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62. Allele-specific histone modifications regulate expression of the Dlk1-Gtl2 imprinted domain. Carr MS, Yevtodiyenko A, Schmidt CL, Schmidt JV. Genomics; 2007 Feb; 89(2):280-90. PubMed ID: 17126526 [Abstract] [Full Text] [Related]
63. Genome-wide allelic methylation analysis reveals disease-specific susceptibility to multiple methylation defects in imprinting syndromes. Court F, Martin-Trujillo A, Romanelli V, Garin I, Iglesias-Platas I, Salafsky I, Guitart M, Perez de Nanclares G, Lapunzina P, Monk D. Hum Mutat; 2013 Apr; 34(4):595-602. PubMed ID: 23335487 [Abstract] [Full Text] [Related]
64. Sequence-specific methylation of the mouse H19 gene in embryonic cells deficient in the Dnmt-1 gene. Warnecke PM, Biniszkiewicz D, Jaenisch R, Frommer M, Clark SJ. Dev Genet; 1998 Apr; 22(2):111-21. PubMed ID: 9581283 [Abstract] [Full Text] [Related]
68. Antisense noncoding RNA promoter regulates the timing of de novo methylation of an imprinting control region. Guseva N, Mondal T, Kanduri C. Dev Biol; 2012 Jan 15; 361(2):403-11. PubMed ID: 22119056 [Abstract] [Full Text] [Related]
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75. An upstream repressor element plays a role in Igf2 imprinting. Eden S, Constancia M, Hashimshony T, Dean W, Goldstein B, Johnson AC, Keshet I, Reik W, Cedar H. EMBO J; 2001 Jul 02; 20(13):3518-25. PubMed ID: 11432838 [Abstract] [Full Text] [Related]
76. Absence of an obvious molecular imprinting mechanism in a human fetus with monoallelic IGF2R expression. Riesewijk AM, Xu YQ, Schepens MT, Mariman EM, Polychronakos C, Ropers HH, Kalscheuer VM. Biochem Biophys Res Commun; 1998 Apr 07; 245(1):272-7. PubMed ID: 9535821 [Abstract] [Full Text] [Related]
77. The MAS proto-oncogene is not imprinted in humans. Riesewijk AM, Schepens MT, Mariman EM, Ropers HH, Kalscheuer VM. Genomics; 1996 Jul 15; 35(2):380-2. PubMed ID: 8661154 [Abstract] [Full Text] [Related]
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