| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1112762819 |
| P356 | DOI | 10.1186/S12920-019-0487-6 |
| P932 | PMC publication ID | 6416829 |
| P698 | PubMed publication ID | 30871545 |
| P50 | author | Peter Sparber | Q92364787 |
| P2093 | author name string | Mikhail Skoblov | |
| Alexandra Filatova | |||
| Mira Khantemirova | |||
| P2860 | cites work | Circular RNA: A new star of noncoding RNAs | Q38519809 |
| The circular RNA ciRS-7 promotes APP and BACE1 degradation in an NF-κB-dependent manner | Q38712195 | ||
| Long noncoding RNA H19 competitively binds miR-17-5p to regulate YES1 expression in thyroid cancer | Q38777108 | ||
| Deficiency in the Ubiquitin Conjugating Enzyme UBE2A in Alzheimer's Disease (AD) is Linked to Deficits in a Natural Circular miRNA-7 Sponge (circRNA; ciRS-7) | Q39120563 | ||
| Genome-wide changes in lncRNA, splicing, and regional gene expression patterns in autism | Q39129795 | ||
| Long noncoding RNAs with snoRNA ends | Q39283383 | ||
| 17A, a novel non-coding RNA, regulates GABA B alternative splicing and signaling in response to inflammatory stimuli and in Alzheimer disease | Q39648917 | ||
| CTCF-binding sites flank CTG/CAG repeats and form a methylation-sensitive insulator at the DM1 locus | Q40789249 | ||
| Paternally inherited microdeletion at 15q11.2 confirms a significant role for the SNORD116 C/D box snoRNA cluster in Prader-Willi syndrome | Q41733066 | ||
| apoE isoform-specific disruption of amyloid beta peptide clearance from mouse brain | Q43243545 | ||
| Oxidative stress potentiates BACE1 gene expression and Abeta generation | Q45198126 | ||
| Mouse RNAase MRP RNA is encoded by a nuclear gene and contains a decamer sequence complementary to a conserved region of mitochondrial RNA substrate. | Q45951314 | ||
| Molecular dissection of the interaction between amyloid precursor protein and its neuronal trafficking receptor SorLA/LR11. | Q48643108 | ||
| Regulation of synaptic responses to high-frequency stimulation and LTP by neurotrophins in the hippocampus | Q59085769 | ||
| Thalassaemia | Q88678149 | ||
| A novel RNA transcript with antiapoptotic function is silenced in fragile X syndrome | Q21562300 | ||
| Potential etiologic and functional implications of genome-wide association loci for human diseases and traits | Q22066284 | ||
| An integrated encyclopedia of DNA elements in the human genome | Q22122150 | ||
| Parental imprinting of the mouse H19 gene | Q22122365 | ||
| An architectural role for a nuclear noncoding RNA: NEAT1 RNA is essential for the structure of paraspeckles | Q24310786 | ||
| The DUX4 gene at the FSHD1A locus encodes a pro-apoptotic protein | Q24313369 | ||
| Neuronal sorting protein-related receptor sorLA/LR11 regulates processing of the amyloid precursor protein | Q24329019 | ||
| An RNA-dependent RNA polymerase formed by TERT and the RMRP RNA | Q24336971 | ||
| A novel endoribonuclease cleaves at a priming site of mouse mitochondrial DNA replication | Q24556370 | ||
| The GENCODE v7 catalog of human long noncoding RNAs: analysis of their gene structure, evolution, and expression | Q24608592 | ||
| A natural antisense transcript at the Huntington's disease repeat locus regulates HTT expression | Q24620388 | ||
| A long ncRNA links copy number variation to a polycomb/trithorax epigenetic switch in FSHD muscular dystrophy | Q24622599 | ||
| A long noncoding RNA controls muscle differentiation by functioning as a competing endogenous RNA | Q24630341 | ||
| miRNA-dependent gene silencing involving Ago2-mediated cleavage of a circular antisense RNA | Q24632605 | ||
| The H19 lincRNA is a developmental reservoir of miR-675 that suppresses growth and Igf1r | Q24633774 | ||
| Expression of a noncoding RNA is elevated in Alzheimer's disease and drives rapid feed-forward regulation of beta-secretase | Q24643985 | ||
| Functional demarcation of active and silent chromatin domains in human HOX loci by noncoding RNAs | Q24673619 | ||
| Apolipoprotein E and Apolipoprotein E Receptors: Normal Biology and Roles in Alzheimer Disease | Q26858870 | ||
| The multilayered complexity of ceRNA crosstalk and competition | Q27025671 | ||
| Silver-Russell Syndrome and Beckwith-Wiedemann Syndrome: Opposite Phenotypes with Heterogeneous Molecular Etiology | Q28079403 | ||
| Spinal Muscular Atrophy | Q28080774 | ||
| H19 RNA binds four molecules of insulin-like growth factor II mRNA-binding protein | Q28139674 | ||
