Thomson JA, Itskovitz-Eldor J, Shapiro SS, Waknitz MA, Swiergiel JJ, Marshall VS, Jones JM: Embryonic stem cell lines derived from human blastocysts. Science. 1998, 282: 1145-1147.
Article
CAS
PubMed
Google Scholar
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: 861-872. 10.1016/j.cell.2007.11.019.
Article
CAS
PubMed
Google Scholar
Blum B, Benvenisty N: The tumorigenicity of human embryonic stem cells. Adv Canc Res. 2008, 100: 133-158.
Article
Google Scholar
Kiuru M, Boyer JL, O’Connor TP, Crystal RG: Genetic control of wayward pluripotent stem cells and their progeny after transplantation. Cell Stem Cell. 2009, 4: 289-300. 10.1016/j.stem.2009.03.010.
Article
PubMed Central
CAS
PubMed
Google Scholar
Izpisua Belmonte JC, Ellis J, Hochedlinger K, Yamanaka S: Induced pluripotent stem cells and reprogramming: seeing the science through the hype. Nat Rev Genet. 2009, 10: 878-883.
Article
CAS
PubMed
Google Scholar
Maherali N, Ahfeldt T, Rigamonti A, Utikal J, Cowan C, Hochedlinger K: A high-efficiency system for the generation and study of human induced pluripotent stem cells. Cell Stem Cell. 2008, 3: 340-345. 10.1016/j.stem.2008.08.003.
Article
PubMed Central
CAS
PubMed
Google Scholar
Mikkelsen TS, Hanna J, Zhang X, Ku M, Wernig M, Schorderet P, Bernstein BE, Jaenisch R, Lander ES, Meissner A: Dissecting direct reprogramming through integrative genomic analysis. Nature. 2008, 454: 49-55. 10.1038/nature07056.
Article
PubMed Central
CAS
PubMed
Google Scholar
Chin MH, Mason MJ, 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 CM, Clark AT, Baxter T, Pyle AD, Teitell MA, Pelegrini M, Plath K, Lowry WE: Induced pluripotent stem cells and embryonic stem cells are distinguished by gene expression signatures. Cell Stem Cell. 2009, 5: 111-123. 10.1016/j.stem.2009.06.008.
Article
PubMed Central
CAS
PubMed
Google Scholar
Marchetto MC, Yeo GW, Kainohana O, Marsala M, Gage FH, Muotri AR: Transcriptional signature and memory retention of human-induced pluripotent stem cells. PLoS One. 2009, 4: e7076-10.1371/journal.pone.0007076.
Article
PubMed Central
PubMed
Google Scholar
Doi A, Park IH, Wen B, Murakami P, Aryee MJ, Irizarry R, Herb B, Ladd-Acosta C, Rho J, Loewer S, Miller J, Schlaeger T, Daley GQ, Feinberg AP: Differential methylation of tissue- and cancer-specific CpG island shores distinguishes human induced pluripotent stem cells, embryonic stem cells and fibroblasts. Nat Genet. 2009, 41: 1350-1353. 10.1038/ng.471.
Article
PubMed Central
CAS
PubMed
Google Scholar
Polo JM, Liu S, Figueroa ME, Kulalert W, Eminli S, Tan KY, Apostolou E, Stadtfeld M, Li Y, Shioda T, Natesan S, Wagers AJ, Melnick A, Evans T, Hochedlinger K: Cell type of origin influences the molecular and functional properties of mouse induced pluripotent stem cells. Nat Biotechnol. 2010, 28: 848-855. 10.1038/nbt.1667.
Article
PubMed Central
CAS
PubMed
Google Scholar
Park TS, Gavina M, Chen CW, Sun B, Teng PN, Huard J, Deasy BM, Zimmerlin L, Peault B: Placental perivascular cells for human muscle regeneration. Stem Cells Dev. 2011, 20: 451-463. 10.1089/scd.2010.0354.
Article
PubMed Central
CAS
PubMed
Google Scholar
Russo A, Calo V, Bruno L, Rizzo S, Bazan V, Di Fede G: Hereditary ovarian cancer. Crit Rev Oncol Hematol. 2009, 69: 28-44. 10.1016/j.critrevonc.2008.06.003.
Article
PubMed
Google Scholar
Balch C, Fang F, Matei DE, Huang TH, Nephew KP: Minireview: epigenetic changes in ovarian cancer. Endocrinology. 2009, 150: 4003-4011. 10.1210/en.2009-0404.
