Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Emiko Matsuzaka"'
Autor:
Tomoyo Yoshida, Tadashi Yokoi, Taku Tanaka, Emiko Matsuzaka, Yuki Saida, Sachiko Nishina, Shuji Takada, Shigeomi Shimizu, Noriyuki Azuma
Publikováno v:
Cells, Vol 13, Iss 2, p 130 (2024)
Retinal ganglion cells (RGCs) are specialized projection neurons that constitute part of the retina, and the death of RGCs causes various eye diseases, but the mechanism of RGC death is still unclear. Here, we induced cell death in human induced plur
Externí odkaz:
https://doaj.org/article/ad7118206a69455aa8368a850ba18c70
Autor:
Satoshi Katagiri, Shin Tanaka, Tadashi Yokoi, Takaaki Hayashi, Emiko Matsuzaka, Kazuko Ueda, Tomoyo Yoshida-Uemura, Akira Arakawa, Sachiko Nishina, Kazuaki Kadonosono, Noriyuki Azuma
Publikováno v:
American Journal of Ophthalmology Case Reports, Vol 5, Iss C, Pp 76-80 (2017)
Purpose: To report the clinical and genetic findings of a male toddler who presented bilateral bullous retinoschisis with a novel RS1 mutation. Observations: This is an observational case report of a patient referred to our hospital with esotropia. A
Externí odkaz:
https://doaj.org/article/fc0e4472d2a4463abe9c6e3f5b375a2c
Autor:
Shohei Yamamoto, Makoto Otsu, Emiko Matsuzaka, Chieko Konishi, Haruna Takagi, Sachiyo Hanada, Shinji Mochizuki, Hiromitsu Nakauchi, Kohzoh Imai, Kohichiro Tsuji, Yasuhiro Ebihara
Publikováno v:
PLoS ONE, Vol 10, Iss 3, p e0120841 (2015)
Induced pluripotent stem (iPS) cells provide powerful tools for studying disease mechanisms and developing therapies for diseases. The 8p11 myeloproliferative syndrome (EMS) is an aggressive chronic myeloproliferative disorder (MPD) that is caused by
Externí odkaz:
https://doaj.org/article/82f6b38e3d2f435fb48a40604239471b
Autor:
Miyuki SHINDO, Miho TERAO, Shuji TAKADA, Minoru ICHINOSE, Emiko MATSUZAKA, Tadashi YOKOI, Noriyuki AZUMA, Seiya MIZUNO, Hideki TSUMURA
Publikováno v:
Experimental Animals; 2024, Vol. 73 Issue 2, p203-210, 8p
Autor:
Noriyuki Azuma, Tadashi Yokoi, Taku Tanaka, Emiko Matsuzaka, Yuki Saida, Sachiko Nishina, Miho Terao, Shuji Takada, Maki Fukami, Kohji Okamura, Kayoko Maehara, Tokiwa Yamasaki, Jun Hirayama, Hiroshi Nishina, Hiroshi Handa, Yuki Yamaguchi
Publikováno v:
Human Molecular Genetics.
The eye and brain are composed of elaborately organized tissues, development of which is supported by spatiotemporally precise expression of a number of transcription factors and developmental regulators. Here we report the molecular and genetic char
Autor:
Nobuhiko Nomura, Hiroshi Otagaki, Hideaki Maseda, Tadaatsu Nakahara, Emiko Matsuzaka, Hiroo Uchiyama, Toshiaki Nakajima-Kambe
Publikováno v:
Microbes and Environments. 18:203-209
The metabolic characteristics of the NO2 - transforming activities of Burkholderia cepacia NH-17, which was isolated as a heterotrophic nitrifying bacterium with O2 tolerant denitrification activity, were characterized. The conversion of NO2- to N2O
Autor:
Kazuhisa Sekimizu, Akiko Wakamoto, Emiko Matsuzaka, Akio Nomoto, Takeo Kubo, Tomoko Fujiyuki, Hideaki Takeuchi, Takayoshi Nakaoka, Seii Ohka
We previously identified a novel insect picorna-like virus, termed Kakugo virus (KV), obtained from the brains of aggressive honeybee worker bees that had counterattacked giant hornets. Here we examined the tissue distribution of KV and alterations o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::68429f42b3ea27a7da33d87793c9f2e7
https://europepmc.org/articles/PMC2772711/
https://europepmc.org/articles/PMC2772711/
Publikováno v:
Zoological science. 24(6)
We previously demonstrated that six genes involved in ecdysteroid signaling are expressed preferentially in Kenyon-cell subtypes in the mushroom bodies of the honeybee (Apis mellifera L.). To further examine the possible involvement of ecdysteroid si
Autor:
Kohichiro Tsuji, Yoko Mizoguchi, Emiko Matsuzaka, Shinji Mochizuki, Kenzaburo Tani, Hiromitsu Nakauchi, Masao Kobayashi, Ryoko Ohnishi, Koji Eto, Takafumi Hiramoto, Yasuhiro Ebihara, Sachiyo Hanada, Kazuhiro Nakamura, Shohei Yamamoto
Publikováno v:
Blood. 118:730-730
Abstract 730 Severe congenital neutropenia (SCN) is a rare disorder characterized by severe neutropenia present at birth, an arrest of neutrophilic differentiation at the promyelocyte or myelocyte stage, and a propensity to develop acute myeloid leuk