Involvement of long noncoding RNAs in diseases affecting the central nervous system

Duplexes of 21-nucleotide RNAs mediate RNA interference in cultured mammalian cells

Elbashir, S. M., Harborth, J., Lendeckel, W., Yalcin, A., Weber, K., & Tuschl, T. (2001) · Nature · doi:10.1038/35078107 · Cited by 9,456 · see citing works

High-Resolution Profiling of Histone Methylations in the Human Genome

Barski, A., Cuddapah, S., Cui, K., Roh, T.-Y., Schones, D. E., Wang, Z., Wei, G., Chepelev, I., & Zhao, K. (2007) · Cell · doi:10.1016/j.cell.2007.05.009 · Cited by 6,845 · see citing works

Long non-coding RNAs: insights into functions

Mercer, T. R., Dinger, M. E., & Mattick, J. S. (2009) · Nature Reviews Genetics · doi:10.1038/nrg2521 · Cited by 5,654 · see citing works

Long non-coding RNA HOTAIR reprograms chromatin state to promote cancer metastasis

Gupta, R. A., Shah, N., Wang, K., Kim, J., Horlings, H. M., Wong, D. J., Tsai, M.-C., Hung, T., Argani, P., Rinn, J. L., et al. (2010) · Nature · doi:10.1038/nature08975 · Cited by 5,203 · see citing works

Non-coding RNAs in human disease

Esteller, M. (2011) · Nature Reviews Genetics · doi:10.1038/nrg3074 · Cited by 4,825 · see citing works

Evolutionarily conserved elements in vertebrate, insect, worm, and yeast genomes

Siepel, A., Bejerano, G., Pedersen, J. S., Hinrichs, A. S., Hou, M., Rosenbloom, K., Clawson, H., Spieth, J., Hillier, L. W., Richards, S., et al. (2005) · Genome Research · doi:10.1101/gr.3715005 · Cited by 4,408 · see citing works

Functional Demarcation of Active and Silent Chromatin Domains in Human HOX Loci by Noncoding RNAs

Rinn, J. L., Kertesz, M., Wang, J. K., Squazzo, S. L., Xu, X. H., Brugmann, S. A., Goodnough, L. H., Helms, J. A., Farnham, P., Segal, E., et al. (2007) · Cell · doi:10.1016/j.cell.2007.05.022 · Cited by 4,246 · see citing works

Chromatin signature reveals over a thousand highly conserved large non-coding RNAs in mammals

Guttman, M., Amit, I., Garber, M., French, C., Lin, M. F., Feldser, D., Huarte, M., Zuk, O., Carey, B. W., Cassady, J. P., et al. (2009) · Nature · doi:10.1038/nature07672 · Cited by 4,098 · see citing works

CpG motifs in bacterial DNA trigger direct B-cell activation

Krieg, A. M., Yi, A.-K., Matson, S., Waldschmidt, T. J., Bishop, G. A., Teasdale, R., Koretzky, G. A., & Klinman, D. M. (1995) · Nature · doi:10.1038/374546a0 · Cited by 3,508 · see citing works

Long Noncoding RNA as Modular Scaffold of Histone Modification Complexes

Tsai, M.-C., Manor, O., Wan, Y., Mosammaparast, N., Wang, J. K., Lan, F., Shi, Y., Segal, E., & Chang, H. Y. (2010) · Science · doi:10.1126/science.1192002 · Cited by 3,290 · see citing works

Genome-Wide Mapping of in Vivo Protein-DNA Interactions

Johnson, D. S., Mortazavi, A., Myers, R. M., & Wold, B. (2007) · Science · doi:10.1126/science.1141319 · Cited by 2,927 · see citing works

Many human large intergenic noncoding RNAs associate with chromatin-modifying complexes and affect gene expression

Khalil, A. M., Guttman, M., Huarte, M., Garber, M., Raj, A., Rivea Morales, D., Thomas, K., Presser, A., Bernstein, B. E., van Oudenaarden, A., et al. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0904715106 · Cited by 2,872 · see citing works

RNA Maps Reveal New RNA Classes and a Possible Function for Pervasive Transcription

Kapranov, P., Cheng, J., Dike, S., Nix, D. A., Duttagupta, R., Willingham, A. T., Stadler, P. F., Jana Hertel, A., Jörg Hackermüller, A., Hofacker, I. L., et al. (2007) · Science · doi:10.1126/science.1138341 · Cited by 2,519 · see citing works

A Large Intergenic Noncoding RNA Induced by p53 Mediates Global Gene Repression in the p53 Response

Huarte, M., Guttman, M., Feldser, D., Garber, M., Koziol, M. J., Kenzelmann-Broz, D., Khalil, A. M., Zuk, O., Amit, I., Rabani, M., et al. (2010) · Cell · doi:10.1016/j.cell.2010.06.040 · Cited by 2,053 · see citing works

Inhibition of Rous sarcoma virus replication and cell transformation by a specific oligodeoxynucleotide.

Zamecnik, P. C., & Stephenson, M. L. (1978) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.75.1.280 · Cited by 1,792 · see citing works

Antisense Transcription in the Mammalian Transcriptome

Katayama, S., Tomaru, Y., Kasukawa, T., Waki, K., Nakanishi, M., Nakamura, M., Nishida, H., Yap, C.-S., Suzuki, M., Kawai, J., et al. (2005) · Science · doi:10.1126/science.1112009 · Cited by 1,661 · see citing works

Molecular Signatures of Natural Selection

Nielsen, R. (2005) · Annual Review of Genetics · doi:10.1146/annurev.genet.39.073003.112420 · Cited by 1,660 · see citing works

Polycomb Proteins Targeted by a Short Repeat RNA to the Mouse X Chromosome

Zhao, J. C., Sun, B. K., Erwin, J. A., Song, J., & Lee, J. T. (2008) · Science · doi:10.1126/science.1163045 · Cited by 1,580 · see citing works

Expression of a noncoding RNA is elevated in Alzheimer's disease and drives rapid feed-forward regulation of β-secretase

Faghihi, M. A., Modarresi, F., Khalil, A. M., Wood, D. E., Sahagan, B. G., Morgan, T. E., Finch, C. E., St. Laurent III, G., Kenny, P. J., & Wahlestedt, C. (2008) · Nature Medicine · doi:10.1038/nm1784 · Cited by 1,416 · see citing works

Molecular Interplay of the Noncoding RNA ANRIL and Methylated Histone H3 Lysine 27 by Polycomb CBX7 in Transcriptional Silencing of INK4a

Yap, K. L., Li, S., Muñoz-Cabello, A. M., Raguz, S., Zeng, L., Mujtaba, S., Gil, J., Walsh, M. J., & Zhou, M.-M. (2010) · Molecular Cell · doi:10.1016/j.molcel.2010.03.021 · Cited by 1,391 · see citing works

UBE3A/E6-AP mutations cause Angelman syndrome

Kishino, T., Lalande, M., & Wagstaff, J. E. (1997) · Nature Genetics · doi:10.1038/ng0197-70 · Cited by 1,304 · see citing works

Disruption of two novel genes by a translocation co-segregating with schizophrenia

Millar, J. K. (2000) · Human Molecular Genetics · doi:10.1093/hmg/9.9.1415 · Cited by 1,254 · see citing works

Kcnq1ot1 Antisense Noncoding RNA Mediates Lineage-Specific Transcriptional Silencing through Chromatin-Level Regulation

Pandey, R. R., Mondal, T., Mohammad, F., Enroth, S., Redrup, L., Komorowski, J., Nagano, T., Mancini‐DiNardo, D., & Kanduri, C. (2008) · Molecular Cell · doi:10.1016/j.molcel.2008.08.022 · Cited by 1,192 · see citing works

Extensive and coordinated transcription of noncoding RNAs within cell-cycle promoters

Hung, T., Wang, Y., Lin, M. F., Koegel, A. K., Kotake, Y., Grant, G. D., Horlings, H. M., Shah, N., Umbricht, C. B., Wang, P., et al. (2011) · Nature Genetics · doi:10.1038/ng.848 · Cited by 1,165 · see citing works

Inactivating mutations of the histone methyltransferase gene EZH2 in myeloid disorders

Ernst, T., Chase, A. J., Score, J., Hidalgo-Curtis, C. E., Bryant, C., Jones, A. V., Waghorn, K., Zoi, K., Ross, F. M., Reiter, A., et al. (2010) · Nature Genetics · doi:10.1038/ng.621 · Cited by 1,139 · see citing works

Non‐coding RNAs: regulators of disease

Taft, R. J., Pang, K. C., Mercer, T. R., Dinger, M. E., & Mattick, J. S. (2009) · The Journal of Pathology · doi:10.1002/path.2638 · Cited by 1,056 · see citing works

Initial impact of the sequencing of the human genome

Lander, E. S. (2011) · Nature · doi:10.1038/nature09792 · Cited by 1,044 · see citing works

Neuroprotective effects of brain-derived neurotrophic factor in rodent and primate models of Alzheimer's disease

Nagahara, A. H., Merrill, D. A., Coppola, G., Tsukada, S., Schroeder, B. E., Shaked, G. M., Wang, L., Blesch, A., Kim, A., Conner, J. M., et al. (2009) · Nature Medicine · doi:10.1038/nm.1912 · Cited by 1,034 · see citing works

Genomewide Analysis of PRC1 and PRC2 Occupancy Identifies Two Classes of Bivalent Domains

