Richard T. Swank
Publications by Year
Research Areas
melanin and skin pigmentation, Biochemical Analysis and Sensing Techniques, Glycosylation and Glycoproteins Research, Cellular transport and secretion, Cell Adhesion Molecules Research
Most-Cited Works
- → Molecular weight analysis of oligopeptides by electrophoresis in polyacrylamide gel with sodium dodecyl sulfate(1971)1,725 cited
- → 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
- → Mutation of a new gene causes a unique form of Hermansky–Pudlak syndrome in a genetic isolate of central Puerto Rico(2001)228 cited
- → Slc7a11 gene controls production of pheomelanin pigment and proliferation of cultured cells(2005)215 cited
- → Mutations in orthologous genes in human spondyloepimetaphyseal dysplasia and the brachymorphic mouse(1998)212 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