Zoekresultaten - Anna Biason‐Lauber

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  1. 1
    Control of sex development

    Control of sex development door Anna Biason‐Lauber

    Gepubliceerd in 2010
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  2. 2
    WNT4, RSPO1, and FOXL2 in Sex Development

    WNT4, RSPO1, and FOXL2 in Sex Development door Anna Biason‐Lauber

    Gepubliceerd in 2012
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  3. 3
    WNT4 and Sex Development

    WNT4 and Sex Development door Anna Biason‐Lauber, Daniel Konrad

    Gepubliceerd in 2008
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  4. 4
    Apparently Normal Ovarian Differentiation in a Prepubertal Girl with Transcriptionally Inactive Steroidogenic Factor 1 (NR5A1/SF-1) and Adrenocortical Insufficiency

    Apparently Normal Ovarian Differentiation in a Prepubertal Girl with Transcriptionally Inactive Steroidogenic Factor 1 (NR5A1/SF-1) and Adrenocortical Insufficiency door Anna Biason‐Lauber, Eugen J. Schoenle

    Gepubliceerd in 2000
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  5. 5
    Genome-Wide Identification of CBX2 Targets: Insights in the Human Sex Development Network

    Genome-Wide Identification of CBX2 Targets: Insights in the Human Sex Development Network door Wassim Eid, Lennart Opitz, Anna Biason‐Lauber

    Gepubliceerd in 2015
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  6. 6
    Effect of Leptin on CYP17 Enzymatic Activities in Human Adrenal Cells: New Insight in the Onset of Adrenarche<sup>1</sup>

    Effect of Leptin on CYP17 Enzymatic Activities in Human Adrenal Cells: New Insight in the Onset of Adrenarche<sup>1</sup> door Anna Biason-Lauber, M. Zachmann, Eugen J. Schoenle

    Gepubliceerd in 2000
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  7. 7
    A<i>WNT4</i>Mutation Associated with Müllerian-Duct Regression and Virilization in a 46,XX Woman

    A<i>WNT4</i>Mutation Associated with Müllerian-Duct Regression and Virilization in a 46,XX Woman door Anna Biason‐Lauber, Daniel Konrad, Francesca Navratil, Eugen J. Schoenle

    Gepubliceerd in 2004
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  8. 8
    Ovaries and Female Phenotype in a Girl with 46,XY Karyotype and Mutations in the CBX2 Gene

    Ovaries and Female Phenotype in a Girl with 46,XY Karyotype and Mutations in the CBX2 Gene door Anna Biason‐Lauber, Daniel Konrad, Monika Meyer, Carine de Beaufort, Eugen J. Schoenle

    Gepubliceerd in 2009
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  9. 9
    WNT4 deficiency—a clinical phenotype distinct from the classic Mayer–Rokitansky–Kuster–Hauser syndrome: A Case Report

    WNT4 deficiency—a clinical phenotype distinct from the classic Mayer–Rokitansky–Kuster–Hauser syndrome: A Case Report door Anna Biason‐Lauber, Gianpaolo De Filippo, Daniel Konrad, Gioacchino Scarano, A. Nazzaro, Ε. Schoenle

    Gepubliceerd in 2006
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  10. 10
    Assembling the jigsaw puzzle: CBX2 isoform 2 and its targets in disorders/differences of sex development

    Assembling the jigsaw puzzle: CBX2 isoform 2 and its targets in disorders/differences of sex development door Patrick Sproll, Eid W, Gomes Cr, Mendonca BB, Gomes Nl, Costa Em, Anna Biason‐Lauber

    Gepubliceerd in 2019
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  11. 11
    Early-Onset Complete Ovarian Failure and Lack of Puberty in a Woman With Mutated Estrogen Receptor β (ESR2)

    Early-Onset Complete Ovarian Failure and Lack of Puberty in a Woman With Mutated Estrogen Receptor β (ESR2) door Mariarosaria Lang‐Muritano, Patrick Sproll, Sascha Wyss, Anne Kolly, Renate Hürlimann, Daniel Konrad, Anna Biason‐Lauber

    Gepubliceerd in 2018
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  12. 12
    Identification and Functional Analysis of a New WNT4 Gene Mutation among 28 Adolescent Girls with Primary Amenorrhea and Müllerian Duct Abnormalities: A French Collaborative Study

    Identification and Functional Analysis of a New WNT4 Gene Mutation among 28 Adolescent Girls with Primary Amenorrhea and Müllerian Duct Abnormalities: A French Collaborative Study... door Pascal Philibert, Anna Biason‐Lauber, Roman Rouzier, Catherine Pienkowski, Françoise Paris, Daniel Konrad, Eugene Schoenle, Charles Sultan

    Gepubliceerd in 2008
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  13. 13
    Molecular analysis of WNT4 gene in four adolescent girls with mullerian duct abnormality and hyperandrogenism (atypical Mayer-Rokitansky-Küster-Hauser syndrome)