Ku, M., Koche, R. P., Rheinbay, E., Mendenhall, E. M., Endoh, M., Mikkelsen, T. S., Aiden, A. P., Nusbaum, C., Xie, X. S., Chi, A. S., et al. (2008) · PLoS Genetics · doi:10.1371/journal.pgen.1000242 · Cited by 1,011 · see citing works

An RNA gene expressed during cortical development evolved rapidly in humans

Pollard, K. S., Salama, S. R., Lambert, N., Lambot, M.-A., Coppens, S., Pedersen, J. S., Katzman, S., King, B., Onodera, C., Siepel, A., et al. (2006) · Nature · doi:10.1038/nature05113 · Cited by 1,005 · see citing works

Long non-coding RNA ANRIL is required for the PRC2 recruitment to and silencing of p15INK4B tumor suppressor gene

Kotake, Y., Nakagawa, T., Kitagawa, K., Suzuki, S., Liu, N., Kitagawa, M., & Xiong, Y. (2011) · Oncogene · doi:10.1038/onc.2010.568 · Cited by 1,001 · see citing works

Induced ncRNAs allosterically modify RNA-binding proteins in cis to inhibit transcription

Wang, X., Arai, S., Song, X., Reichart, D. R., Du, K., Pascual, G., Tempst, P., Rosenfeld, M. G., Glass, C. K., & Kurokawa, R. (2008) · Nature · doi:10.1038/nature06992 · Cited by 988 · see citing works

Expandable DNA repeats and human disease

Mirkin, S. M. (2007) · Nature · doi:10.1038/nature05977 · Cited by 934 · see citing works

Repeat instability: mechanisms of dynamic mutations

Pearson, C. E., Edamura, K. N., & Cleary, J. D. (2005) · Nature Reviews Genetics · doi:10.1038/nrg1689 · Cited by 924 · see citing works

Divergent transcription from active promoters

Seila, A. C., Calabrese, J. M., Levine, S., Yeo, G. W., Rahl, P., Flynn, R. A., Young, R., & Sharp, P. (2008) · Science · doi:10.1126/science.1162253 · Cited by 923 · see citing works

BDNF mRNA is decreased in the hippocampus of individuals with Alzheimer's disease

Phillips, H. S., Hains, J. M., Armanini, M., Laramee, G. R., Johnson, S. A., & Winslow, J. W. (1991) · Neuron · doi:10.1016/0896-6273(91)90273-3 · Cited by 921 · see citing works

The Air Noncoding RNA Epigenetically Silences Transcription by Targeting G9a to Chromatin

Nagano, T., Mitchell, J. A., Sanz, L. A., Pauler, F. M., Ferguson‐Smith, A. C., Feil, R., & Fraser, P. (2008) · Science · doi:10.1126/science.1163802 · Cited by 907 · see citing works

De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome

Matsuura, T., Sutcliffe, J. S., Fang, P., Galjaard, R. H., Jiang, Y., Benton, C. S., Rommens, J. M., & Beaudet, A. L. (1997) · Nature Genetics · doi:10.1038/ng0197-74 · Cited by 858 · see citing works

The neuronal microRNA system

Kosik, K. S. (2006) · Nature reviews. Neuroscience · doi:10.1038/nrn2037 · Cited by 823 · see citing works

Epigenetic silencing of tumour suppressor gene p15 by its antisense RNA

Yu, W., Gius, D. R., Onyango, P. O., Muldoon‐Jacobs, K., Karp, J. E., Feinberg, A. P., & Cui, H. (2008) · Nature · doi:10.1038/nature06468 · Cited by 801 · see citing works

Viral Strategies of Immune Evasion

Ploegh, H. L. (1998) · Science · doi:10.1126/science.280.5361.248 · Cited by 786 · see citing works

RNA Exosome Depletion Reveals Transcription Upstream of Active Human Promoters

Preker, P., Nielsen, J. S., Kammler, S., Lykke‐Andersen, S., Christensen, M. S., Mapendano, C. K., Schierup, M. H., & Jensen, T. H. (2008) · Science · doi:10.1126/science.1164096 · Cited by 777 · see citing works

Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion

David, G., Abbas, N., Stévanin, G., Dürr, A., Yvert, G., Cancel‐Tassin, G., Weber, C., Imbert, G., Saudou, F., Antoniou, E., et al. (1997) · Nature Genetics · doi:10.1038/ng0997-65 · Cited by 769 · see citing works

A long nuclear‐retained non‐coding RNA regulates synaptogenesis by modulating gene expression

Bernard, D., Prasanth, K. V., Tripathi, V., Colasse, S., Nakamura, T., Xuan, Z., Zhang, M. Q., Sedel, F., Jourdren, L., Coulpier, F., et al. (2010) · The EMBO Journal · doi:10.1038/emboj.2010.199 · Cited by 738 · see citing works

Schizophrenia and Affective Disorders—Cosegregation with a Translocation at Chromosome 1q42 That Directly Disrupts Brain-Expressed Genes: Clinical and P300 Findings in a Family

Blackwood, D., Fordyce, A., Walker, M. T., Clair, D. M. S., Porteous, D. J., & Muir, W. J. (2001) · The American Journal of Human Genetics · doi:10.1086/321969 · Cited by 734 · see citing works

Repression of the human dihydrofolate reductase gene by a non-coding interfering transcript

Martianov, I., Ramadass, A., Barros, A. S., Chow, N., & Akoulitchev, A. V. (2007) · Nature · doi:10.1038/nature05519 · Cited by 728 · see citing works

The <i>Evf-2</i> noncoding RNA is transcribed from the Dlx-5/6 ultraconserved region and functions as a Dlx-2 transcriptional coactivator

Feng, J., Bi, C., Clark, B. S., Mady, R., Shah, P., & Kohtz, J. D. (2006) · Genes &amp; Development · doi:10.1101/gad.1416106 · Cited by 712 · see citing works

Repeat instability : mechanisms of dynamic mutations

Pearson, C. E. (2005) · Medical Entomology and Zoology · Cited by 711 · see citing works

Engineering targeted viral vectors for gene therapy

Waehler, R., Russell, S. J., & Curiel, D. T. (2007) · Nature Reviews Genetics · doi:10.1038/nrg2141 · Cited by 687 · see citing works

Identification of an Amplified, Highly Expressed Gene in a Human Glioma

Kinzler, K. W., Bigner, S. H., Bigner, D. D., Trent, J. M., Law, M. L., O’Brien, S. J., Wong, A. J., & Vogelstein, B. (1987) · Science · doi:10.1126/science.3563490 · Cited by 678 · see citing works

Inferring Nonneutral Evolution from Human-Chimp-Mouse Orthologous Gene Trios

Clark, A. G., Glanowski, S., Nielsen, R., Thomas, P. D., Kejariwal, A., Todd, M. A., Tanenbaum, D. M., Civello, D., Lu, F., Murphy, B., et al. (2003) · Science · doi:10.1126/science.1088821 · Cited by 669 · see citing works

Inhibition of natural antisense transcripts in vivo results in gene-specific transcriptional upregulation

Modarresi, F., Faghihi, M. A., López-Toledano, M. A., Fatemi, R. P., Magistri, M., Brothers, S. P., van der Brug, M. P., & Wahlestedt, C. (2012) · Nature Biotechnology · doi:10.1038/nbt.2158 · Cited by 668 · see citing works

Antisense correction of SMN2 splicing in the CNS rescues necrosis in a type III SMA mouse modelPreprint

Hua, Y., Sahashi, K., Hung, G., Rigo, F., Passini, M. A., Bennett, C. F., & Krainer, A. R. (2010) · Genes & Development · doi:10.1101/gad.1941310 · Cited by 665 · see citing works

CTCF is a uniquely versatile transcription regulator linked to epigenetics and disease

Ohlsson, R., Renkawitz, R., & Lobanenkov, V. (2001) · Trends in Genetics · doi:10.1016/s0168-9525(01)02366-6 · Cited by 591 · see citing works

lncRNAdb: a reference database for long noncoding RNAs

Amaral, P., Clark, M. B., Gascoigne, D. K., Dinger, M. E., & Mattick, J. S. (2010) · Nucleic Acids Research · doi:10.1093/nar/gkq1138 · Cited by 584 · see citing works

Aberrations of EZH2 in Cancer

Chase, A., & Cross, N. C. P. (2011) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-10-2156 · Cited by 548 · see citing works

Role of brain-derived neurotrophic factor in Huntington's disease

Zuccato, C., & Cattaneo, E. F. (2007) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2007.01.003 · Cited by 548 · see citing works

Antisense Oligonucleotides Delivered to the Mouse CNS Ameliorate Symptoms of Severe Spinal Muscular Atrophy

Passini, M. A., Bu, J., Richards, A. M., Kinnecom, C., Sardi, S. P., Stanek, L. M., Hua, Y., Rigo, F., Matson, J. E., Hung, G., et al. (2011) · Science Translational Medicine · doi:10.1126/scitranslmed.3001777 · Cited by 547 · see citing works

The Antisense Transcriptomes of Human Cells

He, Y., Vogelstein, B., Velculescu, V. E., Papadopoulos, N., & Kinzler, K. W. (2008) · Science · doi:10.1126/science.1163853 · Cited by 531 · see citing works

Modulation of Anxiety and Neuropeptide Y-Y1 Receptors by Antisense Oligodeoxynucleotides

