BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

173 related articles for article (PubMed ID: 31513304)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. The Fanconi Anemia DNA Repair Pathway Is Regulated by an Interaction between Ubiquitin and the E2-like Fold Domain of FANCL.
    Miles JA; Frost MG; Carroll E; Rowe ML; Howard MJ; Sidhu A; Chaugule VK; Alpi AF; Walden H
    J Biol Chem; 2015 Aug; 290(34):20995-21006. PubMed ID: 26149689
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. [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]  

  • 9. 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]  

  • 10. 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]  

  • 11. 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]  

  • 12. Evidence for subcomplexes in the Fanconi anemia pathway.
    Medhurst AL; Laghmani el H; Steltenpool J; Ferrer M; Fontaine C; de Groot J; Rooimans MA; Scheper RJ; Meetei AR; Wang W; Joenje H; de Winter JP
    Blood; 2006 Sep; 108(6):2072-80. PubMed ID: 16720839
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Hematological consequences of a FANCG founder mutation in Black South African patients with Fanconi anemia.
    Feben C; Kromberg J; Wainwright R; Stones D; Poole J; Haw T; Krause A
    Blood Cells Mol Dis; 2015 Mar; 54(3):270-4. PubMed ID: 25477267
    [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. 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]  

  • 17. 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]  

  • 18. FANCL supports Parkin-mediated mitophagy in a ubiquitin ligase-independent manner.
    Beesetti S; Sirasanagandla S; Sakurada SM; Pruett-Miller SM; Sumpter R; Levine B; Potts MB
    Biochim Biophys Acta Mol Basis Dis; 2022 Sep; 1868(9):166453. PubMed ID: 35644338
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Fanconi Anemia Patients from an Indigenous Community in Mexico Carry a New Founder Pathogenic Variant in
    Reyes P; García-de Teresa B; Juárez U; Pérez-Villatoro F; Fiesco-Roa MO; Rodríguez A; Molina B; Villarreal-Molina MT; Meléndez-Zajgla J; Carnevale A; Torres L; Frias S
    Int J Mol Sci; 2022 Feb; 23(4):. PubMed ID: 35216452
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Comprehensive laboratory diagnosis of Fanconi anaemia: comparison of cellular and molecular analysis.
    Joshi G; Arthur NBJ; Geetha TS; Datari PVR; Modak K; Roy D; Chaudhury AD; Sundaraganesan P; Priyanka S; Na F; Ramprasad V; Abraham A; Srivastava VM; Srivastava A; Kulkarni UP; George B; Velayudhan SR
    J Med Genet; 2023 Aug; 60(8):801-809. PubMed ID: 36894310
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.