Hernández Madrigal, Miguel (Date of defense: 2022-06-17)
Tumours grow in a self-imposed hypoglycaemic microenvironment due to their exacerbated metabolic needs. To thrive in these harsh conditions, malignant cells must adapt their own metabolic routes and ...
Arroyo Solera, Irene (Date of defense: 2017-06-22)
En múltiples tipos tumorales, SERPINA E1 se asocia con una peor evolución clínica de los pacientes. En el carcinoma escamoso de cabeza y cuello (CECC), el aumento del nivel de expresión de SERPINA E1 ...
Núñez Álvarez, Yaiza (Date of defense: 2017-07-26)
HDAC11 is the newest member of the histone deacetylase (HDAC) family and one of the less studied. Its expression was described to be enriched in skeletal muscle tissues from the first moment of its ...
Morcelle Magaña, Carmen (Date of defense: 2017-09-19)
In most human cancers, the c-Myc transcription factor is deregulated and/or its levels are elevated, particularly in colorectal cancer (CRC). Earlier studies suggested a direct relationship between ...
Farrera Sal, Martí (Date of defense: 2020-10-30)
The oncolytic viruses (OVs) preferentially infect tumor and selectively replicate in cancer cells without harming normal tissues. OVs have been tested in clinical trials as monotherapy or combined with ...
Fernández Arévalo, Anna (Date of defense: 2020-11-24)
[spa] Las leishmaniosis son enfermedades causadas por el género Leishmania. Mientras que la clínica visceral se asocia al complejo L. donovani, la clínica tegumentaria puede estar producida por cualquier ...
Coll Iglesias, Laura (Date of defense: 2022-11-23)
[eng] Endometrial cancer represents the most common cancer arising from the uterine cavity and there is little hope for patients with recurrent or metastatic disease. Prior studies of our group reported ...
Marzal Martí, Berta (Date of defense: 2023-12-18)
[spa] El cáncer de mama es el tumor más frecuentemente diagnosticado en mujeres y entre sus diversos subtipos, en esta tesis, nos centraremos particularmente en el cáncer de mama HER2+. Esta patología ...
Lovera Ulecia, Marta (Date of defense: 2023-05-05)
[eng] Cohen syndrome (CS) is an ultra-rare, multi-system, autosomal recessive disorder caused by mutations in the VPS13B gene on chromosome 8q22.2. The most characteristic clinical features of this ...