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Genotoxic Damage to Glioblastoma Cells Treated with 6 MV X-Radiation in The Presence or Absence of Methoxy Estradiol, IUDR or Topotecan.

Cell journal

Eyvazzadeh N, Neshasteh-Riz A, Mahdavi SR, Mohsenifar A.
PMID: 26199910
Cell J. 2015;17(2):312-21. doi: 10.22074/cellj.2016.3738. Epub 2015 Jul 11.

OBJECTIVE: To explore the cumulative genotoxic damage to glioblastoma (GBM) cells, grown as multicellular spheroids, following exposure to 6 MV X-rays (2 Gy, 22 Gy) with or without, 2- methoxy estradiol (2ME2), iododeoxyuridine (IUDR) or topotecan (TPT), using the...

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Eyvazzadeh N, Neshasteh-Riz A, Mahdavi SR, et al. Genotoxic Damage to Glioblastoma Cells Treated with 6 MV X-Radiation in The Presence or Absence of Methoxy Estradiol, IUDR or Topotecan. Cell J. 2015;17(2):312-21doi: 10.22074/cellj.2016.3738.
Eyvazzadeh, N., Neshasteh-Riz, A., Mahdavi, S. R., & Mohsenifar, A. (2015). Genotoxic Damage to Glioblastoma Cells Treated with 6 MV X-Radiation in The Presence or Absence of Methoxy Estradiol, IUDR or Topotecan. Cell journal, 17(2), 312-21. https://doi.org/10.22074/cellj.2016.3738
Eyvazzadeh, Nazila, et al. "Genotoxic Damage to Glioblastoma Cells Treated with 6 MV X-Radiation in The Presence or Absence of Methoxy Estradiol, IUDR or Topotecan." Cell journal vol. 17,2 (2015): 312-21. doi: https://doi.org/10.22074/cellj.2016.3738
Eyvazzadeh N, Neshasteh-Riz A, Mahdavi SR, Mohsenifar A. Genotoxic Damage to Glioblastoma Cells Treated with 6 MV X-Radiation in The Presence or Absence of Methoxy Estradiol, IUDR or Topotecan. Cell J. 2015;17(2):312-21. doi: 10.22074/cellj.2016.3738. Epub 2015 Jul 11. PMID: 26199910; PMCID: PMC4503845.
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DNA and RNA Extraction and Quantitative Real-Time PCR-Based Assays for Biogas Biocenoses in an Interlaboratory Comparison.

Bioengineering (Basel, Switzerland)

Lebuhn M, Derenkó J, Rademacher A, Helbig S, Munk B, Pechtl A, Stolze Y, Prowe S, Schwarz WH, Schlüter A, Liebl W, Klocke M.
PMID: 28952569
Bioengineering (Basel). 2016 Jan 13;3(1). doi: 10.3390/bioengineering3010007.

Five institutional partners participated in an interlaboratory comparison of nucleic acid extraction, RNA preservation and quantitative Real-Time PCR (qPCR) based assays for biogas biocenoses derived from different grass silage digesting laboratory and pilot scale fermenters. A kit format DNA...