| The IC-SNURF-SNRPN transcript serves as a host for multiple small nucleolar RNA species and as an antisense RNA for UBE3A | Q28207947 | ||
| The DISC locus in psychiatric illness | Q28251868 | ||
| X-chromosome inactivation: new insights into cis and trans regulation. | Q38500356 | ||
| H19 acts as a trans regulator of the imprinted gene network controlling growth in mice | Q28505959 | ||
| Kcnq1ot1 noncoding RNA mediates transcriptional gene silencing by interacting with Dnmt1 | Q28507331 | ||
| Genome-wide Identification of Polycomb-Associated RNAs by RIP-seq | Q28513635 | ||
| Polycomb proteins targeted by a short repeat RNA to the mouse X chromosome | Q29547359 | ||
| Identification and characterization of a spinal muscular atrophy-determining gene | Q29547495 | ||
| Long noncoding RNAs with enhancer-like function in human cells | Q29614328 | ||
| Kcnq1ot1 antisense noncoding RNA mediates lineage-specific transcriptional silencing through chromatin-level regulation | Q29614333 | ||
| A single nucleotide in the SMN gene regulates splicing and is responsible for spinal muscular atrophy | Q29617367 | ||
| lncRNAs transactivate STAU1-mediated mRNA decay by duplexing with 3' UTRs via Alu elements | Q29617832 | ||
| Natural RNA circles function as efficient microRNA sponges | Q29617892 | ||
| Inappropriate Gene Activation in FSHD | Q30050619 | ||
| CTCF regulates ataxin-7 expression through promotion of a convergently transcribed, antisense noncoding RNA. | Q30502612 | ||
| High mobility group protein-B1 interacts with sterol regulatory element-binding proteins to enhance their DNA binding | Q33220241 | ||
| Remodeling of the chromatin structure of the facioscapulohumeral muscular dystrophy (FSHD) locus and upregulation of FSHD-related gene 1 (FRG1) expression during human myogenic differentiation | Q33483016 | ||
| RNA gain-of-function in spinocerebellar ataxia type 8. | Q33493406 | ||
| An update of the mutation spectrum of the survival motor neuron gene (SMN1) in autosomal recessive spinal muscular atrophy (SMA). | Q33840923 | ||
| Polyglutamine-expanded ataxin-7 inhibits STAGA histone acetyltransferase activity to produce retinal degeneration | Q33854083 | ||
| Uncoupling antisense-mediated silencing and DNA methylation in the imprinted Gnas cluster. | Q33859387 | ||
| A single nucleotide difference that alters splicing patterns distinguishes the SMA gene SMN1 from the copy gene SMN2. | Q33864982 | ||
| Identification of a methylation imprint mark within the mouse Gnas locus | Q33964982 | ||
| Neurons but not glial cells show reciprocal imprinting of sense and antisense transcripts of Ube3a | Q33965204 | ||
| Deletion of the noncoding GNAS antisense transcript causes pseudohypoparathyroidism type Ib and biparental defects of GNAS methylation in cis | Q34032076 | ||
| H19 lncRNA controls gene expression of the Imprinted Gene Network by recruiting MBD1. | Q34039202 | ||
| Inhibition of natural antisense transcripts in vivo results in gene-specific transcriptional upregulation. | Q34088908 | ||
| Transcription of antisense RNA leading to gene silencing and methylation as a novel cause of human genetic disease | Q34194830 | ||
| An Epidemiological Study of Hirschsprung's Disease | Q34251316 | ||
| Primary structure, neural-specific expression, and dendritic location of human BC200 RNA | Q34306210 | ||
| Activating RNAs associate with Mediator to enhance chromatin architecture and transcription | Q34328232 | ||
| BDNF overexpression in the forebrain rescues Huntington's disease phenotypes in YAC128 mice | Q34338809 | ||
| Quantitative Analyses of SMN1 and SMN2 Based on Real-Time LightCycler PCR: Fast and Highly Reliable Carrier Testing and Prediction of Severity of Spinal Muscular Atrophy | Q34353103 | ||
| Trinucleotide repeat length instability and age of onset in Huntington's disease | Q34357407 | ||
| lncRNAdb v2.0: expanding the reference database for functional long noncoding RNAs | Q34444320 | ||
| A GNAS1 imprinting defect in pseudohypoparathyroidism type IB | Q34457845 | ||
| Bidirectional expression of CUG and CAG expansion transcripts and intranuclear polyglutamine inclusions in spinocerebellar ataxia type 8. | Q34542422 | ||
| An atlas of human long non-coding RNAs with accurate 5' ends. | Q34552181 | ||
| Diagnostic tests in Hirschsprung disease: a systematic review | Q34567605 | ||
| Cross-talking noncoding RNAs contribute to cell-specific neurodegeneration in SCA7 | Q34628905 | ||
