Hasil Pencarian - Reiner A. Veitia

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  1. 1
    Primary ovarian insufficiency, meiosis and DNA repair

    Primary ovarian insufficiency, meiosis and DNA repair oleh Reiner A. Veitia

    Diterbitkan 2020-04-01
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  2. 2
    Whole genome duplications and a 'function' for junk DNA? Facts and hypotheses.

    Whole genome duplications and a 'function' for junk DNA? Facts and hypotheses. oleh Reiner A Veitia, Samuel Bottani

    Diterbitkan 2009-12-01
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  3. 3
    Protein-protein and protein-DNA dosage balance and differential paralog transcription factor retention in polyploids.

    Protein-protein and protein-DNA dosage balance and differential paralog transcription factor retention in polyploids. oleh James A. Birchler, Reiner A. Veitia

    Diterbitkan 2011-10-01
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  4. 4
    Preservation of genes involved in sterol metabolism in cholesterol auxotrophs: facts and hypotheses.

    Preservation of genes involved in sterol metabolism in cholesterol auxotrophs: facts and hypotheses. oleh Giovanna Vinci, Xuhua Xia, Reiner A Veitia

    Diterbitkan 2008-01-01
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  5. 5
    The transcription factor FOXL2 in ovarian function and dysfunction.

    The transcription factor FOXL2 in ovarian function and dysfunction. oleh Elfride De Baere, Marc Fellous, Reiner A Veitia

    Diterbitkan 2010-01-01
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  6. 6
    Genes Encoding Teleost Orthologs of Human Haploinsufficient and Monoallelically Expressed Genes Remain in Duplicate More Frequently Than the Whole Genome

    Genes Encoding Teleost Orthologs of Human Haploinsufficient and Monoallelically Expressed Genes Remain in Duplicate More Frequently Than the Whole Genome oleh Floriane Picolo, Anna Grandchamp, Benoît Piégu, Antoine D. Rolland, Reiner A. Veitia, Philippe Monget

    Diterbitkan 2021-01-01
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  7. 7
    The transcription factor FOXL2 mobilizes estrogen signaling to maintain the identity of ovarian granulosa cells

    The transcription factor FOXL2 mobilizes estrogen signaling to maintain the identity of ovarian granulosa cells oleh Adrien Georges, David L'Hôte, Anne Laure Todeschini, Aurélie Auguste, Bérangère Legois, Alain Zider, Reiner A Veitia

    Diterbitkan 2014-11-01
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  8. 8
    SUMOylation of the Forkhead transcription factor FOXL2 promotes its stabilization/activation through transient recruitment to PML bodies.

    SUMOylation of the Forkhead transcription factor FOXL2 promotes its stabilization/activation through transient recruitment to PML bodies. oleh Adrien Georges, Bérénice A Benayoun, Mara Marongiu, Aurélie Dipietromaria, David L'Hôte, Anne-Laure Todeschini, Jana Auer, Laura Crisponi, Reiner A Veitia

    Diterbitkan 2011-01-01
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  9. 9
    A Hot-spot of In-frame Duplications Activates the Oncoprotein AKT1 in Juvenile Granulosa Cell Tumors

    A Hot-spot of In-frame Duplications Activates the Oncoprotein AKT1 in Juvenile Granulosa Cell Tumors oleh Laurianne Bessière, Anne-Laure Todeschini, Aurélie Auguste, Sabine Sarnacki, Delphine Flatters, Bérangère Legois, Charles Sultan, Nicolas Kalfa, Louise Galmiche, Reiner A. Veitia

    Diterbitkan 2015-05-01
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  10. 10
    FOXL2, GATA4, and SMAD3 co-operatively modulate gene expression, cell viability and apoptosis in ovarian granulosa cell tumor cells.

