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

T Gelbart

Showing results (41-50 of 81) with videos related to

Pageof 9
Sort By:
Blood|October 9, 1999
The molecular basis of a case of gamma-glutamylcysteine synthetase deficiencyE Beutler, T Gelbart, T Kondo, et al.
Acta Haematologica|February 29, 2000
Effect of ozone on red blood cell enzymes and intermediatesA Zimran, G Wasser, L Forman, et al.
Blood Cells, Molecules & Diseases|January 1, 1995
A strategy for cloning the hereditary hemochromatosis geneE Beutler, T Gelbart, C West, et al.
Blood|April 1, 1992
Mutations in Jewish patients with Gaucher diseaseE Beutler, T Gelbart, W Kuhl, et al.
Blood Cells, Molecules & Diseases|February 8, 2000
Commentary on HFE S65C variant is not associated with increased transferrin saturation in voluntary blood donors by Naveen Arya, Subrata Chakrabrati, Robert A. Hegele, Paul C. AdamsE Beutler, V J Felitti, N J Ho, et al.
Blood|January 1, 1990
Gamma-glutamylcysteine synthetase deficiency and hemolytic anemiaE Beutler, R Moroose, L Kramer, et al.
Blood Cells, Molecules & Diseases|January 1, 1995
Five new Gaucher disease mutationsE Beutler, T Gelbart, A Demina, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 1, 1985
Heterogeneity in type I Gaucher disease demonstrated by restriction mapping of the geneJ Sorge, T Gelbart, C West, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1991
Identification of the second common Jewish Gaucher disease mutation makes possible population-based screening for the heterozygous stateE Beutler, T Gelbart, W Kuhl, et al.
Blood|December 1, 1980
In vivo survival studies of 51Cr-labeled methyl acetimidate treated erythrocytes in patients with sickle cell diseaseT G Gabuzda, T L Chao, M R Berenfeld, et al.
Pageof 9

Showing results (41-50 of 81) with videos related to

Sort By:
Pageof 9
Blood|October 9, 1999
The molecular basis of a case of gamma-glutamylcysteine synthetase deficiencyE Beutler, T Gelbart, T Kondo, et al.
Acta Haematologica|February 29, 2000
Effect of ozone on red blood cell enzymes and intermediatesA Zimran, G Wasser, L Forman, et al.
Blood Cells, Molecules & Diseases|January 1, 1995
A strategy for cloning the hereditary hemochromatosis geneE Beutler, T Gelbart, C West, et al.
Blood|April 1, 1992
Mutations in Jewish patients with Gaucher diseaseE Beutler, T Gelbart, W Kuhl, et al.
Blood Cells, Molecules & Diseases|February 8, 2000
Commentary on HFE S65C variant is not associated with increased transferrin saturation in voluntary blood donors by Naveen Arya, Subrata Chakrabrati, Robert A. Hegele, Paul C. AdamsE Beutler, V J Felitti, N J Ho, et al.
Blood|January 1, 1990
Gamma-glutamylcysteine synthetase deficiency and hemolytic anemiaE Beutler, R Moroose, L Kramer, et al.
Blood Cells, Molecules & Diseases|January 1, 1995
Five new Gaucher disease mutationsE Beutler, T Gelbart, A Demina, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 1, 1985
Heterogeneity in type I Gaucher disease demonstrated by restriction mapping of the geneJ Sorge, T Gelbart, C West, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1991
Identification of the second common Jewish Gaucher disease mutation makes possible population-based screening for the heterozygous stateE Beutler, T Gelbart, W Kuhl, et al.
Blood|December 1, 1980
In vivo survival studies of 51Cr-labeled methyl acetimidate treated erythrocytes in patients with sickle cell diseaseT G Gabuzda, T L Chao, M R Berenfeld, et al.
Pageof 9