Audouy S., Hoekstra D. Cationic lipid-mediated transfection in vitro and in vivo (review) // Mol. Membr. Biol. 2001. 18. (2). 129-143.
Bao G. CRISPR/Cas9-based genome editing for treating sickle cell disease // Abstr. AAAS Annual Meeting, Austin, February 15-19, 2018. https://aaas.confex.com/aaas/2018/meetingapp.cgi/Paper/21361
Briggs R., King T.J. Transplantation of living nuclei from blastula cells into enucleated frogs' eggs // Proc. Natl. Acad. Sci. USA. 1952. 38. (5). 455-463.
Bunnell B.A., Flaat M., Gagliardi C., Patel B., Ripoll C. Adipose-derived stem cells: Isolation, expansion and differentiation // Methods. 2008. 45. (2). 115–120.
Chin M.H., Mason M.J., Xie W., Volinia S., Singer M., Peterson C., Ambartsumyan G., Aimiuwu O., Richter L., Zhang J., Khvorostov I., Ott V., Grunstein M., Lavon N., Benvenisty N., Croce C.M., Clark A.T., Baxter T., Pyle A.D., Teitell M.A., Pelegrini M., Plath K., Lowry W.E. Induced pluripotent stem cells and embryonic stem cells are distinguished by gene expression signatures // Cell Stem Cell. 2009. 5. 111–123.
Chou B.K., Mali P., Huang X., Ye Z., Dowey S.N., Resar L.M., Zou C., Zhang Y.A., Tong J., Cheng L. Efficient human iPS cell derivation by a non-integrating plasmid from blood cells with unique epigenetic and gene expression signatures // Cell Res. 2011. 21. (3). 518–529.
Cieslar-Pobuda A., Knoflach V., Ringh M.V., Stark J., Likus W., Siemianowicz K., Ghavami S., Hudecki A., Green J.L., Łos M.J. Transdifferentiation and reprogramming: Overview of the processes, their similarities and differences // Biochim. Biophys. Acta. 2017. 1864. (7). 1359-1369.
de Vries W.N., Evsikov A.V., Brogan L.J., Anderson C.P., Graber J.H., Knowles B.B., Solter D. Reprogramming and differentiation in mammals: motifs and mechanisms // Cold Spring Harb. Symp. Quant. Biol. 2008. 73. 33–38.
Elango N., Elango S., Shivshankar P., Katz M.S. Optimized transfection of mRNA transcribed from a d(A/T)100 tail-containing vector // Biochem. Biophys. Res. Commun. 2005. 330. (3). 958-966.
Evans M.J., Kaufman M.H. Establishment in culture of pluripotential cells from mouse embryos // Nature. 1981. 292. 154–156.
Fu J.D., Stone N.R., Liu L., Delgado-Olguin P., Ding S., Bruneau B.G., Srivastava D. Direct reprogramming of human fibroblasts toward a cardiomyocyte-like state // Stem Cell Reports. 2013. 1. (3). 235-247.
Fusaki N., Ban H., Nishiyama A., Saeki K, Hasegawa M. Efficient induction of transgene-free human pluripotent stem cells using a vector based on Sendai virus, an RNA virus that does not integrate into the host genome // Proc. Jpn. Acad. Ser. B Phys. Biol. Sci. 2009. 85. 348–362.
Gopalakrishnan S., Hor P., Ichida J. K. New approaches for direct conversion of patient fibroblasts into neural cells // Brain Res. 2017. 1656. 2-13.
Gurdon J.B., Byrne J.A. The first half-century of nuclear transplantation // Proc. Natl. Acad. Sci. USA. 2003. 100. (14). 8048-8052.
He T.C., Zhou S., da Costa L.T., Yu J., Kinzler K.W., Vogelstein B. A simplified system for generating recombinant adenoviruses // Proc. Natl. Acad. Sci. USA. 1998. 95. 2509–2514.
Holtkamp S., Kreiter S., Selmi A., Simon P., Koslowski M., Huber C., Türeci O., Sahin U. Modification of antigen-encoding RNA increases stability, translational efficacy, and T-cell stimulatory capacity of dendritic cells // Blood. 2006. 108. (13). 4009-4017.
