Genomic Mosaicism Formed by Somatic Variation in the Aging and Diseased Brain

MIPP-Seq: ultra-sensitive rapid detection and validation of low-frequency mosaic mutations

(2021) Ryan N. Doan et al.   BMC Medical Genomics

Unraveling the features of somatic transposition in the Drosophila intestine

(2021) Katarzyna Siudeja et al.   EMBO JOURNAL

Short antisense oligonucleotides alleviate the pleiotropic toxicity of RNA harboring expanded CGG repeats

(2021) Magdalena Derbis et al.   Nature Communications

The decreased exclusion of nuclear eccDNA: From molecular and subcellular levels to human aging and age-related diseases

(2021) Guo-Hua Qiu et al.   AGEING RESEARCH REVIEWS

Activation of HERV-K(HML-2) disrupts cortical patterning and neuronal differentiation by increasing NTRK3

(2021) Vidya Padmanabhan Nair et al.   Cell Stem Cell

On the wrong DNA track: Molecular mechanisms of repeat-mediated genome instability

(2020) Alexandra N. Khristich et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Restriction Enzyme Based Enriched L1Hs Sequencing (REBELseq): A Scalable Technique for Detection of Ta Subfamily L1Hs in the Human Genome

(2020) Benjamin C. Reiner et al.   G3-Genes Genomes Genetics

Transdifferentiation of Mouse Embryonic Fibroblasts into Dopaminergic Neurons Reactivates LINE-1 Repetitive Elements

(2020) Francesco Della Valle et al.   Stem Cell Reports

Pathogenic mechanisms underlying spinocerebellar ataxia type 1

(2020) Leon Tejwani et al.   CELLULAR AND MOLECULAR LIFE SCIENCES

Extrachromosomal Circular DNA: Current Knowledge and Implications for CNS Aging and Neurodegeneration

(2020) Quratul Ain et al.   INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES

CNS-Derived Blood Exosomes as a Promising Source of Biomarkers: Opportunities and Challenges

(2020) Simon Hornung et al.   Frontiers in Molecular Neuroscience

Mosaic Somatic Gene Recombination as a Potentially Unifying Hypothesis for Alzheimer’s Disease

(2020) Gwendolyn E. Kaeser et al.   Frontiers in Genetics

Patterns of CAG repeat instability in the central nervous system and periphery in Huntington’s disease and in spinocerebellar ataxia type 1

(2020) Ricardo Mouro Pinto et al.   HUMAN MOLECULAR GENETICS

Brain cell somatic gene recombination and its phylogenetic foundations

(2020) Gwendolyn Kaeser et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Parkinson’s disease: etiopathogenesis and treatment

(2020) Joseph Jankovic et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

Reply to: APP gene copy number changes reflect exogenous contamination

(2020) Ming-Hsiang Lee et al.   NATURE

APP gene copy number changes reflect exogenous contamination

(2020) Junho Kim et al.   NATURE

Investigation of Somatic Mutations in Human Brains Targeting Genes Associated With Parkinson's Disease

(2020) Melissa Leija-Salazar et al.   Frontiers in Neurology

Molecular Mechanisms of Neurodegeneration Related to C9orf72 Hexanucleotide Repeat Expansion

(2019) Mirjana Babić Leko et al.   BEHAVIOURAL NEUROLOGY

Detection of Low-Frequency Mutations and Identification of Heat-Induced Artifactual Mutations Using Duplex Sequencing

(2019) Eun Ahn et al.   INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES

ATM orchestrates the DNA-damage response to counter toxic non-homologous end-joining at broken replication forks

(2019) Gabriel Balmus et al.   Nature Communications

Exploring the landscape of focal amplifications in cancer using AmpliconArchitect

(2019) Viraj Deshpande et al.   Nature Communications

Neurons with Complex Karyotypes Are Rare in Aged Human Neocortex

(2019) William D. Chronister et al.   Cell Reports

The use of technical replication for detection of low-level somatic mutations in next-generation sequencing

(2019) Junho Kim et al.   Nature Communications

Motor neuron disease-associated loss of nuclear TDP-43 is linked to DNA double-strand break repair defects

