(Q28243128)

English

DNA-replication checkpoint control at the Drosophila midblastula transition

scientific article (publication date: 3 July 1997)

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scholarly article

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DNA-replication checkpoint control at the Drosophila midblastula transition (English)

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O C Sibon

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V A Stevenson

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W E Theurkauf

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publication date

3 July 1997

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388

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6637

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93-7

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A major developmental transition in early xenopus embryos: I. characterization and timing of cellular changes at the midblastula stage

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Cell cycle control by the nucleo-cytoplasmic ratio in early Drosophila development.

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Temporal regulation of gene expression in the blastoderm Drosophila embryo

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Activation of transcription in Drosophila embryos is a gradual process mediated by the nucleocytoplasmic ratio

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Regulation of the appearance of division asynchrony and microtubule-dependent chromosome cycles in Xenopus laevis embryos

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Completion of DNA replication is monitored by a feedback system that controls the initiation of mitosis in vitro: studies in Xenopus

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Anastral meiotic spindle morphogenesis: role of the non-claret disjunctional kinesin-like protein.

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Distinct molecular mechanism regulate cell cycle timing at successive stages of Drosophila embryogenesis

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Cell cycle checkpoints: preventing an identity crisis

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Zygotic degradation of two maternal Cdc25 mRNAs terminates Drosophila's early cell cycle program.

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Drosophila Wee1 kinase rescues fission yeast from mitotic catastrophe and phosphorylates Drosophila Cdc2 in vitro

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Regulation of runt transcription by Drosophila segmentation genes

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Insertional mutagenesis of the Drosophila genome with single P elements

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p56(chk1) protein kinase is required for the DNA replication checkpoint at 37 degrees C in fission yeast

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rad-dependent response of the chk1-encoded protein kinase at the DNA damage checkpoint.

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Nuclear and cytoplasmic mitotic cycles continue in Drosophila embryos in which DNA synthesis is inhibited with aphidicolin

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Hypersensitivity of Drosophila mei-41 mutants to hydroxyurea is associated with reduced mitotic chromosome stability

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Progression of the cell cycle through mitosis leads to abortion of nascent transcripts

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A non-radioactive in situ hybridization method for the localization of specific RNAs in Drosophila embryos reveals translational control of the segmentation gene hunchback

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