Publications
Found 57 results
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“Association of CD4 SNPs with fat percentage of Holstein cattle”, vol. 15, p. -, 2016.
, “Association of CD4 SNPs with fat percentage of Holstein cattle”, vol. 15, p. -, 2016.
, “De novo assembly and characterization of Gleditsia sinensis transcriptome and subsequent gene identification and SSR mining”, vol. 15, p. -, 2016.
, “De novo assembly and characterization of Gleditsia sinensis transcriptome and subsequent gene identification and SSR mining”, vol. 15, p. -, 2016.
, “De novo assembly and characterization of Gleditsia sinensis transcriptome and subsequent gene identification and SSR mining”, vol. 15, p. -, 2016.
, “Effect of siRNA-induced silencing of cellular prion protein on tyrosine hydroxylase expression in the substantia nigra of a rat model of Parkinson’s disease”, vol. 15, p. -, 2016.
, “Effect of siRNA-induced silencing of cellular prion protein on tyrosine hydroxylase expression in the substantia nigra of a rat model of Parkinson’s disease”, vol. 15, p. -, 2016.
, “Effects of glial cell line-derived neurotrophic factor and leukemia-inhibitory factor on the behavior of two calf testis germline stem cell colony types”, vol. 15, no. 4, p. -, 2016.
,
Conflicts of interest
The authors declare no conflict of interest.
ACKNOWLEDGMENTS
Research supported by the National International Scientific and Technological Cooperation Project (#2011DFA30760-2-1) and the Open Projects of Key Laboratory of Animal Genetics, Breeding and Reproduction, College of Heilongjiang Province, China (#GXZDSYS-2012-07).
REFERENCES
Aponte PM, Soda T, Teerds KJ, Mizrak SC, et al (2008). Propagation of bovine spermatogonial stem cells in vitro. Reproduction 136: 543-557. http://dx.doi.org/10.1530/REP-07-0419
Bain G, Kitchens D, Yao M, Huettner JE, et al (1995). Embryonic stem cells express neuronal properties in vitro. Dev. Biol. 168: 342-357. http://dx.doi.org/10.1006/dbio.1995.1085
Goel S, Fujihara M, Tsuchiya K, Takagi Y, et al (2009). Multipotential ability of primitive germ cells from neonatal pig testis cultured in vitro. Reprod. Fertil. Dev. 21: 696-708. http://dx.doi.org/10.1071/RD08176
Guan K, Nayernia K, Maier LS, Wagner S, et al (2006). Pluripotency of spermatogonial stem cells from adult mouse testis. Nature 440: 1199-1203. http://dx.doi.org/10.1038/nature04697
Herrid M, Vignarajan S, Davey R, Dobrinski I, et al (2006). Successful transplantation of bovine testicular cells to heterologous recipients. Reproduction 132: 617-624. http://dx.doi.org/10.1530/rep.1.01125
Herrid M, Davey RJ, Hutton K, Colditz IG, et al (2009). A comparison of methods for preparing enriched populations of bovine spermatogonia. Reprod. Fertil. Dev. 21: 393-399. http://dx.doi.org/10.1071/RD08129
Honaramooz A, Megee SO, Rathi R, Dobrinski I, et al (2007). Building a testis: formation of functional testis tissue after transplantation of isolated porcine (Sus scrofa) testis cells. Biol. Reprod. 76: 43-47. http://dx.doi.org/10.1095/biolreprod.106.054999
Honaramooz A, Megee S, Zeng W, Destrempes MM, et al (2008). Adeno-associated virus (AAV)-mediated transduction of male germ line stem cells results in transgene transmission after germ cell transplantation. FASEB J. 22: 374-382. http://dx.doi.org/10.1096/fj.07-8935com
Izadyar F, Matthijs-Rijsenbilt JJ, den Ouden K, Creemers LB, et al (2002a). Development of a cryopreservation protocol for type A spermatogonia. J. Androl. 23: 537-545.
