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 (31-40 of 134) with videos related to

Pageof 14
Sort By:
British Journal of Haematology|May 1, 1995
Clonal analysis of haemopoietic cells in essential thrombocythaemiaN el Kassar, G Hetet, Y Li, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1992
A second ferritin L subunit is encoded by an intronless gene in the mouseF Renaudie, A K Yachou, B Grandchamp, et al.
Biochimica Et Biophysica Acta|July 16, 1986
Porphobilinogen deaminase is unstable in the absence of its substrateC Beaumont, B Grandchamp, M Bogard, et al.
European Journal of Immunology|September 1, 1992
Restricted diversity of V gamma 9-JP rearrangements in unstimulated human gamma/delta T lymphocytesM H Delfau, A J Hance, D Lecossier, et al.
Blood|May 1, 1990
Point mutations in the uroporphyrinogen III synthase gene in congenital erythropoietic porphyria (Günther's disease)J C Deybach, H de Verneuil, S Boulechfar, et al.
Leukemia|February 1, 1997
Delineation of a 6 cM commonly deleted region in childhood acute lymphoblastic leukemia on the 6q chromosomal armB Gérard, H Cavé, C Guidal, et al.
Biochimica Et Biophysica Acta|May 22, 1980
Studies of porphyrin synthesis in fibroblasts of patients with congenital erythropoietic porphyria and one patient with homozygous coproporphyriaB Grandchamp, J C Deybach, M Grelier, et al.
Experimental Cell Research|October 10, 1996
Expression of H and L ferritin mRNAs in mouse small intestineB Gérard, N Farman, K B Raja, et al.
The Journal of Clinical Investigation|September 1, 1983
Harderoporphyria: a variant hereditary coproporphyriaY Nordmann, B Grandchamp, H de Verneuil, et al.
Human Mutation|November 26, 1999
Characterization of the 415G>A (E139K) PMM2 mutation in carbohydrate-deficient glycoprotein syndrome type Ia disrupting a splicing enhancer resulting in exon 5 skippingS Vuillaumier-Barrot, A Barnier, M Cuer, et al.
Pageof 14

Showing results (31-40 of 134) with videos related to

Sort By:
Pageof 14
British Journal of Haematology|May 1, 1995
Clonal analysis of haemopoietic cells in essential thrombocythaemiaN el Kassar, G Hetet, Y Li, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1992
A second ferritin L subunit is encoded by an intronless gene in the mouseF Renaudie, A K Yachou, B Grandchamp, et al.
Biochimica Et Biophysica Acta|July 16, 1986
Porphobilinogen deaminase is unstable in the absence of its substrateC Beaumont, B Grandchamp, M Bogard, et al.
European Journal of Immunology|September 1, 1992
Restricted diversity of V gamma 9-JP rearrangements in unstimulated human gamma/delta T lymphocytesM H Delfau, A J Hance, D Lecossier, et al.
Blood|May 1, 1990
Point mutations in the uroporphyrinogen III synthase gene in congenital erythropoietic porphyria (Günther's disease)J C Deybach, H de Verneuil, S Boulechfar, et al.
Leukemia|February 1, 1997
Delineation of a 6 cM commonly deleted region in childhood acute lymphoblastic leukemia on the 6q chromosomal armB Gérard, H Cavé, C Guidal, et al.
Biochimica Et Biophysica Acta|May 22, 1980
Studies of porphyrin synthesis in fibroblasts of patients with congenital erythropoietic porphyria and one patient with homozygous coproporphyriaB Grandchamp, J C Deybach, M Grelier, et al.
Experimental Cell Research|October 10, 1996
Expression of H and L ferritin mRNAs in mouse small intestineB Gérard, N Farman, K B Raja, et al.
The Journal of Clinical Investigation|September 1, 1983
Harderoporphyria: a variant hereditary coproporphyriaY Nordmann, B Grandchamp, H de Verneuil, et al.
Human Mutation|November 26, 1999
Characterization of the 415G>A (E139K) PMM2 mutation in carbohydrate-deficient glycoprotein syndrome type Ia disrupting a splicing enhancer resulting in exon 5 skippingS Vuillaumier-Barrot, A Barnier, M Cuer, et al.
Pageof 14