References analysis of the Wikipedia article "ARN non codificante" in the Galician version

doi.org

dx.doi.org

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Jenny A, Hachet O, Závorszky P, Cyrklaff A, Weston MD, Johnston DS, Erdélyi M, Ephrussi A (2006). "A translation-independent role of oskar RNA in early Drosophila oogenesis". Development 133 (15): 2827–33. PMID 16835436. doi:10.1242/dev.02456.

Gultyaev AP, Roussis A (2007). "Identification of conserved secondary structures and expansion segments in enod40 RNAs reveals new enod40 homologues in plants". Nucleic Acids Res 35 (9): 3144–52. PMC 1888808. PMID 17452360. doi:10.1093/nar/gkm173.

Lu J, Getz G, Miska EA, Alvarez-Saavedra E, Lamb J, Peck D, Sweet-Cordero A, Ebert BL, Mak RH, Ferrando AA, Downing JR, Jacks T, Horvitz HR, Golub TR (2005). "MicroRNA expression profiles classify human cancers". Nature 435 (7043): 834–8. Bibcode:2005Natur.435..834L. PMID 15944708. doi:10.1038/nature03702.

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Fu X, Ravindranath L, Tran N, Petrovics G, Srivastava S (2006). "Regulation of apoptosis by a prostate-specific and prostate cancer-associated noncoding gene, PCGEM1". DNA Cell Biol 25 (3): 135–41. PMID 16569192. doi:10.1089/dna.2006.25.135.

Mourtada-Maarabouni M, Pickard MR, Hedge VL, Farzaneh F, Williams GT (2009). "GAS5, a non-protein-coding RNA, controls apoptosis and is downregulated in breast cancer". Oncogene 28 (2): 195–208. PMID 18836484. doi:10.1038/onc.2008.373.

Dong XY, Guo P, Boyd J, Sun X, Li Q, Zhou W, Dong JT (2009). "Implication of snoRNA U50 in human breast cancer". J Genet Genomics 36 (8): 447–54. PMC 2854654. PMID 19683667. doi:10.1016/S1673-8527(08)60134-4.

Christov CP, Trivier E, Krude T (2008). "Noncoding human Y RNAs are overexpressed in tumours and required for cell proliferation". Br J Cancer 98 (5): 981–8. PMC 2266855. PMID 18283318. doi:10.1038/sj.bjc.6604254.

Farh KK, Grimson A, Jan C, Lewis BP, Johnston WK, Lim LP, Burge CB, Bartel DP (2005). "The widespread impact of mammalian MicroRNAs on mRNA repression and evolution". Science 310 (5755): 1817–21. Bibcode:2005Sci...310.1817F. PMID 16308420. doi:10.1126/science.1121158.

Lim LP, Lau NC, Garrett-Engele P, Grimson A, Schelter JM, Castle J, Bartel DP, Linsley PS, Johnson JM (2005). "Microarray analysis shows that some microRNAs downregulate large numbers of target mRNAs". Nature 433 (7027): 769–73. Bibcode:2005Natur.433..769L. PMID 15685193. doi:10.1038/nature03315.

Christov CP, Gardiner TJ, Szüts D, Krude T (2006). "Functional requirement of noncoding Y RNAs for human chromosomal DNA replication". Mol Cell Biol 26 (18): 6993–7004. PMC 1592862. PMID 16943439. doi:10.1128/MCB.01060-06.

Calin GA, Ferracin M, Cimmino A; et al. (2005). "A MicroRNA signature associated with prognosis and progression in chronic lymphocytic leukemia". N. Engl. J. Med. 353 (17): 1793–801. PMID 16251535. doi:10.1056/NEJMoa050995. Arquivado dende o orixinal o 27 de febreiro de 2009. Consultado o 31 de outubro de 2012.

Calin, GA; Dumitru CD, Shimizu M, Bichi R, Zupo S, Noch E, Aldler H, Rattan S, Keating M, Rai K, Rassenti L, Kipps T, Negrini M, Bullrich F, Croce CM (2002). "Frequent deletions and down-regulation of micro-RNA genes miR15 and miR16 at 13q14 in chronic lymphocytic leukemia". Proc Natl Acad Sci USA 99 (24): 15524–15529. Bibcode:2002PNAS...9915524C. PMC 137750. PMID 12434020. doi:10.1073/pnas.242606799.

Hu Z, Chen J, Tian T, Zhou X, Gu H, Xu L, Zeng Y, Miao R, Jin G, Ma H, Chen Y, Shen H (2008). "Genetic variants of miRNA sequences and non-small cell lung cancer survival". J Clin Invest 118 (7): 2600–8. PMC 2402113. PMID 18521189. doi:10.1172/JCI34934.

Shen J, Ambrosone CB, Zhao H (2009). "Novel genetic variants in microRNA genes and familial breast cancer". Int J Cancer 124 (5): 1178–82. PMID 19048628. doi:10.1002/ijc.24008.

Sahoo T, del Gaudio D, German JR, Shinawi M, Peters SU, Person RE, Garnica A, Cheung SW, Beaudet AL (2008). "Prader–Willi phenotype caused by paternal deficiency for the HBII-85 C/D box small nucleolar RNA cluster". Nat Genet 40 (6): 719–21. PMC 2705197. PMID 18500341. doi:10.1038/ng.158.

Ding F, Li HH, Zhang S, Solomon NM, Camper SA, Cohen P, Francke U (2008). Akbarian, Schahram, ed. "SnoRNA Snord116 (Pwcr1/MBII-85) deletion causes growth deficiency and hyperphagia in mice". PLoS ONE 3 (3): e1709. Bibcode:2008PLoSO...3.1709D. PMC 2248623. PMID 18320030. doi:10.1371/journal.pone.0001709.

