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Revisiting mouse minute virus inactivation by high temperature short time treatment.

Biotechnology and bioengineering

Su J, Rice J, Hoffman J, Alvarado S, Bailey M, Kopp M, Murphy M, Kiss R, Barone PW, Wiebe ME, Springs SL, Dehghani H, Chen D.
PMID: 33913515
Biotechnol Bioeng. 2021 Aug;118(8):2967-2976. doi: 10.1002/bit.27805. Epub 2021 Jun 08.

In recent years, high temperature short time (HTST) treatment technology has been increasingly adopted for medium treatment to mitigate the potential risk of viral contamination in mammalian cell culture GMP manufacturing facilities. Mouse minute virus (MMV), also called minute...

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Su J, Rice J, Hoffman J, et al. Revisiting mouse minute virus inactivation by high temperature short time treatment. Biotechnol Bioeng. 2021;118(8):2967-2976doi: 10.1002/bit.27805.
Su, J., Rice, J., Hoffman, J., Alvarado, S., Bailey, M., Kopp, M., Murphy, M., Kiss, R., Barone, P. W., Wiebe, M. E., Springs, S. L., Dehghani, H., & Chen, D. (2021). Revisiting mouse minute virus inactivation by high temperature short time treatment. Biotechnology and bioengineering, 118(8), 2967-2976. https://doi.org/10.1002/bit.27805
Su, Joleen, et al. "Revisiting mouse minute virus inactivation by high temperature short time treatment." Biotechnology and bioengineering vol. 118,8 (2021): 2967-2976. doi: https://doi.org/10.1002/bit.27805
Su J, Rice J, Hoffman J, Alvarado S, Bailey M, Kopp M, Murphy M, Kiss R, Barone PW, Wiebe ME, Springs SL, Dehghani H, Chen D. Revisiting mouse minute virus inactivation by high temperature short time treatment. Biotechnol Bioeng. 2021 Aug;118(8):2967-2976. doi: 10.1002/bit.27805. Epub 2021 Jun 08. PMID: 33913515.
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Adropin decreases endothelial monolayer permeability after cell-free hemoglobin exposure and reduces MCP-1-induced macrophage transmigration.

Biochemical and biophysical research communications

Dodd WS, Patel D, Lucke-Wold B, Hosaka K, Chalouhi N, Hoh BL.
PMID: 34710824
Biochem Biophys Res Commun. 2021 Dec 10;582:105-110. doi: 10.1016/j.bbrc.2021.10.032. Epub 2021 Oct 16.

BACKGROUND: Cell-free heme-containing proteins mediate endothelial injury in a variety of disease states including subarachnoid hemorrhage and sepsis by increasing endothelial permeability. Inflammatory cells are also attracted to sites of vascular injury by monocyte chemotactic protein 1 (MCP-1) and...

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Dodd WS, Patel D, Lucke-Wold B, et al. Adropin decreases endothelial monolayer permeability after cell-free hemoglobin exposure and reduces MCP-1-induced macrophage transmigration. Biochem Biophys Res Commun. 2021;582:105-110doi: 10.1016/j.bbrc.2021.10.032.
Dodd, W. S., Patel, D., Lucke-Wold, B., Hosaka, K., Chalouhi, N., & Hoh, B. L. (2021). Adropin decreases endothelial monolayer permeability after cell-free hemoglobin exposure and reduces MCP-1-induced macrophage transmigration. Biochemical and biophysical research communications, 582105-110. https://doi.org/10.1016/j.bbrc.2021.10.032
Dodd, William S, et al. "Adropin decreases endothelial monolayer permeability after cell-free hemoglobin exposure and reduces MCP-1-induced macrophage transmigration." Biochemical and biophysical research communications vol. 582 (2021): 105-110. doi: https://doi.org/10.1016/j.bbrc.2021.10.032
Dodd WS, Patel D, Lucke-Wold B, Hosaka K, Chalouhi N, Hoh BL. Adropin decreases endothelial monolayer permeability after cell-free hemoglobin exposure and reduces MCP-1-induced macrophage transmigration. Biochem Biophys Res Commun. 2021 Dec 10;582:105-110. doi: 10.1016/j.bbrc.2021.10.032. Epub 2021 Oct 16. PMID: 34710824.
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Optimization of pre- treatments with Propidium Monoazide and PEMAX™ before real-time quantitative PCR for detection and quantification of viable Helicobacter pylori cells.