Wahlestedt, C., Pich, E. M., Koob, G. F., Yee, F., & Heilig, M. A. (1993) · Science · doi:10.1126/science.8380941 · Cited by 524 · see citing works

Antisense oligonucleotide therapy for neurodegenerative disease

Smith, R. A. (2006) · Journal of Clinical Investigation · doi:10.1172/jci25424 · Cited by 506 · see citing works

Chronic Pharmacological mGlu5 Inhibition Corrects Fragile X in Adult Mice

Michalon, A., Sidorov, M., Ballard, T. M., Ozmen, L., Spooren, W., Wettstein, J. G., Jaeschke, G., Bear, M. F., & Lindemann, L. (2012) · Neuron · doi:10.1016/j.neuron.2012.03.009 · Cited by 489 · see citing works

A Pituitary-Derived MEG3 Isoform Functions as a Growth Suppressor in Tumor Cells

Zhang, X., Zhou, Y., Mehta, K. R., Danila, D. C., Scolavino, S., Johnson, S. R., & Klibanski, A. (2003) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2003-030222 · Cited by 436 · see citing works

Targeted therapy for high-grade glioma with the TGF- 2 inhibitor trabedersen: results of a randomized and controlled phase IIb study

Bogdahn, U., Hau, P., Stockhammer, G., Venkataramana, N. K., Mahapatra, A. K., Suri, A., Balasubramaniam, A., Nair, S., Oliushine, V., Parfenov, V., et al. (2011) · Neuro-Oncology · doi:10.1093/neuonc/noq142 · Cited by 433 · see citing works

Repeat instability as the basis for human diseases and as a potential target for therapy

López Castel, A., Cleary, J. D., & Pearson, C. E. (2010) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2854 · Cited by 429 · see citing works

Long non-coding RNAs in nervous system function and disease

Qureshi, I., Mattick, J. S., & Mehler, M. F. (2010) · Brain Research · doi:10.1016/j.brainres.2010.03.110 · Cited by 426 · see citing works

Bidirectional expression of CUG and CAG expansion transcripts and intranuclear polyglutamine inclusions in spinocerebellar ataxia type 8

Moseley, M. L., Zu, T., Ikeda, Y., Gao, W., Mosemiller, A. K., Daughters, R. S., Chen, G., Weatherspoon, M. R., Clark, H. B., Ebner, T. J., et al. (2006) · Nature Genetics · doi:10.1038/ng1827 · Cited by 422 · see citing works

Small molecule BDNF mimetics activate TrkB signaling and prevent neuronal degeneration in rodents

Massa, S. M., Yang, T., Xie, Y., Shi, J., Bilgen, M., Joyce, J. N., Nehama, D., Rajadas, J., & Longo, F. M. (2010) · Journal of Clinical Investigation · doi:10.1172/jci41356 · Cited by 406 · see citing works

Transcription Regulation Through Promoter-Proximal Pausing of RNA Polymerase II

Core, L. J., & Lis, J. T. (2008) · Science · doi:10.1126/science.1150843 · Cited by 406 · see citing works

Balanced gene regulation by an embryonic brain ncRNA is critical for adult hippocampal GABA circuitry

Bond, A. M., VanGompel, M. J. W., Sametsky, E. A., Clark, M. F., Savage, J. C., Disterhoft, J. F., & Kohtz, J. D. (2009) · Nature Neuroscience · doi:10.1038/nn.2371 · Cited by 399 · see citing works

Long noncoding RNAs in neuronal-glial fate specification and oligodendrocyte lineage maturation

Mercer, T. R., Qureshi, I., Gökhan, Ş., Dinger, M. E., Li, G., Mattick, J. S., & Mehler, M. F. (2010) · BMC Neuroscience · doi:10.1186/1471-2202-11-14 · Cited by 390 · see citing works

Topoisomerase inhibitors unsilence the dormant allele of Ube3a in neurons

Huang, H.-S., Allen, J. A., Mabb, A. M., King, I. F., Miriyala, J., Taylor-Blake, B., Sciaky, N., Dutton, J. W., Lee, H.-M., Chen, X., et al. (2012) · Nature · doi:10.1038/nature10726 · Cited by 387 · see citing works

Genomic imprinting effects on brain development and function

Wilkinson, L. S., Davies, W., & Isles, A. R. (2007) · Nature reviews. Neuroscience · doi:10.1038/nrn2235 · Cited by 373 · see citing works

Epigenetic regulation of gene expression in physiological and pathological brain processes

Gräff, J., Kim, D., Dobbin, M. M., & Tsai, L.-H. (2011) · Physiological Reviews · doi:10.1152/physrev.00012.2010 · Cited by 373 · see citing works

Antisense oligodeoxynucleotides to NMDA-R1 receptor channel protect cortical neurons from excitotoxicity and reduce focal ischaemic infarctions

Wahlestedt, C., Golanov, E. V., Yamamoto, S., Yee, F., Ericson, H., Yoo, H., Inturrisi, C. E., & Reis, D. J. (1993) · Nature · doi:10.1038/363260a0 · Cited by 372 · see citing works

Therapeutic applications of implantable drug delivery systems

Dash, A., & Cudworth, G. (1998) · Journal of Pharmacological and Toxicological Methods · doi:10.1016/s1056-8719(98)00027-6 · Cited by 358 · see citing works

Epigenetics of autism spectrum disorders

Schanen, N. C. (2006) · Human Molecular Genetics · doi:10.1093/hmg/ddl213 · Cited by 341 · see citing works

Bidirectional Transcription Directs Both Transcriptional Gene Activation and Suppression in Human Cells

Morris, K. V., Santoso, S., Turner, A. W., Pastori, C., & Hawkins, P. G. (2008) · PLoS Genetics · doi:10.1371/journal.pgen.1000258 · Cited by 330 · see citing works

Complex Loci in Human and Mouse Genomes

Engström, P. G., Suzuki, H., Ninomiya, N., Akalin, A., Sessa, L., Lavorgna, G., Brozzi, A., Luzi, L., Tan, S. L., Yang, L., et al. (2006) · PLoS Genetics · doi:10.1371/journal.pgen.0020047 · Cited by 294 · see citing works

Noncoding RNAs and RNA Editing in Brain Development, Functional Diversification, and Neurological Disease

Mehler, M. F., & Mattick, J. S. (2007) · Physiological Reviews · doi:10.1152/physrev.00036.2006 · Cited by 293 · see citing works

Activation of human B cells by phosphorothioate oligodeoxynucleotides.

Liang, H., Nishioka, Y., Reich, C. F., Pisetsky, D. S., & Lipsky, P. E. (1996) · Journal of Clinical Investigation · doi:10.1172/jci118894 · Cited by 284 · see citing works

Antisense Transcription and Heterochromatin at the DM1 CTG Repeats Are Constrained by CTCF

Cho, D. H., Thienes, C. P., Mahoney, S. E., Analau, E., Filippova, G. N., & Tapscott, S. J. (2005) · Molecular Cell · doi:10.1016/j.molcel.2005.09.002 · Cited by 283 · see citing works

RNA Gain-of-Function in Spinocerebellar Ataxia Type 8

Daughters, R. S., Tuttle, D. L., Gao, W., Ikeda, Y., Moseley, M. L., Ebner, T. J., Swanson, M. S., & Ranum, L. P. W. (2009) · PLoS Genetics · doi:10.1371/journal.pgen.1000600 · Cited by 278 · see citing works

Understanding microRNAs in neurodegeneration

Eacker, S. M., Dawson, T. M., & Dawson, V. L. (2009) · Nature reviews. Neuroscience · doi:10.1038/nrn2726 · Cited by 275 · see citing works

Calcium signaling cascade links dopamine D1–D2 receptor heteromer to striatal BDNF production and neuronal growth

Hasbi, A., Fan, T., Alijaniaram, M., Nguyen, T., Perreault, M. L., O’Dowd, B. F., & George, S. R. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0903676106 · Cited by 274 · see citing works

Imprinted Genes, Placental Development and Fetal Growth

Fowden, A. L., Sibley, C. P., Reik, W., & Constância, M. (2006) · Hormone Research in Paediatrics · doi:10.1159/000091506 · Cited by 273 · see citing works

Neurons but not glial cells show reciprocal imprinting of sense and antisense transcripts of Ube3a

Yamasaki, K. (2003) · Human Molecular Genetics · doi:10.1093/hmg/ddg106 · Cited by 273 · see citing works

Brain-derived neurotrophic factor (BDNF) gene polymorphisms shape cortical plasticity in humans

Antal, A., Chaieb, L., Moliadze, V., Monte-Silva, K. K., Poreisz, C., Thirugnanasambandam, N., Nitsche, M. A., Shoukier, M., Ludwig, H., & Paulus, W. (2010) · Brain stimulation · doi:10.1016/j.brs.2009.12.003 · Cited by 256 · see citing works

An antisense transcript spanning the CGG repeat region of FMR1 is upregulated in premutation carriers but silenced in full mutation individuals

Ladd, P. D., Smith, L. E., Rabaia, N. A., Moore, J. M., Georges, S. A., Hansen, R. S., Hagerman, R. J., Tassone, F., Tapscott, S. J., & Filippova, G. N. (2007) · Human Molecular Genetics · doi:10.1093/hmg/ddm293 · Cited by 248 · see citing works

Macrophage Delivery of Nanoformulated Antiretroviral Drug to the Brain in a Murine Model of NeuroAIDS

Dou, H., Grotepas, C. B., McMillan, J., Destache, C. J., Chaubal, M. V., Werling, J. O., Kipp, J., Rabinow, B. E., & Gendelman, H. E. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0900274 · Cited by 238 · see citing works

Prelimbic cortical BDNF is required for memory of learned fear but not extinction or innate fear

Choi, D. C., Maguschak, K. A., Ye, K., Jang, S.-W., Myers, K. M., & Ressler, K. J. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0909359107 · Cited by 212 · see citing works

Neurochemical and behavioral consequences of widespread gene knockdown in the adult mouse brain by using nonviral RNA interference

Thakker, D. R., Natt, F., Hüsken, D., Maier, R., Müller, M., van der Putten, H., Hoyer, D., & Cryan, J. F. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0406214101 · Cited by 211 · see citing works

Selective loss of δ opioid analgesia and binding by antisense oligodeoxynucleotides to a δ opioid receptor

Standifer, K. M., Chien, C., Wahlested, C., Brown, G. P., & Pasternak, G. W. (1994) · Neuron · doi:10.1016/0896-6273(94)90333-6 · Cited by 198 · see citing works

Inhibition of c-erbA mRNA splicing by a naturally occurring antisense RNA.