(2019) Joy Mitra et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Ataxia‐telangiectasia: A review of clinical features and molecular pathology

(2019) Parisa Amirifar et al.   PEDIATRIC ALLERGY AND IMMUNOLOGY

Selective vulnerability in α-synucleinopathies

(2019) Javier Alegre-Abarrategui et al.   ACTA NEUROPATHOLOGICA

Somatic mutation that affects transcription factor binding upstream of CD55 in the temporal cortex of a late-onset Alzheimer disease patient

(2019) Hafdis T Helgadottir et al.   HUMAN MOLECULAR GENETICS

Loss of Nuclear TDP-43 Is Associated with Decondensation of LINE Retrotransposons

(2019) Elaine Y. Liu et al.   Cell Reports

Somatic LINE-1 retrotransposition in cortical neurons and non-brain tissues of Rett patients and healthy individuals

(2019) Boxun Zhao et al.   PLoS Genetics

RNA sequence analysis reveals macroscopic somatic clonal expansion across normal tissues

(2019) Keren Yizhak et al.   SCIENCE

Brain somatic mutations observed in Alzheimer’s disease associated with aging and dysregulation of tau phosphorylation

(2019) Jun Sung Park et al.   Nature Communications

Transposable Elements, Inflammation, and Neurological Disease

(2019) Aurian Saleh et al.   Frontiers in Neurology

Antisense oligonucleotide therapeutics in neurodegenerative diseases: the case of polyglutamine disorders

(2019) Ana C Silva et al.   BRAIN

Functional Enhancers Shape Extrachromosomal Oncogene Amplifications

(2019) Andrew R. Morton et al.   CELL

Discovery of autism/intellectual disability somatic mutations in Alzheimer's brains: mutated ADNP cytoskeletal impairments and repair as a case study

(2019) Yanina Ivashko-Pachima et al.   MOLECULAR PSYCHIATRY

Circular ecDNA promotes accessible chromatin and high oncogene expression

(2019) Sihan Wu et al.   NATURE

Postmortem Cortex Samples Identify Distinct Molecular Subtypes of ALS: Retrotransposon Activation, Oxidative Stress, and Activated Glia

(2019) Oliver H. Tam et al.   Cell Reports

Extrachromosomal circular DNA drives oncogenic genome remodeling in neuroblastoma

(2019) Richard P. Koche et al.   NATURE GENETICS

Investigation of somatic CNVs in brains of synucleinopathy cases using targeted SNCA analysis and single cell sequencing

(2019) Diego Perez-Rodriguez et al.   Acta Neuropathologica Communications

NIA-AA Research Framework: Toward a biological definition of Alzheimer's disease

(2018) Clifford R. Jack et al.   Alzheimers & Dementia

Somatic copy number gains of α-synuclein (SNCA) in Parkinson’s disease and multiple system atrophy brains

(2018) Katya Mokretar et al.   BRAIN

A Single-Cell Transcriptome Atlas of the Aging Drosophila Brain

(2018) Kristofer Davie et al.   CELL

Exploring the genetics and non-cell autonomous mechanisms underlying ALS/FTLD

(2018) Hongbo Chen et al.   CELL DEATH AND DIFFERENTIATION

Whole-genome sequencing reveals principles of brain retrotransposition in neurodevelopmental disorders

(2018) Jasmine Jacob-Hirsch et al.   CELL RESEARCH

Transposable elements: genome innovation, chromosome diversity, and centromere conflict

(2018) Savannah J. Klein et al.   CHROMOSOME RESEARCH

Genomic mosaicism in the developing and adult brain

(2018) Suzanne Rohrback et al.   Developmental Neurobiology

Novel applications of array comparative genomic hybridization in molecular diagnostics

