PCGF6-PRC1 suppresses premature differentiation of mouse embryonic stem cells by regulating germ cell-related genes

بواسطة Endoh, M, Endo, T.A, Shinga, J, Hayashi, K, Farcas, A, Ma, K.-W, Ito, S, Sharif, J, Endoh, T, Onaga, N, Nakayama, M, Ishikura, T, Masui, O, Kessler, B.M, Suda, T, Ohara, O, Okuda, A, Klose, R, Koseki, H
منشور في 2020

Recommendations for a nomenclature system for human gene mutations

بواسطة Antonarakis, S.E., Ashburner, M., Auerbach, A.D., Beaudet, A.L., Beckmann, J.S., Beutler, E., Cooper, D.N., Cotton, R.G.H., Den Dunnen, J.T., Desnick, R.J., Eng, C., Fasman, K.H., Goldman, D., Hayashi, K., Hutchinson, F., Kazazian Jr., H.H., Keen, J., King, M.-C., Lehvaslaiho, H., McAlpine, P.J., McKusick, V., Motulski, A.G., Povey, S., Schorderet, D.F., Scriver, C.R., Shows Jr., T.B., Supertifurga, A., Tay, A.H.N., Tsui, L.-C., Valle, D., Vihinen, M.
منشور في 2014

Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci

بواسطة Aung T., Ozaki M., Lee M., Schlötzer-Schrehardt U., Thorleifsson G., Mizoguchi T., Igo R., Haripriya A., Williams S., Astakhov Y., Orr A., Burdon K., Nakano S., Mori K., Abu-Amero K., Hauser M., Li Z., Prakadeeswari G., Bailey J., Cherecheanu A., Kang J., Nelson S., Hayashi K., Manabe S., Kazama S., Zarnowski T., Inoue K., Irkec M., Coca-Prados M., Sugiyama K., Järvelä I., Schlottmann P., Lerner S., Lamari H., Nilgün Y., Bikbov M., Park K., Cha S., Yamashiro K., Zenteno J., Jonas J., Kumar R., Perera S., Chan A., Kobakhidze N., George R., Vijaya L., Do T., Edward D., De Juan Marcos L., Pakravan M., Moghimi S., Ideta R., Bach-Holm D., Kappelgaard P., Wirostko B., Thomas S., Gaston D., Bedard K., Greer W., Yang Z., Chen X., Huang L., Sang J., Jia H., Jia L., Qiao C., Zhang H., Liu X., Zhao B., Wang Y., Xu L., Leruez S., Reynier P., Chichua G., Tabagari S.
منشور في 2017