Zobrazeno 1 - 10
of 112
pro vyhledávání: '"Actinia tenebrosa"'
Autor:
Alaa Haridi
Publikováno v:
PeerJ, Vol 10, p e13292 (2022)
Background Mucins are part of the glycoprotein family and the main proteinaceous component of mucus. The sea anemone species, Actinia tenebrosa (Phylum Cnidaria) produce large amounts of mucus, which have not been studied in detail. Furthermore, ther
Externí odkaz:
https://doaj.org/article/8d0209960e4b496a915b8e48bfc8cf14
Publikováno v:
Bangladesh Journal of Pharmacology, Vol 14, Iss 3 (2019)
Externí odkaz:
https://doaj.org/article/e48c8cd17f91402798713af8f34d3007
Publikováno v:
Ecology and Evolution
Ecology and Evolution, Vol 9, Iss 19, Pp 11314-11328 (2019)
Ecology and Evolution, Vol 9, Iss 19, Pp 11314-11328 (2019)
Sea anemones have a wide array of toxic compounds (peptide toxins found in their venom) which have potential uses as therapeutics. To date, the majority of studies characterizing toxins in sea anemones have been restricted to species from the superfa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f4bd5de12ac957db4956782c69ee876
https://doi.org/10.1002/ece3.5633
https://doi.org/10.1002/ece3.5633
Akademický článek
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Publikováno v:
Ecology and Evolution. 8:5323-5335
The biosynthesis of long‐chain polyunsaturated fatty acids (LC‐PUFAs, ≥ C20) is reliant on the action of desaturase and elongase enzymes, which are encoded by the fatty acyl desaturase (Fad) and elongation of very long‐chain fatty acid (Elovl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b2fb2deb667b08f1bbd60cc5d28a30b5
https://doi.org/10.1002/ece3.4044
https://doi.org/10.1002/ece3.4044
Autor:
Xingchen, Chen, Darren, Leahy, Jessica, Van Haeften, Perry, Hartfield, Peter J, Prentis, Chloé A, van der Burg, Joachim M, Surm, Ana, Pavasovic, Bruno, Madio, Brett R, Hamilton, Glenn F, King, Eivind A B, Undheim, Maria, Brattsand, Jonathan M, Harris
Publikováno v:
Marine Drugs
Serine proteases play pivotal roles in normal physiology and a spectrum of patho-physiological processes. Accordingly, there is considerable interest in the discovery and design of potent serine protease inhibitors for therapeutic applications. This
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::81867c3d6e88db82a327f14a1ad162f1
https://pubmed.ncbi.nlm.nih.gov/31842369
https://pubmed.ncbi.nlm.nih.gov/31842369
Autor:
Christopher A. MacRaild, Raymond S. Norton, Billy J Williams-Noonan, Steve Peigneur, Peter J. Prentis, Alan H. Zhang, Bankala Krishnarjuna, Mehdi Mobli, David K. Chalmers, Khaled A. Elnahriry, Noha N. Badawy, Balasubramanyam Chittoor, Dorothy C.C. Wai, Jan Tytgat, Joachim M. Surm
Publikováno v:
Toxicon : official journal of the International Society on Toxinology. 168
Sea anemone venoms have long been recognised as a rich source of peptides with interesting pharmacological and structural properties. Our recent transcriptomic studies of the Australian sea anemone Actinia tenebrosa have identified a novel 13-residue
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f8026493172c970c430ed39191585a1b
https://pubmed.ncbi.nlm.nih.gov/31302115
https://pubmed.ncbi.nlm.nih.gov/31302115
A non-disruptive method for obtaining DNA samples from sea anemones (Cnidaria: Anthozoa: Actiniaria)
Publikováno v:
Conservation Genetics Resources. 11:19-21
Cnidarian researchers currently lack an established protocol for obtaining DNA samples from animals without requiring wild capture or the disruption of normal behaviour and physiology. Herein we describe a method of obtaining DNA samples from sea ane
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4a5a9efbda5fbb9ef65ede8b08f0b184
https://doi.org/10.1007/s12686-017-0953-4
https://doi.org/10.1007/s12686-017-0953-4
Publikováno v:
Bangladesh Journal of Pharmacology, Vol 14, Iss 3 (2019)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6900c3397553b65321bd76140eeefddc
https://doi.org/10.3329/bjp.v14i3.41472
https://doi.org/10.3329/bjp.v14i3.41472
Autor:
Peter J. Prentis, Maria Brattsand, Eivind A. B. Undheim, Perry J. Hartfield, Glenn F. King, Bruno Madio, Darren Leahy, Jonathan M. Harris, Chloé A. van der Burg, Brett Hamilton, Jessica Van Haeften, Joachim M. Surm, Xingchen Chen, Ana Pavasovic
Publikováno v:
Marine Drugs
Volume 17
Issue 12
Volume 17
Issue 12
Serine proteases play pivotal roles in normal physiology and a spectrum of patho-physiological processes. Accordingly, there is considerable interest in the discovery and design of potent serine protease inhibitors for therapeutic applications. This
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4bc50cb334c1c6145d96105598f5e2a8
https://doi.org/10.3390/md17120701
https://doi.org/10.3390/md17120701