LINGO2
Leucine rich repeat and Ig domain containing 2 is a protein that in humans is encoded by the LINGO2 gene. [1]
References
References
- ↑ “Entrez Gene: Leucine rich repeat and Ig domain containing 2”. Retrieved 2014-03-31.
Further reading
Further reading
- Ferreira, R. C.; Pan-Hammarström, Q; Graham, R. R.; Gateva, V; Fontán, G; Lee, A. T.; Ortmann, W; Urcelay, E; Fernández-Arquero, M; Núñez, C; Jorgensen, G; Ludviksson, B. R.; Koskinen, S; Haimila, K; Clark, H. F.; Klareskog, L; Gregersen, P. K.; Behrens, T. W.; Hammarström, L (2010). “Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency”. Nature Genetics. 42 (9): 777–80. doi:10.1038/ng.644. PMID 20694011.
- Wu, Y. W.; Prakash, K. M.; Rong, T. Y.; Li, H. H.; Xiao, Q; Tan, L. C.; Au, W. L.; Ding, J. Q.; Chen, S. D.; Tan, E. K. (2011). “Lingo2 variants associated with essential tremor and Parkinson’s disease”. Human Genetics. 129 (6): 611–5. doi:10.1007/s00439-011-0955-3. PMID 21287203.
- Su, F. C.; Chen, C. M.; Chen, Y. C.; Wu, Y. R. (2012). “LINGO-2 polymorphism and the risk of Parkinson’s disease in Taiwan”. Parkinsonism & Related Disorders. 18 (5): 609–11. doi:10.1016/j.parkreldis.2011.11.013. PMID 22123311.
- Ichikawa, S; Koller, D. L.; Padgett, L. R.; Lai, D; Hui, S. L.; Peacock, M; Foroud, T; Econs, M. J. (2010). “Replication of previous genome-wide association studies of bone mineral density in premenopausal American women”. Journal of Bone and Mineral Research. 25 (8): 1821–9. doi:10.1002/jbmr.62. PMC 3153352. PMID 20200978.
- Vilariño-Güell, C; Wider, C; Ross, O. A.; Jasinska-Myga, B; Kachergus, J; Cobb, S. A.; Soto-Ortolaza, A. I.; Behrouz, B; Heckman, M. G.; Diehl, N. N.; Testa, C. M.; Wszolek, Z. K.; Uitti, R. J.; Jankovic, J; Louis, E. D.; Clark, L. N.; Rajput, A; Farrer, M. J. (2010). “LINGO1 and LINGO2 variants are associated with essential tremor and Parkinson disease”. Neurogenetics. 11 (4): 401–8. doi:10.1007/s10048-010-0241-x. PMC 3930084. PMID 20369371.
- Carim-Todd, L; Escarceller, M; Estivill, X; Sumoy, L (2003). “LRRN6A/LERN1 (leucine-rich repeat neuronal protein 1), a novel gene with enriched expression in limbic system and neocortex”. The European Journal of Neuroscience. 18 (12): 3167–82. doi:10.1111/j.1460-9568.2003.03003.x. PMID 14686891.
- Speliotes, E. K.; Willer, C. J.; Berndt, S. I.; Monda, K. L.; Thorleifsson, G; Jackson, A. U.; Lango Allen, H; Lindgren, C. M.; Luan, J; Mägi, R; Randall, J. C.; Vedantam, S; Winkler, T. W.; Qi, L; Workalemahu, T; Heid, I. M.; Steinthorsdottir, V; Stringham, H. M.; Weedon, M. N.; Wheeler, E; Wood, A. R.; Ferreira, T; Weyant, R. J.; Segrè, A. V.; Estrada, K; Liang, L; Nemesh, J; Park, J. H.; Gustafsson, S; Kilpeläinen, T. O. (2010). “Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index”. Nature Genetics. 42 (11): 937–48. doi:10.1038/ng.686. PMC 3014648. PMID 20935630.
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