Canlyniadau Chwilio - Etchevers, Heather C. 

The hedgehog pathway and ocular developmental anomalies gan Cavodeassi, Florencia, Creuzet, Sophie, Etchevers, Heather C.

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Outflow Tract Formation—Embryonic Origins of Conotruncal Congenital Heart Disease gan Stefanovic, Sonia, Etchevers, Heather C., Zaffran, Stéphane

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Cutaneous Melanomas Arising during Childhood: An Overview of the Main Entities gan de la Fouchardière, Arnaud, Boivin, Felix, Etchevers, Heather C., Macagno, Nicolas

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Sustained experimental activation of FGF8/ERK in the developing chicken spinal cord models early events in ERK-mediated tumorigenesis gan Wilmerding, Axelle, Bouteille, Lauranne, Caruso, Nathalie, Bidaut, Ghislain, Etchevers, Heather C., Graba, Yacine, Delfini, Marie-Claire

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Human Neural Tube Defects: Developmental Biology, Epidemiology, and Genetics gan Detrait, Eric.R., George, Timothy. M., Etchevers, Heather.C., Gilbert, John.R., Vekemans, Michel., Speer, Marcy. C.

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Epigenetic deregulation of GATA3 in neuroblastoma is associated with increased GATA3 protein expression and with poor outcomes gan Almutairi, Bader, Charlet, Jessica, Dallosso, Anthony R., Szemes, Marianna, Etchevers, Heather C., Malik, Karim T. A., Brown, Keith W.

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ISL1 Directly Regulates FGF10 Transcription during Human Cardiac Outflow Formation gan Golzio, Christelle, Havis, Emmanuelle, Daubas, Philippe, Nuel, Gregory, Babarit, Candice, Munnich, Arnold, Vekemans, Michel, Zaffran, Stéphane, Lyonnet, Stanislas, Etchevers, Heather C.

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Human neural crest cells display molecular and phenotypic hallmarks of stem cells gan Thomas, Sophie, Thomas, Marie, Wincker, Patrick, Babarit, Candice, Xu, Puting, Speer, Marcy C., Munnich, Arnold, Lyonnet, Stanislas, Vekemans, Michel, Etchevers, Heather C.

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Widespread dynamic and pleiotropic expression of the melanocortin‐1‐receptor (MC1R) system is conserved across chick, mouse and human embryonic development gan Thomas, Anna C., Heux, Pauline, Santos, Chloe, Arulvasan, Wisenave, Solanky, Nita, Carey, Magalie E., Gerrelli, Dianne, Kinsler, Veronica A., Etchevers, Heather C.

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Analysis of mouse models carrying the I26T and R160C substitutions in the transcriptional repressor HESX1 as models for septo-optic dysplasia and hypopituitarism gan Sajedi, Ezat, Gaston-Massuet, Carles, Signore, Massimo, Andoniadou, Cynthia L., Kelberman, Daniel, Castro, Sandra, Etchevers, Heather C., Gerrelli, Dianne, Dattani, Mehul T., Martinez-Barbera, Juan Pedro

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Genome‐wide DNA methylation analysis identifies MEGF10 as a novel epigenetically repressed candidate tumor suppressor gene in neuroblastoma gan Charlet, Jessica, Tomari, Ayumi, Dallosso, Anthony R., Szemes, Marianna, Kaselova, Martina, Curry, Thomas J., Almutairi, Bader, Etchevers, Heather C., McConville, Carmel, Malik, Karim T. A., Brown, Keith W.

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A severe clinical phenotype of Noonan syndrome with neonatal hypertrophic cardiomyopathy in the second case worldwide with RAF1 S259Y neomutation gan Jaouadi, Hager, Chehida, Amel Ben, Kraoua, Lilia, Etchevers, Heather C., Argiro, Laurent, Kasdallah, Nadia, Blibech, Sonia, Delague, Valérie, Lévy, Nicolas, Tebib, Néji, Mrad, Ridha, Abdelhak, Sonia, Benkhalifa, Rym, Zaffran, Stéphane

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Matthew-Wood Syndrome Is Caused by Truncating Mutations in the Retinol-Binding Protein Receptor Gene STRA6 gan Golzio, Christelle , Martinovic-Bouriel, Jelena , Thomas, Sophie , Mougou-Zrelli, Soumaya , Grattagliano-Bessières, Bettina , Bonnière, Maryse , Delahaye, Sophie , Munnich, Arnold , Encha-Razavi, Férechté , Lyonnet, Stanislas , Vekemans, Michel , Attié-Bitach, Tania , Etchevers, Heather C. 

