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Elbashir SM, Harborth J, Lendeckel W, Yalcin A, Weber K, Tuschl T (2001. május 1.). „Duplexes of 21-nucleotide RNAs mediate RNA interference in cultured mammalian cells”. Nature411 (6836), 494–498. o. DOI:10.1038/35078107. PMID11373684.
Zhihang Chen, Balaji Krishnamachary, Jesus Pachecho-Torres, Marie-France Penet, Zaver M. Bhujwalla (2020. március 1.). „Theranostic small interfering RNA nanoparticles in cancer precision nanomedicine” (angol nyelven). WIREs Nanomedicine and Nanobiotechnology12 (2), e1595. o. DOI:10.1002/wnan.1595. ISSN1939-5116. PMID31642207. PMC7360334.
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Sharei A, Zoldan J, Adamo A, Sim WY, Cho N, Jackson E, Mao S, Schneider S, Han MJ, Lytton-Jean A, Basto PA, Jhunjhunwala S, Lee J, Heller DA, Kang JW, Hartoularos GC, Kim KS, Anderson DG, Langer R, Jensen KF (2013. február 1.). „A vector-free microfluidic platform for intracellular delivery”. Proceedings of the National Academy of Sciences of the United States of America110 (6), 2082–2087. o. DOI:10.1073/pnas.1218705110. PMID23341631. PMC3568376.
Lee YS, Nakahara K, Pham JW, Kim K, He Z, Sontheimer EJ, Carthew RW (2004. április 1.). „Distinct roles for Drosophila Dicer-1 and Dicer-2 in the siRNA/miRNA silencing pathways”. Cell117 (1), 69–81. o. DOI:10.1016/s0092-8674(04)00261-2. PMID15066283.
Tomari Y, Zamore PD (2005. március 1.). „Perspective: machines for RNAi”. Genes & Development19 (5), 517–529. o. DOI:10.1101/gad.1284105. PMID15741316.
Orban TI, Izaurralde E (2005. április 1.). „Decay of mRNAs targeted by RISC requires XRN1, the Ski complex, and the exosome”. RNA11 (4), 459–469. o. DOI:10.1261/rna.7231505. PMID15703439. PMC1370735.
Marc S. Weinberg, Kevin V. Morris (2016. augusztus 1.). „Transcriptional gene silencing in humans”. Nucleic Acids Research44 (14), 6505–6517. o. DOI:10.1093/nar/gkw139. PMID27060137. PMC5001580.
Jackson AL, Linsley PS (2010. január 1.). „Recognizing and avoiding siRNA off-target effects for target identification and therapeutic application”. Nature Reviews Drug Discovery9 (1), 57–67. o. DOI:10.1038/nrd3010. PMID20043028.
Woolf TM, Melton DA, Jennings CG (1992. augusztus 1.). „Specificity of antisense oligonucleotides in vivo”. Proceedings of the National Academy of Sciences of the United States of America89 (16), 7305–7309. o. DOI:10.1073/pnas.89.16.7305. PMID1380154. PMC49698.
Dua P, Yoo JW, Kim S, Lee DK (2011. szeptember 1.). „Modified siRNA structure with a single nucleotide bulge overcomes conventional siRNA-mediated off-target silencing”. Molecular Therapy19 (9), 1676–1687. o. DOI:10.1038/mt.2011.109. PMID21673662. PMC3182346.
Whitehead KA, Dahlman JE, Langer RS, Anderson DG (2011. június 17.). „Silencing or stimulation? siRNA delivery and the immune system”. Annual Review of Chemical and Biomolecular Engineering2 (1), 77–96. o. DOI:10.1146/annurev-chembioeng-061010-114133. PMID22432611.
Barøy T, Sørensen K, Lindeberg MM, Frengen E (2010. június 1.). „shRNA expression constructs designed directly from siRNA oligonucleotide sequences”. Molecular Biotechnology45 (2), 116–120. o. DOI:10.1007/s12033-010-9247-8. PMID20119685.
