Warning SINEs: Alu elements, evolution of the human brain, and the spectrum of neurological disease

Tau burden and the functional connectome in Alzheimer’s disease and progressive supranuclear palsy

(2018) Thomas E Cope et al.   BRAIN

Contribution of transposable elements and distal enhancers to evolution of human-specific features of interphase chromatin architecture in embryonic stem cells

(2018) Gennadi V. Glinsky   CHROMOSOME RESEARCH

Mitochondria and Mitochondrial Cascades in Alzheimer’s Disease

(2018) Russell H. Swerdlow   JOURNAL OF ALZHEIMERS DISEASE

Genes Linking Mitochondrial Function, Cognitive Impairment and Depression are Associated with Endophenotypes Serving Precision Medicine

(2018) Peter Petschner et al.   NEUROSCIENCE

Regulation of mitochondrial dynamics in astrocytes: Mechanisms, consequences, and unknowns

(2017) Joshua G. Jackson et al.   GLIA

Identification of an atypical microdeletion generating the RNF135-SUZ12 chimeric gene and causing a position effect in an NF1 patient with overgrowth

(2017) Luca Ferrari et al.   HUMAN GENETICS

ADAR RNA editing in human disease; more to it than meets the I

(2017) Angela Gallo et al.   HUMAN GENETICS

Repetitive element transcripts are elevated in the brain of C9orf72 ALS/FTLD patients

(2017) Mercedes Prudencio et al.   HUMAN MOLECULAR GENETICS

Adenosine Deaminase That Acts on RNA 3 (ADAR3) Binding to Glutamate Receptor Subunit B Pre-mRNA Inhibits RNA Editing in Glioblastoma

(2017) Eimile Oakes et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Global, regional, and national burden of neurological disorders during 1990–2015: a systematic analysis for the Global Burden of Disease Study 2015

(2017) Valery L Feigin et al.   LANCET NEUROLOGY

Multiple Innovations in Genetic and Epigenetic Mechanisms Cooperate to Underpin Human Brain Evolution

(2017) Mainá Bitar et al.   MOLECULAR BIOLOGY AND EVOLUTION

Overexpression of LINE-1 Retrotransposons in Autism Brain

(2017) Svitlana Shpyleva et al.   MOLECULAR NEUROBIOLOGY

Dynamic landscape and regulation of RNA editing in mammals

(2017) Meng How Tan et al.   NATURE

Deletion of exons 9 and 10 of the Presenilin 1 gene in a patient with Early-onset Alzheimer Disease generates longer amyloid seeds

(2017) Kilan Le Guennec et al.   NEUROBIOLOGY OF DISEASE

Association of Serotonin Transporter Gene AluJb Methylation with Major Depression, Amygdala Responsiveness, 5-HTTLPR/rs25531 Polymorphism, and Stress

(2017) Ilona Schneider et al.   NEUROPSYCHOPHARMACOLOGY

Genetic variants specific to aging-related verbal memory: Insights from GWASs in a population-based cohort

(2017) Thalida E. Arpawong et al.   PLoS One

Structural variants caused byAluinsertions are associated with risks for many human diseases

(2017) Lindsay M. Payer et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

A to I editing in disease is not fake news

(2017) Prajakta Bajad et al.   RNA Biology

Super-lncRNAs: identification of lncRNAs that target super-enhancers via RNA:DNA:DNA triplex formation

(2017) Benjamin Soibam   RNA

Single-cell transcriptomics reveals specific RNA editing signatures in the human brain

(2017) Ernesto Picardi et al.   RNA

An emerging role for mitochondrial dynamics in schizophrenia

(2017) Kyle H. Flippo et al.   SCHIZOPHRENIA RESEARCH

ALU ternative Regulation for Gene Expression

(2017) Ling-Ling Chen et al.   TRENDS IN CELL BIOLOGY

Mapping Neurodegenerative Disease Onset and Progression

(2017) William W. Seeley   Cold Spring Harbor Perspectives in Biology

Analysis of RP2 and RPGR Mutations in Five X-Linked Chinese Families with Retinitis Pigmentosa

(2017) Jingjing Jiang et al.   Scientific Reports

The association between Alu hypomethylation and severity of type 2 diabetes mellitus

(2017) Jirapan Thongsroy et al.   Clinical Epigenetics

A Multilayered Control of the Human Survival Motor Neuron Gene Expression by Alu Elements

