Zobrazeno 1 - 10
of 74
pro vyhledávání: '"Yui Yamashita"'
Publikováno v:
BMC Ophthalmology, Vol 23, Iss 1, Pp 1-6 (2023)
Abstract Background Posterior scleritis is an inflammatory reaction of the sclera that occurs posterior to the ora serrata. The aim of this study was to present a case of posterior scleritis and to analyze choroidal circulatory and structural changes
Externí odkaz:
https://doaj.org/article/b1b9aed6638840b591959ba0ca43de06
Publikováno v:
Case Reports in Ophthalmology, Vol 12, Iss 3, Pp 899-908 (2021)
Anterior ischemic optic neuropathy (AION) is infrequently complicated with Vogt-Koyanagi-Harada (VKH) disease. We quantitatively examined sequential changes in the morphology and circulation hemodynamics, using a C-scan of optical coherence tomograph
Externí odkaz:
https://doaj.org/article/e122ca0e8d4b4798885f379c1ba4f9da
Autor:
Hiro Takahashi, Noriya Hayashi, Yuta Hiragori, Shun Sasaki, Taichiro Motomura, Yui Yamashita, Satoshi Naito, Anna Takahashi, Kazuyuki Fuse, Kenji Satou, Toshinori Endo, Shoko Kojima, Hitoshi Onouchi
Publikováno v:
BMC Genomics, Vol 21, Iss 1, Pp 1-16 (2020)
Abstract Background Upstream open reading frames (uORFs) in the 5′-untranslated regions (5′-UTRs) of certain eukaryotic mRNAs encode evolutionarily conserved functional peptides, such as cis-acting regulatory peptides that control translation of
Externí odkaz:
https://doaj.org/article/8a3eebde819a4dc4b20f621403cf4bc3
Autor:
Takashi Kurashige, Masahito Kuramochi, Ryosuke Ohsawa, Yui Yamashita, Go Shioi, Hiroyuki Morino, Masaki Kamada, Takashi Ayaki, Hidefumi Ito, Yusuke Sotomaru, Hirofumi Maruyama, Hideshi Kawakami
Publikováno v:
Neurobiology of Disease, Vol 148, Iss , Pp 105215- (2021)
We previously showed that optineurin (OPTN) mutations lead to the development of amyotrophic lateral sclerosis. The association between OPTN mutations and the pathogenesis of amyotrophic lateral sclerosis remains unclear. To investigate the mechanism
Externí odkaz:
https://doaj.org/article/190dffdfc2224b6d86b31a6626a887da
Autor:
Yoshitane Tsukamoto, Hideyuki Iriko, Shohei Matsuo, Yoshihiro Shimono, Junichi Miyazaki, Hironori Tanaka, Toshiya Komatsu, Seiji Azuma, Hiroko Oota, Yui Yamashita, Mizuka Ohkouchi, Yuka Hashikura, Seiichi Hirota
Publikováno v:
Human Pathology: Case Reports, Vol 16, Iss , Pp - (2019)
We report a 20-year-old male with a past history of diarrhea and discharge of a strobila of a broad tapeworm from his anus 3 months ago. He again noticed passing a tapeworm strobila and he visited our hospital with the tapeworm sample. The macroscopi
Externí odkaz:
https://doaj.org/article/4b8f1922c8ec48dd8a3b6ecb47c26949
Autor:
Toshihito Fujii, Keisho Hirota, Akihiro Yasoda, Akiko Takizawa, Naomi Morozumi, Ryuichi Nakamura, Takafumi Yotsumoto, Eri Kondo, Yui Yamashita, Yoriko Sakane, Yugo Kanai, Yohei Ueda, Ichiro Yamauchi, Shigeki Yamanaka, Kazumasa Nakao, Koichiro Kuwahara, Toshimasa Jindo, Mayumi Furuya, Tomoji Mashimo, Nobuya Inagaki, Tadao Serikawa, Kazuwa Nakao
Publikováno v:
PLoS ONE, Vol 13, Iss 3, p e0194812 (2018)
We have previously investigated the physiological role of C-type natriuretic peptide (CNP) on endochondral bone growth, mainly with mutant mouse models deficient in CNP, and reported that CNP is indispensable for physiological endochondral bone growt
Externí odkaz:
https://doaj.org/article/f529792eec9d4297a02abdca277c4211
Autor:
Keita Tsujimura, Koichiro Irie, Hideyuki Nakashima, Yoshihiro Egashira, Yoichiro Fukao, Masayuki Fujiwara, Masayuki Itoh, Masahiro Uesaka, Takuya Imamura, Yasukazu Nakahata, Yui Yamashita, Takaya Abe, Shigeo Takamori, Kinichi Nakashima
Publikováno v:
Cell Reports, Vol 12, Iss 11, Pp 1887-1901 (2015)
Rett syndrome (RTT) is a neurodevelopmental disorder caused by MECP2 mutations. Although emerging evidence suggests that MeCP2 deficiency is associated with dysregulation of mechanistic target of rapamycin (mTOR), which functions as a hub for various
Externí odkaz:
https://doaj.org/article/686c56aae0c14514844775a62c0f01ca
Autor:
Masahito Irie, Masanobu Yoshikawa, Ryuichi Ono, Hirotaka Iwafune, Tamio Furuse, Ikuko Yamada, Shigeharu Wakana, Yui Yamashita, Takaya Abe, Fumitoshi Ishino, Tomoko Kaneko-Ishino
Publikováno v:
PLoS Genetics, Vol 11, Iss 9, p e1005521 (2015)
Gene targeting of mouse Sushi-ichi-related retrotransposon homologue 11/Zinc finger CCHC domain-containing 16 (Sirh11/Zcchc16) causes abnormal behaviors related to cognition, including attention, impulsivity and working memory. Sirh11/Zcchc16 encodes
Externí odkaz:
https://doaj.org/article/808d7aa96ac942c0b8f25f169af38986
Autor:
Shun Sasaki, Toru Murakami, Miharu Yasumuro, Ayaka Makita, Yutaro Oi, Yuta Hiragori, Shun Watanabe, Rin Kudo, Noriya Hayashi, Iwai Ohbayashi, Munetaka Sugiyama, Yui Yamashita, Satoshi Naito, Hitoshi Onouchi
Publikováno v:
Plant biotechnology. 40(1):21-30
Perturbations in ribosome biogenesis cause a type of cellular stress called nucleolar or ribosomal stress, which triggers adaptive responses in both animal and plant cells. The Arabidopsis ANAC082 transcription factor has been identified as a key med
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f127435b05ad2786f4c5d5782beedf2e
http://hdl.handle.net/2115/89239
http://hdl.handle.net/2115/89239
Autor:
Susumu Ishida, Yui Yamashita, Michiyuki Saito, Hideki Koizumi, Nobuhiro Terao, Kousuke Noda, Kiriko Hirooka, Yuki Hashimoto
Publikováno v:
Japanese Journal of Ophthalmology. 66:14-18
PURPOSE Asymmetric dilated vortex vein (ADVV) observed in eyes with pachychoroid spectrum diseases is thought to be due to congestion of choroidal blood flow. The purpose of this study was to quantitatively investigate the blood flow velocity of ADVV
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d77e79b8db6e5a4761847df49fdbb160
https://doi.org/10.1007/s10384-021-00889-7
https://doi.org/10.1007/s10384-021-00889-7