ロード中...

N-ethyl-N-nitrosourea-induced null mutation at the mouse Car-2 locus: an animal model for human carbonic anhydrase II deficiency syndrome.

Electrophoretic screening of (C57BL/6J x DBA/2J)F1 progeny of male mice treated with N-ethyl-N-nitrosourea revealed a mouse that lacked the paternal carbonic anhydrase II (CA II). Breeding tests showed that this trait was heritable and due to a null mutation at the Car-2 locus on chromosome 3. Like...

詳細記述

保存先:
書誌詳細
主要な著者: Lewis, S E, Erickson, R P, Barnett, L B, Venta, P J, Tashian, R E
フォーマット: Artigo
言語:Inglês
出版事項: 1988
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC279901/
https://ncbi.nlm.nih.gov/pubmed/3126501
タグ: タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!