Crossref
journal-article
Elsevier BV
Brain Research (78)
References
137
Referenced
50
10.1038/ncb1335
/ Nat. Cell Biol. / RNA-dependent integrin alpha3 protein localization regulated by the muscleblind-like protein MLP1 by Adereth (2005)10.1007/s00401-013-1149-y
/ Acta Neuropathol. / Modeling key pathological features of frontotemporal dementia with C9ORF72 repeat expansion in iPSC-derived human neurons by Almeida (2013)10.1073/pnas.0901824106
/ Proc. Natl. Acad. Sci. USA / A simple ligand that selectively targets CUG trinucleotide repeats and inhibits MBNL protein binding by Arambula (2009)10.1093/hmg/ddi394
/ Hum. Mol. Genet. / Induction of inclusion formation and disruption of lamin A/C structure by premutation CGG-repeat RNA in human cultured neural cells by Arocena (2005)10.1016/j.neuron.2013.02.004
/ Neuron / Unconventional translation of C9ORF72 GGGGCC expansion generates insoluble polypeptides specific to c9FTD/ALS by Ash (2013)10.1093/hmg/ddq132
/ Hum. Mol. Genet. / Partners in crime: bidirectional transcription in unstable microsatellite disease by Batra (2010)10.1007/s00401-013-1199-1
/ Acta Neuropathol. / Reduced C9orf72 gene expression in c9FTD/ALS is caused by histone trimethylation, an epigenetic event detectable in blood by Belzil (2013)10.1016/j.dnarep.2013.04.019
/ DNA Repair / Bidirectional transcription of trinucleotide repeats: roles for excision repair by Budworth (2013)10.1093/nar/gks068
/ Nucleic Acids Res. / 5′-UTR RNA G-quadruplexes: translation regulation and targeting by Bugaut (2012)10.3389/fnmol.2013.00057
/ Front. Mol. Neurosci. / Brain pathology in myotonic dystrophy: when tauopathy meets spliceopathy and RNAopathy by Caillet-Boudin (2014)10.1016/j.bbadis.2014.01.004
/ Biochim. Biophys. Acta / Tau exon 2 responsive elements deregulated in myotonic dystrophy type I are proximal to exon 2 and synergistically regulated by MBNL1 and MBNL2 by Carpentier (2014)10.1093/hmg/ddq427
/ Hum. Mol. Genet. / Expanded CTG repeat demarcates a boundary for abnormal CpG methylation in myotonic dystrophy patient tissues by Castel (2011)10.1093/hmg/dds306
/ Hum. Mol. Genet. / Mouse model of muscleblind-like 1 overexpression: skeletal muscle effects and therapeutic promise by Chamberlain (2012)10.1016/j.neuron.2012.05.029
/ Neuron / Muscleblind-like 2-mediated alternative splicing in the developing brain and dysregulation in myotonic dystrophy by Charizanis (2012)10.1038/ncomms3044
/ Nat. Commun. / Induction and reversal of myotonic dystrophy type 1 pre-mRNA splicing defects by small molecules by Childs-Disney (2013)10.1002/ana.23946
/ Ann. Neurol. / Loss of function of C9orf72 causes motor deficits in a zebrafish model of amyotrophic lateral sclerosis by Ciura (2013)10.1038/ng870
/ Nat. Genet. / Evidence of cis-acting factors in replication-mediated trinucleotide repeat instability in primate cells by Cleary (2002)10.1093/hmg/ddq432
/ Hum. Mol. Genet. / Premutation CGG-repeat expansion of the Fmr1 gene impairs mouse neocortical development by Cunningham (2011)10.1016/j.neuron.2011.09.011
/ Neuron / Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS by DeJesus-Hernandez (2011)10.1016/j.tig.2009.04.007
/ Trends Genet. / Instability and chromatin structure of expanded trinucleotide repeats by Dion (2009)10.1016/j.neuron.2013.10.015
