296 related articles for article (PubMed ID: 24832598)
21. 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]
22. RNA processing defects of the helicase gene RECQL4 in a compound heterozygous Rothmund-Thomson patient.
Beghini A; Castorina P; Roversi G; Modiano P; Larizza L
Am J Med Genet A; 2003 Jul; 120A(3):395-9. PubMed ID: 12838562
[TBL] [Abstract][Full Text] [Related]
23. Human RecQ Helicases in DNA Double-Strand Break Repair.
Lu H; Davis AJ
Front Cell Dev Biol; 2021; 9():640755. PubMed ID: 33718381
[TBL] [Abstract][Full Text] [Related]
24. Chromosome alignment maintenance requires the MAP RECQL4, mutated in the Rothmund-Thomson syndrome.
Yokoyama H; Moreno-Andres D; Astrinidis SA; Hao Y; Weberruss M; Schellhaus AK; Lue H; Haramoto Y; Gruss OJ; Antonin W
Life Sci Alliance; 2019 Feb; 2(1):. PubMed ID: 30718377
[TBL] [Abstract][Full Text] [Related]
25. 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]
26. Divergent cellular phenotypes of human and mouse cells lacking the Werner syndrome RecQ helicase.
Dhillon KK; Sidorova JM; Albertson TM; Anderson JB; Ladiges WC; Rabinovitch PS; Preston BD; Monnat RJ
DNA Repair (Amst); 2010 Jan; 9(1):11-22. PubMed ID: 19896421
[TBL] [Abstract][Full Text] [Related]
27. RECQL4 localizes to mitochondria and preserves mitochondrial DNA integrity.
Croteau DL; Rossi ML; Canugovi C; Tian J; Sykora P; Ramamoorthy M; Wang ZM; Singh DK; Akbari M; Kasiviswanathan R; Copeland WC; Bohr VA
Aging Cell; 2012 Jun; 11(3):456-66. PubMed ID: 22296597
[TBL] [Abstract][Full Text] [Related]
28. Rothmund-thomson syndrome responsible gene, RECQL4: genomic structure and products.
Kitao S; Lindor NM; Shiratori M; Furuichi Y; Shimamoto A
Genomics; 1999 Nov; 61(3):268-76. PubMed ID: 10552928
[TBL] [Abstract][Full Text] [Related]
29. Loss of p16(Ink4a) function rescues cellular senescence induced by telomere dysfunction.
Zhang X; Wu X; Tang W; Luo Y
Int J Mol Sci; 2012; 13(5):5866-5877. PubMed ID: 22754337
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndrome.
Kitao S; Shimamoto A; Goto M; Miller RW; Smithson WA; Lindor NM; Furuichi Y
Nat Genet; 1999 May; 22(1):82-4. PubMed ID: 10319867
[TBL] [Abstract][Full Text] [Related]
32. Homologous recombination and maintenance of genome integrity: cancer and aging through the prism of human RecQ helicases.
Ouyang KJ; Woo LL; Ellis NA
Mech Ageing Dev; 2008; 129(7-8):425-40. PubMed ID: 18430459
[TBL] [Abstract][Full Text] [Related]
33. ATM activation is impaired in human cells defective in RecQL4 helicase activity.
Park SY; Kim H; Im JS; Lee JK
Biochem Biophys Res Commun; 2019 Feb; 509(2):379-383. PubMed ID: 30594395
[TBL] [Abstract][Full Text] [Related]
34. 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]
35. RecQ family helicases in genome stability: lessons from gene disruption studies in DT40 cells.
Seki M; Otsuki M; Ishii Y; Tada S; Enomoto T
Cell Cycle; 2008 Aug; 7(16):2472-8. PubMed ID: 18719387
[TBL] [Abstract][Full Text] [Related]
36. Acrolein-exposed normal human lung fibroblasts in vitro: cellular senescence, enhanced telomere erosion, and degradation of Werner's syndrome protein.
Jang JH; Bruse S; Huneidi S; Schrader RM; Monick MM; Lin Y; Carter AB; Klingelhutz AJ; Nyunoya T
Environ Health Perspect; 2014 Sep; 122(9):955-62. PubMed ID: 24747221
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. Growth retardation and skin abnormalities of the Recql4-deficient mouse.
Hoki Y; Araki R; Fujimori A; Ohhata T; Koseki H; Fukumura R; Nakamura M; Takahashi H; Noda Y; Kito S; Abe M
Hum Mol Genet; 2003 Sep; 12(18):2293-9. PubMed ID: 12915449
[TBL] [Abstract][Full Text] [Related]
39. The human WRN and BLM RecQ helicases differentially regulate cell proliferation and survival after chemotherapeutic DNA damage.
Mao FJ; Sidorova JM; Lauper JM; Emond MJ; Monnat RJ
Cancer Res; 2010 Aug; 70(16):6548-55. PubMed ID: 20663905
[TBL] [Abstract][Full Text] [Related]
40. 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]
[Previous] [Next] [New Search]
