檢索結果 - Anoop K. Sendamarai

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  1. 1
    Structure of the membrane proximal oxidoreductase domain of human Steap3, the dominant ferrireductase of the erythroid transferrin cycle

    Structure of the membrane proximal oxidoreductase domain of human Steap3, the dominant ferrireductase of the erythroid transferrin cycle 由 Anoop K. Sendamarai, Robert S. Ohgami, Mark D. Fleming, C. Martin Lawrence

    出版 2008
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  2. 2
    The Crystal Structure of Six-transmembrane Epithelial Antigen of the Prostate 4 (Steap4), a Ferri/Cuprireductase, Suggests a Novel Interdomain Flavin-binding Site

    The Crystal Structure of Six-transmembrane Epithelial Antigen of the Prostate 4 (Steap4), a Ferri/Cuprireductase, Suggests a Novel Interdomain Flavin-binding Site 由 George H. Gauss, Mark D. Kleven, Anoop K. Sendamarai, Mark D. Fleming, C. Martin Lawrence

    出版 2013
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  3. 3
    An RNAi therapeutic targeting Tmprss6 decreases iron overload in Hfe−/− mice and ameliorates anemia and iron overload in murine β-thalassemia intermedia

    An RNAi therapeutic targeting Tmprss6 decreases iron overload in Hfe−/− mice and ameliorates anemia and iron overload in murine β-thalassemia intermedia 由 Paul J. Schmidt, Iva Toudjarska, Anoop K. Sendamarai, Tim Racie, Stuart Milstein, Brian R. Bettencourt, Julia Hettinger, David Bumcrot, Mark D. Fleming

    出版 2012
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  4. 4
    Downregulation of ribosome biogenesis during early forebrain development

    Downregulation of ribosome biogenesis during early forebrain development 由 Kevin F. Chau, Morgan L. Shannon, Ryann M. Fame, Erin Fonseca, Hillary Mullan, Matthew B. Johnson, Anoop K. Sendamarai, Mark W. Springel, Benoît Laurent, Maria K. Lehtinen

    出版 2018
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  5. 5
    Lack of Gdf11 does not improve anemia or prevent the activity of RAP-536 in a mouse model of β-thalassemia

    Lack of Gdf11 does not improve anemia or prevent the activity of RAP-536 in a mouse model of β-thalassemia 由 Amaliris Guerra, Paraskevi Rea Oikonomidou, Sayantani Sinha, Jianbing Zhang, Vania Lo Presti, Callum R. Hamilton, Laura Breda, Carla Casu, Ping La, Ana C. Martins, Anoop K. Sendamarai, Mark D. Fleming, Stefano Rivella

    出版 2019
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  6. 6
    Pseudouridine synthase 1 deficient mice, a model for Mitochondrial Myopathy with Sideroblastic Anemia, exhibit muscle morphology and physiology alterations

    Pseudouridine synthase 1 deficient mice, a model for Mitochondrial Myopathy with Sideroblastic Anemia, exhibit muscle morphology and physiology alterations 由 Joshua E. Mangum, Justin P. Hardee, Dennis K. Fix, Melissa Puppa, Johnathon Elkes, Diego Altomare, Yelena Bykhovskaya, Dean R. Campagna, Paul J. Schmidt, Anoop K. Sendamarai, Hart G.W. Lidov, Shayne C. Barlow, Nathan Fischel‐Ghodsian, Mark D. Fleming, James A. Carson, Jeffrey R. Patton

    出版 2016
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  7. 7
    UBE2O remodels the proteome during terminal erythroid differentiation

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

    出版 2017
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  8. 8
    X‐linked sideroblastic anemia due to ALAS2 intron 1 enhancer element GATA‐binding site mutations

    X‐linked sideroblastic anemia due to ALAS2 intron 1 enhancer element GATA‐binding site mutations 由 Dean R. Campagna, Charlotte I. de Bie, Klaus Schmitz‐Abe, Marion Sweeney, Anoop K. Sendamarai, Paul J. Schmidt, Matthew M. Heeney, Helger G. Yntema, Caroline Kannengiesser, Bernard Grandchamp, Charlotte M. Niemeyer, Nine Knoers, Sonia Swart, Gordon Marron, Richard van Wijk, Reinier Raymakers, Alison May, Kyriacos Markianos, Sylvia S. Bottomley, Dorine W. Swinkels, Mark D. Fleming

    出版 2013
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  9. 9
    Bone marrow failure unresponsive to bone marrow transplant is caused by mutations in thrombopoietin

    Bone marrow failure unresponsive to bone marrow transplant is caused by mutations in thrombopoietin 由 Aaron Seo, Miri Ben‐Harosh, Mehtap Sirin, Jerry Stein, Orly Dgany, Joseph Kaplelushnik, Manfred Hoenig, Ulrich Pannicke, Myriam Ricarda Lorenz, Klaus Schwarz, Clemens Stockklausner, Tom Walsh, Süleyman Gülsüner, Ming K. Lee, Anoop K. Sendamarai, Marilyn Sánchez-Bonilla, Mary‐Claire King, Holger Cario, Andreas E. Kulozik, Klaus‐Michael Debatin, Ansgar Schulz, Hannah Tamary, Akiko Shimamura

