BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

140 related articles for article (PubMed ID: 28499504)

  • 1. Williams syndrome deletions and duplications: Genetic windows to understanding anxiety, sociality, autism, and schizophrenia.
    Crespi BJ; Procyshyn TL
    Neurosci Biobehav Rev; 2017 Aug; 79():14-26. PubMed ID: 28499504
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. The Williams syndrome prosociality gene
    Procyshyn TL; Spence J; Read S; Watson NV; Crespi BJ
    Biol Lett; 2017 Apr; 13(4):. PubMed ID: 28424317
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. Variation in the Williams syndrome GTF2I gene and anxiety proneness interactively affect prefrontal cortical response to aversive stimuli.
    Jabbi M; Chen Q; Turner N; Kohn P; White M; Kippenhan JS; Dickinson D; Kolachana B; Mattay V; Weinberger DR; Berman KF
    Transl Psychiatry; 2015 Aug; 5(8):e622. PubMed ID: 26285132
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Intracisternal Gtf2i Gene Therapy Ameliorates Deficits in Cognition and Synaptic Plasticity of a Mouse Model of Williams-Beuren Syndrome.
    Borralleras C; Sahun I; Pérez-Jurado LA; Campuzano V
    Mol Ther; 2015 Nov; 23(11):1691-1699. PubMed ID: 26216516
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. "Intolerance of uncertainty" mediates the relationship between social profile and anxiety in both Williams syndrome and autism.
    South M; Hanley M; Normansell-Mossa K; Russell NCC; Cawthorne T; Riby DM
    Autism Res; 2021 Sep; 14(9):1986-1995. PubMed ID: 34110083
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Oxytocin and Oxytocin Receptor Gene Regulation in Williams Syndrome: A Systematic Review.
    Çalışkan E; Şahin MN; Güldağ MA
    Yale J Biol Med; 2021 Dec; 94(4):623-635. PubMed ID: 34970101
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. Extensive characterization of a Williams syndrome murine model shows Gtf2ird1-mediated rescue of select sensorimotor tasks, but no effect on enhanced social behavior.
    Nygaard KR; Maloney SE; Swift RG; McCullough KB; Wagner RE; Fass SB; Garbett K; Mirnics K; Veenstra-VanderWeele J; Dougherty JD
    Genes Brain Behav; 2023 Aug; 22(4):e12853. PubMed ID: 37370259
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Model syndromes for investigating social cognitive and affective neuroscience: a comparison of Autism and Williams syndrome.
    Tager-Flusberg H; Skwerer DP; Joseph RM
    Soc Cogn Affect Neurosci; 2006 Dec; 1(3):175-82. PubMed ID: 18985104
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Autism and Williams syndrome: Dissimilar socio-cognitive profiles with similar patterns of abnormal gene expression in the blood.
    Niego A; Benítez-Burraco A
    Autism; 2021 Feb; 25(2):464-489. PubMed ID: 33143449
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Gtf2i and Gtf2ird1 mutation do not account for the full phenotypic effect of the Williams syndrome critical region in mouse models.
    Kopp N; McCullough K; Maloney SE; Dougherty JD
    Hum Mol Genet; 2019 Oct; 28(20):3443-3465. PubMed ID: 31418010
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Neuronal deletion of Gtf2i, associated with Williams syndrome, causes behavioral and myelin alterations rescuable by a remyelinating drug.
    Barak B; Zhang Z; Liu Y; Nir A; Trangle SS; Ennis M; Levandowski KM; Wang D; Quast K; Boulting GL; Li Y; Bayarsaihan D; He Z; Feng G
    Nat Neurosci; 2019 May; 22(5):700-708. PubMed ID: 31011227
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Duplication of GTF2I results in separation anxiety in mice and humans.
    Mervis CB; Dida J; Lam E; Crawford-Zelli NA; Young EJ; Henderson DR; Onay T; Morris CA; Woodruff-Borden J; Yeomans J; Osborne LR
    Am J Hum Genet; 2012 Jun; 90(6):1064-70. PubMed ID: 22578324
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.