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Single-cell whole-genome sequencing reveals the functional landscape of somatic mutations in B lymphocytes across the human lifespan

Proceedings of the National Academy of Sciences - PNAS, 2019-04, Vol.116 (18), p.9014-9019

2019

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Somatic mutation burden in relation to aging and functional life span: implications for cellular reprogramming and rejuvenation

Current opinion in genetics & development, 2023-12, Vol.83, p.102132-102132, Article 102132

2023

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Accurate identification of single-nucleotide variants in whole-genome-amplified single cells

Nature methods, 2017-05, Vol.14 (5), p.491

2017

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A note on buyers' behavior in auctions with an outside option

Games, 2020-09, Vol.11 (3), p.1-9

Maslov, Alexander

2020

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SomaMutDB: a database of somatic mutations in normal human tissues

Nucleic acids research, 2022-01, Vol.50 (D1), p.D1100

2022

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Analyzing somatic mutations by single-cell whole-genome sequencing

Nature protocols, 2024-02, Vol.19 (2), p.487-516

2024

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Transcriptional profiling reveals ataxia telangiectasia mutated pathways regulate joint copper and arsenic toxicity for hepatic metalloplasia and anti-cancer therapies

Life sciences (1973), 2022-09, Vol.305, p.120787-120787, Article 120787

2022

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Single-cell analysis of somatic mutations in human bronchial epithelial cells in relation to aging and smoking

Nature genetics, 2022-04, Vol.54 (4), p.492-498

2022

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Genome instability, cancer and aging

Biochimica et biophysica acta, 2009-10, Vol.1790 (10), p.963-969

2009

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Single-cell analysis of somatic mutation burden in mammary epithelial cells of pathogenic BRCA1/2 mutation carriers

The Journal of clinical investigation, 2022-03, Vol.132 (5), p.1-6

2022

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Neural Stem Cell Detection, Characterization, and Age-Related Changes in the Subventricular Zone of Mice

The Journal of neuroscience, 2004-02, Vol.24 (7), p.1726-1733

2004

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FOXO3a acts to suppress DNA double‐strand break‐induced mutations

Aging cell, 2020-09, Vol.19 (9), p.e13184-n/a

2020

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Controlled induction of DNA double-strand breaks in the mouse liver induces features of tissue ageing

Nature communications, 2015-04, Vol.6 (1), p.6790, Article 6790

2015

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Whole Chromosome Instability induces senescence and promotes SASP

Scientific reports, 2016-10, Vol.6 (1), p.35218-35218, Article 35218

2016

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Mitigating age-related somatic mutation burden

Trends in molecular medicine, 2023-07, Vol.29 (7), p.530-540

2023

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Cervical and Vaginal Microbiomes in Early Miscarriages and Ongoing Pregnancy with and without Dydrogesterone Usage

International journal of molecular sciences, 2023-09, Vol.24 (18), p.13836

2023

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Age‐related telomere attrition causes aberrant gene expression in sub‐telomeric regions

Aging cell, 2021-06, Vol.20 (6), p.e13357-n/a

2021

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Fast mitochondrial DNA isolation from mammalian cells for next-generation sequencing

BioTechniques, 2013-09, Vol.55 (3), p.133-136

2013

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High-throughput sequencing in mutation detection: A new generation of genotoxicity tests?

Mutation research, 2015-06, Vol.776, p.136

2015

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Bleomycin-induced genome structural variations in normal, non-tumor cells

Scientific reports, 2018-11, Vol.8 (1), p.16523-7, Article 16523

2018

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Bertrand Duopoly in Online Consumer-to-Consumer Markets

Review of industrial organization, 2023-08, Vol.63 (1), p.97-109

Maslov, Alexander

2023

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Assessing Wood and Soil Carbon Losses from a Forest-Peat Fire in the Boreo-Nemoral Zone

Forests, 2021-07, Vol.12 (7), p.880

2021

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Maintenance of genome sequence integrity in long- and short-lived rodent species

Science advances, 2021-10, Vol.7 (44), p.eabj3284

2021

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Single-molecule, quantitative detection of low-abundance somatic mutations by high-throughput sequencing

Science advances, 2022-04, Vol.8 (14), p.eabm3259-eabm3259

2022

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Quantitative detection of low-abundance somatic structural variants in normal cells by high-throughput sequencing

Nature methods, 2016-07, Vol.13 (7), p.584

2016

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Single-cell whole-genome sequencing reveals the functional landscape of somatic mutations in B lymphocytes across the human lifespan

Somatic mutation burden in relation to aging and functional life span: implications for cellular reprogramming and rejuvenation

Accurate identification of single-nucleotide variants in whole-genome-amplified single cells

A note on buyers' behavior in auctions with an outside option

SomaMutDB: a database of somatic mutations in normal human tissues

Analyzing somatic mutations by single-cell whole-genome sequencing

Transcriptional profiling reveals ataxia telangiectasia mutated pathways regulate joint copper and arsenic toxicity for hepatic metalloplasia and anti-cancer therapies

Single-cell analysis of somatic mutations in human bronchial epithelial cells in relation to aging and smoking

Genome instability, cancer and aging

Single-cell analysis of somatic mutation burden in mammary epithelial cells of pathogenic BRCA1/2 mutation carriers

Neural Stem Cell Detection, Characterization, and Age-Related Changes in the Subventricular Zone of Mice

FOXO3a acts to suppress DNA double‐strand break‐induced mutations

Controlled induction of DNA double-strand breaks in the mouse liver induces features of tissue ageing

Whole Chromosome Instability induces senescence and promotes SASP

Mitigating age-related somatic mutation burden

Cervical and Vaginal Microbiomes in Early Miscarriages and Ongoing Pregnancy with and without Dydrogesterone Usage

Age‐related telomere attrition causes aberrant gene expression in sub‐telomeric regions

Fast mitochondrial DNA isolation from mammalian cells for next-generation sequencing

High-throughput sequencing in mutation detection: A new generation of genotoxicity tests?

Bleomycin-induced genome structural variations in normal, non-tumor cells

Bertrand Duopoly in Online Consumer-to-Consumer Markets

Assessing Wood and Soil Carbon Losses from a Forest-Peat Fire in the Boreo-Nemoral Zone

Maintenance of genome sequence integrity in long- and short-lived rodent species

Single-molecule, quantitative detection of low-abundance somatic mutations by high-throughput sequencing

Quantitative detection of low-abundance somatic structural variants in normal cells by high-throughput sequencing

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