Izadyar F, Spierenberg GT, Creemers LB, den Ouden K, et al (2002b). Isolation and purification of type A spermatogonia from the bovine testis. Reproduction 124: 85-94. http://dx.doi.org/10.1530/rep.0.1240085
Kanatsu-Shinohara M, Inoue K, Lee J, Yoshimoto M, et al (2004). Generation of pluripotent stem cells from neonatal mouse testis. Cell 119: 1001-1012. http://dx.doi.org/10.1016/j.cell.2004.11.011
Kanatsu-Shinohara M, Lee J, Inoue K, Ogonuki N, et al (2008). Pluripotency of a single spermatogonial stem cell in mice. Biol. Reprod. 78: 681-687. http://dx.doi.org/10.1095/biolreprod.107.066068
Kim KJ, Lee YA, Kim BJ, Kim YH, et al (2015). Cryopreservation of putative pre-pubertal bovine spermatogonial stem cells by slow freezing. Cryobiology 70: 175-183. http://dx.doi.org/10.1016/j.cryobiol.2015.02.007
Kossack N, Meneses J, Shefi S, Nguyen HN, et al (2009). Isolation and characterization of pluripotent human spermatogonial stem cell-derived cells. Stem Cells 27: 138-149. http://dx.doi.org/10.1634/stemcells.2008-0439
Kubota H, Brinster RL, et al (2006). Technology insight: In vitro culture of spermatogonial stem cells and their potential therapeutic uses. Nat. Clin. Pract. Endocrinol. Metab. 2: 99-108. http://dx.doi.org/10.1038/ncpendmet0098
Kubota H, Avarbock MR, Brinster RL, et al (2004). Growth factors essential for self-renewal and expansion of mouse spermatogonial stem cells. Proc. Natl. Acad. Sci. USA 101: 16489-16494. http://dx.doi.org/10.1073/pnas.0407063101
Olive V, Cuzin F, et al (2005). The spermatogonial stem cell: from basic knowledge to transgenic technology. Int. J. Biochem. Cell Biol. 37: 246-250. http://dx.doi.org/10.1016/j.biocel.2004.07.017
Seandel M, James D, Shmelkov SV, Falciatori I, et al (2007). Generation of functional multipotent adult stem cells from GPR125+ germline progenitors. Nature 449: 346-350. http://dx.doi.org/10.1038/nature06129
Simon L, Ekman GC, Kostereva N, Zhang Z, et al (2009). Direct transdifferentiation of stem/progenitor spermatogonia into reproductive and nonreproductive tissues of all germ layers. Stem Cells 27: 1666-1675. http://dx.doi.org/10.1002/stem.93
Wrobel KH, Bickel D, Kujat R, Schimmel M, et al (1995). Evolution and ultrastructure of the bovine spermatogonia precursor cell line. Cell Tissue Res. 281: 249-259. http://dx.doi.org/10.1007/BF00583394
Zhang P, Huang ZJ, Lv ZH, Li DX, et al (2009). Study of several factors affecting on preparation of mouse embryonic stem cells. Life Sci. J. 6: 1-4.
Zhao Q, Wang J, Zhang Y, Kou Z, et al (2010). Generation of histocompatible androgenetic embryonic stem cells using spermatogenic cells. Stem Cells 28: 229-239.
Zheng P, Li DX, Tian YG, Huang H, et al (2013). Isolation, purification and cryopreservation of cells from neonatal bovine testis. J. Northeast Agric. Univ. 20: 37-42. http://dx.doi.org/10.1016/S1006-8104(13)60006-9
Zheng P, Zhao XW, Zheng XM, Khalid A, et al (2015). In vitro differentiation of sperm from male germline stem cell. Genet. Mol. Res. 14: 2964-2969. http://dx.doi.org/10.4238/2015.April.10.5
“Effects of glial cell line-derived neurotrophic factor and leukemia-inhibitory factor on the behavior of two calf testis germline stem cell colony types”, vol. 15, no. 4, p. -, 2016.
,
Conflicts of interest
The authors declare no conflict of interest.
ACKNOWLEDGMENTS
Research supported by the National International Scientific and Technological Cooperation Project (#2011DFA30760-2-1) and the Open Projects of Key Laboratory of Animal Genetics, Breeding and Reproduction, College of Heilongjiang Province, China (#GXZDSYS-2012-07).
