نتایج جستجو برای: platyfish

تعداد نتایج: 74  

Journal: :Molecular biology and evolution 2001
J N Volff C Körting A Meyer M Schartl

The fish non–long-terminal-repeat (non-LTR) retrotransposon Rex3 has recently been isolated from the platyfish Xiphophorus maculatus (Volff et al. 1999). Complete versions of Rex3 encode a reverse transcriptase (RT) and an apurinic/apyrimidinic endonuclease (fig. 1). Rex3 belongs to the RTE family of non-LTR retrotransposons (Malik and Eickbush 1998; Volff et al. 1999). From all autonomous fish...

Journal: :IOP conference series 2023

Abstract Mercury (Hg) is a heavy metal that commonly found in waters and sediments. its derivatives are highly toxic ) . Their presence the aquatic environment can be very detrimental. Aspergillus fungi known to reduce Hg levels pollutants. Our research aim was evaluate effect of after being reduced by local isolates Penicillium sp. strain A4. A toxicity test conducted on juvenile Caroline plat...

Journal: :Cancer research 1993
F E Ahmed R B Setlow

Fluence response relationships for the induction of DNA damage in the skin of UV-irradiated Xiphophorus fish were obtained by quantitative gel electrophoresis of unlabeled DNA following extraction and treatment with an enzyme preparation that makes single strand breaks next to cyclobutane pyrimidine dimers. A buffer containing 7 M urea minimized the degradation of DNA during extraction and gave...

Journal: :Cancer research 1981
Y Wakamatsu

A fish melanoma cell line, PSM-1, was established from a hereditary melanoma in an interspecific hybrid of Xiphophorus for cytogenetic studies of this melanoma system. An amelanotic melanoma was obtained from the tail fin of a melanotic F1 hybrid between a spotted platyfish (Xiphophorus maculatus) and an albino swordtail (Xiphophorus helleri). The tumor tissue was dissociated and cultured in Ea...

2006
Farid E. Ahmed R. B. Setlow

Fluence response relationships for the induction of DNA damage in the skin of I \ -irradiali-«!Xiphophorus fish were obtained by quantitative gel electrophoresis of unlabeled DNA following extraction and treatment with an enzyme preparation that makes single strand breaks next to cyclobutane pyrimidine dimers. A buffer containing 7 M urea minimized the degradation of DNA during extraction and ...

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