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Biochimica Et Biophysica Acta|February 11, 1992
Developmental expression of hexokinase 1 in the ratL D Griffin, B D Gelb, V Adams, et al.
American Journal of Diseases of Children (1960)|July 1, 1987
Phenotypic features of patients with congenital adrenal hypoplasia and glycerol kinase deficiencyJ E Wise, R Matalon, A M Morgan, et al.
American Journal of Medical Genetics|September 15, 1991
San Luis Valley recombinant chromosome 8 and tetralogy of Fallot: a review of chromosome 8 anomalies and congenital heart diseaseB D Gelb, J A Towbin, E R McCabe, et al.
Biology of the Neonate|January 1, 1987
Development of enzymes of glycerol metabolism in human fetal liverD Sadava, M Depper, M Gilbert, et al.
Biochemical and Biophysical Research Communications|June 28, 1991
Protein kinase activity of rat brain hexokinaseV Adams, L D Griffin, B D Gelb, et al.
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.
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