Mutation Research-Fundamental and Molecular Mechanisms of Mutagenesis

Papers
(The median citation count of Mutation Research-Fundamental and Molecular Mechanisms of Mutagenesis is 1. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2020-04-01 to 2024-04-01.)
ArticleCitations
Targeting DNA-PK in cancer45
Aurora kinases and DNA damage response34
Chromatin rigidity provides mechanical and genome protection32
Clinical potential of ATM inhibitors30
Nuclear actin: The new normal14
Genome sequencing of ion-beam-induced mutants facilitates detection of candidate genes responsible for phenotypes of mutants in rice12
Therapeutic opportunities for PLK1 inhibitors: Spotlight on BRCA1-deficiency and triple negative breast cancers11
Cell cycle involvement in cancer therapy; WEE1 kinase, a potential target as therapeutic strategy11
The FHA domain of PNKP is essential for its recruitment to DNA damage sites and maintenance of genome stability10
Monitoring global chromatin dynamics in response to DNA damage9
New insight into the biology of R-loops9
Nuclear mechanosensing: mechanism and consequences of a nuclear rupture8
A gain-of-function mutation in CITED2 is associated with congenital heart disease7
Lamin A and telomere maintenance in aging: Two to Tango7
Distribution of copy number variations and rearrangement endpoints in human cancers with a review of literature6
Targeting DNA damage response kinases in cancer therapy6
A novel pathway for the induction of DNA damage in human spermatozoa involving extracellular cell-free DNA6
Biochemical and photochemical mechanisms that produce different UV-induced mutation spectra6
Induction of proliferative and mutagenic activity by benzo(a)pyrene in PC-3 cells via JAK2/STAT3 pathway6
Predicting potential residues associated with lung cancer using deep neural network6
Identification of nsSNPs of transcription factor E2F1 predisposing individuals to lung cancer and head and neck cancer6
Identification and characterization of inheritable structural variations induced by ion beam radiations in rice6
Mutational screening of PKD1 and PKD2 in Indian ADPKD patients identified 95 genetic variants5
Identification and validation of long noncoding RNA AC083900.1 and RP11-283C24.1 for prediction of progression of osteosarcoma5
The long-term effects of exposure to ionising radiation on gene expression in mice5
Genome-wide profiles of UV lesion susceptibility, repair, and mutagenic potential in melanoma5
MiRNA-144–5p down-modulates CDCA3 to regulate proliferation and apoptosis of lung adenocarcinoma cells4
Radiation-induced DNA damage and altered expression of p21, cyclin D1 and Mre11 genes in human fibroblast cell lines with different radiosensitivity4
Mutations induced by Bleomycin, 4-nitroquinoline-1-oxide, and hydrogen peroxide in the rpoB gene of Escherichia coli: Perspective on Mutational Hotspots4
Moving fast and breaking things: Incidence and repair of DNA damage within ribosomal DNA repeats4
Protection of nuclear DNA by lifespan-extending compounds in the yeast Saccharomyces cerevisiae4
Polymer perspective of genome mobilization4
Toxic effect and genotoxicity of carvacrol ethers in Drosophila melanogaster4
Synonymous codon usage and context analysis of genes associated with pancreatic cancer3
Origins of nonsense mutations in human tumor suppressor genes3
Efficient, robust, and versatile fluctuation data analysis using MLE MUtation Rate calculator (mlemur)3
Whole genome analysis of UV-induced mutagenesis in Caulobacter crescentus3
Virtual screening of mutations in antioxidant genes and its putative association with HNSCC: An in silico approach3
Aneuploidy, inflammation and diseases3
Biased distribution of action-at-a-distance mutations by 8-oxo-7,8-dihydroguanine2
Recruitment of MRE-11 to complex DNA damage is modulated by meiosis-specific chromosome organization2
LncRNA CRNDE is involved in the pathogenesis of renal fibrosis by regulating renal epithelial cell mesenchymal-epithelial transition via targeting miR-29a-3p2
Haplotype analysis of the CFTR gene on normal and mutant CFTR genes2
Blood and saliva-derived exomes from healthy Caucasian subjects do not display overt evidence of somatic mosaicism2
Dysregulation of miR-204-5p/APLN axis affects malignant progression and cell stemness of esophageal cancer2
EZH2 affects malignant progression and DNA damage repair of lung adenocarcinoma cells by regulating RAI2 expression2
Impact of glutathione S transferases P1 (Ile105Val) variants on the risk of GSTp, phosphorylated c-Jun kinase, and P53 phenotypic expression and their implications on overall survival outcomes in non-2
Tumor-promoting roles of HMMR in lung adenocarcinoma2
Mutational property of newly identified mutagen l-glutamic acid γ-hydrazide in Escherichia coli2
Recombinational repair in the absence of holliday junction resolvases in E. coli.2
Intronic variants of MITF (rs7623610) and CREB1 (rs10932201) genes may enhance splicing efficiency in human melanoma cell line2
The duration of exposure to 50 Hz magnetic fields: Influence on circadian genes and DNA damage responses in murine hematopoietic FDC-P1 cells2
DNA damage-signaling, homologous recombination and genetic mutation induced by 5-azacytidine and DNA-protein crosslinks in Escherichia coli2
Characterization and implementation of a miniature X-ray system for live cell microscopy1
Characterization of an archaeal recombinase paralog that exhibits novel anti-recombinase activity1
The dose-, LET-, and gene-dependent patterns of DNA changes underlying the point mutations in spermatozoa of Drosophila melanogaster. I. Autosomal gene black1
Analysis of tafazzin and deoxyribonuclease 1 like 1 transcripts and X chromosome sequencing in the evaluation of the effect of mosaicism in the TAZ gene on phenotypes in a family affected by Barth syn1
Mutagenesis induced by protonation of single-stranded DNA is linked to glycolytic sugar metabolism1
Variants in exon 2 of MED12 gene causes uterine leiomyoma’s through over-expression of MMP-9 of ECM pathway1
DinB (DNA polymerase IV), ImuBC and RpoS contribute to the generation of ciprofloxacin-resistance mutations in Pseudomonas aeruginosa1
Association between DNA repair capacity and body mass index in women1
Hepatocarcinogen 4-methylquinoline induced G:C to C:G transversions in the cII gene in the liver of lambda/lacZ transgenic mice (Muta™Mouse)1
Neutrophils and micronuclei: An emerging link between genomic instability and cancer-driven inflammation1
Enhanced characterization of the thyA system for mutational analysis in Escherichia coli: Defining mutationally “hot” regions of the gene1
The accurate bypass of pyrimidine dimers by DNA polymerase eta contributes to ultraviolet-induced mutagenesis1
Expression of the Circadian Clock Gene ARNTL associated with DNA repair gene and prognosis of patient with osteosarcoma1
Evaluation of DNA damages in congenital hearing loss patients1
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