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2-Oxopropanal (Hungarian Wikipedia)

Analysis of information sources in references of the Wikipedia article "2-Oxopropanal" in Hungarian language version.

refsWebsite
Global rank Hungarian rank
18nih.gov
4th place
11th place
15doi.org
2nd place
8th place
1deutsche-apotheker-zeitung.de
low place
low place

deutsche-apotheker-zeitung.de

doi.org

dx.doi.org

  • Loeffler, Kirsten W. (2006). „Oligomer Formation in Evaporating Aqueous Glyoxal and Methyl Glyoxal Solutions”. Environmental Science & Technology 40 (20), 6318–23. o. DOI:10.1021/es060810w. PMID 17120559. 
  • Inoue Y, Kimura A (1995). „Methylglyoxal and regulation of its metabolism in microorganisms”. Adv. Microb. Physiol. 37, 177–227. o. DOI:10.1016/S0065-2911(08)60146-0. PMID 8540421. 
  • Bellier, Justine (2019). „Methylglyoxal, a Potent Inducer of AGEs, Connects between Diabetes and Cancer”. Diabetes Research and Clinical Practice 148, 200–211. o. DOI:10.1016/j.diabres.2019.01.002. PMID 30664892. 
  • Li, YC (2012). „Aristolochic acid-induced accumulation of methylglyoxal and Nε-(carboxymethyl)lysine: an important and novel pathway in the pathogenic mechanism for aristolochic acid nephropathy”. Biochem Biophys Res Commun 423 (4), 832–7. o. DOI:10.1016/j.bbrc.2012.06.049. PMID 22713464. 
  • Thornalley PJ (2003). „Glyoxalase I—structure, function and a critical role in the enzymatic defence against glycation”. Biochem. Soc. Trans. 31 (Pt 6), 1343–8. o. DOI:10.1042/BST0311343. PMID 14641060. 
  • Vander Jagt DL (1993). „Glyoxalase II: molecular characteristics, kinetics and mechanism”. Biochem. Soc. Trans. 21 (2), 522–7. o. DOI:10.1042/bst0210522. PMID 8359524. 
  • Galligan JJ, Wepy JA, Streeter MD, Kingsley PJ, Mitchener MM, Wauchope OR, Beavers WN, Rose KL, Wang T, Spiegel DA, Marnett LJ (2018. szeptember 1.). „Methylglyoxal-derived posttranslational arginine modifications are abundant histone marks”. Proc Natl Acad Sci USA 115 (37), 9228–33. o. DOI:10.1073/pnas.1802901115. PMID 30150385. PMC 6140490. 
  • (2019. március 1.) „Reversible histone glycation is associated with disease-related changes in chromatin architecture”. Nat Commun 10 (1), 1289. o. DOI:10.1038/s41467-019-09192-z. PMID 30894531. PMC 6426841. 
  • Oya, Tomoko (1999). „Methylglyoxal Modification of Protein”. Journal of Biological Chemistry 274 (26), 18492–502. o. DOI:10.1074/jbc.274.26.18492. PMID 10373458. 
  • Richarme G, Liu C, Mihoub M, Abdallah J, Leger T, Joly N, Liebart JC, Jurkunas UV, Nadal M, Bouloc P, Dairou J, Lamouri A (2017. július 14.). „Guanine glycation repair by DJ-1/Park7 and its bacterial homologs”. Science 357 (6347), 208-211. o. DOI:10.1126/science.aag1095. PMID 28596309. 
  • Rabbani N (2011. május 26.). „Glycation of LDL by methylglyoxal increases arterial atherogenicity. A possible contributor to increased risk of cardiovascular disease in diabetes”. Diabetes 60 (7), 1973–80. o. DOI:10.2337/db11-0085. PMID 21617182. PMC 3121424. 
  • (2012) „Methylglyoxal modification of Nav1.8 facilitates nociceptive neuron firing and causes hyperalgesia in diabetic neuropathy”. Nature Medicine 18 (6), 926–33. o. DOI:10.1038/nm.2750. PMID 22581285. 
  • (2014) „Antimicrobial properties of honey.”. American Journal of Therapeutics 21 (4), 304–23. o. DOI:10.1097/MJT.0b013e318293b09b. PMID 23782759. 
  • Wallace A, Eady S, Miles M, Martin H, McLachlan A, Rodier M, Willis J, Scott R, Sutherland J (2010. április 1.). „Demonstrating the safety of manuka honey UMF® 20+ in a human clinical trial with healthy individuals”. Br J Nutr 103 (7), 1023–8. o. DOI:10.1017/S0007114509992777. PMID 20064284. 
  • Degen J, Vogel M, Richter D, Hellwig M, Henle T (2013. október 1.). „Metabolic transit of dietary methylglyoxal”. J Agric Food Chem 61 (43), 10253–60. o. DOI:10.1021/jf304946p. PMID 23451712. 

