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Manfred Gessler

Showing results (31-40 of 115) with videos related to

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Genes, Chromosomes & Cancer|February 9, 2008
New prognostic markers revealed by evaluation of genes correlated with clinical parameters in Wilms tumorsStefanie Wittmann, Christina Wunder, Birgit Zirn, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 25, 2004
Phenotypic variability in Hey2 -/- mice and absence of HEY2 mutations in patients with congenital heart defects or Alagille syndromeAndreas Fischer, Barbara Klamt, Nina Schumacher, et al.
Circulation Research|August 4, 2007
Upregulation of soluble vascular endothelial growth factor receptor 1 contributes to angiogenesis defects in the placenta of alpha 2B-adrenoceptor deficient miceVerena Muthig, Ralf Gilsbach, Miriam Haubold, et al.
Molecular Cancer|November 10, 2011
Retinoic acid pathway activity in Wilms tumors and characterization of biological responses in vitroJenny Wegert, Sabrina Bausenwein, Susanne Kneitz, et al.
Development (Cambridge, England)|October 6, 2006
Developmental patterning of the cardiac atrioventricular canal by Notch and Hairy-related transcription factorsJoshua B Rutenberg, Andreas Fischer, Haibo Jia, et al.
Developmental Cell|January 22, 2009
Hey2 regulation by FGF provides a Notch-independent mechanism for maintaining pillar cell fate in the organ of CortiAngelika Doetzlhofer, Martin L Basch, Takahiro Ohyama, et al.
Nature Communications|April 29, 2014
GATA-dependent regulatory switches establish atrioventricular canal specificity during heart developmentSonia Stefanovic, Phil Barnett, Karel van Duijvenboden, et al.
Carcinogenesis|December 17, 2021
The DGCR8 E518K mutation found in Wilms tumors leads to a partial miRNA processing defect that alters gene expression patterns and biological processesRomina Vardapour, Tim Kehl, Susanne Kneitz, et al.
Experimental Cell Research|October 19, 2006
Hypoxia-mediated activation of Dll4-Notch-Hey2 signaling in endothelial progenitor cells and adoption of arterial cell fateHolger Diez, Andreas Fischer, Anja Winkler, et al.
Genes, Chromosomes & Cancer|July 22, 2014
1q gain is a frequent finding in preoperatively treated Wilms tumors, but of limited prognostic value for risk stratification in the SIOP2001/GPOH trialChristian Vokuhl, Wiebke Vogelgesang, Ivo Leuschner, et al.
Pageof 12

Showing results (31-40 of 115) with videos related to

Sort By:
Pageof 12
Genes, Chromosomes & Cancer|February 9, 2008
New prognostic markers revealed by evaluation of genes correlated with clinical parameters in Wilms tumorsStefanie Wittmann, Christina Wunder, Birgit Zirn, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 25, 2004
Phenotypic variability in Hey2 -/- mice and absence of HEY2 mutations in patients with congenital heart defects or Alagille syndromeAndreas Fischer, Barbara Klamt, Nina Schumacher, et al.
Circulation Research|August 4, 2007
Upregulation of soluble vascular endothelial growth factor receptor 1 contributes to angiogenesis defects in the placenta of alpha 2B-adrenoceptor deficient miceVerena Muthig, Ralf Gilsbach, Miriam Haubold, et al.
Molecular Cancer|November 10, 2011
Retinoic acid pathway activity in Wilms tumors and characterization of biological responses in vitroJenny Wegert, Sabrina Bausenwein, Susanne Kneitz, et al.
Development (Cambridge, England)|October 6, 2006
Developmental patterning of the cardiac atrioventricular canal by Notch and Hairy-related transcription factorsJoshua B Rutenberg, Andreas Fischer, Haibo Jia, et al.
Developmental Cell|January 22, 2009
Hey2 regulation by FGF provides a Notch-independent mechanism for maintaining pillar cell fate in the organ of CortiAngelika Doetzlhofer, Martin L Basch, Takahiro Ohyama, et al.
Nature Communications|April 29, 2014
GATA-dependent regulatory switches establish atrioventricular canal specificity during heart developmentSonia Stefanovic, Phil Barnett, Karel van Duijvenboden, et al.
Carcinogenesis|December 17, 2021
The DGCR8 E518K mutation found in Wilms tumors leads to a partial miRNA processing defect that alters gene expression patterns and biological processesRomina Vardapour, Tim Kehl, Susanne Kneitz, et al.
Experimental Cell Research|October 19, 2006
Hypoxia-mediated activation of Dll4-Notch-Hey2 signaling in endothelial progenitor cells and adoption of arterial cell fateHolger Diez, Andreas Fischer, Anja Winkler, et al.
Genes, Chromosomes & Cancer|July 22, 2014
1q gain is a frequent finding in preoperatively treated Wilms tumors, but of limited prognostic value for risk stratification in the SIOP2001/GPOH trialChristian Vokuhl, Wiebke Vogelgesang, Ivo Leuschner, et al.
Pageof 12