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RFLP for MboI in the human tyrosinase (TYR) gene detected by PCR.

作者信息

Giebel L B, Spritz R A

机构信息

Laboratory of Genetics, University of Wisconsin, Madison 53706.

出版信息

Nucleic Acids Res. 1990 May 25;18(10):3103. doi: 10.1093/nar/18.10.3103-a.

DOI:10.1093/nar/18.10.3103-a
PMID:1971925
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC330887/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79ab/330887/34647f666a15/nar00194-0248-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79ab/330887/e58e3484863c/nar00194-0248-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79ab/330887/34647f666a15/nar00194-0248-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79ab/330887/e58e3484863c/nar00194-0248-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79ab/330887/34647f666a15/nar00194-0248-b.jpg

相似文献

1
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.
2
RFLP for TaqI at the human tyrosinase locus.人类酪氨酸酶基因座TaqI的限制性片段长度多态性
Nucleic Acids Res. 1988 Oct 25;16(20):9890. doi: 10.1093/nar/16.20.9890.
3
RFLP for BgIII at the human tyrosinase (TYR) locus.人类酪氨酸酶(TYR)基因座上BgIII的限制性片段长度多态性
Nucleic Acids Res. 1990 Jun 25;18(12):3672. doi: 10.1093/nar/18.12.3672-a.
4
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.
5
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.
6
A frequent tyrosinase gene mutation in classic, tyrosinase-negative (type IA) oculocutaneous albinism.经典型酪氨酸酶阴性(IA型)眼皮肤白化病中常见的酪氨酸酶基因突变。
Proc Natl Acad Sci U S A. 1990 May;87(9):3255-8. doi: 10.1073/pnas.87.9.3255.
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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.
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One-allele system in the Korean for MboI-RFLP in exon 1 of the human tyrosinase (TYR) gene.韩国人群中人酪氨酸酶(TYR)基因第1外显子MboI限制性片段长度多态性的单等位基因系统。
J Dermatol Sci. 2000 Sep;24(1):1-3. doi: 10.1016/s0923-1811(00)00075-x.
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Human tyrosinase gene, mapped to chromosome 11 (q14----q21), defines second region of homology with mouse chromosome 7.人类酪氨酸酶基因定位于11号染色体(q14----q21),它确定了与小鼠7号染色体同源的第二个区域。
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10
Detection of point mutation in the tyrosinase gene of a Japanese albino patient by a direct sequencing of amplified DNA.
Hum Genet. 1990 Jun;85(1):123-4. doi: 10.1007/BF00276337.

引用本文的文献

1
Association of TYR SNP rs1042602 with Melanoma Risk and Prognosis.TYR基因单核苷酸多态性rs1042602与黑色素瘤风险及预后的关联
Life (Basel). 2022 Dec 1;12(12):2004. doi: 10.3390/life12122004.
2
Molecular analysis of common polymorphisms within the human Tyrosinase locus and genetic association with pigmentation traits.人类酪氨酸酶基因座内常见多态性的分子分析及其与色素沉着性状的遗传关联。
Pigment Cell Melanoma Res. 2014 Jul;27(4):552-64. doi: 10.1111/pcmr.12253. Epub 2014 May 12.
3
Next-generation DNA re-sequencing identifies common variants of TYR and HLA-A that modulate the risk of generalized vitiligo via antigen presentation.

本文引用的文献

1
Molecular basis for the heterogeneity of human tyrosinase.人类酪氨酸酶异质性的分子基础。
Tohoku J Exp Med. 1988 Dec;156(4):403-14. doi: 10.1620/tjem.156.403.
2
Isolation and sequence of a cDNA clone for human tyrosinase that maps at the mouse c-albino locus.定位在小鼠c-白化病基因座上的人类酪氨酸酶cDNA克隆的分离与测序。
Proc Natl Acad Sci U S A. 1987 Nov;84(21):7473-7. doi: 10.1073/pnas.84.21.7473.
3
Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase.使用热稳定DNA聚合酶进行引物引导的DNA酶促扩增。
新一代DNA重测序技术鉴定出TYR和HLA - A的常见变异体,这些变异体通过抗原呈递调节泛发性白癜风的风险。
J Invest Dermatol. 2012 Jun;132(6):1730-3. doi: 10.1038/jid.2012.37. Epub 2012 Mar 8.
4
Prostate cancer risk: associations with ultraviolet radiation, tyrosinase and melanocortin-1 receptor genotypes.前列腺癌风险:与紫外线辐射、酪氨酸酶及黑皮质素-1受体基因分型的关联
Br J Cancer. 2001 Nov 16;85(10):1504-9. doi: 10.1054/bjoc.2001.2097.
5
The 5,6-dihydroxyindole-2-carboxylic acid (DHICA) oxidase activity of human tyrosinase.人酪氨酸酶的5,6-二羟基吲哚-2-羧酸(DHICA)氧化酶活性。
Biochem J. 2001 Feb 15;354(Pt 1):131-9. doi: 10.1042/0264-6021:3540131.
6
Complete sequence and polymorphism study of the human TYRP1 gene encoding tyrosinase-related protein 1.编码酪氨酸酶相关蛋白1的人类TYRP1基因的完整序列及多态性研究
Mamm Genome. 1998 Jan;9(1):50-3. doi: 10.1007/s003359900678.
7
Testing the feasibility of DNA typing for human identification by PCR and an oligonucleotide ligation assay.通过聚合酶链反应(PCR)和寡核苷酸连接测定法检测DNA分型用于人类身份鉴定的可行性。
Am J Hum Genet. 1996 Jun;58(6):1239-46.
8
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.
9
Molecular analyses of a tyrosinase-negative albino family.一个酪氨酸酶阴性白化病家族的分子分析
Am J Hum Genet. 1993 Feb;52(2):406-13.
10
Schizophrenia-associated chromosome 11q21 translocation: identification of flanking markers and development of chromosome 11q fragment hybrids as cloning and mapping resources.精神分裂症相关的11号染色体q21易位:侧翼标记的鉴定以及11号染色体q片段杂种的构建作为克隆和定位资源
Am J Hum Genet. 1993 Mar;52(3):478-90.
Science. 1988 Jan 29;239(4839):487-91. doi: 10.1126/science.2448875.