Hosomichi K - Search Results

1

AMBRA1 p.Gln30Arg Mutation, Identified in a Cowden Syndrome Family, Exhibits Hyperproliferative Potential in hTERT-RPE1 Cells.

Revathidevi S, Hosomichi K, Natsume T, Nakaoka H, Fujito NT, Akatsuka H, Sato T, Munirajan AK, Inoue I. Revathidevi S, et al. Among authors: hosomichi k. Int J Mol Sci. 2022 Sep 22;23(19):11124. doi: 10.3390/ijms231911124. Int J Mol Sci. 2022. PMID: 36232425 Free PMC article.

2

Isolation of ferret astrocytes reveals their morphological, transcriptional, and functional differences from mouse astrocytes.

Roboon J, Hattori T, Nguyen DT, Ishii H, Takarada-Iemata M, Kannon T, Hosomichi K, Maejima T, Saito K, Shinmyo Y, Mieda M, Tajima A, Kawasaki H, Hori O. Roboon J, et al. Among authors: hosomichi k. Front Cell Neurosci. 2022 Oct 6;16:877131. doi: 10.3389/fncel.2022.877131. eCollection 2022. Front Cell Neurosci. 2022. PMID: 36274991 Free PMC article.

3

Positional effects of polymorphisms in probe-target sequences on genoplot images of oligonucleotide microarrays.

Cui TL, Nakaoka H, Akiyama K, Kamura H, Hosomichi K, Bae J, Cheong H, Shin H, Yada T, Inoue I. Cui TL, et al. Among authors: hosomichi k. Genet Mol Res. 2010 Mar 23;9(1):524-31. doi: 10.4238/vol9-1gmr737. Genet Mol Res. 2010. PMID: 20391336 Free article.

4

TRIM39 and RNF39 are associated with Behçet's disease independently of HLA-B∗51 and -A∗26.

Kurata R, Nakaoka H, Tajima A, Hosomichi K, Shiina T, Meguro A, Mizuki N, Ohono S, Inoue I, Inoko H. Kurata R, et al. Among authors: hosomichi k. Biochem Biophys Res Commun. 2010 Oct 29;401(4):533-7. doi: 10.1016/j.bbrc.2010.09.088. Epub 2010 Sep 27. Biochem Biophys Res Commun. 2010. PMID: 20875797

5

Exome resequencing combined with linkage analysis identifies novel PTH1R variants in primary failure of tooth eruption in Japanese.

Yamaguchi T, Hosomichi K, Narita A, Shirota T, Tomoyasu Y, Maki K, Inoue I. Yamaguchi T, et al. Among authors: hosomichi k. J Bone Miner Res. 2011 Jul;26(7):1655-61. doi: 10.1002/jbmr.385. J Bone Miner Res. 2011. PMID: 21404329 Free article.

6

Exact break point of a 50 kb deletion 8 kb centromeric of the HLA-A locus with HLA-A*24:02: the same deletion observed in other A*24 alleles and A*23:01 allele.

Mitsunaga S, Okudaira Y, Kunii N, Cui T, Hosomichi K, Oka A, Suzuki Y, Homma Y, Sato S, Inoue I, Inoko H. Mitsunaga S, et al. Among authors: hosomichi k. Immunogenetics. 2011 Aug;63(8):467-74. doi: 10.1007/s00251-011-0521-0. Epub 2011 Apr 26. Immunogenetics. 2011. PMID: 21519861

7

Next-generation sequencing: impact of exome sequencing in characterizing Mendelian disorders.

Rabbani B, Mahdieh N, Hosomichi K, Nakaoka H, Inoue I. Rabbani B, et al. Among authors: hosomichi k. J Hum Genet. 2012 Oct;57(10):621-32. doi: 10.1038/jhg.2012.91. Epub 2012 Jul 26. J Hum Genet. 2012. PMID: 22832387 Review.

8

Exome sequencing identifies novel rheumatoid arthritis-susceptible variants in the BTNL2.

Mitsunaga S, Hosomichi K, Okudaira Y, Nakaoka H, Kunii N, Suzuki Y, Kuwana M, Sato S, Kaneko Y, Homma Y, Kashiwase K, Azuma F, Kulski JK, Inoue I, Inoko H. Mitsunaga S, et al. Among authors: hosomichi k. J Hum Genet. 2013 Apr;58(4):210-5. doi: 10.1038/jhg.2013.2. Epub 2013 Jan 31. J Hum Genet. 2013. PMID: 23364395

9

Detection of ancestry informative HLA alleles confirms the admixed origins of Japanese population.

Nakaoka H, Mitsunaga S, Hosomichi K, Shyh-Yuh L, Sawamoto T, Fujiwara T, Tsutsui N, Suematsu K, Shinagawa A, Inoko H, Inoue I. Nakaoka H, et al. Among authors: hosomichi k. PLoS One. 2013;8(4):e60793. doi: 10.1371/journal.pone.0060793. Epub 2013 Apr 5. PLoS One. 2013. PMID: 23577161 Free PMC article.

10

A nonsynonymous variant of IL1A is associated with endometriosis in Japanese population.

Hata Y, Nakaoka H, Yoshihara K, Adachi S, Haino K, Yamaguchi M, Nishikawa N, Kashima K, Yahata T, Tajima A, Watanabe A, Akira S, Hosomichi K, Inoue I, Tanaka K. Hata Y, et al. Among authors: hosomichi k. J Hum Genet. 2013 Aug;58(8):517-20. doi: 10.1038/jhg.2013.32. Epub 2013 May 2. J Hum Genet. 2013. PMID: 23635948

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