Suchergebnisse - Etchevers, Heather C. 

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

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

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Cutaneous Melanomas Arising during Childhood: An Overview of the Main Entities von 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 von 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 von 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 von 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 von 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 von 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 von 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 von 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 von 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 von 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 von 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 von 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 von 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 von 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 von 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 von 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 von 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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