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 PMID:6494891  

Heterochronic mutants of the nematode Caenorhabditis elegans.

V Ambros | H R Horvitz
Science (New York, N.Y.) | 1984

Mutations in the Caenorhabditis elegans genes lin-14, lin-28, and lin-29 cause heterochronic developmental defects: the timing of specific developmental events in several tissues is altered relative to the timing of events in other tissues. These defects result from temporal transformations in the fates of specific cells, that is, certain cells express fates normally expressed by cells generated at other developmental stages. The identification and characterization of genes that can be mutated to cause heterochrony support the proposal that heterochrony is a mechanism for phylogenetic change and suggest cellular and genetic bases for heterochronic variation.

Pubmed ID: 6494891

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Associated grants

  • Agency: NIGMS NIH HHS, United States
    Id: GM24663
  • Agency: NIGMS NIH HHS, United States
    Id: GM24943
  • Agency: NICHD NIH HHS, United States
    Id: HD00369

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Caco-2 (cell line)

RRID:CVCL_0025

Cell line Caco-2 is a Cancer cell line with a species of origin Homo sapiens (Human)

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LoVo (cell line)

RRID:CVCL_0399

Cell line LoVo is a Cancer cell line with a species of origin Homo sapiens (Human)

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