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Adenosine-to-inosine RNA editing and human disease
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title
Adenosine-to-inosine RNA editing and human disease
(English)
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PubMed
author name string
William Slotkin
series ordinal
1
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Kazuko Nishikura
series ordinal
2
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language of work or name
English
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PubMed
publication date
2013
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PubMed
published in
Genome Medicine
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volume
5
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PubMed
issue
11
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PubMed
page(s)
105
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PubMed
cites work
ADAR1 forms a complex with Dicer to promote microRNA processing and RNA-induced gene silencing
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Mutations involved in Aicardi-Goutières syndrome implicate SAMHD1 as regulator of the innate immune response
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Frequency and fate of microRNA editing in human brain
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Down-regulation of RNA editing in pediatric astrocytomas: ADAR2 editing activity inhibits cell migration and proliferation
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A microRNA expression signature of human solid tumors defines cancer gene targets
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Widespread A-to-I RNA editing of Alu-containing mRNAs in the human transcriptome
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Underediting of glutamate receptor GluR-B mRNA in malignant gliomas
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Expression and regulation by interferon of a double-stranded-RNA-specific adenosine deaminase from human cells: evidence for two forms of the deaminase
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Ca2+ permeability of KA-AMPA--gated glutamate receptor channels depends on subunit composition
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7 April 2017
The ADAR protein family
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MicroRNAs in stress signaling and human disease
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Quantitative analysis of 5HT(2C) receptor RNA editing patterns in psychiatric disorders
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Liver Disintegration in the Mouse Embryo Caused by Deficiency in the RNA-editing Enzyme ADAR1
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Human spinal motoneurons express low relative abundance of GluR2 mRNA: an implication for excitotoxicity in ALS
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Requirement of dimerization for RNA editing activity of adenosine deaminases acting on RNA
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Altered editing of serotonin 2C receptor pre-mRNA in the prefrontal cortex of depressed suicide victims
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7 April 2017
RNA editing of the human serotonin 5-HT2C receptor. alterations in suicide and implications for serotonergic pharmacotherapy
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A review of central 5-HT receptors and their function
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7 April 2017
RNA editing of the human serotonin 5-hydroxytryptamine 2C receptor silences constitutive activity
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Mutations in ADAR1 cause Aicardi-Goutières syndrome associated with a type I interferon signature
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7 April 2017
Enhancement of replication of RNA viruses by ADAR1 via RNA editing and inhibition of RNA-activated protein kinase
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7 April 2017
Adenosine deaminases acting on RNA (ADARs) are both antiviral and proviral
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7 April 2017
Functions and regulation of RNA editing by ADAR deaminases
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7 April 2017
RNA-specific adenosine deaminase ADAR1 suppresses measles virus-induced apoptosis and activation of protein kinase PKR
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Mutations in the gene encoding the 3'-5' DNA exonuclease TREX1 cause Aicardi-Goutières syndrome at the AGS1 locus
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7 April 2017
Deficient RNA editing of GluR2 and neuronal death in amyotropic lateral sclerosis
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7 April 2017
Regulation of serotonin-2C receptor G-protein coupling by RNA editing
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7 April 2017
RNA editing in brain controls a determinant of ion flow in glutamate-gated channels
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7 April 2017
Induced loss of ADAR2 engenders slow death of motor neurons from Q/R site-unedited GluR2
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7 April 2017
Reprogramming of microRNAs by adenosine-to-inosine editing and the selective elimination of edited microRNA precursors in mouse oocytes and preimplantation embryos
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RNA-interacting proteins act as site-specific repressors of ADAR2-mediated RNA editing and fluctuate upon neuronal stimulation
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7 April 2017
ADAR1 is essential for the maintenance of hematopoiesis and suppression of interferon signaling
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Stress-induced Apoptosis Associated with Null Mutation of ADAR1 RNA Editing Deaminase Gene
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7 April 2017
Redirection of silencing targets by adenosine-to-inosine editing of miRNAs
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Point mutation in an AMPA receptor gene rescues lethality in mice deficient in the RNA-editing enzyme ADAR2
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MicroRNA-mediated loss of ADAR1 in metastatic melanoma promotes tumor growth
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Mapping the human miRNA interactome by CLASH reveals frequent noncanonical binding
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Recoding RNA editing of AZIN1 predisposes to hepatocellular carcinoma
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ADAR1 promotes malignant progenitor reprogramming in chronic myeloid leukemia.
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Comparative RNA editing in autistic and neurotypical cerebella.
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Transcript diversification in the nervous system: a to I RNA editing in CNS function and disease development
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28 September 2017
ADAR2-editing activity inhibits glioblastoma growth through the modulation of the CDC14B/Skp2/p21/p27 axis.
