Conditional inactivation of the peroxisome biogenesis Pex13 gene by Cre-loxP excision

被引：12

作者：

Bjorkman, J

Tonks, I

Maxwell, MA

Paterson, C

Kay, GF

Crane, DI ^{[1
]}

机构：

[1] Griffith Univ, Sch Biomol & Biomed Sci, Nathan, Qld 4111, Australia

[2] Griffith Univ, Sch Biomol & Biomed Sci, Brisbane, Qld 4111, Australia

[3] Univ Queensland, St Lucia, Qld 4067, Australia

[4] Queensland Inst Med Res, Joint Expt Oncol Program, Brisbane, Qld 4006, Australia

来源：

GENESIS | 2002年 / 32卷 / 02期

关键词：

D O I：

10.1002/gene.10044

中图分类号：

Q [生物科学];

学科分类号：

07 ; 0710 ; 09 ;

摘要：

[No abstract available]

引用

页码：179 / 180

页数：2

共 5 条

[1]

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[2] PEX13 is mutated in complementation group 13 of the peroxisome-biogenesis disorders [J].

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[3] High-efficiency deleter mice show that FLPe is an alternative to Cre-loxP [J].

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[5] Nonsense and temperature-sensitive mutations in PEX13 are the cause of complementation group H of peroxisome biogenesis disorders [J].

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Suzuki, Y ;

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Imamura, A ;

Toyama, R ;

Mukai, S ;

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Orii, T ;

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HUMAN MOLECULAR GENETICS, 1999, 8 (06) :1077-1083

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