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Artykuły w czasopismach na temat "Rottlerin"
Chen, Xu‐Ling, Yu Dong i Ji‐Yu Wang. "The Practical Total Synthesis of Rottlerin and Rottlerone". ChemistrySelect 5, nr 29 (4.08.2020): 9206–9. http://dx.doi.org/10.1002/slct.202002245.
Pełny tekst źródłaKim, Hyun Kyung, Eun Young Kang i Gwang-woong Go. "Rottlerin, a Polyphenolic Compound, Alleviate Body Adiposity by Enhancing Lipolysis and Thermogenesis in Diet-Induced Obesity Mice". Current Developments in Nutrition 5, Supplement_2 (czerwiec 2021): 1222. http://dx.doi.org/10.1093/cdn/nzab055_032.
Pełny tekst źródłaShivshankar, Pooja, Lei Lei, Jie Wang i Guangming Zhong. "Rottlerin Inhibits Chlamydial Intracellular Growth and Blocks Chlamydial Acquisition of Sphingolipids from Host Cells". Applied and Environmental Microbiology 74, nr 4 (14.12.2007): 1243–49. http://dx.doi.org/10.1128/aem.02151-07.
Pełny tekst źródłaKim, Ye Jin, i Gwang-woong !Go. "Rottlerin Suppresses Fat Accumulation by Inhibiting Adipogenesis and De Novo Lipogenesis in 3T3-L1 Adipocytes". Current Developments in Nutrition 5, Supplement_2 (czerwiec 2021): 1224. http://dx.doi.org/10.1093/cdn/nzab055_034.
Pełny tekst źródłaOhno, Izumi, Guido Eibl, Irina Odinokova, Mouad Edderkaoui, Robert D. Damoiseaux, Moussa Yazbec, Ravinder Abrol i in. "Rottlerin stimulates apoptosis in pancreatic cancer cells through interactions with proteins of the Bcl-2 family". American Journal of Physiology-Gastrointestinal and Liver Physiology 298, nr 1 (styczeń 2010): G63—G73. http://dx.doi.org/10.1152/ajpgi.00257.2009.
Pełny tekst źródłaMaioli, Emanuela, Lucedio Greci, Karel Soucek, Martina Hyzdalova, Alessandra Pecorelli, Vittoria Fortino i Giuseppe Valacchi. "Rottlerin Inhibits ROS Formation and Prevents NFκB Activation in MCF-7 and HT-29 Cells". Journal of Biomedicine and Biotechnology 2009 (2009): 1–7. http://dx.doi.org/10.1155/2009/742936.
Pełny tekst źródłaMolina, Yessenia L., David García-Seisdedos, Bohdan Babiy, Milagros Lerma, Javier Martínez-Botas, María J. Casarejos, María T. Vallejo i in. "Rottlerin Stimulates Exosome/Microvesicle Release Via the Increase of Ceramide Levels Mediated by Ampk in an In Vitro Model of Intracellular Lipid Accumulation". Biomedicines 10, nr 6 (3.06.2022): 1316. http://dx.doi.org/10.3390/biomedicines10061316.
Pełny tekst źródłaMischitelli, Morena, Mohamed Jemaà, Mustafa Almasry, Caterina Faggio i Florian Lang. "Stimulation of Suicidal Erythrocyte Death by Rottlerin". Cellular Physiology and Biochemistry 40, nr 3-4 (2016): 558–66. http://dx.doi.org/10.1159/000452569.
Pełny tekst źródłaMatschke, Veronika, Ilaria Piccini, Janina Schubert, Eva Wrobel, Florian Lang, Johann Matschke, Elsie Amedonu i in. "The Natural Plant Product Rottlerin Activates Kv7.1/KCNE1 Channels". Cellular Physiology and Biochemistry 40, nr 6 (2016): 1549–58. http://dx.doi.org/10.1159/000453205.
Pełny tekst źródłaKlinger, James R., Josh D. Murray, Brian Casserly, Diego F. Alvarez, Judy A. King, Steven S. An, Gaurav Choudhary, Akua N. Owusu-Sarfo, Rod Warburton i Elizabeth O. Harrington. "Rottlerin causes pulmonary edema in vivo: a possible role for PKCδ". Journal of Applied Physiology 103, nr 6 (grudzień 2007): 2084–94. http://dx.doi.org/10.1152/japplphysiol.00695.2007.