(2018) Sau W Cheung et al.   EXPERT REVIEW OF MOLECULAR DIAGNOSTICS

SOX2 expression diminishes with ageing in several tissues in mice and humans

(2018) Estefania Carrasco-Garcia et al.   MECHANISMS OF AGEING AND DEVELOPMENT

Early life experience drives structural variation of neural genomes in mice

(2018) Tracy A. Bedrosian et al.   SCIENCE

Detecting Somatic Mutations in Normal Cells

(2018) Yanmei Dou et al.   TRENDS IN GENETICS

Circular DNA elements of chromosomal origin are common in healthy human somatic tissue

(2018) Henrik Devitt Møller et al.   Nature Communications

Tau Activates Transposable Elements in Alzheimer’s Disease

(2018) Caiwei Guo et al.   Cell Reports

L1 retrotransposition in the soma: a field jumping ahead

(2018) Geoffrey J. Faulkner et al.   Mobile DNA

Increased DNA Copy Number Variation Mosaicism in Elderly Human Brain

(2018) Darine Villela et al.   NEURAL PLASTICITY

Association Between Autophagy and Neurodegenerative Diseases

(2018) Nobuhiro Fujikake et al.   Frontiers in Neuroscience

Frequency and signature of somatic variants in 1461 human brain exomes

(2018) Wei Wei et al.   GENETICS IN MEDICINE

Somatic Signature of Brain-Specific Single Nucleotide Variations in Sporadic Alzheimer's Disease

(2018) Antoni Parcerisas et al.   JOURNAL OF ALZHEIMERS DISEASE

Transcriptional profiling of HERV-K(HML-2) in amyotrophic lateral sclerosis and potential implications for expression of HML-2 proteins

(2018) Jens Mayer et al.   Molecular Neurodegeneration

Submegabase copy number variations arise during cerebral cortical neurogenesis as revealed by single-cell whole-genome sequencing

(2018) Suzanne Rohrback et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Somatic variants in autosomal dominant genes are a rare cause of sporadic Alzheimer's disease

(2018) Gaël Nicolas et al.   Alzheimers & Dementia

Somatic APP gene recombination in Alzheimer’s disease and normal neurons

(2018) Ming-Hsiang Lee et al.   NATURE

High prevalence of focal and multi-focal somatic genetic variants in the human brain

(2018) Michael J. Keogh et al.   Nature Communications

Memory for relations in the short term and the long term after medial temporal lobe damage

(2017) Larry R. Squire   HIPPOCAMPUS

A modifier of Huntington's disease onset at the MLH1 locus

(2017) Jong-Min Lee et al.   HUMAN MOLECULAR GENETICS

Amyotrophic lateral sclerosis

(2017) Michael A van Es et al.   LANCET

Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study

(2017) Davina J Hensman Moss et al.   LANCET NEUROLOGY

Mechanisms and consequences of aneuploidy and chromosome instability in the aging brain

(2017) Grasiella A. Andriani et al.   MECHANISMS OF AGEING AND DEVELOPMENT

PGBD5 promotes site-specific oncogenic mutations in human tumors

(2017) Anton G Henssen et al.   NATURE GENETICS

Early-Onset Alzheimer Disease

(2017) Mario F. Mendez   NEUROLOGIC CLINICS

Aging and neurodegeneration are associated with increased mutations in single human neurons

(2017) Michael A. Lodato et al.   SCIENCE

Different mutational rates and mechanisms in human cells at pregastrulation and neurogenesis

(2017) Taejeong Bae et al.   SCIENCE

Ultrasensitive and high-efficiency screen of de novo low-frequency mutations by o2n-seq

(2017) Kaile Wang et al.   Nature Communications

Disease Mechanisms of C9ORF72 Repeat Expansions

(2017) Tania F. Gendron et al.   Cold Spring Harbor Perspectives in Medicine

DNA repair pathways underlie a common genetic mechanism modulating onset in polyglutamine diseases

(2016) Conceição Bettencourt et al.   ANNALS OF NEUROLOGY

Human endogenous retroviruses: friend or foe?

