Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Katsuyoshi Fujiwara"'
Publikováno v:
PLoS ONE, Vol 16, Iss 3, p e0248050 (2021)
The vitrification of immature germinal vesicle (GV) oocytes is an important way to preserve genetic resources and female fertility. However, it is well known that cryopreserved GV oocytes have very poor developmental ability and that further improvem
Externí odkaz:
https://doaj.org/article/2b41bd4f50b54c73833ab5147e3de3e0
Autor:
Maki Kamoshita, Tsubasa Kato, Katsuyoshi Fujiwara, Takafumi Namiki, Kazuaki Matsumura, Suong-Hyu Hyon, Junya Ito, Naomi Kashiwazaki
Publikováno v:
PLoS ONE, Vol 12, Iss 4, p e0176711 (2017)
Vitrification is a powerful tool for the efficient production of offspring derived from cryopreserved oocytes or embryos in mammalian species including domestic animals. Genome editing technologies such as transcription activator-like effector nuclea
Externí odkaz:
https://doaj.org/article/18480318dc93404f9294cd78d7543659
Publikováno v:
PLoS ONE, Vol 8, Iss 3, p e58063 (2013)
In mammals, unfertilized oocytes are one of the most available stages for cryopreservation because the cryopreserved oocytes can be used for assisted reproductive technologies, including in vitro fertilization (IVF) and intracytoplasmic sperm injecti
Externí odkaz:
https://doaj.org/article/f8ebbb8338274f20bce95dae6cab6597
Autor:
Hitomi Watanabe, Natsuki Kohaya, Maki Kamoshita, Katsuyoshi Fujiwara, Kazuaki Matsumura, Suong-Hyu Hyon, Junya Ito, Naomi Kashiwazaki
Publikováno v:
PLoS ONE, Vol 8, Iss 12, p e83613 (2013)
In cryopreservation of mammalian germ cells, unfertilized oocytes are one of the most available stages because these cryopreserved oocytes can be used for assisted reproductive technologies, including in vitro fertilization (IVF) and intracytoplasmic
Externí odkaz:
https://doaj.org/article/6a62e37625154812a0a3115176a31700
Autor:
Yuki Kawasaki, Yurie Shibao, Maki Kamoshita, Atsuko Kageyama, Katsuyoshi Fujiwara, Naomi Kashiwazaki, Natsuki Kohaya, Ayumi Suyama, Junya Ito, Suong-Hyu Hyon, Kazuaki Matsumura
Publikováno v:
Cryobiology. 97:245-249
It has been known that different protocols are used for embryo preservation at different stages due to different sensitivity to the physical and physiological stress caused by vitrification. In this study, we developed a common vitrification protocol
Publikováno v:
PLoS ONE
PLoS ONE, Vol 16, Iss 3, p e0248050 (2021)
PLoS ONE, Vol 16, Iss 3, p e0248050 (2021)
The vitrification of immature germinal vesicle (GV) oocytes is an important way to preserve genetic resources and female fertility. However, it is well known that cryopreserved GV oocytes have very poor developmental ability and that further improvem
Publikováno v:
Animal Science Journal. 88:180-184
The objective of this study was to evaluate fertility and full-term development of rat vitrified oocytes after in vitro fertilization (IVF) with cryopreserved sperm. Oocytes with or without surrounding cumulus cells were vitrified with 30% ethylene g
Autor:
Tsubasa Kato, Kazuaki Matsumura, Junya Ito, Maki Kamoshita, Suong-Hyu Hyon, Katsuyoshi Fujiwara, Naomi Kashiwazaki, Takafumi Namiki
Publikováno v:
PLoS ONE
PLoS ONE, Vol 12, Iss 4, p e0176711 (2017)
PLoS ONE, Vol 12, Iss 4, p e0176711 (2017)
Vitrification is a powerful tool for the efficient production of offspring derived from cryopreserved oocytes or embryos in mammalian species including domestic animals. Genome editing technologies such as transcription activator-like effector nuclea
Autor:
Tsubasa Kato, Jan B. Parys, Richard J.H. Wojcikiewicz, Masahiko Hirose, Maki Kamoshita, Anucha Sathanawongs, Junya Ito, Katsuyoshi Fujiwara, Naomi Kashiwazaki
Publikováno v:
Animal Science Journal. 86:138-147
At fertilization, inositol 1,4,5-trisphosphate receptor type 1 (IP3 R1) has a crucial role in Ca(2+) release in mammals. Expression levels, localization and phosphorylation of IP3 R1 are important for its function, but it still remains unclear which
Autor:
Yuki Kawasaki, Suong-Hyu Hyon, Yurie Shibao, Kazuaki Matsumura, Katsuyoshi Fujiwara, Naomi Kashiwazaki, Junya Ito
Publikováno v:
Cryobiology. 68:200-204
Transgenic animals are generally produced by microinjection of exogeneous DNA into embryos at the pronuclear (PN) stage. PN embryos also can be used for knockout animals because artificial nucleases such as zinc-finger nuclease or transcription activ