Esteroide (Galician Wikipedia)

Analysis of information sources in references of the Wikipedia article "Esteroide" in Galician language version.

refsWebsite

Global rank Galician rank

12nih.gov

4^th place

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11doi.org

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4web.archive.org

1^st place

2qmul.ac.uk

1,735^th place

412^th place

2archive.org

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1caslab.com

low place

1britannica.com

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1ias.ac.in

6,086^th place

3,700^th place

archive.org

Schroepfer G (1981). "Sterol biosynthesis". Annu Rev Biochem 50: 585–621. PMID 7023367. doi:10.1146/annurev.bi.50.070181.003101.
Lees N, Skaggs B, Kirsch D, Bard M (1995). "Cloning of the late genes in the ergosterol biosynthetic pathway of Saccharomyces cerevisiae—a review". Lipids 30 (3): 221–6. PMID 7791529. doi:10.1007/BF02537824.

britannica.com

britannica.com > Facts about gonane: steroids, as discussed in steroid (chemical compound): Steroid numbering system and nomenclature Arquivado 29 de xuño de 2011 en Wayback Machine. Retrieved on Feb 13, 2010

caslab.com

PubChem; CAS Number: 203-64-5 Arquivado 08 de xullo de 2011 en Wayback Machine.

doi.org

dx.doi.org

G. P. Moss (1989). "Nomenclature of Steroids (Recommendations 1989)". Pure & Appl. Chem. 61 (10): 1783–1822. doi:10.1351/pac198961101783. Arquivado dende o orixinal o 24 de marzo de 2012. Consultado o 16 de xullo de 2011. "IUPAC-IUB Joint Commission on Biochemical Nomenclature (JCBN). The nomenclature of steroids. Recommendations 1989". Eur. J. Biochem. 186 (3): 429–58. 1989. PMID 2606099. doi:10.1111/j.1432-1033.1989.tb15228.x.
Rossier MF (2006). "T channels and steroid biosynthesis: in search of a link with mitochondria". Cell Calcium. 40 (2): 155–64. PMID 16759697. doi:10.1016/j.ceca.2006.04.020.
Grochowski L, Xu H, White R (2006). "Methanocaldococcus jannaschii uses a modified mevalonate pathway for biosynthesis of isopentenyl diphosphate". J Bacteriol 188 (9): 3192–8. PMC 1447442. PMID 16621811. doi:10.1128/JB.188.9.3192-3198.2006.
Lichtenthaler H (1999). "The 1-Dideoxy-D-xylulose-5-phosphate pathway of isoprenoid biosynthesis in plants". Annu Rev Plant Physiol Plant Mol Biol 50: 47–65. PMID 15012203. doi:10.1146/annurev.arplant.50.1.47.
Kuzuyama T, Seto H (2003). "Diversity of the biosynthesis of the isoprene units". Nat Prod Rep 20 (2): 171–83. PMID 12735695. doi:10.1039/b109860h.
Dubey V, Bhalla R, Luthra R (2003). "An overview of the non-mevalonate pathway for terpenoid biosynthesis in plants" (PDF). J Biosci 28 (5): 637–46. PMID 14517367. doi:10.1007/BF02703339.
Schroepfer G (1981). "Sterol biosynthesis". Annu Rev Biochem 50: 585–621. PMID 7023367. doi:10.1146/annurev.bi.50.070181.003101.
Lees N, Skaggs B, Kirsch D, Bard M (1995). "Cloning of the late genes in the ergosterol biosynthetic pathway of Saccharomyces cerevisiae—a review". Lipids 30 (3): 221–6. PMID 7791529. doi:10.1007/BF02537824.
Pikuleva IA (2006). "Cytochrome P450s and cholesterol homeostasis". Pharmacol. Ther. 112 (3): 761–73. PMID 16872679. doi:10.1016/j.pharmthera.2006.05.014.
Zollner G, Marschall HU, Wagner M, Trauner M (2006). "Role of nuclear receptors in the adaptive response to bile acids and cholestasis: pathogenetic and therapeutic considerations". Mol. Pharm. 3 (3): 231–51. PMID 16749856. doi:10.1021/mp060010s.
Kliewer S, Goodwin B, Willson T (2002). "The nuclear pregnane X receptor: a key regulator of xenobiotic metabolism". Endocr. Rev. 23 (5): 687–702. PMID 12372848. doi:10.1210/er.2001-0038.

ias.ac.in

Dubey V, Bhalla R, Luthra R (2003). "An overview of the non-mevalonate pathway for terpenoid biosynthesis in plants" (PDF). J Biosci 28 (5): 637–46. PMID 14517367. doi:10.1007/BF02703339.

