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Page 1
p53 convergently activates Dux/DUX4 in embryonic stem cells and in facioscapulohumeral muscular dystrophy cell models.
Grow EJ, Weaver BD, Smith CM, Guo J, Stein P, Shadle SC, Hendrickson PG, Johnson NE, Butterfield RJ, Menafra R, Kloet SL, van der Maarel SM, Williams CJ, Cairns BR. Grow EJ, et al. Among authors: johnson ne. Nat Genet. 2021 Aug;53(8):1207-1220. doi: 10.1038/s41588-021-00893-0. Epub 2021 Jul 15. Nat Genet. 2021. PMID: 34267371 Free PMC article.
Neuromuscular Disease.
Butterfield RJ, Johnson NE. Butterfield RJ, et al. Among authors: johnson ne. J Pediatr Rehabil Med. 2016;9(1):1-2. doi: 10.3233/PRM-160354. J Pediatr Rehabil Med. 2016. PMID: 26966793 No abstract available.
Physical function and mobility in children with congenital myotonic dystrophy.
Pucillo EM, Dibella DL, Hung M, Bounsanga J, Crockett B, Dixon M, Butterfield RJ, Campbell C, Johnson NE. Pucillo EM, et al. Among authors: johnson ne. Muscle Nerve. 2017 Aug;56(2):224-229. doi: 10.1002/mus.25482. Epub 2017 Feb 13. Muscle Nerve. 2017. PMID: 27859360 Free PMC article.
Modified dynamic gait index and limits of stability in myotonic dystrophy type 1.
Pucillo EM, Mcintyre MM, Pautler M, Hung M, Bounsanga J, Voss MW, Hayes H, Dibella DL, Trujillo C, Dixon M, Butterfield RJ, Johnson NE. Pucillo EM, et al. Among authors: johnson ne. Muscle Nerve. 2018 Nov;58(5):694-699. doi: 10.1002/mus.26331. Epub 2018 Sep 23. Muscle Nerve. 2018. PMID: 30160307
Clinical trial readiness to solve barriers to drug development in FSHD (ReSolve): protocol of a large, international, multi-center prospective study.
LoRusso S, Johnson NE, McDermott MP, Eichinger K, Butterfield RJ, Carraro E, Higgs K, Lewis L, Mul K, Sacconi S, Sansone VA, Shieh P, van Engelen B, Wagner K, Wang L, Statland JM, Tawil R; ReSolve Investigators and the FSHD CTRN18. LoRusso S, et al. Among authors: johnson ne. BMC Neurol. 2019 Sep 10;19(1):224. doi: 10.1186/s12883-019-1452-x. BMC Neurol. 2019. PMID: 31506080 Free PMC article.
201 results