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Journal Abstract Search

342 related items for PubMed ID: 19057201

  • 1. WHIM syndrome: congenital immune deficiency disease.
    Kawai T, Malech HL.
    Curr Opin Hematol; 2009 Jan; 16(1):20-6. PubMed ID: 19057201
    [Abstract] [Full Text] [Related]

  • 2. WHIM syndrome myelokathexis reproduced in the NOD/SCID mouse xenotransplant model engrafted with healthy human stem cells transduced with C-terminus-truncated CXCR4.
    Kawai T, Choi U, Cardwell L, DeRavin SS, Naumann N, Whiting-Theobald NL, Linton GF, Moon J, Murphy PM, Malech HL.
    Blood; 2007 Jan 01; 109(1):78-84. PubMed ID: 16946301
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  • 3. How I treat warts, hypogammaglobulinemia, infections, and myelokathexis syndrome.
    Badolato R, Donadieu J, WHIM Research Group.
    Blood; 2017 Dec 07; 130(23):2491-2498. PubMed ID: 29066537
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  • 4. Clinical and genetic features of Warts, Hypogammaglobulinemia, Infections and Myelokathexis (WHIM) syndrome.
    Dotta L, Tassone L, Badolato R.
    Curr Mol Med; 2011 Jun 07; 11(4):317-25. PubMed ID: 21506920
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  • 5. Adaptive Immunodeficiency in WHIM Syndrome.
    Majumdar S, Murphy PM.
    Int J Mol Sci; 2018 Dec 20; 20(1):. PubMed ID: 30577453
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  • 6. Severe CD8+ T Lymphopenia in WHIM Syndrome Caused by Selective Sequestration in Primary Immune Organs.
    Majumdar S, Pontejo SM, Jaiswal H, Gao JL, Salancy A, Stassenko E, Yamane H, McDermott DH, Balabanian K, Bachelerie F, Murphy PM.
    J Immunol; 2023 Jun 15; 210(12):1913-1924. PubMed ID: 37133343
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  • 7. CXCL12/CXCR4-axis dysfunctions: Markers of the rare immunodeficiency disorder WHIM syndrome.
    Bachelerie F.
    Dis Markers; 2010 Jun 15; 29(3-4):189-98. PubMed ID: 21178277
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  • 9. CXCR4-Specific Nanobodies as Potential Therapeutics for WHIM syndrome.
    de Wit RH, Heukers R, Brink HJ, Arsova A, Maussang D, Cutolo P, Strubbe B, Vischer HF, Bachelerie F, Smit MJ.
    J Pharmacol Exp Ther; 2017 Oct 15; 363(1):35-44. PubMed ID: 28768817
    [Abstract] [Full Text] [Related]

  • 10. Enhanced function with decreased internalization of carboxy-terminus truncated CXCR4 responsible for WHIM syndrome.
    Kawai T, Choi U, Whiting-Theobald NL, Linton GF, Brenner S, Sechler JM, Murphy PM, Malech HL.
    Exp Hematol; 2005 Apr 15; 33(4):460-8. PubMed ID: 15781337
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  • 11. Stromal-derived factor-1 abolishes constitutive apoptosis of WHIM syndrome neutrophils harbouring a truncating CXCR4 mutation.
    Sanmun D, Garwicz D, Smith CI, Palmblad J, Fadeel B.
    Br J Haematol; 2006 Sep 15; 134(6):640-4. PubMed ID: 16899028
    [Abstract] [Full Text] [Related]

  • 12. Altered leukocyte response to CXCL12 in patients with warts hypogammaglobulinemia, infections, myelokathexis (WHIM) syndrome.
    Gulino AV, Moratto D, Sozzani S, Cavadini P, Otero K, Tassone L, Imberti L, Pirovano S, Notarangelo LD, Soresina R, Mazzolari E, Nelson DL, Notarangelo LD, Badolato R.
    Blood; 2004 Jul 15; 104(2):444-52. PubMed ID: 15026312
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  • 14. Leukocyte analysis from WHIM syndrome patients reveals a pivotal role for GRK3 in CXCR4 signaling.
    Balabanian K, Levoye A, Klemm L, Lagane B, Hermine O, Harriague J, Baleux F, Arenzana-Seisdedos F, Bachelerie F.
    J Clin Invest; 2008 Mar 15; 118(3):1074-84. PubMed ID: 18274673
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  • 15. Familial occurrence of warts, hypogammaglobulinemia, infections, and myelokathexis (WHIM) syndrome.
    Siedlar M, Rudzki Z, Strach M, Trzyna E, Pituch-Noworolska A, Błaut-Szlósarczyk A, Bukowska-Strakova K, Lenart M, Grodzicki T, Zembala M.
    Arch Immunol Ther Exp (Warsz); 2008 Mar 15; 56(6):419-25. PubMed ID: 19043667
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