खोज परिणाम - Anna Biason‐Lauber

  • प्रदर्शित 1 - 20 परिणाम 20
परिणाम को परिष्कृत करें
  1. 1
    Control of sex development

    Control of sex development द्वारा Anna Biason‐Lauber

    प्रकाशित 2010
    पूर्ण पाठ प्राप्त करें
    Revisão
    सूची में सहेजें
    में बचाया:
  2. 2
    WNT4, RSPO1, and FOXL2 in Sex Development

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

    प्रकाशित 2012
    पूर्ण पाठ प्राप्त करें
    Revisão
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    में बचाया:
  3. 3
    WNT4 and Sex Development

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

    प्रकाशित 2008
    पूर्ण पाठ प्राप्त करें
    Revisão
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    में बचाया:
  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 द्वारा Anna Biason‐Lauber, Eugen J. Schoenle

    प्रकाशित 2000
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Artigo
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    में बचाया:
  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 द्वारा Wassim Eid, Lennart Opitz, Anna Biason‐Lauber

    प्रकाशित 2015
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Artigo
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    में बचाया:
  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> द्वारा Anna Biason-Lauber, M. Zachmann, Eugen J. Schoenle

    प्रकाशित 2000
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Artigo
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    में बचाया:
  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 द्वारा Anna Biason‐Lauber, Daniel Konrad, Francesca Navratil, Eugen J. Schoenle

    प्रकाशित 2004
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Artigo
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    में बचाया:
  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 द्वारा Anna Biason‐Lauber, Daniel Konrad, Monika Meyer, Carine de Beaufort, Eugen J. Schoenle

    प्रकाशित 2009
    पूर्ण पाठ प्राप्त करें
    Artigo
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    में बचाया:
  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 द्वारा Anna Biason‐Lauber, Gianpaolo De Filippo, Daniel Konrad, Gioacchino Scarano, A. Nazzaro, Ε. Schoenle

    प्रकाशित 2006
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Artigo
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    में बचाया:
  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 द्वारा Patrick Sproll, Eid W, Gomes Cr, Mendonca BB, Gomes Nl, Costa Em, Anna Biason‐Lauber

    प्रकाशित 2019
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    Artigo
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    में बचाया:
  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) द्वारा Mariarosaria Lang‐Muritano, Patrick Sproll, Sascha Wyss, Anne Kolly, Renate Hürlimann, Daniel Konrad, Anna Biason‐Lauber

    प्रकाशित 2018
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Artigo
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    में बचाया:
  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... द्वारा Pascal Philibert, Anna Biason‐Lauber, Roman Rouzier, Catherine Pienkowski, Françoise Paris, Daniel Konrad, Eugene Schoenle, Charles Sultan

    प्रकाशित 2008
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Artigo
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    में बचाया:
  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) द्वारा Pascal Philibert, Anna Biason‐Lauber, Iva Gueorguieva, Chantal Stuckens, Catherine Pienkowski, Béatrice Lebon-Labich, Françoise Paris, Charles Sultan

    प्रकाशित 2011
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    Artigo
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    में बचाया:
  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 द्वारा Thierry Brun, Isobel Franklin, Luc St‐Onge, Anna Biason‐Lauber, Eugene Schoenle, Claes B. Wollheim, Benoit R. Gauthier

    प्रकाशित 2004
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Artigo
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    में बचाया:
  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 द्वारा Ε. Schoenle, Mariarosaria Lang‐Muritano, Sylvia Gschwend, J Laimbacher, Primus E. Mullis, Toni Torresani, Anna Biason‐Lauber, Luciano Molinari

    प्रकाशित 2001
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Artigo
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    में बचाया:
  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 द्वारा Christa E. Flück, Monika Meyer‐Böni, Amit V. Pandey, Petra Kempná, Walter L. Miller, Eugen J. Schoenle, Anna Biason‐Lauber

    प्रकाशित 2011
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Artigo
    सूची में सहेजें
    में बचाया:
  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 द्वारा Patrick Sproll, Wassim Eid, Camila R. Gomes, Berenice B. Mendonça, Nathália Lisboa Gomes, Elaine Maria Frade Costa, Anna Biason‐Lauber

    प्रकाशित 2018
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Artigo
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    में बचाया:
  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 द्वारा 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

    प्रकाशित 2008
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Artigo
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    में बचाया:
  19. 19
    P450c17 Deficiency: Clinical and Molecular Characterization of Six Patients

    P450c17 Deficiency: Clinical and Molecular Characterization of Six Patients द्वारा 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

    प्रकाशित 2006
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Artigo
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    में बचाया:
  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 द्वारा 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

    प्रकाशित 2013
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    Artigo
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