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Neoplasia (New York, N.Y.)|December 27, 2021
Sustained experimental activation of FGF8/ERK in the developing chicken spinal cord models early events in ERK-mediated tumorigenesisAxelle Wilmerding, Lauranne Bouteille, Nathalie Caruso, et al.
Neurotoxicology and Teratology|June 9, 2005
Human neural tube defects: developmental biology, epidemiology, and geneticsEric R Detrait, Timothy M George, Heather C Etchevers, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|October 8, 2015
Cardiac outflow morphogenesis depends on effects of retinoic acid signaling on multiple cell lineagesNicolas El Robrini, Heather C Etchevers, Lucile Ryckebüsch, et al.
Scientific Reports|December 14, 2019
Epigenetic deregulation of GATA3 in neuroblastoma is associated with increased GATA3 protein expression and with poor outcomesBader Almutairi, Jessica Charlet, Anthony R Dallosso, et al.
Plos One|February 4, 2012
ISL1 directly regulates FGF10 transcription during human cardiac outflow formationChristelle Golzio, Emmanuelle Havis, Philippe Daubas, et al.
Prenatal Diagnosis|November 1, 2006
Cytogenetic and histological features of a human embryo with homogeneous chromosome 8 trisomyChristelle Golzio, Jessica Guirchoun, Catherine Ozilou, et al.
Frontiers in Cell and Developmental Biology|November 10, 2022
Multiple congenital malformations arise from somatic mosaicism for constitutively active Pik3ca signalingElise Marechal, Anne Poliard, Kilian Henry, et al.
Human Molecular Genetics|August 12, 2008
Human neural crest cells display molecular and phenotypic hallmarks of stem cellsSophie Thomas, Marie Thomas, Patrick Wincker, et al.
Birth Defects Research|January 10, 2018
Widespread dynamic and pleiotropic expression of the melanocortin-1-receptor (MC1R) system is conserved across chick, mouse and human embryonic developmentAnna C Thomas, Pauline Heux, Chloe Santos, et al.
Pigment Cell & Melanoma Research|January 10, 2018
Giant congenital melanocytic nevus with vascular malformation and epidermal cysts associated with a somatic activating mutation in BRAFHeather C Etchevers, Christian Rose, Birgit Kahle, et al.
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