/ Neuron / RNA toxicity from the ALS/FTD C9ORF72 expansion is mitigated by antisense intervention by Donnelly (2013)10.1016/j.brainres.2012.02.030
/ Brain Res. / RNA-binding proteins in microsatellite expansion disorders: mediators of RNA toxicity by Echeverria (2012)10.1093/hmg/dds478
/ Hum. Mol. Genet. / Expanded CTG repeats trigger miRNA alterations in Drosophila that are conserved in myotonic dystrophy type 1 patients by Fernandez-Costa (2013)10.1038/srep01016
/ Sci. Rep. / C9orf72 hexanucleotide repeat associated with amyotrophic lateral sclerosis and frontotemporal dementia forms RNA G-quadruplexes by Fratta (2012)10.1093/hmg/ddp497
/ Hum. Mol. Genet. / Fibroblast phenotype in male carriers of FMR1 premutation alleles by Garcia-Arocena (2010)10.1007/s00401-013-1192-8
/ Acta Neuropathol. / Antisense transcripts of the expanded C9ORF72 hexanucleotide repeat form nuclear RNA foci and undergo repeat-associated non-ATG translation in c9FTD/ALS by Gendron (2013)10.1007/s00401-013-1237-z
/ Acta Neuropathol. / Mechanisms of toxicity in C9FTLD/ALS by Gendron (2014)10.1371/journal.pgen.0030052
/ PLoS Genet. / CTG trinucleotide repeat “big jumps”: large expansions, small mice by Gomes-Pereira (2007)10.1016/j.molmed.2011.05.004
/ Trends Mol. Med. / Myotonic dystrophy mouse models: towards rational therapy development by Gomes-Pereira (2011)10.1073/pnas.0800048105
/ Proc. Natl. Acad. Sci. USA / DNA instability in postmitotic neurons by Gonitel (2008)10.1093/brain/awf184
/ Brain / Neuronal intranuclear inclusions in a new cerebellar tremor/ataxia syndrome among Fragile X carriers by Greco (2002)10.1007/s00401-013-1138-1
/ Acta Neuropathol. / Fragile X-associated tremor/ataxia syndrome (FXTAS): pathology and mechanisms by Hagerman (2013)10.1016/S1474-4422(13)70125-X
/ Lancet Neurol. / Advances in clinical and molecular understanding of the FMR1 premutation and Fragile X-associated tremor/ataxia syndrome by Hagerman (2013)10.1073/pnas.94.14.7394
/ Proc. Natl. Acad. Sci. USA / Transcriptional abnormality in myotonic dystrophy affects DMPK but not neighboring genes by Hamshere (1997)10.1371/journal.pgen.1003569
/ PLoS Genet. / Pervasive transcription of the human genome produces thousands of previously unidentified long intergenic noncoding RNAs by Hangauer (2013)10.1093/hmg/ddp182
/ Hum. Mol. Genet. / Ectopic expression of CGG containing mRNA is neurotoxic in mammals by Hashem (2009)10.1093/brain/aws367
/ Brain / Myotonic dystrophy CTG expansion affects synaptic vesicle proteins, neurotransmission and mouse behaviour by Hernandez-Hernandez (2013)10.1016/j.biopsych.2011.05.033
/ Biol. Psychiatry / Decreased Fragile X mental retardation protein expression underlies amygdala dysfunction in carriers of the Fragile X premutation by Hessl (2011)10.1371/journal.pgen.1003043
/ PLoS Genet. / Molecular, physiological, and motor performance defects in DMSXL mice carrying >1,000 CTG repeats from the human DM1 locus by Huguet (2012)10.1007/978-3-642-21649-7_14
/ Results Probl. Cell Differ. / Mouse models of the Fragile X premutation and the Fragile X associated tremor/ataxia syndrome by Hunsaker (2012)10.1093/brain/awh650
/ Brain / Protein composition of the intranuclear inclusions of FXTAS by Iwahashi (2006)10.1021/jm400794z
/ J. Med. Chem. / Developing bivalent ligands to target CUG triplet repeats, the causative agent of myotonic dystrophy type 1 by Jahromi (2013)10.1038/ng0796-316
