Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Miyuki SHINDO"'
Publikováno v:
Biochemistry and Biophysics Reports, Vol 38, Iss , Pp 101733- (2024)
RUNX2 is a transcription factor crucial for bone formation. Mutant mice with varying levels of Runx2 expression display dosage-dependent skeletal abnormalities, underscoring the importance of Runx2 dosage control in skeletal formation. RUNX2 activity
Externí odkaz:
https://doaj.org/article/2af98e2f93c14b058177a4a89c006356
Publikováno v:
Bio-Protocol, Vol 12, Iss 11 (2022)
Superovulation is a method used to reduce the number of mice used per experiment by increasing the egg number. Conventionally, superovulation for obtaining mouse eggs involves the use of equine chorionic gonadotropin (eCG) for stimulation and human C
Externí odkaz:
https://doaj.org/article/568b19e492664ef5898532ffdb2531d9
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:
Miki SUZUKI, Akihiro NAKAMURA, Yu MATSUMOTO, Woojin KANG, Minoru ICHINOSE, Natsuko KAWANO, Mitsutoshi YAMADA, Miyuki SHINDO, Daiki KATANO, Takako SAITO, Yuichirou HARADA, Mami MIYADO, Kenji MIYADO
Publikováno v:
Journal of Veterinary Medical Science; 2023, Vol. 85 Issue 9, p912-920, 9p
Autor:
Kenji Matsumoto, Kenji Miyado, Morihiro Ito, Fumihiro Sugiyama, Kazue Takeda, Miyuki Shindo, Yasuhiko Ito, Akihiro Umezawa, Arisa Igarashi, Takashi Ohkura, Hideki Tsumura
Publikováno v:
Comparative Medicine. 71:285-294
Slc1a5 (ASCT2) encodes a small neutral amino-acid exchanger and is the most well-studied glutamine transporter in cancer cells. To investigate the role of Slc1a5 in osteoclastogenesis, we developed Slc1a5-deficient mice by using a conventional gene-t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::67f2cec24e0f8ac2a8dfc7d85b7eb8d4
https://doi.org/10.30802/aalas-cm-21-000012
https://doi.org/10.30802/aalas-cm-21-000012
Autor:
Yasuhiro Naiki, Mami Miyado, Miyuki Shindo, Reiko Horikawa, Yuichi Hasegawa, Noriyuki Katsumata, Shuji Takada, Hidenori Akutsu, Masafumi Onodera, Maki Fukami
Publikováno v:
Human gene therapy. 33(15-16)
Congenital adrenal hyperplasia (CAH) is an autosomal recessive disorder caused by steroidogenic enzymes containing monogenetic defects. Most steroidogenic enzymes are cytochrome P450 groups that can be categorized as microsomal P450s, including 21-hy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a10db98665ce48f061029212be5c6c68
https://pubmed.ncbi.nlm.nih.gov/35838129
https://pubmed.ncbi.nlm.nih.gov/35838129
Autor:
Youki Takezawa, Maki Iwai, Yukiko Fujiki, Ryo Yokomizo, Harue Kishigami, Mami Miyado, Natsuko Kawano, Mitsutoshi Yamada, Miyuki Shindo, Miki Suzuki, Ban Sato, Daiki Katano, Shintaro Kamijo, Toshio Hamatani, Mamoru Tanaka, Akihiro Umezawa, Woojin Kang, Kenji Miyado
Publikováno v:
Laboratory Investigation. 103:100026
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c3d1008e750620e3d9c46252f81f864b
https://doi.org/10.1016/j.labinv.2022.100026
https://doi.org/10.1016/j.labinv.2022.100026
Autor:
Hideki, Tsumura, Miyuki, Shindo, Morihiro, Ito, Arisa, Igarashi, Kazue, Takeda, Kenji, Matsumoto, Takashi, Ohkura, Kenji, Miyado, Fumihiro, Sugiyama, Akihiro, Umezawa, Yasuhiko, Ito
Publikováno v:
Comp Med
Slc1a5 (ASCT2) encodes a small neutral amino-acid exchanger and is the most well-studied glutamine transporter in cancer cells. To investigate the role of Slc1a5 in osteoclastogenesis, we developed Slc1a5-deficient mice by using a conventional gene-t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::460ccb7a37ae7d6f66bd9dcf5e41291b
https://pubmed.ncbi.nlm.nih.gov/34301346
https://pubmed.ncbi.nlm.nih.gov/34301346
Autor:
Yuko Katoh-Fukui, Yuko Nagakui-Noguchi, Ken Ichirou Morohashi, Hiroyuki Otake, Yasuyuki Ohkawa, Tetsuya Sato, Mikita Suyama, Miyuki Shindo, Hideki Tsumura, Takashi Baba, Maki Fukami
Publikováno v:
Bone. 120:219-231
A set of key developmental genes is essential for skeletal growth from multipotent progenitor cells at weaning. Polycomb group proteins, which regulate such genes contributes to the cell lineage commitment and subsequent differentiation via epigeneti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6bdfbe3cdb2f5f039ee0ded114f93521
https://doi.org/10.1016/j.bone.2018.10.021
https://doi.org/10.1016/j.bone.2018.10.021
Autor:
Natsuko Kawano, Cai Tingwei, Kenji Miyado, Shuji Takada, Hiroshi Okada, Manabu Yoshida, Taku Hibino, Masafumi Inui, Miyuki Shindo, Teruaki Iwamoto, Woojin Kang, Moe Tamano, Kaoru Yoshida
Publikováno v:
International Journal of Molecular Sciences, Vol 20, Iss 18, p 4557 (2019)
International Journal of Molecular Sciences
Volume 20
Issue 18
International Journal of Molecular Sciences
Volume 20
Issue 18
Multiple genes, whose functions or expression are overlapping, compensate for the loss of one gene. A gene cluster in the mouse genome encodes five seminal vesicle proteins (SVS2, SVS3, SVS4, SVS5, and SVS6). These proteins are produced by male roden
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee507497e0accd14343dc3edbc36345b
https://www.mdpi.com/1422-0067/20/18/4557
https://www.mdpi.com/1422-0067/20/18/4557