nih.gov

pubmed.ncbi.nlm.nih.gov

  • Loeffler, Kirsten W. (2006). „Oligomer Formation in Evaporating Aqueous Glyoxal and Methyl Glyoxal Solutions”. Environmental Science & Technology 40 (20), 6318–23. o. DOI:10.1021/es060810w. PMID 17120559. 
  • Inoue Y, Kimura A (1995). „Methylglyoxal and regulation of its metabolism in microorganisms”. Adv. Microb. Physiol. 37, 177–227. o. DOI:10.1016/S0065-2911(08)60146-0. PMID 8540421. 
  • Bellier, Justine (2019). „Methylglyoxal, a Potent Inducer of AGEs, Connects between Diabetes and Cancer”. Diabetes Research and Clinical Practice 148, 200–211. o. DOI:10.1016/j.diabres.2019.01.002. PMID 30664892. 
  • Li, YC (2012). „Aristolochic acid-induced accumulation of methylglyoxal and Nε-(carboxymethyl)lysine: an important and novel pathway in the pathogenic mechanism for aristolochic acid nephropathy”. Biochem Biophys Res Commun 423 (4), 832–7. o. DOI:10.1016/j.bbrc.2012.06.049. PMID 22713464. 
  • Thornalley PJ (2003). „Glyoxalase I—structure, function and a critical role in the enzymatic defence against glycation”. Biochem. Soc. Trans. 31 (Pt 6), 1343–8. o. DOI:10.1042/BST0311343. PMID 14641060. 
  • Vander Jagt DL (1993). „Glyoxalase II: molecular characteristics, kinetics and mechanism”. Biochem. Soc. Trans. 21 (2), 522–7. o. DOI:10.1042/bst0210522. PMID 8359524. 
  • Galligan JJ, Wepy JA, Streeter MD, Kingsley PJ, Mitchener MM, Wauchope OR, Beavers WN, Rose KL, Wang T, Spiegel DA, Marnett LJ (2018. szeptember 1.). „Methylglyoxal-derived posttranslational arginine modifications are abundant histone marks”. Proc Natl Acad Sci USA 115 (37), 9228–33. o. DOI:10.1073/pnas.1802901115. PMID 30150385. PMC 6140490. 
  • (2019. március 1.) „Reversible histone glycation is associated with disease-related changes in chromatin architecture”. Nat Commun 10 (1), 1289. o. DOI:10.1038/s41467-019-09192-z. PMID 30894531. PMC 6426841. 
  • Oya, Tomoko (1999). „Methylglyoxal Modification of Protein”. Journal of Biological Chemistry 274 (26), 18492–502. o. DOI:10.1074/jbc.274.26.18492. PMID 10373458. 
  • Richarme G, Liu C, Mihoub M, Abdallah J, Leger T, Joly N, Liebart JC, Jurkunas UV, Nadal M, Bouloc P, Dairou J, Lamouri A (2017. július 14.). „Guanine glycation repair by DJ-1/Park7 and its bacterial homologs”. Science 357 (6347), 208-211. o. DOI:10.1126/science.aag1095. PMID 28596309. 
  • Rabbani N (2011. május 26.). „Glycation of LDL by methylglyoxal increases arterial atherogenicity. A possible contributor to increased risk of cardiovascular disease in diabetes”. Diabetes 60 (7), 1973–80. o. DOI:10.2337/db11-0085. PMID 21617182. PMC 3121424. 
  • (2012) „Methylglyoxal modification of Nav1.8 facilitates nociceptive neuron firing and causes hyperalgesia in diabetic neuropathy”. Nature Medicine 18 (6), 926–33. o. DOI:10.1038/nm.2750. PMID 22581285. 
  • (2014) „Antimicrobial properties of honey.”. American Journal of Therapeutics 21 (4), 304–23. o. DOI:10.1097/MJT.0b013e318293b09b. PMID 23782759. 
  • Wallace A, Eady S, Miles M, Martin H, McLachlan A, Rodier M, Willis J, Scott R, Sutherland J (2010. április 1.). „Demonstrating the safety of manuka honey UMF® 20+ in a human clinical trial with healthy individuals”. Br J Nutr 103 (7), 1023–8. o. DOI:10.1017/S0007114509992777. PMID 20064284. 
  • Degen J, Vogel M, Richter D, Hellwig M, Henle T (2013. október 1.). „Metabolic transit of dietary methylglyoxal”. J Agric Food Chem 61 (43), 10253–60. o. DOI:10.1021/jf304946p. PMID 23451712. 

ncbi.nlm.nih.gov

  • Galligan JJ, Wepy JA, Streeter MD, Kingsley PJ, Mitchener MM, Wauchope OR, Beavers WN, Rose KL, Wang T, Spiegel DA, Marnett LJ (2018. szeptember 1.). „Methylglyoxal-derived posttranslational arginine modifications are abundant histone marks”. Proc Natl Acad Sci USA 115 (37), 9228–33. o. DOI:10.1073/pnas.1802901115. PMID 30150385. PMC 6140490. 
  • (2019. március 1.) „Reversible histone glycation is associated with disease-related changes in chromatin architecture”. Nat Commun 10 (1), 1289. o. DOI:10.1038/s41467-019-09192-z. PMID 30894531. PMC 6426841. 
  • Rabbani N (2011. május 26.). „Glycation of LDL by methylglyoxal increases arterial atherogenicity. A possible contributor to increased risk of cardiovascular disease in diabetes”. Diabetes 60 (7), 1973–80. o. DOI:10.2337/db11-0085. PMID 21617182. PMC 3121424.