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PLoS ONE, ISSN 1932-6203, 2011, Volume 6, Issue 6, p. e20746
MicroRNAs (miRNAs) are small non-coding RNAs that associate with Argonaute proteins to regulate gene expression at the post-transcriptional level in the... 
5S RIBOSOMAL-RNA | P-BODIES | HUMAN-CELLS | MAMMALIAN MITOCHONDRIA | BIOLOGY | MICRORNA-DEPENDENT LOCALIZATION | PROTEIN COMPLEXES | TARGETING SEQUENCES | SECONDARY STRUCTURE | STRESS GRANULES | WEB SERVER | Cell Line | Conserved Sequence - genetics | Immunoprecipitation | Species Specificity | Chromosomes, Human - genetics | Genomics | Humans | RNA, Messenger - genetics | Gene Expression Regulation | Genome, Mitochondrial - genetics | Gene Expression Profiling | RNA, Messenger - metabolism | Protein Transport | MicroRNAs - isolation & purification | Animals | Cell Nucleus - genetics | Mitochondria - genetics | RNA Interference | RNA Transport - genetics | Models, Biological | Base Sequence | Argonaute Proteins | Eukaryotic Initiation Factor-2 - metabolism | Cytosol - metabolism | Proteins | DNA microarrays | MicroRNA | Analysis | Genes | Genetic aspects | Outsourcing | Genetic transcription | Post-transcription | Dehydrogenases | Pathogenesis | Crosstalk | Gene regulation | Confocal microscopy | Immunoblotting | Identification | Genomes | Mitochondrial DNA | Confocal | Kinases | Cytosol | Nuclei | Liver cancer | Mitochondria | Rodents | Localization | Bioinformatics | Polyclonal antibodies | Enzymes | Fractionation | Wildlife conservation | RNA-mediated interference | Interference | MiRNA | Argonaute 2 protein | Gene expression | Ribonucleic acid--RNA | Studies | Polymerase chain reaction | Acids | Microscopy | Contaminants | MicroRNAs | Computer applications | Cytoplasm | RNA | Ribonucleic acid
Journal Article
Nature Genetics, ISSN 1061-4036, 09/2012, Volume 44, Issue 9, pp. 975 - 977
Journal Article
Nature Medicine, ISSN 1078-8956, 10/2017, Volume 23, Issue 10, pp. 1226 - 1233
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 05/2017, Volume 54, Issue 5, pp. 346 - 356
Journal Article
PLoS ONE, ISSN 1932-6203, 10/2018, Volume 13, Issue 10, p. e0205826
Journal Article
Journal Article
Science, ISSN 0036-8075, 2014, Volume 343, Issue 6170, pp. 506 - 511
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 3/2012, Volume 109, Issue 13, pp. 4980 - 4985
The human genome is densely populated with transposons and transposon-like repetitive elements. Although the impact of these transposons and elements on human... 
Retrotransposons | Nervous system diseases | MicroRNA | Transposons | RNA | Small interfering RNA | Genetic loci | Encephalopathies | Genetic mutation | Sequencing | Pediatrics | Medulla oblongata | Long noncoding RNA | Long interspersed element 1 | Genetic disease | long interspersed element 1 | MULTIDISCIPLINARY SCIENCES | IDENTIFICATION | PREDICTION | ELEMENTS | pediatrics | GENES | SEQUENCE | DISEASE | long noncoding RNA | SIGNAL RECOGNITION PARTICLE | CENTRAL-NERVOUS-SYSTEM | genetic disease | EXPRESSION | medulla oblongata | BRAIN | Geography | Chromosomes, Human, Pair 8 - genetics | Conserved Sequence - genetics | Genes, Recessive - genetics | Humans | Brain Diseases - genetics | Molecular Sequence Data | Nucleotides - genetics | Infant | Anorexia - genetics | Genetic Loci | Anorexia - complications | RNA, Untranslated - genetics | Retroelements - genetics | Young Adult | Base Sequence | RNA, Untranslated - chemistry | Nucleic Acid Conformation | Introns - genetics | Indian Ocean | Chromosome Mapping | Mutation - genetics | Disease Progression | Magnetic Resonance Imaging | Phenotype | Primates - genetics | Animals | Brain Diseases - pathology | Brain Diseases - complications | Chromosome Segregation - genetics | Encephalopathy | Physiological aspects | Development and progression | Genetic aspects | Health aspects | Life Sciences | Human health and pathology | Neurons and Cognition | Neurobiology | Genetics | Human genetics | Biological Sciences
Journal Article
Molecular Therapy - Nucleic Acids, ISSN 2162-2531, 2012, Volume 1, Issue 6, pp. e29 - e29
Leber congenital amaurosis (LCA) is a severe hereditary retinal dystrophy responsible for congenital or early-onset blindness. The most common disease-causing... 
ciliogenesis repair | LCA | antisense oligonucleotide | CEP290 | splice switching-mediated therapy | Ciliogenesis repair | Antisense oligonucleotide | Splice switching-mediated therapy | MEDICINE, RESEARCH & EXPERIMENTAL | Original
Journal Article
Journal of Clinical Immunology, ISSN 0271-9142, 10/2017, Volume 37, Issue 7, pp. 715 - 726
Journal Article
Frontiers in Genetics, ISSN 1664-8021, 11/2019, Volume 10
Despite the astonishing progress in treating chronic hepatitis C virus (HCV) infection with direct-acting antiviral agents, liver fibrosis remains a major... 
Care and treatment | Usage | Genome-wide association studies | Genetic aspects | Diagnosis | High-throughput screening (Biochemical assaying) | Hepatitis C | Risk factors | exome sequencing | TGF-beta | rare-variant association study | endoglin | HCV-related liver fibrosis
Journal Article