Ding F, Prints Y, Dhar MS, Johnson DK, Garnacho-Montero C, Nicholls RD, Francke U (2005). "Lack of Pwcr1/MBII-85 snoRNA is critical for neonatal lethality in Prader–Willi syndrome mouse models". Mamm Genome 16 (6): 424–31. PMID 16075369. doi:10.1007/s00335-005-2460-2.

Bazeley PS, Shepelev V, Talebizadeh Z, Butler MG, Fedorova L, Filatov V, Fedorov A (2008). "snoTARGET shows that human orphan snoRNA targets locate close to alternative splice junctions". Gene 408 (1–2): 172–9. PMID 18160232. doi:10.1016/j.gene.2007.10.037.

Bolton PF, Veltman MW, Weisblatt E; et al. (2004). "Chromosome 15q11-13 abnormalities and other medical conditions in individuals with autism spectrum disorders". Psychiatr. Genet. 14 (3): 131–7. PMID 15318025. doi:10.1097/00041444-200409000-00002.

Cook EH, Scherer SW (2008). "Copy-number variations associated with neuropsychiatric conditions". Nature 455 (7215): 919–23. Bibcode:2008Natur.455..919C. PMID 18923514. doi:10.1038/nature07458.

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Ridanpää M, van Eenennaam H, Pelin K, Chadwick R, Johnson C, Yuan B, vanVenrooij W, Pruijn G, Salmela R, Rockas S, Mäkitie O, Kaitila I, de la Chapelle A (2001). "Mutations in the RNA component of RNase MRP cause a pleiotropic human disease, cartilage-hair hypoplasia". Cell 104 (2): 195–203. PMID 11207361. doi:10.1016/S0092-8674(01)00205-7.

Martin AN, Li Y (2007). "RNase MRP RNA and human genetic diseases". Cell Res 17 (3): 219–26. PMID 17189938. doi:10.1038/sj.cr.7310120.

Kavadas FD, Giliani S, Gu Y, Mazzolari E, Bates A, Pegoiani E, Roifman CM, Notarangelo LD (2008). "Variability of clinical and laboratory features among patients with ribonuclease mitochondrial RNA processing endoribonuclease gene mutations". J Allergy Clin Immunol 122 (6): 1178–84. PMID 18804272. doi:10.1016/j.jaci.2008.07.036.

Faghihi MA, Modarresi F, Khalil AM, Wood DE, Sahagan BG, Morgan TE, Finch CE, St Laurent G, Kenny PJ, Wahlestedt C (2008). "Expression of a noncoding RNA is elevated in Alzheimer's disease and drives rapid feed-forward regulation of beta-secretase". Nat Med 14 (7): 723–30. PMC 2826895. PMID 18587408. doi:10.1038/nm1784.

Mencía A, Modamio-Høybjør S, Redshaw N, Morín M, Mayo-Merino F, Olavarrieta L, Aguirre LA, del Castillo I, Steel KP, Dalmay T, Moreno F, Moreno-Pelayo MA (2009). "Mutations in the seed region of human miR-96 are responsible for nonsyndromic progressive hearing loss". Nat Genet 41 (5): 609–13. PMID 19363479. doi:10.1038/ng.355.

Lewis MA, Quint E, Glazier AM, Fuchs H, De Angelis MH, Langford C, van Dongen S, Abreu-Goodger C, Piipari M, Redshaw N, Dalmay T, Moreno-Pelayo MA, Enright AJ, Steel KP (2009). "An ENU-induced mutation of miR-96 associated with progressive hearing loss in mice". Nat Genet 41 (5): 614–8. PMC 2705913. PMID 19363478. doi:10.1038/ng.369.

Soukup GA (2009). "Little but loud: Small RNAs have a resounding affect on ear development". Brain Res 1277: 104–14. PMC 2700218. PMID 19245798. doi:10.1016/j.brainres.2009.02.027.

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Jeffares DC, Poole AM, Penny D (1998). "Relics from the RNA world". J Mol Evol 46 (1): 18–36. PMID 9419222. doi:10.1007/PL00006280.

Poole AM, Jeffares DC, Penny D (1998). "The path from the RNA world". J Mol Evol 46 (1): 1–17. PMID 9419221. doi:10.1007/PL00006275.

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Shen J, Ambrosone CB, Zhao H (2009). "Novel genetic variants in microRNA genes and familial breast cancer". Int J Cancer 124 (5): 1178–82. PMID 19048628. doi:10.1002/ijc.24008.

Martin AN, Li Y (2007). "RNase MRP RNA and human genetic diseases". Cell Res 17 (3): 219–26. PMID 17189938. doi:10.1038/sj.cr.7310120.

Soukup GA (2009). "Little but loud: Small RNAs have a resounding affect on ear development". Brain Res 1277: 104–14. PMC 2700218. PMID 19245798. doi:10.1016/j.brainres.2009.02.027.

Eddy SR (2001). "Non-coding RNA genes and the modern RNA world". Nat. Rev. Genet. 2 (12): 919–29. PMID 11733745. doi:10.1038/35103511.

Dahm R (2005). "Friedrich Miescher and the discovery of DNA". Dev. Biol. 278 (2): 274–88. PMID 15680349. doi:10.1016/j.ydbio.2004.11.028. Consultado o 2010-09-03.

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ARN non codificante (Galician Wikipedia)

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