| 1. |
Vannier JB, Sarek G, Boulton SJ. RTEL1:functions of adisease-associated helicase[J].Trends Cell Biol, 2014, 24(7):416-425.
|
| 2. |
Zhu L, Hathcock KS, Hande P, et al. Telomere length regulation in mice is linked to a novelchromosome locus[J].Proc Natl Acad Sci USA, 1998, 95(15):8648-8653.
|
| 3. |
Bochman ML, Paeschke K, Zakian VA, et al. DNA secondary structures:stability andfunction of G-quadruplex structures[J].Nat Rev Genet, 2012, 13(11):770-780.
|
| 4. |
Vannier JB, Pavicic-Kaltenbrunner V, Petalcorin MI, et al. RTEL1 dismantles T loops and counteracts telomeric G4-DNA to maintain telomere integrity[J].Cell, 2012, 149(4):795-806.
|
| 5. |
Griffith JD, Comeau L, Rosenfield S, et al. Mammalian telomeres end in a large duplexloop[J].Cell, 1999, 97(4):503-514.
|
| 6. |
Wang RC, Smogorzewska A, De Lange T. Homologous recombination generates T-loop-sized deletions at human telomeres[J].Cell, 2004, 119(3):355-368.
|
| 7. |
Ogawa T, Yu X, Shinohara A, et al. Similarity of the yeast rad51 filament to the bacterial reca filament[J].Science, 1993, 259(513):1896-1899.
|
| 8. |
Shete S, Hosking FJ, Robertson LB, et al. Genome-wide association study identifies fivesusceptibility loci for glioma[J].Nat Genet, 2009, 41(8):899-904.
|
| 9. |
Wrensch M, Jenkins RB, Chang JS, et al. Variants in the CDKN2B and RTEL1 regionsare associated with high-grade glioma susceptibility[J].Nat Genet, 2009, 41(8):905-908.
|
| 10. |
Dehainault C, Michaux D, Pages-Berhouet S, et al. A deep intronic mutation in the RB1 gene leads to intronic sequence exonisation[J].Er J Hum Genet, 2007, 15(4):473-477.
|
| 11. |
Gallus GN, Cardaioli E, Rufa A, et al. Alu-element insertion in an OPA1 intron sequence associated with autosomal dominant optic atrophy[J].Mol Vis, 2010, 16(22-26):178-183.
|
| 12. |
Vannier JB, Sandhu S, Petalcorin MI, et al. RTEL1 is a replisome-associated helicasethat promotes telomere and genome-wide replication[J].Science, 2013, 342(6155):239-242.
|
| 13. |
Du SL, Geng TT, Feng T, et al. The RTEL1 rs6010620 polymorphism and glioma risk:a meta-analysis based on 12 case-control studies[J].Asian Pac J Cancer Prev, 2014, 15(23):10175-10179.
|
| 14. |
Rosenfeld MR, Pruitt AA. Management of malignant gliomas and primary CNS lymphoma:standard of care andfuture directions[J].Continuum (Minneap Minn), 2012, 18(2):406-415.
|
| 15. |
Liu Y, Shete S, Etzel CJ, et al. Polymorphisms of LIG4, BTBD2, HMGA2, and RTEL1 genes involved in the double-strand break repair pathway predict glioblastoma survival[J].Science, 2013, 342(6155):239-242.
|
| 16. |
López-Otín C, Blasco M, Partridge L, et al. The hallmarks of aging[J].Cell, 2013, 153(6):1194-1217.
|
| 17. |
Deng Z, Glousker G, Molczan A, et al. Inherited mutations in the helicase RTEL1 causetelomere dysfunction and Hoyeraal-Hreidarssonsyndrome[J].Proc Natl Acad Sci USA, 2013, 110(36):E3408-E3416.
|
| 18. |
Bai C, Connolly B, Metzker ML. Overexpression of M68yDcR3 in human gastrointestinal tract tumors Independent of gene amplification and its location in a four-gene cluster[J].Proc Natl Acad Sci USA, 2000, 97(3):1230-1235.
|
