Zobrazeno 1 - 10
of 210
pro vyhledávání: '"E. Soeda"'
Autor:
N. Taki, Yuko Kitagawa, Yohei Yamada, Minoru Tanabe, Nobuhiro Takahashi, C. Isobe, T. Turukawa, Naoki Shimojima, S. Nakamaru, A. Takahashi, Y. Nakazawa, Akihiro Fujino, C. Takaoka, Masahiro Shinoda, Yoshikane Izawa, A. Sekiguchi, E Soeda, Tatsuo Kuroda, Ken Hoshino
Publikováno v:
Transplantation Proceedings. 49:115-120
Objectives More than two decades have passed since the first living donor liver transplantation was performed in Japan in 1989. There are many reports about problems in adherence to taking medication and medical follow-ups in children who received li
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37f26ad4f90ee9cf4d5ecf13ce0cc2c4
https://doi.org/10.1016/j.transproceed.2016.10.020
https://doi.org/10.1016/j.transproceed.2016.10.020
Autor:
Valerie A. Trabosh, Ahmad Daher, W.-C. Chen, Cynthia M. Simbulan-Rosenthal, E. Soeda, D. Gerstel, Dean S. Rosenthal
Publikováno v:
Oncogene. 25:3649-3660
Inhibitor of differentiation/DNA binding (Id) proteins comprise a class of helix-loop-helix transcription factors involved in proliferation, differentiation, apoptosis, and carcinogenesis. We have shown that while Id2 is induced by UVB in primary ker
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d78c64d0f6f1464aaf527cbaad43c24
https://doi.org/10.1038/sj.onc.1209407
https://doi.org/10.1038/sj.onc.1209407
Akademický článek
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Publikováno v:
Cytogenetic and Genome Research. 98:67-70
Construction of a comprehensive comparative map between swine and human chromosomes is a prerequisite, in order to select candidate swine genes for traits from the human genome database as well as to understand the evolutionary process of the two spe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0713da7ce5f76ffd7122eac7c3f6aa79
https://doi.org/10.1159/000068537
https://doi.org/10.1159/000068537
Autor:
M, Hattori, A, Fujiyama, T D, Taylor, H, Watanabe, T, Yada, H S, Park, A, Toyoda, K, Ishii, Y, Totoki, D K, Choi, Y, Groner, E, Soeda, M, Ohki, T, Takagi, Y, Sakaki, S, Taudien, K, Blechschmidt, A, Polley, U, Menzel, J, Delabar, K, Kumpf, R, Lehmann, D, Patterson, K, Reichwald, A, Rump, M, Schillhabel, A, Schudy, W, Zimmermann, A, Rosenthal, J, Kudoh, K, Schibuya, K, Kawasaki, S, Asakawa, A, Shintani, T, Sasaki, K, Nagamine, S, Mitsuyama, S E, Antonarakis, S, Minoshima, N, Shimizu, G, Nordsiek, K, Hornischer, P, Brant, M, Scharfe, O, Schon, A, Desario, J, Reichelt, G, Kauer, H, Blocker, J, Ramser, A, Beck, S, Klages, S, Hennig, L, Riesselmann, E, Dagand, T, Haaf, S, Wehrmeyer, K, Borzym, K, Gardiner, D, Nizetic, F, Francis, H, Lehrach, R, Reinhardt, M L, Yaspo
Publikováno v:
Nature, Vol. 405, No 6784 (2000) pp. 311-319
Chromosome 21 is the smallest human autosome. An extra copy of chromosome 21 causes Down syndrome, the most frequent genetic cause of significant mental retardation, which affects up to 1 in 700 live births. Several anonymous loci for monogenic disor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e81de50407c789f78acc3b1dee21c85d
https://doi.org/10.1038/35012518
https://doi.org/10.1038/35012518
Publikováno v:
Scopus-Elsevier
Gene transfer to provide long-term expression of a therapeutic product, without introducing unwelcome genetic information, is a goal being sought for therapy of both hereditary and acquired diseases. Polyoma virus pseudocapsids, generated from a VP1-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7645f04b05304a9cacdead680ff21f77
https://doi.org/10.1038/sj.gt.3300748
https://doi.org/10.1038/sj.gt.3300748
Autor:
H. Yasue, Y. Mizoguchi, Shuichi Asakawa, K. Suzuki, S. Takahashi, S. Fujisaki, N. Shimizu, E. Soeda, Y. Sugimoto, Y. Z. Chen
Publikováno v:
Animal Genetics. 33:379-381
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a262654700b25ba002970b38987a7b69
https://doi.org/10.1046/j.1365-2052.2002.00896_3.x
https://doi.org/10.1046/j.1365-2052.2002.00896_3.x
Publikováno v:
Mammalian Genome. 7:461-463
Down syndrome (DS), the most frequent birth defect, is caused by trisomy of human Chromosome (Chr) 21 and is associated with numerous phenotypic features, including mental retardation. Recently, the major features have been correlated with rare DS pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1592678ef64cfd3be3ef6fb74e13a6e0
https://doi.org/10.1007/s003359900134
https://doi.org/10.1007/s003359900134
Autor:
S, Fujisaki, Y, Mizoguchi, S, Takahashi, Y Z, Chen, K, Suzuki, S, Asakawa, E, Soeda, N, Shimizu, Y, Sugimoto, H, Yasue
Publikováno v:
Animal genetics. 33(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0189dbbf93ef157de5c5054e2fbdb9cf
https://pubmed.ncbi.nlm.nih.gov/12354149
https://pubmed.ncbi.nlm.nih.gov/12354149
Publikováno v:
Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme. 46
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b22597ab4a94a5e16af5a31cfcaf76d5
https://pubmed.ncbi.nlm.nih.gov/11802374
https://pubmed.ncbi.nlm.nih.gov/11802374