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The Journal of Biological Chemistry|February 10, 1983
Turnover of cytochrome c oxidase from Paracoccus denitrificansJ K Reichardt, Q H GibsonHuman Genetics|March 1, 1995
Linkage disequilibrium between a SacI restriction fragment length polymorphism and two galactosemia mutationsH C Lin, J K ReichardtBiotechniques|January 5, 2002
Multiplex automated primer extension analysis: simultaneous genotyping of several polymorphismsN M Makridakis, J K ReichardtThe Journal of Biological Chemistry|August 25, 1982
Spectra of intermediates in oxidation and reduction of cytochrome c oxidaseJ K Reichardt, Q H GibsonJournal of Molecular Endocrinology|August 5, 2004
YY1 binding within the human HSD3B2 gene intron 1 is required for maximal basal promoter activity: identification of YY1 as the 3beta1-A factorD M Foti, J K ReichardtAmerican Journal of Human Genetics|October 1, 1991
Molecular characterization of two galactosemia mutations: correlation of mutations with highly conserved domains in galactose-1-phosphate uridyl transferaseJ K Reichardt, S Packman, S L WooPharmacogenomics|March 22, 2001
Pharmacogenetics of human androgens and prostatic diseasesG Novelli, K Margiotti, F Sangiuolo, et al.Biochemistry|June 23, 1992
Molecular characterization of two galactosemia mutations and one polymorphism: implications for structure-function analysis of human galactose-1-phosphate uridyltransferaseJ K Reichardt, H L Levy, S L WooPharmacogenetics|July 18, 2000
Biochemical and pharmacogenetic dissection of human steroid 5 alpha-reductase type IIN M Makridakis, E di Salle, J K ReichardtMolecular Biology & Medicine|August 1, 1990
Sequence of a cDNA encoding human galactose-1-phosphate uridyl transferaseJ E Flach, J K Reichardt, L J ElsasPageof 5