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Lebuhn M, Derenkó J, Rademacher A, et al. DNA and RNA Extraction and Quantitative Real-Time PCR-Based Assays for Biogas Biocenoses in an Interlaboratory Comparison. Bioengineering (Basel). 2016;3(1)doi: 10.3390/bioengineering3010007.
Lebuhn, M., Derenkó, J., Rademacher, A., Helbig, S., Munk, B., Pechtl, A., Stolze, Y., Prowe, S., Schwarz, W. H., Schlüter, A., Liebl, W., & Klocke, M. (2016). DNA and RNA Extraction and Quantitative Real-Time PCR-Based Assays for Biogas Biocenoses in an Interlaboratory Comparison. Bioengineering (Basel, Switzerland), 3(1), . https://doi.org/10.3390/bioengineering3010007
Lebuhn, Michael, et al. "DNA and RNA Extraction and Quantitative Real-Time PCR-Based Assays for Biogas Biocenoses in an Interlaboratory Comparison." Bioengineering (Basel, Switzerland) vol. 3,1 (2016). doi: https://doi.org/10.3390/bioengineering3010007
Lebuhn M, Derenkó J, Rademacher A, Helbig S, Munk B, Pechtl A, Stolze Y, Prowe S, Schwarz WH, Schlüter A, Liebl W, Klocke M. DNA and RNA Extraction and Quantitative Real-Time PCR-Based Assays for Biogas Biocenoses in an Interlaboratory Comparison. Bioengineering (Basel). 2016 Jan 13;3(1). doi: 10.3390/bioengineering3010007. PMID: 28952569; PMCID: PMC5597165.
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Anti-breast cancer and anti-angiogenic potential of a lichen-derived small-molecule: barbatolic acid.

Cytotechnology

Varol M.
PMID: 30155608
Cytotechnology. 2018 Dec;70(6):1565-1573. doi: 10.1007/s10616-018-0249-x. Epub 2018 Aug 28.

Natural products have been used for centuries as the most potent remedies to cure many diseases including cancer diseases. Angiogenesis is defined as the formation of new capillaries from existing vessels and plays a key role in the tumorigenesis...

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Varol M. Anti-breast cancer and anti-angiogenic potential of a lichen-derived small-molecule: barbatolic acid. Cytotechnology. 2018;70(6):1565-1573doi: 10.1007/s10616-018-0249-x.
Varol, M. (2018). Anti-breast cancer and anti-angiogenic potential of a lichen-derived small-molecule: barbatolic acid. Cytotechnology, 70(6), 1565-1573. https://doi.org/10.1007/s10616-018-0249-x
Varol, Mehmet. "Anti-breast cancer and anti-angiogenic potential of a lichen-derived small-molecule: barbatolic acid." Cytotechnology vol. 70,6 (2018): 1565-1573. doi: https://doi.org/10.1007/s10616-018-0249-x
Varol M. Anti-breast cancer and anti-angiogenic potential of a lichen-derived small-molecule: barbatolic acid. Cytotechnology. 2018 Dec;70(6):1565-1573. doi: 10.1007/s10616-018-0249-x. Epub 2018 Aug 28. PMID: 30155608; PMCID: PMC6269354.
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Combinations of growth factors for human mesenchymal stem cell proliferation and osteogenic differentiation.

Bone & joint research

Hefka Blahnova V, Dankova J, Rampichova M, Filova E.
PMID: 32864112
Bone Joint Res. 2020 Aug 19;9(7):412-420. doi: 10.1302/2046-3758.97.BJR-2019-0183.R2. eCollection 2020 Jul.

AIMS: Here we introduce a wide and complex study comparing effects of growth factors used alone and in combinations on human mesenchymal stem cell (hMSC) proliferation and osteogenic differentiation. Certain ways of cell behaviour can be triggered by specific...

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Hefka Blahnova V, Dankova J, Rampichova M, et al. Combinations of growth factors for human mesenchymal stem cell proliferation and osteogenic differentiation. Bone Joint Res. 2020;9(7):412-420doi: 10.1302/2046-3758.97.BJR-2019-0183.R2.
Hefka Blahnova, V., Dankova, J., Rampichova, M., & Filova, E. (2020). Combinations of growth factors for human mesenchymal stem cell proliferation and osteogenic differentiation. Bone & joint research, 9(7), 412-420. https://doi.org/10.1302/2046-3758.97.BJR-2019-0183.R2
Hefka Blahnova, Veronika, et al. "Combinations of growth factors for human mesenchymal stem cell proliferation and osteogenic differentiation." Bone & joint research vol. 9,7 (2020): 412-420. doi: https://doi.org/10.1302/2046-3758.97.BJR-2019-0183.R2
Hefka Blahnova V, Dankova J, Rampichova M, Filova E. Combinations of growth factors for human mesenchymal stem cell proliferation and osteogenic differentiation. Bone Joint Res. 2020 Aug 19;9(7):412-420. doi: 10.1302/2046-3758.97.BJR-2019-0183.R2. eCollection 2020 Jul. PMID: 32864112; PMCID: PMC7437520.
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Dataset of the absorption, emission and excitation spectra and fluorescence intensity graphs of fluorescent cyanine dyes for the quantification of low amounts of dsDNA.

