BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

307 related articles for article (PubMed ID: 18616953)

  • 21. 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]  

  • 22. Association between osteosarcoma and deleterious mutations in the RECQL4 gene in Rothmund-Thomson syndrome.
    Wang LL; Gannavarapu A; Kozinetz CA; Levy ML; Lewis RA; Chintagumpala MM; Ruiz-Maldanado R; Contreras-Ruiz J; Cunniff C; Erickson RP; Lev D; Rogers M; Zackai EH; Plon SE
    J Natl Cancer Inst; 2003 May; 95(9):669-74. PubMed ID: 12734318
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. RECQ DNA Helicases and Osteosarcoma.
    Lu L; Jin W; Wang LL
    Adv Exp Med Biol; 2020; 1258():37-54. PubMed ID: 32767233
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. RECQL4, mutated in the Rothmund-Thomson and RAPADILINO syndromes, interacts with ubiquitin ligases UBR1 and UBR2 of the N-end rule pathway.
    Yin J; Kwon YT; Varshavsky A; Wang W
    Hum Mol Genet; 2004 Oct; 13(20):2421-30. PubMed ID: 15317757
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Novel pathogenic RECQL4 variants in Chinese patients with Rothmund-Thomson syndrome.
    Gui B; Song Y; Hu X; Li H; Qin Z; Su J; Li C; Fan X; Li M; Luo J; Feng Y; Song L; Chen S; Gong C; Shen Y
    Gene; 2018 May; 654():110-115. PubMed ID: 29462647
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Direct and indirect roles of RECQL4 in modulating base excision repair capacity.
    Schurman SH; Hedayati M; Wang Z; Singh DK; Speina E; Zhang Y; Becker K; Macris M; Sung P; Wilson DM; Croteau DL; Bohr VA
    Hum Mol Genet; 2009 Sep; 18(18):3470-83. PubMed ID: 19567405
    [TBL] [Abstract][Full Text] [Related]  

  • 29. The Rothmund-Thomson syndrome helicase RECQL4 is essential for hematopoiesis.
    Smeets MF; DeLuca E; Wall M; Quach JM; Chalk AM; Deans AJ; Heierhorst J; Purton LE; Izon DJ; Walkley CR
    J Clin Invest; 2014 Aug; 124(8):3551-65. PubMed ID: 24960165
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Rothmund-Thomson syndrome (RTS) with osteosarcoma due to
    Salih A; Inoue S; Onwuzurike N
    BMJ Case Rep; 2018 Jan; 2018():. PubMed ID: 29367366
    [TBL] [Abstract][Full Text] [Related]  

  • 31. The N-terminal region of RECQL4 lacking the helicase domain is both essential and sufficient for the viability of vertebrate cells. Role of the N-terminal region of RECQL4 in cells.
    Abe T; Yoshimura A; Hosono Y; Tada S; Seki M; Enomoto T
    Biochim Biophys Acta; 2011 Mar; 1813(3):473-9. PubMed ID: 21256165
    [TBL] [Abstract][Full Text] [Related]  

  • 32. The human Rothmund-Thomson syndrome gene product, RECQL4, localizes to distinct nuclear foci that coincide with proteins involved in the maintenance of genome stability.
    Petkovic M; Dietschy T; Freire R; Jiao R; Stagljar I
    J Cell Sci; 2005 Sep; 118(Pt 18):4261-9. PubMed ID: 16141230
    [TBL] [Abstract][Full Text] [Related]  

  • 33. RECQL4, the protein mutated in Rothmund-Thomson syndrome, functions in telomere maintenance.
    Ghosh AK; Rossi ML; Singh DK; Dunn C; Ramamoorthy M; Croteau DL; Liu Y; Bohr VA
    J Biol Chem; 2012 Jan; 287(1):196-209. PubMed ID: 22039056
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [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]  

  • 35. The involvement of human RECQL4 in DNA double-strand break repair.
    Singh DK; Karmakar P; Aamann M; Schurman SH; May A; Croteau DL; Burks L; Plon SE; Bohr VA
    Aging Cell; 2010 Jun; 9(3):358-71. PubMed ID: 20222902
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Search for ReCQL4 mutations in 39 patients genotyped for suspected Rothmund-Thomson/Baller-Gerold syndromes.
    Piard J; Aral B; Vabres P; Holder-Espinasse M; Mégarbané A; Gauthier S; Capra V; Pierquin G; Callier P; Baumann C; Pasquier L; Baujat G; Martorell L; Rodriguez A; Brady AF; Boralevi F; González-Enseñat MA; Rio M; Bodemer C; Philip N; Cordier MP; Goldenberg A; Demeer B; Wright M; Blair E; Puzenat E; Parent P; Sznajer Y; Francannet C; DiDonato N; Boute O; Barlogis V; Moldovan O; Bessis D; Coubes C; Tardieu M; Cormier-Daire V; Sousa AB; Franques J; Toutain A; Tajir M; Elalaoui SC; Geneviève D; Thevenon J; Courcet JB; Rivière JB; Collet C; Gigot N; Faivre L; Thauvin-Robinet C
    Clin Genet; 2015 Mar; 87(3):244-51. PubMed ID: 24635570
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Bloom's syndrome: Why not premature aging?: A comparison of the BLM and WRN helicases.
    de Renty C; Ellis NA
    Ageing Res Rev; 2017 Jan; 33():36-51. PubMed ID: 27238185
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Atypical Rothmund-Thomson syndrome in a patient with compound heterozygous mutations in RECQL4 gene and phenotypic features in RECQL4 syndromes.
    Sznajer Y; Siitonen HA; Roversi G; Dangoisse C; Scaillon M; Ziereisen F; Tenoutasse S; Kestilä M; Larizza L
    Eur J Pediatr; 2008 Feb; 167(2):175-81. PubMed ID: 17372760
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Biochemical characterization of the RECQ4 protein, mutated in Rothmund-Thomson syndrome.
    Macris MA; Krejci L; Bussen W; Shimamoto A; Sung P
    DNA Repair (Amst); 2006 Feb; 5(2):172-80. PubMed ID: 16214424
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 16.