BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

238 related articles for article (PubMed ID: 24797903)

  • 1. Mammalian TBX1 preferentially binds and regulates downstream targets via a tandem T-site repeat.
    Castellanos R; Xie Q; Zheng D; Cvekl A; Morrow BE
    PLoS One; 2014; 9(5):e95151. PubMed ID: 24797903
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Variants in a cis-regulatory element of TBX1 in conotruncal heart defect patients impair GATA6-mediated transactivation.
    Jiang X; Li T; Liu S; Fu Q; Li F; Chen S; Sun K; Xu R; Xu Y
    Orphanet J Rare Dis; 2021 Jul; 16(1):334. PubMed ID: 34332615
    [TBL] [Abstract][Full Text] [Related]  

  • 3. TBX1 protein interactions and microRNA-96-5p regulation controls cell proliferation during craniofacial and dental development: implications for 22q11.2 deletion syndrome.
    Gao S; Moreno M; Eliason S; Cao H; Li X; Yu W; Bidlack FB; Margolis HC; Baldini A; Amendt BA
    Hum Mol Genet; 2015 Apr; 24(8):2330-48. PubMed ID: 25556186
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Full spectrum of malformations in velo-cardio-facial syndrome/DiGeorge syndrome mouse models by altering Tbx1 dosage.
    Liao J; Kochilas L; Nowotschin S; Arnold JS; Aggarwal VS; Epstein JA; Brown MC; Adams J; Morrow BE
    Hum Mol Genet; 2004 Aug; 13(15):1577-85. PubMed ID: 15190012
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Novel TBX1 loss-of-function mutation causes isolated conotruncal heart defects in Chinese patients without 22q11.2 deletion.
    Xu YJ; Chen S; Zhang J; Fang SH; Guo QQ; Wang J; Fu QH; Li F; Xu R; Sun K
    BMC Med Genet; 2014 Jul; 15():78. PubMed ID: 24998776
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Identification of a novel nuclear localization signal in Tbx1 that is deleted in DiGeorge syndrome patients harboring the 1223delC mutation.
    Stoller JZ; Epstein JA
    Hum Mol Genet; 2005 Apr; 14(7):885-92. PubMed ID: 15703190
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mice overexpressing genes from the 22q11 region deleted in velo-cardio-facial syndrome/DiGeorge syndrome have middle and inner ear defects.
    Funke B; Epstein JA; Kochilas LK; Lu MM; Pandita RK; Liao J; Bauerndistel R; Schüler T; Schorle H; Brown MC; Adams J; Morrow BE
    Hum Mol Genet; 2001 Oct; 10(22):2549-56. PubMed ID: 11709542
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Reduced dosage of β-catenin provides significant rescue of cardiac outflow tract anomalies in a Tbx1 conditional null mouse model of 22q11.2 deletion syndrome.
    Racedo SE; Hasten E; Lin M; Devakanmalai GS; Guo T; Ozbudak EM; Cai CL; Zheng D; Morrow BE
    PLoS Genet; 2017 Mar; 13(3):e1006687. PubMed ID: 28346476
    [TBL] [Abstract][Full Text] [Related]  

  • 9. MOZ regulates the Tbx1 locus, and Moz mutation partially phenocopies DiGeorge syndrome.
    Voss AK; Vanyai HK; Collin C; Dixon MP; McLennan TJ; Sheikh BN; Scambler P; Thomas T
    Dev Cell; 2012 Sep; 23(3):652-63. PubMed ID: 22921202
    [TBL] [Abstract][Full Text] [Related]  

  • 10. DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1.
    Jerome LA; Papaioannou VE
    Nat Genet; 2001 Mar; 27(3):286-91. PubMed ID: 11242110
    [TBL] [Abstract][Full Text] [Related]  

