Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Takasumi Matsuki"'
Autor:
Jun-ichi Maeyama, Hisakazu Takatsuka, Fumiko Suzuki, Ayumi Kubota, Satomi Horiguchi, Takako Komiya, Ichiroh Shimada, Eri Murata, Youko Osawa, Harukazu Kitagawa, Takasumi Matsuki, Masanori Isaka, Saburo Yamamoto, Sumiko Iho
Publikováno v:
PLoS ONE, Vol 9, Iss 2, p e88846 (2014)
BACKGROUND: CpG oligodeoxynucleotides (ODNs), resembling bacterial DNA, are currently tested in clinical trials as vaccine adjuvants. They have the nuclease-resistant phosphorothioate bond; the immune responses elicited differ according to the CpG OD
Externí odkaz:
https://doaj.org/article/c30f14877ee548c68c65610bec0eed1a
Autor:
Youko Osawa, Hisakazu Takatsuka, Saburo Yamamoto, Shigeharu Fujieda, Sumiko Iho, Takayuki Takahashi, Satomi Horiguchi, Yoshimasa Urasaki, Takasumi Matsuki, Rumiko Takauji
Publikováno v:
The Journal of Immunology. 177:4841-4852
CpG DNA induces plasmacytoid dendritic cells (pDC) to produce type I IFN and chemokines. However, it has not been fully elucidated how the TLR9 signaling pathway is linked to these gene expressions. We examined the mechanisms involving the TLR9 and t
Publikováno v:
Biochimica et Biophysica Acta (BBA) - General Subjects. 1723:302-308
In order to systematically characterize age-related changes in the mtDNA content of various tissues during aging, we analyzed the mtDNA content of eight tissues from mice at five different ages from young to senescent by quantitative real-time PCR an
Autor:
Takasumi Matsuki, Toshihiro Yasuda, Koichiro Kishi, Etsuko Tsubota, Mika Masuyama, Reiko Iida, Hisakazu Takatsuka
Publikováno v:
Experimental Cell Research. 302:22-30
Mpv17-like protein (M-LP) has been identified as a new protein that shows high sequence homology with Mpv17 protein, a peroxisomal membrane protein involved in the development of early onset glomerulosclerosis. We previously showed that the originall
Autor:
Chikahiko Numakura, Takasumi Matsuki, Sumimasa Yamashita, Masayo Kanai, Emi Shirahata, Kiyoshi Hayasaka, Kazuki Kijima
Publikováno v:
Journal of the Neurological Sciences. 210:61-64
Charcot-Marie-Tooth disease type 1 (CMT1) is a heterogeneous disorder. Most CMT1 patients are associated with a duplication of 17p11.2-p12 (CMT1A duplication), but a small number of patients have mutations of peripheral myelin protein 22 (PMP22), mye
Publikováno v:
International Congress Series. 1239:363-366
We mapped human STS UT413 on human chromosome Xq27-q28, renamed it DXS10011 and developed an easy method of analysis using capillary electrophoresis. The probability of discrimination was 0.954 from 1198 chromosomes in the Japanese population. DXS100
Autor:
Hiromichi Iwasaki, Takayuki Takahashi, Sumiko Iho, Rumiko Takauji, Hisakazu Takatsuka, Takashi Yokochi, Saburo Yamamoto, Reiko Iida, Takasumi Matsuki, Harukazu Kitagawa
Publikováno v:
Journal of Leukocyte Biology. 72:1011-1019
Human plasmacytoid or CD4+CD11c− type 2 dendritic cell precursors (PDC) were identified as natural type I interferon (IFN)-producing cells in response to viral and bacterial infection. They represent effector cells of innate immunity and link it to
Autor:
Toshihiro Yasuda, Takasumi Matsuki, Mika Masuyama, Kazumi Sawazaki, Koichiro Kishi, Reiko Iida, Etsuko Tsubota
Publikováno v:
International Journal of Legal Medicine. 116:191-194
From sequence database information we have newly identified three male-specific and polymorphic tetranucleotide STRs, DYS443 (GDB: 10807127), DYS444 (GDB: 10807128) and DYS445 (GDB: 10807129) on the Y chromosome. Analysis of 190 Japanese males reveal
Autor:
Ayumi Kubota, Ichiroh Shimada, Saburo Yamamoto, Takasumi Matsuki, Youko Osawa, Eri Murata, Satomi Horiguchi, Takako Komiya, Jun-ichi Maeyama, Fumiko Suzuki, Masanori Isaka, Hisakazu Takatsuka, Sumiko Iho, Harukazu Kitagawa
Publikováno v:
PLoS ONE, Vol 9, Iss 2, p e88846 (2014)
PLoS ONE
PLoS ONE
Background CpG oligodeoxynucleotides (ODNs), resembling bacterial DNA, are currently tested in clinical trials as vaccine adjuvants. They have the nuclease-resistant phosphorothioate bond; the immune responses elicited differ according to the CpG ODN
Autor:
Takasumi Matsuki, Mitsuhiro Kato, Kiyoshi Hayasaka, Chikahiko Numakura, Shigeki Nakamura, Osamu Soma, Toshiyuki Kimura, Yuichi Takusa, Masayo Kanai
Publikováno v:
Annals of Neurology. 50:547-551
The molecular basis of double cortex syndrome was investigated in 2 male patients. Magnetic resonance imaging of the patients' heads showed diffuse subcortical band heterotopia, as is seen in female patients. We found a heterozygous mutation for Asp5