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12,029 Reviews — All Partners — All Subjects

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Population-level survey of loss-of-function mutations revealed that background dependent fitness genes are rare and functionally related in yeast
Caudal, E., Friedrich, A., Garin, M., Hou, J., Schacherer, J.
10.1101/2021.08.25.457624 — Posted: 2021-08-27 — Discussion: 2022-01-19  Review Commons
Leading edge stability in motile cells is an emergent property of branched actin network growth
Garner, R. M., Theriot, J. A.
10.1101/2020.08.22.262907 — Posted: 2020-08-22 — Discussion: 2022-01-18  eLife
Inter-tissue convergence of gene expression and loss of cellular identity during ageing
Izgi, H., Han, D., Isildak, U., Huang, S., Kocabiyik, E., Khaitovich, P., Somel, M., Dönertas, H. M.
10.1101/2021.03.02.432281 — Posted: 2021-03-02 — Discussion: 2022-01-18  eLife
Parallel pathways for rapid odor processing in lateral entorhinal cortex: Rate and temporal coding by layer 2 subcircuits
Bitzenhofer, S. H., Westeinde, E. A., Zhang, H.-X. B., Isaacson, J. S.
10.1101/2021.08.19.456942 — Posted: 2021-08-19 — Discussion: 2022-01-18  eLife
Skeletal dysplasia-causing TRPV4 mutations suppress the hypertrophic differentiation of human iPSC-derived chondrocytes
Dicks, A. R., Maksaev, G. I., Harissa, Z., Savadipour, A., Tang, R., Steward, N., Liedtke, W., Wu, C.-L., Guilak, F.
10.1101/2021.06.15.448562 — Posted: 2021-06-15 — Discussion: 2022-01-17  eLife
Ancient genomes redate the extinction of Sussemionus, a subgenus of Equus, to late Holocene
Cai, D., Zhu, S., Gong, M., Zhang, N., Wen, J., Liang, Q., Sun, W., Shao, X., Guo, Y., Cai, Y., Zheng, Z., Zhang, W., Hu, S., Wang, X., Tian, H., Li, Y., Liu, W., Yang, M., Yang, J., Wu, D., Orlando, L., Jiang, Y.
10.1101/2021.09.13.460072 — Posted: 2021-09-16 — Discussion: 2022-01-17  eLife
Glypican-1 drives unconventional secretion of Fibroblast Growth Factor 2
Sparn, C., Dimou, E., Meyer, A., Saleppico, R., Wegehingel, S., Gerstner, M., Klaus, S., Ewers, H., Nickel, W.
10.1101/2021.11.11.468179 — Posted: 2021-11-12 — Discussion: 2022-01-17  eLife
A Novel Gene ZNF862 Causes Hereditary Gingival Fibromatosis
Wu, J., Chen, D., Huang, H., Luo, N., Chen, H., Zhao, J., Wang, Y., Ren, Y., Zhai, T., Sun, W., Li, H., Li, W.
10.1101/2020.04.27.20080804 — Posted: 2020-05-01 — Discussion: 2022-01-17  eLife
Genetic Control of Pluripotency Epigenome Determines Differentiation Bias in Mouse Embryonic Stem Cells
Byers, C., Spruce, C., Fortin, H. J., Czechanski, A., Munger, S. C., Reinholdt, L. G., Skelly, D. A., Baker, C. L.
10.1101/2021.01.15.426861 — Posted: 2021-01-16 — Discussion: 2022-01-15  EMBO Press
Unexpected gene activation following CRISPR-Cas9-mediated genome editing
Manjon, A. G., Teunissen, H., de Wit, E., Medema, R. H.
10.1101/2021.06.14.448328 — Posted: 2021-06-14 — Discussion: 2022-01-15  EMBO Press

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