The molecular genetics of sideroblastic anemia von Ducamp, Sarah, Fleming, Mark D.

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Distinct genetic pathways define pre-malignant versus compensatory clonal hematopoiesis in Shwachman-Diamond syndrome von Kennedy, Alyssa L., Myers, Kasiani C., Bowman, James, Gibson, Christopher J., Camarda, Nicholas D., Furutani, Elissa, Muscato, Gwen M., Klein, Robert H., Ballotti, Kaitlyn, Liu, Shanshan, Harris, Chad E., Galvin, Ashley, Malsch, Maggie, Dale, David, Gansner, John M., Nakano, Taizo A., Bertuch, Alison, Vlachos, Adrianna, Lipton, Jeffrey M., Castillo, Paul, Connelly, James, Churpek, Jane, Edwards, John R., Hijiya, Nobuko, Ho, Richard H., Hofmann, Inga, Huang, James N., Keel, Siobán, Lamble, Adam, Lau, Bonnie W., Norkin, Maxim, Stieglitz, Elliot, Stock, Wendy, Walkovich, Kelly, Boettcher, Steffen, Brendel, Christian, Fleming, Mark D., Davies, Stella M., Weller, Edie A., Bahl, Christopher, Carter, Scott L., Shimamura, Akiko, Lindsley, R. Coleman

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Medical neutrality and structural competency in conflict zones: Israeli healthcare professionals' reaction to political violence von Orr, Zvika, Fleming, Mark D.

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Congenital sideroblastic anemias: iron and heme lost in mitochondrial translation von Fleming, Mark D

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Regulation of progenitor cell proliferation and granulocyte function by microRNA-223 von Johnnidis, Jonathan B., Harris, Marian H., Wheeler, Robert T., Stehling-Sun, Sandra, Lam, Michael H., Kirak, Oktay, Brummelkamp, Thijn R., Fleming, Mark D., Camargo, Fernando D.

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HRG1 Is Essential for Heme Transport from the Phagolysosome of Macrophages during Erythrophagocytosis von White, Carine, Yuan, Xiaojing, Schmidt, Paul J., Bresciani, Erica, Samuel, Tamika K., Campagna, Dean, Hall, Caitlin, Bishop, Kevin, Calicchio, Monica L., Lapierre, Ariane, Ward, Diane M., Liu, Paul, Fleming, Mark D., Hamza, Iqbal

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Recurrent BRAF mutations in Langerhans cell histiocytosis von Badalian-Very, Gayane, Vergilio, Jo-Anne, Degar, Barbara A., MacConaill, Laura E., Brandner, Barbara, Calicchio, Monica L., Kuo, Frank C., Ligon, Azra H., Stevenson, Kristen E., Kehoe, Sarah M., Garraway, Levi A., Hahn, William C., Meyerson, Matthew, Fleming, Mark D., Rollins, Barrett J.

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A missense mutation in TFRC, encoding transferrin receptor 1, causes combined immunodeficiency von Jabara, Haifa H, Boyden, Steven E, Chou, Janet, Ramesh, Narayanaswamy, Massaad, Michel J, Benson, Halli, Bainter, Wayne, Fraulino, David, Rahimov, Fedik, Sieff, Colin, Liu, Zhi-Jian, Alshemmari, Salem H, Al-Ramadi, Basel K, Al-Dhekri, Hasan, Arnaout, Rand, Abu-Shukair, Mohammad, Vatsayan, Anant, Silver, Eli, Ahuja, Sanjay, Davies, E Graham, Sola-Visner, Martha, Ohsumi, Toshiro K, Andrews, Nancy C, Notarangelo, Luigi D, Fleming, Mark D, Al-Herz, Waleed, Kunkel, Louis M, Geha, Raif S

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Low iron promotes megakaryocytic commitment of megakaryocytic-erythroid progenitors in humans and mice von Xavier-Ferrucio, Juliana, Scanlon, Vanessa, Li, Xiuqi, Zhang, Ping-Xia, Lozovatsky, Larisa, Ayala-Lopez, Nadia, Tebaldi, Toma, Halene, Stephanie, Cao, Chang, Fleming, Mark D., Finberg, Karin E., Krause, Diane S.

