September 2025
1. PERLA S, Stiegler AL, Yi JS, Enyenihi L, et al
   SHP2 genetic variants in NSML-associated RASopathies disrupt the PZR-IRX transcription factor signaling axis.
   Proc Natl Acad Sci U S A. 2025;122:e2503631122.
   

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   July 2025
2. CROSBY GS, Hei B, Lynn ML, Chakraborti A, et al
   Resolving the structure and dynamics of the disordered C terminus of human cardiac troponin T and effects of cardiomyopathic mutations.
   Proc Natl Acad Sci U S A. 2025;122:e2425343122.
   

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3. CAO T, Feng HZ, Jayasundar JJ, Jin JP, et al
   The highly conserved C-terminal end segment of troponin T binds tropomyosin and actin to function in modulating contractile kinetics.
   Proc Natl Acad Sci U S A. 2025;122:e2507107122.
   

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   May 2024
4. LEE S, Vander Roest AS, Blair CA, Kao K, et al
   Incomplete-penetrant hypertrophic cardiomyopathy MYH7 G256E mutation causes hypercontractility and elevated mitochondrial respiration.
   Proc Natl Acad Sci U S A. 2024;121:e2318413121.
   

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