    Molecular analysis of WNT4 gene in four adolescent girls with mullerian duct abnormality and hyperandrogenism (atypical Mayer-Rokitansky-Küster-Hauser syndrome) door Pascal Philibert, Anna Biason‐Lauber, Iva Gueorguieva, Chantal Stuckens, Catherine Pienkowski, Béatrice Lebon-Labich, Françoise Paris, Charles Sultan

    Gepubliceerd in 2011
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  14. 14
    The diabetes-linked transcription factor PAX4 promotes β-cell proliferation and survival in rat and human islets

    The diabetes-linked transcription factor PAX4 promotes β-cell proliferation and survival in rat and human islets door Thierry Brun, Isobel Franklin, Luc St‐Onge, Anna Biason‐Lauber, Eugene Schoenle, Claes B. Wollheim, Benoit R. Gauthier

    Gepubliceerd in 2004
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  15. 15
    Epidemiology of Type I diabetes mellitus in Switzerland: steep rise in incidence in under 5 year old children in the past decade

    Epidemiology of Type I diabetes mellitus in Switzerland: steep rise in incidence in under 5 year old children in the past decade door Ε. Schoenle, Mariarosaria Lang‐Muritano, Sylvia Gschwend, J Laimbacher, Primus E. Mullis, Toni Torresani, Anna Biason‐Lauber, Luciano Molinari

    Gepubliceerd in 2001
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  16. 16
    Why Boys Will Be Boys: Two Pathways of Fetal Testicular Androgen Biosynthesis Are Needed for Male Sexual Differentiation

    Why Boys Will Be Boys: Two Pathways of Fetal Testicular Androgen Biosynthesis Are Needed for Male Sexual Differentiation door Christa E. Flück, Monika Meyer‐Böni, Amit V. Pandey, Petra Kempná, Walter L. Miller, Eugen J. Schoenle, Anna Biason‐Lauber

    Gepubliceerd in 2011
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  17. 17
    Assembling the jigsaw puzzle: <scp>CBX</scp>2 isoform 2 and its targets in disorders/differences of sex development

    Assembling the jigsaw puzzle: <scp>CBX</scp>2 isoform 2 and its targets in disorders/differences of sex development door Patrick Sproll, Wassim Eid, Camila R. Gomes, Berenice B. Mendonça, Nathália Lisboa Gomes, Elaine Maria Frade Costa, Anna Biason‐Lauber

    Gepubliceerd in 2018
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  18. 18
    Steroid Biomarkers and Genetic Studies Reveal Inactivating Mutations in Hexose-6-Phosphate Dehydrogenase in Patients with Cortisone Reductase Deficiency

    Steroid Biomarkers and Genetic Studies Reveal Inactivating Mutations in Hexose-6-Phosphate Dehydrogenase in Patients with Cortisone Reductase Deficiency door Gareth G. Lavery, Elizabeth A. Walker, Ana Tiganescu, Jon P. Ride, Cedric Shackleton, Jeremy Tomlinson, John Connell, David Ray, Anna Biason‐Lauber, E Małunowicz, Wiebke Arlt, Paul M. Stewart

    Gepubliceerd in 2008
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  19. 19
    P450c17 Deficiency: Clinical and Molecular Characterization of Six Patients

    P450c17 Deficiency: Clinical and Molecular Characterization of Six Patients door Stephanie Rosa, Cameron Duff, Monika Meyer, Mariarosaria Lang‐Muritano, Giancarlo Balercia, Marco Boscaro, A. Kemal Topaloğlu, Roberto Mioni, Francesco Fallo, L. Zuliani, Franco Mantero, Ε. Schoenle, Anna Biason‐Lauber

    Gepubliceerd in 2006
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  20. 20
    Identification of a SIRT1 Mutation in a Family with Type 1 Diabetes

    Identification of a SIRT1 Mutation in a Family with Type 1 Diabetes door Anna Biason‐Lauber, Marianne Böni‐Schnetzler, Basil P. Hubbard, Karim Bouzakri, Andrea Brunner, Claudia Cavelti‐Weder, Cornelia Keller, Monika Meyer‐Böni, Daniel T. Meier, Caroline Brorsson, Katharina Timper, Gil Leibowitz, Andrea Patrignani, Rémy Bruggmann, Gino Boily, Henryk Zulewski, Andreas Geier, J Cermák, Peter J. Elliott, James L. Ellis, Christoph Westphal, Urs Knobel, Jyrki J. Eloranta, Julie Kerr‐Conte, François Pattou, Daniel Konrad, Christian M. Matter, A. Fontana, Gerhard Rogler, Ralph Schlapbach, Camille Regairaz, José M. Carballido, Benjamin Gläser, Michael W. McBurney, Flemming Pociot, David Sinclair, Marc Y. Donath

    Gepubliceerd in 2013
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