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This paper reports the first full-length cDNA sequence of a growth hormone receptor (GHR) from a teleost fish and its functional expression in cultured eukaryotic cells.
In order to develop a sensitive PCR-based assay for the detection of fish-specific amylase in larvae, a complete cDNA and partial genomic sequence, the first reported from a teleost fish, were determined from winter flounder.
In the present work, the molecular cloning of the cDNAs corresponding to slc23a1 and slc23a2 in a teleost fish, the Senegalese sole (Solea senegalensis Kaup, 1858) is first described.
Our research addressed the question of whether or not dutasteride, a pharmaceutical used to treat benign prostatic hyperplasia, may cause adverse effects in a teleost fish, the fathead minnow (Pimephales promelas), by inhibiting the activity of both isoforms of 5α-reductase (5αR), the enzyme that converts testosterone into dihydrotestosterone (DHT).
Taken together, results suggest that uptake and bioactivation are working to enhance diazinon sensitivity in this developmental model of a teleost fish.
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Similar(33)
Additional duplications occurred along the teleost fish lineage, in congruence with the hypothesis of a teleost fish-specific genome duplication – FSGD [ 51, 52].
Importantly, Amh expression was found to be inhibited by 11-ketotestosterone, a teleost fish-specific androgen, and this steroid-mediated suppression of AMH action was sufficient to allow full completion of spermatogenesis in the eel [ 25].
Hence we identify FOBU-12718 as Undichna cf. simplicitas, and it is preliminarily interpreted as a trace made by a swimming teleost fish.
The Nile tilapia is a cultured teleost fish in which males grow faster and larger than females, and mono-sex culturing could avoid unwanted reproduction during grow-out.
In the present study, we identified a new teleost fish class II group called DE.
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