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2022 | 1 |
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PTEN hamartoma tumor syndrome: Clinical and genetic characterization in pediatric patients.
Childs Nerv Syst. 2024 Feb 26. doi: 10.1007/s00381-024-06301-2. Online ahead of print.
Childs Nerv Syst. 2024.
PMID: 38407606
Recurrent NOMO1 Gene Deletion Is a Potential Clinical Marker in Early-Onset Colorectal Cancer and Is Involved in the Regulation of Cell Migration.
Pérez-García J, Martel-Martel A, García-Vallés P, Corchete LA, García JL, Gestoso-Uzal N, Vidal-Tocino R, Blanco Ó, Méndez L, Sánchez-Martín M, Fuentes M, Herrero AB, Holowatyj AN, Perea J, González-Sarmiento R.
Pérez-García J, et al. Among authors: gestoso uzal n.
Cancers (Basel). 2022 Aug 20;14(16):4029. doi: 10.3390/cancers14164029.
Cancers (Basel). 2022.
PMID: 36011023
Free PMC article.
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A mutation in p62 protein (p. R321C), associated to Paget's disease of bone, causes a blockade of autophagy and an activation of NF-kB pathway.
Usategui-Martín R, Gestoso-Uzal N, Calero-Paniagua I, De Pereda JM, Del Pino-Montes J, González-Sarmiento R.
Usategui-Martín R, et al. Among authors: gestoso uzal n.
Bone. 2020 Apr;133:115265. doi: 10.1016/j.bone.2020.115265. Epub 2020 Feb 6.
Bone. 2020.
PMID: 32036052
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