BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

358 related articles for article (PubMed ID: 33959385)

  • 1. CTCF As an Example of DNA-Binding Transcription Factors Containing Clusters of C2H2-Type Zinc Fingers.
    Maksimenko OG; Fursenko DV; Belova EV; Georgiev PG
    Acta Naturae; 2021; 13(1):31-46. PubMed ID: 33959385
    [TBL] [Abstract][Full Text] [Related]  

  • 2. C2H2 Zinc Finger Proteins: The Largest but Poorly Explored Family of Higher Eukaryotic Transcription Factors.
    Fedotova AA; Bonchuk AN; Mogila VA; Georgiev PG
    Acta Naturae; 2017; 9(2):47-58. PubMed ID: 28740726
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The N-terminal dimerization domains of human and Drosophila CTCF have similar functionality.
    Kamalyan S; Kyrchanova O; Klimenko N; Babosha V; Vasileva Y; Belova E; Fursenko D; Maksimenko O; Georgiev P
    Epigenetics Chromatin; 2024 Apr; 17(1):9. PubMed ID: 38561749
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The insulator functions of the
    Kyrchanova O; Maksimenko O; Ibragimov A; Sokolov V; Postika N; Lukyanova M; Schedl P; Georgiev P
    Sci Adv; 2020 Mar; 6(13):eaaz3152. PubMed ID: 32232161
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Study of the N-Terminal Domain Homodimerization in Human Proteins with Zinc Finger Clusters.
    Fursenko DV; Georgiev PG; Bonchuk AN
    Dokl Biochem Biophys; 2021 Jul; 499(1):257-259. PubMed ID: 34426923
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Demarcation of Topologically Associating Domains Is Uncoupled from Enriched CTCF Binding in Developing Zebrafish.
    Pérez-Rico YA; Barillot E; Shkumatava A
    iScience; 2020 May; 23(5):101046. PubMed ID: 32334414
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mechanisms of enhancer-promoter communication and chromosomal architecture in mammals and
    Kyrchanova OV; Bylino OV; Georgiev PG
    Front Genet; 2022; 13():1081088. PubMed ID: 36531247
    [TBL] [Abstract][Full Text] [Related]  

  • 8. C2H2 proteins: Evolutionary aspects of domain architecture and diversification.
    Bonchuk AN; Georgiev PG
    Bioessays; 2024 Jun; ():e2400052. PubMed ID: 38873893
    [TBL] [Abstract][Full Text] [Related]  

  • 9. CTCF, a conserved nuclear factor required for optimal transcriptional activity of the chicken c-myc gene, is an 11-Zn-finger protein differentially expressed in multiple forms.
    Klenova EM; Nicolas RH; Paterson HF; Carne AF; Heath CM; Goodwin GH; Neiman PE; Lobanenkov VV
    Mol Cell Biol; 1993 Dec; 13(12):7612-24. PubMed ID: 8246978
    [TBL] [Abstract][Full Text] [Related]  

  • 10. An exceptionally conserved transcriptional repressor, CTCF, employs different combinations of zinc fingers to bind diverged promoter sequences of avian and mammalian c-myc oncogenes.
    Filippova GN; Fagerlie S; Klenova EM; Myers C; Dehner Y; Goodwin G; Neiman PE; Collins SJ; Lobanenkov VV
    Mol Cell Biol; 1996 Jun; 16(6):2802-13. PubMed ID: 8649389
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Small Drosophila zinc finger C2H2 protein with an N-terminal zinc finger-associated domain demonstrates the architecture functions.
    Maksimenko O; Kyrchanova O; Klimenko N; Zolotarev N; Elizarova A; Bonchuk A; Georgiev P
    Biochim Biophys Acta Gene Regul Mech; 2020 Jan; 1863(1):194446. PubMed ID: 31706027
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Three classes of C2H2 zinc finger proteins.
    Iuchi S
    Cell Mol Life Sci; 2001 Apr; 58(4):625-35. PubMed ID: 11361095
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Evolution of C2H2-zinc finger genes and subfamilies in mammals: species-specific duplication and loss of clusters, genes and effector domains.
    Tadepally HD; Burger G; Aubry M
    BMC Evol Biol; 2008 Jun; 8():176. PubMed ID: 18559114
    [TBL] [Abstract][Full Text] [Related]  

  • 14. N-terminal domain of the architectural protein CTCF has similar structural organization and ability to self-association in bilaterian organisms.
    Bonchuk A; Kamalyan S; Mariasina S; Boyko K; Popov V; Maksimenko O; Georgiev P
    Sci Rep; 2020 Feb; 10(1):2677. PubMed ID: 32060375
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Multiple CTCF sites cooperate with each other to maintain a TAD for enhancer-promoter interaction in the β-globin locus.
    Kang J; Kim YW; Park S; Kang Y; Kim A
    FASEB J; 2021 Aug; 35(8):e21768. PubMed ID: 34245617
    [TBL] [Abstract][Full Text] [Related]  

  • 16. On the prediction of DNA-binding preferences of C2H2-ZF domains using structural models: application on human CTCF.
    Meseguer A; Årman F; Fornes O; Molina-Fernández R; Bonet J; Fernandez-Fuentes N; Oliva B
    NAR Genom Bioinform; 2020 Sep; 2(3):lqaa046. PubMed ID: 33575598
    [TBL] [Abstract][Full Text] [Related]  

  • 17. CTCF modulates allele-specific sub-TAD organization and imprinted gene activity at the mouse Dlk1-Dio3 and Igf2-H19 domains.
    Llères D; Moindrot B; Pathak R; Piras V; Matelot M; Pignard B; Marchand A; Poncelet M; Perrin A; Tellier V; Feil R; Noordermeer D
    Genome Biol; 2019 Dec; 20(1):272. PubMed ID: 31831055
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Variations of the C2H2 zinc finger motif in the yeast genome and classification of yeast zinc finger proteins.
    Böhm S; Frishman D; Mewes HW
    Nucleic Acids Res; 1997 Jun; 25(12):2464-9. PubMed ID: 9171100
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Vertebrate Protein CTCF and its Multiple Roles in a Large-Scale Regulation of Genome Activity.
    Nikolaev LG; Akopov SB; Didych DA; Sverdlov ED
    Curr Genomics; 2009 Aug; 10(5):294-302. PubMed ID: 20119526
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Drosophila architectural protein CTCF is not essential for fly survival and is able to function independently of CP190.
    Kyrchanova O; Klimenko N; Postika N; Bonchuk A; Zolotarev N; Maksimenko O; Georgiev P
    Biochim Biophys Acta Gene Regul Mech; 2021 Oct; 1864(10):194733. PubMed ID: 34311130
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 18.