Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Pau Castillo"'
Autor:
Jordi Minguillón, María José Ramírez, Llorenç Rovirosa, Pilar Bustamante-Madrid, Cristina Camps-Fajol, Gorka Ruiz de Garibay, Hermela Shimelis, Helena Montanuy, Roser Pujol, Gonzalo Hernandez, Massimo Bogliolo, Pau Castillo, Penny Soucy, Griselda Martrat, Antonio Gómez, Daniel Cuadras, María J. García, Javier Gayarre, CIMBA, Conxi Lázaro, Javier Benítez, Fergus J. Couch, Miquel Angel Pujana, Jordi Surrallés
Publikováno v:
Cancers, Vol 14, Iss 2, p 353 (2022)
BRCA2 is essential for homologous recombination DNA repair. BRCA2 mutations lead to genome instability and increased risk of breast and ovarian cancer. Similarly, mutations in BRCA2-interacting proteins are also known to modulate sensitivity to DNA d
Externí odkaz:
https://doaj.org/article/c8c1246b267e45aabc00f05fa6643bca
Publikováno v:
Revista Científica de la Facultad de Ciencias Veterinarias. :1-6
Con el objeto de evaluar la utilización del suero rico en plaquetas (PRP), solo o combinado con otros activadores celulares, como son el cloruro de calcio y/o la trombina, sobre el proceso de cicatrización de la piel en conejos con heridas inducida
Autor:
Pau Castillo Bosch, Puck Knipscheer, James M. Dewar, Marcel Tijsterman, Jane T. van Heteren, Sandra Segura-Bayona, Wouter Koole
Publikováno v:
EMBO Journal, 33(21), 2521-33. Nature Publishing Group
EMBO Journal, 33(21), 2521-2533
The EMBO Journal
EMBO Journal, 33(21), 2521-2533
The EMBO Journal
Our genome contains many G-rich sequences, which have the propensity to fold into stable secondary DNA structures called G4 or G-quadruplex structures. These structures have been implicated in cellular processes such as gene regulation and telomere m
Publikováno v:
DNA Repair. 10:518-525
Fanconi anemia (FA) and ataxia telangiectasia (AT) share common traits such chromosomal instability and proneness to hematological cancers. Both AT and FA cell lines, and patients, are characterized by abnormally high levels of oxidative stress marke
Publikováno v:
Mutation research. Genetic toxicology and environmental mutagenesis. 793
Fanconi anemia (FA) is a rare, clinically heterogeneous autosomal recessive or X-linked genetic disease characterized by chromosome fragility, congenital malformations and cancer susceptibility. FA patients are usually radiosensitive when exposed to
Akademický článek
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Publikováno v:
Mutation Research - Genetic Toxicology & Environmental Mutagenesis. Nov2015, Vol. 793, p9-13. 5p.
Autor:
Bosch PC; Genome Instability and DNA Repair Group, Department of Genetics and Microbiology, Universitat Autònoma de Barcelona (UAB), Barcelona, Spain and Centre for Biomedical Network Research on Rare Diseases (CIBERER), Spain., Bogliolo M; Genome Instability and DNA Repair Group, Department of Genetics and Microbiology, Universitat Autònoma de Barcelona (UAB), Barcelona, Spain and Centre for Biomedical Network Research on Rare Diseases (CIBERER), Spain., Surrallés J; Genome Instability and DNA Repair Group, Department of Genetics and Microbiology, Universitat Autònoma de Barcelona (UAB), Barcelona, Spain and Centre for Biomedical Network Research on Rare Diseases (CIBERER), Spain. Electronic address: jordi.surralles@uab.cat.
Publikováno v:
Mutation research. Genetic toxicology and environmental mutagenesis [Mutat Res Genet Toxicol Environ Mutagen] 2015 Nov; Vol. 793, pp. 9-13. Date of Electronic Publication: 2015 Jun 17.