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Whole-Genome Sequencing of 84 Japanese Eels Reveals Evidence against Panmixia and Support for Sympatric Speciation.
Igarashi Y, Zhang H, Tan E, Sekino M, Yoshitake K, Kinoshita S, Mitsuyama S, Yoshinaga T, Chow S, Kurogi H, Shinoda A, Han YS, Wakiya R, Mochioka N, Yamamoto T, Kuwada H, Kaji Y, Suzuki Y, Gojobori T, Kobayashi T, Saitoh K, Watabe S, Asakawa S. Igarashi Y, et al. Among authors: mitsuyama s. Genes (Basel). 2018 Sep 28;9(10):474. doi: 10.3390/genes9100474. Genes (Basel). 2018. PMID: 30274234 Free PMC article.
A Preliminary Metagenome Analysis Based on a Combination of Protein Domains.
Igarashi Y, Mori D, Mitsuyama S, Yoshitake K, Ono H, Watanabe T, Taniuchi Y, Sakami T, Kuwata A, Kobayashi T, Ishino Y, Watabe S, Gojobori T, Asakawa S. Igarashi Y, et al. Among authors: mitsuyama s. Proteomes. 2019 Apr 29;7(2):19. doi: 10.3390/proteomes7020019. Proteomes. 2019. PMID: 31035705 Free PMC article.
The DNA sequence of human chromosome 21.
Hattori M, Fujiyama A, Taylor TD, Watanabe H, Yada T, Park HS, Toyoda A, Ishii K, Totoki Y, Choi DK, Groner Y, Soeda E, Ohki M, Takagi T, Sakaki Y, Taudien S, Blechschmidt K, Polley A, Menzel U, Delabar J, Kumpf K, Lehmann R, Patterson D, Reichwald K, Rump A, Schillhabel M, Schudy A, Zimmermann W, Rosenthal A, Kudoh J, Schibuya K, Kawasaki K, Asakawa S, Shintani A, Sasaki T, Nagamine K, Mitsuyama S, Antonarakis SE, Minoshima S, Shimizu N, Nordsiek G, Hornischer K, Brant P, Scharfe M, Schon O, Desario A, Reichelt J, Kauer G, Blocker H, Ramser J, Beck A, Klages S, Hennig S, Riesselmann L, Dagand E, Haaf T, Wehrmeyer S, Borzym K, Gardiner K, Nizetic D, Francis F, Lehrach H, Reinhardt R, Yaspo ML; Chromosome 21 mapping and sequencing consortium. Hattori M, et al. Among authors: mitsuyama s. Nature. 2000 May 18;405(6784):311-9. doi: 10.1038/35012518. Nature. 2000. PMID: 10830953
Eye disorder database "KMeyeDB".
Minoshima S, Mitsuyama S, Ohno S, Kawamura T, Shimizu N. Minoshima S, et al. Among authors: mitsuyama s. Hum Mutat. 2000;15(1):95-8. doi: 10.1002/(SICI)1098-1004(200001)15:1<95::AID-HUMU17>3.0.CO;2-3. Hum Mutat. 2000. PMID: 10612828
The KMDB/MutationView: a mutation database for human disease genes.
Minoshima S, Mitsuyama S, Ohtsubo M, Kawamura T, Ito S, Shibamoto S, Ito F, Shimizu N. Minoshima S, et al. Among authors: mitsuyama s. Nucleic Acids Res. 2001 Jan 1;29(1):327-8. doi: 10.1093/nar/29.1.327. Nucleic Acids Res. 2001. PMID: 11125127 Free PMC article.
Keio Mutation Database (KMDB) for human disease gene mutations.
Minoshima S, Mitsuyama S, Ohno S, Kawamura T, Shimizu N. Minoshima S, et al. Among authors: mitsuyama s. Nucleic Acids Res. 2000 Jan 1;28(1):364-8. doi: 10.1093/nar/28.1.364. Nucleic Acids Res. 2000. PMID: 10592275 Free PMC article.
135 results