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Page 1
Novel Nonsense Mutation in the NLRP7 Gene Associated with Recurrent Hydatidiform Mole.
Ito Y, Maehara K, Kaneki E, Matsuoka K, Sugahara N, Miyata T, Kamura H, Yamaguchi Y, Kono A, Nakabayashi K, Migita O, Higashimoto K, Soejima H, Okamoto A, Nakamura H, Kimura T, Wake N, Taniguchi T, Hata K. Ito Y, et al. Among authors: sugahara n. Gynecol Obstet Invest. 2016;81(4):353-8. doi: 10.1159/000441780. Epub 2015 Nov 26. Gynecol Obstet Invest. 2016. PMID: 26606510
Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of human imprinting and suggests a germline methylation-independent mechanism of establishment.
Court F, Tayama C, Romanelli V, Martin-Trujillo A, Iglesias-Platas I, Okamura K, Sugahara N, Simón C, Moore H, Harness JV, Keirstead H, Sanchez-Mut JV, Kaneki E, Lapunzina P, Soejima H, Wake N, Esteller M, Ogata T, Hata K, Nakabayashi K, Monk D. Court F, et al. Among authors: sugahara n. Genome Res. 2014 Apr;24(4):554-69. doi: 10.1101/gr.164913.113. Epub 2014 Jan 8. Genome Res. 2014. PMID: 24402520 Free PMC article.
Decreased serum retinol levels in women with cervical dysplasia.
Shimizu H, Nagata C, Komatsu S, Morita N, Higashiiwai H, Sugahara N, Hisamichi S. Shimizu H, et al. Among authors: sugahara n. Br J Cancer. 1996 Jun;73(12):1600-4. doi: 10.1038/bjc.1996.301. Br J Cancer. 1996. PMID: 8664137 Free PMC article.
Fukuyama type congenital progressive muscular dystrophy.
Osawa M, Arai Y, Ikenaka H, Murasugi H, Sugahara N, Sumida S, Okada N, Shishikura K, Suzuki H, Hirayama Y, et al. Osawa M, et al. Among authors: sugahara n. Acta Paediatr Jpn. 1991 Apr;33(2):261-9. doi: 10.1111/j.1442-200x.1991.tb01552.x. Acta Paediatr Jpn. 1991. PMID: 1957653 Review.
16 results