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Pigment Cell Research|September 11, 2004
Rab27b is up-regulated in human Griscelli syndrome type II melanocytes and linked to the actin cytoskeleton via exon F-Myosin Va transcriptsWendy Westbroek, Jo Lambert, Sofie De Schepper, et al.
Annals of Human Genetics|June 16, 2009
Identifying putative promoter regions of Hermansky-Pudlak syndrome genes by means of phylogenetic footprintingHoria Stanescu, Tyra G Wolfsberg, R Travis Moreland, et al.
Ecology and Evolution|March 28, 2022
Potential for urban agriculture to support accessible and impactful undergraduate biology educationAdam D Kay, Eric J Chapman, Jelagat D Cheruiyot, et al.
The Journal of Investigative Dermatology|December 24, 2005
Neurofibromatosis type 1 protein and amyloid precursor protein interact in normal human melanocytes and colocalize with melanosomesSofie De Schepper, Joachim M A Boucneau, Wendy Westbroek, et al.
The Journal of Biological Chemistry|January 18, 2003
Characterization of the molecular defects in Rab27a, caused by RAB27A missense mutations found in patients with Griscelli syndromePhilippe Bahadoran, Roser Busca, Christine Chiaverini, et al.
Pigment Cell Research|September 16, 2005
Different approaches for assaying melanosome transferWerner Berens, Karolien Van Den Bossche, Tae-Jin Yoon, et al.
Aging Cell|October 22, 2015
Lysosomal storage and impaired autophagy lead to inflammasome activation in Gaucher macrophagesElma Aflaki, Nima Moaven, Daniel K Borger, et al.
Molecular Genetics and Metabolism|April 10, 2008
A novel missense mutation (G43S) in the switch I region of Rab27A causing Griscelli syndromeWendy Westbroek, Maya Tuchman, Bradford Tinloy, et al.
Journal of Medicinal Chemistry|June 1, 2012
Discovery, structure-activity relationship, and biological evaluation of noninhibitory small molecule chaperones of glucocerebrosidaseSamarjit Patnaik, Wei Zheng, Jae H Choi, et al.
Molecular Genetics and Metabolism|July 2, 2010
Novel 47.5-kb deletion in RAB27A results in severe Griscelli Syndrome Type 2Lisa M Vincent, Fred Gilbert, Jennifer I DiPace, et al.
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