Article
PubMed Central
CAS
PubMed
Google Scholar
Knudson AG: Genetics of human cancer. Annu Rev Genet. 1986, 20: 231-251. 10.1146/annurev.ge.20.120186.001311.
Article
PubMed
Google Scholar
Jones PA, Laird PW: Cancer epigenetics comes of age. Nat Genet. 1999, 21: 163-167. 10.1038/5947.
Article
CAS
PubMed
Google Scholar
Feinberg AP: DNA methylation, genomic imprinting and cancer. Curr Top Microbiol Immunol. 2000, 249: 87-99. 10.1007/978-3-642-59696-4_6.
CAS
PubMed
Google Scholar
Joyce JA, Schofield PN: Genomic imprinting and cancer. Mol Pathol. 1998, 51: 185-190. 10.1136/mp.51.4.185.
Article
PubMed Central
CAS
PubMed
Google Scholar
Feinberg AP: Imprinting of a genomic domain of 11p15 and loss of imprinting in cancer: an introduction. Canc Res. 1999, 59 (7 Suppl): 1743s-1746s.
CAS
Google Scholar
Zhang L, Volinia S, Bonome T, Calin GA, Greshock J, Yang N, Liu CG, Giannakakis A, Alexiou P, Hasegawa K, Johnstone CN, Megraw MS, Adams S, Lassus H, Huang J, Kaur S, Liang S, Sethupathy P, Leminen A, Simossis VA, Sandaltzopoulos R, Naomoto Y, Katsaros D, Gimotty PA, DeMichele A, Huang Q, Butzow R, Rustgi AK, Weber BL, Birrer MJ: Genomic and epigenetic alterations deregulate microRNA expression in human epithelial ovarian cancer. Proc Natl Acad Sci USA. 2008, 105: 7004-7009. 10.1073/pnas.0801615105.
Article
PubMed Central
CAS
PubMed
Google Scholar
Kohda T, Asai A, Kuroiwa Y, Kobayashi S, Aisaka K, Nagashima G, Yoshida MC, Kondo Y, Kagiyama N, Kirino T, Kaneko-Ishino T, Ishino F: Tumour suppressor activity of human imprinted gene PEG3 in a glioma cell line. Genes Cells. 2001, 6: 237-247. 10.1046/j.1365-2443.2001.00412.x.
Article
CAS
PubMed
Google Scholar
Nakano S, Murakami K, Meguro M, Soejima H, Higashimoto K, Urano T, Kugoh H, Mukai T, Ikeguchi M, Oshimura M: Expression profile of LIT1/KCNQ1OT1 and epigenetic status at the KvDMR1 in colorectal cancers. Canc Sci. 2006, 97: 1147-1154. 10.1111/j.1349-7006.2006.00305.x.
Article
CAS
Google Scholar
Kamikihara T, Arima T, Kato K, Matsuda T, Kato H, Douchi T, Nagata Y, Nakao M, Wake N: Epigenetic silencing of the imprinted gene ZAC by DNA methylation is an early event in the progression of human ovarian cancer. Int J Canc. 2005, 115: 690-700. 10.1002/ijc.20971.
Article
CAS
Google Scholar
Morison IM, Ramsay JP, Spencer HG: A census of mammalian imprinting. Trends Genet. 2005, 21: 457-465. 10.1016/j.tig.2005.06.008.
Article
CAS
PubMed
Google Scholar
Surani MA: Imprinting and the initiation of gene silencing in the germ line. Cell. 1998, 93: 309-312. 10.1016/S0092-8674(00)81156-3.
Article
CAS
PubMed
Google Scholar
Koerner MV, Barlow DP: Genomic imprinting-an epigenetic gene-regulatory model. Curr Opi Genet Dev. 2010, 20: 164-170. 10.1016/j.gde.2010.01.009.
Article
CAS
Google Scholar
Edwards CA, Ferguson-Smith AC: Mechanisms regulating imprinted genes in clusters. Curr Opi Cell Biol. 2007, 19: 281-289. 10.1016/j.ceb.2007.04.013.
Article
CAS
Google Scholar
Sasaki H, Matsui Y: Epigenetic events in mammalian germ-cell development: reprogramming and beyond. Nat Rev Genet. 2008, 9: 129-140. 10.1038/ni1560.
Article
CAS
PubMed
Google Scholar
Nishino K, Toyoda M, Yamazaki-Inoue M, Fukawatase Y, Chikazawa E, Sakaguchi H, Akutsu H, Umezawa A: DNA methylation dynamics in human induced pluripotent stem cells over time. PLoS Genet. 2011, 7: e1002085-10.1371/journal.pgen.1002085.