Birmingham A, Anderson EM, Reynolds A, Ilsley-Tyree D, Leake D, Fedorov Y, Baskerville S, Maksimova E, Robinson K, Karpilow J, Marshall WS, Khvorova A (2006. március 1.). „3' UTR seed matches, but not overall identity, are associated with RNAi off-targets”. Nature Methods3 (3), 199–204. o. DOI:10.1038/nmeth854. PMID16489337.
Wittrup A, Lieberman J (2015. szeptember 1.). „Knocking down disease: a progress report on siRNA therapeutics”. Nature Reviews. Genetics16 (9), 543–552. o. DOI:10.1038/nrg3978. PMID26281785. PMC4756474.
Grimm D, Streetz KL, Jopling CL, Storm TA, Pandey K, Davis CR, Marion P, Salazar F, Kay MA (2006. május 1.). „Fatality in mice due to oversaturation of cellular microRNA/short hairpin RNA pathways”. Nature441 (7092), 537–41. o. DOI:10.1038/nature04791. PMID16724069.
Dar SA, Thakur A, Qureshi A, Kumar M (2016. január 1.). „siRNAmod: A database of experimentally validated chemically modified siRNAs”. Scientific Reports6 (1), 20031. o. DOI:10.1038/srep20031. PMID26818131. PMC4730238. ; adatbázis: siRNAmod
Hickerson RP, Smith FJ, Reeves RE, Contag CH, Leake D, Leachman SA, Milstone LM, McLean WH, Kaspar RL (2008. március 1.). „Single-nucleotide-specific siRNA targeting in a dominant-negative skin model”. The Journal of Investigative Dermatology128 (3), 594–605. o. DOI:10.1038/sj.jid.5701060. PMID17914454.
Alekseev OM, Richardson RT, Alekseev O, O'Rand MG (2009. május 1.). „Analysis of gene expression profiles in HeLa cells in response to overexpression or siRNA-mediated depletion of NASP”. Reproductive Biology and Endocrinology7 (1), 45. o. DOI:10.1186/1477-7827-7-45. PMID19439102. PMC2686705.
Petrocca F, Lieberman J (2011. február 1.). „Promise and challenge of RNA interference-based therapy for cancer”. Journal of Clinical Oncology29 (6), 747–754. o. DOI:10.1200/JCO.2009.27.6287. PMID21079135.
Hu B, Zhong L, Weng Y, Peng L, Huang Y, Zhao Y, Liang XJ (2020. június 1.). „Therapeutic siRNA: state of the art”. Signal Transduction and Targeted Therapy5 (1), 101. o. DOI:10.1038/s41392-020-0207-x. PMID32561705. PMC7305320.
Shen H, Sun T, Ferrari M (2012. június 1.). „Nanovector delivery of siRNA for cancer therapy”. Cancer Gene Therapy19 (6), 367–373. o. DOI:10.1038/cgt.2012.22. PMID22555511. PMC3842228.
Elbashir SM, Lendeckel W, Tuschl T (2001. január 1.). „RNA interference is mediated by 21- and 22-nucleotide RNAs”. Genes & Development15 (2), 188–200. o. DOI:10.1101/gad.862301. PMID11157775. PMC312613.
Heidel JD, Yu Z, Liu JY, Rele SM, Liang Y, Zeidan RK, Kornbrust DJ, Davis ME (2007. április 1.). „Administration in non-human primates of escalating intravenous doses of targeted nanoparticles containing ribonucleotide reductase subunit M2 siRNA”. Proceedings of the National Academy of Sciences of the United States of America104 (14), 5715–5721. o. DOI:10.1073/pnas.0701458104. PMID17379663. PMC1829492.
Maria João Gomes, Jes Dreier, Jonathan Brewer, Susana Martins, Martin Brandl, Bruno Sarmento (2016. április 1.). „A new approach for a blood-brain barrier model based on phospholipid vesicles: Membrane development and siRNA-loaded nanoparticles permeability”. Journal of Membrane Science503, 8–15. o. DOI:10.1016/j.memsci.2016.01.002.
