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S Sassa

Showing results (141-150 of 248) with videos related to

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Transactions of the Association of American Physicians|January 1, 1979
Studies in porphyria IX: Detection of the gene defect of erythropoietic protoporphyria in mitogen-stimulated human lymphocytesS Sassa, G L Zalar, M B Poh-Fitzpatrick, et al.
Biochemical and Biophysical Research Communications|May 16, 1995
Expression of cytochrome P450 mRNAs in the colon and the rectum in normal human subjectsM G Mercurio, S J Shiff, R A Galbraith, et al.
Hepatology (Baltimore, Md.)|March 8, 2000
Novel molecular defects of the delta-aminolevulinate dehydratase gene in a patient with inherited acute hepatic porphyriaR Akagi, R Shimizu, K Furuyama, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 14, 1996
Complementation analysis of mutants of nitric oxide synthase reveals that the active site requires two hemesQ W Xie, M Leung, M Fuortes, et al.
Human Heredity|January 1, 1982
Absence of close linkage between acute intermittent porphyria and the ABO, Rh, P, acid phosphatase, Pr, orosmucoid and pepsinogen lociK S Dean, P M Conneally, S Sassa, et al.
Photochemistry and Photobiology|June 1, 1995
The effect of ALA and radiation on porphyrin/heme biosynthesis in endothelial cellsD He, S Behar, N Nomura, et al.
Nature Genetics|November 7, 1998
A zebrafish model for hepatoerythropoietic porphyriaH Wang, Q Long, S D Marty, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1992
The molecular defect of ferrochelatase in a patient with erythropoietic protoporphyriaY Nakahashi, H Fujita, S Taketani, et al.
Life Sciences|September 14, 2001
Splenomegaly induced by recombinant human granulocyte-colony stimulating factor in ratsT Nakayama, H Kudo, S Suzuki, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 1, 1974
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 diseaseS Sassa, S Granick, D R Bickers, et al.
Pageof 25

Showing results (141-150 of 248) with videos related to

Sort By:
Pageof 25
Transactions of the Association of American Physicians|January 1, 1979
Studies in porphyria IX: Detection of the gene defect of erythropoietic protoporphyria in mitogen-stimulated human lymphocytesS Sassa, G L Zalar, M B Poh-Fitzpatrick, et al.
Biochemical and Biophysical Research Communications|May 16, 1995
Expression of cytochrome P450 mRNAs in the colon and the rectum in normal human subjectsM G Mercurio, S J Shiff, R A Galbraith, et al.
Hepatology (Baltimore, Md.)|March 8, 2000
Novel molecular defects of the delta-aminolevulinate dehydratase gene in a patient with inherited acute hepatic porphyriaR Akagi, R Shimizu, K Furuyama, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 14, 1996
Complementation analysis of mutants of nitric oxide synthase reveals that the active site requires two hemesQ W Xie, M Leung, M Fuortes, et al.
Human Heredity|January 1, 1982
Absence of close linkage between acute intermittent porphyria and the ABO, Rh, P, acid phosphatase, Pr, orosmucoid and pepsinogen lociK S Dean, P M Conneally, S Sassa, et al.
Photochemistry and Photobiology|June 1, 1995
The effect of ALA and radiation on porphyrin/heme biosynthesis in endothelial cellsD He, S Behar, N Nomura, et al.
Nature Genetics|November 7, 1998
A zebrafish model for hepatoerythropoietic porphyriaH Wang, Q Long, S D Marty, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1992
The molecular defect of ferrochelatase in a patient with erythropoietic protoporphyriaY Nakahashi, H Fujita, S Taketani, et al.
Life Sciences|September 14, 2001
Splenomegaly induced by recombinant human granulocyte-colony stimulating factor in ratsT Nakayama, H Kudo, S Suzuki, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 1, 1974
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 diseaseS Sassa, S Granick, D R Bickers, et al.
Pageof 25