Connecting genotype and phenotype in minor spliceosome diseases

Norppa, A. J., Shcherbii, M. V. & Frilander, M. J., Mar 2025, In: RNA. 31, 3, p. 284-299 16 p.

Research output: Contribution to journal › Article › Scientific › peer-review

Quantitative analysis of electroporation-mediated intracellular delivery via bioorthogonal luminescent reaction

Wang, S., Shcherbii, M. V., Hirvonen, S., Silvennoinen, G., Sarparanta, M. & Santos, H., 15 Aug 2024, In: Communications chemistry. 7, 1, 12 p., 181.

Research output: Contribution to journal › Article › Scientific › peer-review

MCM3AP in recessive axonal neuropathy and mild intellectual disability

Ylikallio, E., Woldegebriel, R., Tumiati, M., Isohanni, P., Ryan, M. M., Stark, Z., Maie, W., Sawyer, S. L., Bell, K. M., Oshlack, A., Lockhart, P. L., Shcherbii, M., Estrada-Cuzcano, A., Atkinson, D., Hartley, T., Tetreault, M., Cuppen, I., van der Pol, W. L., Candayan, A. & Battaloglu, E. & 8 others, Parman, Y., van Gassen, K. L. I., van den Boogaard, M. H., Boycott, K. M., Kauppi, L., Jordanova, A., Lonnqvist, T. & Tyynismaa, H., 2018, In: European Journal of Human Genetics. 26, p. 40-41 2 p.

Research output: Contribution to journal › Meeting Abstract › peer-review