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Somatotroph Tumors and the Epigenetic Status of the GNAS Locus gan Romanet, Pauline, Galluso, Justine, Kamenicky, Peter, Hage, Mirella, Theodoropoulou, Marily, Roche, Catherine, Graillon, Thomas, Etchevers, Heather C., De Murat, Daniel, Mougel, Grégory, Figarella-Branger, Dominique, Dufour, Henry, Cuny, Thomas, Assié, Guillaume, Barlier, Anne

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A Subpopulation of Smooth Muscle Cells, Derived from Melanocyte-Competent Precursors, Prevents Patent Ductus Arteriosus gan Yajima, Ichiro, Colombo, Sophie, Puig, Isabel, Champeval, Delphine, Kumasaka, Mayuko, Belloir, Elodie, Bonaventure, Jacky, Mark, Manuel, Yamamoto, Hiroaki, Taketo, Mark M., Choquet, Philippe, Etchevers, Heather C., Beermann, Friedrich, Delmas, Véronique, Monassier, Laurent, Larue, Lionel

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Loss-of-Function Mutation in the Dioxygenase-Encoding FTO Gene Causes Severe Growth Retardation and Multiple Malformations gan Boissel, Sarah, Reish, Orit, Proulx, Karine, Kawagoe-Takaki, Hiroko, Sedgwick, Barbara, Yeo, Giles S.H., Meyre, David, Golzio, Christelle, Molinari, Florence, Kadhom, Noman, Etchevers, Heather C., Saudek, Vladimir, Farooqi, I. Sadaf, Froguel, Philippe, Lindahl, Tomas, O'Rahilly, Stephen, Munnich, Arnold, Colleaux, Laurence

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SNPs in the neural cell adhesion molecule 1 gene (NCAM1) may be associated with human neural tube defects gan Deak, Kristen L., Boyles, Abee L., Etchevers, Heather C., Melvin, Elizabeth C., Siegel, Deborah G., Graham, Felicia L., Slifer, Susan H., Enterline, David S., George, Timothy M., Vekemans, Michel, McClay, David, Bassuk, Alexander G., Kessler, John A., Linney, Elwood, Gilbert, John R., Speer, Marcy C.

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Targeted resequencing identifies PTCH1 as a major contributor to ocular developmental anomalies and extends the SOX2 regulatory network gan Chassaing, Nicolas, Davis, Erica E., McKnight, Kelly L., Niederriter, Adrienne R., Causse, Alexandre, David, Véronique, Desmaison, Annaïck, Lamarre, Sophie, Vincent-Delorme, Catherine, Pasquier, Laurent, Coubes, Christine, Lacombe, Didier, Rossi, Massimiliano, Dufier, Jean-Louis, Dollfus, Helene, Kaplan, Josseline, Katsanis, Nicholas, Etchevers, Heather C., Faguer, Stanislas, Calvas, Patrick

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Macrophage-derived IL-1β and TNF-α regulate arginine metabolism in neuroblastoma gan Fultang, Livingstone, Gamble, Laura D., Gneo, Luciana, Berry, Andrea M., Egan, Sharon A., De Bie, Fenna, Yogev, Orli, Eden, Georgina L., Booth, Sarah, Brownhill, Samantha, Vardon, Ashley, McConville, Carmel M., Cheng, Paul N., Norris, Murray D., Etchevers, Heather C., Murray, Jayne, Ziegler, David S., Chesler, Louis, Schmidt, Ronny, Burchill, Susan A., Haber, Michelle, De Santo, Carmela, Mussai, Francis

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