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

doi.org

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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.

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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.

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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.

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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.

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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.

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ARN non codificante (Galician Wikipedia)

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