Edward K. Novak
Publications by Year
Research Areas
melanin and skin pigmentation, Biochemical Analysis and Sensing Techniques, Cellular transport and secretion, Cell Adhesion Molecules Research, Skin Protection and Aging
Most-Cited Works
- → Hermansky-Pudlak syndrome type 7 (HPS-7) results from mutant dysbindin, a member of the biogenesis of lysosome-related organelles complex 1 (BLOC-1)(2003)432 cited
- → A mutation in Rab27a causes the vesicle transport defects observed in ashen mice(2000)409 cited
- → Slc7a11 gene controls production of pheomelanin pigment and proliferation of cultured cells(2005)215 cited
- → Murine Hermansky–Pudlak syndrome genes: regulators of lysosome‐related organelles(2004)197 cited
- → Mouse Models of Hermansky Pudlak Syndrome: A Review(1998)191 cited
- → Ru2 and Ru encode mouse orthologs of the genes mutated in human Hermansky-Pudlak syndrome types 5 and 6(2003)190 cited
- → Hermansky-Pudlak syndrome is caused by mutations in HPS4, the human homolog of the mouse light-ear gene(2002)181 cited
- → Rab geranylgeranyl transferase α mutation in the gunmetal mouse reduces Rab prenylation and platelet synthesis(2000)157 cited
- → The mouse pale ear ( ep ) mutation is the homologue of human Hermansky–Pudlak syndrome(1997)133 cited
- → The mouse organellar biogenesis mutant buff results from a mutation inVps33a, a homologue of yeastvps33andDrosophilacarnation(2003)122 cited