Zobrazeno 1 - 10
of 139
pro vyhledávání: '"Kentaro Matsuoka"'
Autor:
Miki Okuno, Yuta Mochimaru, Kentaro Matsuoka, Takahiro Yamabe, Luisa Matiz-Ceron, Takamichi Jogahara, Atsushi Toyoda, Asato Kuroiwa, Takehiko Itoh
Publikováno v:
Scientific Data, Vol 10, Iss 1, Pp 1-10 (2023)
Abstract Herein, we present the first high-quality long-read-based chromosome-level genome assemblies and gene annotations of the genomes of three endangered Tokudaia species: Tokudaia osimensis, Tokudaia tokunoshimensis, and Tokudaia muenninki. Thes
Externí odkaz:
https://doaj.org/article/545bd1014de748eeba5d9d974f1e6621
Autor:
Michio Ozeki, Saori Endo, Shiho Yasue, Akifumi Nozawa, Ryuta Asada, Akiko M. Saito, Hiroya Hashimoto, Takumi Fujimura, Yohei Yamada, Tatsuo Kuroda, Shigeru Ueno, Shoji Watanabe, Shunsuke Nosaka, Mikiko Miyasaka, Akihiro Umezawa, Kentaro Matsuoka, Takanobu Maekawa, Satoshi Hirakawa, Taizo Furukawa, Shigehisa Fumino, Tatsuro Tajiri, Junkichi Takemoto, Ryota Souzaki, Yoshiaki Kinoshita, Akihiro Fujino
Publikováno v:
Frontiers in Medicine, Vol 11 (2024)
IntroductionIntractable lymphatic anomalies (LAs) include cystic lymphatic malformation (LM; macrocystic, microcystic, or mixed), generalized lymphatic anomaly, and Gorham–Stout disease. LAs can present with severe symptoms and poor prognosis. Thus
Externí odkaz:
https://doaj.org/article/75d954cef4394ed4b3e0cce1df803598
Publikováno v:
The Journal of Pediatrics: X, Vol 10, Iss , Pp 100093- (2023)
Externí odkaz:
https://doaj.org/article/35d9f521d8f84b638d671081b96773b0
Publikováno v:
Children, Vol 10, Iss 3, p 506 (2023)
Background: Transplantation-associated thrombotic microangiopathy (TA-TMA) is a severe complication of hematopoietic stem cell transplantation and is sometimes fatal. Observations: A 4-year-old, male patient with stage M neuroblastoma (NBL) who had r
Externí odkaz:
https://doaj.org/article/e9a36b83e35c44509ec8b4dc07a7d368
Autor:
Yuki Mizuno, Naoki Shimojima, Atsushi Makimoto, Yuichi Yokokawa, Kazuaki Miyaguni, Ayano Tsukizaki, Makoto Hashimoto, Miki Ishikawa, Hideo Ishihama, Hirofumi Tomita, Akihiro Shimotakahara, Yuki Yuza, Kentaro Matsuoka, Hirofumi Kawakubo, Seiichi Hirobe
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 78, Iss , Pp 102206- (2022)
Primary rhabdomyosarcoma (RMS) of the diaphragm, especially alveolar RMS, is extremely rare. Because of its rarity, no treatment for it has yet been established, but previous studies have reported long-term survival in recipients of a combination the
Externí odkaz:
https://doaj.org/article/015c01e1b0ac43f7b016301926a6433b
Autor:
Michio Ozeki, Yoko Aoki, Akifumi Nozawa, Shiho Yasue, Saori Endo, Yumiko Hori, Kentaro Matsuoka, Tetsuya Niihori, Ryo Funayama, Matsuyuki Shirota, Keiko Nakayama, Toshiyuki Fukao
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-9 (2019)
Abstract Background Kaposiform lymphangiomatosis (KLA) has recently been distinguished as a novel subtype of generalized lymphatic anomaly (GLA) with foci of spindle endothelial cells. All cases of KLA involve multiple organs and have an unfavorable
Externí odkaz:
https://doaj.org/article/b6246cfbeb3548eaa352aee6bbce0d20
Autor:
Michio Ozeki, Ryuta Asada, Akiko M. Saito, Hiroya Hashimoto, Takumi Fujimura, Tatsuo Kuroda, Shigeru Ueno, Shoji Watanabe, Shunsuke Nosaka, Mikiko Miyasaka, Akihiro Umezawa, Kentaro Matsuoka, Takanobu Maekawa, Yohei Yamada, Akihiro Fujino, Satoshi Hirakawa, Taizo Furukawa, Tatsuro Tajiri, Yoshiaki Kinoshita, Ryota Souzaki, Toshiyuki Fukao
Publikováno v:
Regenerative Therapy, Vol 10, Iss , Pp 84-91 (2019)
Introduction: Lymphatic anomalies (LAs) refer to a group of diseases involving systemic dysplasia of lymphatic vessels. These lesions are classified as cystic lymphatic malformation (macrocystic, microcystic or mixed), generalized lymphatic anomaly,
Externí odkaz:
https://doaj.org/article/aa99aea173204b3ea66d135e1f78b560
Autor:
Masayo Kagami, Atsuhiro Yanagisawa, Miyuki Ota, Kentaro Matsuoka, Akie Nakamura, Keiko Matsubara, Kazuhiko Nakabayashi, Shuji Takada, Maki Fukami, Tsutomu Ogata
Publikováno v:
Clinical Epigenetics, Vol 11, Iss 1, Pp 1-9 (2019)
Abstract Background The human chromosome 14q32.2 imprinted region harbors the primary MEG3/DLK1:IG-differentially methylated region (DMR) and secondary MEG3:TSS-DMR. The MEG3:TSS-DMR can remain unmethylated only in the presence of unmethylated MEG3/D
Externí odkaz:
https://doaj.org/article/105592cf2af643b79b2d926b7f824601
Autor:
Akiyoshi Osaka, Hisamitsu Ide, Kentaro Matsuoka, Toshiyuki Iwahata, Yoshitomo Kobori, Shinichi Ban, Hiroshi Okada, Kazutaka Saito
Publikováno v:
American Journal of Men's Health, Vol 14 (2020)
The risk of a gonadal tumor is high in testicular disorder of sexual development (DSD) with the Y chromosome, but cases of DSD without the Y chromosome are extremely rare. We reported a gonadal tumor in a phenotypically male individual with 46, XX te
Externí odkaz:
https://doaj.org/article/b765d265cc924e21bc39aee33e8d099c
Autor:
Ken Saida, Osamu Miyazaki, Kentaro Matsuoka, Toshihiko Watanabe, Akihiro Fujino, Shunsuke Nosaka
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 3, Iss 8, Pp 344-347 (2015)
We report the first case of a pancreatic desmoid tumor detected during follow-up for hemihypertrophy in a 4-year-old boy. Hemihypertrophy is a rare disorder in which one side of the body grows more than the other, causing asymmetry, and well-known co
Externí odkaz:
https://doaj.org/article/354b2c18dd9843dda68ae71698a7646c