Showing results (1-10 of 43) with videos related to
Sort By:
Pageof 5
Neurogenetics|August 31, 2006
Current perspectives on the genetic causes of neural tube defectsPatrizia De Marco, Elisa Merello, Samantha Mascelli, et al.Birth Defects Research. Part A, Clinical and Molecular Teratology|February 29, 2012
Role of the planar cell polarity gene CELSR1 in neural tube defects and caudal agenesisRedouane Allache, Patrizia De Marco, Elisa Merello, et al.Biofactors (Oxford, England)|June 16, 2011
Human neural tube defects: genetic causes and preventionPatrizia De Marco, Elisa Merello, Armando Cama, et al.European Journal of Medical Genetics|October 8, 2013
Novel MNX1 mutations and clinical analysis of familial and sporadic Currarino casesElisa Merello, Patrizia De Marco, Marcello Ravegnani, et al.Birth Defects Research. Part A, Clinical and Molecular Teratology|September 10, 2014
Genetic studies of ANKRD6 as a molecular switch between Wnt signaling pathways in human neural tube defectsRedouane Allache, Mingqin Wang, Patrizia De Marco, et al.Birth Defects Research. Part A, Clinical and Molecular Teratology|May 20, 2014
Planar cell polarity gene mutations contribute to the etiology of human neural tube defects in our populationPatrizia De Marco, Elisa Merello, Gianluca Piatelli, et al.Birth Defects Research. Part A, Clinical and Molecular Teratology|September 15, 2015
Role of the planar cell polarity gene Protein tyrosine kinase 7 in neural tube defects in humansMingqin Wang, Patrizia De Marco, Elisa Merello, et al.Journal of Leukocyte Biology|December 20, 2007
Hypoxia transcriptionally induces macrophage-inflammatory protein-3alpha/CCL-20 in primary human mononuclear phagocytes through nuclear factor (NF)-kappaBFlorinda Battaglia, Silvana Delfino, Elisa Merello, et al.Birth Defects Research. Part A, Clinical and Molecular Teratology|July 10, 2013
Rare missense variants in DVL1, one of the human counterparts of the Drosophila dishevelled gene, do not confer increased risk for neural tube defectsElisa Merello, Zoha Kibar, Redouane Allache, et al.Human Mutation|November 3, 2011
FZD6 is a novel gene for human neural tube defectsPatrizia De Marco, Elisa Merello, Andrea Rossi, et al.Pageof 5