603 related articles for article (PubMed ID: 31485078)
41. DNMT3L modulates significant and distinct flanking sequence preference for DNA methylation by DNMT3A and DNMT3B in vivo.
Wienholz BL; Kareta MS; Moarefi AH; Gordon CA; Ginno PA; Chédin F
PLoS Genet; 2010 Sep; 6(9):e1001106. PubMed ID: 20838592
[TBL] [Abstract][Full Text] [Related]
42. Base editor scanning charts the DNMT3A activity landscape.
Lue NZ; Garcia EM; Ngan KC; Lee C; Doench JG; Liau BB
Nat Chem Biol; 2023 Feb; 19(2):176-186. PubMed ID: 36266353
[TBL] [Abstract][Full Text] [Related]
43. Murine de novo methyltransferase Dnmt3a demonstrates strand asymmetry and site preference in the methylation of DNA in vitro.
Lin IG; Han L; Taghva A; O'Brien LE; Hsieh CL
Mol Cell Biol; 2002 Feb; 22(3):704-23. PubMed ID: 11784849
[TBL] [Abstract][Full Text] [Related]
44. Further delineation of neuropsychiatric findings in Tatton-Brown-Rahman syndrome due to disease-causing variants in DNMT3A: seven new patients.
Tenorio J; Alarcón P; Arias P; Dapía I; García-Miñaur S; Palomares Bralo M; Campistol J; Climent S; Valenzuela I; Ramos S; Monseny AM; Grondona FL; Botet J; Serrano M; Solís M; Santos-Simarro F; Álvarez S; Teixidó-Tura G; Fernández Jaén A; Gordo G; Bardón Rivera MB; Nevado J; Hernández A; Cigudosa JC; Ruiz-Pérez VL; Tizzano EF; ; Lapunzina P
Eur J Hum Genet; 2020 Apr; 28(4):469-479. PubMed ID: 31685998
[TBL] [Abstract][Full Text] [Related]
45. NSD1 PHD domains bind methylated H3K4 and H3K9 using interactions disrupted by point mutations in human sotos syndrome.
Pasillas MP; Shah M; Kamps MP
Hum Mutat; 2011 Mar; 32(3):292-8. PubMed ID: 21972110
[TBL] [Abstract][Full Text] [Related]
46. Interplay between Histone and DNA Methylation Seen through Comparative Methylomes in Rare Mendelian Disorders.
Velasco G; Ulveling D; Rondeau S; Marzin P; Unoki M; Cormier-Daire V; Francastel C
Int J Mol Sci; 2021 Apr; 22(7):. PubMed ID: 33916664
[TBL] [Abstract][Full Text] [Related]
47. Targeting of EZH2 to a defined genomic site is sufficient for recruitment of Dnmt3a but not de novo DNA methylation.
Rush M; Appanah R; Lee S; Lam LL; Goyal P; Lorincz MC
Epigenetics; 2009 Aug; 4(6):404-14. PubMed ID: 19717977
[TBL] [Abstract][Full Text] [Related]
48. Cooperativity between DNA methyltransferases in the maintenance methylation of repetitive elements.
Liang G; Chan MF; Tomigahara Y; Tsai YC; Gonzales FA; Li E; Laird PW; Jones PA
Mol Cell Biol; 2002 Jan; 22(2):480-91. PubMed ID: 11756544
[TBL] [Abstract][Full Text] [Related]
49. Structural basis for recognition of H3K4 methylation status by the DNA methyltransferase 3A ATRX-DNMT3-DNMT3L domain.
