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Biochemical and Molecular Medicine|December 1, 1995
Comparison of human VDAC1 with streptococcal streptokinase and bovine bactericidal permeability increasing protein: role of structural information in identifying functionally significant domainsK M McCabe, D A Wheeler, V Adams, et al.PCR Methods and Applications|February 1, 1992
Rapid mapping of Escherichia coli::Tn5 insertion mutations by REP-Tn5 PCRP S Subramanian, J Versalovic, E R McCabe, et al.Life Sciences|October 20, 1986
1-Thioglycerol: inhibitor of glycerol kinase activity in vitro and in situW K Seltzer, G Dhariwal, H A Mckelvey, et al.Pediatric Research|January 1, 1980
Multiple acyl-CoA dehydrogenase deficiency (glutaric aciduria type II) with transient hypersarcosinemia and sarcosinuria; possible inherited deficiency of an electron transfer flavoproteinS I Goodman, E R McCabe, P V Fennessey, et al.Genomics|March 1, 1994
Human genes encoding the voltage-dependent anion channel (VDAC) of the outer mitochondrial membrane: mapping and identification of two new isoformsE Blachly-Dyson, A Baldini, M Litt, et al.Obstetrics and Gynecology|September 1, 1988
Teratogenic effects of first-trimester cyclophosphamide therapyB Kirshon, N Wasserstrum, R Willis, et al.The Journal of Pediatrics|August 26, 1998
Minipuberty of infancy and adolescent pubertal function in adrenal hypoplasia congenitaK B Kaiserman, J M Nakamoto, M E Geffner, et al.Human Genetics|March 1, 1987
DNA microextraction from dried blood spots on filter paper blotters: potential applications to newborn screeningE R McCabe, S Z Huang, W K Seltzer, et al.Pediatrician|January 1, 1983
The use of insulin pump therapy in adolescentsG J Klingensmith, B P Giordano, E R McCabe, et al.Human Genetics|August 1, 1991
Isodicentric X chromosome in a patient with Turner syndrome--implications for localization of the X-inactivation centerA L Pettigrew, E R McCabe, F F Elder, et al.Pageof 12