Resultados de procura - Anne Guiochon‐Mantel

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  1. 1
    Nuclear localization signals also mediate the outward movement of proteins from the nucleus.

    Nuclear localization signals also mediate the outward movement of proteins from the nucleus. por Anne Guiochon‐Mantel, Karine Delabre, P. Lescop, Edwin Milgröm

    Publicado 1994
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  2. 2
    Sumoylation of the Progesterone Receptor and of the Steroid Receptor Coactivator SRC-1

    Sumoylation of the Progesterone Receptor and of the Steroid Receptor Coactivator SRC-1 por Anne Chauchereau, Larbi Amazit, Monique Quesne, Anne Guiochon‐Mantel, Edwin Milgröm

    Publicado 2003
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  3. 3
    Mechanisms of Progesterone Receptor Export from Nuclei: Role of Nuclear Localization Signal, Nuclear Export Signal, and Ran Guanosine Triphosphate

    Mechanisms of Progesterone Receptor Export from Nuclei: Role of Nuclear Localization Signal, Nuclear Export Signal, and Ran Guanosine Triphosphate por Rakesh K. Tyagi, Larbi Amazit, P. Lescop, Edwin Milgröm, Anne Guiochon‐Mantel

    Publicado 1998
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  4. 4
    RANK (Receptor Activator of Nuclear Factor kappa B) and RANK Ligand Are Expressed in Giant Cell Tumors of Bone

    RANK (Receptor Activator of Nuclear Factor kappa B) and RANK Ligand Are Expressed in Giant Cell Tumors of Bone por Sophie Roux, Larbi Amazit, Geri Méduri, Anne Guiochon‐Mantel, Edwin Milgröm, Xavier Mariette

    Publicado 2002
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  5. 5
    Human fetal testis: source of estrogen and target of estrogen action

    Human fetal testis: source of estrogen and target of estrogen action por Kahina Boukari, Maria Luisa Ciampi, Anne Guiochon‐Mantel, Jacques Young, Marc Lombès, Geri Méduri

    Publicado 2007
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  6. 6
    Nucleocytoplasmic shuttling of the progesterone receptor.

    Nucleocytoplasmic shuttling of the progesterone receptor. por Anne Guiochon‐Mantel, P. Lescop, Sophie Christin‐Maître, H. Loosfelt, M. Perrot-Applanat, Edwin Milgröm

    Publicado 1991
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  7. 7
    GENETICS IN ENDOCRINOLOGY: Genetic counseling for congenital hypogonadotropic hypogonadism and Kallmann syndrome: new challenges in the era of oligogenism and next-generation sequencing

    GENETICS IN ENDOCRINOLOGY: Genetic counseling for congenital hypogonadotropic hypogonadism and Kallmann syndrome: new challenges in the era of oligogenism and next-generation seque... por Luigi Maione, Andrew Dwyer, Bruno Francou, Anne Guiochon‐Mantel, Nadine Binart, Jérôme Bouligand, Jacques Young

    Publicado 2018
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  8. 8
    Mechanisms of nuclear localization of the progesterone receptor: Evidence for interaction between monomers

    Mechanisms of nuclear localization of the progesterone receptor: Evidence for interaction between monomers por Anne Guiochon‐Mantel, Hugues Loosfelt, P. Lescop, Sokhavuth Sar, M. Atger, Martine Perrot‐Applanat, Edwin Milgröm

    Publicado 1989
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  9. 9
    In vivo functional protein-protein interaction: nuclear targeted hsp90 shifts cytoplasmic steroid receptor mutants into the nucleus.

    In vivo functional protein-protein interaction: nuclear targeted hsp90 shifts cytoplasmic steroid receptor mutants into the nucleus. por Kyucheol Kang, Jocelyne Devin, F. Cadepond, Nicole Jibard, Anne Guiochon‐Mantel, E.E. Baulieu, M.G. Catelli

    Publicado 1994
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  10. 10
    Cloning and sequence analysis of rabbit progesterone-receptor complementary DNA.

    Cloning and sequence analysis of rabbit progesterone-receptor complementary DNA. por H. Loosfelt, M. Atger, Micheline Misrahi, Anne Guiochon‐Mantel, Cécile Mériel, F. Logeat, Richard Bénarous, Edwin Milgröm

    Publicado 1986
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  11. 11
    Germline AIP Mutations in Apparently Sporadic Pituitary Adenomas: Prevalence in a Prospective Single-Center Cohort of 443 Patients

    Germline AIP Mutations in Apparently Sporadic Pituitary Adenomas: Prevalence in a Prospective Single-Center Cohort of 443 Patients por Laure Cazabat, Jérôme Bouligand, Sylvie Salenave, Michèle Bernier, S. Gaillard, Fabrice Parker, Jacques Young, Anne Guiochon‐Mantel, Philippe Chanson

    Publicado 2012
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  12. 12
    RANK (receptor activator of nuclear factor‐κB) and RANKL expression in multiple myeloma

