BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

350 related articles for article (PubMed ID: 27509850)

  • 1. A human neurodevelopmental model for Williams syndrome.
    Chailangkarn T; Trujillo CA; Freitas BC; Hrvoj-Mihic B; Herai RH; Yu DX; Brown TT; Marchetto MC; Bardy C; McHenry L; Stefanacci L; Järvinen A; Searcy YM; DeWitt M; Wong W; Lai P; Ard MC; Hanson KL; Romero S; Jacobs B; Dale AM; Dai L; Korenberg JR; Gage FH; Bellugi U; Halgren E; Semendeferi K; Muotri AR
    Nature; 2016 Aug; 536(7616):338-43. PubMed ID: 27509850
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Haploinsufficiency of BAZ1B contributes to Williams syndrome through transcriptional dysregulation of neurodevelopmental pathways.
    Lalli MA; Jang J; Park JH; Wang Y; Guzman E; Zhou H; Audouard M; Bridges D; Tovar KR; Papuc SM; Tutulan-Cunita AC; Huang Y; Budisteanu M; Arghir A; Kosik KS
    Hum Mol Genet; 2016 Apr; 25(7):1294-306. PubMed ID: 26755828
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Human induced pluripotent stem cell derived neurons as a model for Williams-Beuren syndrome.
    Khattak S; Brimble E; Zhang W; Zaslavsky K; Strong E; Ross PJ; Hendry J; Mital S; Salter MW; Osborne LR; Ellis J
    Mol Brain; 2015 Nov; 8(1):77. PubMed ID: 26603386
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Modeling Williams syndrome with induced pluripotent stem cells.
    Chailangkarn T; Muotri AR
    Neurogenesis (Austin); 2017; 4(1):e1283187. PubMed ID: 28229087
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Smaller and larger deletions of the Williams Beuren syndrome region implicate genes involved in mild facial phenotype, epilepsy and autistic traits.
    Fusco C; Micale L; Augello B; Teresa Pellico M; Menghini D; Alfieri P; Cristina Digilio M; Mandriani B; Carella M; Palumbo O; Vicari S; Merla G
    Eur J Hum Genet; 2014 Jan; 22(1):64-70. PubMed ID: 23756441
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Detection of an atypical 7q11.23 deletion in Williams syndrome patients which does not include the STX1A and FZD3 genes.
    Botta A; Novelli G; Mari A; Novelli A; Sabani M; Korenberg J; Osborne LR; Digilio MC; Giannotti A; Dallapiccola B
    J Med Genet; 1999 Jun; 36(6):478-80. PubMed ID: 10874638
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. Neuron density is decreased in the prefrontal cortex in Williams syndrome.
    Lew CH; Brown C; Bellugi U; Semendeferi K
    Autism Res; 2017 Jan; 10(1):99-112. PubMed ID: 27520580
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Williams syndrome: a genetic deletion disorder presenting clues to the biology of sociability and clinical challenges of hypersociability.
    Deutsch SI; Rosse RB; Schwartz BL
    CNS Spectr; 2007 Dec; 12(12):903-7. PubMed ID: 18163035
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Frizzled 9 knock-out mice have abnormal B-cell development.
    Ranheim EA; Kwan HC; Reya T; Wang YK; Weissman IL; Francke U
    Blood; 2005 Mar; 105(6):2487-94. PubMed ID: 15572594
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Cellular and molecular characterization of multiplex autism in human induced pluripotent stem cell-derived neurons.
    Lewis EMA; Meganathan K; Baldridge D; Gontarz P; Zhang B; Bonni A; Constantino JN; Kroll KL
    Mol Autism; 2019; 10():51. PubMed ID: 31893020
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Heterozygous deletion of the Williams-Beuren syndrome critical interval in mice recapitulates most features of the human disorder.
    Segura-Puimedon M; Sahún I; Velot E; Dubus P; Borralleras C; Rodrigues AJ; Valero MC; Valverde O; Sousa N; Herault Y; Dierssen M; Pérez-Jurado LA; Campuzano V
    Hum Mol Genet; 2014 Dec; 23(24):6481-94. PubMed ID: 25027326
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Conceptualizing neurodevelopmental disorders through a mechanistic understanding of fragile X syndrome and Williams syndrome.
    Fung LK; Quintin EM; Haas BW; Reiss AL
    Curr Opin Neurol; 2012 Apr; 25(2):112-24. PubMed ID: 22395002
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Association between cerebral shape and social use of language in Williams syndrome.
    Gothelf D; Searcy YM; Reilly J; Lai PT; Lanre-Amos T; Mills D; Korenberg JR; Galaburda A; Bellugi U; Reiss AL
    Am J Med Genet A; 2008 Nov; 146A(21):2753-61. PubMed ID: 18924169
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetic contributions to white matter architecture revealed by diffusion tensor imaging in Williams syndrome.
    Marenco S; Siuta MA; Kippenhan JS; Grodofsky S; Chang WL; Kohn P; Mervis CB; Morris CA; Weinberger DR; Meyer-Lindenberg A; Pierpaoli C; Berman KF
    Proc Natl Acad Sci U S A; 2007 Sep; 104(38):15117-22. PubMed ID: 17827280
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The Williams syndrome cognitive profile.
    Mervis CB; Robinson BF; Bertrand J; Morris CA; Klein-Tasman BP; Armstrong SC
    Brain Cogn; 2000 Dec; 44(3):604-28. PubMed ID: 11104544
    [TBL] [Abstract][Full Text] [Related]  

  • 20. VI. Genome structure and cognitive map of Williams syndrome.
    Korenberg JR; Chen XN; Hirota H; Lai Z; Bellugi U; Burian D; Roe B; Matsuoka R
    J Cogn Neurosci; 2000; 12 Suppl 1():89-107. PubMed ID: 10953236
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 18.