Pełny tekst źródłaRozprawy doktorskie na temat "Rottlerin"
Lama, Zoé. "Étude fonctionnelle d'inhibiteurs de kinases réprimant la réplication du virus de la rage". Thesis, Université Paris-Saclay (ComUE), 2017. http://www.theses.fr/2017SACLS490.
Pełny tekst źródłaHowever the rabies viral cycle is fairly well described, the interactions with the cellular machinery are not. This thesis project aimed at identifying and characterizing the cellular signaling pathways involved in the establishment and progress of the viral cycle through the study of cellular kinases. Indeed, kinases are the main actors of these pathways and their effects on certain rabies proteins have already been reported. In order to identify kinases involved in the viral cycle, we screened a kinase inhibitor library for anti-viral activity using a recombinant rabies virus expressing the GFP fluorescent protein. This assay allowed us to isolate two kinase inhibitors that block rabies virus infection: Tyrphostin 9, an inhibitor of the receptor tyrosine kinase platelet-derived growth factor receptor (PDGF.R), and Rottlerin, a PKCδ inhibitor and mitochondrial uncoupler. We confirmed their anti-viral action in different cell types (fibroblast, glioblastoma, neuroblastoma, as well as primary neurons) and on different rabies strains (CVS and SAD-B19). Using various experimental approaches, we found that each inhibitor impairs an early stage of the viral cycle: the viral fusion and more specifically the endosomal acidification by Tyrphostin 9 and the viral replication step by Rottlerin. We observed that Tyrphostin 9 also caused disintegration of the Golgi apparatus. The inhibition of endosomal acidification could therefore result from this effect. Seeking for the mechanisms involved in Rottlerin’s effect, we evidenced that it is independent of PKCδ. Experiments with a well characterized mitochondrial uncoupler (CCCP), revealed that the Rottlerin anti-viral effect is rather due to its mitochondrial uncoupling function, which leads to a decrease of the cellular ATP level. This study allowed the identification of two kinase inhibitors with anti-viral effects acting on early stages of the rabies cycle. The cellular targets as well as the effect on the cellular functions during viral infection remain to be determined. In vivo studies could validate their use in therapeutics as anti-rabies agents
Sivanathan, Sivatharushan [Verfasser]. "Synthese enantiomerenreiner α-Hydroxycarbonsäuren, neuer Cyclooctadepsipeptide sowie Studien zur Totalsynthese von Rottlerin / Sivatharushan Sivanathan". Wuppertal : Universitätsbibliothek Wuppertal, 2015. http://d-nb.info/1076930166/34.
Pełny tekst źródłaHeineck, Lukas [Verfasser], i Christian [Akademischer Betreuer] Kurts. "Der Einfluss von Rottlerin auf T-Zellpräsentation und -aktivierung / Lukas Heineck ; Betreuer: Christian Kurts". Marburg : Philipps-Universität Marburg, 2019. http://d-nb.info/1199537519/34.
Pełny tekst źródłaJuneja, Manisha. "Novel insights into MACC1 transcriptional regulation for identifying small molecule MACC1 inhibitors to restrict colorectal cancer progression". Doctoral thesis, Humboldt-Universität zu Berlin, Mathematisch-Naturwissenschaftliche Fakultät I, 2014. http://dx.doi.org/10.18452/17038.
Pełny tekst źródłaMACC1 has been reported as a prognostic biomarker for tumor progression and metastasis-free survival in CRC along with other solid tumors. It induces cell motility and proliferation in cell culture and metastasis in mouse models. Consequently, targeting MACC1 to intervene in tumor progression and metastasis formation holds a promising approach to treat CRC patients. We designed a strategy to inhibit MACC1 via targeting its transcription. We first identified MACC1 gene promoter by creating various promoter-luciferase constructs. We then established that transcription factors such as Ap-1, Sp1, C/EBPs and GIPC1 bind to the MACC1 promoter and govern MACC1 transcription, expression and thus motility in vitro and in CRC patients. Using a high throughput screening targeting the MACC1 promoter, we identified small molecule MACC1 inhibitors, Rottlerin and Lovastatin. These inhibitors specifically restricted endogenous MACC1 promoter leading to reduced MACC1 expression in a time- and concentration-dependent manner. In vitro functional assays demonstrated the impact of the small molecule inhibitors on retarding cell proliferation and motility. Both inhibitors restricted Sp1 levels and interfered with the binding of c-Jun to the MACC1 promoter, thereby inhibiting MACC1 transcription. The study further described the effect of Rottlerin on a CRC-xenografted mouse model. Daily treatment of xenografted mice with Rottlerin resulted in the inhibition of MACC1 expression in the primary tumor accompanied with the restricted tumor growth. To summarize, this is the first study unraveling the MACC1 promoter, its transcriptional regulation and identification of newly identified MACC1 inhibitors. In clinical settings, inhibition of MACC1 expression using these inhibitors might provide immense potential for the treatment of CRC patients who are at high risk for MACC1-induced metastasis linked to shorter survival.