Article
PubMed Central
CAS
PubMed
Google Scholar
Rugg-Gunn PJ, Ferguson-Smith AC, Pedersen RA: Status of genomic imprinting in human embryonic stem cells as revealed by a large cohort of independently derived and maintained lines. Hum Mol Genet. 2007, 16 Spec No. 2: R243-R251.
Article
PubMed
Google Scholar
Pick M, Stelzer Y, Bar-Nur O, Mayshar Y, Eden A, Benvenisty N: Clone- and gene-specific aberrations of parental imprinting in human induced pluripotent stem cells. Stem Cells. 2009, 27: 2686-2690. 10.1002/stem.205.
Article
CAS
PubMed
Google Scholar
da Rocha ST, Edwards CA, Ito M, Ogata T, Ferguson-Smith AC: Genomic imprinting at the mammalian Dlk1-Dio3 domain. Trends Genet. 2008, 24: 306-316. 10.1016/j.tig.2008.03.011.
Article
PubMed
Google Scholar
Lewis A, Mitsuya K, Umlauf D, Smith P, Dean W, Walter J, Higgins M, Feil R, Reik W: Imprinting on distal chromosome 7 in the placenta involves repressive histone methylation independent of DNA methylation. Nat Genet. 2004, 36: 1291-1295. 10.1038/ng1468.
Article
CAS
PubMed
Google Scholar
Umlauf D, Goto Y, Cao R, Cerqueira F, Wagschal A, Zhang Y, Feil R: Imprinting along the Kcnq1 domain on mouse chromosome 7 involves repressive histone methylation and recruitment of Polycomb group complexes. Nat Genet. 2004, 36: 1296-1300. 10.1038/ng1467.
Article
CAS
PubMed
Google Scholar
Monk D, Wagschal A, Arnaud P, Muller PS, Parker-Katiraee L, Bourc’his D, Scherer SW, Feil R, Stanier P, Moore GE: Comparative analysis of human chromosome 7q21 and mouse proximal chromosome 6 reveals a placental-specific imprinted gene, TFPI2/Tfpi2, which requires EHMT2 and EED for allelic-silencing. Genome Res. 2008, 18: 1270-1281. 10.1101/gr.077115.108.
Article
PubMed Central
CAS
PubMed
Google Scholar
Stadtfeld M, Apostolou E, Akutsu H, Fukuda A, Follett P, Natesan S, Kono T, Shioda T, Hochedlinger K: Aberrant silencing of imprinted genes on chromosome 12qF1 in mouse induced pluripotent stem cells. Nature. 2010, 465: 175-181. 10.1038/nature09017.
Article
PubMed Central
CAS
PubMed
Google Scholar
Stadtfeld M, Apostolou E, Ferrari F, Choi J, Walsh RM, Chen T, Ooi SS, Kim SY, Bestor TH, Shioda T, Park PJ, Hochedlinger K: Ascorbic acid prevents loss of Dlk1-Dio3 imprinting and facilitates generation of all-iPS cell mice from terminally differentiated B cells. Nat Genet. 2012, 44: 398-405. 10.1038/ng.1110. S391-392
Article
PubMed Central
CAS
PubMed
Google Scholar
Sakatani T, Kaneda A, Iacobuzio-Donahue CA, Carter MG, de Boom Witzel S, Okano H, Ko MS, Ohlsson R, Longo DL, Feinberg AP: Loss of imprinting of Igf2 alters intestinal maturation and tumorigenesis in mice. Science. 2005, 307: 1976-1978. 10.1126/science.1108080.
Article
CAS
PubMed
Google Scholar
Nagata S, Toyoda M, Yamaguchi S, Hirano K, Makino H, Nishino K, Miyagawa Y, Okita H, Kiyokawa N, Nakagawa M, Yamanaka S, Akutsu H, Umezawa A, Tada T: Efficient reprogramming of human and mouse primary extra-embryonic cells to pluripotent stem cells. Genes Cells. 2009, 14: 1395-1404. 10.1111/j.1365-2443.2009.01356.x.
