Localization and Kinetics of the Transferrin-Dependent Iron Transport Machinery in the Mouse Placenta

por Cao, Chang, Fleming, Mark D
Publicado 2021

Congenital sideroblastic anemias: From molecular causes to treatment

por Ducamp, Sarah, Fleming, Mark D.
Publicado 2018

Neutrality, conflict, and structural determinants of health in a Jerusalem emergency department

por Orr, Zvika, Jackson, Levi, Alpert, Evan Avraham, Fleming, Mark D.
Publicado 2022

Combination therapy with a Tmprss6 RNAi-therapeutic and the oral iron chelator deferiprone additively diminishes secondary iron overload in a mouse model of β-thalassemia intermedi...

por Schmidt, Paul J, Racie, Tim, Westerman, Mark, Fitzgerald, Kevin, Butler, James S, Fleming, Mark D
Publicado 2015

SIRT3 regulates cellular iron metabolism and cancer growth by repressing iron regulatory protein 1

por Jeong, Seung Min, Lee, Jaewon, Schmidt, Paul J., Fleming, Mark D., Haigis, Marcia C.
Publicado 2014

Radioactive seed localization for excision of non-palpable in-transit metastatic melanoma

por Fleming, Mark D., Pockaj, Barbara A., Hansen, Adam J., Gray, Richard J., Patel, Maitray D.
Publicado 2015

Defining case management success: a qualitative study of case manager perspectives from a large-scale health and social needs support program

por Knox, Margae, Esteban, Emily E, Hernandez, Elizabeth A, Fleming, Mark D, Safaeinilli, Nadia, Brewster, Amanda L
Publicado 2022

Conceptualizing the effective mechanisms of a social needs case management program shown to reduce hospital use: a qualitative study

por Fleming, Mark D., Safaeinili, Nadia, Knox, Margae, Hernandez, Elizabeth, Esteban, Emily E., Sarkar, Urmimala, Brewster, Amanda L.
Publicado 2022

Association of Shelter-in-Place Hotels With Health Services Use Among People Experiencing Homelessness During the COVID-19 Pandemic

por Fleming, Mark D., Evans, Jennifer L., Graham-Squire, Dave, Cawley, Caroline, Kanzaria, Hemal K., Kushel, Margot B., Raven, Maria C.
Publicado 2022

Management of double carotid blowout with definitive repair after temporizing stent graft placement

por Cocca, Alexandra T., Levy, Brittany E., Castle, Jennifer T., Wilt, Wesley S., Fleming, Mark D., Kejner, Alexandra E., Aouad, Rony K., Tyagi, Samuel C.
Publicado 2022

The developmental stage of the hematopoietic niche regulates lineage in MLL-rearranged leukemia

por Rowe, R. Grant, Lummertz da Rocha, Edroaldo, Sousa, Patricia, Missios, Pavlos, Morse, Michael, Marion, William, Yermalovich, Alena, Barragan, Jessica, Mathieu, Ronald, Jha, Deepak Kumar, Fleming, Mark D., North, Trista E., Daley, George Q.
Publicado 2019

NCOA4 maintains murine erythropoiesis via cell autonomous and non-autonomous mechanisms

por Santana-Codina, Naiara, Gableske, Sebastian, del Rey, Maria Quiles, 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.
Publicado 2019

Pseudouridine synthase 1 deficient mice, a model for Mitochondrial Myopathy with Sideroblastic Anemia, exhibit muscle morphology and physiology alterations

por Mangum, Joshua E., Hardee, Justin P., Fix, Dennis K., Puppa, Melissa J., Elkes, Johnathon, Altomare, Diego, Bykhovskaya, Yelena, Campagna, Dean R., Schmidt, Paul J., Sendamarai, Anoop K., Lidov, Hart G. W., Barlow, Shayne C., Fischel-Ghodsian, Nathan, Fleming, Mark D., Carson, James A., Patton, Jeffrey R.
Publicado 2016

Evidence in the UK Biobank for the underdiagnosis of erythropoietic protoporphyria

por Dickey, Amy K., Quick, Corbin, Ducamp, Sarah, Zhu, Zhaozhong, Feng, Yen-Chen A., Naik, Hetanshi, Balwani, Manisha, Anderson, Karl E., Lin, Xihong, Phillips, John E., Rebeiz, Lina, Bonkovsky, Herbert L., McGuire, Brendan M., Wang, Bruce, Chasman, Daniel I., Smoller, Jordan W., Fleming, Mark D., Christiani, David C.
Publicado 2020