    RANK (receptor activator of nuclear factor‐κB) and RANKL expression in multiple myeloma por Sophie Roux, Véronique Meignin, J Quillard, Geri Méduri, Anne Guiochon‐Mantel, Jean‐Paul Fermand, Edwin Milgröm, Xavier Mariette

    Publicado 2002
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  13. 13
    Non-syndromic congenital hypogonadotropic hypogonadism: clinical presentation and genotype–phenotype relationships

    Non-syndromic congenital hypogonadotropic hypogonadism: clinical presentation and genotype–phenotype relationships por Frédéric Brioude, Jérôme Bouligand, Séverine Trabado, Bruno Francou, Sylvie Salenave, Peter Kamenický, Sylvie Brailly‐Tabard, Philippe Chanson, Anne Guiochon‐Mantel, Jacques Young

    Publicado 2010
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  14. 14
    Very low frequency of germline GPR101 genetic variation and no biallelic defects with AIP in a large cohort of patients with sporadic pituitary adenomas

    Very low frequency of germline GPR101 genetic variation and no biallelic defects with AIP in a large cohort of patients with sporadic pituitary adenomas por Anne-Lise Lecoq, Jérôme Bouligand, Mirella Hage, Laure Cazabat, Sylvie Salenave, Agnès Linglart, Jacques Young, Anne Guiochon‐Mantel, Philippe Chanson, Peter Kamenický

    Publicado 2016
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  15. 15
    Kisspeptin Restores Pulsatile LH Secretion in Patients with Neurokinin B Signaling Deficiencies: Physiological, Pathophysiological and Therapeutic Implications

    Kisspeptin Restores Pulsatile LH Secretion in Patients with Neurokinin B Signaling Deficiencies: Physiological, Pathophysiological and Therapeutic Implications por Jacques Young, Jyothis T. George, Javier A. Tello, Bruno Francou, Jérôme Bouligand, Anne Guiochon‐Mantel, Sylvie Brailly‐Tabard, Richard A. Anderson, Robert P. Millar

    Publicado 2012
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  16. 16
    New MCM8 mutation associated with premature ovarian insufficiency and chromosomal instability in a highly consanguineous Tunisian family

    New MCM8 mutation associated with premature ovarian insufficiency and chromosomal instability in a highly consanguineous Tunisian family por Nouha Bouali, Bruno Francou, Jérôme Bouligand, Dilek Imanci, Sarra Dimassi, Lucie Tosca, Monia Zaouali, Soumaya Mougou, Jacques Young, Ali Saâd, Anne Guiochon‐Mantel

    Publicado 2017
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  17. 17
    Familial Glucocorticoid Receptor Haploinsufficiency by Non-Sense Mediated mRNA Decay, Adrenal Hyperplasia and Apparent Mineralocorticoid Excess

    Familial Glucocorticoid Receptor Haploinsufficiency by Non-Sense Mediated mRNA Decay, Adrenal Hyperplasia and Apparent Mineralocorticoid Excess por Jérôme Bouligand, Brigitte Delemer, A.C. Hécart, Geri Méduri, Say Viengchareun, Larbi Amazit, Séverine Trabado, Bruno Fève, Anne Guiochon‐Mantel, Jacques Young, Marc Lombès

    Publicado 2010
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  18. 18
    Isolated Familial Hypogonadotropic Hypogonadism and a<i>GNRH1</i>Mutation

    Isolated Familial Hypogonadotropic Hypogonadism and a<i>GNRH1</i>Mutation por Jérôme Bouligand, Cristina Ghervan, Javier A. Tello, Sylvie Brailly‐Tabard, Sylvie Salenave, Philippe Chanson, Marc Lombès, Robert P. Millar, Anne Guiochon‐Mantel, Jacques Young

    Publicado 2009
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  19. 19
    Three Novel Heterozygous Point Mutations of<i>NR3C1</i>Causing Glucocorticoid Resistance

    Three Novel Heterozygous Point Mutations of<i>NR3C1</i>Causing Glucocorticoid Resistance por Géraldine Vitellius, Jérôme Fagart, Brigitte Delemer, Larbi Amazit, Nelly Ramos, Jérôme Bouligand, Florian Le Billan, Frédéric Castinetti, Anne Guiochon‐Mantel, Séverine Trabado, Marc Lombès

    Publicado 2016
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  20. 20
    <i>TAC3</i>and<i>TACR3</i>Defects Cause Hypothalamic Congenital Hypogonadotropic Hypogonadism in Humans

    <i>TAC3</i>and<i>TACR3</i>Defects Cause Hypothalamic Congenital Hypogonadotropic Hypogonadism in Humans por Jacques Young, Jérôme Bouligand, Bruno Francou, Marie-Laure Raffin-Sanson, Stéphanie Gaillez, Marc Jeanpierre, Michaël Grynberg, Peter Kamenický, Philippe Chanson, Sylvie Brailly‐Tabard, Anne Guiochon‐Mantel

    Publicado 2010
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