Search Results - Mark D Fleming

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  1. 1

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

    Published in Global Public Health (2023-01-01)
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  2. 2

    Congenital sideroblastic anemias: From molecular causes to treatment by Sarah Ducamp, Mark D. Fleming

    Published in HemaSphere (2018-06-01)
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  3. 3

    The ins and outs of erythroid heme transport by Chang Cao, Mark D. Fleming

    Published in Haematologica (2015-06-01)
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  4. 4

    Hemojuvelin is essential for transferrin-dependent and transferrin-independent hepcidin expression in mice by Thomas B. Bartnikas, Mark D. Fleming

    Published in Haematologica (2012-02-01)
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  5. 5

    Defining case management success: a qualitative study of case manager perspectives from a large-scale health and social needs support program by Amanda L Brewster, Margae Knox, Emily E Esteban, Elizabeth A Hernandez, Mark D Fleming, Nadia Safaeinilli

    Published in BMJ Open Quality (2022-06-01)
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  6. 6

    The role of nuclear receptor co-activator 4 in erythropoiesis (Reply to Nai et al.) by Naiara Santana-Codina, Sebastian Gableske, Mark D. Fleming, J. Wade Harper, Alec C. Kimmelman, Joseph D. Mancias

    Published in Haematologica (2019-12-01)
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  7. 7

    Identification and characterization of a novel murine allele of Tmprss6 by Thomas B. Bartnikas, Andrea U. Steinbicker, Dean R. Campagna, Sherika Blevins, Lanette S. Woodward, Carolina Herrera, Kenneth D. Bloch, Monica J. Justice, Mark D. Fleming

    Published in Haematologica (2013-06-01)
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  8. 8

    A competitive enzyme-linked immunosorbent assay specific for murine hepcidin-1: correlation with hepatic mRNA expression in established and novel models of dysregulated iron homeos... by Patrick Gutschow, Paul J. Schmidt, Huiling Han, Vaughn Ostland, Thomas B. Bartnikas, Michael A. Pettiglio, Carolina Herrera, James S. Butler, Elizabeta Nemeth, Tomas Ganz, Mark D. Fleming, Mark Westerman

    Published in Haematologica (2015-02-01)
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  9. 9

    The GLYT1 inhibitor bitopertin mitigates erythroid PPIX production and liver disease in erythroid protoporphyria by Sarah Ducamp, Min Wu, Juan Putra, Dean R. Campagna, Yi Xiang, Vu Hong, Matthew M. Heeney, Amy K. Dickey, Rebecca K. Leaf, Mark D. Fleming, Brian MacDonald, Paul J. Schmidt

    Published in The Journal of Clinical Investigation (2025-09-01)
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  10. 10

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

    Published in Haematologica (2019-07-01)
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  11. 11

    Recurrent heteroplasmy for the MT-ATP6 p.Ser148Asn (m.8969G>A) mutation in patients with syndromic congenital sideroblastic anemia of variable clinical severity by Simon Berhe, Matthew M. Heeney, Dean R. Campagna, John F. Thompson, Eric J. White, Tristen Ross, Roy W. A. Peake, Jeffery D. Hanrahan, Vilmarie Rodriguez, Deborah L. Renaud, Mrinal S. Patnaik, Eugenia Chang, Sylvia S. Bottomley, Mark D. Fleming

    Published in Haematologica (2018-12-01)
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  12. 12

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

    Published in Haematologica (2015-01-01)
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  13. 13

    The phenotypic spectrum of germline YARS2 variants: from isolated sideroblastic anemia to mitochondrial myopathy, lactic acidosis and sideroblastic anemia 2 by Lisa G. Riley, Matthew M. Heeney, Joëlle Rudinger-Thirion, Magali Frugier, Dean R. Campagna, Ronghao Zhou, Gregory A. Hale, Lee M. Hilliard, Joel A. Kaplan, Janet L. Kwiatkowski, Colin A. Sieff, David P. Steensma, Alexander J. Rennings, Annet Simons, Nicolaas Schaap, Richard J. Roodenburg, Tjitske Kleefstra, Leonor Arenillas, Josep Fita-Torró, Rasha Ahmed, Miguel Abboud, Elie Bechara, Roula Farah, Rienk Y. J. Tamminga, Sylvia S. Bottomley, Mayka Sanchez, Gerwin Huls, Dorine W. Swinkels, John Christodoulou, Mark D. Fleming

    Published in Haematologica (2018-12-01)
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  14. 14

    Mitochondrial DNA variant detection in over 6,500 rare disease families by the systematic analysis of exome and genome sequencing data resolves undiagnosed cases by Sarah L. Stenton, Kristen Laricchia, Nicole J. Lake, Sushma Chaluvadi, Vijay Ganesh, Stephanie DiTroia, Ikeoluwa Osei-Owusu, Lynn Pais, Emily O’Heir, Christina Austin-Tse, Melanie O’Leary, Mayada Abu Shanap, Chelsea Barrows, Seth Berger, Carsten G. Bönnemann, Kinga M. Bujakowska, Dean R. Campagna, Alison G. Compton, Sandra Donkervoort, Mark D. Fleming, Lyndon Gallacher, Joseph G. Gleeson, Goknur Haliloglu, Eric A. Pierce, Emily M. Place, Vijay G. Sankaran, Akiko Shimamura, Zornitza Stark, Tiong Yang Tan, David R. Thorburn, Susan M. White, Maha S. Zaki, Eric Vilain, Monkol Lek, Heidi L. Rehm, Anne O’Donnell-Luria

    Published in HGG Advances (2025-07-01)
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