CYSTIC-FIBROSIS - A WELCOME ANIMAL-MODEL

被引：14

作者：

COLLINS, FS ^{[1
]}

WILSON, JM ^{[1
]}

机构：

[1] UNIV NANCY 1,CTR CYST FIBROSIS RDP,F-54506 VANDOEUVRE NANCY,FRANCE

来源：

NATURE | 1992年 / 358卷 / 6389期

关键词：

D O I：

10.1038/358708a0

中图分类号：

O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];

学科分类号：

07 ; 0710 ; 09 ;

摘要：

引用

页码：708 / 709

页数：2

共 14 条

[1]

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[5]

GELEHRTER TD, 1990, PRINCIPLES MED GENET, P125

[6] INTRODUCTION OF A SUBTLE MUTATION INTO THE HOX-2.6 LOCUS IN EMBRYONIC STEM-CELLS [J].

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BRADLEY, A .

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[7] HPRT-DEFICIENT (LESCH-NYHAN) MOUSE EMBRYOS DERIVED FROM GERMLINE COLONIZATION BY CULTURED-CELLS [J].

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[8] IDENTIFICATION OF THE CYSTIC-FIBROSIS GENE - GENETIC-ANALYSIS [J].

KEREM, BS ;

ROMMENS, JM ;

BUCHANAN, JA ;

MARKIEWICZ, D ;

COX, TK ;

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TSUI, LC .

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[9] A POTENTIAL ANIMAL-MODEL FOR LESCH-NYHAN SYNDROME THROUGH INTRODUCTION OF HPRT MUTATIONS INTO MICE [J].

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BRADLEY, A ;

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EVANS, MJ .

NATURE, 1987, 326 (6110) :295-298

[10] SUGGESTION OF AN ABNORMAL ANION-EXCHANGE MECHANISM IN SWEAT GLANDS OF CYSTIC-FIBROSIS PATIENTS [J].

QUINTON, PM .

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