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Similar Items: On the reversibility of RNA deamination versus RNA methylation: exploring the proximate and ultimate causes

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m6A RNA methylation regulatory gene expression in response to ethanol and acetaldehyde exposure and withdrawal
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A novel partial mRNA-derived duplication of the gene identified in NGS carrier screening
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RNA Polymerase III subunit Polr3a is required for craniofacial cartilage and bone development in zebrafish
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Small RNA profiling of virus-infected apple plants
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DNA methylation as a biomarker of prenatal exposures: current challenges and opportunities
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Genome-wide DNA methylation changes after 24 hours at high altitude
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Diazinon may increase the risk of acute lymphoblastic leukemia by inducing MGMT promoter methylation
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Triphenyl phosphate induces coordinated DNA methylation and gene expression changes in aquatic embryonic cells
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DNA methylation mediates the multiple sclerosis onset risk associated with HHV-6 DNA positivity
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Sequence context and methylation interact to shape germline mutation rate variation at CpG sites
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Molecular characterisation of South African isolates of grapevine fanleaf virus and a new, associated satellite RNA
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Impact of a prenatal exposure mixture of metals on DNA methylation-derived cell-type composition in cord blood
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A systematic review investigating the relationship between green and blue spaces and depression in older adults via DNA methylation
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First report of causing cutting rot on in Brazil
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Front Cover: PDMSA: A Web‐Based Tool for Pan‐Cancer Survival Analysis Using DNA Methylation Levels as Biomarkers (Advanced Genetics 2/07)
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First report of pv. causing bacterial leaf spot on ivy () in Iran
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Phenotypic Spectrum of Gastric Adenocarcinoma and Proximal Polyposis of the Stomach (GAPPS) in Denmark: A Case Series Characterizing the First Danish Families With the APC Promotor 1B Variant c.-191T > C
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Cloning, sequencing and expression analysis of the gene encoding the putative RNA polymerase of African Horse sickness virus
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The characterisation of aspects related to the single stranded RNA binding ability of African horsesickness virus nonstructural protein NS2
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A Complex Chromosome Rearrangement Disrupting SYT1 Supports Haploinsufficiency as a Cause of Baker–Gordon Syndrome
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Novel MYH11 Splice Site Variant Causing Exon Skipping in a Family With Thoracic Aortic Aneurysms and Dissections
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Genetic Analysis of Pitt–Hopkins Syndrome Caused by a Novel Splicing Variant (c.1146+3A>T) in the TCF4 Gene
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First Thai Case of Lethal Desbuquois Dysplasia Type I Caused by Novel Compound Heterozygous CANT1 Mutations: Expanding the Molecular Spectrum
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Rare Presentation of Homozygous SLC20A2 Mutations Causing Intra-Arterial Cerebral Vasculopathy and Stroke in Infancy: Case Report and Review of the Literature