Search Results - "Dahl, H.H.M."

The construction of cosmid libraries which can be used to transform eukaryotic cells by Grosveld, F.G., Lund, T., Murray, E.J., Mellor, A.L, Dahl, H.H.M., Flavell, R.A.

“…Cosmid vectors have been developed which carry selective markers for growth in bacteria (β lactamase gene) and animal cells (the Herpes Simplex virus thymidine…”
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Mitochondrial myopathy with tRNALeu(UUR) mutation and complex I deficiency responsive to riboflavin by Ogle, R.F. (Royal Alexandra Hospital for Children, Westmead, New South Wales, Australia.), Christodoulou, J, Fagan, E, Blok, R.B, Kirby, D.M, Seller, K.L, Dahl, H.H.M, Thorburn, D.R

“…Deficiency of complex I (reduced nicotinamide adenine dinucleotide dehydrogenase-ubiquinone oxidoreductase) of the mitochondrial respiratory chain may be seen…”
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Pyruvate dehydrogenase deficiency caused by a 5 base pair duplication in the E1 alpha subunit by Hansen, L L, Brown, G K, Brown, R M, Dahl, H H

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Structure and expression of a cloned β°thalassaemic globin gene by Moschonas, N., de Boer, E., Grosveld, F.G., Dahl, H.H.M., Wright, S., Shewmaker, C.K., Flavell, R.A.

“…We have cloned the single β-globin gene from an Italian patient who is a double heterozygote for (β°/δβ° thalassaemia. RNA isolated from nucleated red cells…”
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Application of DNA-DNA hybridization of dual labeled probes to the detection of trisomy 21, monosomy 21, and sex determination by DAHL, H.-H. M, CHOO, K. H, DANKS, D. M

“…Chromosomal aneuploidy is usually identified by cytogenetic methods. However, for some purposes it would be desirable to have an easier method of recognizing…”
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effect of streptozotocin-induced diabetes on phenylalanine hydroxylase expression in rat liver by Taylor, D.S, Dahl, H.H.M, Mercer, J.F.B, Green, A.K, Fisher, M.J

“…The impact of experimentally induced diabetes on the expression of rat liver phenylalanine hydroxylase has been investigated. A significant elevation in…”
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Purification of four eukaryotic initiation factors required for natural mRNA translation by Dahl, H H, Blair, G E

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mtDNA Deletion in a Patient with Symptoms of Mitochondrial Cytopathy but without Ragged Red Fibers by Blok, R.B., Thorburn, D.R., Danks, D.M., Dahl, H.H.M.

“…We describe a heteroplasmic 4237-bp mitochondrial DNA (mtDNA) deletion in an 11-year-old girl who has suffered from progressive illness since birth. Her…”
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