These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

139 related articles for article (PubMed ID: 30803943)

  • 41. The arterial pole of the mouse heart forms from Fgf10-expressing cells in pharyngeal mesoderm.
    Kelly RG; Brown NA; Buckingham ME
    Dev Cell; 2001 Sep; 1(3):435-40. PubMed ID: 11702954
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Pulmonary endoderm, second heart field and the morphogenesis of distal outflow tract in mouse embryonic heart.
    Liang S; Li HC; Wang YX; Wu SS; Cai YJ; Cui HL; Yang YP; Ya J
    Dev Growth Differ; 2014 May; 56(4):276-92. PubMed ID: 24697670
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Myocardial progenitors in the pharyngeal regions migrate to distinct conotruncal regions.
    Takahashi M; Terasako Y; Yanagawa N; Kai M; Yamagishi T; Nakajima Y
    Dev Dyn; 2012 Feb; 241(2):284-93. PubMed ID: 22184055
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Mesoderm progenitor cells of common origin contribute to the head musculature and the cardiac outflow tract.
    Tirosh-Finkel L; Elhanany H; Rinon A; Tzahor E
    Development; 2006 May; 133(10):1943-53. PubMed ID: 16624859
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Live imaging of heart tube development in mouse reveals alternating phases of cardiac differentiation and morphogenesis.
    Ivanovitch K; Temiño S; Torres M
    Elife; 2017 Dec; 6():. PubMed ID: 29202929
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Inositol 1,4,5-trisphosphate receptors are essential for the development of the second heart field.
    Nakazawa M; Uchida K; Aramaki M; Kodo K; Yamagishi C; Takahashi T; Mikoshiba K; Yamagishi H
    J Mol Cell Cardiol; 2011 Jul; 51(1):58-66. PubMed ID: 21382375
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Numb family proteins: novel players in cardiac morphogenesis and cardiac progenitor cell differentiation.
    Wu M; Li J
    Biomol Concepts; 2015 Apr; 6(2):137-48. PubMed ID: 25883210
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Fgf8 is required for anterior heart field development.
    Ilagan R; Abu-Issa R; Brown D; Yang YP; Jiao K; Schwartz RJ; Klingensmith J; Meyers EN
    Development; 2006 Jun; 133(12):2435-45. PubMed ID: 16720880
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Retinoic acid regulates differentiation of the secondary heart field and TGFbeta-mediated outflow tract septation.
    Li P; Pashmforoush M; Sucov HM
    Dev Cell; 2010 Mar; 18(3):480-5. PubMed ID: 20230754
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Cadm4 restricts the production of cardiac outflow tract progenitor cells.
    Zeng XX; Yelon D
    Cell Rep; 2014 May; 7(4):951-60. PubMed ID: 24813897
    [TBL] [Abstract][Full Text] [Related]  

  • 51.
    Stefanovic S; Laforest B; Desvignes JP; Lescroart F; Argiro L; Maurel-Zaffran C; Salgado D; Plaindoux E; De Bono C; Pazur K; Théveniau-Ruissy M; Béroud C; Puceat M; Gavalas A; Kelly RG; Zaffran S
    Elife; 2020 Aug; 9():. PubMed ID: 32804075
    [TBL] [Abstract][Full Text] [Related]  

  • 52. The contribution of Islet1-expressing splanchnic mesoderm cells to distinct branchiomeric muscles reveals significant heterogeneity in head muscle development.
    Nathan E; Monovich A; Tirosh-Finkel L; Harrelson Z; Rousso T; Rinon A; Harel I; Evans SM; Tzahor E
    Development; 2008 Feb; 135(4):647-57. PubMed ID: 18184728
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Vangl2-regulated polarisation of second heart field-derived cells is required for outflow tract lengthening during cardiac development.
    Ramsbottom SA; Sharma V; Rhee HJ; Eley L; Phillips HM; Rigby HF; Dean C; Chaudhry B; Henderson DJ
    PLoS Genet; 2014 Dec; 10(12):e1004871. PubMed ID: 25521757
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Clonal analysis reveals a common origin between nonsomite-derived neck muscles and heart myocardium.
    Lescroart F; Hamou W; Francou A; Théveniau-Ruissy M; Kelly RG; Buckingham M
    Proc Natl Acad Sci U S A; 2015 Feb; 112(5):1446-51. PubMed ID: 25605943
    [TBL] [Abstract][Full Text] [Related]  

  • 55. The AP-1 transcription factor component Fosl2 potentiates the rate of myocardial differentiation from the zebrafish second heart field.
    Jahangiri L; Sharpe M; Novikov N; González-Rosa JM; Borikova A; Nevis K; Paffett-Lugassy N; Zhao L; Adams M; Guner-Ataman B; Burns CE; Burns CG
    Development; 2016 Jan; 143(1):113-22. PubMed ID: 26732840
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Pbx4 limits heart size and fosters arch artery formation by partitioning second heart field progenitors and restricting proliferation.
    Holowiecki A; Linstrum K; Ravisankar P; Chetal K; Salomonis N; Waxman JS
    Development; 2020 Mar; 147(5):. PubMed ID: 32094112
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Visualization of outflow tract development in the absence of Tbx1 using an FgF10 enhancer trap transgene.
    Kelly RG; Papaioannou VE
    Dev Dyn; 2007 Mar; 236(3):821-8. PubMed ID: 17238155
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Right ventricular myocardium derives from the anterior heart field.
    Zaffran S; Kelly RG; Meilhac SM; Buckingham ME; Brown NA
    Circ Res; 2004 Aug; 95(3):261-8. PubMed ID: 15217909
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Commitment, differentiation, and diversification of avian cardiac progenitor cells.
    Melnik N; Yutzey KE; Gannon M; Bader D
    Ann N Y Acad Sci; 1995 Mar; 752():1-8. PubMed ID: 7755245
    [No Abstract]   [Full Text] [Related]  

  • 60.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.