Associated Papers
Rare MTNR1B variants causing diminished MT2 signalling associate with elevated HbA1c levels but not with type 2 diabetes.
Sørensen KV et al.
Diabetologia, 2025
Association of rs3027178 polymorphism in the circadian clock gene PER1 with susceptibility to Alzheimer's disease and longevity in an Italian population.
Bacalini MG et al.
Geroscience, 2022
34921659 (PubMed )
Supplement: 11357_2021_477_MOESM3_ESM.xlsx › rare_variants_AD
Structural Elements Directing G Proteins and β-Arrestin Interactions with the Human Melatonin Type 2 Receptor Revealed by Natural Variants.
Plouffe B et al.
Acs Pharmacology & Translational Science, 2022
Minireview: Toward the establishment of a link between melatonin and glucose homeostasis: association of melatonin MT2 receptor variants with type 2 diabetes.
Karamitri A et al.
Molecular Endocrinology (baltimore, Md.), 2013
Rare MTNR1B variants impairing melatonin receptor 1B function contribute to type 2 diabetes.
Bonnefond A et al.
Nature Genetics, 2012
MTNR1B G24E variant associates With BMI and fasting plasma glucose in the general population in studies of 22,142 Europeans.
Andersson EA et al.
Diabetes, 2010
[Involvement of melatonin MT2 receptor mutants in type 2 diabetes development].
Karamitri A et al.
Medecine Sciences : M/s, 0
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