Browsing by Author "NOURSHARGH, S"
Now showing items 1-2 of 2
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Development of a CRISPR/Cas9-based therapy for Hutchinson-Gilford progeria syndrome
NOURSHARGH, S; Santiago-Fernández, O; Osorio, F G; Quesada, V; Rodríguez, F; Basso, S; Maeso, D; Rolas, L; Barkaway, A; Folgueras, A R (Nature Research, 2019-02-18)CRISPR/Cas9-based therapies hold considerable promise for the treatment of genetic diseases. Among these, Hutchinson–Gilford progeria syndrome, caused by a point mutation in the LMNA gene, stands out as a potential candidate. ... -
Signatures of Inflammation and Impending Multiple Organ Dysfunction in the Hyperacute Phase of Trauma
CABRERA, CP; MANSON, J; SHEPHERD, JM; TORRANCE, HD; WATSON, D; LONGHI, MP; HOTI, M; PATEL, MB; O'DWYER, M; NOURSHARGH, S (Public Library of Science (PLoS), 2017-07-17)