BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

158 related articles for article (PubMed ID: 34050709)

  • 1. Setd5 is required in cardiopharyngeal mesoderm for heart development and its haploinsufficiency is associated with outflow tract defects in mouse.
    Cheung MY; Roberts C; Scambler P; Stathopoulou A
    Genesis; 2021 Aug; 59(7-8):e23421. PubMed ID: 34050709
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Single cell multi-omic analysis identifies a Tbx1-dependent multilineage primed population in murine cardiopharyngeal mesoderm.
    Nomaru H; Liu Y; De Bono C; Righelli D; Cirino A; Wang W; Song H; Racedo SE; Dantas AG; Zhang L; Cai CL; Angelini C; Christiaen L; Kelly RG; Baldini A; Zheng D; Morrow BE
    Nat Commun; 2021 Nov; 12(1):6645. PubMed ID: 34789765
    [TBL] [Abstract][Full Text] [Related]  

  • 3. HIC2 is a novel dosage-dependent regulator of cardiac development located within the distal 22q11 deletion syndrome region.
    Dykes IM; van Bueren KL; Ashmore RJ; Floss T; Wurst W; Szumska D; Bhattacharya S; Scambler PJ
    Circ Res; 2014 Jun; 115(1):23-31. PubMed ID: 24748541
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Loss of CXCL12/CXCR4 signalling impacts several aspects of cardiovascular development but does not exacerbate Tbx1 haploinsufficiency.
    Page M; Ridge L; Gold Diaz D; Tsogbayar T; Scambler PJ; Ivins S
    PLoS One; 2018; 13(11):e0207251. PubMed ID: 30408103
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Prdm1 functions in the mesoderm of the second heart field, where it interacts genetically with Tbx1, during outflow tract morphogenesis in the mouse embryo.
    Vincent SD; Mayeuf-Louchart A; Watanabe Y; Brzezinski JA; Miyagawa-Tomita S; Kelly RG; Buckingham M
    Hum Mol Genet; 2014 Oct; 23(19):5087-101. PubMed ID: 24821700
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mesodermal expression of Moz is necessary for cardiac septum development.
    Vanyai HK; Thomas T; Voss AK
    Dev Biol; 2015 Jul; 403(1):22-9. PubMed ID: 25912687
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 22q11 deletion syndrome: a role for TBX1 in pharyngeal and cardiovascular development.
    Scambler PJ
    Pediatr Cardiol; 2010 Apr; 31(3):378-90. PubMed ID: 20054531
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Tbx1 regulates fibroblast growth factors in the anterior heart field through a reinforcing autoregulatory loop involving forkhead transcription factors.
    Hu T; Yamagishi H; Maeda J; McAnally J; Yamagishi C; Srivastava D
    Development; 2004 Nov; 131(21):5491-502. PubMed ID: 15469978
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Mapping cellular processes in the mesenchyme during palatal development in the absence of Tbx1 reveals complex proliferation changes and perturbed cell packing and polarity.
    Brock LJ; Economou AD; Cobourne MT; Green JB
    J Anat; 2016 Mar; 228(3):464-73. PubMed ID: 26689739
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Epiblastic Cited2 deficiency results in cardiac phenotypic heterogeneity and provides a mechanism for haploinsufficiency.
    MacDonald ST; Bamforth SD; Chen CM; Farthing CR; Franklyn A; Broadbent C; Schneider JE; Saga Y; Lewandoski M; Bhattacharya S
    Cardiovasc Res; 2008 Aug; 79(3):448-57. PubMed ID: 18440989
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Identification of a Tbx1/Tbx2/Tbx3 genetic pathway governing pharyngeal and arterial pole morphogenesis.
    Mesbah K; Rana MS; Francou A; van Duijvenboden K; Papaioannou VE; Moorman AF; Kelly RG; Christoffels VM
    Hum Mol Genet; 2012 Mar; 21(6):1217-29. PubMed ID: 22116936
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Failed Progenitor Specification Underlies the Cardiopharyngeal Phenotypes in a Zebrafish Model of 22q11.2 Deletion Syndrome.
    Guner-Ataman B; González-Rosa JM; Shah HN; Butty VL; Jeffrey S; Abrial M; Boyer LA; Burns CG; Burns CE
    Cell Rep; 2018 Jul; 24(5):1342-1354.e5. PubMed ID: 30067987
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Tbx1 coordinates addition of posterior second heart field progenitor cells to the arterial and venous poles of the heart.
    Rana MS; Théveniau-Ruissy M; De Bono C; Mesbah K; Francou A; Rammah M; Domínguez JN; Roux M; Laforest B; Anderson RH; Mohun T; Zaffran S; Christoffels VM; Kelly RG
    Circ Res; 2014 Oct; 115(9):790-9. PubMed ID: 25190705
    [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. Mesodermal expression of Tbx1 is necessary and sufficient for pharyngeal arch and cardiac outflow tract development.
    Zhang Z; Huynh T; Baldini A
    Development; 2006 Sep; 133(18):3587-95. PubMed ID: 16914493
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Tbx1 has a dual role in the morphogenesis of the cardiac outflow tract.
    Xu H; Morishima M; Wylie JN; Schwartz RJ; Bruneau BG; Lindsay EA; Baldini A
    Development; 2004 Jul; 131(13):3217-27. PubMed ID: 15175244
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Haploinsufficiency of the intellectual disability gene SETD5 disturbs developmental gene expression and cognition.
    Deliu E; Arecco N; Morandell J; Dotter CP; Contreras X; Girardot C; Käsper EL; Kozlova A; Kishi K; Chiaradia I; Noh KM; Novarino G
    Nat Neurosci; 2018 Dec; 21(12):1717-1727. PubMed ID: 30455454
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Left pulmonary artery in 22q11.2 deletion syndrome. Echocardiographic evaluation in patients without cardiac defects and role of Tbx1 in mice.
    Mastromoro G; Calcagni G; Versacci P; Putotto C; Chinali M; Lambiase C; Unolt M; Pelliccione E; Anaclerio S; Caprio C; Cioffi S; Bilio M; Baban A; Drago F; Digilio MC; Marino B; Baldini A
    PLoS One; 2019; 14(4):e0211170. PubMed ID: 30933971
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.