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  1. 原著論文

Microdissection and microcloning of genomic DNA markers from human chromosomal region 11q23.

https://repo.qst.go.jp/records/43937
https://repo.qst.go.jp/records/43937
e6bef843-4eda-4a96-acac-5072d2033ab6
Item type 学術雑誌論文 / Journal Article(1)
公開日 2005-12-16
タイトル
タイトル Microdissection and microcloning of genomic DNA markers from human chromosomal region 11q23.
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
アクセス権
アクセス権 metadata only access
アクセス権URI http://purl.org/coar/access_right/c_14cb
著者 Seki, Naohiko

× Seki, Naohiko

WEKO 436803

Seki, Naohiko

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Yamauchi, Masatake

× Yamauchi, Masatake

WEKO 436804

Yamauchi, Masatake

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Saito, Toshiyuki

× Saito, Toshiyuki

WEKO 436805

Saito, Toshiyuki

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Katakura, Reiko

× Katakura, Reiko

WEKO 436806

Katakura, Reiko

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Ohta, Tohru

× Ohta, Tohru

WEKO 436807

Ohta, Tohru

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Yoshiura, Koh-ichiro

× Yoshiura, Koh-ichiro

WEKO 436808

Yoshiura, Koh-ichiro

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Jinno, Yoshihiro

× Jinno, Yoshihiro

WEKO 436809

Jinno, Yoshihiro

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Niikawa, Norio

× Niikawa, Norio

WEKO 436810

Niikawa, Norio

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Hori, Tadaaki

× Hori, Tadaaki

WEKO 436811

Hori, Tadaaki

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関 直彦

× 関 直彦

WEKO 436812

en 関 直彦

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山内 正剛

× 山内 正剛

WEKO 436813

en 山内 正剛

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齋藤 俊行

× 齋藤 俊行

WEKO 436814

en 齋藤 俊行

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堀 雅明

× 堀 雅明

WEKO 436815

en 堀 雅明

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抄録
内容記述タイプ Abstract
内容記述 A human genomic DNA library was constructed by using a microdissection-microcloning procedure with polymerase chain reaction (PCR) techniques on DNA from the chromosome 11q23 region. A total of 450 recombinant pUC clones were isolated from the library. Their insert sizes ranged from 150 to 850 bp with a mean of 320 bp. Fifty pUC clones were randomly selected and analyzed in detail. Southern blot analyses showed that 21 (42%) clones were unique DNA sequences, 20 (40%) clones were repetitive sequences, and 9 (18%) clones had no detectable hybridization. The unique sequences were used further in a secondary screening of a partially digested human genomic DNA library constructed in phage vector, and 4 clones were isolated. The chromosomal locations of these phage clones were confirmed to be in the q23 region of chromosome 11 by fluorescence in situ suppression hybridization. These pUC microclones isolated from the chromosomal region-specific genomic DNA library will be useful in the construction of physical contig maps with yeast artificial chromosome and/or cosmid clones and in the positional cloning of disease-associated genes localized to the q23 region of chromosome 11.
書誌情報 Genomics

巻 16, p. 169-172, 発行日 1993-04
ISSN
収録物識別子タイプ ISSN
収録物識別子 0888-7543
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