/ Nat. Genet. / Abnormal myotonic dystrophy protein kinase levels produce only mild myopathy in mice by Jansen (1996)10.1093/hmg/ddh327
/ Hum. Mol. Genet. / Myotonic dystrophy type 1 is associated with nuclear foci of mutant RNA, sequestration of muscleblind proteins and deregulated alternative splicing in neurons by Jiang (2004)10.1016/S0896-6273(03)00533-6
/ Neuron / RNA-mediated neurodegeneration caused by the Fragile X premutation rCGG repeats in Drosophila by Jin (2003)10.1016/j.neuron.2007.07.020
/ Neuron / Pur alpha binds to rCGG repeats and modulates repeat-mediated neurodegeneration in a Drosophila model of Fragile X tremor/ataxia syndrome by Jin (2007)10.1016/j.celrep.2013.12.025
/ Cell Rep. / The Mef2 transcription network is disrupted in myotonic dystrophy heart tissue, dramatically altering miRNA and mRNA expression by Kalsotra (2014)10.1126/science.1088583
/ Science / A muscleblind knockout model for myotonic dystrophy by Kanadia (2003)10.1073/pnas.0604970103
/ Proc. Natl. Acad. Sci. USA / Reversal of RNA missplicing and myotonia after muscleblind overexpression in a mouse poly(CUG) model for myotonic dystrophy by Kanadia (2006)10.1016/j.celrep.2012.06.020
/ Cell Rep. / Msh2-Msh3 interferes with Okazaki fragment processing to promote trinucleotide repeat expansions by Kantartzis (2012)10.1093/hmg/ddg352
/ Hum. Mol. Genet. / Dramatic tissue-specific mutation length increases are an early molecular event in Huntington disease pathogenesis by Kennedy (2003)10.1128/MCB.23.19.6857-6875.2003
/ Mol. Cell. Biol. / Puralpha is essential for postnatal brain development and developmentally coupled cellular proliferation as revealed by genetic inactivation in the mouse by Khalili (2003)10.1093/nar/gkq700
/ Nucleic Acids Res. / Atomic resolution structure of CAG RNA repeats: structural insights and implications for the trinucleotide repeat expansion diseases by Kiliszek (2010)10.1093/nar/gkr368
/ Nucleic Acids Res. / Crystal structures of CGG RNA repeats with implications for Fragile X-associated tremor ataxia syndrome by Kiliszek (2011)10.1093/nar/gki698
/ Nucleic Acids Res. / HnRNP H inhibits nuclear export of mRNA containing expanded CUG repeats and a distal branch point sequence by Kim (2005)10.1093/nar/gkr729
/ Nucleic Acids Res. / Triplet repeat RNA structure and its role as pathogenic agent and therapeutic target by Krzyzosiak (2012)10.1016/j.molcel.2007.07.027
/ Mol. Cell / Increased steady-state levels of CUGBP1 in myotonic dystrophy 1 are due to PKC-mediated hyperphosphorylation by Kuyumcu-Martinez (2007)10.1038/nrg2748
/ Nat. Rev. Genet. / Repeat expansion disease: progress and puzzles in disease pathogenesis by La Spada (2010)10.1093/hmg/ddm293
/ Hum. Mol. Genet. / An antisense transcript spanning the CGG repeat region of FMR1 is upregulated in premutation carriers but silenced in full mutation individuals by Ladd (2007)10.1073/pnas.1318835110
/ Proc. Natl. Acad. Sci. USA / Targeted degradation of sense and antisense C9orf72 RNA foci as therapy for ALS and frontotemporal degeneration by Lagier-Tourenne (2013)10.1093/nar/gkr1228
/ Nucleic Acids Res. / New function for the RNA helicase p68/DDX5 as a modifier of MBNL1 activity on expanded CUG repeats by Laurent (2012)10.1002/emmm.201303275
