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Artykuły w czasopismach na temat "G3BP2 expression"
Scholte, Florine E. M., Ali Tas, Irina C. Albulescu, Eva Žusinaite, Andres Merits, Eric J. Snijder i Martijn J. van Hemert. "Stress Granule Components G3BP1 and G3BP2 Play a Proviral Role Early in Chikungunya Virus Replication". Journal of Virology 89, nr 8 (4.02.2015): 4457–69. http://dx.doi.org/10.1128/jvi.03612-14.
Pełny tekst źródłaZheng, Yinli, Jinjun Wu, Ru Deng, Censhan Lin, Yuhua Huang, Xia Yang, Chunhua Wang i in. "G3BP2 regulated by the lncRNA LINC01554 facilitates esophageal squamous cell carcinoma metastasis through stabilizing HDGF transcript". Oncogene 41, nr 4 (15.11.2021): 515–26. http://dx.doi.org/10.1038/s41388-021-02073-0.
Pełny tekst źródłaGupta, Nisha, Mark Badeaux, Yiqian Liu, Kamila Naxerova, Dennis Sgroi, Lance L. Munn, Rakesh K. Jain i Igor Garkavtsev. "Stress granule-associated protein G3BP2 regulates breast tumor initiation". Proceedings of the National Academy of Sciences 114, nr 5 (17.01.2017): 1033–38. http://dx.doi.org/10.1073/pnas.1525387114.
Pełny tekst źródłaBasu, Gargi D., Kevin Drenner, Audrey Ozols, Candyce M. Bair, Tracey White, Janine R. LoBello, Thomas Royce i Sunil Sharma. "Whole exome and transcriptome sequencing of colorectal and pancreatic cancer." Journal of Clinical Oncology 38, nr 15_suppl (20.05.2020): e15666-e15666. http://dx.doi.org/10.1200/jco.2020.38.15_suppl.e15666.
Pełny tekst źródłaLin, Che-Hsuan, Hsun-Hua Lee, Wei-Min Chang, Fei-Peng Lee, Lung-Che Chen, Long-Sheng Lu i Yuan-Feng Lin. "FOXD1 Repression Potentiates Radiation Effectiveness by Downregulating G3BP2 Expression and Promoting the Activation of TXNIP-Related Pathways in Oral Cancer". Cancers 12, nr 9 (21.09.2020): 2690. http://dx.doi.org/10.3390/cancers12092690.
Pełny tekst źródłaHinton, Shantá D., Michael P. Myers, Vincent R. Roggero, Lizabeth A. Allison i Nicholas K. Tonks. "The pseudophosphatase MK-STYX interacts with G3BP and decreases stress granule formation". Biochemical Journal 427, nr 3 (14.04.2010): 349–57. http://dx.doi.org/10.1042/bj20091383.
Pełny tekst źródłaYang, Ziwei. "Expression of human G3BP1 in E. coli". E3S Web of Conferences 292 (2021): 03087. http://dx.doi.org/10.1051/e3sconf/202129203087.
Pełny tekst źródłaCristea, Ileana M., Heather Rozjabek, Kelly R. Molloy, Sophiya Karki, Laura L. White, Charles M. Rice, Michael P. Rout, Brian T. Chait i Margaret R. MacDonald. "Host Factors Associated with the Sindbis Virus RNA-Dependent RNA Polymerase: Role for G3BP1 and G3BP2 in Virus Replication". Journal of Virology 84, nr 13 (14.04.2010): 6720–32. http://dx.doi.org/10.1128/jvi.01983-09.
Pełny tekst źródłaNeumann, Frank, Daniela C. Bruennert, Anne-Marie Koch, Ingmar Bruns, Norbert Gattermann, Ralf Kronenwett i Rainer Haas. "Transcriptional Changes Induced by Imatinib and Nilotinib in the Chronic Myelogenous Leukemia (CML) Cell Line K562." Blood 110, nr 11 (16.11.2007): 4540. http://dx.doi.org/10.1182/blood.v110.11.4540.4540.
