A hypervariable region 3' to the human apolipoprotein B gene.
作者信息
Knott T J, Wallis S C, Pease R J, Powell L M, Scott J
出版信息
Nucleic Acids Res. 1986 Nov 25;14(22):9215-6. doi: 10.1093/nar/14.22.9215.
Abstract
摘要
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A hypervariable region 3' to the human apolipoprotein B gene.人类载脂蛋白B基因3'端的一个高变区。
Nucleic Acids Res. 1986 Nov 25;14(22):9215-6. doi: 10.1093/nar/14.22.9215.
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A unique length polymorphism in the signal peptide region of the apolipoprotein B gene in Mexican-Americans.墨西哥裔美国人载脂蛋白B基因信号肽区域存在独特的长度多态性。
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引用本文的文献
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Higher alleles of apolipoprotein B gene 3' VNTR: Risk for gallstone disease.载脂蛋白B基因3'端可变数目串联重复序列的高等位基因：胆结石疾病的风险。
Indian J Clin Biochem. 2008 Apr;23(2):123-9. doi: 10.1007/s12291-008-0029-z. Epub 2008 Jun 11.
2
Variant mapping of the Apo(B) AT rich minisatellite. Dependence on nucleotide sequence of the copy number variations. Instability of the non-canonical alleles.载脂蛋白B富含AT的微卫星的变异体定位。拷贝数变异对核苷酸序列的依赖性。非典型等位基因的不稳定性。
Nucleic Acids Res. 1993 May 11;21(9):2179-84. doi: 10.1093/nar/21.9.2179.
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The human apolipoprotein B 3' hypervariable region: detection of eight new alleles and comparisons of allele frequencies in blacks and whites.人类载脂蛋白B 3'高变区：八个新等位基因的检测及黑人和白人等位基因频率的比较。
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DNA fingerprint analysis of a free-range koala population.
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VNTR and microsatellite polymorphisms within the subtelomeric region of 7q.
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Two highly polymorphic minisatellites from the pseudoautosomal region of the human sex chromosomes.来自人类性染色体假常染色体区域的两个高度多态性微卫星。
EMBO J. 1987 Apr;6(4):963-9. doi: 10.1002/j.1460-2075.1987.tb04846.x.
7
Rapid typing of tandemly repeated hypervariable loci by the polymerase chain reaction: application to the apolipoprotein B 3' hypervariable region.通过聚合酶链反应对串联重复高变区进行快速分型：应用于载脂蛋白B 3'高变区。
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New approach for isolation of VNTR markers.分离可变数目串联重复序列（VNTR）标记的新方法。
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Genetic evidence from two families that the apolipoprotein B gene is not involved in abetalipoproteinemia.来自两个家族的基因证据表明载脂蛋白B基因不参与无β脂蛋白血症。
J Clin Invest. 1988 Nov;82(5):1803-6. doi: 10.1172/JCI113795.
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Inference of a molecular defect of apolipoprotein B in hypobetalipoproteinemia by linkage analysis in a large kindred.通过对一个大家系进行连锁分析推断低β脂蛋白血症中载脂蛋白B的分子缺陷
J Clin Invest. 1988 Sep;82(3):847-51. doi: 10.1172/JCI113688.
本文引用的文献
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A highly polymorphic region 3' to the human type II collagen gene.人类II型胶原蛋白基因3'端的一个高度多态性区域。
Nucleic Acids Res. 1985 Jul 11;13(13):4613-22. doi: 10.1093/nar/13.13.4613.
2
RFLP for the human apolipoprotein B gene: V;XbaI.人类载脂蛋白B基因的限制性片段长度多态性：V；XbaI。
Nucleic Acids Res. 1985 Sep 25;13(18):6793. doi: 10.1093/nar/13.18.6793.
3
The origin and evolution of retroposons.反转录转座子的起源与进化。
Int Rev Cytol. 1985;93:187-279. doi: 10.1016/s0074-7696(08)61375-3.
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