Shukla RS, Qin B, Cheng K (2014. október 1.). „Peptides used in the delivery of small noncoding RNA”. Molecular Pharmaceutics11 (10), 3395–3408. o. DOI:10.1021/mp500426r. PMID25157701. PMC4186677.
Tabernero J, Shapiro GI, LoRusso PM, Cervantes A, Schwartz GK, Weiss GJ, Paz-Ares L, Cho DC, Infante JR, Alsina M, Gounder MM, Falzone R, Harrop J, White AC, Toudjarska I, Bumcrot D, Meyers RE, Hinkle G, Svrzikapa N, Hutabarat RM, Clausen VA, Cehelsky J, Nochur SV, Gamba-Vitalo C, Vaishnaw AK, Sah DW, Gollob JA, Burris HA (2013. április 1.). „First-in-humans trial of an RNA interference therapeutic targeting VEGF and KSP in cancer patients with liver involvement”. Cancer Discovery3 (4), 406–417. o. DOI:10.1158/2159-8290.CD-12-0429. PMID23358650.
Geisbert TW, Lee AC, Robbins M, Geisbert JB, Honko AN, Sood V, Johnson JC, de Jong S, Tavakoli I, Judge A, Hensley LE, Maclachlan I (2010. május 1.). „Postexposure protection of non-human primates against a lethal Ebola virus challenge with RNA interference: a proof-of-concept study”. Lancet375 (9729), 1896–905. o. DOI:10.1016/S0140-6736(10)60357-1. PMID20511019. PMC7138079.
Mathieu Guerriaud, Evelyne Kohli (2022). „RNA-based drugs and regulation: Toward a necessary evolution of the definitions issued from the European union legislation”. Frontiers in Medicine9. DOI:10.3389/fmed.2022.1012497. ISSN2296-858X. PMID36325384. PMC9618588.
Rosemary, Kanasty (2013). „Delivery materials for siRNA therapeutics”. Nat Mater12 (11), 967–977. o. DOI:10.1038/nmat3765. PMID24150415.
Jensen K, Anderson JA, Glass EJ (2014. április 1.). „Comparison of small interfering RNA (siRNA) delivery into bovine monocyte-derived macrophages by transfection and electroporation”. Veterinary Immunology and Immunopathology158 (3–4), 224–232. o. DOI:10.1016/j.vetimm.2014.02.002. PMID24598124. PMC3988888.
Morris KV, Rossi JJ (2006. március 1.). „Lentiviral-mediated delivery of siRNAs for antiviral therapy”. Gene Therapy13 (6), 553–558. o. DOI:10.1038/sj.gt.3302688. PMID16397511. PMC7091755.
Cambon K, Déglon N. Lentiviral-Mediated Gene Transfer of siRNAs for the Treatment of Huntington's Disease, Trinucleotide Repeat Protocols, Methods in Molecular Biology, 95–109. o.. DOI: 10.1007/978-1-62703-411-1_7 (2013). ISBN 978-1-62703-410-4
Tiemann K, Rossi JJ (2009. június 1.). „RNAi-based therapeutics-current status, challenges and prospects”. EMBO Molecular Medicine1 (3), 142–151. o. DOI:10.1002/emmm.200900023. PMID20049714. PMC3378126.
Sei Yonezawa, Hiroyuki Koide, Tomohiro Asai (2020. szeptember 13.). „Recent advances in siRNA delivery mediated by lipid-based nanoparticles”. Advanced Drug Delivery Reviews154, 64–78. o. DOI:10.1016/j.addr.2020.07.022. ISSN0169-409X. PMID32768564. PMC7406478.
David Adams, Alejandra Gonzalez-Duarte, William D. O’Riordan, et al. (2018. július 5.). „Patisiran, an RNAi Therapeutic, for Hereditary Transthyretin Amyloidosis”. The New England Journal of Medicine379 (1), 11–21. o. DOI:10.1056/NEJMoa1716153. PMID29972753.
