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2019 | 1 |
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A mutation-independent approach for muscular dystrophy via upregulation of a modifier gene.
Nature. 2019 Aug;572(7767):125-130. doi: 10.1038/s41586-019-1430-x. Epub 2019 Jul 24.
Nature. 2019.
PMID: 31341277
Cortical interneuron-mediated inhibition delays the onset of amyotrophic lateral sclerosis.
Khademullah CS, Aqrabawi AJ, Place KM, Dargaei Z, Liang X, Pressey JC, Bedard S, Yang JW, Garand D, Keramidis I, Gasecka A, Côté D, De Koninck Y, Keith J, Zinman L, Robertson J, Kim JC, Woodin MA.
Khademullah CS, et al. Among authors: place km.
Brain. 2020 Mar 1;143(3):800-810. doi: 10.1093/brain/awaa034.
Brain. 2020.
PMID: 32203578
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Correction of a splicing defect in a mouse model of congenital muscular dystrophy type 1A using a homology-directed-repair-independent mechanism.
Kemaladewi DU, Maino E, Hyatt E, Hou H, Ding M, Place KM, Zhu X, Bassi P, Baghestani Z, Deshwar AG, Merico D, Xiong HY, Frey BJ, Wilson MD, Ivakine EA, Cohn RD.
Kemaladewi DU, et al. Among authors: place km.
Nat Med. 2017 Aug;23(8):984-989. doi: 10.1038/nm.4367. Epub 2017 Jul 17.
Nat Med. 2017.
PMID: 28714989
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