BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

263 related articles for article (PubMed ID: 10552928)

  • 21. Homologous recombination is responsible for cell death in the absence of the Sgs1 and Srs2 helicases.
    Gangloff S; Soustelle C; Fabre F
    Nat Genet; 2000 Jun; 25(2):192-4. PubMed ID: 10835635
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Genomic organization of the JEM-1 (BLZF1) gene on human chromosome 1q24: molecular cloning and analysis of its promoter region.
    Tong JH; Fant X; Benoit G; Chen SJ; Chen Z; Lanotte M
    Genomics; 2000 Nov; 69(3):380-90. PubMed ID: 11056056
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Human RecQL4 helicase plays multifaceted roles in the genomic stability of normal and cancer cells.
    Mo D; Zhao Y; Balajee AS
    Cancer Lett; 2018 Jan; 413():1-10. PubMed ID: 29080750
    [TBL] [Abstract][Full Text] [Related]  

  • 24. p300-mediated acetylation of the Rothmund-Thomson-syndrome gene product RECQL4 regulates its subcellular localization.
    Dietschy T; Shevelev I; Pena-Diaz J; Hühn D; Kuenzle S; Mak R; Miah MF; Hess D; Fey M; Hottiger MO; Janscak P; Stagljar I
    J Cell Sci; 2009 Apr; 122(Pt 8):1258-67. PubMed ID: 19299466
    [TBL] [Abstract][Full Text] [Related]  

  • 25. The Rothmund-Thomson gene product RECQL4 localizes to the nucleolus in response to oxidative stress.
    Woo LL; Futami K; Shimamoto A; Furuichi Y; Frank KM
    Exp Cell Res; 2006 Oct; 312(17):3443-57. PubMed ID: 16949575
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Werner and Bloom helicases are involved in DNA repair in a complementary fashion.
    Imamura O; Fujita K; Itoh C; Takeda S; Furuichi Y; Matsumoto T
    Oncogene; 2002 Jan; 21(6):954-63. PubMed ID: 11840341
    [TBL] [Abstract][Full Text] [Related]  

  • 27. DNA helicases, genomic instability, and human genetic disease.
    van Brabant AJ; Stan R; Ellis NA
    Annu Rev Genomics Hum Genet; 2000; 1():409-59. PubMed ID: 11701636
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A recQ family DNA helicase gene from Aspergillus nidulans.
    Appleyard MV; McPheat WL; Stark MJ
    DNA Seq; 2000; 11(3-4):315-9. PubMed ID: 11092746
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Rothmund-Thomson syndrome, trisomy 8 mosaicism and RECQ4 gene mutation].
    Durand F; Castorina P; Morant C; Delobel B; Barouk E; Modiano P
    Ann Dermatol Venereol; 2002; 129(6-7):892-5. PubMed ID: 12218919
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Cloning of two new human helicase genes of the RecQ family: biological significance of multiple species in higher eukaryotes.
    Kitao S; Ohsugi I; Ichikawa K; Goto M; Furuichi Y; Shimamoto A
    Genomics; 1998 Dec; 54(3):443-52. PubMed ID: 9878247
    [TBL] [Abstract][Full Text] [Related]  

  • 31. RecQL4: a helicase linking formation and maintenance of a replication fork.
    Masai H
    J Biochem; 2011 Jun; 149(6):629-31. PubMed ID: 21436139
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Preparation of the gene targeted knockout mice for human premature aging diseases, Werner syndrome, and Rothmund-Thomson syndrome caused by the mutation of DNA helicases].
    Ichikawa K; Noda T; Furuichi Y
    Nihon Yakurigaku Zasshi; 2002 Apr; 119(4):219-26. PubMed ID: 11979727
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Human RecQL4 as a Novel Molecular Target for Cancer Therapy.
    Balajee AS
    Cytogenet Genome Res; 2021; 161(6-7):305-327. PubMed ID: 34474412
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Sensitivity of RECQL4-deficient fibroblasts from Rothmund-Thomson syndrome patients to genotoxic agents.
    Jin W; Liu H; Zhang Y; Otta SK; Plon SE; Wang LL
    Hum Genet; 2008 Jul; 123(6):643-53. PubMed ID: 18504617
    [TBL] [Abstract][Full Text] [Related]  

  • 35. RECQL4 is essential for the transport of p53 to mitochondria in normal human cells in the absence of exogenous stress.
    De S; Kumari J; Mudgal R; Modi P; Gupta S; Futami K; Goto H; Lindor NM; Furuichi Y; Mohanty D; Sengupta S
    J Cell Sci; 2012 May; 125(Pt 10):2509-22. PubMed ID: 22357944
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Aging in Rothmund-Thomson syndrome and related RECQL4 genetic disorders.
    Lu L; Jin W; Wang LL
    Ageing Res Rev; 2017 Jan; 33():30-35. PubMed ID: 27287744
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Structural and functional characterizations of the 5'-flanking region of the mouse glucagon receptor gene: comparison with the rat gene.
    Geiger A; Decaux JF; Burcelin R; Le Cam A; Salazar G; Charron MJ; Girard J; Kervran A
    Biochem Biophys Res Commun; 2000 Jun; 272(3):912-21. PubMed ID: 10860851
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Genomic organization and expression of the mouse equilibrative, nitrobenzylthioinosine-sensitive nucleoside transporter 1 (ENT1) gene.
    Choi DS; Handa M; Young H; Gordon AS; Diamond I; Messing RO
    Biochem Biophys Res Commun; 2000 Oct; 277(1):200-8. PubMed ID: 11027664
    [TBL] [Abstract][Full Text] [Related]  

  • 39. The Rb/E2F pathway and Ras activation regulate RecQ helicase gene expression.
    Liu Y; El-Naggar S; Clem B; Chesney J; Dean DC
    Biochem J; 2008 Jun; 412(2):299-306. PubMed ID: 18215118
    [TBL] [Abstract][Full Text] [Related]  

  • 40. The versatile RECQL4.
    Kellermayer R
    Genet Med; 2006 Apr; 8(4):213-6. PubMed ID: 16617241
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 14.