• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利：CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法，用中文像聊天一样搜索，搜遍4000万医学文献。AI智能推荐，让科研检索更轻松。

立即免费搜索

文件翻译

保留排版，准确专业，支持PDF/Word/PPT等文件格式，支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述，25分钟生成高质量综述，智能提取关键信息，辅助科研写作。

立即免费体验

相似文献

1
Comparative studies on X-autosome translocations in the mouse. II. Inactivation of autosomal loci, segregation, and mapping of autosomal breakpoints in five T (X;1) S.小鼠X-常染色体易位的比较研究。II. 五个T(X;1)S中常染色体基因座的失活、分离及常染色体断点的定位
Genetics. 1970 Feb;64(2):281-312. doi: 10.1093/genetics/64.2.281.
2
Segmental aneuploidy and the genetic gross structure of the Drosophila genome.节段性非整倍体与果蝇基因组的遗传总体结构。
Genetics. 1972 May;71(1):157-84. doi: 10.1093/genetics/71.1.157.
3
Comparative studies on X-autosome translocations in the mouse. I. Origin, viability, fertility, and weight of five T(X;1)'S.小鼠X染色体与常染色体易位的比较研究。I. 5种T(X;1)的起源、活力、生育力及体重
Genetics. 1969 Sep;63(1):103-20. doi: 10.1093/genetics/63.1.103.
4
Mouse chromosome translocations: visualization and analysis by electron microscopy of the synaptonemal complex.小鼠染色体易位：通过联会复合体的电子显微镜观察与分析
Science. 1977 May 20;196(4292):892-4. doi: 10.1126/science.870966.
5
Meiotic disjunction in mouse translocations and the determination of centromere position.小鼠易位中的减数分裂分离及着丝粒位置的确定。
Genet Res. 1971 Oct;18(2):215-35. doi: 10.1017/s0016672300012611.
6
The genetic analysis of distributive segregation in Drosophila melanogaster. I. Isolation and characterization of Aberrant X segregation (Axs), a mutation defective in chromosome partner choice.黑腹果蝇中分布性分离的遗传分析。I. 异常X染色体分离（Axs）的分离与特性分析，Axs是一种在染色体配对选择中存在缺陷的突变。
Genetics. 1989 Aug;122(4):801-21. doi: 10.1093/genetics/122.4.801.
7
Fine-structure analysis of the chromosome recombinational patterns at the base of the X-chromosome of Drosophila melanogaster.黑腹果蝇X染色体基部染色体重组模式的精细结构分析。
Mutat Res. 1971 Sep;13(1):35-47. doi: 10.1016/0027-5107(71)90123-0.
8
Meiotic behaviour of evolutionary sex-autosome translocations in Bovidae.牛科动物中进化性性染色体-常染色体易位的减数分裂行为。
Chromosome Res. 2016 Sep;24(3):325-38. doi: 10.1007/s10577-016-9524-x. Epub 2016 Apr 30.
9
Genetic mechanisms leading to primary amenorrhea in balanced X-autosome translocations.导致平衡 X-常染色体易位原发性闭经的遗传机制。
Fertil Steril. 2015 May;103(5):1289-96.e2. doi: 10.1016/j.fertnstert.2015.01.030. Epub 2015 Mar 4.
10
A crossover suppressor-enhancer system in the mosquito Aedes aegypti.埃及伊蚊中的一种交叉抑制-增强子系统。
Can J Genet Cytol. 1971 Sep;13(3):561-77. doi: 10.1139/g71-081.

