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An intronic SNP in a RUNX1 binding site of SLC22A4, encoding an organic cation transporter, is associated with rheumatoid arthritis.
Tokuhiro S, Yamada R, Chang X, Suzuki A, Kochi Y, Sawada T, Suzuki M, Nagasaki M, Ohtsuki M, Ono M, Furukawa H, Nagashima M, Yoshino S, Mabuchi A, Sekine A, Saito S, Takahashi A, Tsunoda T, Nakamura Y, Yamamoto K. Tokuhiro S, et al. Among authors: yamada r. Nat Genet. 2003 Dec;35(4):341-8. doi: 10.1038/ng1267. Epub 2003 Nov 9. Nat Genet. 2003. PMID: 14608356
Analysis of single-nucleotide polymorphisms in Japanese rheumatoid arthritis patients shows additional susceptibility markers besides the classic shared epitope susceptibility sequences.
Kochi Y, Yamada R, Kobayashi K, Takahashi A, Suzuki A, Sekine A, Mabuchi A, Akiyama F, Tsunoda T, Nakamura Y, Yamamoto K. Kochi Y, et al. Among authors: yamada r. Arthritis Rheum. 2004 Jan;50(1):63-71. doi: 10.1002/art.11366. Arthritis Rheum. 2004. PMID: 14730600 Free article.
Absence of association between COL1A1 polymorphisms and high myopia in the Japanese population.
Nakanishi H, Yamada R, Gotoh N, Hayashi H, Otani A, Tsujikawa A, Yamashiro K, Shimada N, Ohno-Matsui K, Mochizuki M, Saito M, Saito K, Iida T, Matsuda F, Yoshimura N. Nakanishi H, et al. Among authors: yamada r. Invest Ophthalmol Vis Sci. 2009 Feb;50(2):544-50. doi: 10.1167/iovs.08-2425. Epub 2008 Oct 3. Invest Ophthalmol Vis Sci. 2009. PMID: 18836165
1,876 results