| An antisense transcript spanning the CGG repeat region of FMR1 is upregulated in premutation carriers but silenced in full mutation individuals | Q34699372 | ||
| A global view of genomic information--moving beyond the gene and the master regulator | Q35014896 | ||
| Long non-coding RNA expression profiles in hereditary haemorrhagic telangiectasia | Q35113337 | ||
| Towards a therapy for Angelman syndrome by targeting a long non-coding RNA. | Q35154104 | ||
| Antisense RNA controls LRP1 Sense transcript expression through interaction with a chromatin-associated protein, HMGB2 | Q35607134 | ||
| Human long non-coding RNAs promote pluripotency and neuronal differentiation by association with chromatin modifiers and transcription factors. | Q35739616 | ||
| Pathogenic RNA repeats: an expanding role in genetic disease | Q35885705 | ||
| Translational control at the synapse | Q35919452 | ||
| Dendritic BC200 RNA in aging and in Alzheimer's disease | Q35973450 | ||
| Polyglutamine disease and neuronal cell death. | Q36124665 | ||
| Subcellular partitioning of MRP RNA assessed by ultrastructural and biochemical analysis | Q36233859 | ||
| Long noncoding RNA AK056155 involved in the development of Loeys-Dietz syndrome through AKT/PI3K signaling pathway | Q36261531 | ||
| Ube3a-ATS is an atypical RNA polymerase II transcript that represses the paternal expression of Ube3a | Q36301671 | ||
| LincRNA-p21 suppresses target mRNA translation | Q36431717 | ||
| Long non-coding RNAs display higher natural expression variation than protein-coding genes in healthy humans | Q36517502 | ||
| miR675 upregulates long noncoding RNA H19 through activating EGR1 in human liver cancer | Q36544748 | ||
| An intronic ncRNA-dependent regulation of SORL1 expression affecting Aβ formation is upregulated in post-mortem Alzheimer's disease brain samples. | Q36683066 | ||
| Mediator links epigenetic silencing of neuronal gene expression with x-linked mental retardation | Q36975019 | ||
| The long non-coding RNA nuclear-enriched abundant transcript 1_2 induces paraspeckle formation in the motor neuron during the early phase of amyotrophic lateral sclerosis | Q37060040 | ||
| Transcription is required for establishment of germline methylation marks at imprinted genes | Q37075687 | ||
| Physiological functions of the imprinted Gnas locus and its protein variants Galpha(s) and XLalpha(s) in human and mouse. | Q37078020 | ||
| Central nervous system imprinting of the G protein G(s)alpha and its role in metabolic regulation | Q37233680 | ||
| Paraspeckles: nuclear bodies built on long noncoding RNA | Q37342470 | ||
| Small RNAs derived from lncRNA RNase MRP have gene-silencing activity relevant to human cartilage-hair hypoplasia | Q37406415 | ||
| 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. | Q37503306 | ||
| Genome-wide interrogation reveals hundreds of long intergenic noncoding RNAs that associate with cardiometabolic traits | Q37530111 | ||
| Gene activation of SMN by selective disruption of lncRNA-mediated recruitment of PRC2 for the treatment of spinal muscular atrophy | Q37682281 | ||
| Circular RNA ZNF609 functions as a competitive endogenous RNA to regulate AKT3 expression by sponging miR-150-5p in Hirschsprung's disease | Q37702360 | ||
| RNA-mediated neurodegeneration in repeat expansion disorders | Q37725827 | ||
| Silver-Russell syndrome | Q37846992 | ||
| SREBPs: metabolic integrators in physiology and metabolism | Q37966406 | ||
| The four dimensions of noncoding RNA conservation. | Q38194745 | ||
| Regulation of circRNA biogenesis | Q38369224 | ||
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P433 | issue | Suppl 2 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | long non-coding RNA | Q15087973 |
| Hereditary Disease | Q58704310 | ||
| P304 | page(s) | 42 | |
| P577 | publication date | 2019-03-13 | |
| P13046 | publication type of scholarly work | review article | Q7318358 |
| P1433 | published in | BMC Medical Genomics | Q15754662 |
| P1476 | title | The role of long non-coding RNAs in the pathogenesis of hereditary diseases | |
| P478 | volume | 12 |
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| Q64096921 | Medical genomics research at BGRS-2018 |
| Q101564362 | Molecular landscape of long noncoding RNAs in brain disorders |
| Q91712623 | lncRNA SOX2-OT regulates laryngeal cancer cell proliferation, migration and invasion and induces apoptosis by suppressing miR-654 |
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