BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

256 related articles for article (PubMed ID: 31418010)

  • 21. 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]  

  • 22. GTF2I hemizygosity implicated in mental retardation in Williams syndrome: genotype-phenotype analysis of five families with deletions in the Williams syndrome region.
    Morris CA; Mervis CB; Hobart HH; Gregg RG; Bertrand J; Ensing GJ; Sommer A; Moore CA; Hopkin RJ; Spallone PA; Keating MT; Osborne L; Kimberley KW; Stock AD
    Am J Med Genet A; 2003 Nov; 123A(1):45-59. PubMed ID: 14556246
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A transcriptomic study of Williams-Beuren syndrome associated genes in mouse embryonic stem cells.
    De Cegli R; Iacobacci S; Fedele A; Ballabio A; di Bernardo D
    Sci Data; 2019 Nov; 6(1):262. PubMed ID: 31695049
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Essential role of the N-terminal region of TFII-I in viability and behavior.
    Lucena J; Pezzi S; Aso E; Valero MC; Carreiro C; Dubus P; Sampaio A; Segura M; Barthelemy I; Zindel MY; Sousa N; Barbero JL; Maldonado R; Pérez-Jurado LA; Campuzano V
    BMC Med Genet; 2010 Apr; 11():61. PubMed ID: 20403157
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. 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]  

  • 27. Expression of Gtf2ird1, the Williams syndrome-associated gene, during mouse development.
    Palmer SJ; Tay ES; Santucci N; Cuc Bach TT; Hook J; Lemckert FA; Jamieson RV; Gunnning PW; Hardeman EC
    Gene Expr Patterns; 2007 Feb; 7(4):396-404. PubMed ID: 17239664
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. 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]  

  • 30. GTF2IRD1 in craniofacial development of humans and mice.
    Tassabehji M; Hammond P; Karmiloff-Smith A; Thompson P; Thorgeirsson SS; Durkin ME; Popescu NC; Hutton T; Metcalfe K; Rucka A; Stewart H; Read AP; Maconochie M; Donnai D
    Science; 2005 Nov; 310(5751):1184-7. PubMed ID: 16293761
    [TBL] [Abstract][Full Text] [Related]  

  • 31. An atypical 7q11.23 deletion in a normal IQ Williams-Beuren syndrome patient.
    Ferrero GB; Howald C; Micale L; Biamino E; Augello B; Fusco C; Turturo MG; Forzano S; Reymond A; Merla G
    Eur J Hum Genet; 2010 Jan; 18(1):33-8. PubMed ID: 19568270
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Biallelic GTF2IRD1 variants in brothers with profound neurodevelopmental disorder: A possible novel disorder involving a critical gene for Williams syndrome.
    Cummings CT; Starr LJ
    Am J Med Genet A; 2023 Feb; 191(2):332-337. PubMed ID: 36308390
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Identification of GTF2IRD1, a putative transcription factor within the Williams-Beuren syndrome deletion at 7q11.23.
    Franke Y; Peoples RJ; Francke U
    Cytogenet Cell Genet; 1999; 86(3-4):296-304. PubMed ID: 10575229
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Comparison of TFII-I gene family members deleted in Williams-Beuren syndrome.
    Hinsley TA; Cunliffe P; Tipney HJ; Brass A; Tassabehji M
    Protein Sci; 2004 Oct; 13(10):2588-99. PubMed ID: 15388857
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Genetic contributions to visuospatial cognition in Williams syndrome: insights from two contrasting partial deletion patients.
    Broadbent H; Farran EK; Chin E; Metcalfe K; Tassabehji M; Turnpenny P; Sansbury F; Meaburn E; Karmiloff-Smith A
    J Neurodev Disord; 2014; 6(1):18. PubMed ID: 25057328
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. 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]  

  • 38. Isolation and characterisation of GTF2IRD2, a novel fusion gene and member of the TFII-I family of transcription factors, deleted in Williams-Beuren syndrome.
    Tipney HJ; Hinsley TA; Brass A; Metcalfe K; Donnai D; Tassabehji M
    Eur J Hum Genet; 2004 Jul; 12(7):551-60. PubMed ID: 15100712
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 13.