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Melanocortin 4 receptor mutations become common.
Kühnen P, Biebermann H, Krude H. Kühnen P, et al. Cell Metab. 2021 Aug 3;33(8):1512-1513. doi: 10.1016/j.cmet.2021.07.003. Cell Metab. 2021. PMID: 34348096 Free article.
New pathogenic thyrotropin receptor mutations decipher differentiated activity switching at a conserved helix 6 motif of family A GPCR.
Biebermann H, Winkler F, Handke D, Teichmann A, Gerling B, Cameron F, Eichhorst J, Grüters A, Wiesner B, Kühnen P, Krude H, Kleinau G. Biebermann H, et al. Among authors: kuhnen p. J Clin Endocrinol Metab. 2012 Feb;97(2):E228-32. doi: 10.1210/jc.2011-2106. Epub 2011 Nov 23. J Clin Endocrinol Metab. 2012. PMID: 22112806
Glucose-dependent insulinotropic polypeptide reduces fat-specific expression and activity of 11β-hydroxysteroid dehydrogenase type 1 and inhibits release of free fatty acids.
Gögebakan Ö, Andres J, Biedasek K, Mai K, Kühnen P, Krude H, Isken F, Rudovich N, Osterhoff MA, Kintscher U, Nauck M, Pfeiffer AF, Spranger J. Gögebakan Ö, et al. Among authors: kuhnen p. Diabetes. 2012 Feb;61(2):292-300. doi: 10.2337/db10-0902. Epub 2011 Dec 16. Diabetes. 2012. PMID: 22179810 Free PMC article. Clinical Trial.
Detection of Novel Gene Variants Associated with Congenital Hypothyroidism in a Finnish Patient Cohort.
Löf C, Patyra K, Kuulasmaa T, Vangipurapu J, Undeutsch H, Jaeschke H, Pajunen T, Kero A, Krude H, Biebermann H, Kleinau G, Kühnen P, Rantakari K, Miettinen P, Kirjavainen T, Pursiheimo JP, Mustila T, Jääskeläinen J, Ojaniemi M, Toppari J, Ignatius J, Laakso M, Kero J. Löf C, et al. Among authors: kuhnen p. Thyroid. 2016 Sep;26(9):1215-24. doi: 10.1089/thy.2016.0016. Epub 2016 Aug 2. Thyroid. 2016. PMID: 27373559 Free PMC article.
61 results