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The essential role of AMPA receptor GluR2 subunit RNA editing in the normal and diseased brain
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28 September 2017
Profound downregulation of the RNA editing enzyme ADAR2 in ALS spinal motor neurons
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28 September 2017
Prader-Willi Syndrome: Obesity due to Genomic Imprinting
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A-to-I RNA editing: the "ADAR" side of human cancer
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28 September 2017
ADARs: viruses and innate immunity
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28 September 2017
Editing of neurotransmitter receptor and ion channel RNAs in the nervous system
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28 September 2017
ADARs: allies or enemies? The importance of A-to-I RNA editing in human disease: from cancer to HIV-1.
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28 September 2017
Deficiency in RNA editing enzyme ADAR2 impairs regulated exocytosis
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28 September 2017
Mice with altered serotonin 2C receptor RNA editing display characteristics of Prader-Willi syndrome
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28 September 2017
AMPA receptor-mediated neuronal death in sporadic ALS.
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28 September 2017
Large-scale mRNA sequencing determines global regulation of RNA editing during brain development.
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28 September 2017
Current hypotheses for the underlying biology of amyotrophic lateral sclerosis
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28 September 2017
Dysregulated editing of serotonin 2C receptor mRNAs results in energy dissipation and loss of fat mass
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28 September 2017
Altered adenosine-to-inosine RNA editing in human cancer
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28 September 2017
RNA binding-independent dimerization of adenosine deaminases acting on RNA and dominant negative effects of nonfunctional subunits on dimer functions
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28 September 2017
A-to-I RNA editing and human disease
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28 September 2017
RNA editing by ADAR2 is metabolically regulated in pancreatic islets and beta-cells.
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28 September 2017
Mutations in genes encoding ribonuclease H2 subunits cause Aicardi-Goutières syndrome and mimic congenital viral brain infection
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28 September 2017
Optimal role of temozolomide in the treatment of malignant gliomas.
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28 September 2017
Contributions of 5-HT(2C) receptors to multiple actions of central serotonin systems
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28 September 2017
Mutations of the RNA-specific adenosine deaminase gene (DSRAD) are involved in dyschromatosis symmetrica hereditaria
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28 September 2017
Mutations and A/I hypermutations in measles virus persistent infections
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28 September 2017
Novel ADAR1 mutations including a single amino acid deletion in the deaminase domain underlie dyschromatosis symmetrica hereditaria in Japanese families
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31 May 2018
RNA editing of human microRNAs
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31 May 2018
RNA editing of the human serotonin 5-HT2C receptor alters receptor-mediated activation of G13 protein
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31 May 2018
A-to-I pre-mRNA editing in Drosophila is primarily involved in adult nervous system function and integrity
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31 May 2018
Biased hypermutation and other genetic changes in defective measles viruses in human brain infections
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31 May 2018
Biased hypermutation of viral RNA genomes could be due to unwinding/modification of double-stranded RNA.
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31 May 2018
A role for calpain-dependent cleavage of TDP-43 in amyotrophic lateral sclerosis pathology
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28 November 2018
Ca2+-permeable AMPA receptors regulate growth of human glioblastoma via Akt activation
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28 November 2018
ADAR2-dependent RNA editing of AMPA receptor subunit GluR2 determines vulnerability of neurons in forebrain ischemia
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28 November 2018
Expression of Ca(2+)-permeable AMPA receptor channels primes cell death in transient forebrain ischemia
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28 November 2018
Evidence that the hypermutated M protein of a subacute sclerosing panencephalitis measles virus actively contributes to the chronic progressive CNS disease
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28 November 2018
Q/R RNA editing of the AMPA receptor subunit 2 (GRIA2) transcript evolves no later than the appearance of cartilaginous fishes
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retrieved
28 November 2018
Comparative analysis of the DRADA A-to-I RNA editing gene from mammals, pufferfish and zebrafish
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3979043
retrieved
28 November 2018
RED2, a brain-specific member of the RNA-specific adenosine deaminase family
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3979043
retrieved
28 November 2018
Neurobiology of suicidal behaviour
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/24289319
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Early-onset epilepsy and postnatal lethality associated with an editing-deficient GluR-B allele in mice
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/24289319
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Increased serotonin 2C receptor mRNA editing: a possible risk factor for suicide
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/24289319
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
A novel mutation of the DSRAD gene in a Chinese family with dyschromatosis symmetrica hereditaria
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/24289319
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1186/GM508
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1333808
Dimensions Publication ID
1001672359
0 references
OpenCitations bibliographic resource ID
1333808
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1333808
PMC publication ID
3979043
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1333808
PubMed publication ID
24289319
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1333808
ResearchGate publication ID
259106901
0 references
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