Search Results - "PRAMANIK, Lotta"

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  1. 1

    Charged amino acid patterns of coreceptor use in the major subtypes of human immunodeficiency virus type 1 by PRAMANIK, Lotta, FRIED, Ulrik, CLEVESTIGT, Peter, EHRNST, Anneka

    Published in Journal of general virology (01-08-2011)
    “…Human immunodeficiency virus type 1 has several genetic subtypes and two coreceptor use phenotypes: R5 that uses CCR5, while X4 uses CXCR4. A high amino acid…”
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    Journal Article
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    CD138 and CD31 Double-Positive Cells Comprise the Functional Antibody-Secreting Plasma Cell Compartment in Primate Bone Marrow by Martinez-Murillo, Paola, Pramanik, Lotta, Sundling, Christopher, Hultenby, Kjell, Wretenberg, Per, Spångberg, Mats, Karlsson Hedestam, Gunilla B

    Published in Frontiers in immunology (2016)
    “…Plasma cells (PCs) are defined as terminally differentiated B cells that secrete large amounts of immunoglobulin (Ig). PCs that reside in the bone marrow (BM)…”
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    Journal Article
  4. 4

    CCR5 use by human immunodeficiency virus type 1 is associated closely with the gp120 V3 loop N-linked glycosylation site by Clevestig, Peter, Pramanik, Lotta, Leitner, Thomas, Ehrnst, Anneka

    Published in Journal of general virology (01-03-2006)
    “…1 Microbiology and Tumor Biology Center, Karolinska Institutet, Box 280, SE-171 77 Stockholm, Sweden 2 Theoretical Biology and Biophysics Group, Los Alamos…”
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    Journal Article
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    Amino Acid Predictors of HIV-1 Coreceptor Use in Different Subtypes and Their Application to Antiretroviral Treatment by Sollerkvist, Lotta Pramanik

    Published 01-01-2014
    “…The human immunodeficiency virus type 1 (HIV-1) group M is responsible for the HIV pandemic and has great genetic variability. The main subtypes and…”
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    Dissertation
  7. 7

    Severe Thrombocytopenia Due to Bone Marrow Failure in Children With Dyskeratosis Congenita Does Not Respond to Eltrombopag Treatment: Case Series by Pramanik-Jonsson, Lotta, Borssén, Magnus, Vonlanthen, Sofie, Nilsson, Frans, Sundin, Mikael

    Published in Journal of pediatric hematology/oncology (01-01-2024)
    “…Dyskeratosis congenita is a rare inherited disease with classic cutaneous symptoms, sometimes accompanied with more severe extracutaneous manifestations such…”
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    Journal Article