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The anticancer effects of actinoporin RTX-A from the sea anemone Heteractis crispa (=Radianthus macrodactylus)Meroterpenoids from the alga-derived fungi Penicillium thomii Maire and Penicillium lividum Westling.Sargassopenillines A-G, 6,6-spiroketals from the alga-derived fungi Penicillium thomii and Penicillium lividum.Marine compound rhizochalinin shows high in vitro and in vivo efficacy in castration resistant prostate cancer.Activity of aaptamine and two derivatives, demethyloxyaaptamine and isoaaptamine, in cisplatin-resistant germ cell cancer.Guanidine Alkaloids from the Marine Sponge Monanchora pulchra Show Cytotoxic Properties and Prevent EGF-Induced Neoplastic Transformation in Vitro.Cabazitaxel overcomes cisplatin resistance in germ cell tumour cells.Pretrichodermamides D-F from a Marine Algicolous Fungus Penicillium sp. KMM 4672.Anti-migratory activity of marine alkaloid monanchocidin A - proteomics-based discovery and confirmation.The marine triterpene glycoside frondoside A exhibits activity in vitro and in vivo in prostate cancer.Marine alkaloid Monanchocidin a overcomes drug resistance by induction of autophagy and lysosomal membrane permeabilization.Quinone-carbohydrate nonglucoside conjugates as a new type of cytotoxic agents: synthesis and determination of in vitro activity.Monanchomycalin C, a new pentacyclic guanidine alkaloid from the far-eastern marine sponge Monanchora pulchra.Pallidopenillines: Polyketides from the Alga-Derived Fungus Penicillium thomii Maire KMM 4675.Mycalamide A shows cytotoxic properties and prevents EGF-induced neoplastic transformation through inhibition of nuclear factors.Three new aaptamines from the marine sponge Aaptos sp. and their proapoptotic properties.Monanchocidin: a new apoptosis-inducing polycyclic guanidine alkaloid from the marine sponge Monanchora pulchra.Two new asterosaponins, archasterosides A and B, from the Vietnamese starfish Archaster typicus and their anticancer properties.The Inhibitory Activity of Luzonicosides from the Starfish Echinaster luzonicus against Human Melanoma CellsAaptamines from the marine sponge Aaptos sp. display anticancer activities in human cancer cell lines and modulate AP-1-, NF-κB-, and p53-dependent transcriptional activity in mouse JB6 Cl41 cells.Marine Compounds and Cancer: Where Do We Stand?Oxirapentyns F-K from the marine-sediment-derived fungus Isaria felina KMM 4639.Isolation, structures, and biological activities of triterpenoids from a Penares sp. marine sponge.New meroterpenoids from the marine sponge Aka coralliphaga.Frondoside A induces AIF-associated caspase-independent apoptosis in Burkitt lymphoma cells.Marine Compounds and Cancer: 2017 Updates.[Polar steroids from Solaster endeca starfish and the physiological activity of polar steroids from three starfish species]5-Azacitidine Exerts Prolonged Pro-Apoptotic Effects and Overcomes Cisplatin-Resistance in Non-Seminomatous Germ Cell Tumor CellsAsperindoles A⁻D and a p-Terphenyl Derivative from the Ascidian-Derived Fungus Aspergillus sp. KMM 4676.Aaptamine alkaloids from the Vietnamese sponge Aaptos spMelonoside A: An ω-Glycosylated Fatty Acid Amide from the Far Eastern Marine Sponge Melonanchora kobjakovaePolyphenolic Compounds from Lespedeza Bicolor Root Bark Inhibit Progression of Human Prostate Cancer Cells via Induction of Apoptosis and Cell Cycle ArrestMarine Compounds and Autophagy: Beginning of a New EraBiologically Active Metabolites from the Marine Sediment-Derived Fungus Aspergillus flocculosusSuccessful Targeting of the Warburg Effect in Prostate Cancer by Glucose-Conjugated 1,4-NaphthoquinonesPiltunines A-F from the Marine-Derived Fungus Penicillium piltunense KMM 4668Biologically Active Echinulin-Related Indolediketopiperazines from the Marine Sediment-Derived Fungus Aspergillus niveoglaucusNew Trisulfated Steroids from the Vietnamese Marine Sponge Halichondria vansoesti and Their PSA Expression and Glucose Uptake Inhibitory ActivitiesMarine Compounds and Cancer: The First Two Decades of XXI CenturyMarine Drugs Acting as Autophagy Modulators