    出版 2017
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  10. 10
    Congenital sideroblastic anemia due to mutations in the mitochondrial HSP70 homologue HSPA9

    Congenital sideroblastic anemia due to mutations in the mitochondrial HSP70 homologue HSPA9 由 Klaus Schmitz‐Abe, Szymon J. Ciesielski, Paul J. Schmidt, Dean R. Campagna, Fedik Rahimov, Brenda Schilke, Marloes Cuijpers, Klaus Rieneck, Birgitte Lausen, Michael Linenberger, Anoop K. Sendamarai, Chaoshe Guo, Inga Hofmann, Peter E. Newburger, Dana C. Matthews, Akiko Shimamura, Pieter J.L.M. Snijders, Meghan C. Towne, Charlotte M. Niemeyer, Henry G. Watson, Morten Hanefeld Dziegiel, Matthew M. Heeney, Alison May, Sylvia S. Bottomley, Dorine W. Swinkels, Kyriacos Markianos, Elizabeth A. Craig, Mark D. Fleming

    出版 2015
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  11. 11
    Mutations in TRNT1 cause congenital sideroblastic anemia with immunodeficiency, fevers, and developmental delay (SIFD)

    Mutations in TRNT1 cause congenital sideroblastic anemia with immunodeficiency, fevers, and developmental delay (SIFD) 由 Pranesh Chakraborty, Klaus Schmitz‐Abe, Erin K. Kennedy, Hapsatou Mamady, Thierry Naas, Danielle Durie, Dean R. Campagna, Ashley Lau, Anoop K. Sendamarai, Daniel H. Wiseman, Alison May, Stephen Jolles, Philip Connor, Colin Powell, Matthew M. Heeney, Patricia-Jane Giardina, Robert J. Klaassen, Caroline Kannengiesser, Isabelle Thuret, Alexis A. Thompson, Lino Marques, Stephen Hughes, Denise Bonney, Sylvia S. Bottomley, Robert Wynn, Ronald M. Laxer, Caterina P. Minniti, John Moppett, Victoria Bordon, Michael T. Geraghty, Paul B. M. Joyce, Kyriacos Markianos, Adam D. Rudner, Martin Holčı́k, Mark D. Fleming

    出版 2014
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  12. 12
    Genome-wide association study of thoracic aortic aneurysm and dissection in the Million Veteran Program

    Genome-wide association study of thoracic aortic aneurysm and dissection in the Million Veteran Program 由 Derek Klarin, Poornima Devineni, Anoop K. Sendamarai, Anthony R. Angueira, Sarah E. Graham, Ying H. Shen, Michael G. Levin, James P. Pirruccello, Ida Surakka, Purushotham Karnam, Tanmoy Roychowdhury, Yanming Li, Minxian Wang, Krishna G. Aragam, Kaavya Paruchuri, Verena Zuber, Gabrielle Shakt, Noah L. Tsao, Renae Judy, Ha My T. Vy, Shefali S. Verma, Daniel J. Rader, Ron Do, Joseph E. Bavaria, Girish N. Nadkarni, Marylyn D. Ritchie, Stephen Burgess, Dongchuan Guo, Patrick T. Ellinor, Scott A. LeMaire, Dianna M. Milewicz, Cristen J. Willer, Pradeep Natarajan, Philip S. Tsao, Saiju Pyarajan, Scott M. Damrauer

    出版 2023
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  13. 13
    Regulatory variants in TCF7L2 are associated with thoracic aortic aneurysm

    Regulatory variants in TCF7L2 are associated with thoracic aortic aneurysm 由 Tanmoy Roychowdhury, Haocheng Lu, Whitney Hornsby, Bradley Crone, Gao T. Wang, Dongchuan Guo, Anoop K. Sendamarai, Poornima Devineni, Maoxuan Lin, Wei Zhou, Sarah E. Graham, Brooke N. Wolford, Ida Surakka, Zhenguo Wang, Lin Chang, Jifeng Zhang, Michael R. Mathis, Chad M. Brummett, Tori L. Melendez, Michael J. Shea, Karen Meekyong Kim, G. Michael Deeb, Himanshu J. Patel, Jonathan L. Eliason, Kim A. Eagle, Bo Yang, Santhi K. Ganesh, Ben Brumpton, Bjørn Olav Åsvold, Anne Heidi Skogholt, Kristian Hveem, Saiju Pyarajan, Derek Klarin, Philip S. Tsao, Scott M. Damrauer, Suzanne M. Leal, Dianna M. Milewicz, Y. Eugene Chen, Minerva T. Garcia-Barrio, Cristen J. Willer

    出版 2021
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