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  1. Article

    Open Access

    Author Correction: The HSP90/R2TP assembly chaperone promotes cell proliferation in the intestinal epithelium

    Chloé Maurizy, Claire Abeza, Bénédicte Lemmers, Monica Gabola in Nature Communications (2022)

  2. Article

    Open Access

    The HSP90/R2TP assembly chaperone promotes cell proliferation in the intestinal epithelium

    The R2TP chaperone cooperates with HSP90 to integrate newly synthesized proteins into multi-subunit complexes, yet its role in tissue homeostasis is unknown. Here, we generated conditional, inducible knock-out...

    Chloé Maurizy, Claire Abeza, Bénédicte Lemmers, Monica Gabola in Nature Communications (2021)

  3. No Access

    Article

    Single-cell map** of the thymic stroma identifies IL-25-producing tuft epithelial cells

    T cell development and selection are coordinated in the thymus by a specialized niche of diverse stromal populations13. Although much progress has been made over the years in identifying the functions of the dif...

    Chamutal Bornstein, Shir Nevo, Amir Giladi, Noam Kadouri, Marie Pouzolles in Nature (2018)

  4. No Access

    Article

    Intestinal epithelial tuft cells initiate type 2 mucosal immunity to helminth parasites

    Epithelial tuft cells secretion of IL-25 is shown to regulate type 2 epithelial responses to helminth parasite infection via an IL-13/IL-4Rα-dependent feedback loop.

    François Gerbe, Emmanuelle Sidot, Danielle J. Smyth, Makoto Ohmoto in Nature (2016)

  5. Article

    Random chromosome segregation in mouse intestinal epithelial stem cells

    The mammalian intestinal epithelium is endowed with a high cell turnover sustained by a few stem cells located in the bottoms of millions of crypts. Until recently, it was generally assumed that the extreme se...

    Catherine Legraverend, Philippe Jay in Chromosome Research (2013)

  6. Article

    Open Access

    The intestinal epithelium tuft cells: specification and function

    The intestinal epithelium, composed of at least seven differentiated cell types, represents an extraordinary model to understand the details of multi-lineage differentiation, a question that is highly relevant...

    François Gerbe, Catherine Legraverend, Philippe Jay in Cellular and Molecular Life Sciences (2012)

  7. Article

    Hierarchy and plasticity in the crypt: back to the drawing board

    Catherine Legraverend, Philippe Jay in Cell Research (2011)

  8. Article

    Open Access

    Intestinal epithelial stem cells do not protect their genome by asymmetric chromosome segregation

    The idea that stem cells of adult tissues with high turnover are protected from DNA replication-induced mutations by maintaining the same 'immortal' template DNA strands together through successive divisions h...

    Marion Escobar, Pierre Nicolas, Fatiha Sangar in Nature Communications (2011)

  9. No Access

    Article

    Wnt signalling induces maturation of Paneth cells in intestinal crypts

    Wnt signalling, which is transduced through β-catenin/TCF4, maintains the undifferentiated state of intestinal crypt progenitor cells1,2. Mutational activation of the pathway initiates the adenomacarcinoma sequen...

    Johan H. van Es, Philippe Jay, Alex Gregorieff, Marielle E. van Gijn in Nature Cell Biology (2005)

  10. No Access

    Article

    Diversification Pattern of the HMG and SOX Family Members During Evolution

    From a database containing the published HMG protein sequences, we constructed an alignment of the HMG box functional domain based on sequence identity. Due to the large number of sequences (more than 250) an...

    Stéphan Soullier, Philippe Jay, Francis Poulat in Journal of Molecular Evolution (1999)

  11. No Access

    Article

    The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region

    Prader-Willi syndrome (PWS) is a neurogenetic disorder that results from the absence of a normal paternal contribution to the 15q11–13 region1–3. The clinical manifestations of PWS are a transient severe hypot...

    Philippe Jay, Claire Rougeulle, Annick Massacrier, Anne Moncla in Nature Genetics (1997)

  12. No Access

    Article

    Mutations in the human Sonic Hedgehog gene cause holoprosencephaly

    Holoprosencephaly (HPE) is a common developmental defect of the forebrain and frequently the midface in humans, with both genetic and environmental causes. HPE has a prevalence of 1:250 during embryogenesis an...

    Erich Roessler, Elena Belloni, Karin Gaudenz, Philippe Jay in Nature Genetics (1996)