Associated Papers
Melatonin receptor 1A variants as genetic cause of idiopathic osteoporosis.
Bisikirska B et al.
Science Translational Medicine, 2024
39413162 (PubMed )
Supplement: scitranslmed.adj0085_data_files_s1_to_s10.zip › adj0085_data_file_s1.xlsx › Sheet1
Somatic mutations in tumor-infiltrating lymphocytes impact on antitumor immunity.
Mukohara F et al.
Proceedings of the National Academy of Sciences of the United States of America, 2024
39167601 (PubMed )
Supplement: pnas.2320189121.sd02.xlsx › Dataset_S2
The effects of missense OPN3 mutations in melanocytic lesions on protein structure and light-sensitive function.
Zhang W et al.
Experimental Dermatology, 2022
Identification of OPN3 as associated with non-syndromic oligodontia in a Japanese population.
Inagaki Y et al.
Journal of Human Genetics, 2021
Large-scale polymorphism discovery in macaque G-protein coupled receptors.
Goswami DB et al.
Bmc Genomics, 2013
24119066 (PubMed )
Supplement: 1471-2164-14-703-S4.xlsx › Sheet1
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