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B Grandchamp

Showing results (41-50 of 134) with videos related to

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The Journal of Biological Chemistry|June 5, 1991
Characterization of hypersensitive sites, protein-binding motifs, and regulatory elements in both promoters of the mouse porphobilinogen deaminase geneC Porcher, G Pitiot, M Plumb, et al.
European Journal of Biochemistry|January 2, 1987
Tissue-specific expression of porphobilinogen deaminase. Two isoenzymes from a single geneB Grandchamp, H De Verneuil, C Beaumont, et al.
Blood|March 1, 1996
Overexpression of the ferritin H subunit in cultured erythroid cells changes the intracellular iron distributionV Picard, F Renaudie, C Porcher, et al.
Leukemia|November 22, 1997
Study of the thrombopoitin receptor in essential thrombocythemiaJ J Kiladjian, N Elkassar, G Hetet, et al.
British Journal of Haematology|January 1, 1996
Proto-oncogene c-mpl is involved in spontaneous megakaryocytopoiesis in myeloproliferative disordersY Li, G Hetet, J J Kiladjian, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|October 9, 2002
[Polymorphism of aldose reductase gene and susceptibility to retinopathy and nephropathy in Caucasians with type 1 diabetes]A Fanelli, S Hadjadj, Y Gallois, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 12, 2001
Lack of hepcidin gene expression and severe tissue iron overload in upstream stimulatory factor 2 (USF2) knockout miceG Nicolas, M Bennoun, I Devaux, et al.
British Journal of Haematology|September 1, 2001
Quantification of TEL-AML1 transcript for minimal residual disease assessment in childhood acute lymphoblastic leukaemiaS Drunat, M Olivi, G Brunie, et al.
Biochemical and Biophysical Research Communications|December 16, 1991
Human erythropoietic protoporphyria: two point mutations in the ferrochelatase geneJ Lamoril, S Boulechfar, H de Verneuil, et al.
Human Molecular Genetics|February 1, 1995
A molecular defect in coproporphyrinogen oxidase gene causing harderoporphyria, a variant form of hereditary coproporphyriaJ Lamoril, P Martasek, J C Deybach, et al.
Pageof 14

Showing results (41-50 of 134) with videos related to

Sort By:
Pageof 14
The Journal of Biological Chemistry|June 5, 1991
Characterization of hypersensitive sites, protein-binding motifs, and regulatory elements in both promoters of the mouse porphobilinogen deaminase geneC Porcher, G Pitiot, M Plumb, et al.
European Journal of Biochemistry|January 2, 1987
Tissue-specific expression of porphobilinogen deaminase. Two isoenzymes from a single geneB Grandchamp, H De Verneuil, C Beaumont, et al.
Blood|March 1, 1996
Overexpression of the ferritin H subunit in cultured erythroid cells changes the intracellular iron distributionV Picard, F Renaudie, C Porcher, et al.
Leukemia|November 22, 1997
Study of the thrombopoitin receptor in essential thrombocythemiaJ J Kiladjian, N Elkassar, G Hetet, et al.
British Journal of Haematology|January 1, 1996
Proto-oncogene c-mpl is involved in spontaneous megakaryocytopoiesis in myeloproliferative disordersY Li, G Hetet, J J Kiladjian, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|October 9, 2002
[Polymorphism of aldose reductase gene and susceptibility to retinopathy and nephropathy in Caucasians with type 1 diabetes]A Fanelli, S Hadjadj, Y Gallois, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 12, 2001
Lack of hepcidin gene expression and severe tissue iron overload in upstream stimulatory factor 2 (USF2) knockout miceG Nicolas, M Bennoun, I Devaux, et al.
British Journal of Haematology|September 1, 2001
Quantification of TEL-AML1 transcript for minimal residual disease assessment in childhood acute lymphoblastic leukaemiaS Drunat, M Olivi, G Brunie, et al.
Biochemical and Biophysical Research Communications|December 16, 1991
Human erythropoietic protoporphyria: two point mutations in the ferrochelatase geneJ Lamoril, S Boulechfar, H de Verneuil, et al.
Human Molecular Genetics|February 1, 1995
A molecular defect in coproporphyrinogen oxidase gene causing harderoporphyria, a variant form of hereditary coproporphyriaJ Lamoril, P Martasek, J C Deybach, et al.
Pageof 14