公理
发表于 2025-3-30 10:10:00
Regulation of Sciarid DNA Puffs by Ecdysone: Mechanisms and Perspectivesns coupled to the molecular characterization of DNA puffs revealed that they are sites of disproportional DNA synthesis and abundant transcription. The biological purpose of DNA amplification at these . is to enable the synthesis of large amounts of proteins in short periods of time. Here, the role
大炮
发表于 2025-3-30 16:12:22
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BOLT
发表于 2025-3-30 20:16:37
Applications of RNA Interference in Ecdysone Researchxamples in three insect models. (1) Selective RNAi of the expression of the endogenous messenger RNA encoding EcR of Sf9 tissue culture cells and replacement with EcRs from other insects should permit cell-based screening for potential insecticides against a variety of pests. (2) The applicability o
menopause
发表于 2025-3-31 00:38:03
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教义
发表于 2025-3-31 03:07:01
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完成
发表于 2025-3-31 06:36:41
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陶器
发表于 2025-3-31 09:13:23
20-Hydroxyecdysone, Juvenile Hormone and Biogenic Amines: Mechanisms of Interaction in Control of ,JH and 20-hydroxyecdysone (20E) is of a paramount importance. An imbalance of gonadotropins (shifting the balance either to the side of JH or 20E) leads to reproductive defects: a rise in JH titre leads to oviposition arrest, a rise in 20E level, to the degradation of vitellogenic oocytes. Upon a c
FLIP
发表于 2025-3-31 15:47:18
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headway
发表于 2025-3-31 19:33:19
The Multidimensional Partnership of EcR and USPevidence exists that each participates in a dimerization partnership that is subject to a variety of regulatory interactions and pathways in the cell. Heterologous cell culture has been used to reconstitute and study the transcriptional activity mediated by the EcR/USP heterodimer. These studies hav
愤世嫉俗者
发表于 2025-4-1 00:57:26
Functional Analysis of Ecdysteroid Receptor from , “,”racle (Usp) and to avoid interference with endogenous receptor isoforms. Comparison of different isoforms affords determination of receptor concentration, which was achieved either by determination of ligand binding sites by Scatchard analysis or by quantitative evaluation of specific Western blot s