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 (21-30 of 81) with videos related to

Pageof 9
Sort By:
Human Genetics|June 1, 1994
Tight linkage of pyruvate kinase (PKLR) and glucocerebrosidase (GBA) genesD Glenn, T Gelbart, E Beutler
Proceedings of the National Academy of Sciences of the United States of America|June 1, 1985
6-Phosphogluconolactonase deficiency, a hereditary erythrocyte enzyme deficiency: possible interaction with glucose-6-phosphate dehydrogenase deficiencyE Beutler, W Kuhl, T Gelbart
Genomics|April 1, 1992
Polymorphisms in the human glucocerebrosidase geneE Beutler, C West, T Gelbart
Biotechniques|August 1, 1990
Interference of heparin with the polymerase chain reactionE Beutler, T Gelbart, W Kuhl
Molecular Medicine (Cambridge, Mass.)|November 1, 1994
Glucocerebrosidase mutations in Gaucher diseaseE Beutler, A Demina, T Gelbart
Blood Cells, Molecules & Diseases|January 10, 2002
Synergy between TLR2 and TLR4: a safety mechanismE Beutler, T Gelbart, C West
British Journal of Haematology|March 1, 1986
Blood cell phosphogluconolactonase: assay and propertiesE Beutler, W Kuhl, T Gelbart
Proceedings of the National Academy of Sciences of the United States of America|July 8, 1998
Racial variability in the UDP-glucuronosyltransferase 1 (UGT1A1) promoter: a balanced polymorphism for regulation of bilirubin metabolism?E Beutler, T Gelbart, A Demina
American Journal of Human Genetics|May 1, 1990
Linkage of the PvuII polymorphism with the common Jewish mutation for Gaucher diseaseA Zimran, T Gelbart, E Beutler
Genomics|January 1, 1993
Identification of six new Gaucher disease mutationsE Beutler, T Gelbart, C West
Pageof 9

Showing results (21-30 of 81) with videos related to

Sort By:
Pageof 9
Human Genetics|June 1, 1994
Tight linkage of pyruvate kinase (PKLR) and glucocerebrosidase (GBA) genesD Glenn, T Gelbart, E Beutler
Proceedings of the National Academy of Sciences of the United States of America|June 1, 1985
6-Phosphogluconolactonase deficiency, a hereditary erythrocyte enzyme deficiency: possible interaction with glucose-6-phosphate dehydrogenase deficiencyE Beutler, W Kuhl, T Gelbart
Genomics|April 1, 1992
Polymorphisms in the human glucocerebrosidase geneE Beutler, C West, T Gelbart
Biotechniques|August 1, 1990
Interference of heparin with the polymerase chain reactionE Beutler, T Gelbart, W Kuhl
Molecular Medicine (Cambridge, Mass.)|November 1, 1994
Glucocerebrosidase mutations in Gaucher diseaseE Beutler, A Demina, T Gelbart
Blood Cells, Molecules & Diseases|January 10, 2002
Synergy between TLR2 and TLR4: a safety mechanismE Beutler, T Gelbart, C West
British Journal of Haematology|March 1, 1986
Blood cell phosphogluconolactonase: assay and propertiesE Beutler, W Kuhl, T Gelbart
Proceedings of the National Academy of Sciences of the United States of America|July 8, 1998
Racial variability in the UDP-glucuronosyltransferase 1 (UGT1A1) promoter: a balanced polymorphism for regulation of bilirubin metabolism?E Beutler, T Gelbart, A Demina
American Journal of Human Genetics|May 1, 1990
Linkage of the PvuII polymorphism with the common Jewish mutation for Gaucher diseaseA Zimran, T Gelbart, E Beutler
Genomics|January 1, 1993
Identification of six new Gaucher disease mutationsE Beutler, T Gelbart, C West
Pageof 9