277 related articles for article (PubMed ID: 10678659)
21. [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]
22. Werner syndrome: entering the helicase era.
Epstein CJ; Motulsky AG
Bioessays; 1996 Dec; 18(12):1025-7. PubMed ID: 8976161
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. Intron-size constraint as a mutational mechanism in Rothmund-Thomson syndrome.
Wang LL; Worley K; Gannavarapu A; Chintagumpala MM; Levy ML; Plon SE
Am J Hum Genet; 2002 Jul; 71(1):165-7. PubMed ID: 12016592
[TBL] [Abstract][Full Text] [Related]
25. 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]
26. Homologous recombination is responsible for cell death in the absence of the Sgs1 and Srs2 helicases.
Gangloff S; Soustelle C; Fabre F
Nat Genet; 2000 Jun; 25(2):192-4. PubMed ID: 10835635
[TBL] [Abstract][Full Text] [Related]
27. 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]
28. 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]
29. 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]
30. 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]
31. 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]
32. Sit down, relax and unwind: structural insights into RecQ helicase mechanisms.
Killoran MP; Keck JL
Nucleic Acids Res; 2006; 34(15):4098-105. PubMed ID: 16935877
[TBL] [Abstract][Full Text] [Related]
33. [RecQ family helicases].
Seki M; Enomoto T
Seikagaku; 2004 Feb; 76(2):143-8. PubMed ID: 15049142
[No Abstract] [Full Text] [Related]
34. RecQ helicases: caretakers of the genome.
Hickson ID
Nat Rev Cancer; 2003 Mar; 3(3):169-78. PubMed ID: 12612652
[TBL] [Abstract][Full Text] [Related]
35. 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]
36. Mutations in the consensus helicase domains of the Werner syndrome gene. Werner's Syndrome Collaborative Group.
Yu CE; Oshima J; Wijsman EM; Nakura J; Miki T; Piussan C; Matthews S; Fu YH; Mulligan J; Martin GM; Schellenberg GD
Am J Hum Genet; 1997 Feb; 60(2):330-41. PubMed ID: 9012406
[TBL] [Abstract][Full Text] [Related]
37. Disease-causing missense mutations in human DNA helicase disorders.
Suhasini AN; Brosh RM
Mutat Res; 2013; 752(2):138-152. PubMed ID: 23276657
[TBL] [Abstract][Full Text] [Related]
38. 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]
39. Mutations in ANAPC1, Encoding a Scaffold Subunit of the Anaphase-Promoting Complex, Cause Rothmund-Thomson Syndrome Type 1.
Ajeawung NF; Nguyen TTM; Lu L; Kucharski TJ; Rousseau J; Molidperee S; Atienza J; Gamache I; Jin W; Plon SE; Lee BH; Teodoro JG; Wang LL; Campeau PM
Am J Hum Genet; 2019 Sep; 105(3):625-630. PubMed ID: 31303264
[TBL] [Abstract][Full Text] [Related]
40. 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]
[Previous] [Next] [New Search]