Bernstein E, Caudy AA, Hammond SM, Hannon GJ (2001. január 1.). „Role for a bidentate ribonuclease in the initiation step of RNA interference”. Nature409 (6818), 363–366. o. DOI:10.1038/35053110. PMID11201747.
Hamilton AJ, Baulcombe DC (1999. október 1.). „A species of small antisense RNA in posttranscriptional gene silencing in plants”. Science286 (5441), 950–952. o. DOI:10.1126/science.286.5441.950. PMID10542148.
Elbashir SM, Harborth J, Lendeckel W, Yalcin A, Weber K, Tuschl T (2001. május 1.). „Duplexes of 21-nucleotide RNAs mediate RNA interference in cultured mammalian cells”. Nature411 (6836), 494–498. o. DOI:10.1038/35078107. PMID11373684.
Zhihang Chen, Balaji Krishnamachary, Jesus Pachecho-Torres, Marie-France Penet, Zaver M. Bhujwalla (2020. március 1.). „Theranostic small interfering RNA nanoparticles in cancer precision nanomedicine” (angol nyelven). WIREs Nanomedicine and Nanobiotechnology12 (2), e1595. o. DOI:10.1002/wnan.1595. ISSN1939-5116. PMID31642207. PMC7360334.
Qureshi A, Thakur N, Monga I, Thakur A, Kumar M (2014. január 1.). „VIRmiRNA: a comprehensive resource for experimentally validated viral miRNAs and their targets”. Database2014, bau103. o. DOI:10.1093/database/bau103. PMID25380780. PMC4224276.
Sharei A, Zoldan J, Adamo A, Sim WY, Cho N, Jackson E, Mao S, Schneider S, Han MJ, Lytton-Jean A, Basto PA, Jhunjhunwala S, Lee J, Heller DA, Kang JW, Hartoularos GC, Kim KS, Anderson DG, Langer R, Jensen KF (2013. február 1.). „A vector-free microfluidic platform for intracellular delivery”. Proceedings of the National Academy of Sciences of the United States of America110 (6), 2082–2087. o. DOI:10.1073/pnas.1218705110. PMID23341631. PMC3568376.
Lee YS, Nakahara K, Pham JW, Kim K, He Z, Sontheimer EJ, Carthew RW (2004. április 1.). „Distinct roles for Drosophila Dicer-1 and Dicer-2 in the siRNA/miRNA silencing pathways”. Cell117 (1), 69–81. o. DOI:10.1016/s0092-8674(04)00261-2. PMID15066283.
Tomari Y, Zamore PD (2005. március 1.). „Perspective: machines for RNAi”. Genes & Development19 (5), 517–529. o. DOI:10.1101/gad.1284105. PMID15741316.
Orban TI, Izaurralde E (2005. április 1.). „Decay of mRNAs targeted by RISC requires XRN1, the Ski complex, and the exosome”. RNA11 (4), 459–469. o. DOI:10.1261/rna.7231505. PMID15703439. PMC1370735.
Marc S. Weinberg, Kevin V. Morris (2016. augusztus 1.). „Transcriptional gene silencing in humans”. Nucleic Acids Research44 (14), 6505–6517. o. DOI:10.1093/nar/gkw139. PMID27060137. PMC5001580.
Jackson AL, Linsley PS (2010. január 1.). „Recognizing and avoiding siRNA off-target effects for target identification and therapeutic application”. Nature Reviews Drug Discovery9 (1), 57–67. o. DOI:10.1038/nrd3010. PMID20043028.
Woolf TM, Melton DA, Jennings CG (1992. augusztus 1.). „Specificity of antisense oligonucleotides in vivo”. Proceedings of the National Academy of Sciences of the United States of America89 (16), 7305–7309. o. DOI:10.1073/pnas.89.16.7305. PMID1380154. PMC49698.
Dua P, Yoo JW, Kim S, Lee DK (2011. szeptember 1.). „Modified siRNA structure with a single nucleotide bulge overcomes conventional siRNA-mediated off-target silencing”. Molecular Therapy19 (9), 1676–1687. o. DOI:10.1038/mt.2011.109. PMID21673662. PMC3182346.
