Арчаков А.И. Нанобиотехнологии в медицине. rsmu.ru/fileadmin/rsmu/documents/science/uchenii_sovet/aktovyi _den/Act_rech_13_04_2009_Archakov.pdf
С.Л. Киселев. Гены и генная терапия. http://vivovoco.rsl.ru/VV/JOURNAL/NATURE/01_06/G-THER.HTM немесе http://neovasculgen.ru/index.php?option=com_content&view=artic le&id=85
Мясников А.Д., Артюшкова Е.Б., Пашков Д.В. и др. Комбинированная фармакологическая и хирургическая коррекция хронической ишемии конечности в эксперименте. Курский научно-практический вестник "Человек и его здоровье", 2007, № 4, с. 17-21 (http://neovasculgen.ru/index.php?option=com_content&view=arti cle&id=82)
Aguirre G.K., Komáromy A.M., Cideciyan A.V. e.a. Canine and Human Visual Cortex Intact and Responsive Despite Early Retinal Blindness from RPE65 Mutation. PLoS Med. 2007, v. 4, No. 6, e230. (Published online 2007 June 26).
Escors D., Breckpot R. Lentiviral vectors in gene therapy: their current status and future potential. Arch Immunol Ther Exp (Warsz), 2010, v. 58, No. 2? P. 107–119.
Marangoni F., Bosticardo M., Charrier S. e.a. Evidence for Longterm Efficacy and Safety of Gene Therapy for Wiskott–Aldrich Syndrome in Preclinical Models. Mol. Ther. 2009, v. 17, No. 6, p 1073–1082.
Pluta K, Kacprzak MM. Use of HIV as a gene transfer vector. Acta Biochim Pol. 2009, v. 56, No. 4, p. 531-95.
Templeton N., Lasic D. (2000) Gene Therapy: Therapeutic Mechanisms and Strategies. 584 pp.
Shiguo Zhu, Dean Anthony Lee, Shulin Li. IL12 and IL27 sequential gene therapy via intramuscular electroporation delivery for eliminating distal aggressive tumors. J. Immunol., 2010, v. 184, No. 5, p. 2348–2354.
Zafar R., King M.A., Carney P.R. Adeno associated viral vectormediated expression of somatostatin in rat hippocampus suppresses seizure development. Neurosci Lett., 2012, v. 509, No. 2, p. 87-91.