Journal of microbiological methods

Hortelano I, Moreno MY, García-Hernández J, Ferrús MA.
PMID: 33872638
J Microbiol Methods. 2021 Jun;185:106223. doi: 10.1016/j.mimet.2021.106223. Epub 2021 Apr 16.

Accurate detection of H. pylori in different environmental and clinical samples is essential for public health strtdudies. Now, a big effort is being made to design PCR methodologies that allow for the detection of viable and viable but non-culturable...

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Hortelano I, Moreno MY, García-Hernández J, et al. Optimization of pre- treatments with Propidium Monoazide and PEMAX™ before real-time quantitative PCR for detection and quantification of viable Helicobacter pylori cells. J Microbiol Methods. 2021;185:106223doi: 10.1016/j.mimet.2021.106223.
Hortelano, I., Moreno, M. Y., García-Hernández, J., & Ferrús, M. A. (2021). Optimization of pre- treatments with Propidium Monoazide and PEMAX™ before real-time quantitative PCR for detection and quantification of viable Helicobacter pylori cells. Journal of microbiological methods, 185106223. https://doi.org/10.1016/j.mimet.2021.106223
Hortelano, Irene, et al. "Optimization of pre- treatments with Propidium Monoazide and PEMAX™ before real-time quantitative PCR for detection and quantification of viable Helicobacter pylori cells." Journal of microbiological methods vol. 185 (2021): 106223. doi: https://doi.org/10.1016/j.mimet.2021.106223
Hortelano I, Moreno MY, García-Hernández J, Ferrús MA. Optimization of pre- treatments with Propidium Monoazide and PEMAX™ before real-time quantitative PCR for detection and quantification of viable Helicobacter pylori cells. J Microbiol Methods. 2021 Jun;185:106223. doi: 10.1016/j.mimet.2021.106223. Epub 2021 Apr 16. PMID: 33872638.
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A New Role for Extracellular Vesicles in Cardiac Tissue Engineering and Regenerative Medicine.

Advanced nanobiomed research

Wagner KT, Radisic M.
PMID: 34927167
Adv Nanobiomed Res. 2021 Nov;1(11). doi: 10.1002/anbr.202100047. Epub 2021 Jun 24.

Cardiovascular diseases are the leading cause of death worldwide. Discovering new therapies to treat heart disease requires improved understanding of cardiac physiology at a cellular level. Extracellular vesicles (EVs) are plasma membrane-bound nano- and microparticles secreted by cells and...

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Wagner KT, Radisic M. A New Role for Extracellular Vesicles in Cardiac Tissue Engineering and Regenerative Medicine. Adv Nanobiomed Res. 2021;1(11)doi: 10.1002/anbr.202100047.
Wagner, K. T., & Radisic, M. (2021). A New Role for Extracellular Vesicles in Cardiac Tissue Engineering and Regenerative Medicine. Advanced nanobiomed research, 1(11), . https://doi.org/10.1002/anbr.202100047
Wagner, Karl T, and Radisic, Milica. "A New Role for Extracellular Vesicles in Cardiac Tissue Engineering and Regenerative Medicine." Advanced nanobiomed research vol. 1,11 (2021). doi: https://doi.org/10.1002/anbr.202100047
Wagner KT, Radisic M. A New Role for Extracellular Vesicles in Cardiac Tissue Engineering and Regenerative Medicine. Adv Nanobiomed Res. 2021 Nov;1(11). doi: 10.1002/anbr.202100047. Epub 2021 Jun 24. PMID: 34927167; PMCID: PMC8680295.
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High density bioprocessing of human pluripotent stem cells by metabolic control and in silico modeling.