/ EMBO Mol. Med. / Compound loss of muscleblind-like function in myotonic dystrophy by Lee (2013)10.1016/j.celrep.2013.10.049
/ Cell Rep. / Hexanucleotide repeats in ALS/FTD form length-dependent RNA foci, sequester RNA binding proteins, and are neurotoxic by Lee (2013)10.1093/bioinformatics/bts725
/ Bioinformatics / The product of C9orf72, a gene strongly implicated in neurodegeneration, is structurally related to DENN Rab-GEFs by Levine (2013)10.1371/journal.pgen.1000257
/ PLoS Genet. / CTCF cis-regulates trinucleotide repeat instability in an epigenetic manner: a novel basis for mutational hot spot determination by Libby (2008)10.1038/nsmb1042
/ Nat. Struct. Mol. Biol. / Transcription promotes contraction of CAG repeat tracts in human cells by Lin (2006)10.4161/cc.10.4.14729
/ Cell Cycle / Transcription-induced DNA toxicity at trinucleotide repeats: double bubble Is trouble by Lin (2011)10.1016/j.neuron.2013.07.033
/ Neuron / Converging mechanisms in ALS and FTD: disrupted RNA and protein homeostasis by Ling (2013)10.1126/science.1062125
/ Science / Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9 by Liquori (2001)10.1002/humu.22464
/ Hum. Mutat. / The mismatch repair protein MSH2 is rate limiting for repeat expansion in a Fragile X premutation mouse model by Lokanga (2014)10.1038/nrm2854
/ Nat. Rev. Mol. Cell Biol. / Repeat instability as the basis for human diseases and as a potential target for therapy by Lopez Castel (2010)10.1016/j.jmb.2011.01.006
/ J. Mol. Biol. / Initiation of translation of the FMR1 mRNA occurs predominantly through 5′-end-dependent ribosomal scanning by Ludwig (2011)10.1038/ng1857
/ Nat. Genet. / Reversible model of RNA toxicity and cardiac conduction defects in myotonic dystrophy by Mahadevan (2006)10.1097/WCO.0b013e328357b0d9
/ Curr. Opin. Neurol. / Myotonic dystrophy: is a narrow focus obscuring the rest of the field? by Mahadevan (2012)10.1126/science.289.5485.1769
/ Science / Myotonic dystrophy in transgenic mice expressing an expanded CUG repeat by Mankodi (2000)10.1093/hmg/ddl103
/ Hum. Mol. Genet. / DM2 intronic expansions: evidence for CCUG accumulation without flanking sequence or effects on ZNF9 mRNA processing or protein expression by Margolis (2006)10.4161/rna.7.5.12745
/ RNA Biol. / New insights into repeat instability: role of RNA•DNA hybrids. by McIvor (2010)10.1093/hmg/7.3.423
/ Hum. Mol. Genet. / A tetranucleotide polymorphic microsatellite, located in the first intron of the tyrosine hydroxylase gene, acts as a transcription regulatory element in vitro by Meloni (1998)10.1093/emboj/19.17.4439
/ EMBO J. / Recruitment of human muscleblind proteins to (CUG)(n) expansions associated with myotonic dystrophy by Miller (2000)10.1038/nature05977
/ Nature / Expandable DNA repeats and human disease by Mirkin (2007)10.1007/s00401-013-1200-z
/ Acta Neuropathol. / C9orf72 frontotemporal lobar degeneration is characterised by frequent neuronal sense and antisense RNA foci by Mizielinska (2013)10.1073/pnas.0505873102
/ Proc. Natl. Acad. Sci. USA / The structural basis of myotonic dystrophy from the crystal structure of CUG repeats by Mooers (2005)10.1007/s00401-013-1088-7
/ Acta Neuropathol. / hnRNP A3 binds to GGGGCC repeats and is a constituent of p62-positive/TDP43-negative inclusions in the hippocampus of patients with C9orf72 mutations by Mori (2013)10.1126/science.1232927
