Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

B Grandchamp

Showing results (1-10 of 134) with videos related to

Pageof 14
Sort By:
Seminars in Liver Disease|March 28, 1998
Acute intermittent porphyriaB Grandchamp
Annales De Genetique|January 1, 1994
[New tumor suppressor genes intervening in the regulation of the cycle]B Grandchamp
Enzyme|January 1, 1982
Coproporphyrinogen III oxidase assayB Grandchamp, Y Nordmann
Genomics|January 1, 1995
Structure of the mouse H2A.X gene and physical linkage to the UPS locus on chromosome 9: assignment of the human H2A.X gene to 11q23 by sequence analysisC Porcher, B Grandchamp
Journal of Bioenergetics and Biomembranes|April 1, 1995
Molecular abnormalities of coproporphyrinogen oxidase in patients with hereditary coproporphyriaB Grandchamp, J Lamoril, H Puy
Human Molecular Genetics|March 1, 1994
Homozygous hereditary coproporphyria caused by an arginine to tryptophane substitution in coproporphyrinogen oxidase and common intragenic polymorphismsP Martasek, Y Nordmann, B Grandchamp
The Biochemical Journal|October 15, 1978
The mitochondrial localization of coproporphyrinogen III oxidaseB Grandchamp, N Phung, Y Nordmann
La Nouvelle Presse Medicale|June 14, 1975
[Acute intermittent porphyria. Detection of asymptomatic carriers of the genetic defect]B Grandchamp, M Grelier, Y Nordmann
Biochimica Et Biophysica Acta|January 11, 1980
Some kinetic properties of human red cell uroporphyrinogen decarboxylaseH de Verneuil, B Grandchamp, Y Nordmann
Human Molecular Genetics|August 1, 1994
Coproporphyrinogen oxidase: gene organization and description of a mutation leading to exon 6 skippingM H Delfau-Larue, P Martasek, B Grandchamp
Pageof 14

Showing results (1-10 of 134) with videos related to

Sort By:
Pageof 14
Seminars in Liver Disease|March 28, 1998
Acute intermittent porphyriaB Grandchamp
Annales De Genetique|January 1, 1994
[New tumor suppressor genes intervening in the regulation of the cycle]B Grandchamp
Enzyme|January 1, 1982
Coproporphyrinogen III oxidase assayB Grandchamp, Y Nordmann
Genomics|January 1, 1995
Structure of the mouse H2A.X gene and physical linkage to the UPS locus on chromosome 9: assignment of the human H2A.X gene to 11q23 by sequence analysisC Porcher, B Grandchamp
Journal of Bioenergetics and Biomembranes|April 1, 1995
Molecular abnormalities of coproporphyrinogen oxidase in patients with hereditary coproporphyriaB Grandchamp, J Lamoril, H Puy
Human Molecular Genetics|March 1, 1994
Homozygous hereditary coproporphyria caused by an arginine to tryptophane substitution in coproporphyrinogen oxidase and common intragenic polymorphismsP Martasek, Y Nordmann, B Grandchamp
The Biochemical Journal|October 15, 1978
The mitochondrial localization of coproporphyrinogen III oxidaseB Grandchamp, N Phung, Y Nordmann
La Nouvelle Presse Medicale|June 14, 1975
[Acute intermittent porphyria. Detection of asymptomatic carriers of the genetic defect]B Grandchamp, M Grelier, Y Nordmann
Biochimica Et Biophysica Acta|January 11, 1980
Some kinetic properties of human red cell uroporphyrinogen decarboxylaseH de Verneuil, B Grandchamp, Y Nordmann
Human Molecular Genetics|August 1, 1994
Coproporphyrinogen oxidase: gene organization and description of a mutation leading to exon 6 skippingM H Delfau-Larue, P Martasek, B Grandchamp
Pageof 14