These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
111 related items for PubMed ID: 4672826
1. Microbiological hydroxylation of steroids. IV. The pattern of dihydroxylation of mono-oxygenated 5 -androstanes with cultures of the fungus Calonectria decora. Bell AM, Cherry PC, Clark IM, Denny WA, Jones ER, Meakins GD, Woodgate PD. J Chem Soc Perkin 1; 1972; 16():2081-95. PubMed ID: 4672826 [No Abstract] [Full Text] [Related]
2. Microbiological hydroxylation of steroids. V. The pattern of hydroxylation of dioxygenated 5 -androstanes with cultures of the fungus Calonectria decora. Bell AM, Denny WA, Jones ER, Meakins GD, Müller WE. J Chem Soc Perkin 1; 1972; 21():2759-65. PubMed ID: 4566120 [No Abstract] [Full Text] [Related]
4. Microbiological hydroxylation. Part XVII. C-19 hydroxylation of 17-oxo-5alpha-androstanes and 17-oxo-3alpha, 5-cyclo-5alpha-androstanes by the fungus Calonectria decora. Chambers VE, Denny WA, Jones ER, Meakins GD, Miners JO, Pinhey JT, Wilkins AL. J Chem Soc Perkin 1; 1975; (14):1359-63. PubMed ID: 1172505 [No Abstract] [Full Text] [Related]
5. Microbiological hydroxylation. Part XVII. Introduction of 16alpha-, 9alpha-, and 3alpha-hydroxy-groups into dioxygenated 5alpha-androstanes by the fungus Diaporthe celastrina. Bell AM, Boul AD, Jones ER, Meakins GD, Miners JO, Wilkins AL. J Chem Soc Perkin 1; 1975; (14):1364-6. PubMed ID: 1172506 [No Abstract] [Full Text] [Related]
6. Microbiological hydroxylation. XV, Hydroxylation in the terminal rings of mono- and di-oxygenated 5alpha-androstanes with the fungus Daedalea rufescens. Bell AM, Jones ER, Meakins GD, Miners JO, Pendlebury A. J Chem Soc Perkin 1; 1975; (4):357-60. PubMed ID: 1169247 [No Abstract] [Full Text] [Related]
8. Microbiological hydroxylation. Part XXI. Hydroxylations of 3-halogeno-17-oxo-, 3-halogeno-7-oxo-, and 17-halogeno-3-oxo-androstanes by the fungi Calonectria decora, Rhizopus nigricans, and Aspergillus ochraceus. Jones ER, Meakins GD, Miners JO, Wilkins AL. J Chem Soc Perkin 1; 1975; (22):2308-12. PubMed ID: 1239450 [No Abstract] [Full Text] [Related]
12. Microbiological hydroxylation of steroids. IX. Hydroxylation of diketones and keto-alcohols derived from 5 alpha-androstane with the fungi Rhizopus arrhizus and Rhizopus circinnans. Steroidal 18- and 19-proton magnetic resonance signals. Bell AM, Clark IM, Denny WA, Jones ER, Meakins GD, Müller WE. J Chem Soc Perkin 1; 1973; 19():2131-6. PubMed ID: 4796662 [No Abstract] [Full Text] [Related]
13. Microbiological hydroxylation. XII. Comparative behaviour of D-homogonane (perhydrochrysene) ketones and steroids. Ashton MJ, Bailey AS, Jones ER. J Chem Soc Perkin 1; 1974; 0(14):1658-65. PubMed ID: 4472200 [No Abstract] [Full Text] [Related]
15. Metabolism of androstenedione and progesterone in the isolated perfused rat liver. Eriksson H, Gustafsson JA, Pousette A. Eur J Biochem; 1972 May 23; 27(2):327-34. PubMed ID: 5050977 [No Abstract] [Full Text] [Related]
16. Microbiological hydroxylation of steroids. X. 1 beta, 11 alpha-dihydroxylation of 3 beta-hydroxy-5 alpha-prepnan-20-one and the hydroxylation of other 20-oxo-5 alpha-pregnanes with the fungus Aspergillys ochraceus. Clegg AS, Denny WA, Jones ER, Meakins GD, Pinhey JT. J Chem Soc Perkin 1; 1973 May 23; 19():2137-41. PubMed ID: 4796663 [No Abstract] [Full Text] [Related]
17. [Properties of Rhizopus sp. cultures in the transformation of steroid compounds. II. 11-alpha hydroxylation of delta 4-3 ketosteroids of the pregnane and androstane group]. Eysymontt I, Kotula W, Golonka J, Smolińska J, Iwaszkiewicz M. Acta Pol Pharm; 1975 May 23; 32(5):563-7. PubMed ID: 1199758 [No Abstract] [Full Text] [Related]
18. [Bioconversion of C19- and C21-steroids with parent and mutant strains of Curvularia lunata]. Kollerov VV, Shutov AA, Fokina VV, Sukhodol'skaia GV, Gulevskaia SA, Donova MV. Prikl Biokhim Mikrobiol; 2010 May 23; 46(2):212-20. PubMed ID: 20391766 [Abstract] [Full Text] [Related]
19. The formation of 16,17-dihydroxylated C 19 steroids from 16-dehydro C 19 steroids in liver microsomes from male and female rats. Gustafsson JA. Biochim Biophys Acta; 1973 Jan 19; 296(1):179-88. PubMed ID: 4693504 [No Abstract] [Full Text] [Related]
20. Microbiological hydroxylation. Part XX. Hydroxylation of dioxygenated 5alpha-androstanes with the fungi Absidia regnieri and Syncephelastrum racemosum. Bell AM, Jones ER, Meakins GD, Miners JO, Wilkins AL. J Chem Soc Perkin 1; 1975 Jan 19; (20):2040-3. PubMed ID: 1238423 [No Abstract] [Full Text] [Related] Page: [Next] [New Search]