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1
'ZSTATS'--a statistical analysis for potential Z-DNA sequences.“ZSTATS”——一种针对潜在Z-DNA序列的统计分析方法。
Nucleic Acids Res. 1984 Jan 11;12(1 Pt 2):825-32. doi: 10.1093/nar/12.1part2.825.
2
The DNA sequence of the human beta-globin region is strongly biased in favor of long strings of contiguous purine or pyrimidine residues.人类β-珠蛋白区域的DNA序列强烈偏向于连续嘌呤或嘧啶残基的长串。
Biochemistry. 1987 Dec 1;26(24):7870-5. doi: 10.1021/bi00398a050.
3
Nuclear magnetic resonance structural studies of intramolecular purine.purine.pyrimidine DNA triplexes in solution. Base triple pairing alignments and strand direction.溶液中分子内嘌呤-嘌呤-嘧啶DNA三链体的核磁共振结构研究。碱基三联体配对排列和链方向。
J Mol Biol. 1991 Oct 20;221(4):1403-18.
4
Interactive computer programs for the graphic analysis of nucleotide sequence data.用于核苷酸序列数据图形分析的交互式计算机程序。
Nucleic Acids Res. 1984 Jan 11;12(1 Pt 2):665-73. doi: 10.1093/nar/12.1part2.665.
5
Unusual frequencies of certain alternating purine-pyrimidine runs in natural DNA sequences: relation to Z-DNA.天然DNA序列中特定嘌呤-嘧啶交替序列的异常频率:与Z-DNA的关系。
FEBS Lett. 1985 Jun 3;185(1):197-202. doi: 10.1016/0014-5793(85)80769-9.
6
Conformational DNA transition in the in vitro torsionally strained chicken beta-globin 5' region.体外扭转应变鸡β-珠蛋白5'区域中的构象性DNA转变
Nucleic Acids Res. 1986 Sep 25;14(18):7143-58. doi: 10.1093/nar/14.18.7143.
7
Strong, specific, monodentate G-C base pair recognition by N7-inosine derivatives in the pyrimidine.purine-pyrimidine triple-helical binding motif.嘧啶-嘌呤-嘧啶三螺旋结合基序中N7-肌苷衍生物对G-C碱基对的强特异性单齿识别。
Nucleic Acids Res. 1997 May 15;25(10):1875-82. doi: 10.1093/nar/25.10.1875.
8
Parallel-stranded duplex DNA containing blocks of trans purine-purine and purine-pyrimidine base pairs.含有反式嘌呤-嘌呤和嘌呤-嘧啶碱基对片段的平行链双链DNA。
Nucleic Acids Res. 1994 Aug 25;22(16):3293-303. doi: 10.1093/nar/22.16.3293.
9
DNA sequences preceding the rabbit beta-globin gene are required for formation in mouse L cells of beta-globin RNA with the correct 5' terminus.兔β-珠蛋白基因之前的DNA序列是在小鼠L细胞中形成具有正确5'末端的β-珠蛋白RNA所必需的。
Proc Natl Acad Sci U S A. 1981 Mar;78(3):1411-5. doi: 10.1073/pnas.78.3.1411.
10
Homeodomain protein binding sites, inverted repeats, and nuclear matrix attachment regions along the human beta-globin gene complex.人β-珠蛋白基因复合体中的同源结构域蛋白结合位点、反向重复序列和核基质附着区域。
J Cell Biochem. 1993 May;52(1):23-36. doi: 10.1002/jcb.240520105.

本文引用的文献

1
Left-handed DNA helices.左手DNA螺旋
Nature. 1980 Feb 21;283(5749):743-5. doi: 10.1038/283743a0.
2
A history of the human fetal globin gene duplication.人类胎儿珠蛋白基因复制的历史。
Cell. 1981 Oct;26(2 Pt 2):191-203. doi: 10.1016/0092-8674(81)90302-0.
3
Automation of the computer handling of gel reading data produced by the shotgun method of DNA sequencing.DNA测序鸟枪法产生的凝胶读数数据的计算机处理自动化。
Nucleic Acids Res. 1982 Aug 11;10(15):4731-51. doi: 10.1093/nar/10.15.4731.
4
The DNA sequence of the 5' flanking region of the human beta-globin gene: evolutionary conservation and polymorphic differences.人类β-珠蛋白基因5'侧翼区的DNA序列:进化保守性与多态性差异
Nucleic Acids Res. 1982 Mar 25;10(6):2109-20. doi: 10.1093/nar/10.6.2109.
5
Wrinkled DNA.
Nucleic Acids Res. 1983 Mar 11;11(5):1457-74. doi: 10.1093/nar/11.5.1457.
6
A member of a new repeated sequence family which is conserved throughout eucaryotic evolution is found between the human delta and beta globin genes.在人类δ珠蛋白基因和β珠蛋白基因之间发现了一个新的重复序列家族的成员,该家族在整个真核生物进化过程中都是保守的。
Nucleic Acids Res. 1981 Nov 25;9(22):5931-47. doi: 10.1093/nar/9.22.5931.
7
The nucleotide sequence of the human beta-globin gene.人类β-珠蛋白基因的核苷酸序列。
Cell. 1980 Oct;21(3):647-51. doi: 10.1016/0092-8674(80)90428-6.
8
The primary structure of the human epsilon-globin gene.人类ε-珠蛋白基因的一级结构。
Cell. 1980 Oct;21(3):621-6. doi: 10.1016/0092-8674(80)90425-0.
9
The sequence of the chromosomal mouse beta-globin major gene: homologies in capping, splicing and poly(A) sites.染色体小鼠β-珠蛋白主要基因的序列:帽化、剪接和聚腺苷酸化位点的同源性
Cell. 1978 Dec;15(4):1125-32. doi: 10.1016/0092-8674(78)90040-5.

“ZSTATS”——一种针对潜在Z-DNA序列的统计分析方法。

'ZSTATS'--a statistical analysis for potential Z-DNA sequences.

作者信息

Vass J K, Wilson R H

出版信息

Nucleic Acids Res. 1984 Jan 11;12(1 Pt 2):825-32. doi: 10.1093/nar/12.1part2.825.

DOI:10.1093/nar/12.1part2.825
PMID:6546441
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC321097/
Abstract

We have developed a FORTRAN programme for scanning DNA sequences for potential Z-DNA forming regions using the One-Sample Runs Test. The programme also detects other non-random arrangements of purines and pyrimidines on the same strand and will detect purine- or pyrimidine-rich strands and G:C- or A:T-rich regions. A series of test statistics are produced as a graphical output and these have been used to search a number of beta- type globin DNA sequences for potential Z-DNA regions whose biological significance is briefly discussed.

摘要

我们已经开发了一个FORTRAN程序,用于使用单样本游程检验扫描DNA序列以寻找潜在的Z-DNA形成区域。该程序还能检测同一条链上嘌呤和嘧啶的其他非随机排列,并且能检测富含嘌呤或嘧啶的链以及富含G:C或A:T的区域。一系列检验统计量以图形输出形式生成,并且已被用于在多个β型珠蛋白DNA序列中搜索潜在的Z-DNA区域,本文还简要讨论了这些区域的生物学意义。