Search Results - "Suragani, Rajasekhar NVS"

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    Biological basis for efficacy of activin receptor ligand traps in myelodysplastic syndromes by Verma, Amit, Suragani, Rajasekhar Nvs, Aluri, Srinivas, Shah, Nishi, Bhagat, Tushar D, Alexander, Mark J, Komrokji, Rami, Kumar, Ravi

    Published in The Journal of clinical investigation (01-02-2020)
    “…Signaling by the TGF-β superfamily is important in the regulation of hematopoiesis and is dysregulated in myelodysplastic syndromes (MDSs), contributing to…”
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    Journal Article
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    TGFb1 Antagonist Inhibits Fibrosis in a Murine Model of Myelofibrosis by Suragani, Rajasekhar NVS, Martinez, Pedro A., Cawley, Sharon M, Li, Robert, Pearsall, Robert Scott, Kumar, Ravindra

    Published in Blood (03-12-2015)
    “…Introduction: Myelofibrosis (MF) is a clonal stem cell disorder that originates from acquired mutations in the hematopoietic stem cells leading to abnormal…”
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    Rap-536 (Murine ACE-536/Luspatercept) Inhibits Smad2/3 Signaling and Promotes Erythroid Differentiation By Restoring GATA-1 Function in Murine b-Thalassemia by Martinez, Pedro A., Suragani, Rajasekhar NVS, Bhasin, Manoj, Li, Robert, Pearsall, Robert Scott, Kumar, Ravindra

    Published in Blood (03-12-2015)
    “…We have previously reported that Smad2/3 signaling (of the TGFβ superfamily) is elevated in myelodysplastic syndromes (MDS) and β-thalassemia, diseases that…”
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    Modified Actriib-Fc Fusion Protein (ACE-536) Mitigates Sickling and Red Cell Pathology in a Murine Model of Sickle Cell Disease by Suragani, Rajasekhar NVS, Li, Robert, Cawley, Sharon M, Pearsall, R. Scott, Kumar, Ravindra

    Published in Blood (06-12-2014)
    “…Sickle cell disease (SCD) is a debilitating hereditary disorder caused by a single point mutation in the β-globin gene resulting in the production of sickle…”
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    Genetic Investigation of the Role of GDF11 in the Treatment of β-Thalassemia and MDS by Oikonomidou, Paraskevi Rea, La, Ping, Gupta, Ritama, Lo Presti, Vania, Casu, Carla, Breda, Laura, Watson, Deborah, Suragani, Rajasekhar NVS, Kumar, Ravindra, Rivella, Stefano

    Published in Blood (02-12-2016)
    “…The current treatment of β-thalassemia only partially mitigates the phenotype of the disease, making the need for novel therapeutic agents imperative. The…”
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    Modified Activin Receptor Type IIb-Fc Fusion Protein (RAP-536) Decreases Anemia In a Murine Model Of Myelodysplastic Syndrome and Improves Overall Survival by Suragani, Rajasekhar NVS, Li, Robert, Cawley, Sharon, Pearsall, R. Scott, Kumar, Ravi

    Published in Blood (15-11-2013)
    “…Myelodysplastic syndromes (MDS) are caused due to abnormal proliferation and differentiation of pluripotent hematopoietic stem cells leading to peripheral…”
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    RAP-536 Promotes Terminal Erythroid Differentiation and Reduces Anemia in Myelodysplastic Syndromes by Suragani, Rajasekhar NVS, Mulivor, Aaron, Pearsall, R. Scott, Kumar, Ravindra

    Published in Blood (18-11-2011)
    “…Abstract 610 Myelodysplatic syndromes (MDS) are a heterogeneous group of hematopoietic stem cell disorders characterized by ineffective hematopoiesis. Patients…”
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    ACE-536 Improves Ineffective Erythropoiesis, Anemia and Co-Morbidities in β-Thalassemia by Suragani, Rajasekhar NVS, Li, Robert, Cawley, Sharon, Rivella, Stefano, Pearsall, R. Scott, Kumar, Ravindra

    Published in Blood (16-11-2012)
    “…Abstract 248 β-thalassemia, the most common congenital anemia, is caused by mutations in β-globin gene resulting in partial or complete absence of β-globin…”
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    RAP-536 Promotes Terminal Erythroid Differentiation and Reduces Anemia in a Murine Model of Myelodysplastic Syndromes by Suragani, Rajasekhar NVS, Li, Robert, Sako, Dianne, Grinberg, Asya, Pearsall, R. Scott, Kumar, Ravindra

    Published in Blood (16-11-2012)
    “…Abstract 3796 Myelodysplastic syndromes (MDS) are a group of hematopoietic stem cell disorders characterized by peripheral blood cytopenias such as anemia,…”
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    Haem‐regulated eIF2α kinase is necessary for adaptive gene expression in erythroid precursors under the stress of iron deficiency by Liu, Sijin, Bhattacharya, Sanchita, Han, Anping, Suragani, Rajasekhar N. V. S., Zhao, Wanting, Fry, Rebecca C., Chen, Jane‐Jane

    Published in British journal of haematology (01-10-2008)
    “…Summary Haem‐regulated eIF2α kinase (HRI) is essential for the regulation of globin gene translation and the survival of erythroid precursors in iron/haem…”
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    Oxidative Stress Signaling Pathway of Heme Regulated eIF2α Kinase in mitigating the Severity of β-Thalassemia by Suragani, Rajasekhar NVS, Liu, Sijin, Zhao, Wanting, Chen, Jane-Jane

    Published in Blood (16-11-2008)
    “…Maturation of erythroid precursors requires active synthesis of hemoglobin which consists of two pairs of α- and β-globin subunits with each monomer bound to a…”
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    RAP-536, A Soluble Activin Receptor Type IIb Murine IgG-Fc Fusion Protein, Prevents Myelodysplastic Syndrome Related Anemia by Mulivor, Aaron, Cadena, Samuel M., Suragani, Rajasekhar NVS, Kumar, Ravindra, Underwood, Kathryn, Seehra, Jas, Pearsall, R. Scott

    Published in Blood (19-11-2010)
    “…Abstract 978 Myelodysplastic syndrome (MDS) is a premalignant disease characterized by ineffective hematopoiesis. MDS patients can live for extended periods of…”
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