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7,093 Reviews — eLife — All Subjects

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Heterozygosity for neurodevelopmental disorder-associated TRIO variants yields distinct deficits in behavior, neuronal development, and synaptic transmission in mice
Ishchenko, Y., Jeng, A. T., Feng, S., Nottoli, T., Manriquez-Rodriguez, C., Nguyen, K., Carrizales, M. G., Vitarelli, M. J., Corcoran, E. E., Greer, C. A., Myers, S. A., Koleske, A. J.
10.1101/2024.01.05.574442 — Posted: 2024-01-06 — Discussion: 2024-12-20  eLife
Inhibition of V1a-like receptors disrupts male-male affiliative relationships formed by triadic cohabitation inlarge-billed crows
Seguchi, A., Izawa, E.-I.
10.1101/2024.02.01.578519 — Posted: 2024-02-04 — Discussion: 2024-12-20  eLife
Inferring illness causes recruits the animacy semantic network
Hauptman, M., Bedny, M.
10.1101/2024.07.10.602983 — Posted: 2024-07-13 — Discussion: 2024-12-20  eLife
Assessing the balance between excitation and inhibition in chronic pain through the aperiodic component of EEG
Gil Avila, C., May, E. S., Bott, F. S., Tiemann, L., Hohn, V., Heitmann, H., Zebhauser, P. T., Gross, J., Ploner, M.
10.1101/2024.07.23.604775 — Posted: 2024-07-24 — Discussion: 2024-12-20  eLife
Human formin FHOD3-mediated actin elongation is required for sarcomere integrity in cardiomyocytes
Valencia, D. A., Koeberlein, A. N., Nakano, H., Rudas, A., Harui, A., Spencer, C., Nakano, A., Quinlan, M. E.
10.1101/2024.10.13.618125 — Posted: 2024-10-14 — Discussion: 2024-12-20  eLife
A fat-2(wa17) suppressor screen in C. elegans reveals genetic adaptations to polyunsaturated fatty acid deficiency
Kaper, D., Radovic, U., Bergh, P.-O., Qvist, A., Henricsson, M., Boren, J., Pilon, M.
10.1101/2024.11.08.622646 — Posted: 2024-11-11 — Discussion: 2024-12-20  eLife
Intercellular transport of RNA can limit heritable epigenetic changes
Shugarts, N., Yi, A. L., Chan, W. M., Marre, J. A., Sathya, A., Jose, A. M.
10.1101/2021.10.05.463267 — Posted: 2021-10-06 — Discussion: 2024-12-19  eLife
Exploiting functional regions in the viral RNA genome as druggable entities
Wei, D., Luo, D., Zheng, Y., Huang, Z., Wen, Z., Guo, L., Deng, Y., Li, Q., Bai, Y., Haider, S., Parkinson, G. N.
10.1101/2024.08.11.607475 — Posted: 2024-08-11 — Discussion: 2024-12-19  eLife
Vesiculation pathways in clathrin-mediated endocytosis
Wang, X., Berro, J., Ma, R.
10.1101/2024.08.13.607731 — Posted: 2024-08-13 — Discussion: 2024-12-19  eLife
Defective Neurogenesis in Lowe Syndrome is Caused by Mitochondria Loss and Cilia-related Sonic Hedgehog Defects
Lo, C., Chen, S., Zhao, J., Liu, Z., Wang, B., Wang, Q., Kowal, T. J., Sun, Y.
10.1101/2024.11.01.621496 — Posted: 2024-11-02 — Discussion: 2024-12-19  eLife

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