Munroe, S. H., & Lazar, M. A. (1991) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)54535-x · Cited by 189 · see citing works

The neuronal repressor REST/NRSF is an essential regulator in medulloblastoma cells

Lawinger, P., Radjendirane, V., Guo, Z. S., Immaneni, A., Sengupta, D., Lu, W., Rastelli, L., Carneiro, A. M. D., Levin, V. A., Fuller, G. N., et al. (2000) · Nature Medicine · doi:10.1038/77565 · Cited by 187 · see citing works

MicroRNA dysregulation in psychiatric disease

Miller, B. H., & Wahlestedt, C. (2010) · Brain Research · doi:10.1016/j.brainres.2010.03.035 · Cited by 181 · see citing works

Higher BDNF serum levels predict slower cognitive decline in Alzheimer's disease patients

Laske, C., Stellos, K., Hoffmann, N., Stransky, E., Straten, G., Eschweiler, G. W., & Leyhe, T. (2011) · The International Journal of Neuropsychopharmacology · doi:10.1017/s1461145710001008 · Cited by 180 · see citing works

A Novel RNA Transcript with Antiapoptotic Function Is Silenced in Fragile X Syndrome

Khalil, A. M., Faghihi, M. A., Modarresi, F., Brothers, S. P., & Wahlestedt, C. (2008) · PLoS ONE · doi:10.1371/journal.pone.0001486 · Cited by 172 · see citing works

Dynamics of PhiX174 protein E-mediated lysis of Escherichia coli

Witte, A., Wanner, G., Sulzner, M., & Lubitz, W. (1992) · Archives of Microbiology · doi:10.1007/bf00248685 · Cited by 172 · see citing works

Genetics and Epigenetics of the Multifunctional Protein CTCF

Filippova, G. N. (2007) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/s0070-2153(07)80009-3 · Cited by 170 · see citing works

Expression of HIF‐1α by human macrophages: implications for the use of macrophages in hypoxia‐regulated cancer gene therapy

Burke, B., Tang, N., Corke, K. P., Tazzyman, D., Ameri, K., Wells, M. W., & Lewis, C. E. (2001) · The Journal of Pathology · doi:10.1002/path.1029 · Cited by 169 · see citing works

Transcriptional Regulation: Cancer, Neurons and the REST

Coulson, J. M. (2005) · Current Biology · doi:10.1016/j.cub.2005.08.032 · Cited by 167 · see citing works

An Efficient Intrathecal Delivery of Small Interfering RNA to the Spinal Cord and Peripheral Neurons

Luo, M.-C., Zhang, D.-Q., Ma, S.-W., Huang, Y.-Y., Shuster, S. J., Porreca, F., & Lai, J. Y. (2005) · Molecular Pain · doi:10.1186/1744-8069-1-29 · Cited by 159 · see citing works

Imprinted gene expression in the brain

Davies, W., Isles, A. R., & Wilkinson, L. S. (2005) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2004.11.007 · Cited by 158 · see citing works

A Novel H19 Antisense RNA Overexpressed in Breast Cancer Contributes to Paternal IGF2 Expression

Berteaux, N., Aptel, N., Cathala, G., Genton, C., Coll, J., Daccache, A., Spruyt, N., Hondermarck, H., Dugimont, T., Curgy, J., et al. (2008) · Molecular and Cellular Biology · doi:10.1128/mcb.02103-07 · Cited by 156 · see citing works

Non‐coding RNAs in the nervous system

Mehler, M. F., & Mattick, J. S. (2006) · The Journal of Physiology · doi:10.1113/jphysiol.2006.113191 · Cited by 155 · see citing works

Knockdown of BACE1‐AS Nonprotein‐Coding Transcript Modulates Beta‐Amyloid‐Related Hippocampal Neurogenesis

Modarresi, F., Faghihi, M. A., Patel, N. S., Sahagan, B. G., Wahlestedt, C., & López-Toledano, M. A. (2011) · International Journal of Alzheimer s Disease · doi:10.4061/2011/929042 · Cited by 154 · see citing works

New therapeutic approach for brain tumors: Intranasal delivery of telomerase inhibitor GRN163

Hashizume, R., Ozawa, T., Gryaznov, S. M., Bollen, A. W., Lamborn, K. R., Frey, W. H., & Deen, D. F. (2008) · Neuro-Oncology · doi:10.1215/15228517-2007-052 · Cited by 150 · see citing works

Macrophages in gene therapy: cellular delivery vehicles and in vivo targets

Burke, B., Sumner, S., Maitland, N. J., & Lewis, C. E. (2002) · Journal of Leukocyte Biology · doi:10.1189/jlb.72.3.417 · Cited by 148 · see citing works

CTCF Regulates Ataxin-7 Expression through Promotion of a Convergently Transcribed, Antisense Noncoding RNA

Sopher, B. L., Ladd, P. D., Pineda, V. V., Libby, R. T., Sunkin, S. M., Hurley, J. B., Thienes, C. P., Gaasterland, T., Filippova, G. N., & Spada, A. R. L. (2011) · Neuron · doi:10.1016/j.neuron.2011.05.027 · Cited by 126 · see citing works

REST In Good Times and Bad: Roles In Tumor Suppressor and Oncogenic Activities

Majumader, S. (2006) · Cell Cycle · doi:10.4161/cc.5.17.2982 · Cited by 126 · see citing works

Enhancer of Zeste 2 (EZH2) is up-regulated in malignant gliomas and in glioma stem-like cells

Orzan, F., Pellegatta, S., Poliani, P. L., Pisati, F., Caldera, V., Menghi, F., Kapetis, D., Marras, C. E., Schiffer, D., & Finocchiaro, G. (2010) · Neuropathology and Applied Neurobiology · doi:10.1111/j.1365-2990.2010.01132.x · Cited by 125 · see citing works

Noncoding RNAs in Long-Term Memory Formation

Mercer, T. R., Dinger, M. E., Mariani, J., Kosik, K. S., Mehler, M. F., & Mattick, J. S. (2007) · The Neuroscientist · doi:10.1177/1073858408319187 · Cited by 124 · see citing works

Inhibition of Coagulation by a Phosphorothioate Oligonucleotide

Henry, S. P., Novotny, W. F., LEEDS, J., Auletta, C. S., & Kornbrust, D. J. (1997) · Antisense and Nucleic Acid Drug Development · doi:10.1089/oli.1.1997.7.503 · Cited by 122 · see citing works

Angelman Syndrome, a Genomic Imprinting Disorder of the Brain

Chamberlain, S. J., & Lalande, M. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.1728-10.2010 · Cited by 115 · see citing works

An expanded CAG repeat sequence in spinocerebellar ataxia type 7.Preprint

Lindblad, K., Savontaus, M., Stevanin, G., Holmberg, M., Digre, K., Zander, C., Ehrsson, H., David, G., Benomar, A., Nikoskelainen, E., et al. (1996) · Genome Research · doi:10.1101/gr.6.10.965 · Cited by 111 · see citing works

Bacterial ghosts as novel advanced drug delivery systems: antiproliferative activity of loaded doxorubicin in human Caco-2 cells

Paukner, S., Köhl, G., & Lubitz, W. (2003) · Journal of Controlled Release · doi:10.1016/j.jconrel.2003.09.010 · Cited by 109 · see citing works

Virosomes for antigen and DNA delivery

Daemen, T., DEMARE, A., Bungener, L. B., de Jonge, J., Huckriede, A. L. W., & Wilschut, J. (2004) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2004.09.005 · Cited by 106 · see citing works

Differential Deployment of REST and CoREST Promotes Glial Subtype Specification and Oligodendrocyte Lineage Maturation

Abrajano, J. J., Qureshi, I., Gökhan, Ş., Zheng, D., Bergman, A., & Mehler, M. F. (2009) · PLoS ONE · doi:10.1371/journal.pone.0007665 · Cited by 106 · see citing works

Epigenetics and the nervous system

Mehler, M. F. (2008) · Annals of Neurology · doi:10.1002/ana.21595 · Cited by 100 · see citing works

Partners in crime: bidirectional transcription in unstable microsatellite disease

Batra, R., Charizanis, K., & Swanson, M. S. (2010) · Human Molecular Genetics · doi:10.1093/hmg/ddq132 · Cited by 99 · see citing works

