Cloning and characterization of amphibian cold inducible RNA-binding protein
Comparative Biochemistry and Physiology Part B: Biochemistry and Molecular Biology, ISSN: 1096-4959, Vol: 125, Issue: 2, Page: 237-245
2000
- 31Citations
- 13Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations31
- Citation Indexes31
- 31
- CrossRef22
- Captures13
- Readers13
- 13
Article Description
Gene expression of cold inducible RNA-binding protein (CIRP) was examined in the frog. In Xenopus laevis, expression of CIRP (XCIRP) was observed in both brain and liver at 24°C. Circadian expression of XCIRP was observed in brain. Expression of XCIRP in brain was induced by cold treatment and gradually decreased to the control level at 24°C, but no significant changes were observed in liver. Employing the sequence of murine CIRP, bullfrog ( Rana catesbeiana ) CIRP gene was cloned. The bullfrog CIRP gene, designated BFCIRP, was 706 bp in length and encoded a putative protein of 164 amino acid residues. The deduced protein contained one consensus sequence of RNA-binding domain (CS-RBD) and a glycine rich domain (GRD). The amino acid sequence of BFCIRP was 78.4% identical to XCIRP. Expression of BFCIRP in brain was stronger in winter than that in summer. These findings suggest that BFCIRP expression in brain may link to hibernation.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0305049199001741; http://dx.doi.org/10.1016/s0305-0491(99)00174-1; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=0034015806&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/10817911; http://linkinghub.elsevier.com/retrieve/pii/S0305049199001741; http://api.elsevier.com/content/article/PII:S0305049199001741?httpAccept=text/xml; http://api.elsevier.com/content/article/PII:S0305049199001741?httpAccept=text/plain; https://linkinghub.elsevier.com/retrieve/pii/S0305049199001741; http://dx.doi.org/10.1016/s0305-0491%2899%2900174-1; https://dx.doi.org/10.1016/s0305-0491%2899%2900174-1
Elsevier BV
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