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T Gelbart

Showing results (31-40 of 81) with videos related to

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The Journal of Clinical Investigation|January 1, 1986
Erythrocyte glutathione synthetase deficiency leads not only to glutathione but also to glutathione-S-transferase deficiencyE Beutler, T Gelbart, C Pegelow
Blood|January 9, 1999
Coinheritance of alleles associated with hemochromatosis and hereditary hyperferritinemia-cataract syndromeJ C Barton, E Beutler, T Gelbart
Drug Metabolism and Disposition: the Biological Fate of Chemicals|March 22, 2001
Genetics of iron storage and hemochromatosisE Beutler, V Felitti, T Gelbart, et al.
Biochemical Pharmacology|March 15, 1988
Mechanism of improved maintenance of 2,3-diphosphoglycerate in stored blood by the xanthone compound 2-(2-hydroxyethoxy)-6-(1-H-tetrazole-5-yl)xanthen-9-one (BW A440C)E Beutler, L Forman, C West, et al.
American Journal of Hematology|September 1, 1986
G-6-PD Walter Reed: possible insight into "structural" NADP in G-6-PDE Beutler, K Hartman, T Gelbart, et al.
Annals of Internal Medicine|September 9, 2000
The effect of HFE genotypes on measurements of iron overload in patients attending a health appraisal clinicE Beutler, V Felitti, T Gelbart, et al.
The Journal of Biological Chemistry|March 5, 1991
DNA sequence abnormalities of human glucose-6-phosphate dehydrogenase variantsE Beutler, W Kuhl, T Gelbart, et al.
Acta Haematologica|January 13, 2001
Three Gaucher-disease-producing mutations in a patient with Gaucher disease: mechanism and diagnostic implicationsE Beutler, H Liebman, T Gelbart, et al.
International Journal of Laboratory Hematology|December 17, 2013
Hemolytic anemia associated with a novel heterozygote mutation 1183A in the PK-LR gene (PK- Jordan)N S Karadsheh, T Gelbart, R G Naffa
Clinical Genetics|March 21, 2002
A previously undescribed nonsense mutation of the HFE geneE Beutler, M J Griffin, T Gelbart, et al.
Pageof 9

Showing results (31-40 of 81) with videos related to

Sort By:
Pageof 9
The Journal of Clinical Investigation|January 1, 1986
Erythrocyte glutathione synthetase deficiency leads not only to glutathione but also to glutathione-S-transferase deficiencyE Beutler, T Gelbart, C Pegelow
Blood|January 9, 1999
Coinheritance of alleles associated with hemochromatosis and hereditary hyperferritinemia-cataract syndromeJ C Barton, E Beutler, T Gelbart
Drug Metabolism and Disposition: the Biological Fate of Chemicals|March 22, 2001
Genetics of iron storage and hemochromatosisE Beutler, V Felitti, T Gelbart, et al.
Biochemical Pharmacology|March 15, 1988
Mechanism of improved maintenance of 2,3-diphosphoglycerate in stored blood by the xanthone compound 2-(2-hydroxyethoxy)-6-(1-H-tetrazole-5-yl)xanthen-9-one (BW A440C)E Beutler, L Forman, C West, et al.
American Journal of Hematology|September 1, 1986
G-6-PD Walter Reed: possible insight into "structural" NADP in G-6-PDE Beutler, K Hartman, T Gelbart, et al.
Annals of Internal Medicine|September 9, 2000
The effect of HFE genotypes on measurements of iron overload in patients attending a health appraisal clinicE Beutler, V Felitti, T Gelbart, et al.
The Journal of Biological Chemistry|March 5, 1991
DNA sequence abnormalities of human glucose-6-phosphate dehydrogenase variantsE Beutler, W Kuhl, T Gelbart, et al.
Acta Haematologica|January 13, 2001
Three Gaucher-disease-producing mutations in a patient with Gaucher disease: mechanism and diagnostic implicationsE Beutler, H Liebman, T Gelbart, et al.
International Journal of Laboratory Hematology|December 17, 2013
Hemolytic anemia associated with a novel heterozygote mutation 1183A in the PK-LR gene (PK- Jordan)N S Karadsheh, T Gelbart, R G Naffa
Clinical Genetics|March 21, 2002
A previously undescribed nonsense mutation of the HFE geneE Beutler, M J Griffin, T Gelbart, et al.
Pageof 9