Search Results - Etchevers, Heather C. 

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  1. 1
    The hedgehog pathway and ocular developmental anomalies

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

    Published 2018
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  2. 2
    Outflow Tract Formation—Embryonic Origins of Conotruncal Congenital Heart Disease

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

    Published 2021
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  3. 3
    Cutaneous Melanomas Arising during Childhood: An Overview of the Main Entities

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

    Published 2021
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  4. 4
    Sustained experimental activation of FGF8/ERK in the developing chicken spinal cord models early events in ERK-mediated tumorigenesis

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

    Published 2021
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  5. 5
    Human Neural Tube Defects: Developmental Biology, Epidemiology, and Genetics

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

    Published 2005
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  6. 6
    Epigenetic deregulation of GATA3 in neuroblastoma is associated with increased GATA3 protein expression and with poor outcomes

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

    Published 2019
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  7. 7
    ISL1 Directly Regulates FGF10 Transcription during Human Cardiac Outflow Formation

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

    Published 2012
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  8. 8
    Human neural crest cells display molecular and phenotypic hallmarks of stem cells

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

    Published 2008
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  9. 9
    Widespread dynamic and pleiotropic expression of the melanocortin‐1‐receptor (MC1R) system is conserved across chick, mouse and human embryonic development

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

    Published 2018
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  10. 10
    Analysis of mouse models carrying the I26T and R160C substitutions in the transcriptional repressor HESX1 as models for septo-optic dysplasia and hypopituitarism

    Analysis of mouse models carrying the I26T and R160C substitutions in the transcriptional repressor HESX1 as models for septo-optic dysplasia and hypopituitarism by 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

    Published 2008
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  11. 11
    Genome‐wide DNA methylation analysis identifies MEGF10 as a novel epigenetically repressed candidate tumor suppressor gene in neuroblastoma

    Genome‐wide DNA methylation analysis identifies MEGF10 as a novel epigenetically repressed candidate tumor suppressor gene in neuroblastoma by 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.

    Published 2016
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  12. 12
    A severe clinical phenotype of Noonan syndrome with neonatal hypertrophic cardiomyopathy in the second case worldwide with RAF1 S259Y neomutation

    A severe clinical phenotype of Noonan syndrome with neonatal hypertrophic cardiomyopathy in the second case worldwide with RAF1 S259Y neomutation by 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

    Published 2019
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  13. 13
    Matthew-Wood Syndrome Is Caused by Truncating Mutations in the Retinol-Binding Protein Receptor Gene STRA6

    Matthew-Wood Syndrome Is Caused by Truncating Mutations in the Retinol-Binding Protein Receptor Gene STRA6 by 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. 

    Published 2007
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  14. 14
    Somatotroph Tumors and the Epigenetic Status of the GNAS Locus

    Somatotroph Tumors and the Epigenetic Status of the GNAS Locus by 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

    Published 2021
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  15. 15
    A Subpopulation of Smooth Muscle Cells, Derived from Melanocyte-Competent Precursors, Prevents Patent Ductus Arteriosus

    A Subpopulation of Smooth Muscle Cells, Derived from Melanocyte-Competent Precursors, Prevents Patent Ductus Arteriosus by 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

    Published 2013
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  16. 16
    Loss-of-Function Mutation in the Dioxygenase-Encoding FTO Gene Causes Severe Growth Retardation and Multiple Malformations

    Loss-of-Function Mutation in the Dioxygenase-Encoding FTO Gene Causes Severe Growth Retardation and Multiple Malformations by 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

    Published 2009
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  17. 17
    SNPs in the neural cell adhesion molecule 1 gene (NCAM1) may be associated with human neural tube defects

    SNPs in the neural cell adhesion molecule 1 gene (NCAM1) may be associated with human neural tube defects by 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.

    Published 2005
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  18. 18
    Targeted resequencing identifies PTCH1 as a major contributor to ocular developmental anomalies and extends the SOX2 regulatory network

    Targeted resequencing identifies PTCH1 as a major contributor to ocular developmental anomalies and extends the SOX2 regulatory network by 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

    Published 2016
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  19. 19
    Macrophage-derived IL-1β and TNF-α regulate arginine metabolism in neuroblastoma

    Macrophage-derived IL-1β and TNF-α regulate arginine metabolism in neuroblastoma by 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

    Published 2018
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