Search Results - "Esfandyari, Javanshir"

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  1. 1

    The Iroquois homeobox proteins IRX3 and IRX5 have distinct roles in Wilms tumour development and human nephrogenesis by Holmquist Mengelbier, Linda, Lindell‐Munther, Simon, Yasui, Hiroaki, Jansson, Caroline, Esfandyari, Javanshir, Karlsson, Jenny, Lau, Kimberly, Hui, Chi‐chung, Bexell, Daniel, Hopyan, Sevan, Gisselsson, David

    Published in The Journal of pathology (01-01-2019)
    “…Wilms tumour is a paediatric malignancy with features of halted kidney development. Here, we demonstrate that the Iroquois homeobox genes IRX3 and IRX5 are…”
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    Journal Article
  2. 2

    Anti‐tumor effects of PIM/PI3K/mTOR triple kinase inhibitor IBL‐302 in neuroblastoma by Mohlin, Sofie, Hansson, Karin, Radke, Katarzyna, Martinez, Sonia, Blanco‐Apiricio, Carmen, Garcia‐Ruiz, Cristian, Welinder, Charlotte, Esfandyari, Javanshir, O'Neill, Michael, Pastor, Joaquin, von Stedingk, Kristoffer, Bexell, Daniel

    Published in EMBO molecular medicine (01-08-2019)
    “…The PI3K pathway is a major driver of cancer progression. However, clinical resistance to PI3K inhibition is common. IBL‐302 is a novel highly specific triple…”
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    Anti-tumor effects of rigosertib in high-risk neuroblastoma by Radke, Katarzyna, Hansson, Karin, Sjölund, Jonas, Wolska, Magdalena, Karlsson, Jenny, Esfandyari, Javanshir, Pietras, Kristian, Aaltonen, Kristina, Gisselsson, David, Bexell, Daniel

    Published in Translational oncology (01-08-2021)
    “…•Analysis of multiple tumor types reveal neuroblastoma sensitivity to rigosertib.•Neuroblastoma 2D and 3D organoid models are sensitive to…”
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  5. 5

    Anti‐tumor effects of PIM / PI 3K/ mTOR triple kinase inhibitor IBL ‐302 in neuroblastoma by Mohlin, Sofie, Hansson, Karin, Radke, Katarzyna, Martinez, Sonia, Blanco‐Apiricio, Carmen, Garcia‐Ruiz, Cristian, Welinder, Charlotte, Esfandyari, Javanshir, O'Neill, Michael, Pastor, Joaquin, von Stedingk, Kristoffer, Bexell, Daniel

    Published in EMBO molecular medicine (01-08-2019)
    “…The PI3K pathway is a major driver of cancer progression. However, clinical resistance to PI3K inhibition is common. IBL‐302 is a novel highly specific triple…”
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    Journal Article
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    Effects of COJEC induction on neuroblastoma patient-derived xenografts (PDX) by Manas Nunez, Adriana, Aaltonen, Kristina, Hansson, Karin, Radke, Katarzyna, Esfandyari, Javanshir, Gisselsson, David, Bexell, Daniel

    Published in Journal of clinical oncology (20-05-2019)
    “…Abstract only e21503 Background: Neuroblastoma (NB) is a solid pediatric tumor that causes 15% of childhood cancer deaths. High-risk patients have 50 to 70%…”
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    Abstract A011: Deciphering clonal evolution under chemotherapy in high-risk neuroblastoma using patient derived models by Andersson, Natalie, Nuñez, Adriana Mañas, Aaltonen, Kristina, Hansson, Karin, Seger, Alexandra, Radke, Katarzyna, Esfandyari, Javanshir, Bexell, Daniel, Gisselsson, David

    Published in Cancer research (Chicago, Ill.) (15-05-2022)
    “…This abstract is being presented as a short talk in the scientific program. A full abstract is available in the Proffered Abstracts section (PR001) of the…”
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  12. 12

    Abstract PR001: Deciphering clonal evolution under chemotherapy in high-risk neuroblastoma using patient derived models by Andersson, Natalie, Nuñez, Adriana Mañas, Aaltonen, Kristina, Hansson, Karin, Seger, Alexandra, Radke, Katarzyna, Esfandyari, Javanshir, Bexell, Daniel, Gisselsson, David

    Published in Cancer research (Chicago, Ill.) (15-05-2022)
    “…Neuroblastoma is a pediatric tumor originating from the developing sympathetic nervous system, most often arising in the adrenal medulla in children below 5…”
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  13. 13

    Abstract 3901: Modeling and deciphering COJEC resistance in high risk neuroblastoma by Mañas, Adriana, Aaltonen, Kristina, Andersson, Natalie, Hansson, Karin, Seger, Alexandra, Yasui, Hiroaki, Radke, Katarzyna, Esfandyari, Javanshir, Lindgren, David, Gisselsson, David, Bexell, Daniel

    Published in Cancer research (Chicago, Ill.) (15-06-2022)
    “…Neuroblastoma (NB) is a pediatric cancer of the sympathetic nervous system that accounts for 15% of childhood cancer deaths. High-risk (HR) NB tumors are…”
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    Journal Article