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The Journal of Investigative Dermatology|August 1, 1997
Mutational analysis of copper binding by human tyrosinaseR A Spritz, L Ho, M Furumura, et al.The Biochemical Journal|April 4, 2001
The molecular basis of oculocutaneous albinism type 1 (OCA1): sorting failure and degradation of mutant tyrosinases results in a lack of pigmentationK Toyofuku, I Wada, R A Spritz, et al.The Journal of Biological Chemistry|November 25, 1992
Mutational mapping of the catalytic activities of human tyrosinaseR K Tripathi, V J Hearing, K Urabe, et al.Biochemical and Biophysical Research Communications|February 17, 1998
Metal ligand-binding specificities of the tyrosinase-related proteinsM Furumura, F Solano, N Matsunaga, et al.The Journal of Investigative Dermatology. Symposium Proceedings|October 28, 1999
Biochemical control of melanogenesis and melanosomal organizationV J HearingThe American Journal of Dermatopathology|January 1, 1981
Tumor-specific markers of malignant melanomaV J HearingPigment Cell Research|October 21, 2000
The melanosome: the perfect model for cellular responses to the environmentV J HearingPigment Cell Research|April 13, 2000
Hermansky-Pudlak syndrome and pale ear: melanosome-making for the millenniumR A SpritzJournal of Clinical Immunology|April 9, 1998
Genetic defects in Chediak-Higashi syndrome and the beige mouseR A SpritzCurrent Opinion in Pediatrics|December 26, 2001
The genetics and epigenetics of orofacial cleftsR A SpritzPageof 23