Zobrazeno 1 - 10
of 71
pro vyhledávání: '"Shigeki Mitsunaga"'
Autor:
Shigeki Mitsunaga, Naoko Fujito, Hirofumi Nakaoka, Ryoko Imazeki, Eiichiro Nagata, Ituro Inoue
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-8 (2023)
Abstract The pathogenesis of Alzheimer’s disease (AD) is believed to involve the accumulation of amyloid-β in the brain, which is produced by the sequential cleavage of amyloid precursor protein (APP) by β-secretase and γ-secretase. Recently, an
Externí odkaz:
https://doaj.org/article/4d1ad25c5d094766b037cf99d26682a6
Autor:
Eiichiro Nagata, Natsuko Fujii, Kazuyoshi Hosomichi, Shigeki Mitsunaga, Yoichi Suzuki, Yoichi Mashimo, Hideo Tsukamoto, Tadayuki Satoh, Motoki Osawa, Ituro Inoue, Akira Hata, Shunya Takizawa
Publikováno v:
PLoS ONE, Vol 9, Iss 8, p e105319 (2014)
To identify the genetic causality of migraine and acute, severe melalgia, we performed a linkage analysis and exome sequencing in a family with four affected individuals. We identified a variant (R21L) in exon 2 of the GC globulin gene, which is invo
Externí odkaz:
https://doaj.org/article/f9f6bf6d7591473797c40863b7935963
Autor:
Hirofumi Nakaoka, Shigeki Mitsunaga, Kazuyoshi Hosomichi, Liou Shyh-Yuh, Taiji Sawamoto, Tsutomu Fujiwara, Naohisa Tsutsui, Koji Suematsu, Akira Shinagawa, Hidetoshi Inoko, Ituro Inoue
Publikováno v:
PLoS ONE, Vol 8, Iss 4, p e60793 (2013)
The polymorphisms in the human leukocyte antigen (HLA) region are powerful tool for studying human evolutionary processes. We investigated genetic structure of Japanese by using five-locus HLA genotypes (HLA-A, -B, -C, -DRB1, and -DPB1) of 2,005 indi
Externí odkaz:
https://doaj.org/article/d7f8228b02f24ec9a80f4063b68b00b1
Autor:
Hirofumi Nakaoka, Tailin Cui, Atsushi Tajima, Akira Oka, Shigeki Mitsunaga, Koichi Kashiwase, Yasuhiko Homma, Shinji Sato, Yasuo Suzuki, Hidetoshi Inoko, Ituro Inoue
Publikováno v:
PLoS ONE, Vol 6, Iss 9, p e25389 (2011)
Genome-wide association studies (GWAS) have yielded novel genetic loci underlying common diseases. We propose a systems genetics approach to utilize these discoveries for better understanding of the genetic architecture of rheumatoid arthritis (RA).
Externí odkaz:
https://doaj.org/article/ac1201eef13e4dcdb61988a8f9bac734
Autor:
Kazuyoshi Hosomichi1 (AUTHOR), Shigeki Mitsunaga2 (AUTHOR), Hideki Nagasaki3 (AUTHOR), Ituro Inoue1 (AUTHOR) itinoue@nig.ac.jp
Publikováno v:
BMC Genomics. 2014, Vol. 15 Issue 1, p645-653. 9p. 1 Diagram, 1 Chart, 2 Graphs.
Publikováno v:
Major Histocompatibility Complex. 21:37-44
Autor:
Masao Ota, Jerzy K. Kulski, Yuko Okudaira, Akira Oka, Eri Kikkawa, Shingo Suzuki, Takashi Shiina, Yuki Ozaki, Atsuko Shigenari, Shigeki Mitsunaga, Hidetoshi Inoko
Publikováno v:
Tissue Antigens. 83:10-16
Super high-resolution single molecule sequence-based typing (SS-SBT) is a human leukocyte antigen (HLA) DNA typing method to the field 4 level of allelic resolution (formerly known as eight-digit typing) to efficiently detect new and null alleles wit
Autor:
M Paumen, Hidetoshi Inoko, Y Hayashi, Eri Kikkawa, Yuki Ozaki, Shingo Suzuki, Takeji Umemura, O Takahashi, Satoru Joshita, H Taira, Takashi Shiina, Atsuko Shigenari, Yoshihiko Katsuyama, Masao Ota, Shigeki Mitsunaga, Akira Oka, Jerzy K. Kulski
Publikováno v:
Tissue Antigens. 80:305-316
Current human leukocyte antigen (HLA) DNA typing methods such as the sequence-based typing (SBT) and sequence-specific oligonucleotide (SSO) methods generally yield ambiguous typing results because of oligonucleotide probe design limitations or phase
Autor:
Shingo Suzuki, Shigeki Mitsunaga, Akira Oka, Yuki Ozaki, Atsuko Shigenari, Hidetoshi Inoko, Takashi Shiina, Eri Kikkawa
Publikováno v:
Major Histocompatibility Complex. 19:211-222
Autor:
Shigeki Mitsunaga, Yuko Okudaira, Kazuyoshi Hosomichi, Tailin Cui, Shinji Sato, Akira Oka, Yasuhiko Homma, Nanae Kunii, Ituro Inoue, Hidetoshi Inoko, Yasuo Suzuki
Publikováno v:
Immunogenetics. 63:467-474
In a structural aberration analysis of patients with arthritis mutilans, a 50 kb deletion near the HLA-A locus with HLA-A*24:02 allele was detected. It was previously reported that HLA-A*24:02 haplotype harbored a large-scale deletion telomeric of th