Otani J; Nankumo T; Arita K; Inamoto S; Ariyoshi M; Shirakawa M
EMBO Rep; 2009 Nov; 10(11):1235-41. PubMed ID: 19834512
[TBL] [Abstract][Full Text] [Related]
50. Molecular coupling of DNA methylation and histone methylation.
Hashimoto H; Vertino PM; Cheng X
Epigenomics; 2010 Oct; 2(5):657-69. PubMed ID: 21339843
[TBL] [Abstract][Full Text] [Related]
51. Genome-wide DNA Methylation Signatures Are Determined by DNMT3A/B Sequence Preferences.
Mao SQ; Cuesta SM; Tannahill D; Balasubramanian S
Biochemistry; 2020 Jul; 59(27):2541-2550. PubMed ID: 32543182
[TBL] [Abstract][Full Text] [Related]
52. Constitutive loss of DNMT3A causes morbid obesity through misregulation of adipogenesis.
Tovy A; Reyes JM; Zhang L; Huang YH; Rosas C; Daquinag AC; Guzman A; Ramabadran R; Chen CW; Gu T; Gupta S; Ortinau L; Park D; Cox AR; Rau RE; Hartig SM; Kolonin MG; Goodell MA
Elife; 2022 May; 11():. PubMed ID: 35635747
[TBL] [Abstract][Full Text] [Related]
53. Establishment and maintenance of genomic methylation patterns in mouse embryonic stem cells by Dnmt3a and Dnmt3b.
Chen T; Ueda Y; Dodge JE; Wang Z; Li E
Mol Cell Biol; 2003 Aug; 23(16):5594-605. PubMed ID: 12897133
[TBL] [Abstract][Full Text] [Related]
54. Tatton-Brown-Rahman syndrome due to 2p23 microdeletion.
Okamoto N; Toribe Y; Shimojima K; Yamamoto T
Am J Med Genet A; 2016 May; 170A(5):1339-42. PubMed ID: 26866722
[TBL] [Abstract][Full Text] [Related]
55. Interactions between core histone marks and DNA methyltransferases predict DNA methylation patterns observed in human cells and tissues.
Fu K; Bonora G; Pellegrini M
Epigenetics; 2020 Mar; 15(3):272-282. PubMed ID: 31509087
[TBL] [Abstract][Full Text] [Related]
56. Depletion of H3K36me2 recapitulates epigenomic and phenotypic changes induced by the H3.3K36M oncohistone mutation.
Rajagopalan KN; Chen X; Weinberg DN; Chen H; Majewski J; Allis CD; Lu C
Proc Natl Acad Sci U S A; 2021 Mar; 118(9):. PubMed ID: 33619101
[TBL] [Abstract][Full Text] [Related]
57. A role for LSH in facilitating DNA methylation by DNMT1 through enhancing UHRF1 chromatin association.
Han M; Li J; Cao Y; Huang Y; Li W; Zhu H; Zhao Q; Han JJ; Wu Q; Li J; Feng J; Wong J
Nucleic Acids Res; 2020 Dec; 48(21):12116-12134. PubMed ID: 33170271
[TBL] [Abstract][Full Text] [Related]
58. Aberrant signature methylome by DNMT1 hot spot mutation in hereditary sensory and autonomic neuropathy 1E.
Sun Z; Wu Y; Ordog T; Baheti S; Nie J; Duan X; Hojo K; Kocher JP; Dyck PJ; Klein CJ
Epigenetics; 2014 Aug; 9(8):1184-93. PubMed ID: 25033457
[TBL] [Abstract][Full Text] [Related]
59. NSD1 mutations deregulate transcription and DNA methylation of bivalent developmental genes in Sotos syndrome.
Brennan K; Zheng H; Fahrner JA; Shin JH; Gentles AJ; Schaefer B; Sunwoo JB; Bernstein JA; Gevaert O
Hum Mol Genet; 2022 Jul; 31(13):2164-2184. PubMed ID: 35094088
[TBL] [Abstract][Full Text] [Related]
60. Relationship between gene body DNA methylation and intragenic H3K9me3 and H3K36me3 chromatin marks.
Hahn MA; Wu X; Li AX; Hahn T; Pfeifer GP
PLoS One; 2011 Apr; 6(4):e18844. PubMed ID: 21526191
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]