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Human Mutation|January 1, 1992
In vitro and in vivo correlations for I65T and M1V mutations at the phenylalanine hydroxylase locusS W John, C R Scriver, R Laframboise, et al.Proceedings of the National Academy of Sciences of the United States of America|March 1, 1982
Renal transport of taurine adapts to perturbed taurine homeostasisR Rozen, C R ScriverAmerican Journal of Human Genetics|May 1, 1990
Recurrent mutation, gene conversion, or recombination at the human phenylalanine hydroxylase locus: evidence in French-Canadians and a catalog of mutationsS W John, R Rozen, C R Scriver, et al.American Journal of Human Genetics|December 1, 1989
Novel PKU mutation on haplotype 2 in French-CanadiansS W John, R Rozen, R Laframboise, et al.The American Journal of Physiology|February 1, 1983
Hypertaurinuria in the C57BL/6J mouse: altered transport at the renal basolateral membraneR Rozen, C R Scriver, F MohyuddinThe Biochemical Journal|April 15, 1979
Taurine transport in renal brush-border-membrane vesiclesR Rozen, H S Tenenhouse, C R ScriverBiochimica Et Biophysica Acta|August 8, 1985
A gamma-aminobutyric acid-specific transport mechanism in mammalian kidneyP R Goodyer, R Rozen, C R ScriverClinica Chimica Acta; International Journal of Clinical Chemistry|June 15, 1977
Evaluation of metabolic pathway activity in cultured skin fibroblasts and blood leukocytesR Rozen, S Buhl, F Mohyuddin, et al.American Journal of Human Genetics|August 1, 1994
Mutation profiles of phenylketonuria in Quebec populations: evidence of stratification and novel mutationsR Rozen, A Mascisch, M Lambert, et al.Diabetes Research and Clinical Practice|March 1, 1994
Evidence for different clinical subtypes of type 1 diabetes mellitus: a prospective studyA Schiffrin, A Ciampi, L Hendricks, et al.Pageof 32