 (v1)PublicationUploaded on: December 2, 2022
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February 26, 2016 (v1)Publication
IgaA is a membrane protein that prevents overactivation of the Rcs regulatory system in enteric bacteria. Here we provide evidence that igaA is the first gene in a 70-dependent operon of Salmonella enterica serovar Typhimurium that also includes yrfG, yrfH, and yrfI. We also show that the Lon protease and the MviA response regulator...
Uploaded on: December 4, 2022 -
February 26, 2016 (v1)Publication
Genetic screens based on the use of MudJ-generated lac fusions permitted the identification of novel genes regulated by the Rcs signal transduction system in Salmonella enterica serovar Typhimurium. Besides genes that are also found in the Escherichia coli genome, our screens identified Salmonella-specific genes regulated by RcsB, including...
Uploaded on: March 27, 2023 -
November 7, 2022 (v1)Publication
Fanconi anemia (FA) is a rare hereditary disorder caused by mutations in any one of the FANC genes. FA cells are mainly characterized by extreme hypersensitivity to interstrand crosslink (ICL) agents. Additionally, the FA proteins play a crucial role in concert with homologous recombination (HR) factors to protect stalled replication forks....
Uploaded on: March 24, 2023 -
February 8, 2024 (v1)Publication
Purpose: CAR-T cell therapy has proven to be a disruptive treatment in the hematology field, however, less than 50% of patients maintain long-term response and early predictors of outcome are still inconsistently defined. Here, we aimed to optimize the detection of CD19 CAR-T cells in blood and to identify phenotypic features as early...
Uploaded on: February 11, 2024 -
June 10, 2020 (v1)Publication
Gene therapy is a therapeutic process consisting of the transport of genetic material into cells. The design and preparation of novel carriers to transport DNA is an important research line in the medical field. Hybrid compounds such as metallo-liposomes, containing a mixture of lipids, were prepared and characterized. Cationic metal lipids...
Uploaded on: March 25, 2023 -
February 9, 2024 (v1)Publication
Purpose: Sclerotic chronic GVHD (scGVHD) is characterized by progressive skin fibrosis and frequent refractoriness to available therapies. Aberrant activation of Hedgehog signaling in dermal fibroblasts has been implicated in scGVHD. Here, we report the results of two phase I/II studies (NCT03415867, GETH-TC; NCT04111497, FHD) that evaluated...
Uploaded on: February 11, 2024 -
June 26, 2023 (v1)Publication
Gene therapy is a technique that is currently under expansion and development. Recent advances in genetic medicine have paved the way for a broader range of therapies and laid the groundwork for next-generation technologies. A terminally substituted difluorene-diester Schiff Base calix[4]arene has been studied in this work as possible...
Uploaded on: June 27, 2023 -
August 30, 2021 (v1)Publication
The formation of calixarene-based liposomes was investigated, and the characterization of these nanostructures was carried out using several techniques. Four amphiphilic calixarenes were used. The length of the hydrophobic chains attached to the lower rim as well as the nature of the polar group present in the upper rim of the calixarenes were...
Uploaded on: December 2, 2022