REFERENCES
Aponte PM, Soda T, Teerds KJ, Mizrak SC, et al (2008). Propagation of bovine spermatogonial stem cells in vitro. Reproduction 136: 543-557. http://dx.doi.org/10.1530/REP-07-0419
Bain G, Kitchens D, Yao M, Huettner JE, et al (1995). Embryonic stem cells express neuronal properties in vitro. Dev. Biol. 168: 342-357. http://dx.doi.org/10.1006/dbio.1995.1085
Goel S, Fujihara M, Tsuchiya K, Takagi Y, et al (2009). Multipotential ability of primitive germ cells from neonatal pig testis cultured in vitro. Reprod. Fertil. Dev. 21: 696-708. http://dx.doi.org/10.1071/RD08176
Guan K, Nayernia K, Maier LS, Wagner S, et al (2006). Pluripotency of spermatogonial stem cells from adult mouse testis. Nature 440: 1199-1203. http://dx.doi.org/10.1038/nature04697
Herrid M, Vignarajan S, Davey R, Dobrinski I, et al (2006). Successful transplantation of bovine testicular cells to heterologous recipients. Reproduction 132: 617-624. http://dx.doi.org/10.1530/rep.1.01125
Herrid M, Davey RJ, Hutton K, Colditz IG, et al (2009). A comparison of methods for preparing enriched populations of bovine spermatogonia. Reprod. Fertil. Dev. 21: 393-399. http://dx.doi.org/10.1071/RD08129
Honaramooz A, Megee SO, Rathi R, Dobrinski I, et al (2007). Building a testis: formation of functional testis tissue after transplantation of isolated porcine (Sus scrofa) testis cells. Biol. Reprod. 76: 43-47. http://dx.doi.org/10.1095/biolreprod.106.054999
Honaramooz A, Megee S, Zeng W, Destrempes MM, et al (2008). Adeno-associated virus (AAV)-mediated transduction of male germ line stem cells results in transgene transmission after germ cell transplantation. FASEB J. 22: 374-382. http://dx.doi.org/10.1096/fj.07-8935com
Izadyar F, Matthijs-Rijsenbilt JJ, den Ouden K, Creemers LB, et al (2002a). Development of a cryopreservation protocol for type A spermatogonia. J. Androl. 23: 537-545.
Izadyar F, Spierenberg GT, Creemers LB, den Ouden K, et al (2002b). Isolation and purification of type A spermatogonia from the bovine testis. Reproduction 124: 85-94. http://dx.doi.org/10.1530/rep.0.1240085
Kanatsu-Shinohara M, Inoue K, Lee J, Yoshimoto M, et al (2004). Generation of pluripotent stem cells from neonatal mouse testis. Cell 119: 1001-1012. http://dx.doi.org/10.1016/j.cell.2004.11.011
Kanatsu-Shinohara M, Lee J, Inoue K, Ogonuki N, et al (2008). Pluripotency of a single spermatogonial stem cell in mice. Biol. Reprod. 78: 681-687. http://dx.doi.org/10.1095/biolreprod.107.066068
Kim KJ, Lee YA, Kim BJ, Kim YH, et al (2015). Cryopreservation of putative pre-pubertal bovine spermatogonial stem cells by slow freezing. Cryobiology 70: 175-183. http://dx.doi.org/10.1016/j.cryobiol.2015.02.007
Kossack N, Meneses J, Shefi S, Nguyen HN, et al (2009). Isolation and characterization of pluripotent human spermatogonial stem cell-derived cells. Stem Cells 27: 138-149. http://dx.doi.org/10.1634/stemcells.2008-0439
Kubota H, Brinster RL, et al (2006). Technology insight: In vitro culture of spermatogonial stem cells and their potential therapeutic uses. Nat. Clin. Pract. Endocrinol. Metab. 2: 99-108. http://dx.doi.org/10.1038/ncpendmet0098
Kubota H, Avarbock MR, Brinster RL, et al (2004). Growth factors essential for self-renewal and expansion of mouse spermatogonial stem cells. Proc. Natl. Acad. Sci. USA 101: 16489-16494. http://dx.doi.org/10.1073/pnas.0407063101
Olive V, Cuzin F, et al (2005). The spermatogonial stem cell: from basic knowledge to transgenic technology. Int. J. Biochem. Cell Biol. 37: 246-250. http://dx.doi.org/10.1016/j.biocel.2004.07.017
Seandel M, James D, Shmelkov SV, Falciatori I, et al (2007). Generation of functional multipotent adult stem cells from GPR125+ germline progenitors. Nature 449: 346-350. http://dx.doi.org/10.1038/nature06129
Simon L, Ekman GC, Kostereva N, Zhang Z, et al (2009). Direct transdifferentiation of stem/progenitor spermatogonia into reproductive and nonreproductive tissues of all germ layers. Stem Cells 27: 1666-1675. http://dx.doi.org/10.1002/stem.93
Wrobel KH, Bickel D, Kujat R, Schimmel M, et al (1995). Evolution and ultrastructure of the bovine spermatogonia precursor cell line. Cell Tissue Res. 281: 249-259. http://dx.doi.org/10.1007/BF00583394
Zhang P, Huang ZJ, Lv ZH, Li DX, et al (2009). Study of several factors affecting on preparation of mouse embryonic stem cells. Life Sci. J. 6: 1-4.
