312 related articles for article (PubMed ID: 16271439)
1. 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]
2. 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]
3. 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]
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. 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]
6. 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]
7. 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]
8. 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]
9. Identification of two novel RECQL4exonic SNPs and genomic characterization of the IVS12 minisatellite.
Roversi G; Beghini A; Zambruno G; Paradisi M; Larizza L
J Hum Genet; 2003; 48(2):107-9. PubMed ID: 12601557
[TBL] [Abstract][Full Text] [Related]
10. Initiation of DNA replication requires the RECQL4 protein mutated in Rothmund-Thomson syndrome.
Sangrithi MN; Bernal JA; Madine M; Philpott A; Lee J; Dunphy WG; Venkitaraman AR
Cell; 2005 Jun; 121(6):887-98. PubMed ID: 15960976
[TBL] [Abstract][Full Text] [Related]
11. The versatile RECQL4.
Kellermayer R
Genet Med; 2006 Apr; 8(4):213-6. PubMed ID: 16617241
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. 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]
15. Premature aging and predisposition to cancers caused by mutations in RecQ family helicases.
Furuichi Y
Ann N Y Acad Sci; 2001 Apr; 928():121-31. PubMed ID: 11795503
[TBL] [Abstract][Full Text] [Related]
16. The molecular role of the Rothmund-Thomson-, RAPADILINO- and Baller-Gerold-gene product, RECQL4: recent progress.
Dietschy T; Shevelev I; Stagljar I
Cell Mol Life Sci; 2007 Apr; 64(7-8):796-802. PubMed ID: 17364146
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Analysis of the DNA unwinding activity of RecQ family helicases.
Bachrati CZ; Hickson ID
Methods Enzymol; 2006; 409():86-100. PubMed ID: 16793396
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. DNA helicase deficiencies associated with cancer predisposition and premature ageing disorders.
Mohaghegh P; Hickson ID
Hum Mol Genet; 2001 Apr; 10(7):741-6. PubMed ID: 11257107
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
