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B Grandchamp

Showing results (61-70 of 134) with videos related to

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Experimental Cell Research|October 1, 1984
Effects of succinylacetone on dimethylsulfoxide-mediated induction of heme pathway enzymes in mouse friend virus-transformed erythroleukemia cellsC Beaumont, J C Deybach, B Grandchamp, et al.
Human Genetics|January 1, 1992
Heterogeneity of mutations in the uroporphyrinogen III synthase gene in congenital erythropoietic porphyriaS Boulechfar, V Da Silva, J C Deybach, et al.
Urology|February 25, 2000
Absence of microsatellite instability in transitional cell carcinoma of the bladderC Bonnal, V Ravery, M Toublanc, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 1, 1984
Molecular cloning of a cDNA sequence complementary to porphobilinogen deaminase mRNA from ratB Grandchamp, P H Romeo, A Dubart, et al.
Blood|June 15, 1997
Spectrin St Claude, a splicing mutation of the human alpha-spectrin gene associated with severe poikilocytic anemiaC M Fournier, G Nicolas, P G Gallagher, et al.
The Journal of Biological Chemistry|February 1, 2000
Early embryonic lethality of H ferritin gene deletion in miceC Ferreira, D Bucchini, M E Martin, et al.
Human Mutation|July 20, 2001
Characterization of 11 novel mutations in the X-linked chronic granulomatous disease (CYBB gene)B Gérard, J El Benna, F Alcain, et al.
Blood|March 9, 1999
Inheritance in erythropoietic protoporphyria: a common wild-type ferrochelatase allelic variant with low expression accounts for clinical manifestationL Gouya, H Puy, J Lamoril, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 1, 1984
Isolation and identification of a cDNA clone coding for rat uroporphyrinogen decarboxylaseP H Romeo, A Dubart, B Grandchamp, et al.
La Nouvelle Presse Medicale|April 30, 1977
[Demonstration of hereditary enzyme defect in coproporphyria]B Grandchamp, N Phung, M Grelier, et al.
Pageof 14

Showing results (61-70 of 134) with videos related to

Sort By:
Pageof 14
Experimental Cell Research|October 1, 1984
Effects of succinylacetone on dimethylsulfoxide-mediated induction of heme pathway enzymes in mouse friend virus-transformed erythroleukemia cellsC Beaumont, J C Deybach, B Grandchamp, et al.
Human Genetics|January 1, 1992
Heterogeneity of mutations in the uroporphyrinogen III synthase gene in congenital erythropoietic porphyriaS Boulechfar, V Da Silva, J C Deybach, et al.
Urology|February 25, 2000
Absence of microsatellite instability in transitional cell carcinoma of the bladderC Bonnal, V Ravery, M Toublanc, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 1, 1984
Molecular cloning of a cDNA sequence complementary to porphobilinogen deaminase mRNA from ratB Grandchamp, P H Romeo, A Dubart, et al.
Blood|June 15, 1997
Spectrin St Claude, a splicing mutation of the human alpha-spectrin gene associated with severe poikilocytic anemiaC M Fournier, G Nicolas, P G Gallagher, et al.
The Journal of Biological Chemistry|February 1, 2000
Early embryonic lethality of H ferritin gene deletion in miceC Ferreira, D Bucchini, M E Martin, et al.
Human Mutation|July 20, 2001
Characterization of 11 novel mutations in the X-linked chronic granulomatous disease (CYBB gene)B Gérard, J El Benna, F Alcain, et al.
Blood|March 9, 1999
Inheritance in erythropoietic protoporphyria: a common wild-type ferrochelatase allelic variant with low expression accounts for clinical manifestationL Gouya, H Puy, J Lamoril, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 1, 1984
Isolation and identification of a cDNA clone coding for rat uroporphyrinogen decarboxylaseP H Romeo, A Dubart, B Grandchamp, et al.
La Nouvelle Presse Medicale|April 30, 1977
[Demonstration of hereditary enzyme defect in coproporphyria]B Grandchamp, N Phung, M Grelier, et al.
Pageof 14