eLife

Displaying 51 - 63 of 63
Smith, E. H., Liou, J., Merricks, E. M., Davis, T., Thomson, K., Greger, B., House, P., Emerson, R. G., Goodman, R., McKhann, G. M., Sheth, S., Schevon, C., & Rolston, J. D. (2022). Human interictal epileptiform discharges are bidirectional traveling waves echoing ictal discharges. ELife, 11. CLOCKSS. https://doi.org/10.7554/elife.73541
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Belsky, D. W., Caspi, A., Corcoran, D. L., Sugden, K., Poulton, R., Arseneault, L., Baccarelli, A., Chamarti, K., Gao, X., Hannon, E., Harrington, H. L., Houts, R., Kothari, M., Kwon, D., Mill, J., Schwartz, J., Vokonas, P., Wang, C., Williams, B. S., & Moffitt, T. E. (2022). DunedinPACE, a DNA methylation biomarker of the pace of aging. ELife, 11. CLOCKSS. https://doi.org/10.7554/elife.73420
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Kimura, H., Paranal, R. M., Nanda, N., Wood, L. D., Eshleman, J. R., Hruban, R. H., Goggins, M. G., Klein, A. P., & Roberts, N. J. (2022). Functional CDKN2A assay identifies frequent deleterious alleles misclassified as variants of uncertain significance. ELife, 11. CLOCKSS. https://doi.org/10.7554/elife.71137
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Rousová, D., Nivsarkar, V., Altmannova, V., Raina, V. B., Funk, S. K., Liedtke, D., Janning, P., Müller, F., Reichle, H., Vader, G., & Weir, J. R. (2021). Novel mechanistic insights into the role of Mer2 as the keystone of meiotic DNA break formation. ELife, 10. CLOCKSS. https://doi.org/10.7554/elife.72330
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Loureiro-Campos, E., Mateus-Pinheiro, A., Patrício, P., Soares-Cunha, C., Silva, J., Sardinha, V. M., Mendes-Pinheiro, B., Silveira-Rosa, T., Domingues, A. V., Rodrigues, A. J., Oliveira, J., Sousa, N., Alves, N. D., & Pinto, L. (2021). Constitutive deficiency of the neurogenic hippocampal modulator AP2γ promotes anxiety-like behavior and cumulative memory deficits in mice from juvenile to adult periods. ELife, 10. CLOCKSS. https://doi.org/10.7554/elife.70685
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Gilley, J., Jackson, O., Pipis, M., Estiar, M. A., Al-Chalabi, A., Danzi, M. C., van Eijk, K. R., Goutman, S. A., Harms, M. B., Houlden, H., Iacoangeli, A., Kaye, J., Lima, L., Ravits, J., Rouleau, G. A., Schüle, R., Xu, J., Züchner, S., … Coleman, M. P. (2021). Enrichment of SARM1 alleles encoding variants with constitutively hyperactive NADase in patients with ALS and other motor nerve disorders. ELife, 10. CLOCKSS. https://doi.org/10.7554/elife.70905
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Columbia Affiliation
Bakken, T. E., van Velthoven, C. T., Menon, V., Hodge, R. D., Yao, Z., Nguyen, T. N., Graybuck, L. T., Horwitz, G. D., Bertagnolli, D., Goldy, J., Yanny, A. M., Garren, E., Parry, S., Casper, T., Shehata, S. I., Barkan, E. R., Szafer, A., Levi, B. P., Dee, N., … Tasic, B. (2021). Single-cell and single-nucleus RNA-seq uncovers shared and distinct axes of variation in dorsal LGN neurons in mice, non-human primates, and humans. ELife, 10. CLOCKSS. https://doi.org/10.7554/elife.64875
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Gautheron, J., Morisseau, C., Chung, W. K., Zammouri, J., Auclair, M., Baujat, G., Capel, E., Moulin, C., Wang, Y., Yang, J., Hammock, B. D., Cerame, B., Phan, F., Fève, B., Vigouroux, C., Andreelli, F., & Jeru, I. (2021). EPHX1 mutations cause a lipoatrophic diabetes syndrome due to impaired epoxide hydrolysis and increased cellular senescence. ELife, 10. CLOCKSS. https://doi.org/10.7554/elife.68445
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