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The mechanism of conversion of deletions and insertions.

作者信息

Radding C M

出版信息

Cold Spring Harb Symp Quant Biol. 1979;43 Pt 2:1315-6. doi: 10.1101/sqb.1979.043.01.150.

DOI:10.1101/sqb.1979.043.01.150
PMID:290444
Abstract
摘要

相似文献

1
The mechanism of conversion of deletions and insertions.缺失和插入的转换机制。
Cold Spring Harb Symp Quant Biol. 1979;43 Pt 2:1315-6. doi: 10.1101/sqb.1979.043.01.150.
2
Two mechanisms for directional gene conversion.定向基因转换的两种机制。
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3
Causes of more frequent deletions than insertions in mutations and protein evolution.突变和蛋白质进化中缺失比插入更频繁的原因。
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4
Double-strand cleavage at a two-base deletion mismatch in a DNA heteroduplex by nuclease S1.核酸酶S1在DNA异源双链体中的两碱基缺失错配处产生双链切割。
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5
Targeted Modification of Gene Function Exploiting Homology-Directed Repair of TALEN-Mediated Double-Strand Breaks in Barley.利用同源定向修复大麦中TALEN介导的双链断裂对基因功能进行靶向修饰
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6
Analysis of targeted chromosomal deletions induced by zinc finger nucleases.锌指核酸酶诱导的靶向染色体缺失分析
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7
Analysis of crossover breakpoints yields new insights into the nature of the gene conversion events associated with large NF1 deletions mediated by nonallelic homologous recombination.分析交叉断点为非等位同源重组介导的大 NF1 缺失相关基因转换事件的性质提供了新的见解。
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8
Mismatch repair during pneumococcal transformation of small deletions produced by site-directed mutagenesis.在通过定点诱变产生的小缺失的肺炎球菌转化过程中的错配修复。
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9
Molecular cloning of the uaY regulatory gene of Aspergillus nidulans reveals a favoured region for DNA insertions.
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10
Molecular processes of chromosome 9p21 deletions causing inactivation of the p16 tumor suppressor gene in human cancer: deduction from structural analysis of breakpoints for deletions.导致人类癌症中p16肿瘤抑制基因失活的9号染色体p21缺失的分子过程：从缺失断点的结构分析推断
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A recurrent inversion on the eutherian X chromosome.真兽类X染色体上的一个反复出现的倒位。
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2
Large Heterologies Impose Their Gene Conversion Pattern onto Closely Linked Point Mutations.大片段同源性迫使与之紧密连锁的点突变呈现基因转换模式。
Genetics. 1987 May;116(1):45-53. doi: 10.1093/genetics/116.1.45.
3
Polar branch migration promoted by recA protein: effect of mismatched base pairs.由RecA蛋白促进的极性分支迁移：错配碱基对的影响
Proc Natl Acad Sci U S A. 1982 Feb;79(3):762-6. doi: 10.1073/pnas.79.3.762.
4
Nucleotide sequence of the genetically labile repeated elements 5' to the origin of mouse rRNA transcription.小鼠rRNA转录起始位点上游遗传不稳定重复元件的核苷酸序列。
Nucleic Acids Res. 1983 Jan 11;11(1):211-24. doi: 10.1093/nar/11.1.211.
5
Fungal recombination.真菌重组
Microbiol Rev. 1985 Mar;49(1):33-58. doi: 10.1128/mr.49.1.33-58.1985.
6
Two mechanisms for directional gene conversion.定向基因转换的两种机制。
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7
Mitotic gene conversion of large DNA heterologies in Saccharomyces cerevisiae.
Mol Gen Genet. 1988 Mar;211(3):455-8. doi: 10.1007/BF00425700.
8
Frequency and directionality of gene conversion events involving the CYC7-H3 mutation in Saccharomyces cerevisiae.酿酒酵母中涉及CYC7-H3突变的基因转换事件的频率和方向性
Genetics. 1986 Oct;114(2):347-61. doi: 10.1093/genetics/114.2.347.
9
Recombination hot spot in the human beta-globin gene cluster: meiotic recombination of human DNA fragments in Saccharomyces cerevisiae.人类β-珠蛋白基因簇中的重组热点：酿酒酵母中人类DNA片段的减数分裂重组
Mol Cell Biol. 1985 Aug;5(8):2029-38. doi: 10.1128/mcb.5.8.2029-2038.1985.
10
Homologous recombination catalyzed by human cell extracts.由人类细胞提取物催化的同源重组。
Mol Cell Biol. 1985 Apr;5(4):714-20. doi: 10.1128/mcb.5.4.714-720.1985.