144 related articles for article (PubMed ID: 15523153)
1. Genomic imprinting in mammals.
Wrzeska M; Rejduch B
J Appl Genet; 2004; 45(4):427-33. PubMed ID: 15523153
[TBL] [Abstract][Full Text] [Related]
2. Genomic imprinting: the influence of differential methylation in the two sexes.
Biliya S; Bulla LA
Exp Biol Med (Maywood); 2010 Feb; 235(2):139-47. PubMed ID: 20404028
[TBL] [Abstract][Full Text] [Related]
3. Mechanisms of genomic imprinting.
Brannan CI; Bartolomei MS
Curr Opin Genet Dev; 1999 Apr; 9(2):164-70. PubMed ID: 10322141
[TBL] [Abstract][Full Text] [Related]
4. No loss of genomic imprinting of IGF-II and H19 in placentas of diabetic pregnancies with fetal macrosomia.
Vambergue A; Fajardy I; Dufour P; Valat AS; Vandersippe M; Fontaine P; Danze PM; Rousseaux J
Growth Horm IGF Res; 2007 Apr; 17(2):130-6. PubMed ID: 17306581
[TBL] [Abstract][Full Text] [Related]
5. Imprinting of IGF2, insulin-dependent diabetes, immune function, and apoptosis: a hypothesis.
Polychronakos C; Giannoukakis N; Deal CL
Dev Genet; 1995; 17(3):253-62. PubMed ID: 8565331
[TBL] [Abstract][Full Text] [Related]
6. [Genomic imprinting in mammals].
Koniukhov BV; Platonov ES
Genetika; 2001 Jan; 37(1):5-17. PubMed ID: 11234425
[TBL] [Abstract][Full Text] [Related]
7. Maintenance of normal imprinting of H19 and IGF2 genes in neuroblastoma.
Wada M; Seeger RC; Mizoguchi H; Koeffler HP
Cancer Res; 1995 Aug; 55(15):3386-8. PubMed ID: 7614476
[TBL] [Abstract][Full Text] [Related]
8. Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndrome.
Sparago A; Cerrato F; Vernucci M; Ferrero GB; Silengo MC; Riccio A
Nat Genet; 2004 Sep; 36(9):958-60. PubMed ID: 15314640
[TBL] [Abstract][Full Text] [Related]
9. Manipulations of mouse embryos prior to implantation result in aberrant expression of imprinted genes on day 9.5 of development.
Rivera RM; Stein P; Weaver JR; Mager J; Schultz RM; Bartolomei MS
Hum Mol Genet; 2008 Jan; 17(1):1-14. PubMed ID: 17901045
[TBL] [Abstract][Full Text] [Related]
10. [Short introduction to gene imprinting].
Romer JT
Endokrynol Diabetol Chor Przemiany Materii Wieku Rozw; 2000; 6(1):37-43. PubMed ID: 12818083
[TBL] [Abstract][Full Text] [Related]
11. Alterations of H19 imprinting and IGF2 replication timing are infrequent in Beckwith-Wiedemann syndrome.
Squire JA; Li M; Perlikowski S; Fei YL; Bayani J; Zhang ZM; Weksberg R
Genomics; 2000 May; 65(3):234-42. PubMed ID: 10857747
[TBL] [Abstract][Full Text] [Related]
12. Genomic imprinting in the rat: linkage of Igf2 and H19 genes and opposite parental allele-specific expression during embryogenesis.
Overall M; Bakker M; Spencer J; Parker N; Smith P; Dziadek M
Genomics; 1997 Oct; 45(2):416-20. PubMed ID: 9344669
[TBL] [Abstract][Full Text] [Related]
13. [Genomic imprinting and its role in Prader-Willi and Angelman syndromes].
Mglinets VA; Levina LIa; Konstantinova LM
Genetika; 1996 Dec; 32(12):1605-15. PubMed ID: 9102354
[TBL] [Abstract][Full Text] [Related]
14. Complementation hypothesis: the necessity of a monoallelic gene expression mechanism in mammalian development.
Kaneko-Ishino T; Kohda T; Ono R; Ishino F
Cytogenet Genome Res; 2006; 113(1-4):24-30. PubMed ID: 16575159
[TBL] [Abstract][Full Text] [Related]
15. [Epigenetic modification of the genetic material. Genomic imprinting and its significance for disease in human beings].
Brøndum-Nielsen K; Pedersen ML
Ugeskr Laeger; 2001 Jun; 163(23):3218-22. PubMed ID: 11421188
[TBL] [Abstract][Full Text] [Related]
16. Analysis of the IGF2/H19 imprinting control region uncovers new genetic defects, including mutations of OCT-binding sequences, in patients with 11p15 fetal growth disorders.
Demars J; Shmela ME; Rossignol S; Okabe J; Netchine I; Azzi S; Cabrol S; Le Caignec C; David A; Le Bouc Y; El-Osta A; Gicquel C
Hum Mol Genet; 2010 Mar; 19(5):803-14. PubMed ID: 20007505
[TBL] [Abstract][Full Text] [Related]
17. [Epigenetics and development: genomic imprinting].
Gabory A; Dandolo L
Med Sci (Paris); 2005 Apr; 21(4):390-5. PubMed ID: 15811304
[TBL] [Abstract][Full Text] [Related]
18. Deletion of a silencer element in Igf2 results in loss of imprinting independent of H19.
Constância M; Dean W; Lopes S; Moore T; Kelsey G; Reik W
Nat Genet; 2000 Oct; 26(2):203-6. PubMed ID: 11017078
[TBL] [Abstract][Full Text] [Related]
19. IVF results in de novo DNA methylation and histone methylation at an Igf2-H19 imprinting epigenetic switch.
Li T; Vu TH; Ulaner GA; Littman E; Ling JQ; Chen HL; Hu JF; Behr B; Giudice L; Hoffman AR
Mol Hum Reprod; 2005 Sep; 11(9):631-40. PubMed ID: 16219628
[TBL] [Abstract][Full Text] [Related]
20. Imprinting status of 11p15 genes in Beckwith-Wiedemann syndrome patients with CDKN1C mutations.
Li M; Squire J; Shuman C; Fei YL; Atkin J; Pauli R; Smith A; Nishikawa J; Chitayat D; Weksberg R
Genomics; 2001 Jun; 74(3):370-6. PubMed ID: 11414765
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
