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Showing 13 to 24 of 28 entries
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Preclinical translation of exosomes derived from mesenchymal stem/stromal cells.

Stem cells (Dayton, Ohio)

Elahi FM, Farwell DG, Nolta JA, Anderson JD.
PMID: 31381842
Stem Cells. 2020 Jan;38(1):15-21. doi: 10.1002/stem.3061. Epub 2019 Oct 01.

Exosomes are nanovesicles secreted by virtually all cells. Exosomes mediate the horizontal transfer of various macromolecules previously believed to be cell-autonomous in nature, including nonsecretory proteins, various classes of RNA, metabolites, and lipid membrane-associated factors. Exosomes derived from mesenchymal...

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Elahi FM, Farwell DG, Nolta JA, et al. Preclinical translation of exosomes derived from mesenchymal stem/stromal cells. Stem Cells. 2019;38(1):15-21doi: 10.1002/stem.3061.
Elahi, F. M., Farwell, D. G., Nolta, J. A., & Anderson, J. D. (2020). Preclinical translation of exosomes derived from mesenchymal stem/stromal cells. Stem cells (Dayton, Ohio), 38(1), 15-21. https://doi.org/10.1002/stem.3061
Elahi, Fanny M, et al. "Preclinical translation of exosomes derived from mesenchymal stem/stromal cells." Stem cells (Dayton, Ohio) vol. 38,1 (2020): 15-21. doi: https://doi.org/10.1002/stem.3061
Elahi FM, Farwell DG, Nolta JA, Anderson JD. Preclinical translation of exosomes derived from mesenchymal stem/stromal cells. Stem Cells. 2020 Jan;38(1):15-21. doi: 10.1002/stem.3061. Epub 2019 Oct 01. PMID: 31381842; PMCID: PMC7004029.
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[Drugs and the culturing of hepatocytes].

Bulletin de l'Academie nationale de medecine

Bourel M, Guillouzo A, Guguen-Guillouzo C.
PMID: 2790528
Bull Acad Natl Med. 1989 Apr;173(4):409-12; discussion 412-4.

Two model systems are described for studying isolated hepatocytes in vitro: pure culture for short-term designs and co-culture with epithelial rat liver cells (for long duration procedures). Acute or chronic liver toxicities are discussed as well as indirect toxicities....

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Bourel M, Guillouzo A, Guguen-Guillouzo C. Médicaments et culture d'hépatocytes. [Drugs and the culturing of hepatocytes]. Bull Acad Natl Med. 1989;173(4):409-12; discussion 412-4
Bourel, M., Guillouzo, A., & Guguen-Guillouzo, C. (1989). Médicaments et culture d'hépatocytes. [Drugs and the culturing of hepatocytes]. Bulletin de l'Academie nationale de medecine, 173(4), 409-12; discussion 412-4.
Bourel, M, et al. "Médicaments et culture d'hépatocytes." [Drugs and the culturing of hepatocytes]. Bulletin de l'Academie nationale de medecine vol. 173,4 (1989): 409-12; discussion 412-4.
Bourel M, Guillouzo A, Guguen-Guillouzo C. Médicaments et culture d'hépatocytes. [Drugs and the culturing of hepatocytes]. Bull Acad Natl Med. 1989 Apr;173(4):409-12; discussion 412-4. French. PMID: 2790528.
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[Abstracts of reports presented at the working meeting of the Committee for Cell Culture and the Section on Tissue Culture of the Czech and Slovak Oncology Societies of the J.E. Purkinje Medical Society. Stráznice, 26-29 May 1986].

Ceskoslovenska fysiologie

[No authors listed]
PMID: 3581206
Cesk Fysiol. 1987;36(2):159-79.

No abstract available.

