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. 2000 Sep 18;150(6):1335–1348. doi: 10.1083/jcb.150.6.1335

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© 2000 The Rockefeller University Press

This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).

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Cleavage disruption by DN-p38 is cell autonomous. (A) Cell-tracing dye (rhodamine/biotin-dextran, 2,000 kD) was injected together with DN-p38RNA (125–250 pg) into one of the blastomeres of two-cell embryos. (B) Cross-section of DN/dye-coinjected embryo (A) at 100 μm from the animal pole surface at the 1,000-cell stage. The marginal area, which is the same as that outlined in Fig. 4 D, is shown. Normally divided (N) and enlarged blastomeres (EN) are demarcated by a dotted line. Bar, 4 μm.