Whitehead KA, Dahlman JE, Langer RS, Anderson DG (2011. június 17.). „Silencing or stimulation? siRNA delivery and the immune system”. Annual Review of Chemical and Biomolecular Engineering2 (1), 77–96. o. DOI:10.1146/annurev-chembioeng-061010-114133. PMID22432611.
Barøy T, Sørensen K, Lindeberg MM, Frengen E (2010. június 1.). „shRNA expression constructs designed directly from siRNA oligonucleotide sequences”. Molecular Biotechnology45 (2), 116–120. o. DOI:10.1007/s12033-010-9247-8. PMID20119685.
Birmingham A, Anderson EM, Reynolds A, Ilsley-Tyree D, Leake D, Fedorov Y, Baskerville S, Maksimova E, Robinson K, Karpilow J, Marshall WS, Khvorova A (2006. március 1.). „3' UTR seed matches, but not overall identity, are associated with RNAi off-targets”. Nature Methods3 (3), 199–204. o. DOI:10.1038/nmeth854. PMID16489337.
Wittrup A, Lieberman J (2015. szeptember 1.). „Knocking down disease: a progress report on siRNA therapeutics”. Nature Reviews. Genetics16 (9), 543–552. o. DOI:10.1038/nrg3978. PMID26281785. PMC4756474.
Grimm D, Streetz KL, Jopling CL, Storm TA, Pandey K, Davis CR, Marion P, Salazar F, Kay MA (2006. május 1.). „Fatality in mice due to oversaturation of cellular microRNA/short hairpin RNA pathways”. Nature441 (7092), 537–41. o. DOI:10.1038/nature04791. PMID16724069.
Dar SA, Thakur A, Qureshi A, Kumar M (2016. január 1.). „siRNAmod: A database of experimentally validated chemically modified siRNAs”. Scientific Reports6 (1), 20031. o. DOI:10.1038/srep20031. PMID26818131. PMC4730238. ; adatbázis: siRNAmod
Hickerson RP, Smith FJ, Reeves RE, Contag CH, Leake D, Leachman SA, Milstone LM, McLean WH, Kaspar RL (2008. március 1.). „Single-nucleotide-specific siRNA targeting in a dominant-negative skin model”. The Journal of Investigative Dermatology128 (3), 594–605. o. DOI:10.1038/sj.jid.5701060. PMID17914454.
Alekseev OM, Richardson RT, Alekseev O, O'Rand MG (2009. május 1.). „Analysis of gene expression profiles in HeLa cells in response to overexpression or siRNA-mediated depletion of NASP”. Reproductive Biology and Endocrinology7 (1), 45. o. DOI:10.1186/1477-7827-7-45. PMID19439102. PMC2686705.
Petrocca F, Lieberman J (2011. február 1.). „Promise and challenge of RNA interference-based therapy for cancer”. Journal of Clinical Oncology29 (6), 747–754. o. DOI:10.1200/JCO.2009.27.6287. PMID21079135.
Hu B, Zhong L, Weng Y, Peng L, Huang Y, Zhao Y, Liang XJ (2020. június 1.). „Therapeutic siRNA: state of the art”. Signal Transduction and Targeted Therapy5 (1), 101. o. DOI:10.1038/s41392-020-0207-x. PMID32561705. PMC7305320.
Shen H, Sun T, Ferrari M (2012. június 1.). „Nanovector delivery of siRNA for cancer therapy”. Cancer Gene Therapy19 (6), 367–373. o. DOI:10.1038/cgt.2012.22. PMID22555511. PMC3842228.
Elbashir SM, Lendeckel W, Tuschl T (2001. január 1.). „RNA interference is mediated by 21- and 22-nucleotide RNAs”. Genes & Development15 (2), 188–200. o. DOI:10.1101/gad.862301. PMID11157775. PMC312613.
