(Q28138036)

1

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M Odièvre

2

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Q Wu

3

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A Wilson

4

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J J Huizenga

5

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S W Scherer

7

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R A Gravel

Expression of Bacterial β-Galactosidase in Animal Cells

8

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language of work or name

English

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publication date

15 November 1999

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published in

Gene

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volume

240

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issue

1

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page(s)

75-88

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cites work

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7 January 2021

Escherichia coli ferredoxin NADP+ reductase: activation of E. coli anaerobic ribonucleotide reduction, cloning of the gene (fpr), and overexpression of the protein

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A high-resolution physical and transcript map of the Cri du chat region of human chromosome 5p.

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Cloning, sequencing, gene organization, and localization of the human ribosomal protein RPL23A gene

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CpG islands in vertebrate genomes

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Defects in auxiliary redox proteins lead to functional methionine synthase deficiency

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Databases on transcriptional regulation: TRANSFAC, TRRD and COMPEL

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The mechanism of adenosylmethionine-dependent activation of methionine synthase: a rapid kinetic analysis of intermediates in reductive methylation of Cob(II)alamin enzyme

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Cloning and mapping of a cDNA for methionine synthase reductase, a flavoprotein defective in patients with homocystinuria

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CAT constructions with multiple unique restriction sites for the functional analysis of eukaryotic promoters and regulatory elements

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Construction of plasmids that express E. coli beta-galactosidase in mammalian cells.

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Regulation of the fibroblast growth factor receptor 3 promoter and intron I enhancer by Sp1 family transcription factors

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Transcription initiation from the dihydrofolate reductase promoter is positioned by HIP1 binding at the initiation site

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Isolation, cloning, mapping, and nucleotide sequencing of the gene encoding flavodoxin in Escherichia coli

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NADPH-cytochrome P-450 oxidoreductase gene organization correlates with structural domains of the protein

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Altered vitamin B12 metabolism in fibroblasts from a patient with megaloblastic anemia and homocystinuria due to a new defect in methionine biosynthesis

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Genome sequence of the nematode C. elegans: a platform for investigating biology

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High level transcription of the complement regulatory protein CD59 requires an enhancer located in intron 1.

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A common variant in methionine synthase reductase combined with low cobalamin (vitamin B12) increases risk for spina bifida

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