BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

172 related articles for article (PubMed ID: 26285132)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. High-throughput screening identifies histone deacetylase inhibitors that modulate GTF2I expression in 7q11.23 microduplication autism spectrum disorder patient-derived cortical neurons.
    Cavallo F; Troglio F; Fagà G; Fancelli D; Shyti R; Trattaro S; Zanella M; D'Agostino G; Hughes JM; Cera MR; Pasi M; Gabriele M; Lazzarin M; Mihailovich M; Kooy F; Rosa A; Mercurio C; Varasi M; Testa G
    Mol Autism; 2020 Nov; 11(1):88. PubMed ID: 33208191
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Williams syndrome hemideletion and LIMK1 variation both affect dorsal stream functional connectivity.
    Gregory MD; Mervis CB; Elliott ML; Kippenhan JS; Nash T; B Czarapata J; Prabhakaran R; Roe K; Eisenberg DP; Kohn PD; Berman KF
    Brain; 2019 Dec; 142(12):3963-3974. PubMed ID: 31687737
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. A method for determining haploid and triploid genotypes and their association with vascular phenotypes in Williams syndrome and 7q11.23 duplication syndrome.
    Gregory MD; Kolachana B; Yao Y; Nash T; Dickinson D; Eisenberg DP; Mervis CB; Berman KF
    BMC Med Genet; 2018 Apr; 19(1):53. PubMed ID: 29614955
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 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. 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]  

  • 16. 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]  

  • 17. 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]  

  • 18. Anxiety and autonomic response to social-affective stimuli in individuals with Williams syndrome.
    Ng R; Bellugi U; Järvinen A
    Res Dev Disabil; 2016 Dec; 59():387-398. PubMed ID: 27718424
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Haploinsufficiency of Gtf2i, a gene deleted in Williams Syndrome, leads to increases in social interactions.
    Sakurai T; Dorr NP; Takahashi N; McInnes LA; Elder GA; Buxbaum JD
    Autism Res; 2011 Feb; 4(1):28-39. PubMed ID: 21328569
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Dorsomedial Prefrontal Cortex Mediates the Impact of Serotonin Transporter Linked Polymorphic Region Genotype on Anticipatory Threat Reactions.
    Klumpers F; Kroes MC; Heitland I; Everaerd D; Akkermans SE; Oosting RS; van Wingen G; Franke B; Kenemans JL; Fernández G; Baas JM
    Biol Psychiatry; 2015 Oct; 78(8):582-9. PubMed ID: 25444169
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.