FAP in India: a first genetically proven case

Por Pan, Daniel, Bouligand, Jérôme, Guiochon-Mantel, Anne, Adams, David
Publicado no Orphanet J Rare Dis (2015)

Differential Regulation of Breast Cancer-Associated Genes by Progesterone Receptor Isoforms PRA and PRB in a New Bi-Inducible Breast Cancer Cell Line

Por Khan, Junaid A., Bellance, Catherine, Guiochon-Mantel, Anne, Lombès, Marc, Loosfelt, Hugues
Publicado em 2012

p38 and p42/44 MAPKs Differentially Regulate Progesterone Receptor A and B Isoform Stabilization

Por Khan, Junaid A., Amazit, Larbi, Bellance, Catherine, Guiochon-Mantel, Anne, Lombès, Marc, Loosfelt, Hugues
Publicado em 2011

Progesterone receptor isoforms PRA and PRB differentially contribute to breast cancer cell migration through interaction with focal adhesion kinase complexes

Por Bellance, Catherine, Khan, Junaid A., Meduri, Geri, Guiochon-Mantel, Anne, Lombès, Marc, Loosfelt, Hugues
Publicado em 2013

Congenital Hypogonadotropic Hypogonadism Due to GNRH Receptor Mutations in Three Brothers Reveal Sites Affecting Conformation and Coupling

Por Tello, Javier A., Newton, Claire L., Bouligand, Jerome, Guiochon-Mantel, Anne, Millar, Robert P., Young, Jacques
Publicado em 2012

Ligand-Dependent Degradation of SRC-1 Is Pivotal for Progesterone Receptor Transcriptional Activity

Por Amazit, Larbi, Roseau, Audrey, Khan, Junaid A., Chauchereau, Anne, Tyagi, Rakesh K., Loosfelt, Hugues, Leclerc, Philippe, Lombès, Marc, Guiochon-Mantel, Anne
Publicado em 2011

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

Por Young, Jacques, George, Jyothis T., Tello, Javier A., Francou, Bruno, Bouligand, Jerome, Guiochon-Mantel, Anne, Brailly-Tabard, Sylvie, Anderson, Richard A., Millar, Robert P.
Publicado em 2013

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

Por Bouligand, Jérôme, Delemer, Brigitte, Hecart, Annie-Claude, Meduri, Geri, Viengchareun, Say, Amazit, Larbi, Trabado, Séverine, Fève, Bruno, Guiochon-Mantel, Anne, Young, Jacques, Lombès, Marc
Publicado em 2010

Two Families with Normosmic Congenital Hypogonadotropic Hypogonadism and Biallelic Mutations in KISS1R (KISS1 Receptor): Clinical Evaluation and Molecular Characterization of a Nov...

Por Brioude, Frédéric, Bouligand, Jérôme, Francou, Bruno, Fagart, Jérôme, Roussel, Ronan, Viengchareun, Say, Combettes, Laurent, Brailly-Tabard, Sylvie, Lombès, Marc, Young, Jacques, Guiochon-Mantel, Anne
Publicado em 2013

Women Epidemiology Lung Cancer (WELCA) study: reproductive, hormonal, occupational risk factors and biobank

Por Stücker, Isabelle, Martin, Diane, Neri, Monica, Laurent-Puig, Pierre, Blons, Hélène, Antoine, Martine, Guiochon-Mantel, Anne, Brailly-Tabard, Sylvie, Canonico, Marianne, Wislez, Marie, Trédaniel, Jean
Publicado no BMC Public Health (2017)

Normosmic Congenital Hypogonadotropic Hypogonadism Due to TAC3/TACR3 Mutations: Characterization of Neuroendocrine Phenotypes and Novel Mutations

Por Francou, Bruno, Bouligand, Jérôme, Voican, Adela, Amazit, Larbi, Trabado, Séverine, Fagart, Jérôme, Meduri, Geri, Brailly-Tabard, Sylvie, Chanson, Philippe, Lecomte, Pierre, Guiochon-Mantel, Anne, Young, Jacques
Publicado em 2011

High Level of Plasma Estradiol as a New Predictor of Ischemic Arterial Disease in Older Postmenopausal Women: The Three-City Cohort Study

Por Scarabin-Carré, Valérie, Canonico, Marianne, Brailly-Tabard, Sylvie, Trabado, Séverine, Ducimetière, Pierre, Giroud, Maurice, Ryan, Joanne, Helmer, Catherine, Plu-Bureau, Geneviève, Guiochon-Mantel, Anne, Scarabin, Pierre-Yves
Publicado em 2012

R31C GNRH1 Mutation and Congenital Hypogonadotropic Hypogonadism

Por Maione, Luigi, Albarel, Frederique, Bouchard, Philippe, Gallant, Megan, Flanagan, Colleen A., Bobe, Regis, Cohen-Tannoudji, Joelle, Pivonello, Rosario, Colao, Annamaria, Brue, Thierry, Millar, Robert P., Lombes, Marc, Young, Jacques, Guiochon-Mantel, Anne, Bouligand, Jerome
Publicado em 2013

Correction: R31C GNRH1 Mutation and Congenital Hypogonadotropic Hypogonadism

Por Maione, Luigi, Albarel, Frederique, Bouchard, Philippe, Gallant, Megan, Flanagan, Colleen A., Bobe, Regis, Cohen-Tannoudji, Joelle, Pivonello, Rosario, Colao, Annamaria, Brue, Thierry, Millar, Robert P., Lombes, Marc, Young, Jacques, Guiochon-Mantel, Anne, Bouligand, Jerome
Publicado em 2013

Identification of a human splenic marginal zone B cell precursor with NOTCH2-dependent differentiation properties

Por Descatoire, Marc, Weller, Sandra, Irtan, Sabine, Sarnacki, Sabine, Feuillard, Jean, Storck, Sébastien, Guiochon-Mantel, Anne, Bouligand, Jérôme, Morali, Alain, Cohen, Joseph, Jacquemin, Emmanuel, Iascone, Maria, Bole-Feysot, Christine, Cagnard, Nicolas, Weill, Jean-Claude, Reynaud, Claude-Agnès
Publicado em 2014

Identification of a human splenic marginal zone B cell precursor with NOTCH2-dependent differentiation properties

Por Descatoire, Marc, Weller, Sandra, Irtan, Sabine, Sarnacki, Sabine, Feuillard, Jean, Storck, Sébastien, Guiochon-Mantel, Anne, Bouligand, Jérôme, Morali, Alain, Cohen, Joseph, Jacquemin, Emmanuel, Iascone, Maria, Bole-Feysot, Christine, Cagnard, Nicolas, Weill, Jean-Claude, Reynaud, Claude-Agnès
Publicado em 2014

IGSF10 mutations dysregulate gonadotropin‐releasing hormone neuronal migration resulting in delayed puberty

Por Howard, Sasha R, Guasti, Leonardo, Ruiz‐Babot, Gerard, Mancini, Alessandra, David, Alessia, Storr, Helen L, Metherell, Lousie A, Sternberg, Michael JE, Cabrera, Claudia P, Warren, Helen R, Barnes, Michael R, Quinton, Richard, de Roux, Nicolas, Young, Jacques, Guiochon‐Mantel, Anne, Wehkalampi, Karoliina, André, Valentina, Gothilf, Yoav, Cariboni, Anna, Dunkel, Leo
Publicado no EMBO Mol Med (2016)