Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Masae Takeda"'
Autor:
Yu Ait Bamai, Atsuko Araki, Toshifumi Nomura, Toshio Kawai, Tazuru Tsuboi, Sumitaka Kobayashi, Chihiro Miyashita, Masae Takeda, Hiroshi Shimizu, Reiko Kishi
Publikováno v:
Environment International, Vol 121, Iss , Pp 102-110 (2018)
Background and aim: Exposure to phthalates and phosphorus flame retardants (PFRs) is considered to be a risk factor for asthma and allergies. However, little is known about the contribution of loss-of-function mutations in the gene encoding filaggrin
Externí odkaz:
https://doaj.org/article/115e50ab12cd422cbb60880981c2a1ff
Autor:
Sho Katayama, Toshifumi Nomura, Masae Takeda, Toshinari Miyauchi, Shotaro Suzuki, Jin Teng Peh, Takuma Nohara, Shinya Kitamura, Hiroo Hata, Hiroshi Shimizu
Publikováno v:
Acta Dermato-Venereologica, Vol 99, Iss 13, Pp 1311-1312 (2019)
Externí odkaz:
https://doaj.org/article/20dbb542a16d4064a5978035a2467f8b
Publikováno v:
Plant Production Science, Vol 17, Iss 2, Pp 194-201 (2014)
Greater species diversity in natural ecosystems increases plant biomass production and stability. Intercropping is an agricultural practice that aims to accrue the benefits of species diversity by growing two or more species simultaneously in the sam
Externí odkaz:
https://doaj.org/article/9758d4d276604193bc0ed7b4b279f7df
Autor:
Hiroshi Shimizu, Taiko Sakamoto, Masayuki Aiba, Jin Teng Peh, Yasuyuki Fujita, Ken Natsuga, Shotaro Suzuki, Takuya Takeichi, Toshifumi Nomura, Masashi Akiyama, Toshinari Miyauchi, Masae Takeda
Publikováno v:
Am J Hum Genet
Summary Revertant mosaicism, or “natural gene therapy,” refers to the spontaneous in vivo reversion of an inherited mutation in a somatic cell. Only approximately 50 human genetic disorders exhibit revertant mosaicism, implicating a distinctive r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6101f83f2cc3778ecb92ed6d9be4870c
https://doi.org/10.1016/j.ajhg.2021.04.021
https://doi.org/10.1016/j.ajhg.2021.04.021
Autor:
Jin Teng Peh, Taiko Sakamoto, Toshifumi Nomura, Hiroshi Shimizu, Yasuyuki Fujita, Masae Takeda, Toshinari Miyauchi, Shotaro Suzuki, Masashi Akiyama, Takuya Takeichi, Ken Natsuga, Masayuki Aiba
SummaryRevertant mosaicism, or ‘natural gene therapy’, refers to the spontaneous in vivo reversion of an inherited mutation in a somatic cell1. Only ∼50 human genetic disorders exhibit revertant mosaicism, implicating a distinctive role played
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c5b7ec0c6c1d9bea72696c38c10cc34c
https://doi.org/10.1101/2020.08.19.255430
https://doi.org/10.1101/2020.08.19.255430
Autor:
Toshinari Miyauchi, Toshifumi Nomura, Shotaro Suzuki, Masae Takeda, Hiroshi Shimizu, Reine Moriuchi, Akihiro Orita, Emi Inamura, Jin Teng Peh
Publikováno v:
The Journal of dermatology. 48(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa1a18c0503d7b5a35e9ea94f0918d76
https://pubmed.ncbi.nlm.nih.gov/33340370
https://pubmed.ncbi.nlm.nih.gov/33340370
Autor:
Toshio Kawai, Sumitaka Kobayashi, Atsuko Araki, Yu Ait Bamai, Toshifumi Nomura, Tazuru Tsuboi, Chihiro Miyashita, Reiko Kishi, Masae Takeda, Hiroshi Shimizu
Publikováno v:
Environment International, Vol 121, Iss, Pp 102-110 (2018)
Background and aim: Exposure to phthalates and phosphorus flame retardants (PFRs) is considered to be a risk factor for asthma and allergies. However, little is known about the contribution of loss-of-function mutations in the gene encoding filaggrin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1e77ce0564e4d16d15ab1537b689c76
https://doi.org/10.1016/j.envint.2018.08.046
https://doi.org/10.1016/j.envint.2018.08.046
Autor:
Toshinari Miyauchi, Toshifumi Nomura, Masae Takeda, Hiroshi Shimizu, Takato Sugiyama, Yasuyuki Fujita, Shotaro Suzuki
Publikováno v:
The Journal of Dermatology. 45:1463-1467
TGM1 is the most common gene responsible for lamellar ichthyosis. Previous studies have suggested that patients with lamellar ichthyosis carrying two missense mutations in TGM1 show significantly less severe phenotypes than those with at least one tr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6efd3a2e7d0509156ecd02e0f54f4f9
https://doi.org/10.1111/1346-8138.14675
https://doi.org/10.1111/1346-8138.14675
Autor:
W.H. Irwin McLean, Toshifumi Nomura, Masae Takeda, Kota Ono, Satoru Shinkuma, Hiroshi Shimizu, Shotaro Suzuki, Osamu Nemoto, Osamu Mizuno, Yuka Ohguchi, Toshinari Miyauchi, Yasuyuki Fujita
Publikováno v:
Journal of Investigative Dermatology. 138:836-843
Nagashima-type palmoplantar keratosis (NPPK) is an autosomal recessive skin disorder with a high, unmet medical need that is caused by mutations in SERPINB7. Almost all NPPK patients carry the founder nonsense mutation c.796C>T (p.Arg266Ter) in the l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff532a14513df3cf17afa75d894b458d
https://doi.org/10.1016/j.jid.2017.10.014
https://doi.org/10.1016/j.jid.2017.10.014
Autor:
Takaaki Matsumoto, Hiroshi Shimizu, Masashi Akiyama, Takuya Takeichi, H Niwa, Toshifumi Nomura, Michihiro Kono, Tomoo Ogi, Masae Takeda
Publikováno v:
British Journal of Dermatology. 182:491-493
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9fd3759c6dd21c1abcde633247f57288
https://doi.org/10.1111/bjd.18445
https://doi.org/10.1111/bjd.18445