Ara mostrant els elements 1-10 de 28
Millán Ariño, Lluís (Data de defensa: 2013-11-25)
Seven linker histone H1 variants exist in human somatic cells with distinct prevalence among cell types and during differentiation. Despite being key chromatin structural components, it remains elusive ...
Lloret Llinares, Marta (Data de defensa: 2011-05-17)
La metilació de les lisines de les histones està implicada en les funcions associades a la cromatina, com l’expressió gènica o la formació d’heterocromatina. És una modificació covalent afegida per ...
Mendieta Esteban, Julen (Data de defensa: 2020-12-10)
Genome spatial organisation and transcriptional activity are tightly coordinated to ensure the correct function of the cell. Thus, proper understanding of the chromatin organisation is needed to deepen ...
Ramírez Cuéllar, Angélica Julieta (Data de defensa: 2022-05-12)
In this Thesis we report the successful growth of hormone responsive T47D cells as 3D spheroids in Matrigel mimicking the ECM. A detailed characterization by using a genome-wide approach of the main ...
Arcas Mantas, Aida (Data de defensa: 2013-04-25)
The DNA Damage response is a crucial signaling network that preserves genome integrity. This network is an ensemble of distinct but often overlapping sub-networks, where participating components exert ...
Fraile Beneitez, Rodrigo (Data de defensa: 2021-07-23)
Eukaryotic DNA is condensed inside the nucleus, compacted into chromatin. The structure of chromatin is dynamic, and its accessibility to cellular machinery can be altered depending on the level of ...
Font Mateu, Jofre (Data de defensa: 2016-12-05)
El receptor de la progesterona és un regulador clau per la proliferació de les cèl·lules de càncer de mama dependents d’hormona. El mecanisme d’acció del PR ha tingut un paper important en la resolució ...
Sierra Noguera, Cèsar (Data de defensa: 2022-03-18)
The presence of an extra copy of Human Chromosome 21 (HSA21) in Down syndrome (DS) is one of the most complex genetic perturbations compatible with life and is the most common genetic cause of intellectual ...
Demajo Meseguer, Santiago (Data de defensa: 2014-02-21)
Acute myeloid leukemia (AML) is frequently linked to epigenetic abnormalities and deregulation of gene transcription, which lead to aberrant cell proliferation and accumulation of undifferentiated ...
Iannone, Camilla (Data de defensa: 2014-05-23)
Intron removal is a necessary step for expression of most genes in higher eukaryotes, and alternative splice selection is a highly regulated mechanism that endows a single gene with the possibility to ...
575 - Genètica general. Citogenètica general. Immunogenètica. Evolució. Filogènia (9)
576 - Biologia cel·lular i subcel·lular. Citologia (8)
577 - Bioquímica. Biologia molecular. Biofísica (7)
616 - Patologia. Medicina clínica. Oncologia (2)
616.7 - Patologia dels òrgans de la locomoció. Sistema locomotor i esquelètic (1)