Search Results - "Tomaz, Rute A"

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    Ncoa3 functions as an essential Esrrb coactivator to sustain embryonic stem cell self-renewal and reprogramming by Percharde, Michelle, Lavial, Fabrice, Ng, Jia-Hui, Kumar, Vibhor, Tomaz, Rute A, Martin, Nadine, Yeo, Jia-Chi, Gil, Jesús, Prabhakar, Shyam, Ng, Huck-Hui, Parker, Malcolm G, Azuara, Véronique

    Published in Genes & development (15-10-2012)
    “…Embryonic stem cell (ESC) pluripotency depends on a well-characterized gene regulatory network centered on Oct4, Sox2, and Nanog. In contrast, little is known…”
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    Journal Article
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    Bmi1 facilitates primitive endoderm formation by stabilizing Gata6 during early mouse development by Lavial, Fabrice, Bessonnard, Sylvain, Ohnishi, Yusuke, Tsumura, Akiko, Chandrashekran, Anil, Fenwick, Mark A, Tomaz, Rute A, Hosokawa, Hiroyuki, Nakayama, Toshinori, Chambers, Ian, Hiiragi, Takashi, Chazaud, Claire, Azuara, Véronique

    Published in Genes & development (01-07-2012)
    “…The transcription factors Nanog and Gata6 are critical to specify the epiblast versus primitive endoderm (PrE) lineages. However, little is known about the…”
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    Journal Article
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    Modeling Disease with Human Inducible Pluripotent Stem Cells by Grandy, Rodrigo, Tomaz, Rute A, Vallier, Ludovic

    Published in Annual review of pathology (24-01-2019)
    “…Understanding the physiopathology of disease remains an essential step in developing novel therapeutics. Although animal models have certainly contributed to…”
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    Journal Article
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    FOXE1 polymorphisms are associated with familial and sporadic nonmedullary thyroid cancer susceptibility by Tomaz, Rute A., Sousa, Inês, Silva, Joana G., Santos, Catarina, Teixeira, Manuel R., Leite, Valeriano, Cavaco, Branca M.

    Published in Clinical endocrinology (Oxford) (01-12-2012)
    “…Summary Objective FOXE1 is a transcription factor required for thyroid differentiation and function. FOXE1 locus polymorphisms (chromosome 9q22.33) were…”
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    Differential methylation as a cause of allele dropout at the imprinted GNAS locus by Tomaz, Rute A, Cavaco, Branca M, Leite, Valeriano

    Published in Genetic testing and molecular biomarkers (01-08-2010)
    “…We detected false homozygosity at the NESP55 differentially methylated region of the imprinted GNAS locus while analyzing the segregation of single-nucleotide…”
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    Journal Article
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