204 related articles for article (PubMed ID: 10985851)
1. X inactivation in the mouse embryo deficient for Dnmt1: distinct effect of hypomethylation on imprinted and random X inactivation.
Sado T; Fenner MH; Tan SS; Tam P; Shioda T; Li E
Dev Biol; 2000 Sep; 225(2):294-303. PubMed ID: 10985851
[TBL] [Abstract][Full Text] [Related]
2. Expression of an X-linked HMG-lacZ transgene in mouse embryos: implication of chromosomal imprinting and lineage-specific X-chromosome activity.
Tam PP; Williams EA; Tan SS
Dev Genet; 1994; 15(6):491-503. PubMed ID: 7834909
[TBL] [Abstract][Full Text] [Related]
3. X chromosome inactivation revealed by the X-linked lacZ transgene activity in periimplantation mouse embryos.
Sugimoto M; Tan SS; Takagi N
Int J Dev Biol; 2000 Feb; 44(2):177-82. PubMed ID: 10794075
[TBL] [Abstract][Full Text] [Related]
4. Retarded postimplantation development of X0 mouse embryos: impact of the parental origin of the monosomic X chromosome.
Jamieson RV; Tan SS; Tam PP
Dev Biol; 1998 Sep; 201(1):13-25. PubMed ID: 9733570
[TBL] [Abstract][Full Text] [Related]
5. De novo DNA methylation independent establishment of maternal imprint on X chromosome in mouse oocytes.
Chiba H; Hirasawa R; Kaneda M; Amakawa Y; Li E; Sado T; Sasaki H
Genesis; 2008 Dec; 46(12):768-74. PubMed ID: 18932249
[TBL] [Abstract][Full Text] [Related]
6. X-chromosome inactivation occurs at different times in different tissues of the post-implantation mouse embryo.
Tan SS; Williams EA; Tam PP
Nat Genet; 1993 Feb; 3(2):170-4. PubMed ID: 8499950
[TBL] [Abstract][Full Text] [Related]
7. Dynamics of Dnmt1 methyltransferase expression and intracellular localization during oogenesis and preimplantation development.
Ratnam S; Mertineit C; Ding F; Howell CY; Clarke HJ; Bestor TH; Chaillet JR; Trasler JM
Dev Biol; 2002 May; 245(2):304-14. PubMed ID: 11977983
[TBL] [Abstract][Full Text] [Related]
8. Global hypomethylation of the genome in XX embryonic stem cells.
Zvetkova I; Apedaile A; Ramsahoye B; Mermoud JE; Crompton LA; John R; Feil R; Brockdorff N
Nat Genet; 2005 Nov; 37(11):1274-9. PubMed ID: 16244654
[TBL] [Abstract][Full Text] [Related]
9. Imprinted X-inactivation in extra-embryonic endoderm cell lines from mouse blastocysts.
Kunath T; Arnaud D; Uy GD; Okamoto I; Chureau C; Yamanaka Y; Heard E; Gardner RL; Avner P; Rossant J
Development; 2005 Apr; 132(7):1649-61. PubMed ID: 15753215
[TBL] [Abstract][Full Text] [Related]
10. Imprinted X inactivation maintained by a mouse Polycomb group gene.
Wang J; Mager J; Chen Y; Schneider E; Cross JC; Nagy A; Magnuson T
Nat Genet; 2001 Aug; 28(4):371-5. PubMed ID: 11479595
[TBL] [Abstract][Full Text] [Related]
11. Imprinted X inactivation and reprogramming in the preimplantation mouse embryo.
Sado T; Ferguson-Smith AC
Hum Mol Genet; 2005 Apr; 14 Spec No 1():R59-64. PubMed ID: 15809274
[TBL] [Abstract][Full Text] [Related]
12. X-chromosome activity: impact of imprinting and chromatin structure.
Jamieson RV; Tam PP; Gardiner-Garden M
Int J Dev Biol; 1996 Dec; 40(6):1065-80. PubMed ID: 9032012
[TBL] [Abstract][Full Text] [Related]
13. DNA methylation is a primary mechanism for silencing postmigratory primordial germ cell genes in both germ cell and somatic cell lineages.
Maatouk DM; Kellam LD; Mann MR; Lei H; Li E; Bartolomei MS; Resnick JL
Development; 2006 Sep; 133(17):3411-8. PubMed ID: 16887828
[TBL] [Abstract][Full Text] [Related]
14. XIST repression in the absence of DNMT1 and DNMT3B.
Vasques LR; Stabellini R; Xue F; Tian XC; Soukoyan M; Pereira LV
DNA Res; 2005; 12(5):373-8. PubMed ID: 16769694
[TBL] [Abstract][Full Text] [Related]
15. Reactivation of the paternal X chromosome in early mouse embryos.
Mak W; Nesterova TB; de Napoles M; Appanah R; Yamanaka S; Otte AP; Brockdorff N
Science; 2004 Jan; 303(5658):666-9. PubMed ID: 14752160
[TBL] [Abstract][Full Text] [Related]
16. X-inactivation is stably maintained in mouse embryos deficient for histone methyl transferase G9a.
Ohhata T; Tachibana M; Tada M; Tada T; Sasaki H; Shinkai Y; Sado T
Genesis; 2004 Nov; 40(3):151-6. PubMed ID: 15493016
[TBL] [Abstract][Full Text] [Related]
17. DNMT1 is required to maintain CpG methylation and aberrant gene silencing in human cancer cells.
Robert MF; Morin S; Beaulieu N; Gauthier F; Chute IC; Barsalou A; MacLeod AR
Nat Genet; 2003 Jan; 33(1):61-5. PubMed ID: 12496760
[TBL] [Abstract][Full Text] [Related]
18. Imprinting analysis of the mouse chromosome 7C region in DNMT1-null embryos.
Nakagaki A; Osanai H; Kishino T
Gene; 2014 Dec; 553(1):63-8. PubMed ID: 25300248
[TBL] [Abstract][Full Text] [Related]
19. Specific differentially methylated domain sequences direct the maintenance of methylation at imprinted genes.
Reinhart B; Paoloni-Giacobino A; Chaillet JR
Mol Cell Biol; 2006 Nov; 26(22):8347-56. PubMed ID: 16954379
[TBL] [Abstract][Full Text] [Related]
20. The SRA protein Np95 mediates epigenetic inheritance by recruiting Dnmt1 to methylated DNA.
Sharif J; Muto M; Takebayashi S; Suetake I; Iwamatsu A; Endo TA; Shinga J; Mizutani-Koseki Y; Toyoda T; Okamura K; Tajima S; Mitsuya K; Okano M; Koseki H
Nature; 2007 Dec; 450(7171):908-12. PubMed ID: 17994007
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]