Progesteron (Slovenian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Progesteron" in Slovenian language version.

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10doi.org

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6nih.gov

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3archive.org

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1hmdb.ca

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1amebis.si

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1archive.today

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1jst.go.jp

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1elsevier.com

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1webmd.com

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amebis.si

lsm1.amebis.si

http://lsm1.amebis.si/lsmeds/novPogoj.aspx?pPogoj=progesteron^{[mrtva povezava]}, Slovenski medicinski e-slovar, vpogled: 8. 9. 2013.

archive.org

Allen WM (1970). »Progesterone: how did the name originate?«. South. Med. J. 63 (10): 1151–5. doi:10.1097/00007611-197010000-00012. PMID 4922128.
Dewick, Paul M. (2002). Medicinal natural products: a biosynthetic approach. New York: Wiley. str. 244. ISBN 0-471-49641-3.
Duport C; Spagnoli R; Degryse E; Pompon D (Februar 1998). »Self-sufficient biosynthesis of pregnenolone and progesterone in engineered yeast«. Nat. Biotechnol. 16 (2): 186–189. doi:10.1038/nbt0298-186. PMID 9487528.

archive.today

Numazawa M; Nagaoka M; Kunitama Y (1986). »Regiospecific deoxygenation of the dihydroxyacetone moiety at C-17 of corticoid steroids with iodotrimethylsilane«. Chem. Pharm. Bull. 34 (9): 3722–3726. doi:10.1248/cpb.34.3722. PMID 3815593. Arhivirano iz prvotnega spletišča dne 9. decembra 2012. Pridobljeno 8. septembra 2013.

doi.org

Allen WM (1935). »The isolation of crystalline progestin«. Science. 82 (2118): 89–93. doi:10.1126/science.082.2118.89. PMID 17747122.
Butenandt A; Westphal U (1934). »Zur Isolierung und Charakterisierung des Corpusluteum-Hormons«. Berichte Deu0tsche chemische Gesellschaft. 67 (8): 1440–1442. doi:10.1002/cber.19340670831.
Hartmann M; Wettstein A (1934). »Ein krystallisiertes Hormon aus Corpus luteum«. Helvetica Chimica Acta. 17: 878–882. doi:10.1002/hlca.193401701111.
Slotta KH; Ruschig H; Fels E (1934). »Reindarstellung der Hormone aus dem Corpusluteum«. Berichte Deutsche chemische Gesellschaft. 67 (7): 1270–1273. doi:10.1002/cber.19340670729.
Allen WM (1970). »Progesterone: how did the name originate?«. South. Med. J. 63 (10): 1151–5. doi:10.1097/00007611-197010000-00012. PMID 4922128.
Duport C; Spagnoli R; Degryse E; Pompon D (Februar 1998). »Self-sufficient biosynthesis of pregnenolone and progesterone in engineered yeast«. Nat. Biotechnol. 16 (2): 186–189. doi:10.1038/nbt0298-186. PMID 9487528.
Marker RE; Krueger J (1940). »Sterols. CXII. Sapogenins. XLI. The Preparation of Trillin and its Conversion to Progesterone«. J. Am. Chem. Soc. 62 (12): 3349–3350. doi:10.1021/ja01869a023.
Numazawa M; Nagaoka M; Kunitama Y (1986). »Regiospecific deoxygenation of the dihydroxyacetone moiety at C-17 of corticoid steroids with iodotrimethylsilane«. Chem. Pharm. Bull. 34 (9): 3722–3726. doi:10.1248/cpb.34.3722. PMID 3815593. Arhivirano iz prvotnega spletišča dne 9. decembra 2012. Pridobljeno 8. septembra 2013.
Johnson WS; Gravestock MB; McCarry BE (1971). »Acetylenic bond participation in biogenetic-like olefinic cyclizations. II. Synthesis of dl-progesterone«. J. Am. Chem. Soc. 93 (17): 4332–4334. doi:10.1021/ja00746a062. PMID 5131151.
Schindler AE; Campagnoli C; Druckmann R; Huber J; Pasqualini JR; Schweppe KW; Thijssen JH (2008). »Classification and pharmacology of progestins« (PDF). Maturitas. 61 (1–2): 171–80. doi:10.1016/j.maturitas.2003.09.014. PMID 19434889.^{[mrtva povezava]}

elsevier.com

www1.elsevier.com

Schindler AE; Campagnoli C; Druckmann R; Huber J; Pasqualini JR; Schweppe KW; Thijssen JH (2008). »Classification and pharmacology of progestins« (PDF). Maturitas. 61 (1–2): 171–80. doi:10.1016/j.maturitas.2003.09.014. PMID 19434889.^{[mrtva povezava]}

hmdb.ca

»Metabocard for Hydroxyprogesterone«. Human Metabolome Database. Pridobljeno 31. julija 2013.

jst.go.jp

journalarchive.jst.go.jp

Numazawa M; Nagaoka M; Kunitama Y (1986). »Regiospecific deoxygenation of the dihydroxyacetone moiety at C-17 of corticoid steroids with iodotrimethylsilane«. Chem. Pharm. Bull. 34 (9): 3722–3726. doi:10.1248/cpb.34.3722. PMID 3815593. Arhivirano iz prvotnega spletišča dne 9. decembra 2012. Pridobljeno 8. septembra 2013.

nih.gov

pubmed.ncbi.nlm.nih.gov

Allen WM (1935). »The isolation of crystalline progestin«. Science. 82 (2118): 89–93. doi:10.1126/science.082.2118.89. PMID 17747122.
Allen WM (1970). »Progesterone: how did the name originate?«. South. Med. J. 63 (10): 1151–5. doi:10.1097/00007611-197010000-00012. PMID 4922128.
Duport C; Spagnoli R; Degryse E; Pompon D (Februar 1998). »Self-sufficient biosynthesis of pregnenolone and progesterone in engineered yeast«. Nat. Biotechnol. 16 (2): 186–189. doi:10.1038/nbt0298-186. PMID 9487528.
Numazawa M; Nagaoka M; Kunitama Y (1986). »Regiospecific deoxygenation of the dihydroxyacetone moiety at C-17 of corticoid steroids with iodotrimethylsilane«. Chem. Pharm. Bull. 34 (9): 3722–3726. doi:10.1248/cpb.34.3722. PMID 3815593. Arhivirano iz prvotnega spletišča dne 9. decembra 2012. Pridobljeno 8. septembra 2013.
Johnson WS; Gravestock MB; McCarry BE (1971). »Acetylenic bond participation in biogenetic-like olefinic cyclizations. II. Synthesis of dl-progesterone«. J. Am. Chem. Soc. 93 (17): 4332–4334. doi:10.1021/ja00746a062. PMID 5131151.
Schindler AE; Campagnoli C; Druckmann R; Huber J; Pasqualini JR; Schweppe KW; Thijssen JH (2008). »Classification and pharmacology of progestins« (PDF). Maturitas. 61 (1–2): 171–80. doi:10.1016/j.maturitas.2003.09.014. PMID 19434889.^{[mrtva povezava]}

webmd.com

http://www.webmd.com/vitamins-supplements/ingredientmono-760-progesterone.aspx?activeIngredientId=760&activeIngredientName=progesterone, vpogled: 8. 9. 2013.