Ets-1 is essential for connective tissue growth factor (CTGF/CCN2) induction by TGF-β1 in osteoblasts von Geisinger, Max T, Astaiza, Randy, Butler, Tiffany, Popoff, Steven N, Planey, Sonia Lobo, Arnott, John A

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AFAP1 Is a Novel Downstream Mediator of TGF-β1 for CCN2 Induction in Osteoblasts von Cho, Youngjin, Silverstein, Rachel, Geisinger, Max T, Martinkovich, Stephen, Corkill, Holly, Cunnick, Jess M, Planey, Sonia L, Arnott, John A

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Natural history of the aortic root in Tetralogy of Fallot after repair von Kim, Yuli Y., Geisinger, Max T., Bhamare, Tanmay, Wasserman, Melissa, Min, Jungwon, Goldmuntz, Elizabeth

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CCN2 induction by TGF‐β1 requires osteoblast specific promoter motifs (541.6) von Martinkovich, Stephen, Silverstein, Rachel, Geisinger, Max, Planey, Sonia, Arnott, John

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AFAP1 Is a Novel Downstream Mediator of TGF-[beta]1 for CCN2 Induction in Osteoblasts von Cho, Youngjin, Silverstein, Rachel, Geisinger, Max T, Martinkovich, Stephen, Corkill, Holly, Cunnick, Jess M, Planey, Sonia L, Arnott, John A

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Ets-1 Is Essential for Connective Tissue Growth Factor Induction by TGF-[beta]1 in Osteoblasts von Geisinger, Max T, Astaiza, Randy, Butler, Tiffany, Popoff, Steven N, Planey, Sonia Lobo, Arnott, John A

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Ets-1 Is Essential for Connective Tissue Growth Factor von Geisinger, Max T, Astaiza, Randy, Butler, Tiffany, Popoff, Steven N, Planey, Sonia Lobo, Arnott, John A

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CTGF/CCN2 induction by TGF‐1 β requires Ets‐1 in osteoblasts von Arnott, John, Geisinger, Max, Astaiza, Randy, Butler, Tiffany, Popoff, Steven, Planey, Sonia

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Abstract 16273: Natural History of Aortic Growth After Tetralogy of Fallot Repair von Geisinger, Max T, Min, Jungwon W, Bhamare, Tanmay, Awh, Katherine, Edman, Sharon, Wasserman, Melissa, Goldmuntz, Elizabeth, Kim, Yuli Y

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AFAP1 Is a Novel Downstream Mediator of TGF- square 1 for CCN2 Induction in Osteoblasts: e0136712 von Cho, Youngjin, Silverstein, Rachel, Geisinger, Max T, Martinkovich, Stephen, Corkill, Holly, Cunnick, Jess M, Planey, Sonia L, Arnott, John A

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GWAS of serum ALT and AST reveals an association of SLC30A10 Thr95Ile with hypermanganesemia symptoms von Ward, Lucas D., Tu, Ho-Chou, Quenneville, Chelsea B., Tsour, Shira, Flynn-Carroll, Alexander O., Parker, Margaret M., Deaton, Aimee M., Haslett, Patrick A. J., Lotta, Luca A., Verweij, Niek, Ferreira, Manuel A. R., Baras, Aris, Hinkle, Gregory, Nioi, Paul

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Gene-level analysis of rare variants in 379,066 whole exome sequences identifies an association of GIGYF1 loss of function with type 2 diabetes von Deaton, Aimee M., Parker, Margaret M., Ward, Lucas D., Flynn-Carroll, Alexander O., BonDurant, Lucas, Hinkle, Gregory, Akbari, Parsa, Lotta, Luca A., Baras, Aris, Nioi, Paul

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