Data in brief

Bruijns B, Tiggelaar R, Gardeniers H.
PMID: 27957521
Data Brief. 2016 Nov 28;10:132-143. doi: 10.1016/j.dib.2016.11.090. eCollection 2017 Feb.

This article describes data related to a research article entitled "Fluorescent cyanine dyes for the quantification of low amounts of dsDNA" (B. Bruijns, R. Tiggelaar, J. Gardeniers, 2016) [1]. Six cyanine dsDNA dyes - EvaGreen, SYBR Green, PicoGreen, AccuClear,...

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Bruijns B, Tiggelaar R, Gardeniers H. Dataset of the absorption, emission and excitation spectra and fluorescence intensity graphs of fluorescent cyanine dyes for the quantification of low amounts of dsDNA. Data Brief. 2016;10:132-143doi: 10.1016/j.dib.2016.11.090.
Bruijns, B., Tiggelaar, R., & Gardeniers, H. (2017). Dataset of the absorption, emission and excitation spectra and fluorescence intensity graphs of fluorescent cyanine dyes for the quantification of low amounts of dsDNA. Data in brief, 10132-143. https://doi.org/10.1016/j.dib.2016.11.090
Bruijns, Brigitte, et al. "Dataset of the absorption, emission and excitation spectra and fluorescence intensity graphs of fluorescent cyanine dyes for the quantification of low amounts of dsDNA." Data in brief vol. 10 (2017): 132-143. doi: https://doi.org/10.1016/j.dib.2016.11.090
Bruijns B, Tiggelaar R, Gardeniers H. Dataset of the absorption, emission and excitation spectra and fluorescence intensity graphs of fluorescent cyanine dyes for the quantification of low amounts of dsDNA. Data Brief. 2016 Nov 28;10:132-143. doi: 10.1016/j.dib.2016.11.090. eCollection 2017 Feb. PMID: 27957521; PMCID: PMC5143369.
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Real-time PCR.

Forensic science, medicine, and pathology

Bowyer VL.
PMID: 25868892
Forensic Sci Med Pathol. 2007 Mar;3(1):61-3. doi: 10.1385/FSMP:3:1:61.

Research into the field of DNA has increased dramatically in the years since DNA profiling was first identified. Since then, techniques have been developed to identify individuals from DNA samples equivalent to a single cell. Development of these techniques...

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Bowyer VL. Real-time PCR. Forensic Sci Med Pathol. 2007;3(1):61-3doi: 10.1385/FSMP:3:1:61.
Bowyer, V. L. (2007). Real-time PCR. Forensic science, medicine, and pathology, 3(1), 61-3. https://doi.org/10.1385/FSMP:3:1:61
Bowyer, Victoria L. "Real-time PCR." Forensic science, medicine, and pathology vol. 3,1 (2007): 61-3. doi: https://doi.org/10.1385/FSMP:3:1:61
Bowyer VL. Real-time PCR. Forensic Sci Med Pathol. 2007 Mar;3(1):61-3. doi: 10.1385/FSMP:3:1:61. PMID: 25868892.
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Cryptic Streptococcus mutans 5.6-kb plasmids encode a toxin-antitoxin system for plasmid stabilization.

