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B Grandchamp

Showing results (71-80 of 134) with videos related to

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American Journal of Human Genetics|February 1, 1996
Modulation of the phenotype in dominant erythropoietic protoporphyria by a low expression of the normal ferrochelatase alleleL Gouya, J C Deybach, J Lamoril, et al.
Annals of Human Genetics|May 1, 1984
Assignment of the human gene for delta aminolevulinate dehydrase to chromosome 9 by somatic cell hybridization and specific enzyme immunoassayC Beaumont, C Foubert, B Grandchamp, et al.
Blood|June 25, 1998
Microsatellite instability and frameshift mutations in BAX and transforming growth factor-beta RII genes are very uncommon in acute lymphoblastic leukemia in vivo but not in cell linesJ J Molenaar, B Gérard, C Chambon-Pautas, et al.
Human Genetics|February 1, 1980
Prenatal exclusion of congenital erythropoietic porphyria (Günther's disease) in a fetus at riskJ C Deybach, B Grandchamp, M Grelier, et al.
Biochemical and Biophysical Research Communications|January 13, 1984
Cell-free translation of human uroporphyrinogen decarboxylase mRNAsB Grandchamp, P H Roméo, H de Verneuil, et al.
Nucleic Acids Research|August 25, 1989
A point mutation G----A in exon 12 of the porphobilinogen deaminase gene results in exon skipping and is responsible for acute intermittent porphyriaB Grandchamp, C Picat, F de Rooij, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
A retrospective study of a patient with homozygous form of acute intermittent porphyriaG J Beukeveld, B G Wolthers, Y Nordmann, et al.
Molecular Microbiology|July 1, 1989
Detection and identification of mycobacteria by amplification of mycobacterial DNAA J Hance, B Grandchamp, V Lévy-Frébault, et al.
Leukemia|July 17, 1998
High-resolution allelotype analysis of childhood B-lineage acute lymphoblastic leukemiaC Chambon-Pautas, H Cavé, B Gérard, et al.
British Journal of Haematology|February 1, 1996
Deletion mapping indicates that MTS1 is the target of frequent deletions at chromosome 9p21 in paediatric acute lymphoblastic leukaemiasC Guidal-Giroux, B Gérard, H Cavé, et al.
Pageof 14

Showing results (71-80 of 134) with videos related to

Sort By:
Pageof 14
American Journal of Human Genetics|February 1, 1996
Modulation of the phenotype in dominant erythropoietic protoporphyria by a low expression of the normal ferrochelatase alleleL Gouya, J C Deybach, J Lamoril, et al.
Annals of Human Genetics|May 1, 1984
Assignment of the human gene for delta aminolevulinate dehydrase to chromosome 9 by somatic cell hybridization and specific enzyme immunoassayC Beaumont, C Foubert, B Grandchamp, et al.
Blood|June 25, 1998
Microsatellite instability and frameshift mutations in BAX and transforming growth factor-beta RII genes are very uncommon in acute lymphoblastic leukemia in vivo but not in cell linesJ J Molenaar, B Gérard, C Chambon-Pautas, et al.
Human Genetics|February 1, 1980
Prenatal exclusion of congenital erythropoietic porphyria (Günther's disease) in a fetus at riskJ C Deybach, B Grandchamp, M Grelier, et al.
Biochemical and Biophysical Research Communications|January 13, 1984
Cell-free translation of human uroporphyrinogen decarboxylase mRNAsB Grandchamp, P H Roméo, H de Verneuil, et al.
Nucleic Acids Research|August 25, 1989
A point mutation G----A in exon 12 of the porphobilinogen deaminase gene results in exon skipping and is responsible for acute intermittent porphyriaB Grandchamp, C Picat, F de Rooij, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
A retrospective study of a patient with homozygous form of acute intermittent porphyriaG J Beukeveld, B G Wolthers, Y Nordmann, et al.
Molecular Microbiology|July 1, 1989
Detection and identification of mycobacteria by amplification of mycobacterial DNAA J Hance, B Grandchamp, V Lévy-Frébault, et al.
Leukemia|July 17, 1998
High-resolution allelotype analysis of childhood B-lineage acute lymphoblastic leukemiaC Chambon-Pautas, H Cavé, B Gérard, et al.
British Journal of Haematology|February 1, 1996
Deletion mapping indicates that MTS1 is the target of frequent deletions at chromosome 9p21 in paediatric acute lymphoblastic leukaemiasC Guidal-Giroux, B Gérard, H Cavé, et al.
Pageof 14