Heidel JD, Yu Z, Liu JY, Rele SM, Liang Y, Zeidan RK, Kornbrust DJ, Davis ME (2007. április 1.). „Administration in non-human primates of escalating intravenous doses of targeted nanoparticles containing ribonucleotide reductase subunit M2 siRNA”. Proceedings of the National Academy of Sciences of the United States of America104 (14), 5715–5721. o. DOI:10.1073/pnas.0701458104. PMID17379663. PMC1829492.
Shukla RS, Qin B, Cheng K (2014. október 1.). „Peptides used in the delivery of small noncoding RNA”. Molecular Pharmaceutics11 (10), 3395–3408. o. DOI:10.1021/mp500426r. PMID25157701. PMC4186677.
Tabernero J, Shapiro GI, LoRusso PM, Cervantes A, Schwartz GK, Weiss GJ, Paz-Ares L, Cho DC, Infante JR, Alsina M, Gounder MM, Falzone R, Harrop J, White AC, Toudjarska I, Bumcrot D, Meyers RE, Hinkle G, Svrzikapa N, Hutabarat RM, Clausen VA, Cehelsky J, Nochur SV, Gamba-Vitalo C, Vaishnaw AK, Sah DW, Gollob JA, Burris HA (2013. április 1.). „First-in-humans trial of an RNA interference therapeutic targeting VEGF and KSP in cancer patients with liver involvement”. Cancer Discovery3 (4), 406–417. o. DOI:10.1158/2159-8290.CD-12-0429. PMID23358650.
Geisbert TW, Lee AC, Robbins M, Geisbert JB, Honko AN, Sood V, Johnson JC, de Jong S, Tavakoli I, Judge A, Hensley LE, Maclachlan I (2010. május 1.). „Postexposure protection of non-human primates against a lethal Ebola virus challenge with RNA interference: a proof-of-concept study”. Lancet375 (9729), 1896–905. o. DOI:10.1016/S0140-6736(10)60357-1. PMID20511019. PMC7138079.
Mathieu Guerriaud, Evelyne Kohli (2022). „RNA-based drugs and regulation: Toward a necessary evolution of the definitions issued from the European union legislation”. Frontiers in Medicine9. DOI:10.3389/fmed.2022.1012497. ISSN2296-858X. PMID36325384. PMC9618588.
Rosemary, Kanasty (2013). „Delivery materials for siRNA therapeutics”. Nat Mater12 (11), 967–977. o. DOI:10.1038/nmat3765. PMID24150415.
Jensen K, Anderson JA, Glass EJ (2014. április 1.). „Comparison of small interfering RNA (siRNA) delivery into bovine monocyte-derived macrophages by transfection and electroporation”. Veterinary Immunology and Immunopathology158 (3–4), 224–232. o. DOI:10.1016/j.vetimm.2014.02.002. PMID24598124. PMC3988888.
Morris KV, Rossi JJ (2006. március 1.). „Lentiviral-mediated delivery of siRNAs for antiviral therapy”. Gene Therapy13 (6), 553–558. o. DOI:10.1038/sj.gt.3302688. PMID16397511. PMC7091755.
Tiemann K, Rossi JJ (2009. június 1.). „RNAi-based therapeutics-current status, challenges and prospects”. EMBO Molecular Medicine1 (3), 142–151. o. DOI:10.1002/emmm.200900023. PMID20049714. PMC3378126.
Sei Yonezawa, Hiroyuki Koide, Tomohiro Asai (2020. szeptember 13.). „Recent advances in siRNA delivery mediated by lipid-based nanoparticles”. Advanced Drug Delivery Reviews154, 64–78. o. DOI:10.1016/j.addr.2020.07.022. ISSN0169-409X. PMID32768564. PMC7406478.
David Adams, Alejandra Gonzalez-Duarte, William D. O’Riordan, et al. (2018. július 5.). „Patisiran, an RNAi Therapeutic, for Hereditary Transthyretin Amyloidosis”. The New England Journal of Medicine379 (1), 11–21. o. DOI:10.1056/NEJMoa1716153. PMID29972753.
