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Items: 8

1.

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;112(3):450-6. Erratum in: J Clin Invest. 2005 Apr;115(4):1100.

2.

Griscelli syndrome: a model system to study vesicular trafficking.

Van Gele M, Dynoodt P, Lambert J.

Pigment Cell Melanoma Res. 2009 Jun;22(3):268-82. doi: 10.1111/j.1755-148X.2009.00558.x. Epub 2009 Feb 25. Review.

PMID:
19243575
3.
4.

The melanosome as a model to study organelle motility in mammals.

Barral DC, Seabra MC.

Pigment Cell Res. 2004 Apr;17(2):111-8. Review.

PMID:
15016299
5.

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. Review.

6.

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. Review.

PMID:
11601653
7.

[Hypomelanoses transmitted from generation to generation].

Otręba M, Buszman E, Miliński M, Wrześniok D.

Postepy Hig Med Dosw (Online). 2014 Sep 3;68:1081-90. Review. Polish.

8.

An overview and online registry of microvillus inclusion disease patients and their MYO5B mutations.

van der Velde KJ, Dhekne HS, Swertz MA, Sirigu S, Ropars V, Vinke PC, Rengaw T, van den Akker PC, Rings EH, Houdusse A, van Ijzendoorn SC.

Hum Mutat. 2013 Dec;34(12):1597-605. doi: 10.1002/humu.22440. Epub 2013 Oct 16. Review.

PMID:
24014347
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