P50
Q33663904-C604A994-94ED-40D5-8D89-BD4F3FF93EF6Q34421037-513B8BF1-37E6-44C3-B27E-4762889247B8Q34453518-3F379015-83AB-47AD-968B-5939F5C85770Q37688428-4C9A3622-8387-4658-807D-7F56FBB2177EQ38482989-F7B9951F-CD26-479B-9AE2-AA3CC5E34EDCQ38757470-322CAB02-DF44-44CD-A935-85DA8E1E0956Q38757753-06652365-4681-43A1-ABA1-09BF70F084FCQ38760985-5D63920D-3623-4DD7-BFE3-469E708C54D9Q38784326-70B31FB8-DAF5-4815-B0EA-7C057D17C912Q38809660-AE76ED3C-AA42-427B-99C7-11DB242EAF93Q38861914-CB5DC36C-F293-41A9-8748-7867732AF494Q39015286-AE791820-1BB7-43E4-8D68-B12020F6D3CEQ39041915-1AFF91EE-4493-49C3-8C9A-74A381AF319CQ39071715-13246F43-7290-4EF3-8582-0211A0FA2B2EQ39309996-90552B15-84DA-4006-A591-FDE410CD560FQ39596786-75A1423E-941F-465B-BC9D-F2B36B285D37Q39661823-662C2977-273B-45C4-AA64-B5DEAFF9540BQ39701386-2161D4FA-0C02-4D1A-9C1E-8C84EB357BBBQ41162034-AD88BC2A-91E8-4A3D-A0B5-C385D3789CAAQ41872927-3B0E385D-D5FB-4C9C-965C-198710937012Q43239058-507CFD25-4376-4134-B1C8-C94918F37B29Q43643661-CF49FCAA-52F8-4461-9B9C-B90AC38B5D15Q44031635-221BE1ED-9B6F-4773-B3F0-506062584A1BQ45183526-AB582B99-6E20-41E1-A4C2-619237AEAA2FQ48138574-4D4BB4D8-DC68-4537-AFEB-A972B0B3AC3EQ48175871-F4D78674-A228-4F58-8683-18489D1E6AE9Q53319863-F4ED9781-8226-4678-B8B9-3F3DFC5E9925Q60939710-6839AE1F-3DA6-4044-A7CB-FABB2967A4ACQ64890317-915F8BB2-D292-495F-961E-FF6572D8BA2FQ84575755-42C747C7-23FF-4C84-99D9-63F5DE3BBBF1Q87783957-C0D9C2EC-F616-40F0-80A3-727FC93227CAQ90399344-3B16431A-3F7C-4A76-8AEE-94912612B668Q90672290-9D736432-0710-41BE-B5B5-B91FC8777988Q90721175-BDA39AE1-3F8F-49D2-B74D-ADBE57260FFAQ91037473-6628B65D-8934-48F8-ABE7-1B98AC9A0017Q91377047-6D176312-0A86-47A5-B6D9-E3FD11FC85E7Q92257646-704E0491-354D-49B2-945F-A4E1FA58010DQ92257811-A897BA12-72D2-4B00-9B44-BC82CEC73F6BQ92326170-9F53D4F5-EB5C-440F-A786-7B2CE9568E99Q92701980-8D342336-C00A-4802-8AB8-1EDEE05EBC08
P50
description
hulumtues
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researcher
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wetenschapper
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հետազոտող
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name
Sergey A Dyshlovoy
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Sergey A Dyshlovoy
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Sergey A Dyshlovoy
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Sergey A Dyshlovoy
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Sergey A Dyshlovoy
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type
label
Sergey A Dyshlovoy
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Sergey A Dyshlovoy
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Sergey A Dyshlovoy
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Sergey A Dyshlovoy
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Sergey A Dyshlovoy
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prefLabel
Sergey A Dyshlovoy
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Sergey A Dyshlovoy
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Sergey A Dyshlovoy
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Sergey A Dyshlovoy
@nl
Sergey A Dyshlovoy
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P1053
B-3586-2013
P106
P21
P31
P3829
P496
0000-0002-7155-9245