(2016) Robin A. Weiss   APMIS

From Mendel to epigenetics: History of genetics

(2016) Jean Gayon   COMPTES RENDUS BIOLOGIES

The amyloid hypothesis of Alzheimer's disease at 25 years

(2016) Dennis J Selkoe et al.   EMBO Molecular Medicine

Genetic compendium of 1511 human brains available through the UK Medical Research Council Brain Banks Network Resource

(2016) Michael J. Keogh et al.   GENOME RESEARCH

Assessment of megabase-scale somatic copy number variation using single-cell sequencing

(2016) Kristin A. Knouse et al.   GENOME RESEARCH

Engineered LINE-1 retrotransposition in nondividing human neurons

(2016) Angela Macia et al.   GENOME RESEARCH

The search for true numbers of neurons and glial cells in the human brain: A review of 150 years of cell counting

(2016) Christopher S. von Bartheld et al.   JOURNAL OF COMPARATIVE NEUROLOGY

L1-associated genomic regions are deleted in somatic cells of the healthy human brain

(2016) Jennifer A Erwin et al.   NATURE NEUROSCIENCE

Genome-wide quantification of rare somatic mutations in normal human tissues using massively parallel sequencing

(2016) Margaret L. Hoang et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Discovery of unfixed endogenous retrovirus insertions in diverse human populations

(2016) Julia Halo Wildschutte et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Retrotransposons as regulators of gene expression

(2016) R. A. Elbarbary et al.   SCIENCE

Resolving rates of mutation in the brain using single-neuron genomics

(2016) Gilad D Evrony et al.   eLife

Restricting retrotransposons: a review

(2016) John L. Goodier   Mobile DNA

Regional mosaic genomic heterogeneity in the elderly and in Alzheimer’s disease as a correlate of neuronal vulnerability

(2015) Thomas Arendt et al.   ACTA NEUROPATHOLOGICA

On the identification of low allele frequency mosaic mutations in the brains of Alzheimer's disease patients

(2015) Carlo Sala Frigerio et al.   Alzheimers & Dementia

Ubiquitous L1 Mosaicism in Hippocampal Neurons

(2015) Kyle R. Upton et al.   CELL

Extensive size variability of the GGGGCC expansion in C9orf72 in both neuronal and non-neuronal tissues in 18 patients with ALS or FTD

(2015) Angelica Nordin et al.   HUMAN MOLECULAR GENETICS

The Roles of the Stem Cell-Controlling Sox2 Transcription Factor: from Neuroectoderm Development to Alzheimer’s Disease?

(2015) Golmaryam Sarlak et al.   MOLECULAR NEUROBIOLOGY

Genomic integrity and the ageing brain

(2015) Hei-man Chow et al.   NATURE REVIEWS NEUROSCIENCE

A genetic cause of Alzheimer disease: mechanistic insights from Down syndrome

(2015) Frances K. Wiseman et al.   NATURE REVIEWS NEUROSCIENCE

The current state of eukaryotic DNA base damage and repair

(2015) Nicholas C. Bauer et al.   NUCLEIC ACIDS RESEARCH

Somatic mutation in single human neurons tracks developmental and transcriptional history

(2015) M. A. Lodato et al.   SCIENCE

Human endogenous retrovirus-K contributes to motor neuron disease

(2015) Wenxue Li et al.   Science Translational Medicine

Genomic mosaicism with increased amyloid precursor protein (APP) gene copy number in single neurons from sporadic Alzheimer's disease brains

(2015) Diane M Bushman et al.   eLife

RNA Sequence Analysis of Human Huntington Disease Brain Reveals an Extensive Increase in Inflammatory and Developmental Gene Expression

(2015) Adam Labadorf et al.   PLoS One

Analysis of Parkinson's disease brain-derived DNA for alpha-synuclein coding somatic mutations

(2014) Christos Proukakis et al.   MOVEMENT DISORDERS

Detecting ultralow-frequency mutations by Duplex Sequencing

(2014) Scott R Kennedy et al.   Nature Protocols

DNA Damage and Its Links to Neurodegeneration

(2014) Ram Madabhushi et al.   NEURON

Potential for genomic instability associated with retrotranspositionally-incompetent L1 loci

