| An RNAi therapeutic targeting Tmprss6 decreases iron overload in Hfe−/− mice and ameliorates anemia and iron overload in murine β-thalassemia intermedia PJ Schmidt, I Toudjarska, AK Sendamarai, T Racie, S Milstein, ... Blood, The Journal of the American Society of Hematology 121 (7), 1200-1208, 2013 | 210 | 2013 |
| Mutations in TRNT1 cause congenital sideroblastic anemia with immunodeficiency, fevers, and developmental delay (SIFD) PK Chakraborty, K Schmitz-Abe, EK Kennedy, H Mamady, T Naas, ... Blood, The Journal of the American Society of Hematology 124 (18), 2867-2871, 2014 | 194 | 2014 |
| UBE2O remodels the proteome during terminal erythroid differentiation AT Nguyen, MA Prado, PJ Schmidt, AK Sendamarai, JT Wilson-Grady, ... Science 357 (6350), eaan0218, 2017 | 129 | 2017 |
| Structure of the membrane proximal oxidoreductase domain of human Steap3, the dominant ferrireductase of the erythroid transferrin cycle AK Sendamarai, RS Ohgami, MD Fleming, CM Lawrence Proceedings of the National Academy of Sciences 105 (21), 7410-7415, 2008 | 107 | 2008 |
| Atomic structure of the 75 MDa extremophile Sulfolobus turreted icosahedral virus determined by CryoEM and X-ray crystallography D Veesler, TS Ng, AK Sendamarai, BJ Eilers, CM Lawrence, SM Lok, ... Proceedings of the National Academy of Sciences 110 (14), 5504-5509, 2013 | 94 | 2013 |
| Downregulation of ribosome biogenesis during early forebrain development KF Chau, ML Shannon, RM Fame, E Fonseca, H Mullan, MB Johnson, ... Elife 7, e36998, 2018 | 92 | 2018 |
| Congenital sideroblastic anemia due to mutations in the mitochondrial HSP70 homologue HSPA9 K Schmitz-Abe, SJ Ciesielski, PJ Schmidt, DR Campagna, F Rahimov, ... Blood, The Journal of the American Society of Hematology 126 (25), 2734-2738, 2015 | 80 | 2015 |
| Lack of Gdf11 does not improve anemia or prevent the activity of RAP-536 in a mouse model of β-thalassemia A Guerra, PR Oikonomidou, S Sinha, J Zhang, V Lo Presti, CR Hamilton, ... Blood, The Journal of the American Society of Hematology 134 (6), 568-572, 2019 | 55 | 2019 |
| X‐linked sideroblastic anemia due to ALAS2 intron 1 enhancer element GATA‐binding site mutations DR Campagna, CI de Bie, K Schmitz‐Abe, M Sweeney, AK Sendamarai, ... American journal of hematology 89 (3), 315-319, 2014 | 49 | 2014 |
| Bone marrow failure unresponsive to bone marrow transplant is caused by mutations in thrombopoietin A Seo, M Ben-Harosh, M Sirin, J Stein, O Dgany, J Kaplelushnik, ... Blood, The Journal of the American Society of Hematology 130 (7), 875-880, 2017 | 48 | 2017 |
| A recurring mutation in the respiratory complex 1 protein NDUFB11 is responsible for a novel form of X-linked sideroblastic anemia DA Lichtenstein, AW Crispin, AK Sendamarai, DR Campagna, ... Blood, The Journal of the American Society of Hematology 128 (15), 1913-1917, 2016 | 46 | 2016 |
| The crystal structure of six-transmembrane epithelial antigen of the prostate 4 (Steap4), a ferri/cuprireductase, suggests a novel interdomain flavin-binding site GH Gauss, MD Kleven, AK Sendamarai, MD Fleming, CM Lawrence Journal of Biological Chemistry 288 (28), 20668-20682, 2013 | 41 | 2013 |
| Pseudouridine synthase 1 deficient mice, a model for Mitochondrial Myopathy with Sideroblastic Anemia, exhibit muscle morphology and physiology alterations JE Mangum, JP Hardee, DK Fix, MJ Puppa, J Elkes, D Altomare, ... Scientific reports 6 (1), 26202, 2016 | 32 | 2016 |
| Indolent T-lymphoblastic proliferation with disseminated multinodal involvement and partial CD33 expression RS Ohgami, AK Sendamarai, SK Atwater, M Liedtke, MD Fleming, ... The American Journal of Surgical Pathology 38 (9), 1298-1304, 2014 | 24 | 2014 |
| Mutations in the iron-sulfur cluster biogenesis protein HSCB cause congenital sideroblastic anemia A Crispin, C Guo, C Chen, DR Campagna, PJ Schmidt, D Lichtenstein, ... The Journal of clinical investigation 130 (10), 5245-5256, 2020 | 20 | 2020 |
| Hscb, a Mitochondrial Iron-Sulfur Cluster Assembly Co-Chaperone, Is a Novel Candidate Gene for Congenital Sideroblastic Anemia A Crispin, P Schmidt, D Campagna, C Cao, D Lichtenstein, A Sendamarai, ... Blood, The Journal of the American Society of Hematology 130 (Suppl_1), 79-79, 2017 | 7 | 2017 |
| Mutations in TRNT1, encoding the CCA-adding enzyme, cause congenital sideroblastic anemia with B cell immunodeficiency, periodic fevers and developmental delay (SIFD) PK Chakraborty, K Schmitz-Abe, EK Kennedy, H Mamady, T Naas, ... Blood 5 (2014), 08, 2014 | 4 | 2014 |
| Conditional Synthetic Lethality between the Initial Steps of Heme Biosynthesis and Pyridoxine Metabolism during Erythropoiesis S Ducamp, A Sendamarai, MD Fleming Blood 140 (Supplement 1), 5346-5347, 2022 | 2 | 2022 |
| X-linked sideroblastic anemia due to ALAS2 intron 1 enhancer element GATA-binding site mutations (vol 89, pg 315, 2014) DR Campagna, CI de Bie, K Schmitz-Abe, M Sweeney, AK Sendamarai, ... AMERICAN JOURNAL OF HEMATOLOGY 89 (6), 670-670, 2014 | 2 | 2014 |
| Abstract PR10: FBXO11 is recurrently mutated in Burkitt lymphoma and its inactivation accelerates lymphomagenesis in Eμ-myc mice C Pighi, M Compagno, TC Cheong, T Poggio, Q Wang, F Langellotto, ... Clinical Cancer Research 23 (24_Supplement), PR10-PR10, 2017 | 1 | 2017 |
John E. JohnsonThe Scripps Research InstituteVerified email at scripps.edu
