Searching journal content for articles similar to Chembazhi et al. 31 (4): 576.

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  1. Resource: Epigenomics of embryogenesis in turbot
    • Oscar Aramburu,
    • Belen G Pardo,
    • Ada Jimenez-Gonzalez,
    • Andrés Blanco-Hortas,
    • Daniel Macqueen,
    • Carmen Bouza,
    • and Paulino Martinez
    Genome Res. November 4, 2025 gr.280355.124; Published in Advance November 4, 2025, doi:10.1101/gr.280355.124
    ...dynamics were revealed for many 30 orthologous Hox genes, notable cross-species differences were identified from 31 pre-ZGA leading up to hatching. This multi-omics investigation provides a novel 32 atlas of non-coding regulatory elements controlling turbot development, with key 33 applications...
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  2. Research: A systems-level approach to parental genomic imprinting: the imprinted gene network includes extracellular matrix genes and regulates cell cycle exit and differentiation
    • Hala Al Adhami,
    • Brendan Evano,
    • Anne Le Digarcher,
    • Charlotte Gueydan,
    • Emeric Dubois,
    • Hugues Parrinello,
    • Christelle Dantec,
    • Tristan Bouschet,
    • Annie Varrault,
    • and Laurent Journot
    Genome Res. March 2015 25: 353-367; Published in Advance January 22, 2015, doi:10.1101/gr.175919.114
    ...from proliferation to quiescence and differentiation during fibroblast cell cycle withdrawal, adipogenesis in vitro, and muscle regeneration in vivo. Imprinted gene regulation is not linked to alteration of DNA methylation or to perturbation of monoallelic, parent-of-origin-dependent expression...
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  3. Method: A metabolomic and systems biology perspective on the brain of the Fragile X syndrome mouse model
    • Laetitia Davidovic,
    • Vincent Navratil,
    • Carmela M. Bonaccorso,
    • Maria Vincenza Catania,
    • Barbara Bardoni,
    • and Marc-Emmanuel Dumas
    Genome Res. December 2011 21: 2190-2202; Published in Advance September 7, 2011, doi:10.1101/gr.116764.110
    ..., a dynamic mutation increasing abnormally the number of CGG repeats in the first exon of the FMR1 gene leads to their hypermethylation and the subsequent absence of its gene product, FMRP (Penagarikano et al. 2007). Although a monogenic disorder, FXS is a disease of complex etiology accompanied by behavioral...
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