引用本文的文献

1
-Acting Factors and Elements Involved in the Human Inactive X Chromosome Organization and Compaction.人类失活 X 染色体组织和压缩的作用因素和元素。
Genet Res (Camb). 2021 May 7;2021:6683460. doi: 10.1155/2021/6683460. eCollection 2021.
2
X chromosome inactivation and Xist evolution in a rodent lacking LINE-1 activity.缺乏LINE-1活性的啮齿动物中的X染色体失活与Xist进化
PLoS One. 2009 Jul 15;4(7):e6252. doi: 10.1371/journal.pone.0006252.
3
High-resolution analysis of epigenetic changes associated with X inactivation.与X染色体失活相关的表观遗传变化的高分辨率分析。
Genome Res. 2009 Aug;19(8):1361-73. doi: 10.1101/gr.092643.109. Epub 2009 Jul 6.
4
Somatic cells as indicators of germinal mutations in the mouse.体细胞作为鼠种系突变的指示剂。
Environ Health Perspect. 1978 Jun;24:113-6. doi: 10.1289/ehp.7824113.
5
Do LINEs have a role in X-chromosome inactivation?长散在重复序列（LINEs）在X染色体失活中起作用吗？
J Biomed Biotechnol. 2006;2006(1):59746. doi: 10.1155/JBB/2006/59746.
6
Molecular evidence for a relationship between LINE-1 elements and X chromosome inactivation: the Lyon repeat hypothesis.LINE-1元件与X染色体失活之间关系的分子证据：莱昂重复假说。
Proc Natl Acad Sci U S A. 2000 Jun 6;97(12):6634-9. doi: 10.1073/pnas.97.12.6634.
7
X-chromosome inactivation spreads itself: effects in autosomes.X染色体失活会自我扩展：对常染色体的影响。
Am J Hum Genet. 1998 Jul;63(1):17-9. doi: 10.1086/301940.
8
Coordinate control and variation in X-linked gene expression among female mice.雌性小鼠中X连锁基因表达的协调控制与变异
Mamm Genome. 1997;8(11):818-22. doi: 10.1007/s003359900585.
9
The X-autosome translocation in the common shrew (Sorex araneus L.): late replication in female somatic cells and pairing in male meiosis.普通鼩鼱（Sorex araneus L.）中的X-常染色体易位：雌性体细胞中的晚期复制和雄性减数分裂中的配对。
Chromosoma. 1993 May;102(5):355-60. doi: 10.1007/BF00661279.
10
Primary and secondary nonrandom X chromosome inactivation in early female mouse embryos carrying Searle's translocation T(X; 16)16H.携带塞尔易位T(X;16)16H的早期雌性小鼠胚胎中的原发性和继发性非随机X染色体失活
Chromosoma. 1980;81(3):439-59. doi: 10.1007/BF00368155.

本文引用的文献

1
The Effects of Genotype and Cell Environment on Melanoblast Differentiation in the House Mouse.基因型和细胞环境对家鼠成黑素细胞分化的影响。
Genetics. 1956 May;41(3):429-50. doi: 10.1093/genetics/41.3.429.
2
The phenomenon of position effect.位置效应现象
Adv Genet. 1950;3:73-115. doi: 10.1016/s0065-2660(08)60083-8.
3
Surgical treatment of sudden hemiplegia due to complete occlusion of the internal carotid artery.
J Indiana State Med Assoc. 1959 Nov;52:1962-5.
4
CYTOLOGICAL STUDY OF SEARLE'S X-AUTOSOME TRANSLOCATION IN MUS MUSCULUS.小家鼠中塞尔氏X染色体-常染色体易位的细胞学研究。
Chromosoma. 1965 Jan 30;16:90-100. doi: 10.1007/BF00320564.
5
A MOUSE TRANSLOCATION SUPPRESSING SEX-LINKED VARIEGATION.一种抑制性连锁斑驳的小鼠易位
Cytogenetics. 1964;3:306-23. doi: 10.1159/000129820.
6
Cytological study of an X-autosome translocation in Mus musculus.小家鼠X-常染色体易位的细胞学研究。
Cytogenetics. 1962;1:129-40.
7
Genetics of mammalian sex chromosomes.哺乳动物性染色体的遗传学
Science. 1961 Jun 9;133(3467):1795-803. doi: 10.1126/science.133.3467.1795.
8
The genetic extent of the insertion involved in the flecked translocation in the mouse.小鼠斑点易位所涉及插入的基因范围。
Genetics. 1967 Feb;55(2):203-12. doi: 10.1093/genetics/55.2.203.
9
Multiple congenital anomalies associated with a ring 3 chromosome and translocated 3/X chromosome.与3号环状染色体和3/X易位染色体相关的多种先天性异常。
Nature. 1966 Oct 8;212(5058):153-5. doi: 10.1038/212153a0.
10
The location of Cattanach's translocation in the X-chromosome linkage map of the mouse.卡塔纳赫易位在小鼠X染色体连锁图谱中的位置。
Genet Res. 1966 Oct;8(2):253-6. doi: 10.1017/s0016672300010107.

Comparative studies on X-autosome translocations in the mouse. II. Inactivation of autosomal loci, segregation, and mapping of autosomal breakpoints in five T (X;1) S.

作者信息

Russell L B, Montgomery C S

出版信息

Genetics. 1970 Feb;64(2):281-312. doi: 10.1093/genetics/64.2.281.

DOI:10.1093/genetics/64.2.281
PMID:5470482
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1212403/
Abstract
摘要