(2017) Eric W. Ottesen et al.   Frontiers in Microbiology

The Alzheimer's Disease Mitochondrial Cascade Hypothesis

(2017) Russell H. Swerdlow et al.   JOURNAL OF ALZHEIMERS DISEASE

Abnormalities in A-to-I RNA editing patterns in CNS injuries correlate with dynamic changes in cell type composition

(2017) Nurit Gal-Mark et al.   Scientific Reports

Mutations underlying Episodic Ataxia type-1 antagonize Kv1.1 RNA editing

(2017) Elizabeth A. Ferrick-Kiddie et al.   Scientific Reports

Therapeutic strategies for the treatment of tauopathies: Hopes and challenges

(2016) Mansi R. Khanna et al.   Alzheimers & Dementia

Understanding the genetics of APOE and TOMM40 and role of mitochondrial structure and function in clinical pharmacology of Alzheimer's disease

(2016) Allen Roses et al.   Alzheimers & Dementia

Repetitive element hypermethylation in multiple sclerosis patients

(2016) K. Y. Neven et al.   BMC GENETICS

How retrotransposons shape genome regulation

(2016) Paolo Mita et al.   CURRENT OPINION IN GENETICS & DEVELOPMENT

Structural variants can be more informative for disease diagnostics, prognostics and translation than current SNP mapping and exon sequencing

(2016) Allen D. Roses et al.   Expert Opinion on Drug Metabolism & Toxicology

Network analysis of mitonuclear GWAS reveals functional networks and tissue expression profiles of disease-associated genes

(2016) Simon C. Johnson et al.   HUMAN GENETICS

The Activity of Menkes Disease Protein ATP7A Is Essential for Redox Balance in Mitochondria

(2016) Ashima Bhattacharjee et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Alu RNA accumulation in hyperglycemia augments oxidative stress and impairs eNOS and SOD2 expression in endothelial cells

(2016) Wei Wang et al.   MOLECULAR AND CELLULAR ENDOCRINOLOGY

Regulatory Role of Circular RNAs and Neurological Disorders

(2016) Gabriele Floris et al.   MOLECULAR NEUROBIOLOGY

A multi-modal parcellation of human cerebral cortex

(2016) Matthew F. Glasser et al.   NATURE

Dynamic regulation of RNA editing in human brain development and disease

(2016) Taeyoung Hwang et al.   NATURE NEUROSCIENCE

Retrotransposons jump into alternative-splicing regulation via a long noncoding RNA

(2016) Reini F Luco   NATURE STRUCTURAL & MOLECULAR BIOLOGY

A TOMM40 poly-T variant modulates gene expression and is associated with vocabulary ability and decline in nonpathologic aging

(2016) A. Payton et al.   NEUROBIOLOGY OF AGING

REDIportal: a comprehensive database of A-to-I RNA editing events in humans

(2016) Ernesto Picardi et al.   NUCLEIC ACIDS RESEARCH

Increased complexity of circRNA expression during species evolution

(2016) Rui Dong et al.   RNA Biology

One brain, many genomes

(2016) G. D. Evrony   SCIENCE

Retrotransposons as regulators of gene expression

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

RNA Editing: A Contributor to Neuronal Dynamics in the Mammalian Brain

(2016) Mikaela Behm et al.   TRENDS IN GENETICS

Circular RNAs in Brain and Other Tissues: A Functional Enigma

(2016) Wei Chen et al.   TRENDS IN NEUROSCIENCES

The dynamic genome: transposons and environmental adaptation in the nervous system

(2016) Hannah E Lapp et al.   Epigenomics

Retrotransposons jump into alternative-splicing regulation via a long noncoding RNA

(2016) Reini F Luco   NATURE STRUCTURAL & MOLECULAR BIOLOGY

Environment-driven somatic mosaicism in brain disorders

(2016) Tracy A. Bedrosian et al.   Genome Medicine

Staufen1 Regulates Multiple Alternative Splicing Events either Positively or Negatively in DM1 Indicating Its Role as a Disease Modifier

(2016) Emma Bondy-Chorney et al.   PLoS Genetics

Restricting retrotransposons: a review

(2016) John L. Goodier   Mobile DNA

Roles for retrotransposon insertions in human disease

(2016) Dustin C. Hancks et al.   Mobile DNA

Region-specific alterations of A-to-I RNA editing of serotonin 2c receptor in the cortex of suicides with major depression

