167 related articles for article (PubMed ID: 16949575)
1. 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]
2. 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]
3. 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]
4. 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]
5. Nuclear import and retention domains in the amino terminus of RECQL4.
Burks LM; Yin J; Plon SE
Gene; 2007 Apr; 391(1-2):26-38. PubMed ID: 17250975
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. RECQL4-deficient cells are hypersensitive to oxidative stress/damage: Insights for osteosarcoma prevalence and heterogeneity in Rothmund-Thomson syndrome.
Werner SR; Prahalad AK; Yang J; Hock JM
Biochem Biophys Res Commun; 2006 Jun; 345(1):403-9. PubMed ID: 16678792
[TBL] [Abstract][Full Text] [Related]
8. Molecular defect of RAPADILINO syndrome expands the phenotype spectrum of RECQL diseases.
Siitonen HA; Kopra O; Kääriäinen H; Haravuori H; Winter RM; Säämänen AM; Peltonen L; Kestilä M
Hum Mol Genet; 2003 Nov; 12(21):2837-44. PubMed ID: 12952869
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. Rothmund-Thomson syndrome and RECQL4 defect: splitting and lumping.
Larizza L; Magnani I; Roversi G
Cancer Lett; 2006 Jan; 232(1):107-20. PubMed ID: 16271439
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. 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]
15. Cooperation of the Cockayne syndrome group B protein and poly(ADP-ribose) polymerase 1 in the response to oxidative stress.
Thorslund T; von Kobbe C; Harrigan JA; Indig FE; Christiansen M; Stevnsner T; Bohr VA
Mol Cell Biol; 2005 Sep; 25(17):7625-36. PubMed ID: 16107709
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Cloning, genomic structure and chromosomal localization of the gene encoding mouse DNA helicase RecQ helicase protein-like 4.
Ohhata T; Araki R; Fukumura R; Kuroiwa A; Matsuda Y; Tatsumi K; Abe M
Gene; 2000 Dec; 261(2):251-8. PubMed ID: 11167012
[TBL] [Abstract][Full Text] [Related]
18. Defective sister-chromatid cohesion, aneuploidy and cancer predisposition in a mouse model of type II Rothmund-Thomson syndrome.
Mann MB; Hodges CA; Barnes E; Vogel H; Hassold TJ; Luo G
Hum Mol Genet; 2005 Mar; 14(6):813-25. PubMed ID: 15703196
[TBL] [Abstract][Full Text] [Related]
19. Poly(ADP-ribose) polymerase 1 regulates both the exonuclease and helicase activities of the Werner syndrome protein.
von Kobbe C; Harrigan JA; Schreiber V; Stiegler P; Piotrowski J; Dawut L; Bohr VA
Nucleic Acids Res; 2004; 32(13):4003-14. PubMed ID: 15292449
[TBL] [Abstract][Full Text] [Related]
20. Identification of new RECQL4 mutations in Caucasian Rothmund-Thomson patients and analysis of sensitivity to a wide range of genotoxic agents.
Cabral RE; Queille S; Bodemer C; de Prost Y; Neto JB; Sarasin A; Daya-Grosjean L
Mutat Res; 2008 Aug; 643(1-2):41-7. PubMed ID: 18616953
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]