Publications
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“Generation of four myotonic dystrophy type 1 patient iPSC lines (CBRCULi002-A, CBRCULi003-A, CBRCULi004-A, CBRCULi005-A) and a control (CBRCULi001-A) derived from lymphoblastoids cell lines.”, Stem Cell Res, vol. 67, p. 103037, 2023.
“Lymphoblastoid cell lines derived from iPSCs of a myotonic dystrophy type 1 patient carrying 700 CTG repeats (CBRCULi007-A) and a control (CBRCULi006-A).”, Stem Cell Res, vol. 71, p. 103148, 2023.
“Antisense oligonucleotides as a potential treatment for brain deficits observed in myotonic dystrophy type 1.”, Gene Ther, vol. 29, no. 12, pp. 698-709, 2022.
“Combining NGN2 programming and dopaminergic patterning for a rapid and efficient generation of hiPSC-derived midbrain neurons.”, Sci Rep, vol. 12, no. 1, p. 17176, 2022.
“Deciphering the mechanisms underlying brain alterations and cognitive impairment in congenital myotonic dystrophy.”, Neurobiol Dis, vol. 160, p. 105532, 2021.
, “Na1.5 knockout in iPSCs: a novel approach to study Na1.5 variants in a human cardiomyocyte environment.”, Sci Rep, vol. 11, no. 1, p. 17168, 2021.
