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Indian Journal of Biochemistry & Biophysics|October 1, 1991
Tyrosinase exhibits lag at pH 6.8 under steady state concentrations of tyrosine and 3,4-dihydroxy phenyl alanine in melanoma tissueC Chintamaneni, A R Nadimpalli, R AbburiBiochemical and Biophysical Research Communications|May 30, 1989
Molecular basis of mouse Himalayan mutationB S Kwon, R Halaban, C ChintamaneniMolecular and Cellular Biology|June 1, 1996
Participation of the yeast activator Abf1 in meiosis-specific expression of the HOP1 geneV Gailus-Durner, J Xie, C Chintamaneni, et al.Molecular and Cellular Biology|July 1, 1997
Analysis of a meiosis-specific URS1 site: sequence requirements and involvement of replication protein AV Gailus-Durner, C Chintamaneni, R Wilson, 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.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|October 15, 1991
A melanocyte-specific gene, Pmel 17, maps near the silver coat color locus on mouse chromosome 10 and is in a syntenic region on human chromosome 12B S Kwon, C Chintamaneni, C A Kozak, et al.Pageof 1