Sassa, Shigeru

Studies in lead poisoning

Granick, J. L., Sassa, S., Granick, S., Levere, R. D., & Kappas, A. (1973) · Biochemical Medicine

Heavy Metal Exposure and ToxicityPorphyrin Metabolism and Disorders

Cited by 173

Hereditary Tyrosinemia and the Heme Biosynthetic Pathway: Profound Inhibition of δ-Aminolevulinic Acid Dehydratase Activity by Succinylacetone

Sassa, S., & Kappas, A. (1983) · Journal of Clinical Investigation

Porphyrin Metabolism and DisordersMetabolism and Genetic Disorders

Cited by 145

A Microassay for Uroporphyrinogen I Synthase, One of Three Abnormal Enzyme Activities in Acute Intermittent Porphyria, and its Application to the Study of the Genetics of this Disease

Sassa, S., Granick, S., Bickers, D. R., Bradlow, H. L., & Kappas, A. (1974) · Proceedings of the National Academy of Sciences

Porphyrin Metabolism and DisordersMetabolism and Genetic Disorders

Cited by 97

Cytoprotective Effects of Heme Oxygenase in Acute Renal Failure

Akagi, R., Takahashi, T., & Sassa, S. (2005) · Contributions to Nephrology

Heme Oxygenase-1 and Carbon MonoxideAcute Kidney Injury Research

Cited by 53

Phenotypic variation in human HepG2 hepatoma cells: alterations in cell growth, plasma protein synthesis and heme pathway enzymes

Fuyuki, I., Galbraith, R. A., & Sassa, S. (1990) · International Journal of Biochemistry

Cancer and biochemical researchLiver physiology and pathology

Cited by 24

Accumulation of protoporphyrin IX from delta-aminolevulinic acid in bovine skin fibroblasts with hereditary erythropoietic protoporphyria. A gene-dosage effect.

Sassa, S., Schwartz, S., & Ruth, G. (1981) · The Journal of experimental medicine

Porphyrin Metabolism and DisordersNeonatal Health and Biochemistry

Cited by 19