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Generation of five induced pluripotent stem cell lines from patients with MECP2 Duplication Syndrome. | LitMetric

Generation of five induced pluripotent stem cell lines from patients with MECP2 Duplication Syndrome.

Stem Cell Res

Department of Pediatrics-Neurology, Baylor College of Medicine, Houston, TX 77030, USA; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston, TX 77030, USA; Department of Neuroscience, Baylor College of Medicine, Houston, TX 77030, USA. Electronic address: Mirjana.M

Published: February 2024


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Article Abstract

MECP2 Duplication Syndrome (MDS) is a rare, severe neurodevelopmental disorder arising from duplications in the Xq28 region containing the MECP2 gene that predominantly affects males. We generated five human induced pluripotent stem cell (iPSC) lines from the fibroblasts of individuals carrying between 0.355 and 11.2 Mb size duplications in the chromosomal locus containing MECP2. All lines underwent extensive testing to confirm MECP2 duplication and iPSC-related features such as morphology, pluripotency markers, and trilineage differentiation potential. These lines are a valuable resource for molecular and functional studies of MDS as well as screening for a variety of therapeutic approaches.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10898976PMC
http://dx.doi.org/10.1016/j.scr.2023.103292DOI Listing

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