/ Science / The C9orf72 GGGGCC repeat is translated into aggregating dipeptide-repeat proteins in FTLD/ALS by Mori (2013)10.1093/hmg/ddq501
/ Hum. Mol. Genet. / Bidirectional transcription stimulates expansion and contraction of expanded (CTG)•(CAG) repeats by Nakamori (2011)10.1038/cddis.2013.276
/ Cell Death Dis. / Mechanisms of RNA-induced toxicity in CAG repeat disorders by Nalavade (2013)10.1074/jbc.R800025200
/ J. Biol. Chem. / Mechanisms of RNA-mediated disease by O׳Rourke (2009)10.1073/pnas.0708519105
/ Proc. Natl. Acad. Sci. USA / Expanded CTG repeats within the DMPK 3′ UTR causes severe skeletal muscle wasting in an inducible mouse model for myotonic dystrophy by Orengo (2008)10.1093/hmg/ddl181
/ Hum. Mol. Genet. / RNA-dominant diseases by Osborne (2006)10.1074/jbc.M910165199
/ J. Biol. Chem. / Splicing factors induce cystic fibrosis transmembrane regulator exon 9 skipping through a nonevolutionary conserved intronic element by Pagani (2000)10.1007/s00439-013-1356-6
/ Hum. Genet. / Comprehensive analysis of the transcriptional landscape of the human FMR1 gene reveals two new long noncoding RNAs differentially expressed in Fragile X syndrome and Fragile X-associated tremor/ataxia syndrome by Pastori (2014)10.1038/sj.emboj.7601296
/ EMBO J. / Interaction of muscleblind, CUG-BP1 and hnRNP H proteins in DM1-associated aberrant IR splicing by Paul (2006)10.1038/nrg1689
/ Nat. Rev. Genet. / Repeat instability: mechanisms of dynamic mutations by Pearson (2005)10.1371/journal.pgen.1003930
/ PLoS Genet. / Mismatch repair genes Mlh1 and Mlh3 modify CAG instability in Huntington׳s disease mice: genome-wide and candidate approaches by Pinto (2013)10.1101/cshperspect.a000778
/ Cold Spring Harb. Perspect. Biol. / Developments in RNA splicing and disease by Poulos (2011)10.1002/emmm.201000064
/ EMBO Mol. Med. / Long intronic GAA repeats causing Friedreich ataxia impede transcription elongation by Punga (2010)10.1242/jcs.073270
/ J. Cell Sci. / Stochastic and reversible aggregation of mRNA with expanded CUG-triplet repeats by Querido (2011)10.1146/annurev.neuro.29.051605.113014
/ Annu. Rev. Neurosci. / RNA-mediated neuromuscular disorders by Ranum (2006)10.1038/nsmb.2067
/ Nat. Struct. Mol. Biol. / Misregulation of miR-1 processing is associated with heart defects in myotonic dystrophy by Rau (2011)10.1083/jcb.201108113
/ J. Cell Biol. / The RNA-binding protein Staufen1 is increased in DM1 skeletal muscle and promotes alternative pre-mRNA splicing by Ravel-Chapuis (2012)10.1074/jbc.C113.452532
/ J. Biol. Chem. / The disease-associated r(GGGGCC)n repeat from the C9orf72 gene forms tract length-dependent uni- and multimolecular RNA G-quadruplex structures by Reddy (2013)10.1038/ng0796-325
/ Nat. Genet. / Mice lacking the myotonic dystrophy protein kinase develop a late onset progressive myopathy by Reddy (1996)10.1016/j.neuron.2011.09.010
/ Neuron / A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD by Renton (2011)10.1038/emboj.2010.21
/ EMBO J. / Sam68 sequestration and partial loss of function are associated with splicing alterations in FXTAS patients by Sellier (2010)10.1016/j.celrep.2013.02.004
/ Cell Rep. / Sequestration of DROSHA and DGCR8 by expanded CGG RNA repeats alters microRNA processing in Fragile X-associated tremor/ataxia syndrome by Sellier (2013)10.1093/hmg/10.19.2143