Hematologic complications with age in Shwachman-Diamond syndrome

por Furutani, Elissa, Liu, Shanshan, Galvin, Ashley, Steltz, Sarah, Malsch, Maggie M., Loveless, Sara K., Mount, Leann, Larson, Jordan H., Queenan, Kelan, Bertuch, Alison A., Fleming, Mark D., Gansner, John M., Geddis, Amy E., Hanna, Rabi, Keel, Sioban B., Lau, Bonnie W., Lipton, Jeffrey M., Lorsbach, Robert, Nakano, Taizo A., Vlachos, Adrianna, Wang, Winfred C., Davies, Stella M., Weller, Edie, Myers, Kasiani C., Shimamura, Akiko
Publicado 2022

A missense mutation in TFRC, encoding transferrin receptor 1, causes combined immunodeficiency

por 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.
Publicado 2015

Mitochondrial Atpif1 regulates heme synthesis in developing erythroblasts

por Shah, Dhvanit I., Takahashi-Makise, Naoko, Cooney, Jeffrey D., Li, Liangtao, Schultz, Iman J., Pierce, Eric L., Narla, Anupama, Seguin, Alexandra, Hattangadi, Shilpa M., Medlock, Amy E., Langer, Nathaniel B., Dailey, Tamara A., Hurst, Slater N., Faccenda, Danilo, Wiwczar, Jessica M., Heggers, Spencer K., Vogin, Guillaume, Chen, Wen, Chen, Caiyong, Campagna, Dean R., Brugnara, Carlo, Zhou, Yi, Ebert, Benjamin L., Danial, Nika N., Fleming, Mark D., Ward, Diane M., Campanella, Michelangelo, Dailey, Harry A., Kaplan, Jerry, Paw, Barry H.
Publicado 2012

The phenotypic spectrum of germline YARS2 variants: from isolated sideroblastic anemia to mitochondrial myopathy, lactic acidosis and sideroblastic anemia 2

por Riley, Lisa G., Heeney, Matthew M., Rudinger-Thirion, Joëlle, Frugier, Magali, Campagna, Dean R., Zhou, Ronghao, Hale, Gregory A., Hilliard, Lee M., Kaplan, Joel A., Kwiatkowski, Janet L., Sieff, Colin A., Steensma, David P., Rennings, Alexander J., Simons, Annet, Schaap, Nicolaas, Roodenburg, Richard J., Kleefstra, Tjitske, Arenillas, Leonor, Fita-Torró, Josep, Ahmed, Rasha, Abboud, Miguel, Bechara, Elie, Farah, Roula, Tamminga, Rienk Y. J., Bottomley, Sylvia S., Sanchez, Mayka, Huls, Gerwin, Swinkels, Dorine W., Christodoulou, John, Fleming, Mark D.
Publicado 2018

Hepcidin-Mediated Hypoferremia Disrupts Immune Responses to Vaccination and Infection

por Frost, Joe N., Tan, Tiong Kit, Abbas, Munawar, Wideman, Sarah K., Bonadonna, Michael, Stoffel, Nicole U., Wray, Katherine, Kronsteiner, Barbara, Smits, Gaby, Campagna, Dean R., Duarte, Tiago L., Lopes, José M., Shah, Akshay, Armitage, Andrew E., Arezes, João, Lim, Pei Jin, Preston, Alexandra E., Ahern, David, Teh, Megan, Naylor, Caitlin, Salio, Mariolina, Gileadi, Uzi, Andrews, Simon C., Dunachie, Susanna J., Zimmermann, Michael B., van der Klis, Fiona R.M., Cerundolo, Vincenzo, Bannard, Oliver, Draper, Simon J., Townsend, Alain R.M., Galy, Bruno, Fleming, Mark D., Lewis, Marie C., Drakesmith, Hal
Publicado 2021

Distinct genetic pathways define pre-malignant versus compensatory clonal hematopoiesis in Shwachman-Diamond syndrome

por 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
Publicado 2021