Search Results - Naveh, Natali

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  1. 1
    The role of CTCF in the organization of the centromeric 11p15 imprinted domain interactome

    The role of CTCF in the organization of the centromeric 11p15 imprinted domain interactome by Naveh, Natali S Sobel, Deegan, Daniel F, Huhn, Jacklyn, Traxler, Emily, Lan, Yemin, Weksberg, Rosanna, Ganguly, Arupa, Engel, Nora, Kalish, Jennifer M

    Published in Nucleic acids research
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  2. 2
    Cancer predisposition signaling in Beckwith-Wiedemann Syndrome drives Wilms tumor development

    Cancer predisposition signaling in Beckwith-Wiedemann Syndrome drives Wilms tumor development by Nirgude, Snehal, Naveh, Natali S. Sobel, Kavari, Sanam L., Traxler, Emily M., Kalish, Jennifer M.

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  3. 3
    Derivation and investigation of the first human cell-based model of Beckwith-Wiedemann syndrome

    Derivation and investigation of the first human cell-based model of Beckwith-Wiedemann syndrome by Chang, Suhee, Hur, Stella K., Naveh, Natali S. Sobel, Thorvaldsen, Joanne L., French, Deborah L., Gagne, Alyssa L, Jobaliya, Chintan D., Anguera, Montserrat C., Bartolomei, Marisa S., Kalish, Jennifer M

    Published in Epigenetics
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  4. 4
    Molecular networks of hepatoblastoma predisposition and oncogenesis in Beckwith‐Wiedemann syndrome

    Molecular networks of hepatoblastoma predisposition and oncogenesis in Beckwith‐Wiedemann syndrome by Sobel Naveh, Natali S., Traxler, Emily M., Duffy, Kelly A., Kalish, Jennifer M.

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  5. 5
    Abstract A008: Cancer predisposition signaling pathways drive Beckwith-Wiedemann syndrome Wilms tumor oncogenesis

    Abstract A008: Cancer predisposition signaling pathways drive Beckwith-Wiedemann syndrome Wilms tumor oncogenesis by Nirgude, Snehal Dinkar, Naveh, Natali Sobel, Kavai, Sanam, Kalish, Jennifer

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  6. 6
    Abstract 6045: Methylation differences in cancer signaling pathways drive Beckwith-Wiedemann Syndrome Wilms Tumor oncogenesis

    Abstract 6045: Methylation differences in cancer signaling pathways drive Beckwith-Wiedemann Syndrome Wilms Tumor oncogenesis by Naveh, Natali Sobel, Traxler, Emily, Nirgude, Snehal, Kalish, Jennifer

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  7. 7
    PSMD11 loss-of-function variants correlate with a neurobehavioral phenotype, obesity, and increased interferon response

    PSMD11 loss-of-function variants correlate with a neurobehavioral phenotype, obesity, and increased interferon response by Deb, Wallid, Rosenfelt, Cory, Vignard, Virginie, Papendorf, Jonas Johannes, Möller, Sophie, Wendlandt, Martin, Studencka-Turski, Maja, Cogné, Benjamin, Besnard, Thomas, Ruffier, Léa, Toutain, Bérénice, Poirier, Léa, Cuinat, Silvestre, Kritzer, Amy, Crunk, Amy, diMonda, Janette, Vengoechea, Jaime, Mercier, Sandra, Kleinendorst, Lotte, van Haelst, Mieke M., Zuurbier, Linda, Sulem, Telma, Katrínardóttir, Hildigunnur, Friðriksdóttir, Rún, Sulem, Patrick, Stefansson, Kari, Jonsdottir, Berglind, Zeidler, Shimriet, Sinnema, Margje, Stegmann, Alexander P.A., Naveh, Natali, Skraban, Cara M., Gray, Christopher, Murrell, Jill R., Isikay, Sedat, Pehlivan, Davut, Calame, Daniel G., Posey, Jennifer E., Nizon, Mathilde, McWalter, Kirsty, Lupski, James R., Isidor, Bertrand, Bolduc, François V., Bézieau, Stéphane, Krüger, Elke, Küry, Sébastien, Ebstein, Frédéric

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