BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

176 related articles for article (PubMed ID: 14751286)

  • 21. A complete physical contig and partial transcript map of the Williams syndrome critical region.
    Hockenhull EL; Carette MJ; Metcalfe K; Donnai D; Read AP; Tassabehji M
    Genomics; 1999 Jun; 58(2):138-45. PubMed ID: 10366445
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. 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]  

  • 24. 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]  

  • 25. 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]  

  • 26. Molecular basis of Williams-Beuren syndrome: TFII-I regulated targets involved in craniofacial development.
    Makeyev AV; Bayarsaihan D
    Cleft Palate Craniofac J; 2011 Jan; 48(1):109-16. PubMed ID: 20500075
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. 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]  

  • 29. Alternative splicing and promoter use in TFII-I genes.
    Makeyev AV; Bayarsaihan D
    Gene; 2009 Mar; 433(1-2):16-25. PubMed ID: 19111598
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Identification of genes from a 500-kb region at 7q11.23 that is commonly deleted in Williams syndrome patients.
    Osborne LR; Martindale D; Scherer SW; Shi XM; Huizenga J; Heng HH; Costa T; Pober B; Lew L; Brinkman J; Rommens J; Koop B; Tsui LC
    Genomics; 1996 Sep; 36(2):328-36. PubMed ID: 8812460
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A novel human gene, WSTF, is deleted in Williams syndrome.
    Lu X; Meng X; Morris CA; Keating MT
    Genomics; 1998 Dec; 54(2):241-9. PubMed ID: 9828126
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Disparities in visuo-spatial constructive abilities in Williams syndrome patients with typical deletion on chromosome 7q11.23.
    Muramatsu Y; Tokita Y; Mizuno S; Nakamura M
    Brain Dev; 2017 Feb; 39(2):145-153. PubMed ID: 27692871
    [TBL] [Abstract][Full Text] [Related]  

  • 33. The early embryonic expression of TFII-I during mouse preimplantation development.
    Enkhmandakh B; Bitchevaia N; Ruddle F; Bayarsaihan D
    Gene Expr Patterns; 2004 Jan; 4(1):25-8. PubMed ID: 14678824
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. Comparative mapping of the region of human chromosome 7 deleted in williams syndrome.
    DeSilva U; Massa H; Trask BJ; Green ED
    Genome Res; 1999 May; 9(5):428-36. PubMed ID: 10330122
    [TBL] [Abstract][Full Text] [Related]  

  • 36. A novel human homologue of the Drosophila frizzled wnt receptor gene binds wingless protein and is in the Williams syndrome deletion at 7q11.23.
    Wang YK; Samos CH; Peoples R; Pérez-Jurado LA; Nusse R; Francke U
    Hum Mol Genet; 1997 Mar; 6(3):465-72. PubMed ID: 9147651
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. Integration of a c-myc transgene results in disruption of the mouse Gtf2ird1 gene, the homologue of the human GTF2IRD1 gene hemizygously deleted in Williams-Beuren syndrome.
    Durkin ME; Keck-Waggoner CL; Popescu NC; Thorgeirsson SS
    Genomics; 2001 Apr; 73(1):20-7. PubMed ID: 11352562
    [TBL] [Abstract][Full Text] [Related]  

  • 39. From genes to brain development to phenotypic behavior: "dorsal-stream vulnerability" in relation to spatial cognition, attention, and planning of actions in Williams syndrome (WS) and other developmental disorders.
    Atkinson J; Braddick O
    Prog Brain Res; 2011; 189():261-83. PubMed ID: 21489394
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Expression analysis and protein localization of the human HPC-1/syntaxin 1A, a gene deleted in Williams syndrome.
    Botta A; Sangiuolo F; Calza L; Giardino L; Potenza S; Novelli G; Dallapiccola B
    Genomics; 1999 Dec; 62(3):525-8. PubMed ID: 10644452
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.