人类载脂蛋白CII基因位点的NcoI限制性片段长度多态性 - Suppr

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NcoI RFLP at the human apolipoprotein CII gene locus.

作者信息

Frossard P M, Coleman R T, Assmann G

出版信息

Nucleic Acids Res. 1986 Jun 25;14(12):5120. doi: 10.1093/nar/14.12.5120.

DOI:10.1093/nar/14.12.5120

PMID:3014445

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC311522/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/703d/311522/af43e4785638/nar00281-0418-a.jpg

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NcoI RFLP at the human apolipoprotein CII gene locus.人类载脂蛋白CII基因位点的NcoI限制性片段长度多态性

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The isolation of a genomic clone containing the apolipoprotein CII gene and the detection of linkage disequilibrium between two common DNA polymorphisms around the gene.包含载脂蛋白CII基因的基因组克隆的分离以及该基因周围两个常见DNA多态性之间连锁不平衡的检测。

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Dimorphic markers for the human apolipoprotein CII gene locus.人类载脂蛋白CII基因位点的双态标记

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The apolipoprotein CII gene: subchromosomal localisation and linkage to the myotonic dystrophy locus.载脂蛋白CII基因：亚染色体定位及与强直性肌营养不良基因座的连锁关系

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A DNA polymorphism adjacent to the human apolipoprotein CII gene.人类载脂蛋白CII基因附近的DNA多态性。

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The gene for apolipoprotein C-II is closely linked to the gene for apolipo-protein E on chromosome 19.载脂蛋白C-II基因与19号染色体上的载脂蛋白E基因紧密连锁。

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Localization of genes encoding apolipoproteins CI, CII, and E to the p13----cen region of human chromosome 19.

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The locus for apolipoprotein CII is closely linked to the apolipoprotein E locus on chromosome 19 in man.载脂蛋白CII基因座与人第19号染色体上的载脂蛋白E基因座紧密连锁。

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引用本文的文献

The 1.5-Mb region spanning the myotonic dystrophy locus shows uniform recombination frequency.跨越强直性肌营养不良基因座的150万个碱基对区域显示出均匀的重组频率。

Am J Hum Genet. 1994 Jan;54(1):104-13.

Tight linkage between myotonic dystrophy and apolipoprotein E genes revealed with allele-specific oligonucleotides.

Hum Genet. 1988 Sep;80(1):49-52. doi: 10.1007/BF00451455.

Myotonic dystrophy is closely linked to the gene for muscle-type creatine kinase (CKMM).强直性肌营养不良症与肌肉型肌酸激酶（CKMM）基因密切相关。

Hum Genet. 1989 Mar;81(4):308-10. doi: 10.1007/BF00283680.

Linkage disequilibrium detected between dystrophia myotonica and APOC2 locus in the Finnish population.在芬兰人群中检测到强直性肌营养不良与载脂蛋白C2基因座之间的连锁不平衡。

Hum Genet. 1990 Oct;85(5):541-5. doi: 10.1007/BF00194234.

A new polymorphic probe which defines the region of chromosome 19 containing the myotonic dystrophy locus.

Am J Hum Genet. 1990 Jun;46(6):1073-81.

A polymorphic PstI site in intron 2 of the human apolipoprotein C-II gene detected by polymerase chain reaction.通过聚合酶链反应检测到人类载脂蛋白C-II基因内含子2中的一个多态性PstI位点。

Hum Genet. 1992 May;89(3):361. doi: 10.1007/BF00220562.

本文引用的文献

Isolation and sequence of a human apolipoprotein CII cDNA clone and its use to isolate and map to human chromosome 19 the gene for apolipoprotein CII.人载脂蛋白CII cDNA克隆的分离、测序及其用于分离载脂蛋白CII基因并将其定位于人第19号染色体上。

Proc Natl Acad Sci U S A. 1984 May;81(10):2945-9. doi: 10.1073/pnas.81.10.2945.

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