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 *

192 related articles for article (PubMed ID: 28419882)

  • 1. Novel homozygous FANCL mutation and somatic heterozygous SETBP1 mutation in a Chinese girl with Fanconi Anemia.
    Wu W; Liu Y; Zhou Q; Wang Q; Luo F; Xu Z; Geng Q; Li P; Zhang HZ; Xie J
    Eur J Med Genet; 2017 Jul; 60(7):369-373. PubMed ID: 28419882
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Assessing the spectrum of germline variation in Fanconi anemia genes among patients with head and neck carcinoma before age 50.
    Chandrasekharappa SC; Chinn SB; Donovan FX; Chowdhury NI; Kamat A; Adeyemo AA; Thomas JW; Vemulapalli M; Hussey CS; Reid HH; Mullikin JC; Wei Q; Sturgis EM
    Cancer; 2017 Oct; 123(20):3943-3954. PubMed ID: 28678401
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Characterization of FANCL variants observed in patient cancer cells.
    Frost MG; Mazloumi Aboukheili AM; Toth R; Walden H
    Biosci Rep; 2020 Jun; 40(6):. PubMed ID: 32420600
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The causes of Fanconi anemia in South Asia and the Middle East: A case series and review of the literature.
    Thompson AS; Saba N; McReynolds LJ; Munir S; Ahmed P; Sajjad S; Jones K; Yeager M; Donovan FX; Chandrasekharappa SC; Alter BP; Savage SA; Rehman S
    Mol Genet Genomic Med; 2021 Jul; 9(7):e1693. PubMed ID: 33960719
    [TBL] [Abstract][Full Text] [Related]  

  • 5. An acquired BMF with FANCL gene heterozygous mutation: Case report.
    Zhang N; Wang X; Miao XJ; Zhang XP; Xia XY; Li L; Sun HP
    Medicine (Baltimore); 2023 Jun; 102(24):e34036. PubMed ID: 37327301
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Identification and characterization of mutations in FANCL gene: a second case of Fanconi anemia belonging to FA-L complementation group.
    Ali AM; Kirby M; Jansen M; Lach FP; Schulte J; Singh TR; Batish SD; Auerbach AD; Williams DA; Meetei AR
    Hum Mutat; 2009 Jul; 30(7):E761-70. PubMed ID: 19405097
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Loss-of-Function FANCL Mutations Associate with Severe Fanconi Anemia Overlapping the VACTERL Association.
    Vetro A; Iascone M; Limongelli I; Ameziane N; Gana S; Della Mina E; Giussani U; Ciccone R; Forlino A; Pezzoli L; Rooimans MA; van Essen AJ; Messa J; Rizzuti T; Bianchi P; Dorsman J; de Winter JP; Lalatta F; Zuffardi O
    Hum Mutat; 2015 May; 36(5):562-8. PubMed ID: 25754594
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Association of complementation group and mutation type with clinical outcome in fanconi anemia. European Fanconi Anemia Research Group.
    Faivre L; Guardiola P; Lewis C; Dokal I; Ebell W; Zatterale A; Altay C; Poole J; Stones D; Kwee ML; van Weel-Sipman M; Havenga C; Morgan N; de Winter J; Digweed M; Savoia A; Pronk J; de Ravel T; Jansen S; Joenje H; Gluckman E; Mathew CG
    Blood; 2000 Dec; 96(13):4064-70. PubMed ID: 11110674
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A founder variant in the South Asian population leads to a high prevalence of FANCL Fanconi anemia cases in India.
    Donovan FX; Solanki A; Mori M; Chavan N; George M; C SK; Okuno Y; Muramastsu H; Yoshida K; Shimamoto A; Takaori-Kondo A; Yabe H; Ogawa S; Kojima S; Yabe M; Ramanagoudr-Bhojappa R; Smogorzewska A; Mohan S; Rajendran A; Auerbach AD; Takata M; Chandrasekharappa SC; Vundinti BR
    Hum Mutat; 2020 Jan; 41(1):122-128. PubMed ID: 31513304
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Severe telomere shortening in Fanconi anemia complementation group L.
    Shah A; George M; Dhangar S; Rajendran A; Mohan S; Vundinti BR
    Mol Biol Rep; 2021 Jan; 48(1):585-593. PubMed ID: 33394227
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mutational analysis of FANCL, FANCM and the recently identified FANCI suggests that among the 13 known Fanconi Anemia genes, only FANCD1/BRCA2 plays a major role in high-risk breast cancer predisposition.
    García MJ; Fernández V; Osorio A; Barroso A; Fernández F; Urioste M; Benítez J
    Carcinogenesis; 2009 Nov; 30(11):1898-902. PubMed ID: 19737859
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Functions of FANCL in primordial germ cell formation and Fanconi anemia].
    Zhao QG; Lu BS; Huang PT
    Yi Chuan Xue Bao; 2005 Sep; 32(9):993-1000. PubMed ID: 16201245
    [TBL] [Abstract][Full Text] [Related]  

  • 13. FANCL gene mutations in premature ovarian insufficiency.
    Yang Y; Guo T; Liu R; Ke H; Xu W; Zhao S; Qin Y
    Hum Mutat; 2020 May; 41(5):1033-1041. PubMed ID: 32048394
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Profiling Fanconi Anemia Gene Mutations among Iranian Patients.
    Esmail Nia G; Fadaee M; Royer R; Najmabadi H; Akbari MR
    Arch Iran Med; 2016 Apr; 19(4):236-40. PubMed ID: 27041517
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The WD40 repeats of FANCL are required for Fanconi anemia core complex assembly.
    Gurtan AM; Stuckert P; D'Andrea AD
    J Biol Chem; 2006 Apr; 281(16):10896-905. PubMed ID: 16474167
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Deficiency of UBE2T, the E2 Ubiquitin Ligase Necessary for FANCD2 and FANCI Ubiquitination, Causes FA-T Subtype of Fanconi Anemia.
    Rickman KA; Lach FP; Abhyankar A; Donovan FX; Sanborn EM; Kennedy JA; Sougnez C; Gabriel SB; Elemento O; Chandrasekharappa SC; Schindler D; Auerbach AD; Smogorzewska A
    Cell Rep; 2015 Jul; 12(1):35-41. PubMed ID: 26119737
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Drosophila homologs of FANCD2 and FANCL function in DNA repair.
    Marek LR; Bale AE
    DNA Repair (Amst); 2006 Nov; 5(11):1317-26. PubMed ID: 16860002
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A requirement of FancL and FancD2 monoubiquitination in DNA repair.
    Seki S; Ohzeki M; Uchida A; Hirano S; Matsushita N; Kitao H; Oda T; Yamashita T; Kashihara N; Tsubahara A; Takata M; Ishiai M
    Genes Cells; 2007 Mar; 12(3):299-310. PubMed ID: 17352736
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Structural analysis of human FANCL, the E3 ligase in the Fanconi anemia pathway.
    Hodson C; Cole AR; Lewis LP; Miles JA; Purkiss A; Walden H
    J Biol Chem; 2011 Sep; 286(37):32628-37. PubMed ID: 21775430
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Hypermethylation of the FANCC and FANCL promoter regions in sporadic acute leukaemia.
    Hess CJ; Ameziane N; Schuurhuis GJ; Errami A; Denkers F; Kaspers GJ; Cloos J; Joenje H; Reinhardt D; Ossenkoppele GJ; Zwaan CM; Waisfisz Q
    Cell Oncol; 2008; 30(4):299-306. PubMed ID: 18607065
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.