首页 > 按专业查询名词 > 查询PubMed相关文献
名词信息
Pubmed相关的文献
DNA double strand break repair,DSBR相关文献:
ARID1A is involved in DNA double-strand break repair in gastric cancer.
Zhang Y, Qian HS, Hu G, Wang L, Zhu Y.
J Gastrointest Oncol. 2024 Jun 30;15(3):862-872. doi: 10.21037/jgo-24-283. Epub 2024 Jun 27.
PMID:38989399
XRCC1 protein; Form and function.
Caldecott KW.
DNA Repair (Amst). 2019 Sep;81:102664. doi: 10.1016/j.dnarep.2019.102664. Epub 2019 Jul 8.
PMID:31324530
Double-strand break repair plays a role in repeat instability in a fragile X mouse model.
Gazy I, Hayward B, Potapova S, Zhao X, Usdin K.
DNA Repair (Amst). 2019 Feb;74:63-69. doi: 10.1016/j.dnarep.2018.12.004. Epub 2018 Dec 21.
PMID:30606610
Double-strand break repair and colorectal cancer: gene variants within 3' UTRs and microRNAs binding as modulators of cancer risk and clinical outcome.
Naccarati A, Rosa F, Vymetalkova V, Barone E, Jiraskova K, Di Gaetano C, Novotny J, Levy M, Vodickova L, Gemignani F, Buchler T, Landi S, Vodicka P, Pardini B.
Oncotarget. 2016 Apr 26;7(17):23156-69. doi: 10.18632/oncotarget.6804.
PMID:26735576
High mobility group (HMG) proteins: Modulators of chromatin structure and DNA repair in mammalian cells.
Reeves R.
DNA Repair (Amst). 2015 Dec;36:122-136. doi: 10.1016/j.dnarep.2015.09.015. Epub 2015 Sep 16.
PMID:26411874
Maintenance of Genome Integrity by Mi2 Homologs CHD-3 and LET-418 in Caenorhabditis elegans.
Turcotte CA, Sloat SA, Rigothi JA, Rosenkranse E, Northrup AL, Andrews NP, Checchi PM.
Genetics. 2018 Mar;208(3):991-1007. doi: 10.1534/genetics.118.300686. Epub 2018 Jan 16.
PMID:29339410
Repeat Instability in the Fragile X-Related Disorders: Lessons from a Mouse Model.
Zhao X, Gazy I, Hayward B, Pintado E, Hwang YH, Tassone F, Usdin K.
Brain Sci. 2019 Mar 1;9(3):52. doi: 10.3390/brainsci9030052.
PMID:30832215
Environmental Stress Induces Trinucleotide Repeat Mutagenesis in Human Cells by Alt-Nonhomologous End Joining Repair.
Chatterjee N, Lin Y, Yotnda P, Wilson JH.
J Mol Biol. 2016 Jul 31;428(15):2978-80. doi: 10.1016/j.jmb.2016.06.004. Epub 2016 Jun 15.
PMID:27318194
Sequence analysis of European maize inbred line F2 provides new insights into molecular and chromosomal characteristics of presence/absence variants.
Darracq A, Vitte C, Nicolas S, Duarte J, Pichon JP, Mary-Huard T, Chevalier C, Bérard A, Le Paslier MC, Rogowsky P, Charcosset A, Joets J.
BMC Genomics. 2018 Feb 5;19(1):119. doi: 10.1186/s12864-018-4490-7.
PMID:29402214
© Copyright 2021 鸿泰茂源  版权所有All Rights Reserved京ICP备11040441号-3