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Pigment Cell Research|May 23, 2007
Informatic and genomic analysis of melanocyte cDNA libraries as a resource for the study of melanocyte development and functionLaura L Baxter, Benjamin J Hsu, Lowell Umayam, et al.Genome Research|June 24, 2003
Human disease genes and their cloned mouse orthologs: exploration of the FANTOM2 cDNA sequence data setLynn M Schriml, David P Hill, Judith A Blake, et al.Elife|September 11, 2023
Transcriptomic profiling of tissue environments critical for post-embryonic patterning and morphogenesis of zebrafish skinAndrew J Aman, Lauren M Saunders, August A Carr, et al.Human Molecular Genetics|November 1, 2016
Systemic AAV9 gene therapy improves the lifespan of mice with Niemann-Pick disease, type C1Randy J Chandler, Ian M Williams, Alana L Gibson, et al.Iscience|October 1, 2024
Quiescence and aging of melanocyte stem cells and a novel association with programmed death-ligand 1Joseph W Palmer, Kyrene M Villavicencio, Misgana Idris, et al.Human Molecular Genetics|April 10, 2008
A sensitized mutagenesis screen identifies Gli3 as a modifier of Sox10 neurocristopathyIvana Matera, Dawn E Watkins-Chow, Stacie K Loftus, et al.Plos Genetics|September 27, 2005
Acinar cell apoptosis in Serpini2-deficient mice models pancreatic insufficiencyStacie K Loftus, Jennifer L Cannons, Arturo Incao, et al.Molecular Genetics and Metabolism|July 16, 2013
A somatic cell defect is associated with the onset of neurological symptoms in a lysosomal storage diseaseJorge L Rodriguez-Gil, Denise M Larson, Christopher A Wassif, et al.Human Molecular Genetics|December 7, 2005
Deletion of long-range sequences at Sox10 compromises developmental expression in a mouse model of Waardenburg-Shah (WS4) syndromeAnthony Antonellis, William R Bennett, Trevelyan R Menheniott, et al.Scientific Reports|February 27, 2015
Highly stable and sensitive fluorescent probes (LysoProbes) for lysosomal labeling and trackingNazmiye B Yapici, Yue Bi, Pengfei Li, et al.Pageof 13