  • 11. TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome.
    Merscher S; Funke B; Epstein JA; Heyer J; Puech A; Lu MM; Xavier RJ; Demay MB; Russell RG; Factor S; Tokooya K; Jore BS; Lopez M; Pandita RK; Lia M; Carrion D; Xu H; Schorle H; Kobler JB; Scambler P; Wynshaw-Boris A; Skoultchi AI; Morrow BE; Kucherlapati R
    Cell; 2001 Feb; 104(4):619-29. PubMed ID: 11239417
    [TBL] [Abstract][Full Text] [Related]  

  • 12. TBX1 mutation identified by exome sequencing in a Japanese family with 22q11.2 deletion syndrome-like craniofacial features and hypocalcemia.
    Ogata T; Niihori T; Tanaka N; Kawai M; Nagashima T; Funayama R; Nakayama K; Nakashima S; Kato F; Fukami M; Aoki Y; Matsubara Y
    PLoS One; 2014; 9(3):e91598. PubMed ID: 24637876
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Decreased levels of embryonic retinoic acid synthesis accelerate recovery from arterial growth delay in a mouse model of DiGeorge syndrome.
    Ryckebüsch L; Bertrand N; Mesbah K; Bajolle F; Niederreither K; Kelly RG; Zaffran S
    Circ Res; 2010 Mar; 106(4):686-94. PubMed ID: 20110535
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A Tbx1-Six1/Eya1-Fgf8 genetic pathway controls mammalian cardiovascular and craniofacial morphogenesis.
    Guo C; Sun Y; Zhou B; Adam RM; Li X; Pu WT; Morrow BE; Moon A; Li X
    J Clin Invest; 2011 Apr; 121(4):1585-95. PubMed ID: 21364285
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Tbx1 affects asymmetric cardiac morphogenesis by regulating Pitx2 in the secondary heart field.
    Nowotschin S; Liao J; Gage PJ; Epstein JA; Campione M; Morrow BE
    Development; 2006 Apr; 133(8):1565-73. PubMed ID: 16556915
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The 22q11 deletion: DiGeorge and velocardiofacial syndromes and the role of TBX1.
    Papangeli I; Scambler P
    Wiley Interdiscip Rev Dev Biol; 2013; 2(3):393-403. PubMed ID: 23799583
    [TBL] [Abstract][Full Text] [Related]  

  • 17. p53 Suppression partially rescues the mutant phenotype in mouse models of DiGeorge syndrome.
    Caprio C; Baldini A
    Proc Natl Acad Sci U S A; 2014 Sep; 111(37):13385-90. PubMed ID: 25197075
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genotype and cardiovascular phenotype correlations with TBX1 in 1,022 velo-cardio-facial/DiGeorge/22q11.2 deletion syndrome patients.
    Guo T; McDonald-McGinn D; Blonska A; Shanske A; Bassett AS; Chow E; Bowser M; Sheridan M; Beemer F; Devriendt K; Swillen A; Breckpot J; Digilio MC; Marino B; Dallapiccola B; Carpenter C; Zheng X; Johnson J; Chung J; Higgins AM; Philip N; Simon TJ; Coleman K; Heine-Suner D; Rosell J; Kates W; Devoto M; Goldmuntz E; Zackai E; Wang T; Shprintzen R; Emanuel B; Morrow B;
    Hum Mutat; 2011 Nov; 32(11):1278-89. PubMed ID: 21796729
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Differential DNA binding and transcription modulation by three T-box proteins, T, TBX1 and TBX2.
    Sinha S; Abraham S; Gronostajski RM; Campbell CE
    Gene; 2000 Nov; 258(1-2):15-29. PubMed ID: 11111039
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Dissection of Tbx1 and Fgf interactions in mouse models of 22q11DS suggests functional redundancy.
    Aggarwal VS; Liao J; Bondarev A; Schimmang T; Lewandoski M; Locker J; Shanske A; Campione M; Morrow BE
    Hum Mol Genet; 2006 Nov; 15(21):3219-28. PubMed ID: 17000704
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.