226 related articles for article (PubMed ID: 38291337)
1. DNMT3B PWWP mutations cause hypermethylation of heterochromatin.
Taglini F; Kafetzopoulos I; Rolls W; Musialik KI; Lee HY; Zhang Y; Marenda M; Kerr L; Finan H; Rubio-Ramon C; Gautier P; Wapenaar H; Kumar D; Davidson-Smith H; Wills J; Murphy LC; Wheeler A; Wilson MD; Sproul D
EMBO Rep; 2024 Mar; 25(3):1130-1155. PubMed ID: 38291337
[TBL] [Abstract][Full Text] [Related]
2. The PWWP domain of Dnmt3a and Dnmt3b is required for directing DNA methylation to the major satellite repeats at pericentric heterochromatin.
Chen T; Tsujimoto N; Li E
Mol Cell Biol; 2004 Oct; 24(20):9048-58. PubMed ID: 15456878
[TBL] [Abstract][Full Text] [Related]
3. Structural basis for recognition of histone H3K36me3 nucleosome by human de novo DNA methyltransferases 3A and 3B.
Rondelet G; Dal Maso T; Willems L; Wouters J
J Struct Biol; 2016 Jun; 194(3):357-67. PubMed ID: 26993463
[TBL] [Abstract][Full Text] [Related]
4. Chromatin targeting of de novo DNA methyltransferases by the PWWP domain.
Ge YZ; Pu MT; Gowher H; Wu HP; Ding JP; Jeltsch A; Xu GL
J Biol Chem; 2004 Jun; 279(24):25447-54. PubMed ID: 14998998
[TBL] [Abstract][Full Text] [Related]
5. Dnmt3a and Dnmt3b are transcriptional repressors that exhibit unique localization properties to heterochromatin.
Bachman KE; Rountree MR; Baylin SB
J Biol Chem; 2001 Aug; 276(34):32282-7. PubMed ID: 11427539
[TBL] [Abstract][Full Text] [Related]
6. DNMT3B Functions: Novel Insights From Human Disease.
Gagliardi M; Strazzullo M; Matarazzo MR
Front Cell Dev Biol; 2018; 6():140. PubMed ID: 30406101
[TBL] [Abstract][Full Text] [Related]
7. Mutations in DNA methyltransferase DNMT3B in ICF syndrome affect its regulation by DNMT3L.
Xie ZH; Huang YN; Chen ZX; Riggs AD; Ding JP; Gowher H; Jeltsch A; Sasaki H; Hata K; Xu GL
Hum Mol Genet; 2006 May; 15(9):1375-85. PubMed ID: 16543361
[TBL] [Abstract][Full Text] [Related]
8. Structure of DNMT3B homo-oligomer reveals vulnerability to impairment by ICF mutations.
Gao L; Guo Y; Biswal M; Lu J; Yin J; Fang J; Chen X; Shao Z; Huang M; Wang Y; Wang GG; Song J
Nat Commun; 2022 Jul; 13(1):4249. PubMed ID: 35869095
[TBL] [Abstract][Full Text] [Related]
9. Structural basis for the allosteric regulation and dynamic assembly of DNMT3B.
Lu J; Fang J; Zhu H; Liang KL; Khudaverdyan N; Song J
Nucleic Acids Res; 2023 Dec; 51(22):12476-12491. PubMed ID: 37941146
[TBL] [Abstract][Full Text] [Related]
10. DNA methyltransferases Dnmt3a and Dnmt3b are essential for de novo methylation and mammalian development.
Okano M; Bell DW; Haber DA; Li E
Cell; 1999 Oct; 99(3):247-57. PubMed ID: 10555141
[TBL] [Abstract][Full Text] [Related]
11. The Dnmt3a PWWP domain reads histone 3 lysine 36 trimethylation and guides DNA methylation.
Dhayalan A; Rajavelu A; Rathert P; Tamas R; Jurkowska RZ; Ragozin S; Jeltsch A
J Biol Chem; 2010 Aug; 285(34):26114-20. PubMed ID: 20547484
[TBL] [Abstract][Full Text] [Related]
12. Genomic profiling of DNA methyltransferases reveals a role for DNMT3B in genic methylation.
Baubec T; Colombo DF; Wirbelauer C; Schmidt J; Burger L; Krebs AR; Akalin A; Schübeler D
Nature; 2015 Apr; 520(7546):243-7. PubMed ID: 25607372
[TBL] [Abstract][Full Text] [Related]
13. Two competing mechanisms of DNMT3A recruitment regulate the dynamics of de novo DNA methylation at PRC1-targeted CpG islands.
Weinberg DN; Rosenbaum P; Chen X; Barrows D; Horth C; Marunde MR; Popova IK; Gillespie ZB; Keogh MC; Lu C; Majewski J; Allis CD
Nat Genet; 2021 Jun; 53(6):794-800. PubMed ID: 33986537
[TBL] [Abstract][Full Text] [Related]
14. Three novel DNMT3B mutations in Japanese patients with ICF syndrome.
Shirohzu H; Kubota T; Kumazawa A; Sado T; Chijiwa T; Inagaki K; Suetake I; Tajima S; Wakui K; Miki Y; Hayashi M; Fukushima Y; Sasaki H
Am J Med Genet; 2002 Sep; 112(1):31-7. PubMed ID: 12239717
[TBL] [Abstract][Full Text] [Related]
15. DNA methyltransferase 3B (DNMT3B) mutations in ICF syndrome lead to altered epigenetic modifications and aberrant expression of genes regulating development, neurogenesis and immune function.
Jin B; Tao Q; Peng J; Soo HM; Wu W; Ying J; Fields CR; Delmas AL; Liu X; Qiu J; Robertson KD
Hum Mol Genet; 2008 Mar; 17(5):690-709. PubMed ID: 18029387
[TBL] [Abstract][Full Text] [Related]
16. Molecular enzymology of the catalytic domains of the Dnmt3a and Dnmt3b DNA methyltransferases.
Gowher H; Jeltsch A
J Biol Chem; 2002 Jun; 277(23):20409-14. PubMed ID: 11919202
[TBL] [Abstract][Full Text] [Related]
17. ICF1-Syndrome-Associated
Verma A; Poondi Krishnan V; Cecere F; D'Angelo E; Lullo V; Strazzullo M; Selig S; Angelini C; Matarazzo MR; Riccio A
Biomolecules; 2023 Nov; 13(12):. PubMed ID: 38136588
[TBL] [Abstract][Full Text] [Related]
18. A DNMT3A PWWP mutation leads to methylation of bivalent chromatin and growth retardation in mice.
Sendžikaitė G; Hanna CW; Stewart-Morgan KR; Ivanova E; Kelsey G
Nat Commun; 2019 Apr; 10(1):1884. PubMed ID: 31015495
[TBL] [Abstract][Full Text] [Related]
19. DNA replication is altered in Immunodeficiency Centromeric instability Facial anomalies (ICF) cells carrying DNMT3B mutations.
Lana E; Mégarbané A; Tourrière H; Sarda P; Lefranc G; Claustres M; De Sario A
Eur J Hum Genet; 2012 Oct; 20(10):1044-50. PubMed ID: 22378288
[TBL] [Abstract][Full Text] [Related]
20. Domain Structure of the Dnmt1, Dnmt3a, and Dnmt3b DNA Methyltransferases.
Tajima S; Suetake I; Takeshita K; Nakagawa A; Kimura H; Song J
Adv Exp Med Biol; 2022; 1389():45-68. PubMed ID: 36350506
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