nih.gov

ncbi.nlm.nih.gov

G. P. Moss (1989). "Nomenclature of Steroids (Recommendations 1989)". Pure & Appl. Chem. 61 (10): 1783–1822. doi:10.1351/pac198961101783. Arquivado dende o orixinal o 24 de marzo de 2012. Consultado o 16 de xullo de 2011. "IUPAC-IUB Joint Commission on Biochemical Nomenclature (JCBN). The nomenclature of steroids. Recommendations 1989". Eur. J. Biochem. 186 (3): 429–58. 1989. PMID 2606099. doi:10.1111/j.1432-1033.1989.tb15228.x.
Rossier MF (2006). "T channels and steroid biosynthesis: in search of a link with mitochondria". Cell Calcium. 40 (2): 155–64. PMID 16759697. doi:10.1016/j.ceca.2006.04.020.
Grochowski L, Xu H, White R (2006). "Methanocaldococcus jannaschii uses a modified mevalonate pathway for biosynthesis of isopentenyl diphosphate". J Bacteriol 188 (9): 3192–8. PMC 1447442. PMID 16621811. doi:10.1128/JB.188.9.3192-3198.2006.
Lichtenthaler H (1999). "The 1-Dideoxy-D-xylulose-5-phosphate pathway of isoprenoid biosynthesis in plants". Annu Rev Plant Physiol Plant Mol Biol 50: 47–65. PMID 15012203. doi:10.1146/annurev.arplant.50.1.47.
Kuzuyama T, Seto H (2003). "Diversity of the biosynthesis of the isoprene units". Nat Prod Rep 20 (2): 171–83. PMID 12735695. doi:10.1039/b109860h.
Dubey V, Bhalla R, Luthra R (2003). "An overview of the non-mevalonate pathway for terpenoid biosynthesis in plants" (PDF). J Biosci 28 (5): 637–46. PMID 14517367. doi:10.1007/BF02703339.
Schroepfer G (1981). "Sterol biosynthesis". Annu Rev Biochem 50: 585–621. PMID 7023367. doi:10.1146/annurev.bi.50.070181.003101.
Lees N, Skaggs B, Kirsch D, Bard M (1995). "Cloning of the late genes in the ergosterol biosynthetic pathway of Saccharomyces cerevisiae—a review". Lipids 30 (3): 221–6. PMID 7791529. doi:10.1007/BF02537824.
Pikuleva IA (2006). "Cytochrome P450s and cholesterol homeostasis". Pharmacol. Ther. 112 (3): 761–73. PMID 16872679. doi:10.1016/j.pharmthera.2006.05.014.
Zollner G, Marschall HU, Wagner M, Trauner M (2006). "Role of nuclear receptors in the adaptive response to bile acids and cholestasis: pathogenetic and therapeutic considerations". Mol. Pharm. 3 (3): 231–51. PMID 16749856. doi:10.1021/mp060010s.
Kliewer S, Goodwin B, Willson T (2002). "The nuclear pregnane X receptor: a key regulator of xenobiotic metabolism". Endocr. Rev. 23 (5): 687–702. PMID 12372848. doi:10.1210/er.2001-0038.

pubchem.ncbi.nlm.nih.gov

PubChem; CAS Number: 203-64-5 Arquivado 08 de xullo de 2011 en Wayback Machine.

qmul.ac.uk

chem.qmul.ac.uk

G. P. Moss (1989). "Nomenclature of Steroids (Recommendations 1989)". Pure & Appl. Chem. 61 (10): 1783–1822. doi:10.1351/pac198961101783. Arquivado dende o orixinal o 24 de marzo de 2012. Consultado o 16 de xullo de 2011. "IUPAC-IUB Joint Commission on Biochemical Nomenclature (JCBN). The nomenclature of steroids. Recommendations 1989". Eur. J. Biochem. 186 (3): 429–58. 1989. PMID 2606099. doi:10.1111/j.1432-1033.1989.tb15228.x.
"Lanosterol biosynthesis". Arquivado dende o orixinal o 08 de marzo de 2011. Consultado o 16 de xullo de 2011.

web.archive.org

G. P. Moss (1989). "Nomenclature of Steroids (Recommendations 1989)". Pure & Appl. Chem. 61 (10): 1783–1822. doi:10.1351/pac198961101783. Arquivado dende o orixinal o 24 de marzo de 2012. Consultado o 16 de xullo de 2011. "IUPAC-IUB Joint Commission on Biochemical Nomenclature (JCBN). The nomenclature of steroids. Recommendations 1989". Eur. J. Biochem. 186 (3): 429–58. 1989. PMID 2606099. doi:10.1111/j.1432-1033.1989.tb15228.x.
"Lanosterol biosynthesis". Arquivado dende o orixinal o 08 de marzo de 2011. Consultado o 16 de xullo de 2011.
PubChem; CAS Number: 203-64-5 Arquivado 08 de xullo de 2011 en Wayback Machine.
britannica.com > Facts about gonane: steroids, as discussed in steroid (chemical compound): Steroid numbering system and nomenclature Arquivado 29 de xuño de 2011 en Wayback Machine. Retrieved on Feb 13, 2010