(2014) Kristine J. Kines et al.   NUCLEIC ACIDS RESEARCH

Single cell sequencing reveals low levels of aneuploidy across mammalian tissues

(2014) Kristin A. Knouse et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

A Brief History of Epigenetics

(2014) G. Felsenfeld   Cold Spring Harbor Perspectives in Biology

Processed pseudogenes acquired somatically during cancer development

(2014) Susanna L. Cooke et al.   Nature Communications

Autophagy supports genomic stability by degrading retrotransposon RNA

(2014) Huishan Guo et al.   Nature Communications

Single-Cell, Genome-wide Sequencing Identifies Clonal Somatic Copy-Number Variation in the Human Brain

(2014) Xuyu Cai et al.   Cell Reports

X chromosome aneuploidy in the Alzheimer’s disease brain

(2014) Yuri B Yurov et al.   Molecular Cytogenetics

Characterization of the repeat expansion size in C9orf72 in amyotrophic lateral sclerosis and frontotemporal dementia

(2013) O. Dols-Icardo et al.   HUMAN MOLECULAR GENETICS

The Role of Transposable Elements in Health and Diseases of the Central Nervous System

(2013) M. T. Reilly et al.   JOURNAL OF NEUROSCIENCE

Simultaneous and independent detection of C9ORF72 alleles with low and high number of GGGGCC repeats using an optimised protocol of Southern blot hybridisation

(2013) Vladimir L Buchman et al.   Molecular Neurodegeneration

Rare autosomal copy number variations in early-onset familial Alzheimer’s disease

(2013) B V Hooli et al.   MOLECULAR PSYCHIATRY

Somatic alpha-synuclein mutations in Parkinson's disease: Hypothesis and preliminary data

(2013) Christos Proukakis et al.   MOVEMENT DISORDERS

Massively parallel polymerase cloning and genome sequencing of single cells using nanoliter microwells

(2013) Jeff Gole et al.   NATURE BIOTECHNOLOGY

Mosaicism of alpha-synuclein gene rearrangements: Report of two unrelated cases of early-onset parkinsonism

(2013) C. Perandones et al.   PARKINSONISM & RELATED DISORDERS

Mosaic Copy Number Variation in Human Neurons

(2013) M. J. McConnell et al.   SCIENCE

The genomically mosaic brain: Aneuploidy and more in neural diversity and disease

(2013) Diane M. Bushman et al.   SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY

MSH3 Polymorphisms and Protein Levels Affect CAG Repeat Instability in Huntington's Disease Mice

(2013) Stéphanie Tomé et al.   PLoS Genetics

Cell division promotes efficient retrotransposition in a stable L1 reporter cell line

(2013) Yi Xie et al.   Mobile DNA

What does complement do in Alzheimer’s disease? Old molecules with new insights

(2013) Yong Shen et al.   Translational Neurodegeneration

Changes in neuronal DNA content variation in the human brain during aging

(2012) Hans-Georg Fischer et al.   AGING CELL

Single-Neuron Sequencing Analysis of L1 Retrotransposition and Somatic Mutation in the Human Brain

(2012) Gilad D. Evrony et al.   CELL

How do C9ORF72 repeat expansions cause amyotrophic lateral sclerosis and frontotemporal dementia

(2012) Marka van Blitterswijk et al.   CURRENT OPINION IN NEUROLOGY

A genome-wide analysis of common fragile sites: What features determine chromosomal instability in the human genome?

(2012) Arkarachai Fungtammasan et al.   GENOME RESEARCH

Aneuploid Cells Are Differentially Susceptible to Caspase-Mediated Death during Embryonic Cerebral Cortical Development

(2012) S. E. Peterson et al.   JOURNAL OF NEUROSCIENCE

SINE Retrotransposons Cause Epigenetic Reprogramming of Adjacent Gene Promoters

(2012) M. R. H. Estecio et al.   MOLECULAR CANCER RESEARCH

Performance comparison of benchtop high-throughput sequencing platforms

(2012) Nicholas J Loman et al.   NATURE BIOTECHNOLOGY

David Hubel and Torsten Wiesel

(2012) David Hubel et al.   NEURON

Transposable Elements in TDP-43-Mediated Neurodegenerative Disorders

(2012) Wanhe Li et al.   PLoS One

The remarkable, yet not extraordinary, human brain as a scaled-up primate brain and its associated cost