Cordeiro, Thuany de Moura. "Efeitos da rottlerin na esquizogonia eritrocitária de Plasmodium falciparum e implementação e avaliação de teste in vitro por fluorescência de atividade antiplasmodial". reponame:Repositório Institucional da UnB, 2014. http://repositorio.unb.br/handle/10482/15666.
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A malária é uma doença infecciosa causada por protozoários Plasmodium spp. O P. falciparum é considerado o mais severo por ser o responsável pela maioria dos casos de morte causados pela doença. Devido ao rápido surgimento de cepas de P. falciparum resistentes às drogas antimalariais dá-se a importância de realizar um screening de compostos da biodiversidade, além de elucidar os mecanismos de ação de substâncias com comprovada ação antiplasmodial, como por exemplo, a rottlerin, um inibidor da proteína quinase C. As proteínas quinases desempenham um papel essencial em muitas funções celulares, o que as tornam alvos muito atraentes para o desenvolvimento de novas drogas. A metodologia considerada padrão ouro para avaliar a atividade antimalárica de drogas é o ensaio com incorporação de hipoxantina tritiada. No entanto, o alto custo, a adoção de medidas de segurança e a produção de lixo radioativo limitam a utilização desta técnica. Desta forma, os objetivos deste trabalho foram à implementação do teste de atividade antiplasmodial baseado em fluorescência com SYBR Green I®, avaliação da atividade antimalárica das subfrações cromatográficas de sílica-gel do extrato de acetato de etila de Qualea grandiflora, uma planta típica do Cerrado brasileiro, e avaliação dos efeitos da rottlerin no ciclo intra-eritrocitário do P. falciparum por métodos bioquímicos e citofluorimétricos. Três subfrações de Q. grandiflora apresentaram atividade antiplasmodial moderada, sem atividade citotóxica e hemolítica aparentes. Foi demonstrado o efeito da rottlerin, um potencial efetor da autofagia, sobre o ciclo eritrocitário de P. falciparum por citometria de fluxo. De fato, a análise da população enriquecida de esquizonte de P. falciparum em cultura tratada por rottlerin comparada com a não tratada revelou que houve inibição da diferenciação dos merozoítos, acarretando na morte rápida do parasito. A fim de entender quais eram os alvos proteicos de ação desta molécula, foi realizada uma análise proteômica comparativa preliminar por eletroforese bidimensional. Três proteínas, Heat Shock Protein 90 (HSP90), 3-fosfoglicerato quinase (3-PGK) e lactato desidrogenase (LDH), superexpressas na população de esquizontes não tratada com a rottlerin foram identificadas. Estas proteínas pertencem à classe de proteínas quinases ou possuem um domínio de interação com quinase. A HSP90 está envolvida no processo de enovelamento proteico com um papel fundamental no crescimento e desenvolvimento do parasito e, consequentemente, estudada como potencial alvo de droga antiplasmodial. A LDH e a 3-PGK são enzimas do metabolismo da glicose, e assim, potenciais alvos bem conhecidos para compostos antimaláricos devido à dependência deste parasito à glicólise para produção de energia. O estudo da biodiversidade do Cerrado pode contribuir para a descoberta de compostos antimalariais e a conservação deste bioma ameaçado. A não detecção das proteínas identificadas na presença de rottlerin pode estar relacionada à indução da autofagia na esquizogonia eritrocitária e constituem potenciais alvos de drogas antimaláricas. _______________________________________________________________________________________ ABSTRACT
Malaria is an infectious disease caused by Plasmodium spp protozoa. The P. falciparum is considered the most severe, since it is responsible for the majority of deaths related to this disease. Due to the rapid emergence of resistant strains of P. falciparum against antimalarial drugs, a great importance can be given to the screening of biodiversity compounds in addition to elucidate the mechanisms of action of substances with demonstrated antiplasmodial action such as rottlerin, an inhibitor of protein kinase C. Protein kinases play a pivotal role in many cellular functions, which make them very attractive targets for the development of new drugs. The methodology considered the gold standard for assessing antimalarial drug activity is the [3H]hypoxanthine incorporation assay. However, the high cost, adoption of safety regulations and the production of radioactive waste limit the application of this technique. Therefore, the objectives of this study were to implement the antiplasmodial activity test based on SYBR® Green I fluorescence, assessment of