Journal of oral microbiology

Rheinberg A, Swierzy IJ, Nguyen TD, Horz HP, Conrads G.
PMID: 23330057
J Oral Microbiol. 2013;5. doi: 10.3402/jom.v5i0.19729. Epub 2013 Jan 15.

BACKGROUND: In all Streptococcus mutans strains, 5-13% carry a 5.6-kb plasmid. Despite its frequency, little is known about its mediated functions with most of the information coming from a single study focussing on plasmid pUA140.OBJECTIVE: Here, we describe the...

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Rheinberg A, Swierzy IJ, Nguyen TD, et al. Cryptic Streptococcus mutans 5.6-kb plasmids encode a toxin-antitoxin system for plasmid stabilization. J Oral Microbiol. 2013;5doi: 10.3402/jom.v5i0.19729.
Rheinberg, A., Swierzy, I. J., Nguyen, T. D., Horz, H. P., & Conrads, G. (2013). Cryptic Streptococcus mutans 5.6-kb plasmids encode a toxin-antitoxin system for plasmid stabilization. Journal of oral microbiology, 5. https://doi.org/10.3402/jom.v5i0.19729
Rheinberg, Anke, et al. "Cryptic Streptococcus mutans 5.6-kb plasmids encode a toxin-antitoxin system for plasmid stabilization." Journal of oral microbiology vol. 5 (2013). doi: https://doi.org/10.3402/jom.v5i0.19729
Rheinberg A, Swierzy IJ, Nguyen TD, Horz HP, Conrads G. Cryptic Streptococcus mutans 5.6-kb plasmids encode a toxin-antitoxin system for plasmid stabilization. J Oral Microbiol. 2013;5. doi: 10.3402/jom.v5i0.19729. Epub 2013 Jan 15. PMID: 23330057; PMCID: PMC3547324.
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Quantitative analysis of cell-free DNA in the plasma of gastric cancer patients.

Oncology letters

Park JL, Kim HJ, Choi BY, Lee HC, Jang HR, Song KS, Noh SM, Kim SY, Han DS, Kim YS.
PMID: 22741019
Oncol Lett. 2012 Apr 01;3(4):921-926. doi: 10.3892/ol.2012.592. Epub 2012 Feb 03.

In the present study, an accurate and reproducible method for quantifying cell-free DNA (cfDNA) in human blood was established and tested for its ability to predict gastric cancer in patients. Using 'Alu81-qPCR' to amplify 81-bp Alu DNA sequences, we...

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Park JL, Kim HJ, Choi BY, et al. Quantitative analysis of cell-free DNA in the plasma of gastric cancer patients. Oncol Lett. 2012;3(4):921-926doi: 10.3892/ol.2012.592.
Park, J. L., Kim, H. J., Choi, B. Y., Lee, H. C., Jang, H. R., Song, K. S., Noh, S. M., Kim, S. Y., Han, D. S., & Kim, Y. S. (2012). Quantitative analysis of cell-free DNA in the plasma of gastric cancer patients. Oncology letters, 3(4), 921-926. https://doi.org/10.3892/ol.2012.592
Park, Jong-Lyul, et al. "Quantitative analysis of cell-free DNA in the plasma of gastric cancer patients." Oncology letters vol. 3,4 (2012): 921-926. doi: https://doi.org/10.3892/ol.2012.592
Park JL, Kim HJ, Choi BY, Lee HC, Jang HR, Song KS, Noh SM, Kim SY, Han DS, Kim YS. Quantitative analysis of cell-free DNA in the plasma of gastric cancer patients. Oncol Lett. 2012 Apr 01;3(4):921-926. doi: 10.3892/ol.2012.592. Epub 2012 Feb 03. PMID: 22741019; PMCID: PMC3362424.
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Evidence for simvastatin anti-inflammatory actions based on quantitative analyses of NETosis and other inflammation/oxidation markers.