    FOXL2, GATA4, and SMAD3 co-operatively modulate gene expression, cell viability and apoptosis in ovarian granulosa cell tumor cells. oleh Mikko Anttonen, Marjut Pihlajoki, Noora Andersson, Adrien Georges, David L'hôte, Sanna Vattulainen, Anniina Färkkilä, Leila Unkila-Kallio, Reiner A Veitia, Markku Heikinheimo

    Diterbitkan 2014-01-01
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  11. 11
    A truncating MEIOB mutation responsible for familial primary ovarian insufficiency abolishes its interaction with its partner SPATA22 and their recruitment to DNA double-strand breaksResearch in context

    A truncating MEIOB mutation responsible for familial primary ovarian insufficiency abolishes its interaction with its partner SPATA22 and their recruitment to DNA double-strand bre... oleh Sandrine Caburet, Anne-Laure Todeschini, Cynthia Petrillo, Emmanuelle Martini, Nada D. Farran, Bérangère Legois, Gabriel Livera, Johnny S. Younis, Stavit Shalev, Reiner A. Veitia

    Diterbitkan 2019-04-01
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  12. 12
    Genome-wide linkage in a highly consanguineous pedigree reveals two novel loci on chromosome 7 for non-syndromic familial Premature Ovarian Failure.

    Genome-wide linkage in a highly consanguineous pedigree reveals two novel loci on chromosome 7 for non-syndromic familial Premature Ovarian Failure. oleh Sandrine Caburet, Petra Zavadakova, Ziva Ben-Neriah, Kamal Bouhali, Aurélie Dipietromaria, Céline Charon, Céline Besse, Paul Laissue, Vered Chalifa-Caspi, Sophie Christin-Maitre, Daniel Vaiman, Giovanni Levi, Reiner A Veitia, Marc Fellous

    Diterbitkan 2012-01-01
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  13. 13
    Functional exploration of the adult ovarian granulosa cell tumor-associated somatic FOXL2 mutation p.Cys134Trp (c.402C>G).

    Functional exploration of the adult ovarian granulosa cell tumor-associated somatic FOXL2 mutation p.Cys134Trp (c.402C>G). oleh Bérénice A Benayoun, Sandrine Caburet, Aurélie Dipietromaria, Adrien Georges, Barbara D'Haene, P J Eswari Pandaranayaka, David L'Hôte, Anne-Laure Todeschini, Sankaran Krishnaswamy, Marc Fellous, Elfride De Baere, Reiner A Veitia

    Diterbitkan 2010-01-01
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  14. 14
    A homozygous FANCM mutation underlies a familial case of non-syndromic primary ovarian insufficiency

    A homozygous FANCM mutation underlies a familial case of non-syndromic primary ovarian insufficiency oleh Baptiste Fouquet, Patrycja Pawlikowska, Sandrine Caburet, Celine Guigon, Marika Mäkinen, Laura Tanner, Marja Hietala, Kaja Urbanska, Laura Bellutti, Bérangère Legois, Bettina Bessieres, Alain Gougeon, Alexandra Benachi, Gabriel Livera, Filippo Rosselli, Reiner A Veitia, Micheline Misrahi

    Diterbitkan 2017-12-01
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  15. 15
    A missense in HSF2BP causing primary ovarian insufficiency affects meiotic recombination by its novel interactor C19ORF57/BRME1

    A missense in HSF2BP causing primary ovarian insufficiency affects meiotic recombination by its novel interactor C19ORF57/BRME1 oleh Natalia Felipe-Medina, Sandrine Caburet, Fernando Sánchez-Sáez, Yazmine B Condezo, Dirk G de Rooij, Laura Gómez-H, Rodrigo Garcia-Valiente, Anne Laure Todeschini, Paloma Duque, Manuel Adolfo Sánchez-Martin, Stavit A Shalev, Elena Llano, Reiner A Veitia, Alberto M Pendás

    Diterbitkan 2020-08-01
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  16. 16
    Association of FOXD1 variants with adverse pregnancy outcomes in mice and humans

    Association of FOXD1 variants with adverse pregnancy outcomes in mice and humans oleh Paul Laissue, Besma Lakhal, Magalie Vatin, Frank Batista, Gaëtan Burgio, Eric Mercier, Esther Dos Santos, Christophe Buffat, Diana Carolina Sierra-Diaz, Gilles Renault, Xavier Montagutelli, Jane Salmon, Philippe Monget, Reiner A. Veitia, Céline Méhats, Marc Fellous, Jean-Christophe Gris, Julie Cocquet, Daniel Vaiman

    Diterbitkan 2016-01-01
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