antimalarial activity of silica gel chromatographic subfractions of Qualea grandiflora ethyl acetate extract, a typical plant of the Brazilian Cerrado, and assessment of the rottlerin‟s effects in erythrocytic cycle of P. falciparum by biochemical and cytofluorimetric methods. Three subfractions of Q.grandiflora showed moderate antiplasmodial activity without apparent cytotoxic and hemolytic activities. It was demonstrated the effect of rottlerin, a potencial autophagy effector, on P. falciparum erythrocytic cycle by flow cytometry. In fact, analysis of the schizont enriched population of P. falciparum in rottlerin-treated culture compared to untreated ones revealed that there was an inhibition of merozoites differentiation, resulting in the rapid death of the parasite. In order to elucidate which proteins were the targets of rottlerin action, a preliminary comparative proteomic analysis by two-dimensional electrophoresis was performed. Three proteins, heat shock protein 90 (HSP90), 3- phosphoglycerate kinase (PGK-3) and lactate dehydrogenase (LDH), upregulated in schizont population non treated with rottlerin were identified. These proteins belong to the class of protein kinases or possess domains that interact with them. The HSP90 is involved in the protein folding process with a critic role in parasite growth and development, thus being studied as a potential target for antiplasmodial drugs. The 3- PGK and LDH are enzymes of glucose metabolism, hence well known potential targets for antimalarial compounds due to parasite dependence on glycolysis to produce energy. The study of Cerrado biodiversity can contribute to the discovery of antimalarial compounds and to the conservation of this threatened biome. The not detection of these proteins identified in the presence of rottlerin may be related to autophagy induction in erythrocytic schizogony and constitute potential targets for antimalarial drugs.
Nguyen, Khoa Thuy Diem. "Energy metabolism in the brain and rapid distribution of glutamate transporter GLAST in astrocytes". Thesis, The University of Sydney, 2008. http://hdl.handle.net/2123/3996.
Pełny tekst źródłaNguyen, Khoa Thuy Diem. "Energy metabolism in the brain and rapid distribution of glutamate transporter GLAST in astrocytes". University of Sydney, 2008. http://hdl.handle.net/2123/3996.
Pełny tekst źródłaGlutamate transporters play a role in removing extracellular excitatory neurotransmitter, L-glutamate into the cells. The rate of the uptake depends on the density of the transporters at the membrane. Some studies claimed that glutamate transporters could transit between the cytoplasm and the membrane on a time-scale of minutes. The present study examined the distribution of glutamate transporter GLAST predominantly expressed in rat cortical cultured astrocytes between the membrane and the cytoplasm by using deconvolution microscopy and then analyzing the images. The regulation of the distribution of GLAST was studied in the presence of glutamate transporter substrate (D-aspartate), purinergic receptor activators (α,β-methylene ATP, adenosine), neuroleptic drugs (clozapine, haloperidol), ammonia (hyperammonia) and Na+/K+-ATPase inhibitors (ouabain, digoxin and FCCP). It was demonstrated that the translocation of GLAST towards the plasma membrane was induced by D-aspartate, α,β-methylene ATP, adenosine, clozapine and ammonia (at 100 μM and very high concentrations of 10 mM). However, the inhibition of Na+/K+-ATPase activity had an opposite effect, resulting in redistribution of GLAST away from the membrane. It has previously been claimed that the membrane-cytoplasm trafficking of GLAST was regulated by phosphorylation catalysed by protein kinase C delta (PKC-delta). Involvement of this mechanism has, however, been put to doubt when rottlerin, a PKC-delta inhibitor, used to test the hypothesis showed to inhibit Na+/K+-ATPase-mediated uptake of Rb+, suggesting that rottlerin influenced the activity of Na+/K+-ATPase. As Na+/K+-ATPase converts ATP to energy and pumps Na+, K+ ions, thus helping to maintain normal electrochemical and ionic gradients across the cell membrane. Its inhibition also reduced D-aspartate transport and could impact on the cytoplasm-to-membrane traffic of GLAST molecules. Furthermore, rottlerin decreased the activity of Na+/K+-ATPase by acting as a mitochondrial inhibitor. The present study has focused on the inhibition of Na+/K+-ATPase activity by rottlerin, ouabain and digoxin in homogenates prepared from rat kidney and cultured astrocytes. The activity of Na+/K+-ATPase was measured by the absorption of inorganic