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Journal Abstract Search
209 related items for PubMed ID: 18397837
1. A novel missense mutation (G43S) in the switch I region of Rab27A causing Griscelli syndrome. Westbroek W, Tuchman M, Tinloy B, De Wever O, Vilboux T, Hertz JM, Hasle H, Heilmann C, Helip-Wooley A, Kleta R, Gahl WA. Mol Genet Metab; 2008 Jun; 94(2):248-54. PubMed ID: 18397837 [Abstract] [Full Text] [Related]
2. Rab27a and MyoVa are the primary Mlph interactors regulating melanosome transport in melanocytes. Hume AN, Ushakov DS, Tarafder AK, Ferenczi MA, Seabra MC. J Cell Sci; 2007 Sep 01; 120(Pt 17):3111-22. PubMed ID: 17698919 [Abstract] [Full Text] [Related]
3. The adaptor protein melanophilin regulates dynamic myosin-Va:cargo interaction and dendrite development in melanocytes. Robinson CL, Evans RD, Sivarasa K, Ramalho JS, Briggs DA, Hume AN. Mol Biol Cell; 2019 Mar 15; 30(6):742-752. PubMed ID: 30699046 [Abstract] [Full Text] [Related]
4. The leaden gene product is required with Rab27a to recruit myosin Va to melanosomes in melanocytes. Hume AN, Collinson LM, Hopkins CR, Strom M, Barral DC, Bossi G, Griffiths GM, Seabra MC. Traffic; 2002 Mar 15; 3(3):193-202. PubMed ID: 11886590 [Abstract] [Full Text] [Related]
5. Melanophilin directly links Rab27a and myosin Va through its distinct coiled-coil regions. Nagashima K, Torii S, Yi Z, Igarashi M, Okamoto K, Takeuchi T, Izumi T. FEBS Lett; 2002 Apr 24; 517(1-3):233-8. PubMed ID: 12062444 [Abstract] [Full Text] [Related]
6. The GTPase-deficient Rab27A(Q78L) mutant inhibits melanosome transport in melanocytes through trapping of Rab27A effector protein Slac2-a/melanophilin in their cytosol: development of a novel melanosome-targetinG tag. Ishida M, Arai SP, Ohbayashi N, Fukuda M. J Biol Chem; 2014 Apr 18; 289(16):11059-11067. PubMed ID: 24584932 [Abstract] [Full Text] [Related]
8. The actin-binding domain of Slac2-a/melanophilin is required for melanosome distribution in melanocytes. Kuroda TS, Ariga H, Fukuda M. Mol Cell Biol; 2003 Aug 18; 23(15):5245-55. PubMed ID: 12861011 [Abstract] [Full Text] [Related]
13. A coiled-coil domain of melanophilin is essential for Myosin Va recruitment and melanosome transport in melanocytes. Hume AN, Tarafder AK, Ramalho JS, Sviderskaya EV, Seabra MC. Mol Biol Cell; 2006 Nov 18; 17(11):4720-35. PubMed ID: 16914517 [Abstract] [Full Text] [Related]
14. A family of Rab27-binding proteins. Melanophilin links Rab27a and myosin Va function in melanosome transport. Strom M, Hume AN, Tarafder AK, Barkagianni E, Seabra MC. J Biol Chem; 2002 Jul 12; 277(28):25423-30. PubMed ID: 11980908 [Abstract] [Full Text] [Related]
15. Rab27a: A key to melanosome transport in human melanocytes. Bahadoran P, Aberdam E, Mantoux F, Buscà R, Bille K, Yalman N, de Saint-Basile G, Casaroli-Marano R, Ortonne JP, Ballotti R. J Cell Biol; 2001 Feb 19; 152(4):843-50. PubMed ID: 11266474 [Abstract] [Full Text] [Related]
16. Functional characterization of two RAB27A missense mutations found in Griscelli syndrome type 2. Ohbayashi N, Mamishi S, Ishibashi K, Maruta Y, Pourakbari B, Tamizifar B, Mohammadpour M, Fukuda M, Parvaneh N. Pigment Cell Melanoma Res; 2010 Jun 19; 23(3):365-74. PubMed ID: 20370853 [Abstract] [Full Text] [Related]
17. Functional analysis of Slac2-c/MyRIP as a linker protein between melanosomes and myosin VIIa. Kuroda TS, Fukuda M. J Biol Chem; 2005 Jul 29; 280(30):28015-22. PubMed ID: 15927964 [Abstract] [Full Text] [Related]
18. The absence of Rab27a accelerates the degradation of Melanophilin. Park JI, Lee JE, Myung CH, Jo CS, Jang HS, Hwang JS. Exp Dermatol; 2019 Jan 29; 28(1):90-93. PubMed ID: 30417443 [Abstract] [Full Text] [Related]
19. Griscelli syndrome restricted to hypopigmentation results from a melanophilin defect (GS3) or a MYO5A F-exon deletion (GS1). Ménasché G, Ho CH, Sanal O, Feldmann J, Tezcan I, Ersoy F, Houdusse A, Fischer A, de Saint Basile G. J Clin Invest; 2003 Aug 29; 112(3):450-6. PubMed ID: 12897212 [Abstract] [Full Text] [Related]
20. Griscelli syndrome: a model system to study vesicular trafficking. Van Gele M, Dynoodt P, Lambert J. Pigment Cell Melanoma Res; 2009 Jun 29; 22(3):268-82. PubMed ID: 19243575 [Abstract] [Full Text] [Related] Page: [Next] [New Search]