These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

320 related articles for article (PubMed ID: 28334952)

  • 1. DNMT1 mutations found in HSANIE patients affect interaction with UHRF1 and neuronal differentiation.
    Smets M; Link S; Wolf P; Schneider K; Solis V; Ryan J; Meilinger D; Qin W; Leonhardt H
    Hum Mol Genet; 2017 Apr; 26(8):1522-1534. PubMed ID: 28334952
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing loss.
    Klein CJ; Botuyan MV; Wu Y; Ward CJ; Nicholson GA; Hammans S; Hojo K; Yamanishi H; Karpf AR; Wallace DC; Simon M; Lander C; Boardman LA; Cunningham JM; Smith GE; Litchy WJ; Boes B; Atkinson EJ; Middha S; B Dyck PJ; Parisi JE; Mer G; Smith DI; Dyck PJ
    Nat Genet; 2011 Jun; 43(6):595-600. PubMed ID: 21532572
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The Ubiquitin-like with PHD and Ring Finger Domains 1 (UHRF1)/DNA Methyltransferase 1 (DNMT1) Axis Is a Primary Regulator of Cell Senescence.
    Jung HJ; Byun HO; Jee BA; Min S; Jeoun UW; Lee YK; Seo Y; Woo HG; Yoon G
    J Biol Chem; 2017 Mar; 292(9):3729-3739. PubMed ID: 28100769
    [TBL] [Abstract][Full Text] [Related]  

  • 5. S phase-dependent interaction with DNMT1 dictates the role of UHRF1 but not UHRF2 in DNA methylation maintenance.
    Zhang J; Gao Q; Li P; Liu X; Jia Y; Wu W; Li J; Dong S; Koseki H; Wong J
    Cell Res; 2011 Dec; 21(12):1723-39. PubMed ID: 22064703
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Defects of mutant DNMT1 are linked to a spectrum of neurological disorders.
    Baets J; Duan X; Wu Y; Smith G; Seeley WW; Mademan I; McGrath NM; Beadell NC; Khoury J; Botuyan MV; Mer G; Worrell GA; Hojo K; DeLeon J; Laura M; Liu YT; Senderek J; Weis J; Van den Bergh P; Merrill SL; Reilly MM; Houlden H; Grossman M; Scherer SS; De Jonghe P; Dyck PJ; Klein CJ
    Brain; 2015 Apr; 138(Pt 4):845-61. PubMed ID: 25678562
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The DNA methyltransferase Dnmt1 directly interacts with the SET and RING finger-associated (SRA) domain of the multifunctional protein Uhrf1 to facilitate accession of the catalytic center to hemi-methylated DNA.
    Berkyurek AC; Suetake I; Arita K; Takeshita K; Nakagawa A; Shirakawa M; Tajima S
    J Biol Chem; 2014 Jan; 289(1):379-86. PubMed ID: 24253042
    [TBL] [Abstract][Full Text] [Related]  

  • 8. DNA methylation requires a DNMT1 ubiquitin interacting motif (UIM) and histone ubiquitination.
    Qin W; Wolf P; Liu N; Link S; Smets M; La Mastra F; Forné I; Pichler G; Hörl D; Fellinger K; Spada F; Bonapace IM; Imhof A; Harz H; Leonhardt H
    Cell Res; 2015 Aug; 25(8):911-29. PubMed ID: 26065575
    [TBL] [Abstract][Full Text] [Related]  

  • 9. SET8 prevents excessive DNA methylation by methylation-mediated degradation of UHRF1 and DNMT1.
    Zhang H; Gao Q; Tan S; You J; Lyu C; Zhang Y; Han M; Chen Z; Li J; Wang H; Liao L; Qin J; Li J; Wong J
    Nucleic Acids Res; 2019 Sep; 47(17):9053-9068. PubMed ID: 31400111
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The UHRF1 protein stimulates the activity and specificity of the maintenance DNA methyltransferase DNMT1 by an allosteric mechanism.
    Bashtrykov P; Jankevicius G; Jurkowska RZ; Ragozin S; Jeltsch A
    J Biol Chem; 2014 Feb; 289(7):4106-15. PubMed ID: 24368767
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The USP7/Dnmt1 complex stimulates the DNA methylation activity of Dnmt1 and regulates the stability of UHRF1.
    Felle M; Joppien S; Németh A; Diermeier S; Thalhammer V; Dobner T; Kremmer E; Kappler R; Längst G
    Nucleic Acids Res; 2011 Oct; 39(19):8355-65. PubMed ID: 21745816
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Dual Functions of the RFTS Domain of Dnmt1 in Replication-Coupled DNA Methylation and in Protection of the Genome from Aberrant Methylation.
    Garvilles RG; Hasegawa T; Kimura H; Sharif J; Muto M; Koseki H; Takahashi S; Suetake I; Tajima S
    PLoS One; 2015; 10(9):e0137509. PubMed ID: 26383849
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Autosomal dominant cerebellar ataxia, deafness, and narcolepsy (ADCA-DN) associated with progressive cognitive and behavioral deterioration.
    Walker LA; Bourque P; Smith AM; Warman Chardon J
    Neuropsychology; 2017 Mar; 31(3):292-303. PubMed ID: 27869457
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Usp7 and Uhrf1 control ubiquitination and stability of the maintenance DNA methyltransferase Dnmt1.
    Qin W; Leonhardt H; Spada F
    J Cell Biochem; 2011 Feb; 112(2):439-44. PubMed ID: 21268065
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Enhanced processivity of Dnmt1 by monoubiquitinated histone H3.
    Mishima Y; Brueckner L; Takahashi S; Kawakami T; Otani J; Shinohara A; Takeshita K; Garvilles RG; Watanabe M; Sakai N; Takeshima H; Nachtegael C; Nishiyama A; Nakanishi M; Arita K; Nakashima K; Hojo H; Suetake I
    Genes Cells; 2020 Jan; 25(1):22-32. PubMed ID: 31680384
    [TBL] [Abstract][Full Text] [Related]  

  • 17. UHRF1 plays a role in maintaining DNA methylation in mammalian cells.
    Bostick M; Kim JK; Estève PO; Clark A; Pradhan S; Jacobsen SE
    Science; 2007 Sep; 317(5845):1760-4. PubMed ID: 17673620
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mutations in human DNA methyltransferase DNMT1 induce specific genome-wide epigenomic and transcriptomic changes in neurodevelopment.
    Davis KN; Qu PP; Ma S; Lin L; Plastini M; Dahl N; Plazzi G; Pizza F; O'Hara R; Wong WH; Hallmayer J; Mignot E; Zhang X; Urban AE
    Hum Mol Genet; 2023 Oct; 32(21):3105-3120. PubMed ID: 37584462
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy.
    Winkelmann J; Lin L; Schormair B; Kornum BR; Faraco J; Plazzi G; Melberg A; Cornelio F; Urban AE; Pizza F; Poli F; Grubert F; Wieland T; Graf E; Hallmayer J; Strom TM; Mignot E
    Hum Mol Genet; 2012 May; 21(10):2205-10. PubMed ID: 22328086
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Recruitment of Dnmt1 roles of the SRA protein Np95 (Uhrf1) and other factors.
    Sharif J; Koseki H
    Prog Mol Biol Transl Sci; 2011; 101():289-310. PubMed ID: 21507355
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.