phosphate product generated from the hydrolysis of ATP and the fluorescent transition of the dye RH421 induced by the movement of Na+/K+-ATPase. This approach has a potential to test whether the rottlerin effect on Na+/K+-ATPase is a direct inhibition of the enzyme activity. Rottlerin has been found to block the activity of Na+/K+-ATPase in a dose-dependent manner in both rat kidney and astrocyte homogenates. Therefore, rottlerin inhibited the activity of Na+/K+-ATPase directly in a cell-free preparation, thus strongly indicating that the effect was direct on the enzyme. In parallel experiments, ouabain and digoxin produced similar inhibitions of Na+/K+-ATPase activity in rat kidney while digoxin blocked the activity of Na+/K+-ATPase to a greater extent than ouabain in rat cortical cultured astrocytes. In a separate set of experiments, Na+/K+-ATPase in the astrocytic membrane was found to be unsaturated in E1(Na+)3 conformation in the presence of Na+ ions and this could explain the differences between the effects of digoxin and ouabain on the activity of Na+/K+-ATPase in rat astrocytes. In addition, it was found that at low concentrations of rottlerin, the activity of Na+/K+-ATPase was increased rather than inhibited. This effect was further investigated by studying rottlerin interactions with membrane lipids. The activity of Na+/K+-ATPase has been reported to be regulated by membrane lipids. The enzyme activity can be enhanced by increasing fluidity of the lipid membrane. I have, therefore, proposed that rottlerin binds to the membrane lipids and the effects of rottlerin on Na+/K+-ATPase are mediated by changes in the properties (fluidity) of the membrane. The hypothesis was tested by comparing rottlerin and a detergent, DOC (sodium deoxycholate), for their binding to the lipids by using a DMPC (1,2-Dimyristoyl-sn-Glycero-3-Phosphocholine) monolayer technique. DOC has been shown to both increase and inhibit activity of Na+/K+-ATPase in a manner similar to that displayed by rottlerin. The effects of rottlerin and DOC on the DMPC monolayers were studied by measuring the surface pressure of DMPC monolayers and surface area per DMPC molecule. I established that both rottlerin and DOC decreased the surface pressure of DMPC monolayers and increased the surface area per DMPC molecule. This indicates that both rottlerin and DOC penetrated into the DMPC monolayers. If rottlerin can interact with the lipids, changes in fluidity of the lipid membrane cannot be ruled out and should be considered as a possible factor contributing to the effects of rottlerin on the activity of Na+/K+-ATPase. Overall, the study demonstrates that rottlerin is not only a PKC-delta inhibitor but can have additional effects, both on the enzyme activities (Na+/K+-ATPase) and/or on lipid-containing biological structures such as membranes. The findings have implication not only for studies where rottlerin was used as a supposedly specific PKC-delta inhibitor but also for mechanisms of its toxicity.
Contreras, Xavier. "Rôle des voies PKC et calcium dans les productions de TNF-alpha et d'IL-10 induites par la protéine Tat du Virus de l'immuodéficience humaine chez le monocyte humain et dans la réplication de virus R5-tropiques dans le macrophage". Toulouse 3, 2005. http://www.theses.fr/2005TOU30012.
Pełny tekst źródłaThe goals of this study are on the one hand the characterization of signaling pathways involved in TNF-a and IL-10 productions by human monocytes/macrophages stimulated by Tat protein of HIV-1 and on the other hand the evaluation of the role of these signaling pathways in viral replication. Thus, Tat protein activates the calcium and PKC pathways in the monocyte/macrophage to stimulate TNF-a and IL-10 productions via its 1-45 N-terminal domain. The 20-45 region stimulates calcium entry in monocytes via DHP-sensitive calcium channels. Tat induces the activation of a, bI, bII, d, and e PKC isozymes, but only d and bII PKC isozymes activation is essential for IL-10 production. The selective inhibition of PKC d activation by rottlerin blocks CCR5-tropic HIV-1 BaL virus replication in human macrophage by acting probably at the level of an early step of the virus life cycle involving the cytoskeleton
Koterba, Kristen L. "Regulation of Autophagy and Cell Death in Breast Carcinoma Cells". University of Toledo Health Science Campus / OhioLINK, 2010. http://rave.ohiolink.edu/etdc/view?acc_num=mco1276005638.
Pełny tekst źródłaRottler, Andreas [Verfasser]. "Investigation of Radial Metamaterials / Andreas Rottler". München : Verlag Dr. Hut, 2013. http://d-nb.info/1037286847/34.