Zhao Q, Wang J, Zhang Y, Kou Z, et al (2010). Generation of histocompatible androgenetic embryonic stem cells using spermatogenic cells. Stem Cells 28: 229-239.
Zheng P, Li DX, Tian YG, Huang H, et al (2013). Isolation, purification and cryopreservation of cells from neonatal bovine testis. J. Northeast Agric. Univ. 20: 37-42. http://dx.doi.org/10.1016/S1006-8104(13)60006-9
Zheng P, Zhao XW, Zheng XM, Khalid A, et al (2015). In vitro differentiation of sperm from male germline stem cell. Genet. Mol. Res. 14: 2964-2969. http://dx.doi.org/10.4238/2015.April.10.5
“Fas-FasL expression and myocardial cell apoptosis in patients with viral myocarditis”, vol. 15, p. -, 2016.
, “Fas-FasL expression and myocardial cell apoptosis in patients with viral myocarditis”, vol. 15, p. -, 2016.
, “Histone H3K9 acetylation influences growth characteristics of goat adipose-derived stem cells in vitro”, vol. 15, no. 4, p. -, 2016.
,
Conflicts of interest
The authors declare no conflict of interest.
ACKNOWLEDGMENTS
Research supported by a High Yield Transgenic Cashmere Goats Breeding grant (#2014ZX08008-002).
REFERENCES
Ahmadi N, Razavi S, Kazemi M, Oryan S, et al (2012). Stability of neural differentiation in human adipose derived stem cells by two induction protocols. Tissue Cell 44: 87-94. http://dx.doi.org/10.1016/j.tice.2011.11.006
Ali A, Bluteau O, Messaoudi K, Palazzo A, et al (2013). Thrombocytopenia induced by the histone deacetylase inhibitor abexinostat involves p53-dependent and -independent mechanisms. Cell Death Dis. 4: e738. http://dx.doi.org/10.1038/cddis.2013.260
Baltus GA, Kowalski MP, Tutter AV, Kadam S, et al (2009). A positive regulatory role for the mSin3A-HDAC complex in pluripotency through Nanog and Sox2. J. Biol. Chem. 284: 6998-7006. http://dx.doi.org/10.1074/jbc.M807670200
Collas P, et al (2010). Programming differentiation potential in mesenchymal stem cells. Epigenetics 5: 476-482. http://dx.doi.org/10.4161/epi.5.6.12517
Culmes M, Eckstein HH, Burgkart R, Nüssler AK, et al (2013). Endothelial differentiation of adipose-derived mesenchymal stem cells is improved by epigenetic modifying drug BIX-01294. Eur. J. Cell Biol. 92: 70-79. http://dx.doi.org/10.1016/j.ejcb.2012.11.001
Dudakovic A, Camilleri ET, Lewallen EA, McGee-Lawrence ME, et al (2015). Histone deacetylase inhibition destabilizes the multi-potent state of uncommitted adipose-derived mesenchymal stromal cells. J. Cell. Physiol. 230: 52-62. http://dx.doi.org/10.1002/jcp.24680
Fan QD, Wu G, Liu ZR, et al (2014). Dynamics of posttranslational modifications of p53. Comput. Math. Methods Med. 2014: 245610. http://dx.doi.org/10.1155/2014/245610
Ge W, Liu Y, Chen T, Zhang X, et al (2014). The epigenetic promotion of osteogenic differentiation of human adipose-derived stem cells by the genetic and chemical blockade of histone demethylase LSD1. Biomaterials 35: 6015-6025. http://dx.doi.org/10.1016/j.biomaterials.2014.04.055
Huang Y, Liang P, Liu D, Huang J, et al (2014). Telomere regulation in pluripotent stem cells. Protein Cell 5: 194-202. http://dx.doi.org/10.1007/s13238-014-0028-1
