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S Sassa

Showing results (131-140 of 248) with videos related to

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The Journal of Biological Chemistry|February 10, 1979
Heme biosynthesis and drug metabolism in mice with hereditary hemolytic anemia. Heme oxygenase induction as an adaptive response for maintaining cytochrome P-450 in chronic hemolysisS Sassa, A Kappas, S E Bernstein, et al.
Blood|May 1, 1983
Tin-protoporphyrin suppression of hyperbilirubinemia in mutant mice with severe hemolytic anemiaS Sassa, G S Drummond, S E Bernstein, et al.
The Journal of Investigative Dermatology|September 1, 1989
Erythrocyte uroporphyrinogen decarboxylase activity in porphyria cutanea tarda: a study of 40 consecutive patientsJ L Held, S Sassa, A Kappas, et al.
Nihon Naibunpi Gakkai Zasshi|October 20, 1984
[The extraction of biologically active substances from hop]A Kumai, R Asakai, S Sassa, et al.
Biochemical and Biophysical Research Communications|January 29, 1988
Tin-protoporphyrin inhibits heme oxygenase and prevents the decline in hepatic heme and cytochrome P-450 contents produced in nude mice by tumor transplantationP S Wissel, R A Galbraith, S Sassa, et al.
Blood|November 1, 1996
Five new mutations in the uroporphyrinogen decarboxylase gene identified in families with cutaneous porphyriaJ F McManus, C G Begley, S Sassa, et al.
Placenta|April 15, 2004
Marked developmental changes in heme oxygenase-1 (HO-1) expression in the mouse placenta: correlation between HO-1 expression and placental developmentS Watanabe, R Akagi, M Mori, et al.
Blood|August 1, 1995
The role of the erythroid-specific delta-aminolevulinate synthase gene expression in erythroid heme synthesisK Meguro, K Igarashi, M Yamamoto, et al.
Pharmacology|January 1, 1981
The potent heme oxygenase inducing action of arsenic and parasiticidal arsenicalsM K Sardana, G S Drummond, S Sassa, et al.
The American Journal of Medicine|April 1, 1979
Studies in porphyria. VIII. Relationship of the 5 alpha-reductive metabolism of steroid hormones to clinical expression of the genetic defect in acute intermittent porphyriaK E Anderson, H L Bradlow, S Sassa, et al.
Pageof 25

Showing results (131-140 of 248) with videos related to

Sort By:
Pageof 25
The Journal of Biological Chemistry|February 10, 1979
Heme biosynthesis and drug metabolism in mice with hereditary hemolytic anemia. Heme oxygenase induction as an adaptive response for maintaining cytochrome P-450 in chronic hemolysisS Sassa, A Kappas, S E Bernstein, et al.
Blood|May 1, 1983
Tin-protoporphyrin suppression of hyperbilirubinemia in mutant mice with severe hemolytic anemiaS Sassa, G S Drummond, S E Bernstein, et al.
The Journal of Investigative Dermatology|September 1, 1989
Erythrocyte uroporphyrinogen decarboxylase activity in porphyria cutanea tarda: a study of 40 consecutive patientsJ L Held, S Sassa, A Kappas, et al.
Nihon Naibunpi Gakkai Zasshi|October 20, 1984
[The extraction of biologically active substances from hop]A Kumai, R Asakai, S Sassa, et al.
Biochemical and Biophysical Research Communications|January 29, 1988
Tin-protoporphyrin inhibits heme oxygenase and prevents the decline in hepatic heme and cytochrome P-450 contents produced in nude mice by tumor transplantationP S Wissel, R A Galbraith, S Sassa, et al.
Blood|November 1, 1996
Five new mutations in the uroporphyrinogen decarboxylase gene identified in families with cutaneous porphyriaJ F McManus, C G Begley, S Sassa, et al.
Placenta|April 15, 2004
Marked developmental changes in heme oxygenase-1 (HO-1) expression in the mouse placenta: correlation between HO-1 expression and placental developmentS Watanabe, R Akagi, M Mori, et al.
Blood|August 1, 1995
The role of the erythroid-specific delta-aminolevulinate synthase gene expression in erythroid heme synthesisK Meguro, K Igarashi, M Yamamoto, et al.
Pharmacology|January 1, 1981
The potent heme oxygenase inducing action of arsenic and parasiticidal arsenicalsM K Sardana, G S Drummond, S Sassa, et al.
The American Journal of Medicine|April 1, 1979
Studies in porphyria. VIII. Relationship of the 5 alpha-reductive metabolism of steroid hormones to clinical expression of the genetic defect in acute intermittent porphyriaK E Anderson, H L Bradlow, S Sassa, et al.
Pageof 25