These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

187 related articles for article (PubMed ID: 25628358)

  • 1. Human regulator of telomere elongation helicase 1 (RTEL1) is required for the nuclear and cytoplasmic trafficking of pre-U2 RNA.
    Schertzer M; Jouravleva K; Perderiset M; Dingli F; Loew D; Le Guen T; Bardoni B; de Villartay JP; Revy P; Londoño-Vallejo A
    Nucleic Acids Res; 2015 Feb; 43(3):1834-47. PubMed ID: 25628358
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Inherited mutations in the helicase RTEL1 cause telomere dysfunction and Hoyeraal-Hreidarsson syndrome.
    Deng Z; Glousker G; Molczan A; Fox AJ; Lamm N; Dheekollu J; Weizman OE; Schertzer M; Wang Z; Vladimirova O; Schug J; Aker M; Londoño-Vallejo A; Kaestner KH; Lieberman PM; Tzfati Y
    Proc Natl Acad Sci U S A; 2013 Sep; 110(36):E3408-16. PubMed ID: 23959892
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Human RTEL1 deficiency causes Hoyeraal-Hreidarsson syndrome with short telomeres and genome instability.
    Le Guen T; Jullien L; Touzot F; Schertzer M; Gaillard L; Perderiset M; Carpentier W; Nitschke P; Picard C; Couillault G; Soulier J; Fischer A; Callebaut I; Jabado N; Londono-Vallejo A; de Villartay JP; Revy P
    Hum Mol Genet; 2013 Aug; 22(16):3239-49. PubMed ID: 23591994
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Full length RTEL1 is required for the elongation of the single-stranded telomeric overhang by telomerase.
    Awad A; Glousker G; Lamm N; Tawil S; Hourvitz N; Smoom R; Revy P; Tzfati Y
    Nucleic Acids Res; 2020 Jul; 48(13):7239-7251. PubMed ID: 32542379
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [RTEL1 (regulator of telomere elongation helicase 1), a DNA helicase essential for genome stability].
    Le Guen T; Jullien L; Schertzer M; Lefebvre A; Kermasson L; de Villartay JP; Londoño-Vallejo A; Revy P
    Med Sci (Paris); 2013 Dec; 29(12):1138-44. PubMed ID: 24356145
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Compound heterozygous mutations in the helicase RTEL1 causing Hoyeraal-Hreidarsson syndrome with Blake`s pouch cyst: a case report.
    He M; Lian G; Hu H; He H; Wang M
    Turk J Pediatr; 2023; 65(5):845-852. PubMed ID: 37853975
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Constitutional mutations in RTEL1 cause severe dyskeratosis congenita.
    Walne AJ; Vulliamy T; Kirwan M; Plagnol V; Dokal I
    Am J Hum Genet; 2013 Mar; 92(3):448-53. PubMed ID: 23453664
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Germline mutations of regulator of telomere elongation helicase 1, RTEL1, in Dyskeratosis congenita.
    Ballew BJ; Yeager M; Jacobs K; Giri N; Boland J; Burdett L; Alter BP; Savage SA
    Hum Genet; 2013 Apr; 132(4):473-80. PubMed ID: 23329068
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A recessive founder mutation in regulator of telomere elongation helicase 1, RTEL1, underlies severe immunodeficiency and features of Hoyeraal Hreidarsson syndrome.
    Ballew BJ; Joseph V; De S; Sarek G; Vannier JB; Stracker T; Schrader KA; Small TN; O'Reilly R; Manschreck C; Harlan Fleischut MM; Zhang L; Sullivan J; Stratton K; Yeager M; Jacobs K; Giri N; Alter BP; Boland J; Burdett L; Offit K; Boulton SJ; Savage SA; Petrini JH
    PLoS Genet; 2013 Aug; 9(8):e1003695. PubMed ID: 24009516
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Human RTEL1 stabilizes long G-overhangs allowing telomerase-dependent over-extension.
    Porreca RM; Glousker G; Awad A; Matilla Fernandez MI; Gibaud A; Naucke C; Cohen SB; Bryan TM; Tzfati Y; Draskovic I; Londoño-Vallejo A
    Nucleic Acids Res; 2018 May; 46(9):4533-4545. PubMed ID: 29522136
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The C-terminal extension of human RTEL1, mutated in Hoyeraal-Hreidarsson syndrome, contains harmonin-N-like domains.
    Faure G; Revy P; Schertzer M; Londono-Vallejo A; Callebaut I
    Proteins; 2014 Jun; 82(6):897-903. PubMed ID: 24130156
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The Arabidopsis thaliana homolog of the helicase RTEL1 plays multiple roles in preserving genome stability.
    Recker J; Knoll A; Puchta H
    Plant Cell; 2014 Dec; 26(12):4889-902. PubMed ID: 25516598
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The many faces of the helicase RTEL1 at telomeres and beyond.
    Hourvitz N; Awad A; Tzfati Y
    Trends Cell Biol; 2024 Feb; 34(2):109-121. PubMed ID: 37532653
    [TBL] [Abstract][Full Text] [Related]  

  • 14. RTEL1: functions of a disease-associated helicase.
    Vannier JB; Sarek G; Boulton SJ
    Trends Cell Biol; 2014 Jul; 24(7):416-25. PubMed ID: 24582487
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Resonance assignment and secondary structure of the tandem harmonin homology domains of human RTEL1.
    Kumar N; Ghosh M; Manikandan P; Basak S; Deepa A; Singh M
    Biomol NMR Assign; 2022 Apr; 16(1):159-164. PubMed ID: 35320499
    [TBL] [Abstract][Full Text] [Related]  

  • 16. TRF2 recruits RTEL1 to telomeres in S phase to promote t-loop unwinding.
    Sarek G; Vannier JB; Panier S; Petrini JHJ; Boulton SJ
    Mol Cell; 2015 Feb; 57(4):622-635. PubMed ID: 25620558
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Heterozygous
    Marsh JCW; Gutierrez-Rodrigues F; Cooper J; Jiang J; Gandhi S; Kajigaya S; Feng X; Ibanez MDPF; Donaires FS; Lopes da Silva JP; Li Z; Das S; Ibanez M; Smith AE; Lea N; Best S; Ireland R; Kulasekararaj AG; McLornan DP; Pagliuca A; Callebaut I; Young NS; Calado RT; Townsley DM; Mufti GJ
    Blood Adv; 2018 Jan; 2(1):36-48. PubMed ID: 29344583
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mutations of the RTEL1 Helicase in a Hoyeraal-Hreidarsson Syndrome Patient Highlight the Importance of the ARCH Domain.
    Jullien L; Kannengiesser C; Kermasson L; Cormier-Daire V; Leblanc T; Soulier J; Londono-Vallejo A; de Villartay JP; Callebaut I; Revy P
    Hum Mutat; 2016 May; 37(5):469-72. PubMed ID: 26847928
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Heterozygous RTEL1 mutations are associated with familial pulmonary fibrosis.
    Kannengiesser C; Borie R; Ménard C; Réocreux M; Nitschké P; Gazal S; Mal H; Taillé C; Cadranel J; Nunes H; Valeyre D; Cordier JF; Callebaut I; Boileau C; Cottin V; Grandchamp B; Revy P; Crestani B
    Eur Respir J; 2015 Aug; 46(2):474-85. PubMed ID: 26022962
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Regulator of telomere elongation helicase 1 gene and its association with malignancy.
    Hassani MA; Murid J; Yan J
    Cancer Rep (Hoboken); 2023 Jan; 6(1):e1735. PubMed ID: 36253342
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.