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The N-terminus of obscurin is flexible in solution.
Mauriello GE, Moncure GE, Nowzari RA, Miller CJ, Wright NT. Mauriello GE, et al. Among authors: wright nt. Proteins. 2023 Apr;91(4):485-496. doi: 10.1002/prot.26442. Epub 2022 Nov 4. Proteins. 2023. PMID: 36306263
Patient mutations linked to arrhythmogenic cardiomyopathy enhance calpain-mediated desmoplakin degradation.
Ng R, Manring H, Papoutsidakis N, Albertelli T, Tsai N, See CJ, Li X, Park J, Stevens TL, Bobbili PJ, Riaz M, Ren Y, Stoddard CE, Janssen PM, Bunch TJ, Hall SP, Lo YC, Jacoby DL, Qyang Y, Wright N, Ackermann MA, Campbell SG. Ng R, et al. JCI Insight. 2019 Jun 13;5(14):e128643. doi: 10.1172/jci.insight.128643. JCI Insight. 2019. PMID: 31194698 Free PMC article.
SOS1 Gain-of-Function Variants in Dilated Cardiomyopathy.
Cowan JR, Salyer L, Wright NT, Kinnamon DD, Amaya P, Jordan E, Bamshad MJ, Nickerson DA, Hershberger RE. Cowan JR, et al. Among authors: wright nt. Circ Genom Precis Med. 2020 Aug;13(4):e002892. doi: 10.1161/CIRCGEN.119.002892. Epub 2020 Jun 30. Circ Genom Precis Med. 2020. PMID: 32603605 Free PMC article.
Inherited Variants in SCARB1 Cause Severe Early-Onset Coronary Artery Disease.
Koenig SN, Sucharski HC, Jose EM, Dudley EK, Madiai F, Cavus O, Argall AD, Williams JL, Murphy NP, Keith CBR, El Refaey M, Gumina RJ, Boudoulas KD, Milks MW, Sofowora G, Smith SA, Hund TJ, Wright NT, Bradley EA, Zareba KM, Wold LE, Mazzaferri EL Jr, Mohler PJ. Koenig SN, et al. Among authors: wright nt. Circ Res. 2021 Jul 9;129(2):296-307. doi: 10.1161/CIRCRESAHA.120.318793. Epub 2021 May 12. Circ Res. 2021. PMID: 33975440 Free PMC article.
66 results