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Pre-implantation diagnosis of HPRT-deficient male and carrier female mouse embryos by trophectoderm biopsy.

作者信息

Monk M, Muggleton-Harris A L, Rawlings E, Whittingham D G

机构信息

MRC Experimental Embryology and Teratology Unit, Medical Research Council Laboratories, Carshalton, Surrey, UK.

出版信息

Hum Reprod. 1988 Apr;3(3):377-81. doi: 10.1093/oxfordjournals.humrep.a136711.

DOI:10.1093/oxfordjournals.humrep.a136711
PMID:3372699
Abstract

In an animal model for Lesch-Nyhan syndrome, the affected male embryos, as well as the carrier female embryos, have been successfully identified by biochemical microassay of a sample of trophectoderm cells taken from the mouse embryos at the blastocyst stage. The embryos were removed from the uterus, diagnosed and returned to the uterus within 2 days without the need for cryopreservation. The diagnosis was confirmed at 14 days gestation by analysis of the hypoxanthine phosphoribosyl transferase (HPRT) status of the fetuses. Live young were obtained from biopsied embryos after transfer.

摘要

相似文献

1
Pre-implantation diagnosis of HPRT-deficient male and carrier female mouse embryos by trophectoderm biopsy.
Hum Reprod. 1988 Apr;3(3):377-81. doi: 10.1093/oxfordjournals.humrep.a136711.
2
Preimplantation diagnosis of deficiency of hypoxanthine phosphoribosyl transferase in a mouse model for Lesch-Nyhan syndrome.
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Preimplantation sexing and diagnosis of hypoxanthine phosphoribosyl transferase deficiency in mice by biochemical microassay.通过生化微量测定法对小鼠进行植入前性别鉴定和次黄嘌呤磷酸核糖基转移酶缺乏症的诊断。
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HPRT-deficient (Lesch-Nyhan) mouse embryos derived from germline colonization by cultured cells.通过培养细胞进行种系定殖产生的次黄嘌呤磷酸核糖基转移酶缺陷型(莱施-奈恩)小鼠胚胎。
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Production of a model for Lesch-Nyhan syndrome in hypoxanthine phosphoribosyltransferase-deficient mice.次黄嘌呤磷酸核糖基转移酶缺陷小鼠中莱施-奈恩综合征模型的构建。
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A potential animal model for Lesch-Nyhan syndrome through introduction of HPRT mutations into mice.通过将次黄嘌呤磷酸核糖基转移酶(HPRT)突变引入小鼠建立莱施-奈恩综合征潜在动物模型。
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Genetic analysis of the HPRT mutation of Lesch-Nyhan syndrome in a Chinese family.一个中国家庭中莱施-奈恩综合征HPRT突变的基因分析。
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Selection against blood cells deficient in hypoxanthine phosphoribosyltransferase (HPRT) in Lesch-Nyhan heterozygotes occurs at the level of multipotent stem cells.在莱施-奈恩杂合子中,针对缺乏次黄嘌呤磷酸核糖基转移酶(HPRT)的血细胞的选择发生在多能干细胞水平。
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[Complete and partial deficiency of HPRT].[次黄嘌呤磷酸核糖转移酶的完全和部分缺乏]
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Successful preimplantation genetic diagnosis for sex Link Lesch--Nyhan Syndrome using specific diagnosis.采用特异性诊断对性连锁莱施-奈恩综合征进行成功的植入前基因诊断。
Prenat Diagn. 1999 Dec;19(13):1237-41. doi: 10.1002/(sici)1097-0223(199912)19:13<1237::aid-pd726>3.0.co;2-o.

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