Jia F., Wilson K. D., Sun N., Gupta D.M., Huang M., Li Z., Panetta N.J., Chen Z.Y., Robbins R.C., Kay M.A., Longaker M.T., Wu J.C. A nonviral minicircle vector for deriving human iPS cells // Nat. Methods. 2010. 7. (3). 197–199.
Jungverdorben J., Till A., Brustle O. Induced pluripotent stem cell-based modeling of neurodegenerative diseases: a focus on autophagy // J. Mol. Med. 2017. 95. (7). 705-718.
Kumano K., Arai S., Hosoi M., Taoka K., Takayama N., Otsu M., Nagae G., Ueda K., Nakazaki K., Kamikubo Y., Eto K., Aburatani H., Nakauchi H., Kurokawa M. Generation of induced pluripotent stem cells from primary chronic myelogenous leukemia patient samples // Blood. 2012. 119. (26). 6234-6242.
Li X., Zhang P., Wei C., Zhang Y. Generation of pluripotent stem cells via protein transduction // J. Dev. Biol. 2014. 58. 21–27.
Liu H., Zhaohui Y., Kim Y., Sharkis S., Jang Y.Y. Generation of endoderm-derived human induced pluripotent stem cells from primary hepatocytes // Hepatology. 2010. 51. (5). 1810–1819.
Markoulaki S., Hanna J., Beard C., Carey B. W, Cheng A. W., Lengner C. J., Dausman J A., Fu D., Gao Q., Wu S., Cassady J. P., Jaenisch R. Transgenic mice with defined combinations of drug-inducible reprogramming factors // Nat. Biotechnol. 2009. 27. 169–171.
Martin G.R. Isolation of a pluripotent cell line from early mouse embryos cultured in medium conditioned by teratocarcinoma stem cells // Proc. Natl. Acad. Sci. USA. 1981. 78. 7634–8.
Maureen L. Condic totipotency: What it is and what it is not // Stem Cells Dev. 2014. 23. (8). 796–812.
Mendez-Ferrer S., Scadden D.T., Sanchez-Aguilera A. Bone marrow stem cells: Current and emerging concepts // Ann. N. Y. Acad. Sci. 2015. 1335. 32–44.
Meraviglia V., Zanon A., Lavdas A.A., Schwienbacher C., Silipigni R., Di Segni M., Chen H.S., Pramstaller P.P., Hicks A.A., Rossini A. Generation of induced pluripotent stem cells from frozen buffy coats using non-integrating episomal plasmids // J. Vis. Exp. 2015. 100. e52885.
Mitalipov S., Wolf D. Totipotency, pluripotency and nuclear reprogramming // Adv. Biochem. Eng. Biotechnol. 2009. 114. 185–199.
Nakhaei-Rad S., Bahrami A.R., Mirahmadi M., Matin M.M. New windows to enhance direct reprogramming of somatic cells towards induced pluripotent stem cells // Biochem. Cell Biol. 2012. 90. (2). 115-123.
Novak A., Shtrichman R., Germanguz I., Segev H., Zeevi-Levin N., Fishman B., Mandel Y.E., Barad L., Domev H., Kotton D., Mostoslavsky G., Binah O., Itskovitz-Eldor J. Enhanced reprogramming and cardiac differentiation of human keratinocytes derived from plucked hair follicles, using a single excisable lentivirus // Cell. Reprogram. 2010. 12. (6). 665-678.
Okita K., Ichisaka T., Yamanaka S. Generation of germline-competent induced pluripotent stem cells. Nature. 2007. 448. 313–7.
Okita K., Nakagawa M., Hyenjong H., Ichisaka T, Yamanaka S. Generation of mouse induced pluripotent stem cells without viral vectors // Science. 2008. 322. (5903). 949-953.
Okita K., Yamakawa T., MatsumuraY., Sato Y., Amano N., Watanabe A., Goshima N., Yamanaka S. An efficient nonviral method to generate integration-free human-induced pluripotent stem cells from cord blood and peripheral blood cells // Stem Cells. 2013. 31. 458–466.
Pasque V., Karnik R., Chronis C., Petrella P., Langerman J., Bonora G., Song J., Vanheer L., Sadhu Dimashkie A., Meissner A., Plath K. X Chromosome dosage influences DNA methylation dynamics during reprogramming to mouse iPSCs // Stem Cell Reports. 2018. 10. (5). 1537-1550.