Applications of Bacterial Ghosts in Biomedicine

Lubitz, P., Mayr, U. B., & Lubitz, W. (2009) · Advances in experimental medicine and biology · doi:10.1007/978-1-4419-1132-2_12 · Cited by 82 · see citing works

Parent-of-origin effects on handedness and schizophrenia susceptibility on chromosome 2p12-q11

Francks, C. (2003) · Human Molecular Genetics · doi:10.1093/hmg/ddg362 · Cited by 71 · see citing works

Associations between Brain-Derived Neurotrophic Factor Plasma Levels and Severity of the Illness, Recurrence and Symptoms in Depressed Patients

Dell’Osso, L., Debbio, A. D., Veltri, A., Bianchi, C., Roncaglia, I., Carlini, M., Massimetti, G., Dell’Osso, M. C., Vizzaccaro, C., Marazziti, D., et al. (2010) · Neuropsychobiology · doi:10.1159/000319946 · Cited by 68 · see citing works

DNA-Loaded Bacterial Ghosts Efficiently Mediate Reporter Gene Transfer and Expression in Macrophages

Paukner, S., Kudela, P., Köhl, G., Schlapp, T., Friedrichs, S., & Lubitz, W. (2004) · Molecular Therapy · doi:10.1016/j.ymthe.2004.09.024 · Cited by 68 · see citing works

Loci on chromosomes 6q and 6p interact to increase susceptibility to bipolar affective disorder in the national institute of mental health genetics initiative pedigrees

Schulze, T. G., Buervenich, S., Badner, J. A., Steele, C. J. M., Detera‐Wadleigh, S. D., Dick, D. M., Foroud, T., Cox, N. J., MacKinnon, D. F., Potash, J. B., et al. (2004) · Biological Psychiatry · doi:10.1016/j.biopsych.2004.04.004 · Cited by 68 · see citing works

Antisense Transcription in the Mammalian Transcriptome RIKEN Genome Exploration Research Group and Genome Science Group (Genome Network Project Core Group) and the FANTOM Consortium

Katayama, S., Tomaru, Y., Kasukawa, T., Waki, K., Nakanishi, M., Nakamura, M., Nishida, H., Yap, C.-S., Kawai, J., Suzuki, H., et al. (2005) · Cited by 63 · see citing works

The RAY1/ST7 Tumor-Suppressor Locus on Chromosome 7q31 Represents a Complex Multi-transcript System

Vincent, J. B., Petek, E., Thevarkunnel, S., Kolozsvari, D., Cheung, J., Patel, M., & Scherer, S. W. (2002) · Genomics · doi:10.1006/geno.2002.6835 · Cited by 58 · see citing works

Bacterial Ghosts as Novel Efficient Targeting Vehicles for DNA Delivery to the Human Monocyte-Derived Dendritic Cells

Kudela, P., Paukner, S., Mayr, U. B., Cholujová, D., Schwarczova, Z., Sedlák, J., Bízik, J., & Lubitz, W. (2005) · Journal of Immunotherapy · doi:10.1097/01.cji.0000154246.89630.6f · Cited by 52 · see citing works

Mouse brain gene expression changes after acute and chronic amphetamine

Sokolov, B. P., Polesskaya, O. O., & Uhl, G. R. (2003) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2003.01523.x · Cited by 50 · see citing works

Using attenuated salmonella typhi as tumor targeting vector for MDR1 siRNA delivery: An experimental study

Jiang, Z.-M., Zhao, P., Zhou, Z., Liu, J., Qin, L., & Wang, H. (2007) · Cancer Biology & Therapy · doi:10.4161/cbt.6.4.3850 · Cited by 43 · see citing works

Toxicologic Effects of an Oligodeoxynucleotide Phosphorothioate and Its Analogs Following Intravenous Administration in Rats

Agrawal, S., Zhao, Q., JIANG, Z., OLIVER, C., GILES, H., HEATH, J., & Serota, D. G. (1997) · Antisense and Nucleic Acid Drug Development · doi:10.1089/oli.1.1997.7.575 · Cited by 41 · see citing works

Antisense inhibition at the β-secretase-site of β-amyloid precursor protein reduces cerebral amyloid and acetyl cholinesterase activity in Tg2576

Chauhan, N. B., & Siegel, G. J. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2007.01.008 · Cited by 40 · see citing works

Localizing hotspots of antisense transcription

Finocchiaro, G., Carro, M. S., François, S., Parise, P., Ninni, V. D., & Müller, H. (2007) · Nucleic Acids Research · doi:10.1093/nar/gkm027 · Cited by 38 · see citing works

Oligonucleotides Tethered to a Short Polyguanylic Acid Stretch Are Targeted to Macrophages: Enhanced Antiviral Activity of a Vesicular Stomatitis Virus-Specific Antisense Oligonucleotide

Prasad, V., Hashim, S., Mukhopadhyay, A., Basu, S. K., & Roy, R. P. (1999) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.43.11.2689 · Cited by 30 · see citing works

Spinocerebellar ataxia type 8 larger triplet expansion alters histone modification and induces RNA foci

Chen, I., Lin, H.-Y., Lee, G.-C., Kao, S.-H., Chen, C., Wu, Y., Hsieh-Li, H.-M., Su, M., & Lee‐Chen, G. (2009) · BMC Molecular Biology · doi:10.1186/1471-2199-10-9 · Cited by 29 · see citing works

DNA Delivery to Cells in Culture Using Peptides

Zhang, L., Ambulos, N. P., & Mixson, A. J. (2004) · Humana Press eBooks · doi:10.1385/1-59259-649-5:33 · Cited by 13 · see citing works

GABAergic Circuit Development and Its Implication for CNS Disorders

Cristo, G. D., Pizzorusso, T., Cancedda, L., & Sernagor, E. (2011) · Neural Plasticity · doi:10.1155/2011/623705 · Cited by 9 · see citing works

Targeting long non-coding RNA to therapeutically upregulate gene expression

Wahlestedt, C. (2013) · Nature Reviews Drug Discovery · doi:10.1038/nrd4018 · Cited by 524 · see citing works

From Discovery to Function: The Expanding Roles of Long NonCoding RNAs in Physiology and Disease

Sun, M., & Kraus, W. L. (2014) · Endocrine Reviews · doi:10.1210/er.2014-1034 · Cited by 392 · see citing works

Personalized medicine in psychiatry: problems and promises

Ozomaro, U., Wahlestedt, C., & Nemeroff, C. B. (2013) · BMC Medicine · doi:10.1186/1741-7015-11-132 · Cited by 237 · see citing works

The Bromodomain protein BRD4 controls HOTAIR, a long noncoding RNA essential for glioblastoma proliferation

Pastori, C., Kapranov, P., Penas, C., Peschansky, V. J., Volmar, C., Sarkaria, J. N., Bregy, A., Komotar, R. J., Laurent, G. S., Ayad, N. G., et al. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1424220112 · Cited by 212 · see citing works

Regulation of the Apolipoprotein Gene Cluster by a Long Noncoding RNA

Halley, P., Kadakkuzha, B. M., Faghihi, M. A., Magistri, M., Zeier, Z. R., Khorkova, O., Coito, C., Hsiao, J. H., Lawrence, M. S., & Wahlestedt, C. (2014) · Cell Reports · doi:10.1016/j.celrep.2013.12.015 · Cited by 200 · see citing works

The Role of Long Noncoding RNAs in Neurodegenerative Diseases

Wan, P., Su, W., & Zhuo, Y. (2016) · Molecular Neurobiology · doi:10.1007/s12035-016-9793-6 · Cited by 174 · see citing works

Gene regulation of mammalian long non-coding RNA

Bunch, H. (2017) · Molecular Genetics and Genomics · doi:10.1007/s00438-017-1370-9 · Cited by 162 · see citing works

The Clinical Relevance of Long Non-Coding RNAs in Cancer

da Silva, A. M., Bullock, M. D., & Călin, G. A. (2015) · Cancers · doi:10.3390/cancers7040884 · Cited by 150 · see citing works

Long non‐coding RNA MALAT1 regulates retinal neurodegeneration through CREB signaling

Yao, J., Wang, X. Q., Li, Y., Shan, K., Yang, H., Wang, Y., Yao, M., Liu, C., Li, X., Shen, Y., et al. (2016) · EMBO Molecular Medicine · doi:10.15252/emmm.201505725 · Cited by 127 · see citing works

LncRNA NONRATT021972 siRNA regulates neuropathic pain behaviors in type 2 diabetic rats through the P2X7 receptor in dorsal root ganglia

Liu, S., Zou, L., Xie, J., Xie, W., Wen, S., Xie, Q., Gao, Y., Li, G., Zhang, C., Xu, C., et al. (2016) · Molecular Brain · doi:10.1186/s13041-016-0226-2 · Cited by 126 · see citing works

Long noncoding RNAs: regulation, function and cancer

Rafiee, A., Riazi‐Rad, F., Havaskary, M., & Nuri, F. (2018) · Biotechnology and Genetic Engineering Reviews · doi:10.1080/02648725.2018.1471566 · Cited by 126 · see citing works

Emerging epigenetic mechanisms of long non-coding RNAs

Schaukowitch, K., & Kim, T.-K. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.12.009 · Cited by 122 · see citing works

Long noncoding RNAs, emerging players in muscle differentiation and disease

Neguembor, M. V., Jothi, M., & Gabellini, D. (2014) · Skeletal Muscle · doi:10.1186/2044-5040-4-8 · Cited by 115 · see citing works

