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European Journal of Endocrinology|October 23, 2013
Systematic screening for PRKAR1A gene rearrangement in Carney complex: identification and functional characterization of a new in-frame deletionM Guillaud Bataille, Y Rhayem, S B Sousa, et al.
Human Mutation|January 15, 1999
Mutation analyses of North American APS-1 patientsM Heino, H S Scott, Q Chen, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 1, 2009
Expression of neuropeptide hormone receptors in human adrenal tumors and cell lines: antiproliferative effects of peptide analoguesC G Ziegler, J W Brown, A V Schally, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|October 30, 2010
A novel device for islet transplantation providing immune protection and oxygen supplyB Ludwig, B Zimerman, A Steffen, et al.
The Journal of Clinical Endocrinology and Metabolism|August 26, 1998
Carney complex, Peutz-Jeghers syndrome, Cowden disease, and Bannayan-Zonana syndrome share cutaneous and endocrine manifestations, but not genetic lociC A Stratakis, L S Kirschner, S E Taymans, et al.
Molecular Psychiatry|October 26, 2016
The PHF21B gene is associated with major depression and modulates the stress responseM-L Wong, M Arcos-Burgos, S Liu, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|November 4, 2014
Oxygen supply by photosynthesis to an implantable islet cell deviceY Evron, B Zimermann, B Ludwig, et al.
Molecular Psychiatry|September 13, 2017
DHEA inhibits acute microglia-mediated inflammation through activation of the TrkA-Akt1/2-CREB-Jmjd3 pathwayV I Alexaki, G Fodelianaki, A Neuwirth, et al.
The Pharmacogenomics Journal|December 25, 2013
Lipidomic profiling before and after Roux-en-Y gastric bypass in obese patients with diabetesJ Graessler, T D Bornstein, D Goel, et al.
Clinical Genetics|May 29, 2010
The role of germline AIP, MEN1, PRKAR1A, CDKN1B and CDKN2C mutations in causing pituitary adenomas in a large cohort of children, adolescents, and patients with genetic syndromesC A Stratakis, M A Tichomirowa, S Boikos, et al.
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