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JCI Insight|June 13, 2023
Calcineurin regulates aldosterone production via dephosphorylation of NFATC4Mesut Berber, Sining Leng, Agnieszka Wengi, et al.
BMC Primary Care|August 31, 2022
Family doctors' attitudes toward peer support programs for type 2 diabetes and/or coronary artery disease: an exploratory survey among German practitionersK Majjouti, L Küppers, A Thielmann, et al.
Infection and Immunity|July 19, 2000
Cloning of genes of nontypeable Haemophilus influenzae involved in penetration between human lung epithelial cellsM van Schilfgaarde, P van Ulsen, W van Der Steeg, et al.
Human Heredity|November 1, 1993
Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency: the prevalent mutation G985 (K304E) is subject to a strong founder effect from northwestern EuropeN Gregersen, V Winter, D Curtis, et al.
Biorxiv : the Preprint Server for Biology|September 15, 2025
Alterations in glucocorticoid homeostasis following sleeve gastrectomySeraina O Moser, Andrei Moscalu, Cullen F Roberts, et al.
Human Genetics|April 1, 1991
Molecular characterization of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency: identification of a lys329 to glu mutation in the MCAD gene, and expression of inactive mutant enzyme protein in E. coliN Gregersen, B S Andresen, P Bross, et al.
Marine Environmental Research|April 26, 2025
An egg case study: Chronic exposure to AC electromagnetic fields results in hyperactivity in thornback ray (Raja clavata L.) embryosAnnemiek Hermans, Diede L Maas, Lydia M V de Barros Neta, et al.
Biochimica Et Biophysica Acta|October 20, 1993
Co-overexpression of bacterial GroESL chaperonins partly overcomes non-productive folding and tetramer assembly of E. coli-expressed human medium-chain acyl-CoA dehydrogenase (MCAD) carrying the prevalent disease-causing K304E mutationP Bross, B S Andresen, V Winter, et al.
British Journal of Pharmacology|September 23, 2023
Identification of a human blood biomarker of pharmacological 11β-hydroxysteroid dehydrogenase 1 inhibitionCristina Gómez, Zerin Alimajstorovic, Nantia Othonos, et al.
European Journal of Neurology|March 13, 2018
A novel heterozygous variant in ERLIN2 causes autosomal dominant pure hereditary spastic paraplegiaS L Rydning, A Dudesek, F Rimmele, et al.
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