Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Moe Kitazawa"'
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 11 (2023)
PEG10 and PEG11/RTL1 are paternally expressed, imprinted genes that play essential roles in the current eutherian developmental system and are therefore associated with developmental abnormalities caused by aberrant genomic imprinting. They are also
Externí odkaz:
https://doaj.org/article/6eb84e264d734121ab944baed7d86816
Autor:
Moe Kitazawa
Publikováno v:
Genes & Genetic Systems; Dec2023, Vol. 98 Issue 6, p321-336, 16p
Publikováno v:
Genes to Cells
RTL1 (also termed paternal expressed 11 (PEG11)) is considered the major imprinted gene responsible for the placental and fetal/neonatal muscle defects that occur in the Kagami–Ogata and Temple syndromes (KOS14 and TS14, respectively). However, it
Autor:
Yumiko Oishi, Shinichiro Hayashi, Fumitoshi Ishino, Moe Kitazawa, Tomoko Kaneko-Ishino, Michihiro Imamura, Shin'ichi Takeda
Publikováno v:
Development (Cambridge, England)
article-version (VoR) Version of Record
article-version (VoR) Version of Record
Temple and Kagami-Ogata syndromes are genomic imprinting diseases caused by maternal and paternal duplication of human chromosome 14, respectively. They exhibit different postnatal muscle-related symptoms as well as prenatal placental problems. Using
Autor:
Masahiro Hatasa, Kazuki Watanabe, Tomomitsu Hirota, Satoshi Yokose, Akira Aoki, Hiroshi Kadokura, Takanori Iwata, Sayaka Katagiri, Koji Mizutani, Moe Kitazawa, Hiromi Niimi, Yujin Ohsugi, Tsuyoshi Shimohira, Ayumi Matsuzawa
Publikováno v:
FASEB journal : official publication of the Federation of American Societies for Experimental BiologyREFERENCES. 34(9)
Anti-sclerostin monoclonal antibody romosozumab, a treatment for osteoporosis, reduced vertebral fracture risk and clinical fracture. Laser irradiation triggers various effects, including bio-stimulation, which can induce beneficial therapeutic effec
Publikováno v:
Genes to Cells. 22:174-188
Paternally expressed 11/Retrotransposon-like 1 (Peg11/Rtl1) knockout (KO) mice show mid- to late fetal lethality or late fetal growth retardation associated with frequent neonatal lethality. The lethal phenotype is largely dependent on genetic backgr
Autor:
Moe Kitazawa, Shinichiro Hayashi, Michihiro Imamura, Shin'ichi Takeda, Yumiko Oishi, Tomoko Kaneko-Ishino, Fumitoshi Ishino
Publikováno v:
Development (09501991); Nov2020, Vol. 147 Issue 23, p1-10, 10p
Autor:
Yujin Ohsugi, Sayaka Katagiri, Tomomitsu Hirota, Hiromi Niimi, Masahiro Hatasa, Kazuki Watanabe, Tsuyoshi Shimohira, Koji Mizutani, Moe Kitazawa, Ayumi Matsuzawa, Hiroshi Kadokura, Satoshi Yokose, Takanori Iwata, Akira Aoki
Publikováno v:
FASEB Journal; Sep2020, Vol. 34 Issue 9, p12877-12893, 17p
Autor:
Fumitoshi Ishino, Masayuki Ishii, Jun Kanno, Ryuichi Ono, Masahito Ikawa, Tomoko Kaneko-Ishino, Takako Usami, Moe Kitazawa, Yoshitaka Fujihara
Publikováno v:
Scientific Reports
Ono, R., Ishii, M., Fujihara, Y. et al. Double strand break repair by capture of retrotransposon sequences and reverse-transcribed spliced mRNA sequences in mouse zygotes. Sci Rep 5, 12281 (2015). https://doi.org/10.1038/srep12281
The CRISPR/Cas
The CRISPR/Cas
Autor:
Mitsuteru Ito, Carol A. Edwards, Tsui-Han Loo, Sarah E. Allen, Amanda N. Sferruzzi-Perri, Tomoko Kaneko-Ishino, Anne C. Ferguson-Smith, Fumitoshi Ishino, Moe Kitazawa, Colin L. Stewart, Bjorn T. Adalsteinsson
Publikováno v:
Development (Cambridge, England). 142(14)
The paternally expressed imprinted Retrotransposon-like 1 (Rtl1/Peg11) is a retrotransposon-derived gene that has evolved a function in eutherian placentation. Seven miRNAs, including miR-127, are processed from a maternally expressed antisense Rtl1