Pełny tekst źródłaKsiążki na temat "Rottlerin"
Misaca, Constantin. How I escaped from Communist Romania, or... the Story of My Rottlen Life. Lulu Press, Inc., 2010.
Znajdź pełny tekst źródłaCzęści książek na temat "Rottlerin"
Bhandari, Khadka B., Suresh Subedi, Ripu M. Kunwar, Rainer W. Bussmann i Narel Y. Paniagua-Zambrana. "Grewia disperma Rottler ex Spreng. Malvaceae". W Ethnobotany of the Himalayas, 1–13. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-45597-2_112-1.
Pełny tekst źródłaBhandari, Khadka B., Suresh Subedi, Ripu M. Kunwar, Rainer W. Bussmann i Narel Y. Paniagua-Zambrana. "Grewia disperma Rottler ex Spreng. Malvaceae". W Ethnobotany of the Himalayas, 1001–13. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-57408-6_112.
Pełny tekst źródła"ROTTLERA". W Directory Of Plants Containing Secondary Metabolites, 1034. CRC Press, 1991. http://dx.doi.org/10.1201/b12561-426.
Pełny tekst źródła"Kachri (Cucumis callosus [Rottler] Cogn.)". W Handbook of Cucurbits, 519–32. CRC Press, 2016. http://dx.doi.org/10.1201/b19233-48.
Pełny tekst źródłaStreszczenia konferencji na temat "Rottlerin"
Goldklang, Monica P., Nazish Sayed, Takwi Nkyimbeng, Jordis Trischler, Tina Zelonina, A. J. Dabo, Sergey Zakharov i in. "Rottlerin Suppresses Airway Hyperreactivity And Inflammation In Mouse Models Of Experimental Asthma". W American Thoracic Society 2012 International Conference, May 18-23, 2012 • San Francisco, California. American Thoracic Society, 2012. http://dx.doi.org/10.1164/ajrccm-conference.2012.185.1_meetingabstracts.a3580.
Pełny tekst źródłaSu, Hsin-Yuan, Richard Waldron, Raymond Gong, Stephen Pandol i Aurelia Lugea. "Abstract 1769: Rottlerin induces ER stress-mediated cell death in pancreatic stellate cells". W Proceedings: AACR 106th Annual Meeting 2015; April 18-22, 2015; Philadelphia, PA. American Association for Cancer Research, 2015. http://dx.doi.org/10.1158/1538-7445.am2015-1769.
Pełny tekst źródłaJoeckel, Matthias W., Elke Schneider, Frederik C. Roos, Christian Hampel, Joachim W. Thueroff i Walburgis Brenner. "Abstract 1041: Sorafenib in combination with rottlerin show an additive effects in renal cell carcinoma (RCC) cells." W Proceedings: AACR 104th Annual Meeting 2013; Apr 6-10, 2013; Washington, DC. American Association for Cancer Research, 2013. http://dx.doi.org/10.1158/1538-7445.am2013-1041.
Pełny tekst źródłaKumar, Dhruv. "Abstract 329: Rottlerin induced autophagy by targeting multiple sites that leads to the apoptosis in cancer stem cells". W Proceedings: AACR Annual Meeting 2014; April 5-9, 2014; San Diego, CA. American Association for Cancer Research, 2014. http://dx.doi.org/10.1158/1538-7445.am2014-329.
Pełny tekst źródłaPrudnikova, Tatiana, i Jonathan Chernoff. "Abstract LB-011: PAK1 inhibitor FRAX1036 sensitizes ovarian cancer cells with amplified 11q13 to cytotoxic effect of rottlerin". W Proceedings: AACR 107th Annual Meeting 2016; April 16-20, 2016; New Orleans, LA. American Association for Cancer Research, 2016. http://dx.doi.org/10.1158/1538-7445.am2016-lb-011.
Pełny tekst źródłaAshour, Ahmed A., Abdel-Aziz H. Abdel-Aziz, Ahmed M. Mansour, Sultan N. Alpay, Kevin Dalby i Bulent Ozpolat. "Abstract 848: Inhibition of eukaryotic elongation factor-2 kinase mediates Rottlerin induced effects in apoptosis and cell proliferation inhibition in human pancreatic cancer cells." W Proceedings: AACR 104th Annual Meeting 2013; Apr 6-10, 2013; Washington, DC. American Association for Cancer Research, 2013. http://dx.doi.org/10.1158/1538-7445.am2013-848.
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