Kwon MJ, Kang SJ, Park YI, Yang YH, et al (2015). Hepatic differentiation of human adipose tissue-derived mesenchymal stem cells and adverse effects of arsanilic acid and acetaminophen during in vitro hepatic developmental stage. Cell Biol. Toxicol. 31: 149-159. http://dx.doi.org/10.1007/s10565-015-9300-2
Lagutina I, Fulka H, Lazzari G, Galli C, et al (2013). Interspecies somatic cell nuclear transfer: advancements and problems. Cell. Reprogram. 15: 374-384. http://dx.doi.org/10.1089/cell.2013.0036
Latella L, Palacios D, Forcales S, Puri PL, et al (2012). Epigenetic control of reprogramming and cellular differentiation. Comp. Funct. Genomics 2012: 538639. http://dx.doi.org/10.1155/2012/538639
Lee K, Kim H, Kim JM, Kim JR, et al (2011). Systemic transplantation of human adipose-derived stem cells stimulates bone repair by promoting osteoblast and osteoclast function. J. Cell. Mol. Med. 15: 2082-2094. http://dx.doi.org/10.1111/j.1582-4934.2010.01230.x
Leu S, Lin YC, Yuen CM, Yen CH, et al (2010). Adipose-derived mesenchymal stem cells markedly attenuate brain infarct size and improve neurological function in rats. J. Transl. Med. 8: 63. http://dx.doi.org/10.1186/1479-5876-8-63
Lin T, Chao C, Saito S, Mazur SJ, et al (2005). p53 induces differentiation of mouse embryonic stem cells by suppressing Nanog expression. Nat. Cell Biol. 7: 165-171. http://dx.doi.org/10.1038/ncb1211
Long CR, Westhusin ME, Golding MC, et al (2014). Reshaping the transcriptional frontier: epigenetics and somatic cell nuclear transfer. Mol. Reprod. Dev. 81: 183-193. http://dx.doi.org/10.1002/mrd.22271
Makarova AV, Burgers PM, et al (2015). Eukaryotic DNA polymerase ζ. DNA Repair (Amst.) 29: 47-55. http://dx.doi.org/10.1016/j.dnarep.2015.02.012
Mejlvang J, Feng Y, Alabert C, Neelsen KJ, et al (2014). New histone supply regulates replication fork speed and PCNA unloading. J. Cell Biol. 204: 29-43. http://dx.doi.org/10.1083/jcb.201305017
Ogura A, Inoue K, Wakayama T, et al (2013). Recent advancements in cloning by somatic cell nuclear transfer. Philos. Trans. R. Soc. Lond. B Biol. Sci. 368: 20110329. http://dx.doi.org/10.1098/rstb.2011.0329
Oh ET, Park MT, Choi BH, Ro S, et al (2012). Novel histone deacetylase inhibitor CG200745 induces clonogenic cell death by modulating acetylation of p53 in cancer cells. Invest. New Drugs 30: 435-442. http://dx.doi.org/10.1007/s10637-010-9568-2
Oh HJ, Park JE, Kim MJ, Hong SG, et al (2011). Recloned dogs derived from adipose stem cells of a transgenic cloned beagle. Theriogenology 75: 1221-1231. http://dx.doi.org/10.1016/j.theriogenology.2010.11.035
Oh HJ, Park JE, Park EJ, Kim MJ, et al (2014). Analysis of cell growth and gene expression of porcine adipose tissue-derived mesenchymal stem cells as nuclear donor cell. Dev. Growth Differ. 56: 595-604. http://dx.doi.org/10.1111/dgd.12159
Peterson DR, Mok HO, Au DW, et al (2015). Modulation of telomerase activity in fish muscle by biological and environmental factors. Comp. Biochem. Physiol. C Toxicol. Pharmacol. 178: 51-59.