Stem cells translational medicine

Manstein F, Ullmann K, Kropp C, Halloin C, Triebert W, Franke A, Farr CM, Sahabian A, Haase A, Breitkreuz Y, Peitz M, Brüstle O, Kalies S, Martin U, Olmer R, Zweigerdt R.
PMID: 33660952
Stem Cells Transl Med. 2021 Jul;10(7):1063-1080. doi: 10.1002/sctm.20-0453. Epub 2021 Mar 04.

To harness the full potential of human pluripotent stem cells (hPSCs) we combined instrumented stirred tank bioreactor (STBR) technology with the power of in silico process modeling to overcome substantial, hPSC-specific hurdles toward their mass production. Perfused suspension culture...

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Manstein F, Ullmann K, Kropp C, et al. High density bioprocessing of human pluripotent stem cells by metabolic control and in silico modeling. Stem Cells Transl Med. 2021;10(7):1063-1080doi: 10.1002/sctm.20-0453.
Manstein, F., Ullmann, K., Kropp, C., Halloin, C., Triebert, W., Franke, A., Farr, C. M., Sahabian, A., Haase, A., Breitkreuz, Y., Peitz, M., Brüstle, O., Kalies, S., Martin, U., Olmer, R., & Zweigerdt, R. (2021). High density bioprocessing of human pluripotent stem cells by metabolic control and in silico modeling. Stem cells translational medicine, 10(7), 1063-1080. https://doi.org/10.1002/sctm.20-0453
Manstein, Felix, et al. "High density bioprocessing of human pluripotent stem cells by metabolic control and in silico modeling." Stem cells translational medicine vol. 10,7 (2021): 1063-1080. doi: https://doi.org/10.1002/sctm.20-0453
Manstein F, Ullmann K, Kropp C, Halloin C, Triebert W, Franke A, Farr CM, Sahabian A, Haase A, Breitkreuz Y, Peitz M, Brüstle O, Kalies S, Martin U, Olmer R, Zweigerdt R. High density bioprocessing of human pluripotent stem cells by metabolic control and in silico modeling. Stem Cells Transl Med. 2021 Jul;10(7):1063-1080. doi: 10.1002/sctm.20-0453. Epub 2021 Mar 04. PMID: 33660952; PMCID: PMC8235132.
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Retinoprotective Effects Of Crocin And Crocetin via Anti-Angiogenic Mechanism in High Glucose-Induced Human Retinal Pigment Epithelium Cells.

Current molecular pharmacology

Sepahi S, Soheili ZS, Tavakkol-Afshari J, Mehri S, Hosseini SM, Mohajeri SA, Khodaverdi E.
PMID: 33881975
Curr Mol Pharmacol. 2021;14(5):883-893. doi: 10.2174/1874467214666210420111232.

BACKGROUND: Diabetic retinopathy (DR) is one of the most common side effects of diabetes. We aimed to investigate the effects of crocin and crocetin (as a deglycosylated form of crocin in blood stream) in gene expression or protein levels...