(2016) D Weissmann et al.   Translational Psychiatry

Epigenetics and aging

(2016) S. Pal et al.   Science Advances

Type 3 Diabetes: Cross Talk between Differentially Regulated Proteins of Type 2 Diabetes Mellitus and Alzheimer’s Disease

(2016) Khyati Mittal et al.   Scientific Reports

Immunoinflammatory diseases of the central nervous system - the tale of two cytokines

(2015) M J Hofer et al.   BRITISH JOURNAL OF PHARMACOLOGY

Wilson's disease caused by alternative splicing and Alu exonization due to a homozygous 3039-bp deletion spanning from intron 1 to exon 2 of the ATP7B gene

(2015) Eva Mameli et al.   GENE

The role of combined SNV and CNV burden in patients with distal symmetric polyneuropathy

(2015) Davut Pehlivan et al.   GENETICS IN MEDICINE

Alu-mediated diverse and complex pathogenic copy-number variants within human chromosome 17 at p13.3

(2015) Shen Gu et al.   HUMAN MOLECULAR GENETICS

Evidence of Distinct Channel Conformations and Substrate Binding Affinities for the Mitochondrial Outer Membrane Protein Translocase Pore Tom40

(2015) Adam J. Kuszak et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Circular RNAs in the Mammalian Brain Are Highly Abundant, Conserved, and Dynamically Expressed

(2015) Agnieszka Rybak-Wolf et al.   MOLECULAR CELL

Tau missorting and spastin-induced microtubule disruption in neurodegeneration: Alzheimer Disease and Hereditary Spastic Paraplegia

(2015) Hans Zempel et al.   Molecular Neurodegeneration

The case for rejecting the amyloid cascade hypothesis

(2015) Karl Herrup   NATURE NEUROSCIENCE

A-to-I editing of coding and non-coding RNAs by ADARs

(2015) Kazuko Nishikura   NATURE REVIEWS MOLECULAR CELL BIOLOGY

Intragenic deletions ofALDH7A1in pyridoxine-dependent epilepsy caused byAlu-Alurecombination

(2015) Heather C. Mefford et al.   NEUROLOGY

MitoCarta2.0: an updated inventory of mammalian mitochondrial proteins

(2015) Sarah E. Calvo et al.   NUCLEIC ACIDS RESEARCH

Aberrant alternative splicing pattern of ADAR2 downregulates adenosine-to-inosine editing in glioma

(2015) ZHAOHUI LI et al.   ONCOLOGY REPORTS

Reduced levels of protein recoding by A-to-I RNA editing in Alzheimer's disease

(2015) Khen Khermesh et al.   RNA

Molecular architecture of the active mitochondrial protein gate

(2015) T. Shiota et al.   SCIENCE

Novel PRD-like homeodomain transcription factors and retrotransposon elements in early human development

(2015) Virpi Töhönen et al.   Nature Communications

Profiling RNA editing in human tissues: towards the inosinome Atlas

(2015) Ernesto Picardi et al.   Scientific Reports

Brain metabolic stress and neuroinflammation at the basis of cognitive impairment in Alzheimer’s disease

(2015) Fernanda G. De Felice et al.   Frontiers in Aging Neuroscience

Alu Elements as Novel Regulators of Gene Expression in Type 1 Diabetes Susceptibility Genes?

(2015) Simranjeet Kaur et al.   Genes

The Evidence for Increased L1 Activity in the Site of Human Adult Brain Neurogenesis

(2015) Alexey A. Kurnosov et al.   PLoS One

Positive correlation between ADAR expression and its targets suggests a complex regulation mediated by RNA editing in the human brain

(2015) Noa Liscovitch et al.   RNA Biology

The Alu-Rich Genomic Architecture of SPAST Predisposes to Diverse and Functionally Distinct Disease-Associated CNV Alleles

(2014) Philip M. Boone et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Brain metabolic dysfunction at the core of Alzheimer's disease

(2014) Suzanne M. de la Monte et al.   BIOCHEMICAL PHARMACOLOGY

The Protein Import Machinery of Mitochondria—A Regulatory Hub in Metabolism, Stress, and Disease

