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Intron retention induced by microsatellite expansions as a disease biomarker.
Sznajder ŁJ, Thomas JD, Carrell EM, Reid T, McFarland KN, Cleary JD, Oliveira R, Nutter CA, Bhatt K, Sobczak K, Ashizawa T, Thornton CA, Ranum LPW, Swanson MS. Sznajder ŁJ, et al. Among authors: bhatt k. Proc Natl Acad Sci U S A. 2018 Apr 17;115(16):4234-4239. doi: 10.1073/pnas.1716617115. Epub 2018 Apr 2. Proc Natl Acad Sci U S A. 2018. PMID: 29610297 Free PMC article.
Transcriptome alterations in myotonic dystrophy skeletal muscle and heart.
Wang ET, Treacy D, Eichinger K, Struck A, Estabrook J, Olafson H, Wang TT, Bhatt K, Westbrook T, Sedehizadeh S, Ward A, Day J, Brook D, Berglund JA, Cooper T, Housman D, Thornton C, Burge C. Wang ET, et al. Among authors: bhatt k. Hum Mol Genet. 2019 Apr 15;28(8):1312-1321. doi: 10.1093/hmg/ddy432. Hum Mol Genet. 2019. PMID: 30561649 Free PMC article.
TWEAK/Fn14, a pathway and novel therapeutic target in myotonic dystrophy.
Yadava RS, Foff EP, Yu Q, Gladman JT, Kim YK, Bhatt KS, Thornton CA, Zheng TS, Mahadevan MS. Yadava RS, et al. Among authors: bhatt ks. Hum Mol Genet. 2015 Apr 1;24(7):2035-48. doi: 10.1093/hmg/ddu617. Epub 2014 Dec 11. Hum Mol Genet. 2015. PMID: 25504044 Free PMC article.
449 results