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Sepahi S, Soheili ZS, Tavakkol-Afshari J, et al. Retinoprotective Effects Of Crocin And Crocetin via Anti-Angiogenic Mechanism in High Glucose-Induced Human Retinal Pigment Epithelium Cells. Curr Mol Pharmacol. 2021;14(5):883-893doi: 10.2174/1874467214666210420111232.
Sepahi, S., Soheili, Z. S., Tavakkol-Afshari, J., Mehri, S., Hosseini, S. M., Mohajeri, S. A., & Khodaverdi, E. (2021). Retinoprotective Effects Of Crocin And Crocetin via Anti-Angiogenic Mechanism in High Glucose-Induced Human Retinal Pigment Epithelium Cells. Current molecular pharmacology, 14(5), 883-893. https://doi.org/10.2174/1874467214666210420111232
Sepahi, Samaneh, et al. "Retinoprotective Effects Of Crocin And Crocetin via Anti-Angiogenic Mechanism in High Glucose-Induced Human Retinal Pigment Epithelium Cells." Current molecular pharmacology vol. 14,5 (2021): 883-893. doi: https://doi.org/10.2174/1874467214666210420111232
Sepahi S, Soheili ZS, Tavakkol-Afshari J, Mehri S, Hosseini SM, Mohajeri SA, Khodaverdi E. Retinoprotective Effects Of Crocin And Crocetin via Anti-Angiogenic Mechanism in High Glucose-Induced Human Retinal Pigment Epithelium Cells. Curr Mol Pharmacol. 2021;14(5):883-893. doi: 10.2174/1874467214666210420111232. PMID: 33881975.
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Measuring the density and viscosity of culture media for optimized computational fluid dynamics analysis of in vitro devices.

Journal of the mechanical behavior of biomedical materials

Poon C.
PMID: 34911025
J Mech Behav Biomed Mater. 2021 Dec 07;126:105024. doi: 10.1016/j.jmbbm.2021.105024. Epub 2021 Dec 07.

Culture medium is frequently modelled as water in computational fluid dynamics (CFD) analysis of in vitro culture systems involving flow, such as bioreactors and organ-on-chips. However, culture medium can be expected to have different properties to water due to...

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Poon C. Measuring the density and viscosity of culture media for optimized computational fluid dynamics analysis of in vitro devices. J Mech Behav Biomed Mater. 2021;126:105024doi: 10.1016/j.jmbbm.2021.105024.
Poon, C. (2021). Measuring the density and viscosity of culture media for optimized computational fluid dynamics analysis of in vitro devices. Journal of the mechanical behavior of biomedical materials, 126105024. https://doi.org/10.1016/j.jmbbm.2021.105024
Poon, Christine. "Measuring the density and viscosity of culture media for optimized computational fluid dynamics analysis of in vitro devices." Journal of the mechanical behavior of biomedical materials vol. 126 (2021): 105024. doi: https://doi.org/10.1016/j.jmbbm.2021.105024
Poon C. Measuring the density and viscosity of culture media for optimized computational fluid dynamics analysis of in vitro devices. J Mech Behav Biomed Mater. 2021 Dec 07;126:105024. doi: 10.1016/j.jmbbm.2021.105024. Epub 2021 Dec 07. PMID: 34911025.
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Docosahexaenoic Acid Modulates Paracellular Absorption of Testosterone and Claudin-1 Expression in a Tissue-Engineered Skin Model.

International journal of molecular sciences

Tremblay A, Simard M, Morin S, Pouliot R.
PMID: 34884896
Int J Mol Sci. 2021 Dec 03;22(23). doi: 10.3390/ijms222313091.

Healthy skin moLEdels produced by tissue-engineering often present a suboptimal skin barrier function as compared with normal human skin. Moreover, skin substitutes reconstructed according to the self-assembly method were found to be deficient in polyunsaturated fatty acids (PUFAs). Therefore,...

