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1. A parthenogenetic quasi-program causes teratoma-like tumors during aging in wild-type C. elegans

2. C. elegans flavin-containing monooxygenase-4 is essential for osmoregulation in hypotonic stress

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3. A parthenogenetic quasi-program causes teratoma-like tumors during aging in wild-type

4. The fmo genes of Caenorhabditis elegans and C. briggsae: characterisation, gene expression and comparative genomic analysis

5. Distribution of mRNAs Encoding the Peroxisome Proliferator-Activated Receptor α, β, and γ and the Retinoid X Receptor α, β, and γ in Rat Central Nervous System

6. Quantification and cellular localization of expression in human skin of genes encoding flavin-containing monooxygenases and cytochromes P450 2 2Abbreviations: FMO, flavin-containing monooxygenase; CYP, cytochrome P450; KGM, keratinocyte growth medium; DMEM, Dulbecco’s modified Eagle’s medium

7. Compound heterozygosity for missense mutations in the flavin-containing monooxygenase 3 (FMO3) gene in patients with fish-odour syndrome

8. Ethnic Differences in Human Flavin-Containing Monooxygenase 2 (FMO2) Polymorphisms: Detection of Expressed Protein in African-Americans

9. A novel mutation in the flavin-containing monooxygenase 3 gene, FMO3, that causes fish-odour syndrome: activity of the mutant enzyme assessed by proton NMR spectroscopy

10. Localization of Human Flavin-Containing Monooxygenase GenesFMO2andFMO5to Chromosome 1q

11. Differential Developmental and Tissue-Specific Regulation of Expression of the Genes Encoding Three Members of the Flavin-Containing Monooxygenase Family of Man, FMO1, FMO3 and FMO4

12. Seamless replacement of Autographa californica multiple nucleopolyhedrovirus gp64 with each of five novel type II alphabaculovirus fusion sequences generates pseudotyped virus that fails to transduce mammalian cells

13. Localization of Genes Encoding Three Distinct Flavin-Containing Monooxygenases to Human Chromosome 1q

14. Escherichia coli MW005: lambda Red-mediated recombineering and copy-number induction of oriV-equipped constructs in a single host

15. Cloning, primary sequence, and chromosomal mapping of a human flavin-containing monooxygenase (FMO1)

16. RNA interference mediated in human primary cells via recombinant baculoviral vectors

17. Genetic polymorphisms of flavin-containing monooxygenase (FMO)

18. The peroxisome proliferator-activated receptor alpha-selective activator ciprofibrate upregulates expression of genes encoding fatty acid oxidation and ketogenesis enzymes in rat brain

19. Regulation of the Ketogenic Enzyme Mitochondrial 3-Hydroxy-3-Methylglutaryl-COA Synthase in Astrocytes and Meningeal Fibroblasts

20. The flavin-containing monooxygenase 2 gene (FMO2) of humans, but not of other primates, encodes a truncated, nonfunctional protein

21. Structural organization of the human flavin-containing monooxygenase 3 gene (FMO3), the favored candidate for fish-odor syndrome, determined directly from genomic DNA

22. Missense mutation in flavin-containing mono-oxygenase 3 gene, FMO3, underlies fish-odour syndrome

23. A simplified counter-selection recombineering protocol for creating fluorescent protein reporter constructs directly from C. elegans fosmid genomic clones

24. The molecular biology of the flavin-containing monooxygenases of man

25. A nomenclature for the mammalian flavin-containing monooxygenase gene family based on amino acid sequence identities

26. Counter-selection recombineering of the baculovirus genome: a strategy for seamless modification of repeat-containing BACs

27. Cloning, primary sequence and chromosomal localization of human FMO2, a new member of the flavin-containing mono-oxygenase family

29. Effect of poly rI:rC treatment upon the metabolism of [14C]-paracetamol in the BALB/cJ mouse

30. The role of intestinal microflora in the formation of the methylthio adduct metabolites of paracetamol

31. Effect of interferon synthesis upon the metabolism of [carboxyl-14C]-aspirin in the mouse

32. Depression of oxidative metabolism of aspirin in mice via an interferon-associated mechanism in relation to Reye's syndrome