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Journal Abstract Search

146 related items for PubMed ID: 23025459

  • 1. Molecular determinants of platelet delta storage pool deficiencies: an update.
    Masliah-Planchon J, Darnige L, Bellucci S.
    Br J Haematol; 2013 Jan; 160(1):5-11. PubMed ID: 23025459
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  • 2. Mutation analysis of HPS1, the gene mutated in Hermansky-Pudlak syndrome, in patients with isolated platelet dense-granule deficiency.
    Corral J, González-Conejero R, Pujol-Moix N, Domenech P, Vicente V.
    Haematologica; 2004 Mar; 89(3):325-9. PubMed ID: 15020272
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  • 4. Electron-dense chains and clusters in platelets from patients with storage pool-deficiency disorders.
    White JG.
    J Thromb Haemost; 2003 Jan; 1(1):74-9. PubMed ID: 12871542
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  • 5. Hermansky-Pudlak syndrome and Chediak-Higashi syndrome: disorders of vesicle formation and trafficking.
    Huizing M, Anikster Y, Gahl WA.
    Thromb Haemost; 2001 Jul; 86(1):233-45. PubMed ID: 11487012
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  • 7. Heterogeneous abnormalities of platelet dense granule ultrastructure in 20 patients with congenital storage pool deficiency.
    Weiss HJ, Lages B, Vicic W, Tsung LY, White JG.
    Br J Haematol; 1993 Feb; 83(2):282-95. PubMed ID: 8457477
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  • 9. Platelet granule disorders.
    White JG.
    Crit Rev Oncol Hematol; 1986 Feb; 4(4):337-77. PubMed ID: 3513985
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  • 11. Molecular genetics of the Hermansky-Pudlak and Chediak-Higashi syndromes.
    Spritz RA.
    Platelets; 1998 Feb; 9(1):21-9. PubMed ID: 16793741
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  • 14. 5'-UTR structural organization, transcript expression, and mutational analysis of the human Rab geranylgeranyl transferase alpha-subunit (RABGGTA) gene.
    Li W, Detter JC, Weiss HJ, Cramer EM, Zhang Q, Novak EK, Favier R, Kingsmore SF, Swank RT.
    Mol Genet Metab; 2000 Dec; 71(4):599-608. PubMed ID: 11136552
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  • 15. Correction of symptoms of platelet storage pool deficiency in animal models for Chediak-Higashi syndrome and Hermansky-Pudlak syndrome.
    Novak EK, McGarry MP, Swank RT.
    Blood; 1985 Nov; 66(5):1196-201. PubMed ID: 3902123
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  • 16. Congenital disorders associated with platelet dysfunctions.
    Nurden P, Nurden AT.
    Thromb Haemost; 2008 Feb; 99(2):253-63. PubMed ID: 18278172
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  • 17. Enhanced increases in cytosolic Ca2+ in ADP-stimulated platelets from patients with delta-storage pool deficiency--a possible indicator of interactions between granule-bound ADP and the membrane ADP receptor.
    Lages B, Weiss HJ.
    Thromb Haemost; 1997 Feb; 77(2):376-82. PubMed ID: 9157599
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  • 18. Quantification of a novel dense granule protein (granulophysin) in platelets of patients with dense granule storage pool deficiency.
    Shalev A, Michaud G, Israels SJ, McNicol A, Singhroy S, McMillan EM, White JG, Witkop CJ, Nichols WL, Greenberg AH.
    Blood; 1992 Sep 01; 80(5):1231-7. PubMed ID: 1515640
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  • 19. Rapid detection of hereditary and acquired platelet storage pool deficiency by flow cytometry.
    Gordon N, Thom J, Cole C, Baker R.
    Br J Haematol; 1995 Jan 01; 89(1):117-23. PubMed ID: 7833250
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  • 20. Platelet aggregation, storage pool deficiency, and protein phosphorylation in mice with Chediak-Higashi syndrome.
    Pratt HL, Carroll RC, Jones JB, Lothrop CD.
    Am J Vet Res; 1991 Jun 01; 52(6):945-50. PubMed ID: 1652907
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