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UBE2O remodels the proteome during terminal erythroid differentiation von Nguyen, Anthony T., Prado, Miguel A., Schmidt, Paul J., Sendamarai, Anoop K., Wilson-Grady, Joshua T., Min, Mingwei, Campagna, Dean R., Tian, Geng, Shi, Yuan, Dederer, Verena, Kawan, Mona, Kuehnle, Nathalie, Paulo, Joao A., Yao, Yu, Weiss, Mitchell J., Justice, Monica J., Gygi, Steven P., Fleming, Mark D., Finley, Daniel

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The Steap proteins are metalloreductases von Ohgami, Robert S., Campagna, Dean R., McDonald, Alice, Fleming, Mark D.

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NCOA4 maintains murine erythropoiesis via cell autonomous and non-autonomous mechanisms von Santana-Codina, Naiara, Gableske, Sebastian, Rey, Maria Quiles Del, Małachowska, Beata, Jedrychowski, Mark P, Biancur, Douglas E, Schmidt, Paul J, Fleming, Mark D, Fendler, Wojciech, Harper, J Wade, Kimmelman, Alec C, Mancias, Joseph D

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The IRP1-HIF-2α Axis Coordinates Iron and Oxygen Sensing with Erythropoiesis and Iron Absorption von Anderson, Sheila A., Nizzi, Christopher P., Chang, Yuan-I., Deck, Kathryn M., Schmidt, Paul J., Galy, Bruno, Damnernsawad, Alisa, Broman, Aimee T., Kendziorski, Christina, Hentze, Matthias W., Fleming, Mark D., Zhang, Jing, Eisenstein, Richard S.

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Mutations in TMPRSS6 cause iron-refractory iron deficiency anemia (IRIDA) von Finberg, Karin E, Heeney, Matthew M, Campagna, Dean R, Aydınok, Yeşim, Pearson, Howard A, Hartman, Kip R, Mayo, Mary M, Samuel, Stewart M, Strouse, John J, Markianos, Kyriacos, Andrews, Nancy C, Fleming, Mark D

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Cdk5rap2 regulates centrosome function and chromosome segregation in neuronal progenitors von Lizarraga, Sofia B, Margossian, Steven P, Harris, Marian H, Campagna, Dean R, Han, An-Ping, Blevins, Sherika, Mudbhary, Raksha, Barker, Jane E, Walsh, Christopher A, Fleming, Mark D

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Differing impact of the deletion of hemochromatosis‐associated molecules HFE and transferrin receptor‐2 on the iron phenotype of mice lacking bone morphogenetic protein 6 or hemoju... von Latour, Chloé, Besson‐Fournier, Céline, Meynard, Delphine, Silvestri, Laura, Gourbeyre, Ophélie, Aguilar‐Martinez, Patricia, Schmidt, Paul J., Fleming, Mark D., Roth, Marie‐Paule, Coppin, Hélène

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Neutrality, conflict, and structural determinants of health in a Jerusalem emergency department von Orr, Zvika, Jackson, Levi, Alpert, Evan Avraham, Fleming, Mark D

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Genomic analysis of bone marrow failure and myelodysplastic syndromes reveals phenotypic and diagnostic complexity von Zhang, Michael Y, Keel, Siobán B, Walsh, Tom, Lee, Ming K, Gulsuner, Suleyman, Watts, Amanda C, Pritchard, Colin C, Salipante, Stephen J, Jeng, Michael R, Hofmann, Inga, Williams, David A, Fleming, Mark D, Abkowitz, Janis L, King, Mary-Claire, Shimamura, Akiko

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Perturbation of hepcidin expression by BMP type I receptor deletion induces iron overload in mice von Steinbicker, Andrea U., Bartnikas, Thomas B., Lohmeyer, Lisa K., Leyton, Patricio, Mayeur, Claire, Kao, Sonya M., Pappas, Alexandra E., Peterson, Randall T., Bloch, Donald B., Yu, Paul B., Fleming, Mark D., Bloch, Kenneth D.

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Conceptualizing the effective mechanisms of a social needs case management program shown to reduce hospital use: a qualitative study von Fleming, Mark D, Safaeinili, Nadia, Knox, Margae, Hernandez, Elizabeth, Esteban, Emily E, Sarkar, Urmimala, Brewster, Amanda L

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