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B Grandchamp

Showing results (81-90 of 134) with videos related to

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Genomics|July 1, 1991
Mouse ferritin H multigene family is polymorphic and contains a single multiallelic functional gene located on chromosome 19A K Yachou, F Renaudie, J L Guenet, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1988
Alternative transcription and splicing of the human porphobilinogen deaminase gene result either in tissue-specific or in housekeeping expressionS Chretien, A Dubart, D Beaupain, et al.
Human Genetics|January 1, 1983
Assignment of the human coproporphyrinogen oxidase to chromosome 9B Grandchamp, D Weil, Y Nordmann, et al.
American Journal of Human Genetics|August 1, 1991
Molecular heterogeneity of acute intermittent porphyria: identification of four additional mutations resulting in the CRIM-negative subtype of the diseaseM H Delfau, C Picat, F De Rooij, et al.
Journal of Biochemical and Biophysical Methods|May 1, 1989
An efficient laboratory made apparatus for DNA amplificationO Bertrand, M H Delfau, M Garbarz, et al.
The Journal of Clinical Investigation|July 17, 1998
Cytotoxic T cell response against the chimeric ETV6-AML1 protein in childhood acute lymphoblastic leukemiaP Yotnda, F Garcia, M Peuchmaur, et al.
Human Genetics|January 1, 1988
Prevalence of the 281 (Gly----Glu) mutation in hepatoerythropoietic porphyria and porphyria cutanea tardaH de Verneuil, J Hansen, C Picat, et al.
British Journal of Haematology|February 5, 1998
A 5' splice region G-->C mutation in exon 3 of the human beta-spectrin gene leads to decreased levels of beta-spectrin mRNA and is responsible for dominant hereditary spherocytosis (spectrin Guemene-Penfao)M Garbarz, C Galand, D Bibas, et al.
European Journal of Clinical Investigation|April 1, 1991
Identification of a new mutation responsible for hepatoerythropoietic porphyriaM Romana, B Grandchamp, A Dubart, et al.
Human Molecular Genetics|March 1, 1996
Mutations in the protoporphyrinogen oxidase gene in patients with variegate porphyriaJ C Deybach, H Puy, A M Robréau, et al.
Pageof 14

Showing results (81-90 of 134) with videos related to

Sort By:
Pageof 14
Genomics|July 1, 1991
Mouse ferritin H multigene family is polymorphic and contains a single multiallelic functional gene located on chromosome 19A K Yachou, F Renaudie, J L Guenet, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1988
Alternative transcription and splicing of the human porphobilinogen deaminase gene result either in tissue-specific or in housekeeping expressionS Chretien, A Dubart, D Beaupain, et al.
Human Genetics|January 1, 1983
Assignment of the human coproporphyrinogen oxidase to chromosome 9B Grandchamp, D Weil, Y Nordmann, et al.
American Journal of Human Genetics|August 1, 1991
Molecular heterogeneity of acute intermittent porphyria: identification of four additional mutations resulting in the CRIM-negative subtype of the diseaseM H Delfau, C Picat, F De Rooij, et al.
Journal of Biochemical and Biophysical Methods|May 1, 1989
An efficient laboratory made apparatus for DNA amplificationO Bertrand, M H Delfau, M Garbarz, et al.
The Journal of Clinical Investigation|July 17, 1998
Cytotoxic T cell response against the chimeric ETV6-AML1 protein in childhood acute lymphoblastic leukemiaP Yotnda, F Garcia, M Peuchmaur, et al.
Human Genetics|January 1, 1988
Prevalence of the 281 (Gly----Glu) mutation in hepatoerythropoietic porphyria and porphyria cutanea tardaH de Verneuil, J Hansen, C Picat, et al.
British Journal of Haematology|February 5, 1998
A 5' splice region G-->C mutation in exon 3 of the human beta-spectrin gene leads to decreased levels of beta-spectrin mRNA and is responsible for dominant hereditary spherocytosis (spectrin Guemene-Penfao)M Garbarz, C Galand, D Bibas, et al.
European Journal of Clinical Investigation|April 1, 1991
Identification of a new mutation responsible for hepatoerythropoietic porphyriaM Romana, B Grandchamp, A Dubart, et al.
Human Molecular Genetics|March 1, 1996
Mutations in the protoporphyrinogen oxidase gene in patients with variegate porphyriaJ C Deybach, H Puy, A M Robréau, et al.
Pageof 14