(2014) Angelika B. Harbauer et al.   Cell Metabolism

Aberrant signature methylome by DNMT1 hot spot mutation in hereditary sensory and autonomic neuropathy 1E

(2014) Zhifu Sun et al.   Epigenetics

The TOMM40 poly-T rs10524523 variant is associated with cognitive performance among non-demented elderly with type 2 diabetes

(2014) Lior Greenbaum et al.   EUROPEAN NEUROPSYCHOPHARMACOLOGY

Sequence-Level Mechanisms of Human Epigenome Evolution

(2014) James G.D. Prendergast et al.   Genome Biology and Evolution

A biochemical landscape of A-to-I RNA editing in the human brain transcriptome

(2014) M. Sakurai et al.   GENOME RESEARCH

Serotonin transporter gene methylation is associated with hippocampal gray matter volume

(2014) Udo Dannlowski et al.   HUMAN BRAIN MAPPING

Deletions in the 3′ Part of theNFIXGene Including a Recurrent Alu-Mediated Deletion of Exon 6 and 7 Account for Previously Unexplained Cases of Marshall-Smith Syndrome

(2014) Denny Schanze et al.   HUMAN MUTATION

DJ-1 Is a Copper Chaperone Acting on SOD1 Activation

(2014) Stefania Girotto et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Mobile DNA elements in the generation of diversity and complexity in the brain

(2014) Jennifer A. Erwin et al.   NATURE REVIEWS NEUROSCIENCE

Alzheimer's disease susceptibility genes APOE and TOMM40, and brain white matter integrity in the Lothian Birth Cohort 1936

(2014) Donald M. Lyall et al.   NEUROBIOLOGY OF AGING

Characterization of Alu and recombination-associated motifs mediating a large homozygous SPG7 gene rearrangement causing hereditary spastic paraplegia

(2014) Eva López et al.   NEUROGENETICS

Increased L1 Retrotransposition in the Neuronal Genome in Schizophrenia

(2014) Miki Bundo et al.   NEURON

The RNA-centred view of the synapse: non-coding RNAs and synaptic plasticity

(2014) N. R. Smalheiser   PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES

Effects of GWAS-Associated Genetic Variants on lncRNAs within IBD and T1D Candidate Loci

(2014) Aashiq H. Mirza et al.   PLoS One

DICER1/AluRNA dysmetabolism induces Caspase-8–mediated cell death in age-related macular degeneration

(2014) Younghee Kim et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Stress and the dynamic genome: Steroids, epigenetics, and the transposome: Fig. 1.

(2014) Richard G. Hunter et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

A role of ADAR2 and RNA editing of glutamate receptors in mood disorders and schizophrenia

(2014) Mie Kubota-Sakashita et al.   Molecular Brain

Alu elements shape the primate transcriptome by cis-regulation of RNA editing

(2014) Chammiran Daniel et al.   GENOME BIOLOGY

Alport syndrome caused by aCOL4A5deletion and exonization of an adjacentAluY

(2014) Kandai Nozu et al.   Molecular Genetics & Genomic Medicine

A-to-I RNA editing occurs at over a hundred million genomic sites, located in a majority of human genes

(2013) L. Bazak et al.   GENOME RESEARCH

The mitochondrial solute carrier SLC25A5 at Xq24 is a novel candidate gene for non-syndromic intellectual disability

(2013) Joke Vandewalle et al.   HUMAN GENETICS

The ALS disease-associated mutant TDP-43 impairs mitochondrial dynamics and function in motor neurons

(2013) Wenzhang Wang et al.   HUMAN MOLECULAR GENETICS

Deciphering the functions and regulation of brain-enriched A-to-I RNA editing

(2013) Jin Billy Li et al.   NATURE NEUROSCIENCE

Functional regulation of Alu element of human angiotensin-converting enzyme gene in neuron cells

(2013) Shyh-Jong Wu et al.   NEUROBIOLOGY OF AGING

Aberrant Schwann Cell Lipid Metabolism Linked to Mitochondrial Deficits Leads to Axon Degeneration and Neuropathy

(2013) Andreu Viader et al.   NEURON

Hypomethylation of Alu Elements in Post-Menopausal Women with Osteoporosis

(2013) Pornrutsami Jintaridth et al.   PLoS One

Rates and patterns of great ape retrotransposition

(2013) F. Hormozdiari et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Network hubs in the human brain

