Холестерол (Serbian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Холестерол" in Serbian language version.

refsWebsite

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12doi.org

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11nih.gov

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2web.archive.org

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2archive.org

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2books.google.com

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1wiley.com

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1sciencedirect.com

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1wikipedia.org

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1ox.ac.uk

613^th place

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1lipidmaps.org

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1zenodo.org

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1semanticscholar.org

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1upenn.edu

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1mcgraw-hill.com

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1harvard.edu

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archive.org

Razin S, Tully JG (мај 1970). „Cholesterol Requirement of Mycoplasmas”. Journal of Bacteriology. 102 (2): 306—310. PMC 247552 . PMID 4911537. doi:10.1128/JB.102.2.306-310.1970.
Lopez-Garcia, E. (2005). „"Consumption of trans-fatty acids is related to plasma biomarkers of inflammation and endothelial dysfunction"”. J. Nutr. 135 (3): 562—566. PMID 15735094. doi:10.1093/jn/135.3.562.

books.google.com

Chevreul (1816) "Recherches chimiques sur les corps gras, et particulièrement sur leurs combinaisons avec les alcalis. Sixième mémoire. Examen des graisses d'homme, de mouton, de boeuf, de jaguar et d'oie" (Chemical researches on fatty substances, and particularly on their combinations o filippos ine kapios with alkalis. Sixth memoir. Study of human, sheep, beef, jaguar and goose fat), (París), Crochard; Arago, François; Gay-Lussac, Joseph Louis (1816). Annales de chimie et de physique. стр. 346. : "Je nommerai cholesterine, de χολη, bile, et στερεος, solide, la substance cristallisée des calculs biliares humains, ... " (I will name cholesterine — from χολη (bile) and στερεος (solid) — the crystalized substance from human gallstones ... )
Thomas L. Lemke; David A. Williams, ур. (2007). „Chapter: Adrenocorticoids”. Foye's Principles of Medicinal Chemistry (6. изд.). Baltimore: Lippincott Willams & Wilkins. ISBN 0781768799.

doi.org

Joanne Wixon; Douglas Kell (2000). „Website Review: The Kyoto Encyclopedia of Genes and Genomes — KEGG”. Yeast. 17 (1): 48—55. doi:10.1002/(SICI)1097-0061(200004)17:1<48::AID-YEA2>3.0.CO;2-H.
Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today. 15 (23-24): 1052—7. PMID 20970519. doi:10.1016/j.drudis.2010.10.003. уреди
Evan E. Bolton; Yanli Wang; Paul A. Thiessen; Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry. 4: 217—241. doi:10.1016/S1574-1400(08)00012-1.
Emma Leah (2009). „Cholesterol”. Lipidomics Gateway. doi:10.1038/lipidmaps.2009.3. Архивирано из оригинала 13. 6. 2011. г. Приступљено 1. 7. 2010.
Hanukoglu I (децембар 1992). „Steroidogenic enzymes: structure, function, and role in regulation of steroid hormone biosynthesis”. J Steroid Biochem Mol Biol. 43 (8): 779—804. PMID 22217824. S2CID 112729. doi:10.1016/0960-0760(92)90307-5.
Razin S, Tully JG (мај 1970). „Cholesterol Requirement of Mycoplasmas”. Journal of Bacteriology. 102 (2): 306—310. PMC 247552 . PMID 4911537. doi:10.1128/JB.102.2.306-310.1970.
Olson RE (фебруар 1998). „Discovery of the lipoproteins, their role in fat transport and their significance as risk factors”. J. Nutr. 128 (2 Suppl): 439S—443S. PMID 9478044. doi:10.1093/jn/128.2.439S.
Lopez-Garcia, E. (2005). „"Consumption of trans-fatty acids is related to plasma biomarkers of inflammation and endothelial dysfunction"”. J. Nutr. 135 (3): 562—566. PMID 15735094. doi:10.1093/jn/135.3.562.
Ascherio, A.; Willett, W. C. (1997). „"Health effects of trans fatty acids" (review article)”. American Journal of Clinical Nutrition. 66 (4 Suppl): 1006S—1010S. PMID 9322581. doi:10.1093/ajcn/66.4.1006S.
Pearson A, Budin M, Brocks JJ (2003). „Phylogenetic and biochemical evidence for sterol synthesis in the bacterium Gemmata obscuriglobus”. Proc. Natl. Acad. Sci. U.S.A. 100 (26): 15352—7. Bibcode:2003PNAS..10015352P. PMC 307571 . PMID 14660793. doi:10.1073/pnas.2536559100 .
Westover EJ, Covey DF, Brockman HL, Brown RE, Pike LJ (децембар 2003). „Cholesterol depletion results in site-specific increases in epidermal growth factor receptor phosphorylation due to membrane level effects. Studies with cholesterol enantiomers”. J. Biol. Chem. 278 (51): 51125—33. PMC 2593805 . PMID 14530278. doi:10.1074/jbc.M304332200 .
Kristiana I, Luu W, Stevenson J, Cartland S, Jessup W, Belani JD, Rychnovsky SD, Brown AJ (септембар 2012). „Cholesterol through the looking glass: ability of its enantiomer also to elicit homeostatic responses”. J. Biol. Chem. 287 (40): 33897—904. PMC 3460484 . PMID 22869373. doi:10.1074/jbc.M112.360537 .

harvard.edu

adsabs.harvard.edu

Pearson A, Budin M, Brocks JJ (2003). „Phylogenetic and biochemical evidence for sterol synthesis in the bacterium Gemmata obscuriglobus”. Proc. Natl. Acad. Sci. U.S.A. 100 (26): 15352—7. Bibcode:2003PNAS..10015352P. PMC 307571 . PMID 14660793. doi:10.1073/pnas.2536559100 .

