Suppr超能文献

相似文献

1
Characterization of terminal deletions at 7q32 and 22q13.3 healed by De novo telomere addition.
Am J Hum Genet. 2000 Sep;67(3):610-22. doi: 10.1086/303050. Epub 2000 Aug 1.
3
AT-rich palindromes mediate the constitutional t(11;22) translocation.
Am J Hum Genet. 2001 Jan;68(1):1-13. doi: 10.1086/316952. Epub 2000 Nov 28.
5
Disruption of the ProSAP2 gene in a t(12;22)(q24.1;q13.3) is associated with the 22q13.3 deletion syndrome.
Am J Hum Genet. 2001 Aug;69(2):261-8. doi: 10.1086/321293. Epub 2001 Jun 18.

引用本文的文献

1
ATR blocks telomerase from converting DNA breaks into telomeres.
Science. 2024 Feb 16;383(6684):763-770. doi: 10.1126/science.adg3224. Epub 2024 Feb 15.
2
Centromere scission drives chromosome shuffling and reproductive isolation.
Proc Natl Acad Sci U S A. 2020 Apr 7;117(14):7917-7928. doi: 10.1073/pnas.1918659117. Epub 2020 Mar 19.
3
Telomeres and genomic evolution.
Philos Trans R Soc Lond B Biol Sci. 2018 Mar 5;373(1741). doi: 10.1098/rstb.2016.0437.
4
Terminal 18q deletions are stabilized by neotelomeres.
Mol Cytogenet. 2015 May 13;8:32. doi: 10.1186/s13039-015-0135-6. eCollection 2015.
5
Regulation of telomere addition at DNA double-strand breaks.
Chromosoma. 2013 Jun;122(3):159-73. doi: 10.1007/s00412-013-0404-2. Epub 2013 Mar 17.
7
Multiple pathways suppress telomere addition to DNA breaks in the Drosophila germline.
Genetics. 2012 Jun;191(2):407-17. doi: 10.1534/genetics.112.138818. Epub 2012 Mar 23.
10
Telomere dysfunction and chromosome instability.
Mutat Res. 2012 Feb 1;730(1-2):28-36. doi: 10.1016/j.mrfmmm.2011.04.008. Epub 2011 May 7.

本文引用的文献

1
The Stability of Broken Ends of Chromosomes in Zea Mays.
Genetics. 1941 Mar;26(2):234-82. doi: 10.1093/genetics/26.2.234.
3
The DNA sequence of human chromosome 22.
Nature. 1999 Dec 2;402(6761):489-95. doi: 10.1038/990031.
9

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验