(2013) Martijn P. van den Heuvel et al.   TRENDS IN COGNITIVE SCIENCES

Mitochondrial Trafficking in Neurons

(2013) T. L. Schwarz   Cold Spring Harbor Perspectives in Biology

Alu elements: an intrinsic source of human genome instability

(2013) Catherine Ade et al.   Current Opinion in Virology

DICER1 Loss and Alu RNA Induce Age-Related Macular Degeneration via the NLRP3 Inflammasome and MyD88

(2012) Valeria Tarallo et al.   CELL

Mitochondrial quality control: a matter of life and death for neurons

(2012) Elena I Rugarli et al.   EMBO JOURNAL

Alu-mediated deletion of SOX10 regulatory elements in Waardenburg syndrome type 4

(2012) Nadége Bondurand et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Alu elements mediate large SPG11 gene rearrangements: further spatacsin mutations

(2012) Maria Conceição Pereira et al.   GENETICS IN MEDICINE

The bonobo genome compared with the chimpanzee and human genomes

(2012) Kay Prüfer et al.   NATURE

Topological domains in mammalian genomes identified by analysis of chromatin interactions

(2012) Jesse R. Dixon et al.   NATURE

Mutations in ADAR1 cause Aicardi-Goutières syndrome associated with a type I interferon signature

(2012) Gillian I Rice et al.   NATURE GENETICS

Transposable Elements in TDP-43-Mediated Neurodegenerative Disorders

(2012) Wanhe Li et al.   PLoS One

Circular RNAs are abundant, conserved, and associated with ALU repeats

(2012) W. R. Jeck et al.   RNA

The essential role of AMPA receptor GluR2 subunit RNA editing in the normal and diseased brain

(2012) Amanda Wright et al.   Frontiers in Molecular Neuroscience

The diagnosis of dementia due to Alzheimer’s disease: Recommendations from the National Institute on Aging-Alzheimer’s Association workgroups on diagnostic guidelines for Alzheimer's disease

(2011) Guy M. McKhann et al.   Alzheimers & Dementia

A mitochondrial etiology of Alzheimer and Parkinson disease

(2011) Pinar Coskun et al.   BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS

Genetic and epigenetic variations contributed by Alu retrotransposition

(2011) Alexandre de Andrade et al.   BMC GENOMICS

Abnormal tau, mitochondrial dysfunction, impaired axonal transport of mitochondria, and synaptic deprivation in Alzheimer's disease

(2011) P. Hemachandra Reddy   BRAIN RESEARCH

Contributions of Brain Insulin Resistance and Deficiency in Amyloid-Related Neurodegeneration in Alzheimerʼs Disease

(2011) Suzanne M. de la Monte   DRUGS

Novel Alu retrotransposon insertion leading to Alström syndrome

(2011) Mustafa Taşkesen et al.   HUMAN GENETICS

Detection of large gene rearrangements in X-linked genes by dosage analysis: identification of novel α-galactosidase A (GLA) deletions causing Fabry disease

(2011) Robert Dobrovolny et al.   HUMAN MUTATION

Functional Refolding and Characterization of Two Tom40 Isoforms from Human Mitochondria

(2011) Frauke Mager et al.   JOURNAL OF MEMBRANE BIOLOGY

Schwann Cell Mitochondrial Metabolism Supports Long-Term Axonal Survival and Peripheral Nerve Function

(2011) A. Viader et al.   JOURNAL OF NEUROSCIENCE

DICER1 deficit induces Alu RNA toxicity in age-related macular degeneration

(2011) Hiroki Kaneko et al.   NATURE

Somatic retrotransposition alters the genetic landscape of the human brain

(2011) J. Kenneth Baillie et al.   NATURE

ATP7A-related copper transport diseases—emerging concepts and future trends

(2011) Stephen G. Kaler   Nature Reviews Neurology

Regulation of axonal mitochondrial transport and its impact on synaptic transmission

