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Journal Abstract Search

203 related items for PubMed ID: 12531900

  • 41. The dilute locus and Griscelli syndrome: gateways towards a better understanding of melanosome transport.
    Westbroek W, Lambert J, Naeyaert JM.
    Pigment Cell Res; 2001 Oct; 14(5):320-7. PubMed ID: 11601653
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  • 42. A novel function of Prohibitin on melanosome transport in melanocytes.
    Jo CS, Park HI, Jung HJ, Park JI, Lee JE, Myung CH, Hwang JS.
    Theranostics; 2020 Oct; 10(9):3880-3891. PubMed ID: 32226526
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  • 43. The roles of Rab27 and its effectors in the regulated secretory pathways.
    Izumi T, Gomi H, Kasai K, Mizutani S, Torii S.
    Cell Struct Funct; 2003 Oct; 28(5):465-74. PubMed ID: 14745138
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  • 48. Structural basis for the exclusive specificity of Slac2-a/melanophilin for the Rab27 GTPases.
    Kukimoto-Niino M, Sakamoto A, Kanno E, Hanawa-Suetsugu K, Terada T, Shirouzu M, Fukuda M, Yokoyama S.
    Structure; 2008 Oct 08; 16(10):1478-90. PubMed ID: 18940604
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  • 50. The ternary Rab27a-Myrip-Myosin VIIa complex regulates melanosome motility in the retinal pigment epithelium.
    Lopes VS, Ramalho JS, Owen DM, Karl MO, Strauss O, Futter CE, Seabra MC.
    Traffic; 2007 May 08; 8(5):486-99. PubMed ID: 17451552
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  • 51. The Slp homology domain of synaptotagmin-like proteins 1-4 and Slac2 functions as a novel Rab27A binding domain.
    Kuroda TS, Fukuda M, Ariga H, Mikoshiba K.
    J Biol Chem; 2002 Mar 15; 277(11):9212-8. PubMed ID: 11773082
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  • 52. Interactions of human Myosin Va isoforms, endogenously expressed in human melanocytes, are tightly regulated by the tail domain.
    Westbroek W, Lambert J, Bahadoran P, Busca R, Herteleer MC, Smit N, Mommaas M, Ballotti R, Naeyaert JM.
    J Invest Dermatol; 2003 Mar 15; 120(3):465-75. PubMed ID: 12603861
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  • 54. Rab27a targeting to melanosomes requires nucleotide exchange but not effector binding.
    Tarafder AK, Wasmeier C, Figueiredo AC, Booth AE, Orihara A, Ramalho JS, Hume AN, Seabra MC.
    Traffic; 2011 Aug 15; 12(8):1056-66. PubMed ID: 21554507
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  • 55. Patients with Griscelli syndrome and normal pigmentation identify RAB27A mutations that selectively disrupt MUNC13-4 binding.
    Cetica V, Hackmann Y, Grieve S, Sieni E, Ciambotti B, Coniglio ML, Pende D, Gilmour K, Romagnoli P, Griffiths GM, Aricò M.
    J Allergy Clin Immunol; 2015 May 15; 135(5):1310-8.e1. PubMed ID: 25312756
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  • 58. Griscelli syndrome: characterization of a new mutation and rescue of T-cytotoxic activity by retroviral transfer of RAB27A gene.
    Bizario JC, Feldmann J, Castro FA, Ménasché G, Jacob CM, Cristofani L, Casella EB, Voltarelli JC, de Saint-Basile G, Espreafico EM.
    J Clin Immunol; 2004 Jul 15; 24(4):397-410. PubMed ID: 15163896
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  • 59. Mutations in Mlph, encoding a member of the Rab effector family, cause the melanosome transport defects observed in leaden mice.
    Matesic LE, Yip R, Reuss AE, Swing DA, O'Sullivan TN, Fletcher CF, Copeland NG, Jenkins NA.
    Proc Natl Acad Sci U S A; 2001 Aug 28; 98(18):10238-43. PubMed ID: 11504925
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  • 60. Rab7 and Rab27a control two motor protein activities involved in melanosomal transport.
    Jordens I, Westbroek W, Marsman M, Rocha N, Mommaas M, Huizing M, Lambert J, Naeyaert JM, Neefjes J.
    Pigment Cell Res; 2006 Oct 28; 19(5):412-23. PubMed ID: 16965270
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