Showing results (1-10 of 183) with videos related to

Sort By:
Pageof 19
Biochemical and Biophysical Research Communications|May 30, 1989
Molecular basis of mouse Himalayan mutationB S Kwon, R Halaban, C Chintamaneni
Nucleic Acids Research|January 11, 1995
Mouse silver mutation is caused by a single base insertion in the putative cytoplasmic domain of Pmel 17B S Kwon, R Halaban, S Ponnazhagan, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 1, 1987
Isolation and sequence of a cDNA clone for human tyrosinase that maps at the mouse c-albino locusB S Kwon, A K Haq, S H Pomerantz, et al.
Pigment Cell Research|December 1, 1994
Characterization of mouse Pmel 17 gene and silver locusB S Kwon, K K Kim, R Halaban, et al.
Oncogene Research|September 1, 1988
bFGF as an autocrine growth factor for human melanomasR Halaban, B S Kwon, S Ghosh, et al.
Biochemical and Biophysical Research Communications|June 30, 1988
Sequence analysis of mouse tyrosinase cDNA and the effect of melanotropin on its gene expressionB S Kwon, M Wakulchik, A K Haq, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 25, 1991
A single base insertion in the putative transmembrane domain of the tyrosinase gene as a cause for tyrosinase-negative oculocutaneous albinismC D Chintamaneni, R Halaban, Y Kobayashi, et al.
American Journal of Human Genetics|February 1, 1993
Molecular analyses of a tyrosinase-negative albino familyK C Park, C D Chintamaneni, R Halaban, et al.
The Journal of Experimental Medicine|February 1, 1990
Genomic organization of the mouse pore-forming protein (perforin) gene and localization to chromosome 10. Similarities to and differences from C9J A Trapani, B S Kwon, C A Kozak, et al.
Molecular Biology & Medicine|December 1, 1987
A melanocyte-specific complementary DNA clone whose expression is inducible by melanotropin and isobutylmethyl xanthineB S Kwon, R Halaban, G S Kim, et al.
Pageof 19