Epigenetic variation: amount, causes, and consequences
作者： Elena de la Casa-Esper������n , Carmen Sapienza
DOI: 10.1002/047001153X.G103227
关键词: Variation (linguistics) 、 Allele 、 Chromatin 、 Phenotype 、 DNA methylation 、 X-inactivation 、 Epigenetic code 、 Genetics 、 Biology 、 Epigenetics
摘要: Epigenetic variation is the result of biochemical and spatial modifications that affect the function of chromosomes. The diversity of phenotypes that we observe in all organisms is …
sci-hub.se 参考文章(91)
Itamar Simon, Toyoaki Tenzen, Benjamin E. Reubinoff, Dahlia Hillman, John R. McCarrey, Howard Cedar, Asynchronous replication of imprinted genes is established in the gametes and maintained during development. Nature. ,vol. 401, pp. 929- 932 ,(1999) , 10.1038/44866
Joseph H. Nadeau, Christopher J. Krapp, Ivona Percec, Ivona Percec, Marisa S. Bartolomei, Joanne L. Thorvaldsen, Robert M. Plenge, Huntington F. Willard, Huntington F. Willard, An N-Ethyl-N-Nitrosourea Mutagenesis Screen for Epigenetic Mutations in the Mouse Genetics. ,vol. 164, pp. 1481- 1494 ,(2003) , 10.1093/GENETICS/164.4.1481
J Messing, O P Das, Variegated Phenotype and Developmental Methylation Changes of a Maize Allele Originating from Epimutation Genetics. ,vol. 136, pp. 1121- 1141 ,(1994) , 10.1093/GENETICS/136.3.1121
Jane Halliday, Kay Oke, Sue Breheny, Elizabeth Algar, David J. Amor, Beckwith-Wiedemann Syndrome and IVF: A Case-Control Study American Journal of Human Genetics. ,vol. 75, pp. 526- 528 ,(2004) , 10.1086/423902
F. Pagani, D. Toniolo, C. Vergani, Stability of DNA methylation of X-chromosome genes during aging. Somatic Cell and Molecular Genetics. ,vol. 16, pp. 79- 84 ,(1990) , 10.1007/BF01650482
Roland Bunzel, Ingmar Blümcke, Sven Cichon, Sabine Normann, Johannes Schramm, Peter Propping, Markus M Nöthen, None, Polymorphic imprinting of the serotonin-2A (5-HT2A) receptor gene in human adult brain Molecular Brain Research. ,vol. 59, pp. 90- 92 ,(1998) , 10.1016/S0169-328X(98)00146-6
Stefan Kochanek, Doris Renz, Walter Doerfler, Variability in allelic DNA methylation in spermatozoa Human Genetics. ,vol. 94, pp. 203- 206 ,(1994) , 10.1007/BF00202872
Christine M. Disteche, Escape from X inactivation in human and mouse Trends in Genetics. ,vol. 11, pp. 17- 22 ,(1995) , 10.1016/S0168-9525(00)88981-7
Emily L. Niemitz, Michael R. DeBaun, Jonathan Fallon, Kazuhiro Murakami, Hiroyuki Kugoh, Mitsuo Oshimura, Andrew P. Feinberg, Microdeletion of LIT1 in familial Beckwith-Wiedemann syndrome. American Journal of Human Genetics. ,vol. 75, pp. 844- 849 ,(2004) , 10.1086/425343
Takashi Sakatani, Michelle Wei, Motonobu Katoh, Chiga Okita, Daisuke Wada, Kohzoh Mitsuya, Makiko Meguro, Masahide Ikeguchi, Hisao Ito, Benjamin Tycko, Mitsuo Oshimura, Epigenetic Heterogeneity at Imprinted Loci in Normal Populations Biochemical and Biophysical Research Communications. ,vol. 283, pp. 1124- 1130 ,(2001) , 10.1006/BBRC.2001.4916