A novel Rab27a mutation binds melanophilin, but not Munc13-4, causing immunodeficiency without albinism-Reference-Cited by-同舟云学术

A novel Rab27a mutation binds melanophilin, but not Munc13-4, causing immunodeficiency without albinism

Published:2016-08 Issue:2 Volume:138 Page:599-601.e3
ISSN:0091-6749
Container-title:Journal of Allergy and Clinical Immunology
language:en
Short-container-title:Journal of Allergy and Clinical Immunology

Author:

Netter Petra,Chan Sanny K.,Banerjee Pinaki P.,Monaco-Shawver Linda,Noroski Lenora M.,Hanson Imelda C.,Forbes Lisa R.,Mace Emily M.,Chinen Javier,Gaspar H. Bobby,Sleiman Patrick,Hakonarson Hakon,Klein Christoph,Ehlayel Mohammad S.,Orange Jordan S.

Publisher

Elsevier BV

Subject

Immunology,Immunology and Allergy

Reference7 articles.

1. A family of Rab27-binding proteins. Melanophilin links Rab27a and myosin Va function in melanosome transport;Strom;J Biol Chem,2002

2. Secretory cytotoxic granule maturation and exocytosis require the effector protein hMunc13-4;Menager;Nat Immunol,2007

3. Munc13-4 is an effector of Rab27a and controls secretion of lysosomes in hematopoietic cells;Neeft;Mol Biol Cell,2005

4. Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome;Menasche;Nat Genet,2000

5. Patients with Griscelli syndrome and normal pigmentation identify RAB27A mutations that selectively disrupt MUNC13-4 binding;Cetica;J Allergy Clin Immunol,2015

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