Results in immunology

Al-Ghoul WM, Kim MS, Fazal N, Azim AC, Ali A.
PMID: 24809006
Results Immunol. 2014 Mar 25;4:14-22. doi: 10.1016/j.rinim.2014.03.001. eCollection 2014.

Simvastatin (SMV) has been shown to exhibit promising anti-inflammatory properties alongside its classic cholesterol lowering action. We tested these emerging effects in a major thermal injury mouse model (3rd degree scald, ~20% TBSA) with previously documented, inflammation-mediated intestinal defects....

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Al-Ghoul WM, Kim MS, Fazal N, et al. Evidence for simvastatin anti-inflammatory actions based on quantitative analyses of NETosis and other inflammation/oxidation markers. Results Immunol. 2014;4:14-22doi: 10.1016/j.rinim.2014.03.001.
Al-Ghoul, W. M., Kim, M. S., Fazal, N., Azim, A. C., & Ali, A. (2014). Evidence for simvastatin anti-inflammatory actions based on quantitative analyses of NETosis and other inflammation/oxidation markers. Results in immunology, 414-22. https://doi.org/10.1016/j.rinim.2014.03.001
Al-Ghoul, Walid M, et al. "Evidence for simvastatin anti-inflammatory actions based on quantitative analyses of NETosis and other inflammation/oxidation markers." Results in immunology vol. 4 (2014): 14-22. doi: https://doi.org/10.1016/j.rinim.2014.03.001
Al-Ghoul WM, Kim MS, Fazal N, Azim AC, Ali A. Evidence for simvastatin anti-inflammatory actions based on quantitative analyses of NETosis and other inflammation/oxidation markers. Results Immunol. 2014 Mar 25;4:14-22. doi: 10.1016/j.rinim.2014.03.001. eCollection 2014. PMID: 24809006; PMCID: PMC4009405.
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Multiple-Monitor HPLC Assays for Rapid Process Development, In-Process Monitoring, and Validation of AAV Production and Purification.

Pharmaceutics

Gagnon P, Goricar B, Mencin N, Zvanut T, Peljhan S, Leskovec M, Strancar A.
PMID: 33477351
Pharmaceutics. 2021 Jan 17;13(1). doi: 10.3390/pharmaceutics13010113.

HPLC is established as a fast convenient analytical technology for characterizing the content of empty and full capsids in purified samples containing adeno-associated virus (AAV). UV-based monitoring unfortunately over-estimates the proportion of full capsids and offers little value for...

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Gagnon P, Goricar B, Mencin N, et al. Multiple-Monitor HPLC Assays for Rapid Process Development, In-Process Monitoring, and Validation of AAV Production and Purification. Pharmaceutics. 2021;13(1)doi: 10.3390/pharmaceutics13010113.
Gagnon, P., Goricar, B., Mencin, N., Zvanut, T., Peljhan, S., Leskovec, M., & Strancar, A. (2021). Multiple-Monitor HPLC Assays for Rapid Process Development, In-Process Monitoring, and Validation of AAV Production and Purification. Pharmaceutics, 13(1), . https://doi.org/10.3390/pharmaceutics13010113
Gagnon, Pete, et al. "Multiple-Monitor HPLC Assays for Rapid Process Development, In-Process Monitoring, and Validation of AAV Production and Purification." Pharmaceutics vol. 13,1 (2021). doi: https://doi.org/10.3390/pharmaceutics13010113
Gagnon P, Goricar B, Mencin N, Zvanut T, Peljhan S, Leskovec M, Strancar A. Multiple-Monitor HPLC Assays for Rapid Process Development, In-Process Monitoring, and Validation of AAV Production and Purification. Pharmaceutics. 2021 Jan 17;13(1). doi: 10.3390/pharmaceutics13010113. PMID: 33477351; PMCID: PMC7830902.
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Evaluation of silk sericin as a biomaterial: in vitro growth of human corneal limbal epithelial cells on Bombyx mori sericin membranes.

