Differential Regulation of Human 3β-Hydroxysteroid Dehydrogenase Type 2 for Steroid Hormone Biosynthesis by Starvation and Cyclic Amp Stimulation: Studies in the Human Adrenal NCI-...

por Udhane, Sameer, Kempna, Petra, Hofer, Gaby, Mullis, Primus E., Flück, Christa E.
Publicado 2013

Retinoic acid receptor beta and angiopoietin-like protein 1 are involved in the regulation of human androgen biosynthesis

por Udhane, Sameer S., Pandey, Amit V., Hofer, Gaby, Mullis, Primus E., Flück, Christa E.
Publicado 2015

Butyrate Increases Intracellular Calcium Levels and Enhances Growth Hormone Release from Rat Anterior Pituitary Cells via the G-Protein-Coupled Receptors GPR41 and 43

por Miletta, Maria Consolata, Petkovic, Vibor, Eblé, Andrée, Ammann, Roland A., Flück, Christa E., Mullis, Primus-E.
Publicado 2014

Role of AMP-Activated Protein Kinase on Steroid Hormone Biosynthesis in Adrenal NCI-H295R Cells

por Hirsch, Andrea, Hahn, Dagmar, Kempná, Petra, Hofer, Gaby, Mullis, Primus E., Nuoffer, Jean-Marc, Flück, Christa E.
Publicado 2012

Children’s and adolescent’s self - assessment of metabolic control versus professional judgment: a cross-sectional retrospective and prospective cohort study

por Bieri, Andreas, Oser-Meier, Monika, Janner, Marco, Cripe-Mamie, Chantal, Pipczynski-Suter, Kathrin, Mullis, Primus E, Flück, Christa E
Publicado 2013

Transient Neonatal Zinc Deficiency Caused by a Heterozygous G87R Mutation in the Zinc Transporter ZnT-2 (SLC30A2) Gene in the Mother Highlighting the Importance of Zn(2+) for Norm...

por Miletta, Maria Consolata, Bieri, Andreas, Kernland, Kristin, Schöni, Martin H., Petkovic, Vibor, Flück, Christa E., Eblé, Andrée, Mullis, Primus E.
Publicado 2013

Characterization of Novel StAR (Steroidogenic Acute Regulatory Protein) Mutations Causing Non-Classic Lipoid Adrenal Hyperplasia

por Flück, Christa E., Pandey, Amit V., Dick, Bernhard, Camats, Núria, Fernández-Cancio, Mónica, Clemente, María, Gussinyé, Miquel, Carrascosa, Antonio, Mullis, Primus E., Audi, Laura
Publicado 2011

Human MAMLD1 Gene Variations Seem Not Sufficient to Explain a 46,XY DSD Phenotype

por Camats, Núria, Fernández-Cancio, Mónica, Audí, Laura, Mullis, Primus E., Moreno, Francisca, González Casado, Isabel, López-Siguero, Juan Pedro, Corripio, Raquel, Bermúdez de la Vega, José Antonio, Blanco, José Antonio, Flück, Christa E.
Publicado 2015

Description of the SAGhE Cohort: A Large European Study of Mortality and Cancer Incidence Risks after Childhood Treatment with Recombinant Growth Hormone

por Swerdlow, Anthony J, Cooke, Rosi, Albertsson-Wikland, Kersti, Borgström, Birgi, Butler, Gar, Cianfarani, Stefan, Clayton, Pete, Coste, Joë, Deodati, Annalis, Ecosse, Emmanue, Gausche, Rut, Giacomozzi, Claudi, Kiess, Wielan, Hokken-Koelega, Anita C.S, Kuehni, Claudia E, Landier, Fabienn, Maes, Mar, Mullis, Primus-E, Pfaffle, Rolan, Sävendahl, Lar, Sommer, Gri, Thomas, Murie, Tollerfield, Sall, Zandwijken, Gladys R.J, Carel, Jean-Claud
Publicado 2015

De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy

por Syrbe, Steffen, Hedrich, Ulrike B.S., Riesch, Erik, Djémié, Tania, Müller, Stephan, Møller, Rikke S., Maher, Bridget, Hernandez-Hernandez, Laura, Synofzik, Matthis, Caglayan, Hande S., Arslan, Mutluay, Serratosa, José M., Nothnagel, Michael, May, Patrick, Krause, Roland, Löffler, Heidrun, Detert, Katja, Dorn, Thomas, Vogt, Heinrich, Krämer, Günter, Schöls, Ludger, Mullis, Primus E., Linnankivi, Tarja, Lehesjoki, Anna-Elina, Sterbova, Katalin, Craiu, Dana C., Hoffman-Zacharska, Dorota, Korff, Christian M., Weber, Yvonne G., Steinlin, Maja, Gallati, Sabina, Bertsche, Astrid, Bernhard, Matthias K., Merkenschlager, Andreas, Kiess, Wieland, Gonzalez, Michael, Züchner, Stephan, Palotie, Aarno, Suls, Arvid, De Jonghe, Peter, Helbig, Ingo, Biskup, Saskia, Wolff, Markus, Maljevic, Snezana, Schüle, Rebecca, Sisodiya, Sanjay M., Weckhuysen, Sarah, Lerche, Holger, Lemke, Johannes R.
Publicado 2015