Creating animal models of genetic disease.
作者信息
Erickson R P
机构信息
Department of Human Genetics, University of Michigan School of Medicine, Ann Arbor 48109-0618.
出版信息
Am J Hum Genet. 1988 Nov;43(5):582-6.
Abstract
摘要
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本文引用的文献
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Establishment in culture of pluripotential cells from mouse embryos.从小鼠胚胎中建立多能细胞的培养方法。
Nature. 1981 Jul 9;292(5819):154-6. doi: 10.1038/292154a0.
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Electrophoretically detected germinal mutations induced in the mouse by ethylnitrosourea.电泳检测到的乙基亚硝基脲在小鼠中诱导产生的生殖细胞突变。
Proc Natl Acad Sci U S A. 1981 May;78(5):3138-41. doi: 10.1073/pnas.78.5.3138.
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Carbonic anhydrase II deficiency identified as the primary defect in the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral calcification.碳酸酐酶II缺乏被确定为伴有肾小管酸中毒和脑钙化的常染色体隐性骨硬化综合征的主要缺陷。
Proc Natl Acad Sci U S A. 1983 May;80(9):2752-6. doi: 10.1073/pnas.80.9.2752.
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Mouse trisomy 16 as an animal model of human trisomy 21 (Down syndrome): production of viable trisomy 16 diploid mouse chimeras.小鼠16三体作为人类21三体（唐氏综合征）的动物模型：可存活的16三体二倍体小鼠嵌合体的产生。
Dev Biol. 1984 Feb;101(2):416-24. doi: 10.1016/0012-1606(84)90156-8.
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Linkage of genes for adult alpha-globin and embryonic alpha-like globin chains.成人α-珠蛋白基因与胚胎α-样珠蛋白链基因的连锁
Proc Natl Acad Sci U S A. 1980 Feb;77(2):1087-90. doi: 10.1073/pnas.77.2.1087.
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Trisomy in the fetal backcross progeny of male and female metacentric heterozygotes of the mouse. i.小鼠雄性和雌性中着丝粒杂合子的胎儿回交后代中的三体性。一。
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Targetted correction of a mutant HPRT gene in mouse embryonic stem cells.对小鼠胚胎干细胞中突变的次黄嘌呤磷酸核糖转移酶（HPRT）基因进行靶向校正。
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