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Tremblay A, Simard M, Morin S, et al. Docosahexaenoic Acid Modulates Paracellular Absorption of Testosterone and Claudin-1 Expression in a Tissue-Engineered Skin Model. Int J Mol Sci. 2021;22(23)doi: 10.3390/ijms222313091.
Tremblay, A., Simard, M., Morin, S., & Pouliot, R. (2021). Docosahexaenoic Acid Modulates Paracellular Absorption of Testosterone and Claudin-1 Expression in a Tissue-Engineered Skin Model. International journal of molecular sciences, 22(23), . https://doi.org/10.3390/ijms222313091
Tremblay, Andréa, et al. "Docosahexaenoic Acid Modulates Paracellular Absorption of Testosterone and Claudin-1 Expression in a Tissue-Engineered Skin Model." International journal of molecular sciences vol. 22,23 (2021). doi: https://doi.org/10.3390/ijms222313091
Tremblay A, Simard M, Morin S, Pouliot R. Docosahexaenoic Acid Modulates Paracellular Absorption of Testosterone and Claudin-1 Expression in a Tissue-Engineered Skin Model. Int J Mol Sci. 2021 Dec 03;22(23). doi: 10.3390/ijms222313091. PMID: 34884896; PMCID: PMC8658185.
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Chemical susceptibility testing of non-tuberculous mycobacterium strains and other aquatic bacteria: Results of a study for the development of a more sensitive and simple method for the detection of NTM in environmental samples.

Journal of microbiological methods

Ditommaso S, Giacomuzzi M, Memoli G, Garlasco J, Curtoni A, Iannaccone M, Zotti CM.
PMID: 34990646
J Microbiol Methods. 2022 Jan 03;193:106405. doi: 10.1016/j.mimet.2021.106405. Epub 2022 Jan 03.

The methods employed to detect non-tuberculous mycobacteria on environmental samples are essentially those classically used in clinical microbiology, which envisage a decontamination step to reduce the overgrowth of non-mycobacterial organisms before plating them on the culture medium. The aim...

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Ditommaso S, Giacomuzzi M, Memoli G, et al. Chemical susceptibility testing of non-tuberculous mycobacterium strains and other aquatic bacteria: Results of a study for the development of a more sensitive and simple method for the detection of NTM in environmental samples. J Microbiol Methods. 2022;193:106405doi: 10.1016/j.mimet.2021.106405.
Ditommaso, S., Giacomuzzi, M., Memoli, G., Garlasco, J., Curtoni, A., Iannaccone, M., & Zotti, C. M. (2022). Chemical susceptibility testing of non-tuberculous mycobacterium strains and other aquatic bacteria: Results of a study for the development of a more sensitive and simple method for the detection of NTM in environmental samples. Journal of microbiological methods, 193106405. https://doi.org/10.1016/j.mimet.2021.106405
Ditommaso, Savina, et al. "Chemical susceptibility testing of non-tuberculous mycobacterium strains and other aquatic bacteria: Results of a study for the development of a more sensitive and simple method for the detection of NTM in environmental samples." Journal of microbiological methods vol. 193 (2022): 106405. doi: https://doi.org/10.1016/j.mimet.2021.106405
Ditommaso S, Giacomuzzi M, Memoli G, Garlasco J, Curtoni A, Iannaccone M, Zotti CM. Chemical susceptibility testing of non-tuberculous mycobacterium strains and other aquatic bacteria: Results of a study for the development of a more sensitive and simple method for the detection of NTM in environmental samples. J Microbiol Methods. 2022 Jan 03;193:106405. doi: 10.1016/j.mimet.2021.106405. Epub 2022 Jan 03. PMID: 34990646.
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Engineering novel designer glycopeptides as molecular carriers for boosting protein secretion in plant cell culture.

[No authors listed]
UIID-NSF: 430

1605564 Xu, Jianfeng With increasing needs for high-value protein-based therapeutics, plant cells offer a safe and cost-effective alternative bioproduction platform. However, low protein productivity is a common bottleneck in the commercialization of this technology. This project engineers plant cells...

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Engineering novel designer glycopeptides as molecular carriers for boosting protein secretion in plant cell culture. ;
(). Engineering novel designer glycopeptides as molecular carriers for boosting protein secretion in plant cell culture. .
"Engineering novel designer glycopeptides as molecular carriers for boosting protein secretion in plant cell culture." vol. ().
Engineering novel designer glycopeptides as molecular carriers for boosting protein secretion in plant cell culture. UIID-NSF: 430.
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Showing 2197 to 2206 of 2206 entries