Zhihang Chen, Balaji Krishnamachary, Jesus Pachecho-Torres, Marie-France Penet, Zaver M. Bhujwalla (2020. március 1.). „Theranostic small interfering RNA nanoparticles in cancer precision nanomedicine” (angol nyelven). WIREs Nanomedicine and Nanobiotechnology12 (2), e1595. o. DOI:10.1002/wnan.1595. ISSN1939-5116. PMID31642207. PMC7360334.
Qureshi A, Thakur N, Monga I, Thakur A, Kumar M (2014. január 1.). „VIRmiRNA: a comprehensive resource for experimentally validated viral miRNAs and their targets”. Database2014, bau103. o. DOI:10.1093/database/bau103. PMID25380780. PMC4224276.
Sharei A, Zoldan J, Adamo A, Sim WY, Cho N, Jackson E, Mao S, Schneider S, Han MJ, Lytton-Jean A, Basto PA, Jhunjhunwala S, Lee J, Heller DA, Kang JW, Hartoularos GC, Kim KS, Anderson DG, Langer R, Jensen KF (2013. február 1.). „A vector-free microfluidic platform for intracellular delivery”. Proceedings of the National Academy of Sciences of the United States of America110 (6), 2082–2087. o. DOI:10.1073/pnas.1218705110. PMID23341631. PMC3568376.
Orban TI, Izaurralde E (2005. április 1.). „Decay of mRNAs targeted by RISC requires XRN1, the Ski complex, and the exosome”. RNA11 (4), 459–469. o. DOI:10.1261/rna.7231505. PMID15703439. PMC1370735.
Marc S. Weinberg, Kevin V. Morris (2016. augusztus 1.). „Transcriptional gene silencing in humans”. Nucleic Acids Research44 (14), 6505–6517. o. DOI:10.1093/nar/gkw139. PMID27060137. PMC5001580.
Woolf TM, Melton DA, Jennings CG (1992. augusztus 1.). „Specificity of antisense oligonucleotides in vivo”. Proceedings of the National Academy of Sciences of the United States of America89 (16), 7305–7309. o. DOI:10.1073/pnas.89.16.7305. PMID1380154. PMC49698.
Dua P, Yoo JW, Kim S, Lee DK (2011. szeptember 1.). „Modified siRNA structure with a single nucleotide bulge overcomes conventional siRNA-mediated off-target silencing”. Molecular Therapy19 (9), 1676–1687. o. DOI:10.1038/mt.2011.109. PMID21673662. PMC3182346.
Wittrup A, Lieberman J (2015. szeptember 1.). „Knocking down disease: a progress report on siRNA therapeutics”. Nature Reviews. Genetics16 (9), 543–552. o. DOI:10.1038/nrg3978. PMID26281785. PMC4756474.
Dar SA, Thakur A, Qureshi A, Kumar M (2016. január 1.). „siRNAmod: A database of experimentally validated chemically modified siRNAs”. Scientific Reports6 (1), 20031. o. DOI:10.1038/srep20031. PMID26818131. PMC4730238. ; adatbázis: siRNAmod
Alekseev OM, Richardson RT, Alekseev O, O'Rand MG (2009. május 1.). „Analysis of gene expression profiles in HeLa cells in response to overexpression or siRNA-mediated depletion of NASP”. Reproductive Biology and Endocrinology7 (1), 45. o. DOI:10.1186/1477-7827-7-45. PMID19439102. PMC2686705.
Hu B, Zhong L, Weng Y, Peng L, Huang Y, Zhao Y, Liang XJ (2020. június 1.). „Therapeutic siRNA: state of the art”. Signal Transduction and Targeted Therapy5 (1), 101. o. DOI:10.1038/s41392-020-0207-x. PMID32561705. PMC7305320.
Shen H, Sun T, Ferrari M (2012. június 1.). „Nanovector delivery of siRNA for cancer therapy”. Cancer Gene Therapy19 (6), 367–373. o. DOI:10.1038/cgt.2012.22. PMID22555511. PMC3842228.
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