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

Pastori, C., Peschansky, V. J., Barbouth, D., Mehta, A., Silva, J., & Wahlestedt, C. (2013) · Human Genetics · doi:10.1007/s00439-013-1356-6 · Cited by 102 · see citing works

Antisense RNA Controls LRP1 Sense Transcript Expression through Interaction with a Chromatin-Associated Protein, HMGB2

Yamanaka, Y., Faghihi, M. A., Magistri, M., Álvarez-García, Ó., Lotz, M., & Wahlestedt, C. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.04.011 · Cited by 99 · see citing works

Genome-wide differential expression of synaptic long noncoding RNAs in autism spectrum disorder

Wang, Y., Zhao, X., Ju, W., Flory, M. J., Zhong, J. L., Jiang, S., Wang, P., Dong, X., Tao, X., Chen, Q., et al. (2015) · Translational Psychiatry · doi:10.1038/tp.2015.144 · Cited by 97 · see citing works

lncRNA NONRATT021972 siRNA Decreases Diabetic Neuropathic Pain Mediated by the P2X3 Receptor in Dorsal Root Ganglia

Peng, H., Zou, L., Xie, J., Wu, H., Wu, B., Zhu, G., Lv, Q., Zhang, X., Liu, S., Li, G., et al. (2016) · Molecular Neurobiology · doi:10.1007/s12035-015-9632-1 · Cited by 88 · see citing works

Anticancer Properties of Fenofibrate: A Repurposing Use

Lian, X., Wang, G., Zhou, H., Zheng, Z., Fu, Y., & Cai, L. (2018) · Journal of Cancer · doi:10.7150/jca.24488 · Cited by 86 · see citing works

RNA delivery biomaterials for the treatment of genetic and rare diseases

Zhao, W., Hou, X., Vick, O. G., & Dong, Y. (2019) · Biomaterials · doi:10.1016/j.biomaterials.2019.119291 · Cited by 82 · see citing works

Comprehensive Identification of Long Non-coding RNAs in Purified Cell Types from the Brain Reveals Functional LncRNA in OPC Fate Determination

Dong, X., Chen, K., Durán, R. C., You, Y., Sloan, S. A., Zhang, Y., Zong, S., Cao, Q., Barres, B. A., & Wu, J. Q. (2015) · PLoS Genetics · doi:10.1371/journal.pgen.1005669 · Cited by 82 · see citing works

Long Non-Coding RNAs in Cancer and Development: Where Do We Go from Here?

Hämmerle, M., & Gutschner, T. (2015) · International Journal of Molecular Sciences · doi:10.3390/ijms16011395 · Cited by 79 · see citing works

Epigenetics, a key for unlocking complex CNS disorders? Therapeutic implications

Szyf, M. (2015) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2014.01.009 · Cited by 76 · see citing works

Long noncoding RNA MRAK009713 is a novel regulator of neuropathic pain in rats

Li, G., Jiang, H., Zheng, C., Zhu, G., Xu, Y., Sheng, X., Wu, B., Guo, J., Zhu, S., Zhan, Y., et al. (2017) · Pain · doi:10.1097/j.pain.0000000000001013 · Cited by 74 · see citing works

Invited Review: Long non‐coding RNA s: important regulators in the development, function and disorders of the central nervous system

Durán, R. C., Wei, H., Kim, D. H., & Wu, J. Q. (2019) · Neuropathology and Applied Neurobiology · doi:10.1111/nan.12541 · Cited by 74 · see citing works

Pharmacological Insights into Halophyte Bioactive Extract Action on Anti-Inflammatory, Pain Relief and Antibiotics-Type Mechanisms

Giordano, R., Saii, Z., Fredsgaard, M., Hulkko, L. S. S., Poulsen, T. B. G., Thomsen, M. E., Henneberg, N. C., Zucolotto, S. M., Arendt‐Nielsen, L., Papenbrock, J., et al. (2021) · Molecules · doi:10.3390/molecules26113140 · Cited by 75 · see citing works

Developmental Changes in the Transcriptome of Human Cerebral Cortex Tissue: Long Noncoding RNA Transcripts

Lipovich, L., Tarca, A. L., Cai, J., Jia, H., Chugani, H. T., Sterner, K. N., Grossman, L. I., Uddin, M., Hof, P. R., Sherwood, C. C., et al. (2013) · Cerebral Cortex · doi:10.1093/cercor/bhs414 · Cited by 72 · see citing works

Increased Binding of Stroke-Induced Long Non-Coding RNAs to the Transcriptional Corepressors Sin3A and coREST

Dharap, A. A., Pokrzywa, C. J., & Vemuganti, R. (2013) · ASN NEURO · doi:10.1042/an20130029 · Cited by 71 · see citing works

LncRNAs, MALAT1 and lnc-DC as potential biomarkers for multiple sclerosis diagnosis

Shaker, O. G., Mahmoud, R. H., Abdelaleem, O. O., Ibrahem, E. G., Mohamed, A. A., Zaki, O. M., Abdelghaffar, N. K., Ahmed, T. I., Hemeda, N. F., Ahmed, N. A., et al. (2018) · Bioscience Reports · doi:10.1042/bsr20181335 · Cited by 69 · see citing works

Knockdown of a novel lincRNA AATBC suppresses proliferation and induces apoptosis in bladder cancer

Zhao, F., Lin, T., He, W., Han, J., Zhu, D., Hu, K., Li, W., Zheng, Z., Huang, J., & Xie, W. (2014) · Oncotarget · doi:10.18632/oncotarget.2833 · Cited by 68 · see citing works

Knockdown of linc-POU3F3 suppresses the proliferation, apoptosis, and migration resistance of colorectal cancer

Shan, T., Xu, J., Yu, T., Li, J., Zhao, L.-N., Ouyang, H., Luo, S., Lu, X.-J., Huang, C., Lan, Q.-S., et al. (2015) · Oncotarget · doi:10.18632/oncotarget.5830 · Cited by 58 · see citing works

Relationship between schizophrenia and changes in the expression of the long non-coding RNAs Meg3, Miat, Neat1 and Neat2

Li, J., Zhu, L., Guan, F., Yan, Z., Liu, D., Han, W., & Chen, T. (2018) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2018.09.005 · Cited by 57 · see citing works

LncRNA-DQ786227-mediated cell malignant transformation induced by benzo(a)pyrene

Gao, L., Mai, A., Li, X., Lai, Y., Zheng, J., Yang, Q., Wu, J., Nan, A., Ye, S., & Jiang, Y. (2013) · Toxicology Letters · doi:10.1016/j.toxlet.2013.09.015 · Cited by 52 · see citing works

Expression of non-protein-coding antisense RNAs in genomic regions related to autism spectrum disorders

Velmeshev, D., Magistri, M., & Faghihi, M. A. (2013) · Molecular Autism · doi:10.1186/2040-2392-4-32 · Cited by 52 · see citing works

Effects of LncRNA BC168687 siRNA on Diabetic Neuropathic Pain Mediated by P2X7 Receptor on SGCs in DRG of Rats

Liu, C., Tao, J., Wu, H., Yang, Y., Chen, Q., Deng, Z., Liu, J., & Xu, C. (2017) · BioMed Research International · doi:10.1155/2017/7831251 · Cited by 52 · see citing works

Identification of long noncoding RNA s dysregulated in the midbrain of human cocaine abusers

Bannon, M. J., Savonen, C., Jia, H., Dachet, F., Halter, S. D., Schmidt, C. J., Lipovich, L., & Kapatos, G. (2015) · Journal of Neurochemistry · doi:10.1111/jnc.13255 · Cited by 49 · see citing works

Noncoding RNAs in ischemic stroke: time to translate

Kaur, H., Sarmah, D., Saraf, J., Vats, K., Kalia, K., Borah, A., Yavagal, D. R., Dave, K. R., Ghosh, Z., & Bhattacharya, P. (2018) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.13612 · Cited by 48 · see citing works

Feature extraction approaches for biological sequences: a comparative study of mathematical features

Bonidia, R. P., Sampaio, L. D. H., Domingues, D. S., Paschoal, A. R., Lopes, F. M., de Carvalho, A. C. P. L. F., & Sanches, D. S. (2021) · Briefings in Bioinformatics · doi:10.1093/bib/bbab011 · Cited by 48 · see citing works

Circular and long non-coding RNAs and their role in ophthalmologic diseases

Wawrzyniak, O., Zarębska, Ż., Rolle, K., & Gotz‐Więckowska, A. (2018) · Acta Biochimica Polonica · doi:10.18388/abp.2018_2639 · Cited by 47 · see citing works

CRNDE enhances neuropathic pain via modulating miR‐136/IL6R axis in CCI rat models

Zhang, D., Mou, J., Wang, F., Liu, J., & Hu, X. (2019) · Journal of Cellular Physiology · doi:10.1002/jcp.28790 · Cited by 45 · see citing works

LncRNA-MIAT promotes neural cell autophagy and apoptosis in ischemic stroke by up-regulating REDD1

Guo, X., Wang, Y., Zheng, D.-L., Cheng, X., & Sun, Y. (2021) · Brain Research · doi:10.1016/j.brainres.2021.147436 · Cited by 42 · see citing works