/ Hum. Mol. Genet. / Dysregulation of human brain microtubule-associated tau mRNA maturation in myotonic dystrophy type 1 by Sergeant (2001)10.1093/hmg/9.8.1185
/ Hum. Mol. Genet. / Transgenic mice carrying large human genomic sequences with expanded CTG repeat mimic closely the DM CTG repeat intergenerational and somatic instability by Seznec (2000)10.1093/hmg/10.23.2717
/ Hum. Mol. Genet. / Mice transgenic for the human myotonic dystrophy region with expanded CTG repeats display muscular and brain abnormalities by Seznec (2001)10.1016/j.bbadis.2013.03.002
/ Biochim. Biophys. Acta / RNA toxicity in human disease and animal models: from the uncovering of a new mechanism to the development of promising therapies by Sicot (2013)10.1093/nar/gkg766
/ Nucleic Acids Res. / RNA structure of trinucleotide repeats associated with human neurological diseases by Sobczak (2003)10.1074/jbc.M109.078790
/ J. Biol. Chem. / Structural diversity of triplet repeat RNAs by Sobczak (2010)10.1016/j.neuron.2007.07.021
/ Neuron / RNA-binding proteins hnRNP A2/B1 and CUGBP1 suppress Fragile X CGG premutation repeat-induced neurodegeneration in a Drosophila model of FXTAS by Sofola (2007)10.1038/nn.3566
/ Nat. Neurosci. / The mouse C9ORF72 ortholog is enriched in neurons known to degenerate in ALS and FTD by Suzuki (2013)10.1128/MCB.8.5.2237
/ Mol. Cell. Biol. / Classification and purification of proteins of heterogeneous nuclear ribonucleoprotein particles by RNA-binding specificities by Swanson (1988)10.1083/jcb.128.6.995
/ J. Cell Biol. / Foci of trinucleotide repeat transcripts in nuclei of myotonic-dystrophy cells and tissues by Taneja (1995)10.1086/302720
/ Am. J. Hum. Genet. / Elevated levels of FMR1 mRNA in carrier males: a new mechanism of involvement in the fragile-X syndrome by Tassone (2000)10.1038/nsmb.1519
/ Nat. Struct. Mol. Biol. / Structural insights into RNA recognition by the alternative-splicing regulator muscleblind-like MBNL1 by Teplova (2008)10.1371/journal.pone.0083450
/ PLoS One / Deletion of C9ORF72 results in motor neuron degeneration and stress sensitivity in C. elegans by Therrien (2013)10.1016/j.neuron.2013.03.026
/ Neuron / CGG repeat-associated translation mediates neurodegeneration in Fragile X tremor ataxia syndrome by Todd (2013)10.1371/journal.pgen.1003280
/ PLoS Genet. / MSH3 polymorphisms and protein levels affect CAG repeat instability in Huntington׳s disease mice by Tome (2013)10.1074/jbc.M110.194928
/ J. Biol. Chem. / Analysis of exonic regions involved in nuclear localization, splicing activity, and dimerization of muscleblind-like-1 isoforms by Tran (2011)10.1038/nrg3117
/ Nat. Rev. Genet. / Repetitive DNA and next-generation sequencing: computational challenges and solutions by Treangen (2012)10.1016/S1474-4422(12)70204-1
/ Lancet Neurol. / The myotonic dystrophies: molecular, clinical, and therapeutic challenges by Udd (2012)10.1101/gr.070409.107
/ Genome Res. / The biological effects of simple tandem repeats: lessons from the repeat expansion diseases by Usdin (2008)10.1007/s00401-013-1240-4
/ Acta Neuropathol. / TMEM106B protects C9ORF72 expansion carriers against frontotemporal dementia by van Blitterswijk (2014)10.1038/ng.536
/ Nat. Genet. / Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions by Van Deerlin (2010)10.1016/j.cell.2012.06.041