(2012) S. Herculano-Houzel   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Extrachromosomal MicroDNAs and Chromosomal Microdeletions in Normal Tissues

(2012) Y. Shibata et al.   SCIENCE

ATM and the Molecular Pathogenesis of Ataxia Telangiectasia

(2011) Peter J. McKinnon   Annual Review of Pathology-Mechanisms of Disease

Looking for differences in copy number between blood and brain in sporadic amyotrophic lateral sclerosis

(2011) Roger Pamphlett et al.   MUSCLE & NERVE

Somatic retrotransposition alters the genetic landscape of the human brain

(2011) J. Kenneth Baillie et al.   NATURE

An approach to finding brain-situated mutations in sporadic Parkinson's disease

(2011) Roger Pamphlett et al.   PARKINSONISM & RELATED DISORDERS

Ataxia telangiectasia mutated (ATM) modulates long interspersed element-1 (L1) retrotransposition in human neural stem cells

(2011) N. G. Coufal et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

TDP-43 functions and pathogenic mechanisms implicated in TDP-43 proteinopathies

(2011) Todd J. Cohen et al.   TRENDS IN MOLECULAR MEDICINE

Identification of active loci of a human endogenous retrovirus in neurons of patients with amyotrophic lateral sclerosis

(2010) Renée Douville et al.   ANNALS OF NEUROLOGY

Neuronal DNA content variation (DCV) with regional and individual differences in the human brain

(2010) Jurjen W. Westra et al.   JOURNAL OF COMPARATIVE NEUROLOGY

L1 retrotransposition in neurons is modulated by MeCP2

(2010) Alysson R. Muotri et al.   NATURE

Somatic expansion of the Huntington's disease CAG repeat in the brain is associated with an earlier age of disease onset

(2009) Meera Swami et al.   HUMAN MOLECULAR GENETICS

Increased chromosome instability dramatically disrupts neural genome integrity and mediates cerebellar degeneration in the ataxia-telangiectasia brain

(2009) Ivan Y. Iourov et al.   HUMAN MOLECULAR GENETICS

L1 retrotransposition in human neural progenitor cells

(2009) Nicole G. Coufal et al.   NATURE

Wnt-mediated activation of NeuroD1 and retro-elements during adult neurogenesis

(2009) Tomoko Kuwabara et al.   NATURE NEUROSCIENCE

The impact of retrotransposons on human genome evolution

(2009) Richard Cordaux et al.   NATURE REVIEWS GENETICS

Aneuploidy in the normal, Alzheimer's disease and ataxia-telangiectasia brain: Differential expression and pathological meaning

(2009) Ivan Y. Iourov et al.   NEUROBIOLOGY OF DISEASE

A Reevaluation of Tetraploidy in the Alzheimer’s Disease Brain

(2009) Jurjen W. Westra et al.   Neurodegenerative Diseases

The Role of Copy Number Variation in Susceptibility to Amyotrophic Lateral Sclerosis: Genome-Wide Association Study and Comparison with Published Loci

(2009) Louise V. Wain et al.   PLoS One

Somatic evolutionary genomics: Mutations during development cause highly variable genetic mosaicism with risk of cancer and neurodegeneration

(2009) S. A. Frank   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Identification of candidate genes for sporadic amyotrophic lateral sclerosis by array comparative genomic hybridization

(2008) Sarah A. Shoichet et al.   Amyotrophic Lateral Sclerosis

Analysis of genome-wide copy number variation in Irish and Dutch ALS populations

(2008) S. Cronin et al.   HUMAN MOLECULAR GENETICS

Somatic mosaicism for copy number variation in differentiated human tissues

(2008) Arkadiusz Piotrowski et al.   HUMAN MUTATION

Transcription destabilizes triplet repeats

(2008) Yunfu Lin et al.   MOLECULAR CARCINOGENESIS

Quantification of reverse transcriptase in ALS and elimination of a novel retroviral candidate

(2008) A. L. McCormick et al.   NEUROLOGY