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Journal Abstract Search

207 related items for PubMed ID: 11882363

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  • 7. Unique CD18 mutations involving a deletion in the extracellular stalk region and a major truncation of the cytoplasmic domain in a patient with leukocyte adhesion deficiency type 1.
    Hixson P, Smith CW, Shurin SB, Tosi MF.
    Blood; 2004 Feb 01; 103(3):1105-13. PubMed ID: 14512306
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  • 9. A novel CD18 genomic deletion in a patient with severe leucocyte adhesion deficiency: a possible CD2/lymphocyte function-associated antigen-1 functional association in humans.
    Allende LM, Hernández M, Corell A, García-Pérez MA, Varela P, Moreno A, Caragol I, García-Martín F, Guillén-Perales J, Olivé T, Español T, Arnaiz-Villena A.
    Immunology; 2000 Mar 01; 99(3):440-50. PubMed ID: 10712675
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  • 11. A novel point mutation in CD18 causing leukocyte adhesion deficiency in a Chinese patient.
    Li L, Jin YY, Cao RM, Chen TX.
    Chin Med J (Engl); 2010 May 20; 123(10):1278-82. PubMed ID: 20529581
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  • 13. Retroviral-mediated gene transfer of the leukocyte integrin CD18 into peripheral blood CD34+ cells derived from a patient with leukocyte adhesion deficiency type 1.
    Bauer TR, Schwartz BR, Liles WC, Ochs HD, Hickstein DD.
    Blood; 1998 Mar 01; 91(5):1520-6. PubMed ID: 9473215
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  • 14. Genetic analysis of integrin function in man: LAD-1 and other syndromes.
    Hogg N, Bates PA.
    Matrix Biol; 2000 Jul 01; 19(3):211-22. PubMed ID: 10936446
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  • 16. The effect of gentamicin-induced readthrough on a novel premature termination codon of CD18 leukocyte adhesion deficiency patients.
    Simon AJ, Lev A, Wolach B, Gavrieli R, Amariglio N, Rosenthal E, Gazit E, Eyal E, Rechavi G, Somech R.
    PLoS One; 2010 Nov 16; 5(11):e13659. PubMed ID: 21103413
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  • 18. Leukocyte Adhesion Deficiency-I: Clinical and Molecular Characterization in an Indian Population.
    Deshpande P, Kathirvel K, Alex AA, Korula A, George B, Shaji RV, Mathews V.
    Indian J Pediatr; 2016 Aug 16; 83(8):799-804. PubMed ID: 26924654
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  • 20. Molecular characterization of leukocyte adhesion deficiency-I in Indian patients: identification of 9 novel mutations.
    Madkaikar M, Italia K, Gupta M, Chavan S, Mishra A, Rao M, Mhatre S, Desai M, Manglani M, Singh S, Suri D, Agrawal A, Ghosh K.
    Blood Cells Mol Dis; 2015 Mar 16; 54(3):217-23. PubMed ID: 25703682
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