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Journal Abstract Search

589 related items for PubMed ID: 25518736

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  • 3. FLI1 Induces Megakaryopoiesis Gene Expression Through WAS/WIP-Dependent and Independent Mechanisms; Implications for Wiskott-Aldrich Syndrome.
    Wang C, Sample KM, Gajendran B, Kapranov P, Liu W, Hu A, Zacksenhaus E, Li Y, Hao X, Ben-David Y.
    Front Immunol; 2021; 12():607836. PubMed ID: 33717090
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  • 6. Autonomous role of Wiskott-Aldrich syndrome platelet deficiency in inducing autoimmunity and inflammation.
    Sereni L, Castiello MC, Marangoni F, Anselmo A, di Silvestre D, Motta S, Draghici E, Mantero S, Thrasher AJ, Giliani S, Aiuti A, Mauri P, Notarangelo LD, Bosticardo M, Villa A.
    J Allergy Clin Immunol; 2018 Oct; 142(4):1272-1284. PubMed ID: 29421274
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  • 7. Megakaryocyte-specific Profilin1-deficiency alters microtubule stability and causes a Wiskott-Aldrich syndrome-like platelet defect.
    Bender M, Stritt S, Nurden P, van Eeuwijk JM, Zieger B, Kentouche K, Schulze H, Morbach H, Stegner D, Heinze KG, Dütting S, Gupta S, Witke W, Falet H, Fischer A, Hartwig JH, Nieswandt B.
    Nat Commun; 2014 Sep 04; 5():4746. PubMed ID: 25187265
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  • 8. WASP is involved in proliferation and differentiation of human haemopoietic progenitors in vitro.
    Kajiwara M, Nonoyama S, Eguchi M, Morio T, Imai K, Okawa H, Kaneko M, Sako M, Ohga S, Maeda M, Hibi S, Hashimito H, Shibuya A, Ochs HD, Nakahata T, Yata JI.
    Br J Haematol; 1999 Nov 04; 107(2):254-62. PubMed ID: 10583210
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  • 9. Development of hematopoietic stem cell gene therapy for Wiskott-Aldrich syndrome.
    Boztug K, Dewey RA, Klein C.
    Curr Opin Mol Ther; 2006 Oct 04; 8(5):390-5. PubMed ID: 17078381
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  • 12. Retroviral WASP gene transfer into human hematopoietic stem cells reconstitutes the actin cytoskeleton in myeloid progeny cells differentiated in vitro.
    Dewey RA, Avedillo Díez I, Ballmaier M, Filipovich A, Greil J, Güngör T, Happel C, Maschan A, Noyan F, Pannicke U, Schwarz K, Snapper S, Welte K, Klein C.
    Exp Hematol; 2006 Sep 04; 34(9):1161-9. PubMed ID: 16939809
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  • 13. A peptide derived from the Wiskott-Aldrich syndrome (WAS) protein-interacting protein (WIP) restores WAS protein level and actin cytoskeleton reorganization in lymphocytes from patients with WAS mutations that disrupt WIP binding.
    Massaad MJ, Ramesh N, Le Bras S, Giliani S, Notarangelo LD, Al-Herz W, Notarangelo LD, Geha RS.
    J Allergy Clin Immunol; 2011 Apr 04; 127(4):998-1005.e1-2. PubMed ID: 21376381
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  • 14. Platelet actin nodules are podosome-like structures dependent on Wiskott-Aldrich syndrome protein and ARP2/3 complex.
    Poulter NS, Pollitt AY, Davies A, Malinova D, Nash GB, Hannon MJ, Pikramenou Z, Rappoport JZ, Hartwig JH, Owen DM, Thrasher AJ, Watson SP, Thomas SG.
    Nat Commun; 2015 Jun 01; 6():7254. PubMed ID: 26028144
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  • 15. [Identification of two novel WASP gene mutations in 3 boys with Wiskott-Aldrich syndrome].
    Jiang LP, Xu YH, Yang XQ, Liu EM, Wang LJ, Lau YL, Chan KW.
    Zhonghua Er Ke Za Zhi; 2003 Aug 01; 41(8):590-3. PubMed ID: 14744380
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  • 16. Wiskott-Aldrich syndrome: a disorder of haematopoietic cytoskeletal regulation.
    Thrasher AJ, Burns S.
    Microsc Res Tech; 1999 Oct 15; 47(2):107-13. PubMed ID: 10523789
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