Progress in biomaterials

Chirila TV, Suzuki S, Bray LJ, Barnett NL, Harkin DG.
PMID: 29470674
Prog Biomater. 2013 Nov 28;2(1):14. doi: 10.1186/2194-0517-2-14.

Sericin and fibroin are the two major proteins in the silk fibre produced by the domesticated silkworm, Bombyx mori. Fibroin has been extensively investigated as a biomaterial. We have previously shown that fibroin can function successfully as a substratum...

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Chirila TV, Suzuki S, Bray LJ, et al. Evaluation of silk sericin as a biomaterial: in vitro growth of human corneal limbal epithelial cells on Bombyx mori sericin membranes. Prog Biomater. 2013;2(1):14doi: 10.1186/2194-0517-2-14.
Chirila, T. V., Suzuki, S., Bray, L. J., Barnett, N. L., & Harkin, D. G. (2013). Evaluation of silk sericin as a biomaterial: in vitro growth of human corneal limbal epithelial cells on Bombyx mori sericin membranes. Progress in biomaterials, 2(1), 14. https://doi.org/10.1186/2194-0517-2-14
Chirila, Traian V, et al. "Evaluation of silk sericin as a biomaterial: in vitro growth of human corneal limbal epithelial cells on Bombyx mori sericin membranes." Progress in biomaterials vol. 2,1 (2013): 14. doi: https://doi.org/10.1186/2194-0517-2-14
Chirila TV, Suzuki S, Bray LJ, Barnett NL, Harkin DG. Evaluation of silk sericin as a biomaterial: in vitro growth of human corneal limbal epithelial cells on Bombyx mori sericin membranes. Prog Biomater. 2013 Nov 28;2(1):14. doi: 10.1186/2194-0517-2-14. PMID: 29470674; PMCID: PMC5151120.
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Pleiotropic Roles of NOTCH1 Signaling in the Loss of Maturational Arrest of Human Osteoarthritic Chondrocytes.

International journal of molecular sciences

Minguzzi M, Panichi V, D'Adamo S, Cetrullo S, Cattini L, Flamigni F, Mariani E, Borzì RM.
PMID: 34769441
Int J Mol Sci. 2021 Nov 05;22(21). doi: 10.3390/ijms222112012.

Notch signaling has been identified as a critical regulator of cartilage development and homeostasis. Its pivotal role was established by both several joint specific Notch signaling loss of function mouse models and transient or sustained overexpression. NOTCH1 is the...

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Minguzzi M, Panichi V, D'Adamo S, et al. Pleiotropic Roles of NOTCH1 Signaling in the Loss of Maturational Arrest of Human Osteoarthritic Chondrocytes. Int J Mol Sci. 2021;22(21)doi: 10.3390/ijms222112012.
Minguzzi, M., Panichi, V., D'Adamo, S., Cetrullo, S., Cattini, L., Flamigni, F., Mariani, E., & Borzì, R. M. (2021). Pleiotropic Roles of NOTCH1 Signaling in the Loss of Maturational Arrest of Human Osteoarthritic Chondrocytes. International journal of molecular sciences, 22(21), . https://doi.org/10.3390/ijms222112012
Minguzzi, Manuela, et al. "Pleiotropic Roles of NOTCH1 Signaling in the Loss of Maturational Arrest of Human Osteoarthritic Chondrocytes." International journal of molecular sciences vol. 22,21 (2021). doi: https://doi.org/10.3390/ijms222112012
Minguzzi M, Panichi V, D'Adamo S, Cetrullo S, Cattini L, Flamigni F, Mariani E, Borzì RM. Pleiotropic Roles of NOTCH1 Signaling in the Loss of Maturational Arrest of Human Osteoarthritic Chondrocytes. Int J Mol Sci. 2021 Nov 05;22(21). doi: 10.3390/ijms222112012. PMID: 34769441; PMCID: PMC8585104.
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Showing 1 to 12 of 30 entries