Article
CAS
PubMed
Google Scholar
Makino H, Toyoda M, Matsumoto K, Saito H, Nishino K, Fukawatase Y, Machida M, Akutsu H, Uyama T, Miyagawa Y, Okita H, Kiyokawa N, Fujino T, Ishikawa Y, Nakamura T, Umezawa A: Mesenchymal to embryonic incomplete transition of human cells by chimeric OCT4/3 (POU5F1) with physiological co-activator EWS. Exp Cell Res. 2009, 315: 2727-2740. 10.1016/j.yexcr.2009.06.016.
Article
CAS
PubMed
Google Scholar
Cui CH, Uyama T, Miyado K, Terai M, Kyo S, Kiyono T, Umezawa A: Menstrual blood-derived cells confer human dystrophin expression in the murine model of Duchenne muscular dystrophy via cell fusion and myogenic transdifferentiation. Mol Biol Cell. 2007, 18: 1586-1594. 10.1091/mbc.E06-09-0872.
Article
PubMed Central
CAS
PubMed
Google Scholar
Vambergue A, Fajardy I, Dufour P, Valat AS, Vandersippe M, Fontaine P, Danze PM, Rousseaux J: No loss of genomic imprinting of IGF-II and H19 in placentas of diabetic pregnancies with fetal macrosomia. Growth Horm IGF Res. 2007, 17: 130-136. 10.1016/j.ghir.2007.01.001.
Article
CAS
PubMed
Google Scholar
Wylie AA, Murphy SK, Orton TC, Jirtle RL: Novel imprinted DLK1/GTL2 domain on human chromosome 14 contains motifs that mimic those implicated in IGF2/H19 regulation. Genome Res. 2000, 10: 1711-1718. 10.1101/gr.161600.
Article
PubMed Central
CAS
PubMed
Google Scholar
Ogawa O, Eccles MR, Szeto J, McNoe LA, Yun K, Maw MA, Smith PJ, Reeve AE: Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms’ tumour. Nature. 1993, 362: 749-751. 10.1038/362749a0.
Article
CAS
PubMed
Google Scholar
Maegawa S, Yoshioka H, Itaba N, Kubota N, Nishihara S, Shirayoshi Y, Nanba E, Oshimura M: Epigenetic silencing of PEG3 gene expression in human glioma cell lines. Mol Carcinog. 2001, 31: 1-9. 10.1002/mc.1034.
Article
CAS
PubMed
Google Scholar
Pedersen IS, Dervan PA, Broderick D, Harrison M, Miller N, Delany E, O’Shea D, Costello P, McGoldrick A, Keating G, Tobin B, Gorey T, McCann A: Frequent loss of imprinting of PEG1/MEST in invasive breast cancer. Cancer Res. 1999, 59: 5449-5451.
CAS
PubMed
Google Scholar
Higashimoto K, Soejima H, Yatsuki H, Katsuki T, Mukai T: An NsiI RFLP in the human long QT intronic transcript 1 (LIT1). J Hum Genet. 2000, 45: 96-97. 10.1007/s100380050020.
Article
CAS
PubMed
Google Scholar
Mitsuya K, Meguro M, Lee MP, Katoh M, Schulz TC, Kugoh H, Yoshida MA, Niikawa N, Feinberg AP, Oshimura M: LIT1, an imprinted antisense RNA in the human KvLQT1 locus identified by screening for differentially expressed transcripts using monochromosomal hybrids. Hum Mol Genet. 1999, 8: 1209-1217. 10.1093/hmg/8.7.1209.
Article
CAS
PubMed
Google Scholar
MacDonald HR, Wevrick R: The necdin gene is deleted in Prader-Willi syndrome and is imprinted in human and mouse. Hum Mol Genet. 1997, 6: 1873-1878. 10.1093/hmg/6.11.1873.
Article
CAS
PubMed
Google Scholar
Kobayashi H, Sato A, Otsu E, Hiura H, Tomatsu C, Utsunomiya T, Sasaki H, Yaegashi N, Arima T: Aberrant DNA methylation of imprinted loci in sperm from oligospermic patients. Hum Mol Genet. 2007, 16: 2542-2551. 10.1093/hmg/ddm187.
Article
CAS
PubMed
Google Scholar
Hiura H, Sugawara A, Ogawa H, John RM, Miyauchi N, Miyanari Y, Horiike T, Li Y, Yaegashi N, Sasaki H, Kono T, Arima T: A tripartite paternally methylated region within the Gpr1-Zdbf2 imprinted domain on mouse chromosome 1 identified by meDIP-on-chip. Nucleic Acids Res. 2010, 38: 4929-4945. 10.1093/nar/gkq200.
Article
PubMed Central
CAS
PubMed
Google Scholar