The multiple molecular facets of fragile X-associated tremor/ataxia syndrome

Sellier, C., Usdin, K., Pastori, C., Peschansky, V. J., Tassone, F., & Charlet‐Berguerand, N. (2014) · Journal of Neurodevelopmental Disorders · doi:10.1186/1866-1955-6-23 · Cited by 41 · see citing works

The long non-coding RNA FMR4 promotes proliferation of human neural precursor cells and epigenetic regulation of gene expression in trans

Peschansky, V. J., Pastori, C., Zeier, Z. R., Wentzel, K., Velmeshev, D., Magistri, M., Silva, J., & Wahlestedt, C. (2016) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2016.03.008 · Cited by 40 · see citing works

Molecular mechanisms of long ncRNAs in neurological disorders

Vučićević, D., Schrewe, H., & Ørom, U. A. (2014) · Frontiers in Genetics · doi:10.3389/fgene.2014.00048 · Cited by 39 · see citing works

Non-Coding RNAs as Potential Neuroprotectants against Ischemic Brain Injury

Kaur, P., Liu, F., Tan, J., Lim, K. J., Sepramaniam, S., Karolina, D. S., Armugam, A., & Jeyaseelan, K. (2013) · Brain Sciences · doi:10.3390/brainsci3010360 · Cited by 38 · see citing works

Epigenetics of Alzheimer's Disease and Frontotemporal Dementia

Veerappan, C. S., Sleiman, S. F., & Coppola, G. (2013) · Neurotherapeutics · doi:10.1007/s13311-013-0219-0 · Cited by 37 · see citing works

LINC00657 expedites neuropathic pain development by modulating miR‐136/ZEB1 axis in a rat model

Shen, F., Zheng, H., Zhou, L., Li, W., Zhang, Y., & Xu, X. (2018) · Journal of Cellular Biochemistry · doi:10.1002/jcb.27466 · Cited by 36 · see citing works

Noncoding RNA Ginir functions as an oncogene by associating with centrosomal proteins

Panda, S., Setia, M., Kaur, N., Shepal, V., Arora, V., Singh, D. K., Mondal, A., Teli, A., Tathode, M., Gajula, R. P., et al. (2018) · PLoS Biology · doi:10.1371/journal.pbio.2004204 · Cited by 36 · see citing works

Noncoding RNAs Databases: Current Status and Trends

Maracaja‐Coutinho, V., Paschoal, A. R., Caris-Maldonado, J. C., Borges, P. V., Ferreira, A. J., & Durham, A. M. (2019) · Methods in molecular biology · doi:10.1007/978-1-4939-8982-9_10 · Cited by 36 · see citing works

Analysis of long non-coding RNA expression profiles following focal cerebral ischemia in mice

Liu, C., Yang, J., Chencheng, Z., Liu, M., Geng, X., Ji, X., Du, H., & Zhao, H. (2017) · Neuroscience Letters · doi:10.1016/j.neulet.2017.11.058 · Cited by 35 · see citing works

Systematic analysis of purified astrocytes after SCI unveils Zeb2os function during astrogliosis

Wei, H., Wu, X., You, Y., Durán, R. C., Zheng, Y., Narayanan, K. L., Hai, B., Li, X., Tallapragada, N., Prajapati, T. J., et al. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.108721 · Cited by 34 · see citing works

Circulating Long Noncoding RNAs as Novel Biomarkers of Human Diseases

Jiang, X., Lei, R., & Ning, Q. (2016) · Biomarkers in Medicine · doi:10.2217/bmm-2016-0039 · Cited by 34 · see citing works

Role of Long Noncoding RNA Gas5 in Cocaine Action

Xu, H., Brown, A. N., Waddell, N. J., Liu, X., Kaplan, G. J., Chitaman, J. M., Stockman, V., Hedinger, R. L., Adams, R., Abreu, K., et al. (2020) · Biological Psychiatry · doi:10.1016/j.biopsych.2020.05.004 · Cited by 33 · see citing works

NONRATT021972 long-noncoding RNA: A promising lncRNA in diabetes-related diseases

Suwal, A., Hao, J., Liu, X., Zhou, D.-D., Pant, O. P., Gao, Y., Hui, P., Dai, X.-X., & Lu, C. (2019) · International Journal of Medical Sciences · doi:10.7150/ijms.34200 · Cited by 32 · see citing works

Coding and long non-coding gene expression changes in the CNS traumatic injuries

Wu, X., Wei, H., & Wu, J. Q. (2022) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-021-04092-2 · Cited by 28 · see citing works

Peripheral expression of long non-coding RNAs in bipolar patients

Sayad, A., Taheri, M. N., Omrani, M. D., Fallah, H., Oskooei, V. K., & Ghafouri‐Fard, S. (2019) · Journal of Affective Disorders · doi:10.1016/j.jad.2019.02.034 · Cited by 27 · see citing works

Long non-coding RNAs and their involvement in bipolar disorders

Bella, F., & Campo, S. (2021) · Gene · doi:10.1016/j.gene.2021.145803 · Cited by 24 · see citing works

Building an RNA Sequencing Transcriptome of the Central Nervous System

Dong, X., You, Y., & Wu, J. Q. (2015) · The Neuroscientist · doi:10.1177/1073858415610541 · Cited by 24 · see citing works

Suppression of MALAT1 ameliorates chronic constriction injury‐induced neuropathic pain in rats via modulating miR‐206 and ZEB2

Chen, Z., Liu, J., Wang, F., & Xu, J. (2019) · Journal of Cellular Physiology · doi:10.1002/jcp.28213 · Cited by 24 · see citing works

Non-coding RNAs in Ischemic Stroke: Roles in the Neuroinflammation and Cell Death

Lü, M., Xingang, D., Zhang, Z., Li, W., & Khoshnam, S. E. (2020) · Neurotoxicity Research · doi:10.1007/s12640-020-00236-7 · Cited by 24 · see citing works

OLIG2 regulates lncRNAs and its own expression during oligodendrocyte lineage formation

Wei, H., Dong, X., You, Y., Hai, B., Durán, R. C., Wu, X., Kharas, N., & Wu, J. Q. (2021) · BMC Biology · doi:10.1186/s12915-021-01057-6 · Cited by 21 · see citing works

FAM72, Glioblastoma Multiforme (GBM) and Beyond

Ho, N. T. T., Rahane, C. S., Pramanik, S., Kim, P., Kutzner, A., & Heese, K. (2021) · Cancers · doi:10.3390/cancers13051025 · Cited by 20 · see citing works

A Novel Decomposing Model With Evolutionary Algorithms for Feature Selection in Long Non-Coding RNAs

Bonidia, R. P., Machida, J. S., Negri, T. D. C., Alves, W. A. L., Kashiwabara, A. Y., Domingues, D. S., de Carvalho, A. C. P. L. F., Paschoal, A. R., & Sanches, D. S. (2020) · IEEE Access · doi:10.1109/access.2020.3028039 · Cited by 20 · see citing works

LncRNA NONRATT021972 siRNA rescued decreased heart rate variability in diabetic rats in superior cervical ganglia

Xu, H., Liu, C., Rao, S., He, L., Zhang, T., Sun, S., Wu, B., Zou, L., Wang, S., Xue, Y., et al. (2016) · Autonomic Neuroscience · doi:10.1016/j.autneu.2016.07.012 · Cited by 19 · see citing works

Long Non-Coding RNA Associated with Cholesterol Homeostasis and Its Involvement in Metabolic Diseases

Lee, K.-H., Hwang, H., & Cho, J. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21218337 · Cited by 19 · see citing works

Identification of Potential Long Noncoding RNA Biomarker of Mercury Compounds in Zebrafish Embryos

Cao, M., Song, F., Yang, X., Peng, L., Yang, C., Zheng, Q., Liang, Y., & Wang, C. (2019) · Chemical Research in Toxicology · doi:10.1021/acs.chemrestox.9b00029 · Cited by 18 · see citing works

Neurobiological Opportunities in Diabetic Polyneuropathy

Poitras, T. M., Munchrath, E., & Zochodne, D. W. (2021) · Neurotherapeutics · doi:10.1007/s13311-021-01138-y · Cited by 18 · see citing works

All-Trans Retinoic Acid Induces Expression of a Novel Intergenic Long Noncoding RNA in Adult rat Primary Hippocampal Neurons

Kour, S., & Rath, P. C. (2015) · Journal of Molecular Neuroscience · doi:10.1007/s12031-015-0671-x · Cited by 18 · see citing works

Expression and diagnostic values of MIAT, H19, and NRON long non-coding RNAs in multiple sclerosis patients

Amiri, M., Mokhtari, M. J., Bayat, M., Safari, A., Dianatpuor, M., Tabrizi, R., & Borhani‐Haghighi, A. (2022) · Egyptian Journal of Medical Human Genetics · doi:10.1186/s43042-022-00260-6 · Cited by 16 · see citing works

Anticancer Effects of I-BET151, an Inhibitor of Bromodomain and Extra-Terminal Domain Proteins

Lai, J.-C., Liu, Z., Zhao, Y.-L., Ma, C.-C., & Huang, H.-Y. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2021.716830 · Cited by 14 · see citing works

Methionine Restriction Improves Cognitive Ability by Alleviating Hippocampal Neuronal Apoptosis through H19 in Middle-Aged Insulin-Resistant Mice

Feng, C., Jiang, Y., Li, S., Ge, Y., Shi, Y., Xue Ming, T. A. N. G., & Le, G. (2022) · Nutrients · doi:10.3390/nu14214503 · Cited by 15 · see citing works

