Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Keisuke Ishiwata"'
Autor:
Atsushi Hattori, Atsuhito Seki, Naoto Inaba, Kazuhiko Nakabayashi, Kazue Takeda, Kuniko Tatsusmi, Yasuhiro Naiki, Akie Nakamura, Keisuke Ishiwata, Kenji Matsumoto, Michiyo Nasu, Kohji Okamura, Toshimi Michigami, Yuko Katoh-Fukui, Akihiro Umezawa, Tsutomu Ogata, Masayo Kagami, Maki Fukami
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-7 (2024)
Abstract All attempts to identify male-specific growth genes in humans have failed. This study aimed to clarify why men are taller than women. Microarray-based transcriptome analysis of the cartilage tissues of four adults and chondrocytes of 12 chil
Externí odkaz:
https://doaj.org/article/3019d22edd4d4c8dbe4a7506cd74d8be
Autor:
Fumiya Takahashi, Takashi Baba, Antonius Christianto, Shogo Yanai, Hyeon-Cheol Lee-Okada, Keisuke Ishiwata, Kazuhiko Nakabayashi, Kenichiro Hata, Tomohiro Ishii, Tomonobu Hasegawa, Takehiko Yokomizo, Man Ho Choi, Ken-ichirou Morohashi
Publikováno v:
Cell Reports, Vol 43, Iss 2, Pp 113715- (2024)
Summary: The zona fasciculata (zF) in the adrenal cortex contributes to multiple physiological actions through glucocorticoid synthesis. The size, proliferation, and glucocorticoid synthesis characteristics are all female biased, and sexual dimorphis
Externí odkaz:
https://doaj.org/article/9961e1b280314f7cbbce9266e2036088
Autor:
Keita Hasegawa, Kazuhiko Nakabayashi, Keisuke Ishiwata, Yoshifumi Kasuga, Kenichiro Hata, Mamoru Tanaka
Publikováno v:
BMC Research Notes, Vol 16, Iss 1, Pp 1-6 (2023)
Abstract Objective The opportunities for sequencing-based methylome analysis of clinical samples are increasing. To reduce its cost and the amount of genomic DNA required for library preparation, we aimed to establish a capture methyl-seq protocol, w
Externí odkaz:
https://doaj.org/article/3d4eb7f99c8142a89e8228718c73f7a0
Autor:
Masanori Yoshida, Kazuhiko Nakabayashi, Wentao Yang, Aiko Sato‐Otsubo, Shin‐ichi Tsujimoto, Hiroko Ogata‐Kawata, Tomoko Kawai, Keisuke Ishiwata, Mika Sakamoto, Kohji Okamura, Kaoru Yoshida, Ryota Shirai, Tomoo Osumi, Chikako Kiyotani, Yoko Shioda, Keita Terashima, Sae Ishimaru, Yuki Yuza, Masatoshi Takagi, Yuki Arakawa, Toshihiko Imamura, Daisuke Hasegawa, Akiko Inoue, Takako Yoshioka, Shuichi Ito, Daisuke Tomizawa, Katsuyoshi Koh, Kimikazu Matsumoto, Nobutaka Kiyokawa, Seishi Ogawa, Atsushi Manabe, Akira Niwa, Kenichiro Hata, Jun J. Yang, Motohiro Kato
Publikováno v:
Cancer Medicine, Vol 12, Iss 10, Pp 11264-11273 (2023)
Abstract Background Second malignant neoplasms (SMNs) are one of the most severe late complications after pediatric cancer treatment. However, the effect of genetic variation on SMNs remains unclear. In this study, we revealed germline genetic factor
Externí odkaz:
https://doaj.org/article/cb1a6a18425b4649bbcf7f5cbbacef02
Autor:
Masanori Yoshida, Daisuke Tomizawa, Satoshi Yoshimura, Tomoo Osumi, Kazuhiko Nakabayashi, Hiroko Ogata‐Kawata, Keisuke Ishiwata, Aiko Sato‐Otsubo, Yui Kimura, Shuichi Ito, Kimikazu Matsumoto, Takao Deguchi, Nobutaka Kiyokawa, Takako Yoshioka, Kenichiro Hata, Motohiro Kato
