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127 related items for PubMed ID: 9648734

  • 1. Identification of elicitor-induced cytochrome P450s of soybean (Glycine max L.) using differential display of mRNA.
    Schopfer CR, Ebel J.
    Mol Gen Genet; 1998 May; 258(4):315-22. PubMed ID: 9648734
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  • 2. Cloning of wound-induced cytochrome P450 monooxygenases expressed in pea.
    Frank MR, Deyneka JM, Schuler MA.
    Plant Physiol; 1996 Mar; 110(3):1035-46. PubMed ID: 8819874
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  • 3. Whole genome co-expression analysis of soybean cytochrome P450 genes identifies nodulation-specific P450 monooxygenases.
    Guttikonda SK, Trupti J, Bisht NC, Chen H, An YQ, Pandey S, Xu D, Yu O.
    BMC Plant Biol; 2010 Nov 09; 10():243. PubMed ID: 21062474
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  • 4. Molecular characterization and functional expression of dihydroxypterocarpan 6a-hydroxylase, an enzyme specific for pterocarpanoid phytoalexin biosynthesis in soybean (Glycine max L.).
    Schopfer CR, Kochs G, Lottspeich F, Ebel J.
    FEBS Lett; 1998 Aug 07; 432(3):182-6. PubMed ID: 9720921
    [Abstract] [Full Text] [Related]

  • 5. Cytochrome P450 superfamily in Arabidopsis thaliana: isolation of cDNAs, differential expression, and RFLP mapping of multiple cytochromes P450.
    Mizutani M, Ward E, Ohta D.
    Plant Mol Biol; 1998 May 07; 37(1):39-52. PubMed ID: 9620263
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  • 11. Molecular cloning and characterization of a cDNA for pterocarpan 4-dimethylallyltransferase catalyzing the key prenylation step in the biosynthesis of glyceollin, a soybean phytoalexin.
    Akashi T, Sasaki K, Aoki T, Ayabe S, Yazaki K.
    Plant Physiol; 2009 Feb 07; 149(2):683-93. PubMed ID: 19091879
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  • 12. Cloning, heterologous expression, and functional characterization of 5-epi-aristolochene-1,3-dihydroxylase from tobacco (Nicotiana tabacum).
    Ralston L, Kwon ST, Schoenbeck M, Ralston J, Schenk DJ, Coates RM, Chappell J.
    Arch Biochem Biophys; 2001 Sep 15; 393(2):222-35. PubMed ID: 11556809
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  • 13. Induction of phytoalexin synthesis in soybean. Stereospecific 3,9-dihydroxypterocarpan 6a-hydroxylase from elicitor-induced soybean cell cultures.
    Hagmann ML, Heller W, Grisebach H.
    Eur J Biochem; 1984 Jul 02; 142(1):127-31. PubMed ID: 6540173
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  • 14. Regiospecific cytochrome P450 limonene hydroxylases from mint (Mentha) species: cDNA isolation, characterization, and functional expression of (-)-4S-limonene-3-hydroxylase and (-)-4S-limonene-6-hydroxylase.
    Lupien S, Karp F, Wildung M, Croteau R.
    Arch Biochem Biophys; 1999 Aug 01; 368(1):181-92. PubMed ID: 10415126
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  • 15. The primary sequence of cytochrome P450tyr, the multifunctional N-hydroxylase catalyzing the conversion of L-tyrosine to p-hydroxyphenylacetaldehyde oxime in the biosynthesis of the cyanogenic glucoside dhurrin in Sorghum bicolor (L.) Moench.
    Koch BM, Sibbesen O, Halkier BA, Svendsen I, Møller BL.
    Arch Biochem Biophys; 1995 Oct 20; 323(1):177-86. PubMed ID: 7487064
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  • 16. Further characterization of cytochrome P450 involved in phytoalexin synthesis in soybean: cytochrome P450 cinnamate 4-hydroxylase and 3,9-dihydroxypterocarpan 6a-hydroxylase.
    Kochs G, Werck-Reichhart D, Grisebach H.
    Arch Biochem Biophys; 1992 Feb 14; 293(1):187-94. PubMed ID: 1731635
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  • 17. Defense response in slash pine: chitosan treatment alters the abundance of specific mRNAs.
    Mason ME, Davis JM.
    Mol Plant Microbe Interact; 1997 Jan 14; 10(1):135-7. PubMed ID: 9002276
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  • 18. Isolation and sequence of a cDNA encoding the Jerusalem artichoke cinnamate 4-hydroxylase, a major plant cytochrome P450 involved in the general phenylpropanoid pathway.
    Teutsch HG, Hasenfratz MP, Lesot A, Stoltz C, Garnier JM, Jeltsch JM, Durst F, Werck-Reichhart D.
    Proc Natl Acad Sci U S A; 1993 May 01; 90(9):4102-6. PubMed ID: 8097885
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  • 19. Phytoalexin synthesis in soybean: purification and reconstitution of cytochrome P450 3,9-dihydroxypterocarpan 6a-hydroxylase and separation from cytochrome P450 cinnamate 4-hydroxylase.
    Kochs G, Grisebach H.
    Arch Biochem Biophys; 1989 Sep 01; 273(2):543-53. PubMed ID: 2505672
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  • 20. Identification of a cytochrome P450 cDNA (CYP98A5) from Phaseolus vulgaris, inducible by 3,5-dichlorosalicylic acid and 2,6-dichloro isonicotinic acid.
    Basson AE, Dubery IA.
    J Plant Physiol; 2007 Apr 01; 164(4):421-8. PubMed ID: 16584810
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