Rajaei B., Shamsara M., Amirabad L.M., Massumi M., Sanati M.H. Pancreatic endoderm-derived from diabetic patient-specific induced pluripotent stem cell generates glucose-responsive insulin-secreting cells // J. Cell. Physiol. 2017. 232. (10). 2616-2625.
Rivera T., Haggblom C., Cosconati S., Karlseder J. A balance between elongation and trimming regulates telomere stability in stem cells // Nat. Struct. Mol. Biol. 2017. 24. (1). 30-39.
Sandmaier S.E.S., Telugu B.P.L. MicroRNA-mediated reprogramming of somatic cells into induced pluripotent stem cells // Cell. Reprogram. 2015. 1330. 29-36.
Seki T., Yuase S., Fukuda K. Generation of induced pluripotent stem cells from a small amount of human peripheral blood using a combination of activated T cells and Sendai virus // Nat. Protocols. 2012. 7. 718–728.
Shizuru J. A., NegrinR. S., Weissman I.L. Hematopoietic stem and progenitor cells: Clinical and preclinical regeneration of the hematolymphoid system // Annu. Rev. Med. 2005. 56. 509-538.
Takahashi K., Tanabe K., Ohnuki M., Narita M, Ichisaka T, Tomoda K, Yamanaka S. Induction of pluripotent stem cells from adult human fibroblasts by defined factors // Cell. 2007. 131. (5). 861–872.
Takahashi K., Yamanaka S. Induction of pluripotent stem cells from mouse embryonic and adult fibroblast cultures by defined factors // Cell. 2006. 126. 663–676.
Takahashi K., Yamanaka S. A developmental framework for induced pluripotency // Development. 2015. 142. 3274–3285.
Tang R., Jing L., Willard V.P., Wu C., Guilak F., Chen J., Setton L. A. Differentiation of human induced pluripotent stem cells into nucleus pulposus-like cells // Stem Cell Res. Ther. 2018. 9. 61.
Thomson J.A., Itskovitz-Eldor J., Shapiro S.S., Waknitz M.A., Swiergiel J.J., Marshall V.S., Jones J.M. Embryonic stem cell lines derived from human blastocysts // Science. 1998. 282. 1145–1147.
Warren L., Manos P.D., Ahfeldt T., Loh Y.H., Li H., Lau F., Ebina W., Mandal P.K., Smith Z.D., Meissner A., Daley G.Q., Brack A.S., Collins J.J., Cowan C., Schlaeger T.M., Rossi D.J. Highly efficient reprogramming to pluripotency and directed differentiation of human cells with synthetic modified mRNA // Cell Stem Cell. 2010. 7. (5). 618-30.
Wernig M., Meissner A., Cassady J.P., Jaenisch R. c-Myc is dispensable for direct reprogramming of mouse fibroblasts // Cell Stem Cell. 2008. 2. 10–12.
Wu Y.M., Huang Y.J., Chen P., Hsu Y.C., Lin S.W., Lai H.S., Lee H.S. Hepatocyte-like cells derived from mouse induced pluripotent stem cells produce functional coagulation factor IX in a hemophilia B mouse model // Cell Transpl. 2016. 25. (7). 1237-1246.
Xie M., Tang S.B., Li K., Ding S. Pharmacological reprogramming of somatic cells for regenerative medicine //Acc. Chem. Res. 2017. 50. (5). 1202-1211.
Yu J., Hu K., Smuga-Otto K., Tian S., Stewart R., Slukvin I.I., Thomson J.A. Human induced pluripotent stem cells free of vector and transgene sequences // Science. 2009. 324. (5928). 797-801.
Zang X., Gruz F.D., Remotti F., Matushasky I. Terminal differentiation and loss of tumorigenicity of human cancers via pluripotency-based reprogramming // Oncogene. 2013. 32. 2249–2260.
Zhou H., Wu S., Joo J.Y., Zhu S., Han D.W., Lin T., Trauger S., Bien G., Yao S., Zhu Y., Siuzdak G., Schöler H.R., Duan L., Ding S. Generation of induced pluripotent stem cells using recombinant proteins // Cell Stem Cell. 2009. 4. (5). 381–384.