Publikováno v:
Cancer Reports, Vol 5, Iss 7, Pp n/a-n/a (2022)
Abstract Background An atypical form of Burkitt leukemia/lymphoma (BL), BL with a phenotype of precursor B‐cells (preBLL), is listed in the WHO Classification. Recent reports suggested that preBLL and classical BL could be distinguished by the diff
Externí odkaz:
https://doaj.org/article/4a9767631d7847e9ba01ca7bd1e40b6d
Autor:
Ryota Shirai, Tomoo Osumi, Aiko Sato‐Otsubo, Kazuhiko Nakabayashi, Keisuke Ishiwata, Yuji Yamada, Masanori Yoshida, Kaoru Yoshida, Yoko Shioda, Chikako Kiyotani, Keita Terashima, Daisuke Tomizawa, Nao Takasugi, Junko Takita, Osamu Miyazaki, Nobutaka Kiyokawa, Akihiro Yoneda, Yutaka Kanamori, Tomoro Hishiki, Kimikazu Matsumoto, Kenichiro Hata, Takako Yoshioka, Motohiro Kato
Publikováno v:
Genes, Chromosomes and Cancer. 61:662-669
Liquid biopsy, a method of detecting genomic alterations using blood specimens, has recently attracted attention as a noninvasive alternative to surgical tissue biopsy. We attempted quantitative analysis to detect amplification of MYCN (MYCNamp) and
Autor:
Fumiya Takahashi, Takashi Baba, Antonius Christianto, Shogo Yanai, Keisuke Ishiwata, Kazuhiko Nakabayashi, Kenichiro Hata, Tomohiro Ishii, Tomonobu Hasegawa, Man Ho Choi, Ken-ichirou Morohashi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4f522723d9fe8417d1512a06fdf2c940
https://doi.org/10.2139/ssrn.4425878
https://doi.org/10.2139/ssrn.4425878
Autor:
Keita Hasegawa, Kazuhiko Nakabayashi, Keisuke Ishiwata, Yoshifumi Kasuga, Kenichiro Hata, Mamoru Tanaka
Objective The opportunities for sequencing-based methylome analysis of clinical samples are increasing. To reduce its cost and the amount of genomic DNA required for library preparation, we aimed to establish a capture methyl-seq protocol, which adop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b83319db40af4949fee6fba910aa6270
https://doi.org/10.21203/rs.3.rs-2173809/v1
https://doi.org/10.21203/rs.3.rs-2173809/v1
Autor:
Sayaka Kawashima, Akiko Yuno, Shinichiro Sano, Akie Nakamura, Keisuke Ishiwata, Tomoyuki Kawasaki, Kazuyoshi Hosomichi, Kazuhiko Nakabayashi, Hidenori Akutsu, Hirotomo Saitsu, Maki Fukami, Takeshi Usui, Tsutomu Ogata, Masayo Kagami
Publikováno v:
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral ResearchReferences. 37(10)
Loss of methylation (LOM) at GNAS-A/B:TSS-differentially methylated regions (DMRs) in the GNAS locus is observed in pseudohypoparathyroidism type 1B (PHP1B). Many PHP1B cases are sporadic, but autosomal dominant-PHP1B has a deletion involving NESP55
Autor:
null Sayaka Kawashima, null Akiko Yuno, null Shinichiro Sano, null Akie Nakamura, null Keisuke Ishiwata, null Tomoyuki Kawasaki, null Kazuyoshi Hosomichi, null Kazuhiko Nakabayashi, null Hidenori Akutsu, null Hirotomo Saitsu, null Maki Fukami, null Takeshi Usui, null Tsutomu Ogata, null Masayo Kagami
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84bbecb7218172fa90f6e08c5b225ad7
https://doi.org/10.1002/jbmr.4652/v2/response1
https://doi.org/10.1002/jbmr.4652/v2/response1