330 related articles for article (PubMed ID: 9738504)
21. Baseline levels of chromosome instability in the human lymphoblastoid cell TK6.
Schwartz JL; Jordan R; Evans HH; Lenarczyk M; Liber HL
Mutagenesis; 2004 Nov; 19(6):477-82. PubMed ID: 15548760
[TBL] [Abstract][Full Text] [Related]
22. Development of a novel mouse tk+/- embryonic stem cell line for use in mutagenicity studies.
Dobrovolsky VN; Casciano DA; Heflich RH
Environ Mol Mutagen; 1996; 28(4):483-9. PubMed ID: 8991081
[TBL] [Abstract][Full Text] [Related]
23. Mutagenicity of the mycotoxin alternariol in cultured mammalian cells.
Brugger EM; Wagner J; Schumacher DM; Koch K; Podlech J; Metzler M; Lehmann L
Toxicol Lett; 2006 Jul; 164(3):221-30. PubMed ID: 16464542
[TBL] [Abstract][Full Text] [Related]
24. DNMT3B mutations and DNA methylation defect define two types of ICF syndrome.
Jiang YL; Rigolet M; Bourc'his D; Nigon F; Bokesoy I; Fryns JP; Hultén M; Jonveaux P; Maraschio P; Mégarbané A; Moncla A; Viegas-Péquignot E
Hum Mutat; 2005 Jan; 25(1):56-63. PubMed ID: 15580563
[TBL] [Abstract][Full Text] [Related]
25. Deletion, rearrangement, and gene conversion; genetic consequences of chromosomal double-strand breaks in human cells.
Honma M; Izumi M; Sakuraba M; Tadokoro S; Sakamoto H; Wang W; Yatagai F; Hayashi M
Environ Mol Mutagen; 2003; 42(4):288-98. PubMed ID: 14673874
[TBL] [Abstract][Full Text] [Related]
26. Differential repetitive DNA methylation in multiple myeloma molecular subgroups.
Bollati V; Fabris S; Pegoraro V; Ronchetti D; Mosca L; Deliliers GL; Motta V; Bertazzi PA; Baccarelli A; Neri A
Carcinogenesis; 2009 Aug; 30(8):1330-5. PubMed ID: 19531770
[TBL] [Abstract][Full Text] [Related]
27. 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]
28. Reduced rates of gene loss, gene silencing, and gene mutation in Dnmt1-deficient embryonic stem cells.
Chan MF; van Amerongen R; Nijjar T; Cuppen E; Jones PA; Laird PW
Mol Cell Biol; 2001 Nov; 21(22):7587-600. PubMed ID: 11604495
[TBL] [Abstract][Full Text] [Related]
29. Major and essential role for the DNA methylation mark in mouse embryogenesis and stable association of DNMT1 with newly replicated regions.
Takebayashi S; Tamura T; Matsuoka C; Okano M
Mol Cell Biol; 2007 Dec; 27(23):8243-58. PubMed ID: 17893328
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. Severe global DNA hypomethylation blocks differentiation and induces histone hyperacetylation in embryonic stem cells.
Jackson M; Krassowska A; Gilbert N; Chevassut T; Forrester L; Ansell J; Ramsahoye B
Mol Cell Biol; 2004 Oct; 24(20):8862-71. PubMed ID: 15456861
[TBL] [Abstract][Full Text] [Related]
32. DNA methyltransferase Dnmt1 and mismatch repair.
Wang KY; James Shen CK
Oncogene; 2004 Oct; 23(47):7898-902. PubMed ID: 15378011
[TBL] [Abstract][Full Text] [Related]
33. Characterization of Hprt mutations in cDNA and genomic DNA of T-cell mutants from control and 1,3-butadiene-exposed male B6C3F1 mice and F344 rats.
Meng Q; Walker DM; Scott BR; Seilkop SK; Aden JK; Walker VE
Environ Mol Mutagen; 2004; 43(2):75-92. PubMed ID: 14991748
[TBL] [Abstract][Full Text] [Related]
34. [Role and significance of DNA methylation].
Kowal M; Wojcierowski J
Pol Merkur Lekarski; 2003 Apr; 14(82):364-8. PubMed ID: 12868204
[TBL] [Abstract][Full Text] [Related]
35. Mutagenicity of gamma-radiation, mitomycin C, and etoposide in the Hprt and Tk genes of Tk(+/-) mice.
Dobrovolsky VN; Shaddock JG; Heflich RH
Environ Mol Mutagen; 2002; 39(4):342-7. PubMed ID: 12112386
[TBL] [Abstract][Full Text] [Related]
36. Mechanisms for changing gene expression and their possible relationship to carcinogenesis.
Holliday R; Jeggo PA
Cancer Surv; 1985; 4(3):557-81. PubMed ID: 3916656
[TBL] [Abstract][Full Text] [Related]
37. Analysis of in vivo mutation in the hprt and tk genes of mouse lymphocytes.
Dobrovolsky VN; Shaddock JG; Heflich RH
Methods Mol Biol; 2005; 291():133-44. PubMed ID: 15502218
[TBL] [Abstract][Full Text] [Related]
38. Analysis of In Vivo Mutation in the Hprt and Tk Genes of Mouse Lymphocytes.
Dobrovolsky VN; Shaddock JG; Heflich RH
Methods Mol Biol; 2020; 2102():333-348. PubMed ID: 31989565
[TBL] [Abstract][Full Text] [Related]
39. The DNMT3B DNA methyltransferase gene is mutated in the ICF immunodeficiency syndrome.
Hansen RS; Wijmenga C; Luo P; Stanek AM; Canfield TK; Weemaes CM; Gartler SM
Proc Natl Acad Sci U S A; 1999 Dec; 96(25):14412-7. PubMed ID: 10588719
[TBL] [Abstract][Full Text] [Related]
40. Clonally derived cell lines with altered DNA methylation as models for error correction and mutation in tumours.
Diver WP; Woodcock DM
Mutagenesis; 1989 Nov; 4(6):462-6. PubMed ID: 2695760
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
