Irene E. Zohn Center for Neuroscience Research, Children's Research Institute Children's National Medical Center Biography Publications Institution JoVE Articles Irene E. Zohn has not added a biography. If you are Irene E. Zohn and would like to personalize this page please email our Author Liaison for assistance. Publications HectD1 E3 Ligase Modifies Adenomatous Polyposis Coli (APC) with Polyubiquitin to Promote the APC-Axin Interaction The Journal of Biological Chemistry. Dec, 2012 | Pubmed ID: 23277359 Does the Cranial Mesenchyme Contribute to Neural Fold Elevation During Neurulation? Birth Defects Research. Part A, Clinical and Molecular Teratology. Oct, 2012 | Pubmed ID: 22945385 Mouse As a Model for Multifactorial Inheritance of Neural Tube Defects Birth Defects Research. Part C, Embryo Today : Reviews. Jun, 2012 | Pubmed ID: 22692891 Hectd1 Regulates Intracellular Localization and Secretion of Hsp90 to Control Cellular Behavior of the Cranial Mesenchyme The Journal of Cell Biology. Mar, 2012 | Pubmed ID: 22431752 The Coiled-coil Domain Containing Protein CCDC40 is Essential for Motile Cilia Function and Left-right Axis Formation Nature Genetics. Jan, 2011 | Pubmed ID: 21131974 The Iron Exporter Ferroportin 1 is Essential for Development of the Mouse Embryo, Forebrain Patterning and Neural Tube Closure Development (Cambridge, England). Sep, 2010 | Pubmed ID: 20702562 The Visceral Yolk Sac Endoderm Provides for Absorption of Nutrients to the Embryo During Neurulation Birth Defects Research. Part A, Clinical and Molecular Teratology. Aug, 2010 | Pubmed ID: 20672346 Transformation by a Nucleotide-activated P2Y Receptor is Mediated by Activation of Galphai, Galphaq and Rho-dependent Signaling Pathways Journal of Molecular Signaling. 2010 | Pubmed ID: 20653955 Modeling Neural Tube Defects in the Mouse Current Topics in Developmental Biology. 2008 | Pubmed ID: 19186242 The Hectd1 Ubiquitin Ligase is Required for Development of the Head Mesenchyme and Neural Tube Closure Developmental Biology. Jun, 2007 | Pubmed ID: 17442300 The Flatiron Mutation in Mouse Ferroportin Acts As a Dominant Negative to Cause Ferroportin Disease Blood. May, 2007 | Pubmed ID: 17289807 P38 and a P38-interacting Protein Are Critical for Downregulation of E-cadherin During Mouse Gastrulation Cell. Jun, 2006 | Pubmed ID: 16751104 Using Genomewide Mutagenesis Screens to Identify the Genes Required for Neural Tube Closure in the Mouse Birth Defects Research. Part A, Clinical and Molecular Teratology. Sep, 2005 | Pubmed ID: 15971254 Cell Polarity Pathways Converge and Extend to Regulate Neural Tube Closure Trends in Cell Biology. Sep, 2003 | Pubmed ID: 12946622 Um ensaio de explante para avaliar o comportamento celular do mesênquima craniana Anjali A. Sarkar1, Irene E. Zohn1 1Center for Neuroscience Research, Children's Research Institute, Children's National Medical Center JoVE 4245 Biologia
Um ensaio de explante para avaliar o comportamento celular do mesênquima craniana Anjali A. Sarkar1, Irene E. Zohn1 1Center for Neuroscience Research, Children's Research Institute, Children's National Medical Center JoVE 4245 Biologia