Julia C. Wedel
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View article: Haplotype-based analysis resolves missing heritability in oculocutaneous albinism type 1B
Haplotype-based analysis resolves missing heritability in oculocutaneous albinism type 1B Open
View article: Genetic background modifies phenotypic severity and longevity in a mouse model of Niemann-Pick disease type C1
Genetic background modifies phenotypic severity and longevity in a mouse model of Niemann-Pick disease type C1 Open
Niemann-Pick disease type C1 (NPC1) is a rare, fatal neurodegenerative disorder characterized by lysosomal accumulation of unesterified cholesterol and glycosphingolipids. These subcellular pathologies lead to phenotypes of hepatosplenomeg…
View article: MEK inhibition remodels the active chromatin landscape and induces SOX10 genomic recruitment in BRAF(V600E) mutant melanoma cells
MEK inhibition remodels the active chromatin landscape and induces SOX10 genomic recruitment in BRAF(V600E) mutant melanoma cells Open
View article: MOESM2 of MEK inhibition remodels the active chromatin landscape and induces SOX10 genomic recruitment in BRAF(V600E) mutant melanoma cells
MOESM2 of MEK inhibition remodels the active chromatin landscape and induces SOX10 genomic recruitment in BRAF(V600E) mutant melanoma cells Open
Additional file 2: Table S1. Genes exhibiting significantly different expression changes in 501mel cells in response to AZD6244 treatment. Table S2. The 250 pigmentation genes with differential expression in 501mel cells under AZD6244 trea…