Ren Y, Wu H, Zhou X, Wen J, et al (2012). Isolation, expansion, and differentiation of goat adipose-derived stem cells. Res. Vet. Sci. 93: 404-411. http://dx.doi.org/10.1016/j.rvsc.2011.08.014
Rinaldi L, Benitah SA, et al (2015). Epigenetic regulation of adult stem cell function. FEBS J. 282: 1589-1604. http://dx.doi.org/10.1111/febs.12946
Rizzino A, et al (2013). Concise review: The Sox2-Oct4 connection: critical players in a much larger interdependent network integrated at multiple levels. Stem Cells 31: 1033-1039. http://dx.doi.org/10.1002/stem.1352
Rodriguez J, Boucher F, Lequeux C, Josset-Lamaugarny A, et al (2015). Intradermal injection of human adipose-derived stem cells accelerates skin wound healing in nude mice. Stem Cell Res. Ther. 6: 241. http://dx.doi.org/10.1186/s13287-015-0238-3
Saunders A, Faiola F, Wang J, et al (2013). Concise review: pursuing self-renewal and pluripotency with the stem cell factor Nanog. Stem Cells 31: 1227-1236. http://dx.doi.org/10.1002/stem.1384
Teven CM, Liu X, Hu N, Tang N, et al (2011). Epigenetic regulation of mesenchymal stem cells: a focus on osteogenic and adipogenic differentiation. Stem Cells Int. 2011: 201371. http://dx.doi.org/10.4061/2011/201371
Wang S, Hu C, Zhu J, et al (2007). Transcriptional silencing of a novel hTERT reporter locus during in vitro differentiation of mouse embryonic stem cells. Mol. Biol. Cell 18: 669-677. http://dx.doi.org/10.1091/mbc.E06-09-0840
Wang Z, Oron E, Nelson B, Razis S, et al (2012). Distinct lineage specification roles for NANOG, OCT4, and SOX2 in human embryonic stem cells. Cell Stem Cell 10: 440-454. http://dx.doi.org/10.1016/j.stem.2012.02.016
Wankhade UD, Shen M, Kolhe R, Fulzele S, et al (2016). Advances in adipose-derived stem cells isolation, characterization, and application in regenerative tissue engineering. Stem Cells Int. 2016: 3206807. http://dx.doi.org/10.1155/2016/3206807
Yang H, Yan B, Liao D, Huang S, et al (2015). Acetylation of HDAC1 and degradation of SIRT1 form a positive feedback loop to regulate p53 acetylation during heat-shock stress. Cell Death Dis. 6: e1747. http://dx.doi.org/10.1038/cddis.2015.106
Yannarelli G, Pacienza N, Cuniberti L, Medin J, et al (2013). Brief report: The potential role of epigenetics on multipotent cell differentiation capacity of mesenchymal stromal cells. Stem Cells 31: 215-220. http://dx.doi.org/10.1002/stem.1262
Yoon DS, Choi Y, Jang Y, Lee M, et al (2014). SIRT1 directly regulates SOX2 to maintain self-renewal and multipotency in bone marrow-derived mesenchymal stem cells. Stem Cells 32: 3219-3231. http://dx.doi.org/10.1002/stem.1811
Zhang C, Qu S, Wei X, Feng Y, et al (2016). HSP25 down-regulation enhanced p53 acetylation by dissociation of SIRT1 from p53 in doxorubicin-induced H9c2 cell apoptosis. Cell Stress Chaperones 21: 251-260. http://dx.doi.org/10.1007/s12192-015-0655-3
Zhang Q, Ramlee MK, Brunmeir R, Villanueva CJ, et al (2012). Dynamic and distinct histone modifications modulate the expression of key adipogenesis regulatory genes. Cell Cycle 11: 4310-4322. http://dx.doi.org/10.4161/cc.22224
Zhang S, Cui W, et al (2014). Sox2, a key factor in the regulation of pluripotency and neural differentiation. World J. Stem Cells 6: 305-311. http://dx.doi.org/10.4252/wjsc.v6.i3.305
Zhang Y, Zhang A, Shen C, Zhang B, et al (2014). E2F1 acts as a negative feedback regulator of c-Myc‑induced hTERT transcription during tumorigenesis. Oncol. Rep. 32: 1273-1280.
Zhu Y, Song X, Han F, Li Y, et al (2015). Alteration of histone acetylation pattern during long-term serum-free culture conditions of human fetal placental mesenchymal stem cells. PLoS One 10: e0117068. http://dx.doi.org/10.1371/journal.pone.0117068
“Histone H3K9 acetylation influences growth characteristics of goat adipose-derived stem cells in vitro”, vol. 15, no. 4, p. -, 2016.
,
Conflicts of interest
The authors declare no conflict of interest.
ACKNOWLEDGMENTS
Research supported by a High Yield Transgenic Cashmere Goats Breeding grant (#2014ZX08008-002).