Pełny tekst źródłaSomasekharan, Syam Prakash, Amal El-Naggar, Gabriel Leprivier, Hongwei Cheng, Shamil Hajee, Thomas G. P. Grunewald, Fan Zhang i in. "YB-1 regulates stress granule formation and tumor progression by translationally activating G3BP1". Journal of Cell Biology 208, nr 7 (23.03.2015): 913–29. http://dx.doi.org/10.1083/jcb.201411047.
Pełny tekst źródłaRozprawy doktorskie na temat "G3BP2 expression"
Alam, Umber. "Translational Regulation Of Target Gene Expression By G3BPs In Breast Cancer Cells". Thesis, Griffith University, 2018. http://hdl.handle.net/10072/380057.
Pełny tekst źródłaThesis (PhD Doctorate)
Doctor of Philosophy (PhD)
School of Environment and Sc
Science, Environment, Engineering and Technology
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Stirling, Susan Renee, i n/a. "The Roles of RasGAP SH3 Domain Binding Proteins (G3BPs) in RNA Metabolism, the Cellular Stress Response and Tumorigenesis". Griffith University. School of Biomolecular and Biomedical Science, 2006. http://www4.gu.edu.au:8080/adt-root/public/adt-QGU20070705.175459.
Pełny tekst źródłaStirling, Susan Renee. "The Roles of RasGAP SH3 Domain Binding Proteins (G3BPs) in RNA Metabolism, the Cellular Stress Response and Tumorigenesis". Thesis, Griffith University, 2006. http://hdl.handle.net/10072/366889.
Pełny tekst źródłaThesis (PhD Doctorate)
Doctor of Philosophy (PhD)
School of Biomolecular and Biomedical Sciences
Full Text
Barbeta, Lilian Pires. "Avaliação da expressão gênica da proteína 2 ligante de SH3 ativadora da GTPase de Ras (G3BP2), do fator da tecidual (TF) e da isoforma asHTF como possíveis marcadores prognósticos em carcinoma epidermóide de cabeça e pescoço". Universidade de São Paulo, 2009. http://www.teses.usp.br/teses/disponiveis/5/5155/tde-18022010-145012/.
Pełny tekst źródłaGTPase activating protein (SH3 domain) binding protein 2 (G3BP2) seems to be involved in pathways important for cell survival as NF- B pathway. Tissue factor (TF) and its isoform asHTF appear to be involved in angiogenesis, proliferation and metastasis. Thus, the genes G3BP2, TF and asHTF seem possible prognostic factors in head and neck squamous cell carcinoma (SCC). To assess the importance of these genes in this type of cancer, we performed mRNA expression analysis of these markers by real time PCR (polymerase chain reaction) in primary tumors and adjacent mucosa of 148 patients with oral cavity, tongue and larynx SCC. TF and asHTF protein was determined by Western blotting in 17 patients with oral cavity SCC. mRNA expression levels were correlated with clinical and pathological variables and survival of patients. G3BP2 mRNA expression was lower in primary tumors as compared to adjacent mucosa at all sites analyzed. No difference was found between TF and asHTF expression in primary tumors and adjacent mucosa in the whole group. TF and asHTF levels mRNA expression were higher in pN+ tumors as compared to pN0 in oral cavity (P=0.003, P = 0.004, respectively) and tongue (P= 0.033, P= 0.018, respectively - Mann-Whitney test) tumors. For Kaplan Meier survival analysis patients were categorized positive (expression > tumor median relative expression) and negative (expression tumor median relative expression). For oral cavity SCC, patients with positive expression of TF (P =0.034 - log-rank test) and asHTF (P =0.010) genes presented shorter disease-free survival in univariate analysis. In multivariate analysis both TF as asHTF retained statistical significance (P=0.002 for both genes), suggesting, therefore, are independent prognostic factors. Protein analysis showed 76.4% agreement with mRNA expression for TF and 58.8% for asHTF. In patients with tongue and larynx tumors there correlation were not found. Thus, we suggest that the TF and asHTF expression seem to be prognostic markers in oral cavity SCC especially in relation to disease-free survival. Supported by FAPESP 06/53755-5
Irvine, Katharine Margaret. "The expression and function of G3BPs in macrophages /". [St. Lucia, Qld], 2004. http://www.library.uq.edu.au/pdfserve.php?image=thesisabs/absthe18195.pdf.
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