Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Elena Díaz-Santiago"'
Autor:
Elena Díaz-Santiago, M. Gonzalo Claros, Raquel Yahyaoui, Yolanda de Diego-Otero, Rocío Calvo, Janet Hoenicka, Francesc Palau, Juan A. G. Ranea, James R. Perkins
Publikováno v:
Frontiers in Molecular Biosciences, Vol 8 (2021)
Neuromuscular disorders (NMDs) represent an important subset of rare diseases associated with elevated morbidity and mortality whose diagnosis can take years. Here we present a novel approach using systems biology to produce functionally-coherent phe
Externí odkaz:
https://doaj.org/article/0b1a57da523a479ebbf16cd47b3994b9
Autor:
Elena Díaz-Santiago, Fernando M Jabato, Elena Rojano, Pedro Seoane, Florencio Pazos, James R Perkins, Juan A G Ranea
Publikováno v:
PLoS Genetics, Vol 16, Iss 10, p e1009054 (2020)
Genetic and molecular analysis of rare disease is made difficult by the small numbers of affected patients. Phenotypic comorbidity analysis can help rectify this by combining information from individuals with similar phenotypes and looking for overla
Externí odkaz:
https://doaj.org/article/6dd3ee164edf4928a8b351983cede7ae
Publikováno v:
RIUMA. Repositorio Institucional de la Universidad de Málaga
instname
instname
Network and systemic approaches to studying human pathologies are helping us to gain insight into the molecular mechanisms of and potential therapeutic interventions for human diseases, especially for complex diseases where large numbers of genes are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::828dea5366c38654e30bc45df9002c2c
https://hdl.handle.net/10630/24543
https://hdl.handle.net/10630/24543
Autor:
Florencio Pazos, Elena Rojano, Fernando M. Jabato, Elena Díaz-Santiago, James R. Perkins, Pedro Seoane, Juan A. G. Ranea
Publikováno v:
PLoS Genetics, Vol 16, Iss 10, p e1009054 (2020)
Digital.CSIC. Repositorio Institucional del CSIC
instname
PLoS Genetics
Digital.CSIC. Repositorio Institucional del CSIC
instname
PLoS Genetics
© 2020 Díaz-Santiago et al.
Genetic and molecular analysis of rare disease is made difficult by the small numbers of affected patients. Phenotypic comorbidity analysis can help rectify this by combining information from individuals with simila
Genetic and molecular analysis of rare disease is made difficult by the small numbers of affected patients. Phenotypic comorbidity analysis can help rectify this by combining information from individuals with simila
Autor:
Elena Díaz-Santiago, Casimiro Cárdenas, Ana R. Quesada, José J. Serrano, Luis Rodríguez-Caso, Miguel Ángel Medina
Publikováno v:
Redox Report. 22:183-189
Objective: We studied the modulatory effects of homocysteine pre-treatment on the disulfide reduction capacity of tumor and endothelial cells. Methods: Human MDA-MB-231 breast carcinoma and bovine aorta endothelial cells were pre-treated for 1–24 h
Autor:
Díaz-Santiago, Elena1 (AUTHOR), Jabato, Fernando M.1 (AUTHOR), Rojano, Elena1 (AUTHOR), Seoane, Pedro1,2 (AUTHOR), Pazos, Florencio3 (AUTHOR), Perkins, James R.1,2,4 (AUTHOR) jimrperkins@uma.es, Ranea, Juan A. G.1,2,4 (AUTHOR)
Publikováno v:
PLoS Genetics. 10/1/2020, Vol. 16 Issue 10, p1-33. 33p.
Publikováno v:
Genes; Jun2022, Vol. 13 Issue 6, p1081-1081, 15p
Autor:
Díaz-Santiago, Elena1 (AUTHOR), Rodríguez-Caso, Luis1 (AUTHOR), Cárdenas, Casimiro1,2 (AUTHOR), Serrano, José J.1 (AUTHOR), Quesada, Ana R.1,3 (AUTHOR), Medina, Miguel Ángel1,3 (AUTHOR) medina@uma.es
Publikováno v:
Redox Report. Jul2017, Vol. 22 Issue 4, p183-189. 7p.