✦ LIBER ✦

Ecdysteroids in snails

✍ Scribed by F. Romer

Book ID: 104757215
Publisher: Springer
Year: 1979
Tongue: English
Weight: 224 KB
Volume: 66
Category: Article
ISSN: 0028-1042
DOI: 10.1007/bf00399009

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Ecdysteroid biosynthesis in crayfish Y-o

Ecdysteroid biosynthesis in crayfish Y-organs: Feedback regulation by circulating ecdysteroids

✍ Susanne Dell; Dietrich Sedlmeier; Detlef Böcking; Chantal Dauphin-Villemant 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 147 KB

In crustaceans, ecdysteroid synthesis in the Y-organs is negatively regulated by the molt-inhibiting hormone (MIH). Reduction or cessation of MIH release from the sinus gland in the eyestalk, probably due to environmental cues, is one of possibly several signals for an increase of edysteroid product

Prehistoric snails

✍ RENFREW, JANE M. 📂 Article 📅 1974 🏛 Nature Publishing Group 🌐 English ⚖ 128 KB

Snails, slugs …

✍ Rigby, Joyce E. 📂 Article 📅 1975 🏛 Nature Publishing Group 🌐 English ⚖ 115 KB

Biosynthesis of ecdysteroids in Zea mays

✍ Timothy P. Devarenne; Banalata Sen-Michael; John H. Adler 📂 Article 📅 1995 🏛 Elsevier Science 🌐 English ⚖ 607 KB

Nongenomic effects of ecdysteroids

✍ Karl-Heinz Tomaschko 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 105 KB

The classical mode of action of ecdysteroids (ES) is the receptor-mediated control of gene activity, influencing transcription, and, subsequently, protein synthesis. Most of these actions occur after a lag phase of 10 min or more, usually after several hours. During the last three decades evidence h

Ecdysteroids from Silene viridiflora

✍ András Simon; Noémi Tóth; Gábor Tóth; Zoltán Kele; Judit Groska; Mária Báthori 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 German ⚖ 213 KB

## Abstract magnified image Two new ecdysteroid acetonide derivatives, 5__α__‐2‐deoxy‐20‐hydroxyecdysone 20,22‐acetonide (**6**) and makisterone C 2,3;20,22‐diacetonide (**8**), were isolated from the dried herb of __Silene viridiflora.__ The already known 5__β__‐2‐deoxy‐20‐hydroxyecdysone 20,22‐a