Ribose 5-phosphate (Vietnamese Wikipedia)

Analysis of information sources in references of the Wikipedia article "Ribose 5-phosphate" in Vietnamese language version.

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15doi.org

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10nih.gov

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3archive.org

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1jbc.org

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1iupac.org

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archive.org

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. doi:10.1086/383204. PMC 1181951. PMID 14988808.
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. doi:10.1016/b978-1-4377-2864-4.10003-x. ISBN 978-1-4377-2864-4.
Singer HS, Mink JW, Gilbert DL, Jankovic J (2010). “Inherited Metabolic Disorders Associated with Extrapyramidal Symptoms”. Movement Disorders in Childhood. tr. 164–204. doi:10.1016/B978-0-7506-9852-8.00015-1. ISBN 978-0-7506-9852-8.

doi.org

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. doi:10.1016/s1369-5266(03)00039-6. PMID 12753973.
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. doi:10.1016/s0969-2126(02)00933-4. PMC 2792023. PMID 12517338.
Coleman JP, Smith CJ (2007). X Pharm: The Comprehensive Pharmacology Reference. tr. 1–6. doi:10.1016/b978-008055232-3.60227-2. ISBN 9780080552323.
“Nucleotides”. IUPAC Compendium of Chemical Terminology. International Union of Pure and Applied Chemistry. 2009. doi:10.1351/goldbook.n04255. ISBN 978-0-9678550-9-7.
Engelking LR (2015). “Purine Biosynthesis”. Textbook of Veterinary Physiological Chemistry . tr. 88–92. doi:10.1016/b978-0-12-391909-0.50015-3. ISBN 978-0-12-391909-0.
Pelley JW (2011). “Purine, Pyrimidine, and Single-Carbon Metabolism”. Elsevier's Integrated Review Biochemistry (ấn bản thứ 2). tr. 119–124. doi:10.1016/b978-0-323-07446-9.00014-3. ISBN 9780323074469.
Engelking LR (2015). “Chapter 31 — Carbohydrate Metabolism in Erythrocytes”. Textbook of Veterinary Physiological Chemistry . tr. 190–194. doi:10.1016/b978-0-12-391909-0.50031-1. ISBN 978-0-12-391909-0.
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. doi:10.1016/s0079-6603(04)78007-1. ISBN 9780125400787. PMID 15210333.
Ingle RA (tháng 1 năm 2011). “Histidine biosynthesis”. The Arabidopsis Book. 9: e0141. doi:10.1199/tab.0141. PMC 3266711. PMID 22303266.
Evans WR, San Pietro A (tháng 1 năm 1966). “Phosphorolysis of adenosine diphosphoribose”. Archives of Biochemistry and Biophysics. 113 (1): 236–44. doi:10.1016/0003-9861(66)90178-0. PMID 4287446.
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. doi:10.1007/s00109-010-0634-1. PMID 20499043.
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. doi:10.1086/383204. PMC 1181951. PMID 14988808.
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. doi:10.1016/b978-1-4377-2864-4.10003-x. ISBN 978-1-4377-2864-4.
Ichida K, Hosoyamada M, Hosoya T, Endou H (2009). “Primary Metabolic and Renal Hyperuricemia”. Genetic Diseases of the Kidney. tr. 651–660. doi:10.1016/b978-0-12-449851-8.00038-3. ISBN 978-0-12-449851-8.
Singer HS, Mink JW, Gilbert DL, Jankovic J (2010). “Inherited Metabolic Disorders Associated with Extrapyramidal Symptoms”. Movement Disorders in Childhood. tr. 164–204. doi:10.1016/B978-0-7506-9852-8.00015-1. ISBN 978-0-7506-9852-8.

iupac.org

goldbook.iupac.org

“Nucleotides”. IUPAC Compendium of Chemical Terminology. International Union of Pure and Applied Chemistry. 2009. doi:10.1351/goldbook.n04255. ISBN 978-0-9678550-9-7.

jbc.org

Levene PA, Stiller ET (tháng 2 năm 1934). “The Synthesis of Ribose-5-Phosphoric Acid”. Journal of Biological Chemistry. 104 (2): 299–306.

nih.gov

pubmed.ncbi.nlm.nih.gov

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. doi:10.1016/s1369-5266(03)00039-6. PMID 12753973.
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. doi:10.1016/s0969-2126(02)00933-4. PMC 2792023. PMID 12517338.
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. doi:10.1016/s0079-6603(04)78007-1. ISBN 9780125400787. PMID 15210333.
Ingle RA (tháng 1 năm 2011). “Histidine biosynthesis”. The Arabidopsis Book. 9: e0141. doi:10.1199/tab.0141. PMC 3266711. PMID 22303266.
Evans WR, San Pietro A (tháng 1 năm 1966). “Phosphorolysis of adenosine diphosphoribose”. Archives of Biochemistry and Biophysics. 113 (1): 236–44. doi:10.1016/0003-9861(66)90178-0. PMID 4287446.
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. doi:10.1007/s00109-010-0634-1. PMID 20499043.
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. doi:10.1086/383204. PMC 1181951. PMID 14988808.

ncbi.nlm.nih.gov

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. doi:10.1016/s0969-2126(02)00933-4. PMC 2792023. PMID 12517338.
Ingle RA (tháng 1 năm 2011). “Histidine biosynthesis”. The Arabidopsis Book. 9: e0141. doi:10.1199/tab.0141. PMC 3266711. PMID 22303266.
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. doi:10.1086/383204. PMC 1181951. PMID 14988808.