Taliaferro, J. Matthew
University of Colorado Anschutz
3 papers on CoChatORCID 0000-0001-7580-1433
Most cited papers
- Verified
Cell-type-specific profiling of human cellular models of fragile X syndrome reveal PI3K-dependent defects in translation and neurogenesis.
Raj, N., McEachin, Z. T., Harousseau, W., Zhou, Y., Zhang, F., Merritt-Garza, M. E., Taliaferro, J. M., Kalinowska, M., Marro, S. G., Hales, C. M., et al. (2021) · Cell Reports
Genetics and Neurodevelopmental DisordersNeurogenesis and neuroplasticity mechanisms
Cited by 54
- Verified
Selected humanization of yeast U1 snRNP leads to global suppression of pre-mRNA splicing and mitochondrial dysfunction in the budding yeast
Chalivendra, S., Shi, S., Li, X., Kuang, Z., Giovinazzo, J., Zhang, L., Rossi, J., Wang, J., Saviola, A. J., Welty, R., et al. (2024) · RNA
RNA Research and SplicingRNA and protein synthesis mechanisms
Cited by 5
- Verified
Selected humanization of yeast U1 snRNP leads to global suppression of pre-mRNA splicing and mitochondrial dysfunction in the budding yeast
Chalivendra, S., Shi, S., Li, X., Kuang, Z., Giovinazzo, J., Zhang, L., Rossi, J., Saviola, A. J., Wang, J., Welty, R., et al. (2023) · RNA
RNA Research and SplicingRNA and protein synthesis mechanisms
Cited by 5
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