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] Boat TF., 1989, CYSTIC FIBROSIS META, V6th, P2649
[2] DEFECTIVE EPITHELIAL CHLORIDE TRANSPORT IN A GENE-TARGETED MOUSE MODEL OF CYSTIC-FIBROSIS
CLARKE, LL
GRUBB, BR
GABRIEL, SE
SMITHIES, O
KOLLER, BH
BOUCHER, RC
[J]. SCIENCE, 1992, 257 (5073) : 1125 - 1128
[3] CYSTIC-FIBROSIS - MOLECULAR-BIOLOGY AND THERAPEUTIC IMPLICATIONS
COLLINS, FS
[J]. SCIENCE, 1992, 256 (5058) : 774 - 779
[4] MICE DEFICIENT FOR P53 ARE DEVELOPMENTALLY NORMAL BUT SUSCEPTIBLE TO SPONTANEOUS TUMORS
DONEHOWER, LA
HARVEY, M
SLAGLE, BL
MCARTHUR, MJ
MONTGOMERY, CA
BUTEL, JS
BRADLEY, A
[J]. NATURE, 1992, 356 (6366) : 215 - 221
[5] GELEHRTER TD, 1990, PRINCIPLES MED GENET, P125
[6] INTRODUCTION OF A SUBTLE MUTATION INTO THE HOX-2.6 LOCUS IN EMBRYONIC STEM-CELLS
HASTY, P
RAMIREZSOLIS, R
KRUMLAUF, R
BRADLEY, A
[J]. NATURE, 1991, 350 (6315) : 243 - 246
[7] HPRT-DEFICIENT (LESCH-NYHAN) MOUSE EMBRYOS DERIVED FROM GERMLINE COLONIZATION BY CULTURED-CELLS
HOOPER, M
HARDY, K
HANDYSIDE, A
HUNTER, S
MONK, M
[J]. NATURE, 1987, 326 (6110) : 292 - 295
[8] IDENTIFICATION OF THE CYSTIC-FIBROSIS GENE - GENETIC-ANALYSIS
KEREM, BS
ROMMENS, JM
BUCHANAN, JA
MARKIEWICZ, D
COX, TK
CHAKRAVARTI, A
BUCHWALD, M
TSUI, LC
[J]. SCIENCE, 1989, 245 (4922) : 1073 - 1080
[9] A POTENTIAL ANIMAL-MODEL FOR LESCH-NYHAN SYNDROME THROUGH INTRODUCTION OF HPRT MUTATIONS INTO MICE
KUEHN, MR
BRADLEY, A
ROBERTSON, EJ
EVANS, MJ
[J]. NATURE, 1987, 326 (6110) : 295 - 298
[10] SUGGESTION OF AN ABNORMAL ANION-EXCHANGE MECHANISM IN SWEAT GLANDS OF CYSTIC-FIBROSIS PATIENTS
QUINTON, PM
[J]. PEDIATRIC RESEARCH, 1982, 16 (07) : 533 - 537

← 1 2 →