(2011) Qian Cai et al.   NEUROSCIENCE RESEARCH

Widespread establishment and regulatory impact of Alu exons in human genes

(2011) S. Shen et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

The NF1 Gene Contains Hotspots for L1 Endonuclease-Dependent De Novo Insertion

(2011) Katharina Wimmer et al.   PLoS Genetics

Alu elements: know the SINEs

(2011) Prescott Deininger   GENOME BIOLOGY

Mobile DNA and the TE-Thrust hypothesis: supporting evidence from the primates

(2011) Keith R Oliver et al.   Mobile DNA

Genetic variation at a single locus and age of onset for Alzheimer's disease

(2010) Michael W. Lutz et al.   Alzheimers & Dementia

An Inherited Variable Poly-T Repeat Genotype in TOMM40 in Alzheimer Disease

(2010) Allen D. Roses   ARCHIVES OF NEUROLOGY

Gene regulation by SINES and inosines: biological consequences of A-to-I editing of Alu element inverted repeats

(2010) Ling-Ling Chen et al.   CELL CYCLE

An Alu-like RNA promotes cell differentiation and reduces malignancy of human neuroblastoma cells

(2010) Manuele Castelnuovo et al.   FASEB JOURNAL

Mitochondrial loss, dysfunction and altered dynamics in Huntington's disease

(2010) J. Kim et al.   HUMAN MOLECULAR GENETICS

L1 retrotransposition in neurons is modulated by MeCP2

(2010) Alysson R. Muotri et al.   NATURE

Amyloid-β and tau — a toxic pas de deux in Alzheimer's disease

(2010) Lars M. Ittner et al.   NATURE REVIEWS NEUROSCIENCE

Inheritance of Charcot–Marie–Tooth disease 1A with rare nonrecurrent genomic rearrangement

(2010) Byung-Ok Choi et al.   NEUROGENETICS

Distinctive patterns of age-dependent hypomethylation in interspersed repetitive sequences

(2010) Pornrutsami Jintaridth et al.   PHYSIOLOGICAL GENOMICS

All y’all need to know ‘bout retroelements in cancer

(2010) Victoria P. Belancio et al.   SEMINARS IN CANCER BIOLOGY

Mitochondrial dynamics and neurodegeneration

(2009) Bingwei Lu   Current Neurology and Neuroscience Reports

Repetitive DNA elements, nucleosome binding and human gene expression

(2009) Ahsan Huda et al.   GENE

Loss of epigenetic silencing in tumors preferentially affects primate-specific retroelements

(2009) Sebastian Szpakowski et al.   GENE

Adenosine deamination in human transcripts generates novel microRNA binding sites

(2009) Glen M. Borchert et al.   HUMAN MOLECULAR GENETICS

Altered Nuclear Retention of mRNAs Containing Inverted Repeats in Human Embryonic Stem Cells: Functional Role of a Nuclear Noncoding RNA

(2009) Ling-Ling Chen et al.   MOLECULAR CELL

The impact of retrotransposons on human genome evolution

(2009) Richard Cordaux et al.   NATURE REVIEWS GENETICS

A TOMM40 variable-length polymorphism predicts the age of late-onset Alzheimer's disease

(2009) A D Roses et al.   PHARMACOGENOMICS JOURNAL

Evidence for Co-Evolution between Human MicroRNAs and Alu-Repeats

(2009) Stefan Lehnert et al.   PLoS One

Dynamic regulation of RNA editing of ion channels and receptors in the mammalian nervous system

(2009) Bao Tan et al.   Molecular Brain

Alu and B1 Repeats Have Been Selectively Retained in the Upstream and Intronic Regions of Genes of Specific Functional Classes

(2009) Aristotelis Tsirigos et al.   PLoS Computational Biology

A clinical, genetic, and biochemical characterization ofSPG7mutations in a large cohort of patients with hereditary spastic paraplegia

(2008) Alessia Arnoldi et al.   HUMAN MUTATION

Decline in genomic DNA methylation through aging in a cohort of elderly subjects

(2008) Valentina Bollati et al.   MECHANISMS OF AGEING AND DEVELOPMENT

Human Alu RNA Is a Modular Transacting Repressor of mRNA Transcription during Heat Shock

(2008) Peter D. Mariner et al.   MOLECULAR CELL

Mitochondrial Dysfunction and Psychiatric Disorders

(2008) Gislaine T. Rezin et al.   NEUROCHEMICAL RESEARCH

RNA editing, DNA recoding and the evolution of human cognition

(2008) John S. Mattick et al.   TRENDS IN NEUROSCIENCES

Diverse Splicing Patterns of Exonized Alu Elements in Human Tissues

(2008) Lan Lin et al.   PLoS Genetics