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An MboI polymorphism at codon 192 of the human tyrosinase gene is present in Asians and Afrocaribbeans.

作者信息

Johnston J D, Winder A F, Breimer L H

机构信息

Chemical Pathology, Royal Free Hospital School of Medicine, London, UK.

出版信息

Nucleic Acids Res. 1992 Mar 25;20(6):1433. doi: 10.1093/nar/20.6.1433.

DOI:10.1093/nar/20.6.1433
PMID:1348580
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC312212/
Abstract
摘要

相似文献

1
An MboI polymorphism at codon 192 of the human tyrosinase gene is present in Asians and Afrocaribbeans.人类酪氨酸酶基因第192密码子处的MboI多态性存在于亚洲人和非洲加勒比人当中。
Nucleic Acids Res. 1992 Mar 25;20(6):1433. doi: 10.1093/nar/20.6.1433.
2
The MboI polymorphism at codon 192 of the human tyrosinase gene is present in Asians and Afrocaribbeans.
Biochem Soc Trans. 1992 Feb;20(1):41S. doi: 10.1042/bst020041s.
3
PCR detection of a TaqI polymorphism at the CCAATT box of the human tyrosinase (TYR) gene.聚合酶链反应检测人酪氨酸酶(TYR)基因CCAATT盒处的TaqI多态性
Nucleic Acids Res. 1991 Oct 25;19(20):5800. doi: 10.1093/nar/19.20.5800-a.
4
RFLP for MboI in the human tyrosinase (TYR) gene detected by PCR.通过聚合酶链反应(PCR)检测人酪氨酸酶(TYR)基因中MboI的限制性片段长度多态性(RFLP)。
Nucleic Acids Res. 1990 May 25;18(10):3103. doi: 10.1093/nar/18.10.3103-a.
5
PCR-based detection of a polymorphic HaeIII site in intron VII of the human albumin (ALB) gene.基于聚合酶链反应(PCR)检测人白蛋白(ALB)基因内含子VII中一个多态性HaeIII位点。
Nucleic Acids Res. 1991 Dec 25;19(24):6972. doi: 10.1093/nar/19.24.6972-a.
6
TaqI RFLP at the c-kit oncogene locus (KIT).原癌基因c-kit位点(KIT)处的TaqI限制性片段长度多态性
Nucleic Acids Res. 1991 Dec 25;19(24):6975. doi: 10.1093/nar/19.24.6975.
7
AcyI-RFLP in intron 8 of hTPO gene.人甲状腺过氧化物酶(hTPO)基因第8内含子的酰基限制性片段长度多态性
Nucleic Acids Res. 1992 Mar 11;20(5):1162. doi: 10.1093/nar/20.5.1162-a.
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PCR detection of a BglII polymorphism in intron I of the human p53 gene (TP53).聚合酶链反应(PCR)检测人类p53基因(TP53)内含子I中的BglII多态性。
Nucleic Acids Res. 1992 Mar 11;20(5):1172. doi: 10.1093/nar/20.5.1172-a.
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AhaII polymorphism in human X-linked proteolipid protein gene (PLP).人类X连锁蛋白脂蛋白基因(PLP)中的AhaII多态性。
Nucleic Acids Res. 1991 Nov 11;19(21):6057. doi: 10.1093/nar/19.21.6057-a.
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HLA-DP distribution in Shanghai Chinese--a study by polymerase chain reaction--restriction fragment length polymorphism.上海汉族人群中HLA-DP分布——聚合酶链反应-限制性片段长度多态性研究
Hum Immunol. 1992 Feb;33(2):129-32. doi: 10.1016/0198-8859(92)90063-s.

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Screening and validation of double allele-specific binding F-primers for the measurement of antihypertensive pharmacogenomics.用于抗高血压药物基因组学检测的双等位基因特异性结合F引物的筛选与验证
Front Med (Lausanne). 2023 Dec 20;10:1269221. doi: 10.3389/fmed.2023.1269221. eCollection 2023.
2
A frequent tyrosinase gene mutation associated with type I-A (tyrosinase-negative) oculocutaneous albinism in Puerto Rico.与波多黎各I-A型(酪氨酸酶阴性)眼皮肤白化病相关的常见酪氨酸酶基因突变。
Am J Hum Genet. 1993 Jan;52(1):17-23.

本文引用的文献

1
Detection of mutations in the tyrosinase gene in a patient with type IA oculocutaneous albinism.IA型眼皮肤白化病患者酪氨酸酶基因突变的检测
N Engl J Med. 1990 Jun 14;322(24):1724-8. doi: 10.1056/NEJM199006143222407.
2
RFLP for MboI in the human tyrosinase (TYR) gene detected by PCR.通过聚合酶链反应(PCR)检测人酪氨酸酶(TYR)基因中MboI的限制性片段长度多态性(RFLP)。
Nucleic Acids Res. 1990 May 25;18(10):3103. doi: 10.1093/nar/18.10.3103-a.
3
Non-random distribution of missense mutations within the human tyrosinase gene in type I (tyrosinase-related) oculocutaneous albinism.I型(酪氨酸酶相关)眼皮肤白化病患者中,人类酪氨酸酶基因错义突变的非随机分布。
Mol Biol Med. 1991 Feb;8(1):19-29.