BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

161 related articles for article (PubMed ID: 28424317)

  • 1. 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]  

  • 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. 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]  

  • 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. 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]  

  • 6. An Exploration of Social Cognition in Children with Different Degrees of Genetic Deletion in Williams Syndrome.
    Serrano-Juárez CA; Prieto-Corona B; Rodríguez-Camacho M; Venegas-Vega CA; Yáñez-Téllez MG; Silva-Pereyra J; Salgado-Ceballos H; Arias-Trejo N; De León Miranda MA
    J Autism Dev Disord; 2021 May; 51(5):1695-1704. PubMed ID: 32812194
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Oxytocin receptor activation does not mediate associative fear deficits in a Williams Syndrome model.
    Nygaard KR; Swift RG; Glick RM; Wagner RE; Maloney SE; Gould GG; Dougherty JD
    Genes Brain Behav; 2022 Jan; 21(1):e12750. PubMed ID: 33978321
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. Is it Williams syndrome? GTF2IRD1 implicated in visual-spatial construction and GTF2I in sociability revealed by high resolution arrays.
    Dai L; Bellugi U; Chen XN; Pulst-Korenberg AM; Järvinen-Pasley A; Tirosh-Wagner T; Eis PS; Graham J; Mills D; Searcy Y; Korenberg JR
    Am J Med Genet A; 2009 Mar; 149A(3):302-14. PubMed ID: 19205026
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The Role of the Oxytocin System in Anxiety Disorders.
    Yoon S; Kim YK
    Adv Exp Med Biol; 2020; 1191():103-120. PubMed ID: 32002925
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. 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]  

  • 16. Neuronal deletion of Gtf2i results in developmental microglial alterations in a mouse model related to Williams syndrome.
    Bar E; Fischer I; Rokach M; Elad-Sfadia G; Shirenova S; Ophir O; Trangle SS; Okun E; Barak B
    Glia; 2024 Jun; 72(6):1117-1135. PubMed ID: 38450767
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Impact of maternal depression across the first 6 years of life on the child's mental health, social engagement, and empathy: The moderating role of oxytocin.
    Apter-Levy Y; Feldman M; Vakart A; Ebstein RP; Feldman R
    Am J Psychiatry; 2013 Oct; 170(10):1161-8. PubMed ID: 23846912
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. Transposons in the Williams-Beuren Syndrome Critical Region are Associated with Social Behavior in Assistance Dogs.
    Gnanadesikan GE; Tandon D; Bray EE; Kennedy BS; Tennenbaum SR; MacLean EL; vonHoldt BM
    Behav Genet; 2024 Mar; 54(2):196-211. PubMed ID: 38091228
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.