Anti-differentiation non-coding RNA, ANCR, is differentially expressed in different types of brain tumors

Malakootian, M., Azad, F. M., Fouani, Y., Bajgan, E. T., Saberi, H., & Mowla, S. J. (2018) · Journal of Neuro-Oncology · doi:10.1007/s11060-018-2809-5 · Cited by 15 · see citing works

DLX6-AS1: A Long Non-coding RNA With Oncogenic Features

Ghafouri‐Fard, S., Najafi, S., Hussen, B. M., Ganjo, A. R., Taheri, M. N., & Samadian, M. M. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.746443 · Cited by 15 · see citing works

Long non-coding RNA H19 deficiency ameliorates bleomycin-induced pulmonary inflammation and fibrosis

Wan, X., Tian, X., Du, J., Lu, Y., & Xiao, Y. (2020) · Respiratory Research · doi:10.1186/s12931-020-01534-6 · Cited by 14 · see citing works

Oligonucleotide Analogues as Modulators of the Expression and Function of Noncoding RNAs (ncRNAs): Emerging Therapeutics Applications

Avitabile, C., Cimmino, A., & Romanelli, A. (2014) · Journal of Medicinal Chemistry · doi:10.1021/jm5006594 · Cited by 14 · see citing works

Virosomes as Novel drug delivery System: An Overview

Singh, N., Gautam, S. P., Kumari, N., Kaur, R., & Kaur, M. (2017) · Pharmatutor · Cited by 13 · see citing works

Sex-based dimorphisms in expression of BDNF and BACE1 in bipolar patients

Ghafouri‐Fard, S., Taheri, M. N., Arsang‐Jang, S., Oskooei, V. K., & Omrani, M. D. (2019) · Comprehensive Psychiatry · doi:10.1016/j.comppsych.2019.02.008 · Cited by 8 · see citing works

Pathophysiology Mechanisms in Fragile-X Primary Ovarian Insufficiency

Elizur, S. E., Friedman-Gohas, M., Dratviman‐Storobinsky, O., & Cohen, Y. (2019) · Methods in molecular biology · doi:10.1007/978-1-4939-9080-1_14 · Cited by 8 · see citing works

On the identification of long non-coding RNAs from RNA-seq

Cristiano, F., Veltri, P., Prosperi, M., & Tradigo, G. (2016) · IEEE International Conference on Bioinformatics and Biomedicine (BIBM) · doi:10.1109/bibm.2016.7822675 · Cited by 6 · see citing works

Long Non-coding RNA Uc.48+ Small Interfering RNA Alleviates Neuroinflammatory Hyperalgesia in Gp120-Treated Rats via the P2Y12 Receptor

Peng, L., Wu, B., Shi, L., Zou, L., Li, L., Yang, R., Xu, X., Li, G., Liu, S., Zhang, C., et al. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.663962 · Cited by 6 · see citing works

Genetics of neurosarcoidosis

Hardin, A., Dawkins, B. A., Pezant, N. P., Rasmussen, A., & Montgomery, C. G. (2022) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2022.577957 · Cited by 5 · see citing works

Implication of P2Y12 receptor in uc.48+-mediated abnormal sympathoexcitatory reflex via superior cervical ganglia in myocardial ischemic rats

Zou, L., Liu, S., Li, L., Yang, R., Xu, X., Li, G., Zhang, C., Li, G., & Liang, S. (2022) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2022.175049 · Cited by 4 · see citing works

The expression analysis of long noncoding RNAs PCAT-1, PCAT-29, and MER11C in bipolar disorder

Dini, N., Taheri, M. N., & Shirvani-Farsani, Z. (2024) · BMC Psychiatry · doi:10.1186/s12888-024-05974-y · Cited by 4 · see citing works

Effects of myo-inositol on regulating glucose and lipid metabolism and alternative splicing events coexpressed with lncRNAs in the liver tissues of diabetic mice

Li, J., Huang, Q., Nie, Q., Luo, Y., Zeng, H., Zhang, Y., He, X., & Liu, J. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e32460 · Cited by 4 · see citing works

MiR-107 Activates NF- κ B versus A β Analysis of the regulatory effect of 1-42 induced apoptosis in Alzheimer's disease cells

Peng, Y., Du, Z., Duan, J., Shao, Y., & Nie, S. (2023) · Cellular and Molecular Biology · doi:10.14715/cmb/2023.69.3.5 · Cited by 3 · see citing works

Reading and writing: the evolution of molecular pain genetics

Bullock, D., Jesuthasan, A., González‐Cano, R., & Costigan, M. (2019) · Pain · doi:10.1097/j.pain.0000000000001608 · Cited by 2 · see citing works

Genome-Wide Identification of lncRNA and mRNA for Diagnosing Type 2 Diabetes in Saudi Arabia

Albogami, S. M. (2023) · Pharmacogenomics and Personalized Medicine · doi:10.2147/pgpm.s427977 · Cited by 1 · see citing works

A comprehensive study on the review of virosomes As a novel drug delivery system

Medarametla, R. T., Gopaiah, K. V., J, N. S. K., Kumar Sai, A., Mohana chari, G., Kranti Kiran, A., Koteswarao Naik, B., & Sandya rani, K. (2023) · UPI Journal of Pharmaceutical Medical and Health Sciences · doi:10.37022/jpmhs.v6i4.94 · Cited by 1 · see citing works

lncRNA profiling in NCI-H292 cells after stimulation with Dermatophagoides farinae extracts

Wang, L., Zhou, Y., & Cui, Y. (2018) · International Journal of Immunopathology and Pharmacology · doi:10.1177/0394632017750997 · Cited by 1 · see citing works

Molecular Analysis of the Involvements of lncRNA in Cancer Development

Bagchi, A. (2021) · Springer eBooks · doi:10.1007/978-981-15-4501-6_153-1 · Cited by 1 · see citing works

Extracellular Vesicles and RNA interference in tumors

Lunavat, T. R. (2016) · Gothenburg University Publications Electronic Archive (Gothenburg University)

Noncoding RNAs as Critical Players in Regulatory Accuracy, Redox Signaling, and Immune Cell Functions

Gomes, A. Q., Real, C., Antunes, F., Marinho, H. S., Nolasco, S., & Soares, H. (2016) · Elsevier eBooks · doi:10.1016/b978-0-444-63660-7.00010-3

Genetic approaches to neurodegenerative disease

Takada, L. T. (2016) · Cambridge University Press eBooks · doi:10.1017/9781139924771.006

MicroRNA involvement in breast cancer susceptibility and progression

Gomes, B. C. (2016) · Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT)

Lack of association between LincRNA-Pou3f gene expression and clinicopathological features in gastric cancer tissue

Asgharzadeh, S., Tafvizi, F., Chaleshi, V., & Iravani, S. (2020) · Gene Reports · doi:10.1016/j.genrep.2020.100700

Inference and Validation of an Integrated Regulatory Network of AutismPreprint

Ganji, M., Emadi‐Baygi, M., Mohammadtaheri, F., Mirmohammadsadeghi, N., Malek, M., & Nikpour, P. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.06.08.139733

Epigenetic mechanisms of drug addiction vulnerability

Milian, A. A., Bendersky, C. J., & Walker, D. M. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-823577-5.00008-8

Molecular Analysis of the Involvements of lncRNA in Cancer Development

Bagchi, A. (2022) · Springer eBooks · doi:10.1007/978-981-15-9411-3_153

LNCRNA LY86-AS1 EXPRESSION ON T2DM AGED 40 YEARS OVER IN MUNGGU SOCIETY

Ayu Saka Laksmita, W., Widayanti, N. P., Apriyanthi, D. P. R. V., & Arijana, I. G. K. N. (2020) · LIFE International Journal of Health and Life-Sciences · doi:10.20319/lijhls.2020.61.7382

Explorando o papel dos RNAs longos não codificadores na doença de Alzheimer

Vasquez, F. J. D. A. (2022) · doi:10.11606/d.17.2022.tde-08082022-105803

Additional file 1 of The expression analysis of long noncoding RNAs PCAT-1, PCAT-29, and MER11C in bipolar disorder

Dini, N., Taheri, M., & Shirvani-Farsani, Z. (2024) · Figshare · doi:10.6084/m9.figshare.26752804

Invited Review: Long non‐coding RNA s: important regulators in the development, function and disorders of the central nervous system

Durán, R. C., Wei, H., Kim, D. H., & Wu, J. Q. (2019) · Neuropathology and Applied Neurobiology · doi:10.1111/nan.12541 · Cited by 74 · see citing works

Long noncoding RNAs and human disease

Wapinski, O. L., & Chang, H. Y. (2011) · Trends in Cell Biology · doi:10.1016/j.tcb.2011.04.001 · Cited by 1,900 · see citing works

Non-coding RNAs in Nervous System Development and Disease

Salvatori, B., Biscarini, S., & Morlando, M. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.00273 · Cited by 73 · see citing works

Non-coding RNAs in the brain: new class of prospective biomarkers and therapeutics

Goel, R. (2023) · International Journal of Research in Medical Sciences · doi:10.18203/2320-6012.ijrms20232822 · Cited by 2 · see citing works

Long Noncoding RNAs: Emerging Stars in Gene Regulation, Epigenetics and Human Disease

Bhan, A., & Mandal, S. S. (2014) · ChemMedChem · doi:10.1002/cmdc.201300534 · Cited by 283 · see citing works