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AN00069296-20060300-0029.pdf
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Title |
Title |
神経病原性レトロウイルスA8-Vのenv遺伝子発現に見られた奇妙なスプライシング
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Kana |
シンケイ ビョウゲンセイ レトロウイルス A8 - V ノ env イデンシ ハツゲン ニ ミラレタ キミョウナ スプライシング
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Romanization |
shinkei byogensei retoroirusu A8 - V no env idenshi hatsugen ni mirareta kimyona supuraishingu
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Title |
Eccentric splicing found in env gene expression of neuropathogenic A8-V
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Creator |
Name |
渡辺, 里仁
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Kana |
ワタナベ, リヒト
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Romanization |
Watanabe, Rihito
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Affiliation |
創価大学工学部生命情報工学科
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Affiliation (Translated) |
Department of Bioinformatics Faculty of Engineering, Soka University, Tangi-cho 1-236, Hachioji, Tokyo
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Name |
高瀬(余田), 明
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Kana |
タカセ (ヨデン), サヤカ
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Romanization |
Takase (Yoden), Sayaka
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Affiliation |
創価大学工学部生命情報工学科
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Affiliation (Translated) |
Department of Bioinformatics Faculty of Engineering, Soka University, Tangi-cho 1-236, Hachioji, Tokyo
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山川, 圭
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Kana |
ヤマカワ, ケイ
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Romanization |
Yamakawa, Kei
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Affiliation |
創価大学工学部生命情報工学科
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Affiliation (Translated) |
Department of Bioinformatics Faculty of Engineering, Soka University, Tangi-cho 1-236, Hachioji, Tokyo
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池田, 富夫
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Kana |
イケダ, トミオ
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Romanization |
Ikeda, Tomio
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Affiliation |
デンカ生研株式会社
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Affiliation (Translated) |
Denka Seiken Co., LTD.1-2-2 Minami Honcho, Gosen-shi, Niigata
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慶應医学会
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Kana |
ケイオウ イガッカイ
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Romanization |
Keio igakkai
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Issued (from:yyyy) |
2006
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Physical description |
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Source Title |
Name |
慶應医学
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Name (Translated) |
Journal of the Keio Medical Society
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Volume |
83
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Issue |
1
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Year |
2006
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Month |
3
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Start page |
29
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End page |
35
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Abstract |
Packaging cell lines PacNIH/A8β and PacNIH/A8δ, which were introduced by the DNA of expression vectors pA8(Ψ-)βand pA8(Ψ-)δ re spective1y, to produce pseud-retroviral particles in the retroviral vector system, were established. Both the expression vectors were constructed using the genes of A8-V, which is an isolate from Friend murine leukemia virus(F-MLV) and shows higher proliferation rates in the central nervous system(CNS) of rats and mice compared with original F-MLV. These two expression vectors utilize a different polyadenylation signal (polyA signal) for the expression of retroviral genes. The former employs a 0.85kb fragment in the SV40 early region as a polyA signal, and the latter, a 0.13kb of the same
region. PacNIH/A8β showed an unstable expression of the env gene in the A8-V genome, whereas all of the retroviral gene expressions in the PacNIH/A8δ were perfect. An occurrence of abnormal splicing in the mRNA for the env gene in the PacNIH/A8β cells was suggested.
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