Tham khảo Ribose 5-phosphate

  1. ↑ Levene PA, Stiller ET (tháng 2 năm 1934). “The Synthesis of Ribose-5-Phosphoric Acid”. Journal of Biological Chemistry 104 (2): 299–306. 
  2. 1 2 3 4 5 6 Berg JM, Tymoczko JL, Stryer L (2015). Biochemistry (ấn bản 7). W.H. Freeman. tr. 589–613. ISBN 978-1-4292-7635-1. 
  3. ↑ Kruger NJ, von Schaewen A (tháng 6 năm 2003). “The oxidative pentose phosphate pathway: structure and organisation”. Current Opinion in Plant Biology 6 (3): 236–46. PMID 12753973. doi:10.1016/s1369-5266(03)00039-6. 
  4. ↑ Zhang R, Andersson CE, Savchenko A, Skarina T, Evdokimova E, Beasley S, Arrowsmith CH, Edwards AM, Joachimiak A, Mowbray SL (tháng 1 năm 2003). “Structure of Escherichia coli ribose-5-phosphate isomerase: a ubiquitous enzyme of the pentose phosphate pathway and the Calvin cycle”. Structure 11 (1): 31–42. PMC 2792023. PMID 12517338. doi:10.1016/s0969-2126(02)00933-4. 
  5. ↑ Coleman JP, Smith CJ (2007). X Pharm: The Comprehensive Pharmacology Reference. tr. 1–6. ISBN 9780080552323. doi:10.1016/b978-008055232-3.60227-2. 
  6. ↑ “Nucleotides”. IUPAC Compendium of Chemical Terminology. International Union of Pure and Applied Chemistry. 2009. ISBN 978-0-9678550-9-7. doi:10.1351/goldbook.n04255. 
  7. ↑ Engelking LR (2015). “Purine Biosynthesis”. Textbook of Veterinary Physiological Chemistry . tr. 88–92. ISBN 978-0-12-391909-0. doi:10.1016/b978-0-12-391909-0.50015-3. 
  8. 1 2 3 Pelley JW (2011). “Purine, Pyrimidine, and Single-Carbon Metabolism”. Elsevier's Integrated Review Biochemistry (ấn bản 2). tr. 119–124. ISBN 9780323074469. doi:10.1016/b978-0-323-07446-9.00014-3. 
  9. ↑ Engelking LR (2015). “Chapter 31  — Carbohydrate Metabolism in Erythrocytes”. Textbook of Veterinary Physiological Chemistry . tr. 190–194. ISBN 978-0-12-391909-0. doi:10.1016/b978-0-12-391909-0.50031-1. 
  10. ↑ Schramm VL, Grubmeyer C (2004). Phosphoribosyltransferase Mechanisms and Roles in Nucleic Acid Metabolism. Progress in Nucleic Acid Research and Molecular Biology 78. tr. 261–304. ISBN 9780125400787. PMID 15210333. doi:10.1016/s0079-6603(04)78007-1. 
  11. ↑ Ingle RA (tháng 1 năm 2011). “Histidine biosynthesis”. The Arabidopsis Book 9: e0141. PMC 3266711. PMID 22303266. doi:10.1199/tab.0141. 
  12. ↑ Evans WR, San Pietro A (tháng 1 năm 1966). “Phosphorolysis of adenosine diphosphoribose”. Archives of Biochemistry and Biophysics 113 (1): 236–44. PMID 4287446. doi:10.1016/0003-9861(66)90178-0. 
  13. ↑ Wamelink MM, Grüning NM, Jansen EE, Bluemlein K, Lehrach H, Jakobs C, Ralser M (tháng 9 năm 2010). “The difference between rare and exceptionally rare: molecular characterization of ribose 5-phosphate isomerase deficiency”. Journal of Molecular Medicine 88 (9): 931–9. PMID 20499043. doi:10.1007/s00109-010-0634-1. 
  14. ↑ Huck JH, Verhoeven NM, Struys EA, Salomons GS, Jakobs C, van der Knaap MS (tháng 4 năm 2004). “Ribose-5-phosphate isomerase deficiency: new inborn error in the pentose phosphate pathway associated with a slowly progressive leukoencephalopathy”. American Journal of Human Genetics 74 (4): 745–51. PMC 1181951. PMID 14988808. doi:10.1086/383204. 
  15. ↑ Jiménez RT, Puig JG (2012). “Purine Metabolism in the Pathogenesis of Hyperuricemia and Inborn Errors of Purine Metabolism Associated With Disease”. Gout & Other Crystal Arthropathies. tr. 36–50. ISBN 978-1-4377-2864-4. doi:10.1016/b978-1-4377-2864-4.10003-x. 
  16. ↑ Ichida K, Hosoyamada M, Hosoya T, Endou H (2009). “Primary Metabolic and Renal Hyperuricemia”. Genetic Diseases of the Kidney. tr. 651–660. ISBN 978-0-12-449851-8. doi:10.1016/b978-0-12-449851-8.00038-3. 
  17. ↑ Singer HS, Mink JW, Gilbert DL, Jankovic J (2010). “Inherited Metabolic Disorders Associated with Extrapyramidal Symptoms”. Movement Disorders in Childhood. tr. 164–204. ISBN 978-0-7506-9852-8. doi:10.1016/B978-0-7506-9852-8.00015-1. 

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