lipidmaps.org

Emma Leah (2009). „Cholesterol”. Lipidomics Gateway. doi:10.1038/lipidmaps.2009.3. Архивирано из оригинала 13. 6. 2011. г. Приступљено 1. 7. 2010.

mcgraw-hill.com

books.mcgraw-hill.com

Keith Parker; Laurence Brunton; Goodman, Louis Sanford; Lazo, John S.; Gilman, Alfred (2006). Goodman & Gilman's The Pharmacological Basis of Therapeutics (11. изд.). New York: McGraw-Hill. ISBN 0071422803.

nih.gov

ncbi.nlm.nih.gov

Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today. 15 (23-24): 1052—7. PMID 20970519. doi:10.1016/j.drudis.2010.10.003. уреди
Hanukoglu I (децембар 1992). „Steroidogenic enzymes: structure, function, and role in regulation of steroid hormone biosynthesis”. J Steroid Biochem Mol Biol. 43 (8): 779—804. PMID 22217824. S2CID 112729. doi:10.1016/0960-0760(92)90307-5.
Razin S, Tully JG (мај 1970). „Cholesterol Requirement of Mycoplasmas”. Journal of Bacteriology. 102 (2): 306—310. PMC 247552 . PMID 4911537. doi:10.1128/JB.102.2.306-310.1970.
Olson RE (фебруар 1998). „Discovery of the lipoproteins, their role in fat transport and their significance as risk factors”. J. Nutr. 128 (2 Suppl): 439S—443S. PMID 9478044. doi:10.1093/jn/128.2.439S.
Lopez-Garcia, E. (2005). „"Consumption of trans-fatty acids is related to plasma biomarkers of inflammation and endothelial dysfunction"”. J. Nutr. 135 (3): 562—566. PMID 15735094. doi:10.1093/jn/135.3.562.
Ascherio, A.; Willett, W. C. (1997). „"Health effects of trans fatty acids" (review article)”. American Journal of Clinical Nutrition. 66 (4 Suppl): 1006S—1010S. PMID 9322581. doi:10.1093/ajcn/66.4.1006S.
Pearson A, Budin M, Brocks JJ (2003). „Phylogenetic and biochemical evidence for sterol synthesis in the bacterium Gemmata obscuriglobus”. Proc. Natl. Acad. Sci. U.S.A. 100 (26): 15352—7. Bibcode:2003PNAS..10015352P. PMC 307571 . PMID 14660793. doi:10.1073/pnas.2536559100 .
Westover EJ, Covey DF, Brockman HL, Brown RE, Pike LJ (децембар 2003). „Cholesterol depletion results in site-specific increases in epidermal growth factor receptor phosphorylation due to membrane level effects. Studies with cholesterol enantiomers”. J. Biol. Chem. 278 (51): 51125—33. PMC 2593805 . PMID 14530278. doi:10.1074/jbc.M304332200 .
Kristiana I, Luu W, Stevenson J, Cartland S, Jessup W, Belani JD, Rychnovsky SD, Brown AJ (септембар 2012). „Cholesterol through the looking glass: ability of its enantiomer also to elicit homeostatic responses”. J. Biol. Chem. 287 (40): 33897—904. PMC 3460484 . PMID 22869373. doi:10.1074/jbc.M112.360537 .

pubchem.ncbi.nlm.nih.gov

„Cholesterol, 57-88-5”. PubChem, National Library of Medicine, US National Institutes of Health. 9. 11. 2019. Приступљено 14. 11. 2019.

meshb.nlm.nih.gov

Cholesterol на US National Library of Medicine Medical Subject Headings (MeSH)

ox.ac.uk

physchem.ox.ac.uk

„Safety (MSDS) data for cholesterol”. Архивирано из оригинала 12. 7. 2007. г. Приступљено 20. 10. 2007.

sciencedirect.com

Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today. 15 (23-24): 1052—7. PMID 20970519. doi:10.1016/j.drudis.2010.10.003. уреди

semanticscholar.org

api.semanticscholar.org

Hanukoglu I (децембар 1992). „Steroidogenic enzymes: structure, function, and role in regulation of steroid hormone biosynthesis”. J Steroid Biochem Mol Biol. 43 (8): 779—804. PMID 22217824. S2CID 112729. doi:10.1016/0960-0760(92)90307-5.

upenn.edu

chem.upenn.edu

Donald Voet; Judith G. Voet (2005). Biochemistry (3 изд.). Wiley. стр. 394. ISBN 9780471193500.

web.archive.org

„Safety (MSDS) data for cholesterol”. Архивирано из оригинала 12. 7. 2007. г. Приступљено 20. 10. 2007.
Emma Leah (2009). „Cholesterol”. Lipidomics Gateway. doi:10.1038/lipidmaps.2009.3. Архивирано из оригинала 13. 6. 2011. г. Приступљено 1. 7. 2010.

wikipedia.org

sr.wikipedia.org

Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today. 15 (23-24): 1052—7. PMID 20970519. doi:10.1016/j.drudis.2010.10.003. уреди

wiley.com

onlinelibrary.wiley.com

Joanne Wixon; Douglas Kell (2000). „Website Review: The Kyoto Encyclopedia of Genes and Genomes — KEGG”. Yeast. 17 (1): 48—55. doi:10.1002/(SICI)1097-0061(200004)17:1<48::AID-YEA2>3.0.CO;2-H.

zenodo.org

Hanukoglu I (децембар 1992). „Steroidogenic enzymes: structure, function, and role in regulation of steroid hormone biosynthesis”. J Steroid Biochem Mol Biol. 43 (8): 779—804. PMID 22217824. S2CID 112729. doi:10.1016/0960-0760(92)90307-5.