BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

132 related articles for article (PubMed ID: 32907914)

  • 1. Gene of the month:
    Nathany S; Tripathi R; Mehta A
    J Clin Pathol; 2021 Jan; 74(1):1-4. PubMed ID: 32907914
    [TBL] [Abstract][Full Text] [Related]  

  • 2.
    Tarrini G; Ciabatti E; Pacini S; Galimberti S; Petrini I
    Anticancer Res; 2017 Oct; 37(10):5459-5462. PubMed ID: 28982856
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A specific missense mutation in GTF2I occurs at high frequency in thymic epithelial tumors.
    Petrini I; Meltzer PS; Kim IK; Lucchi M; Park KS; Fontanini G; Gao J; Zucali PA; Calabrese F; Favaretto A; Rea F; Rodriguez-Canales J; Walker RL; Pineda M; Zhu YJ; Lau C; Killian KJ; Bilke S; Voeller D; Dakshanamurthy S; Wang Y; Giaccone G
    Nat Genet; 2014 Aug; 46(8):844-9. PubMed ID: 24974848
    [TBL] [Abstract][Full Text] [Related]  

  • 4. GTF2I mutation frequently occurs in more indolent thymic epithelial tumors and predicts better prognosis.
    Feng Y; Lei Y; Wu X; Huang Y; Rao H; Zhang Y; Wang F
    Lung Cancer; 2017 Aug; 110():48-52. PubMed ID: 28676218
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Thymic epithelial tumors: examining the GTF2I mutation and developing a novel prognostic signature with LncRNA pairs to predict tumor recurrence.
    Liu W; Yang HS; Zheng SY; Weng JH; Luo HH; Lei YY; Feng YF
    BMC Genomics; 2022 Sep; 23(1):656. PubMed ID: 36114454
    [TBL] [Abstract][Full Text] [Related]  

  • 6. GTF2I-RARA is a novel fusion transcript in a t(7;17) variant of acute promyelocytic leukaemia with clinical resistance to retinoic acid.
    Li J; Zhong HY; Zhang Y; Xiao L; Bai LH; Liu SF; Zhou GB; Zhang GS
    Br J Haematol; 2015 Mar; 168(6):904-8. PubMed ID: 25284716
    [No Abstract]   [Full Text] [Related]  

  • 7. A novel GTF2I/NCOA2 fusion gene emphasizes the role of NCOA2 in soft tissue angiofibroma development.
    Arbajian E; Magnusson L; Mertens F; Domanski HA; Vult von Steyern F; Nord KH
    Genes Chromosomes Cancer; 2013 Mar; 52(3):330-1. PubMed ID: 23225380
    [No Abstract]   [Full Text] [Related]  

  • 8. The contribution of GTF2I haploinsufficiency to Williams syndrome.
    Chailangkarn T; Noree C; Muotri AR
    Mol Cell Probes; 2018 Aug; 40():45-51. PubMed ID: 29305905
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A Knock-In Mouse Model of Thymoma With the GTF2I L424H Mutation.
    He Y; Kim IK; Bian J; Polyzos A; Di Giammartino DC; Zhang YW; Luo J; Hernandez MO; Kedei N; Cam M; Borczuk AC; Lee T; Han Y; Conner EA; Wong M; Tillo DC; Umemura S; Chen V; Ruan L; White JB; Miranda IC; Awasthi PP; Altorki NK; Divakar P; Elemento O; Apostolou E; Giaccone G
    J Thorac Oncol; 2022 Dec; 17(12):1375-1386. PubMed ID: 36049655
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Consistent hypersocial behavior in mice carrying a deletion of
    Martin LA; Iceberg E; Allaf G
    Brain Behav; 2018 Jan; 8(1):e00895. PubMed ID: 29568691
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Unique correlation between GTF2I mutation and spindle cell morphology in thymomas (type A and AB thymomas).
    Wells K; Lamrca A; Papaxoinis G; Wallace A; Quinn AM; Summers Y; Nonaka D
    J Clin Pathol; 2023 Jul; 76(7):463-466. PubMed ID: 35039450
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Cognitive-behavioral phenotypes of Williams syndrome are associated with genetic variation in the GTF2I gene, in a healthy population.
    Crespi BJ; Hurd PL
    BMC Neurosci; 2014 Nov; 15():127. PubMed ID: 25429715
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mutant GTF2I induces cell transformation and metabolic alterations in thymic epithelial cells.
    Kim IK; Rao G; Zhao X; Fan R; Avantaggiati ML; Wang Y; Zhang YW; Giaccone G
    Cell Death Differ; 2020 Jul; 27(7):2263-2279. PubMed ID: 32034314
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A mouse single-copy gene, Gtf2i, the homolog of human GTF2I, that is duplicated in the Williams-Beuren syndrome deletion region.
    Wang YK; Pérez-Jurado LA; Francke U
    Genomics; 1998 Mar; 48(2):163-70. PubMed ID: 9521869
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Loss of GTF2I promotes neuronal apoptosis and synaptic reduction in human cellular models of neurodevelopment.
    Adams JW; Vinokur A; de Souza JS; Austria C; Guerra BS; Herai RH; Wahlin KJ; Muotri AR
    Cell Rep; 2024 Mar; 43(3):113867. PubMed ID: 38416640
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Essential functions of the Williams-Beuren syndrome-associated TFII-I genes in embryonic development.
    Enkhmandakh B; Makeyev AV; Erdenechimeg L; Ruddle FH; Chimge NO; Tussie-Luna MI; Roy AL; Bayarsaihan D
    Proc Natl Acad Sci U S A; 2009 Jan; 106(1):181-6. PubMed ID: 19109438
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The Integrated Genomic Landscape of Thymic Epithelial Tumors.
    Radovich M; Pickering CR; Felau I; Ha G; Zhang H; Jo H; Hoadley KA; Anur P; Zhang J; McLellan M; Bowlby R; Matthew T; Danilova L; Hegde AM; Kim J; Leiserson MDM; Sethi G; Lu C; Ryan M; Su X; Cherniack AD; Robertson G; Akbani R; Spellman P; Weinstein JN; Hayes DN; Raphael B; Lichtenberg T; Leraas K; Zenklusen JC; ; Fujimoto J; Scapulatempo-Neto C; Moreira AL; Hwang D; Huang J; Marino M; Korst R; Giaccone G; Gokmen-Polar Y; Badve S; Rajan A; Ströbel P; Girard N; Tsao MS; Marx A; Tsao AS; Loehrer PJ
    Cancer Cell; 2018 Feb; 33(2):244-258.e10. PubMed ID: 29438696
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Association of GTF2i in the Williams-Beuren syndrome critical region with autism spectrum disorders.
    Malenfant P; Liu X; Hudson ML; Qiao Y; Hrynchak M; Riendeau N; Hildebrand MJ; Cohen IL; Chudley AE; Forster-Gibson C; Mickelson EC; Rajcan-Separovic E; Lewis ME; Holden JJ
    J Autism Dev Disord; 2012 Jul; 42(7):1459-69. PubMed ID: 22048961
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Gene mutation may signal indolent thymus cancer.
    Cancer Discov; 2014 Sep; 4(9):OF4. PubMed ID: 25185203
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A Common Polymorphism in a Williams Syndrome Gene Predicts Amygdala Reactivity and Extraversion in Healthy Adults.
    Swartz JR; Waller R; Bogdan R; Knodt AR; Sabhlok A; Hyde LW; Hariri AR
    Biol Psychiatry; 2017 Feb; 81(3):203-210. PubMed ID: 26853120
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.