/ Cell / Transcriptome-wide regulation of pre-mRNA splicing and mRNA localization by muscleblind proteins by Wang (2012)10.1172/JCI32308
/ J. Clin. Investig. / Elevation of RNA-binding protein CUGBP1 is an early event in an inducible heart-specific mouse model of myotonic dystrophy by Wang (2007)10.1073/pnas.0903234106
/ Proc. Natl. Acad. Sci. USA / Pentamidine reverses the splicing defects associated with myotonic dystrophy by Warf (2009){'key': '10.1016/j.brainres.2014.03.039_bib130', 'first-page': '3952', 'article-title': 'Correction of ClC-1 splicing eliminates chloride channelopathy and myotonia in mouse models of myotonic dystrophy', 'volume': '117', 'author': 'Wheeler', 'year': '2007', 'journal-title': 'J. Clin. Investig.'}
/ J. Clin. Investig. / Correction of ClC-1 splicing eliminates chloride channelopathy and myotonia in mouse models of myotonic dystrophy by Wheeler (2007)10.1038/nature11362
/ Nature / Targeting nuclear RNA for in vivo correction of myotonic dystrophy by Wheeler (2012)10.1093/hmg/ddg114
/ Hum. Mol. Genet. / The FMR1 CGG repeat mouse displays ubiquitin-positive intranuclear neuronal inclusions; implications for the cerebellar tremor/ataxia syndrome by Willemsen (2003)10.1093/hmg/ddr299
/ Hum. Mol. Genet. / Cellular toxicity of expanded RNA repeats: focus on RNA foci by Wojciechowska (2011)10.1073/pnas.1219643110
/ Proc. Natl. Acad. Sci. USA / Expanded GGGGCC repeat RNA associated with amyotrophic lateral sclerosis and frontotemporal dementia causes neurodegeneration by Xu (2013)10.1093/nar/gkm601
/ Nucleic Acids Res. / Muscleblind-like 1 interacts with RNA hairpins in splicing target and pathogenic RNAs by Yuan (2007)10.1073/pnas.1013343108
/ Proc. Natl. Acad. Sci. USA / Non-ATG-initiated translation directed by microsatellite expansions by Zu (2011)10.1073/pnas.1315438110
/ Proc. Natl. Acad. Sci. USA / RAN proteins and RNA foci from antisense transcripts in C9ORF72 ALS and frontotemporal dementia by Zu (2013)
Dates
Type | When |
---|---|
Created | 11 years, 4 months ago (April 4, 2014, 4 p.m.) |
Deposited | 1 year, 2 months ago (May 25, 2024, 1:26 p.m.) |
Indexed | 2 months, 4 weeks ago (May 26, 2025, 3:26 a.m.) |
Issued | 10 years, 10 months ago (Oct. 1, 2014) |
Published | 10 years, 10 months ago (Oct. 1, 2014) |
Published Print | 10 years, 10 months ago (Oct. 1, 2014) |
Funders
4
National Institutes of Health
10.13039/100000002
Region: Americas
gov (National government)
Labels
3
- Institutos Nacionales de la Salud
- US National Institutes of Health
- NIH
Awards
2
- NS058901
- AR046799
Muscular Dystrophy Association
10.13039/100005202
Region: Americas
gov (Associations and societies (private and public))
Labels
2
- Muscular Dystrophy Association, Inc.
- MDA
Awards
1
- MDA276063
W.M. Keck Foundation
10.13039/100000888
W. M. Keck FoundationRegion: Americas
pri (Trusts, charities, foundations (both public and private))
Labels
3
- Keck Foundation
- The W. M. Keck Foundation
- WMKF
Marigold Foundation
@article{Mohan_2014, title={RNA–protein interactions in unstable microsatellite diseases}, volume={1584}, ISSN={0006-8993}, url={http://dx.doi.org/10.1016/j.brainres.2014.03.039}, DOI={10.1016/j.brainres.2014.03.039}, journal={Brain Research}, publisher={Elsevier BV}, author={Mohan, Apoorva and Goodwin, Marianne and Swanson, Maurice S.}, year={2014}, month=oct, pages={3–14} }