REFERENCES
Ahmadi N, Razavi S, Kazemi M, Oryan S, et al (2012). Stability of neural differentiation in human adipose derived stem cells by two induction protocols. Tissue Cell 44: 87-94. http://dx.doi.org/10.1016/j.tice.2011.11.006
Ali A, Bluteau O, Messaoudi K, Palazzo A, et al (2013). Thrombocytopenia induced by the histone deacetylase inhibitor abexinostat involves p53-dependent and -independent mechanisms. Cell Death Dis. 4: e738. http://dx.doi.org/10.1038/cddis.2013.260
Baltus GA, Kowalski MP, Tutter AV, Kadam S, et al (2009). A positive regulatory role for the mSin3A-HDAC complex in pluripotency through Nanog and Sox2. J. Biol. Chem. 284: 6998-7006. http://dx.doi.org/10.1074/jbc.M807670200
Collas P, et al (2010). Programming differentiation potential in mesenchymal stem cells. Epigenetics 5: 476-482. http://dx.doi.org/10.4161/epi.5.6.12517
Culmes M, Eckstein HH, Burgkart R, Nüssler AK, et al (2013). Endothelial differentiation of adipose-derived mesenchymal stem cells is improved by epigenetic modifying drug BIX-01294. Eur. J. Cell Biol. 92: 70-79. http://dx.doi.org/10.1016/j.ejcb.2012.11.001
Dudakovic A, Camilleri ET, Lewallen EA, McGee-Lawrence ME, et al (2015). Histone deacetylase inhibition destabilizes the multi-potent state of uncommitted adipose-derived mesenchymal stromal cells. J. Cell. Physiol. 230: 52-62. http://dx.doi.org/10.1002/jcp.24680
Fan QD, Wu G, Liu ZR, et al (2014). Dynamics of posttranslational modifications of p53. Comput. Math. Methods Med. 2014: 245610. http://dx.doi.org/10.1155/2014/245610
Ge W, Liu Y, Chen T, Zhang X, et al (2014). The epigenetic promotion of osteogenic differentiation of human adipose-derived stem cells by the genetic and chemical blockade of histone demethylase LSD1. Biomaterials 35: 6015-6025. http://dx.doi.org/10.1016/j.biomaterials.2014.04.055
Huang Y, Liang P, Liu D, Huang J, et al (2014). Telomere regulation in pluripotent stem cells. Protein Cell 5: 194-202. http://dx.doi.org/10.1007/s13238-014-0028-1
Kwon MJ, Kang SJ, Park YI, Yang YH, et al (2015). Hepatic differentiation of human adipose tissue-derived mesenchymal stem cells and adverse effects of arsanilic acid and acetaminophen during in vitro hepatic developmental stage. Cell Biol. Toxicol. 31: 149-159. http://dx.doi.org/10.1007/s10565-015-9300-2
Lagutina I, Fulka H, Lazzari G, Galli C, et al (2013). Interspecies somatic cell nuclear transfer: advancements and problems. Cell. Reprogram. 15: 374-384. http://dx.doi.org/10.1089/cell.2013.0036
Latella L, Palacios D, Forcales S, Puri PL, et al (2012). Epigenetic control of reprogramming and cellular differentiation. Comp. Funct. Genomics 2012: 538639. http://dx.doi.org/10.1155/2012/538639
Lee K, Kim H, Kim JM, Kim JR, et al (2011). Systemic transplantation of human adipose-derived stem cells stimulates bone repair by promoting osteoblast and osteoclast function. J. Cell. Mol. Med. 15: 2082-2094. http://dx.doi.org/10.1111/j.1582-4934.2010.01230.x
Leu S, Lin YC, Yuen CM, Yen CH, et al (2010). Adipose-derived mesenchymal stem cells markedly attenuate brain infarct size and improve neurological function in rats. J. Transl. Med. 8: 63. http://dx.doi.org/10.1186/1479-5876-8-63
Lin T, Chao C, Saito S, Mazur SJ, et al (2005). p53 induces differentiation of mouse embryonic stem cells by suppressing Nanog expression. Nat. Cell Biol. 7: 165-171. http://dx.doi.org/10.1038/ncb1211
Long CR, Westhusin ME, Golding MC, et al (2014). Reshaping the transcriptional frontier: epigenetics and somatic cell nuclear transfer. Mol. Reprod. Dev. 81: 183-193. http://dx.doi.org/10.1002/mrd.22271
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