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Souhrny referátů prednesených na pracovní schůzi komise pro kultivaci tkání pri Ceské a Sekce pracovníků s tkánovými kulturami pri Slovenské onkologické spolecnosti Lékarské spolecnosti J. E. Purkynĕ ve Stráznici 26.-29. 5. 1986. [Abstracts of reports presented at the working meeting of the Committee for Cell Culture and the Section on Tissue Culture of the Czech and Slovak Oncology Societies of the J.E. Purkinje Medical Society. Stráznice, 26-29 May 1986]. Cesk Fysiol. 1987;36(2):159-79
(1987). Souhrny referátů prednesených na pracovní schůzi komise pro kultivaci tkání pri Ceské a Sekce pracovníků s tkánovými kulturami pri Slovenské onkologické spolecnosti Lékarské spolecnosti J. E. Purkynĕ ve Stráznici 26.-29. 5. 1986. [Abstracts of reports presented at the working meeting of the Committee for Cell Culture and the Section on Tissue Culture of the Czech and Slovak Oncology Societies of the J.E. Purkinje Medical Society. Stráznice, 26-29 May 1986]. Ceskoslovenska fysiologie, 36(2), 159-79.
"Souhrny referátů prednesených na pracovní schůzi komise pro kultivaci tkání pri Ceské a Sekce pracovníků s tkánovými kulturami pri Slovenské onkologické spolecnosti Lékarské spolecnosti J. E. Purkynĕ ve Stráznici 26.-29. 5. 1986." [Abstracts of reports presented at the working meeting of the Committee for Cell Culture and the Section on Tissue Culture of the Czech and Slovak Oncology Societies of the J.E. Purkinje Medical Society. Stráznice, 26-29 May 1986]. Ceskoslovenska fysiologie vol. 36,2 (1987): 159-79.
Souhrny referátů prednesených na pracovní schůzi komise pro kultivaci tkání pri Ceské a Sekce pracovníků s tkánovými kulturami pri Slovenské onkologické spolecnosti Lékarské spolecnosti J. E. Purkynĕ ve Stráznici 26.-29. 5. 1986. [Abstracts of reports presented at the working meeting of the Committee for Cell Culture and the Section on Tissue Culture of the Czech and Slovak Oncology Societies of the J.E. Purkinje Medical Society. Stráznice, 26-29 May 1986]. Cesk Fysiol. 1987;36(2):159-79. Czech, Slovak. PMID: 3581206.
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[Liver cell culture and physiopathology of the liver].

Nihon rinsho. Japanese journal of clinical medicine

Nagamori S, Fujise K, Hasumura S, Kameda H.
PMID: 691698
Nihon Rinsho. 1978 May;2208-9.

No abstract available.

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Nagamori S, Fujise K, Hasumura S, et al. [Liver cell culture and physiopathology of the liver]. Nihon Rinsho. 1978;2208-9
Nagamori, S., Fujise, K., Hasumura, S., & Kameda, H. (1978). [Liver cell culture and physiopathology of the liver]. Nihon rinsho. Japanese journal of clinical medicine, 2208-9.
Nagamori, S, et al. "[Liver cell culture and physiopathology of the liver]." Nihon rinsho. Japanese journal of clinical medicine vol. (1978): 2208-9.
Nagamori S, Fujise K, Hasumura S, Kameda H. [Liver cell culture and physiopathology of the liver]. Nihon Rinsho. 1978 May;2208-9. Japanese. PMID: 691698.
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Time delay in simple chemostat models.

Biotechnology and bioengineering

MacDonald N.
PMID: 1268333
Biotechnol Bioeng. 1976 Jun;18(6):805-12. doi: 10.1002/bit.260180604.

The models of Monod and Williams, for the growth of unicellular organisms in chemostats, give strongly damped transients in the biomass and cell number when the flow rate of the chemostat is changed. A simple trick is used to...

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MacDonald N. Time delay in simple chemostat models. Biotechnol Bioeng. 1976;18(6):805-12doi: 10.1002/bit.260180604.
MacDonald, N. (1976). Time delay in simple chemostat models. Biotechnology and bioengineering, 18(6), 805-12. https://doi.org/10.1002/bit.260180604
MacDonald, N. "Time delay in simple chemostat models." Biotechnology and bioengineering vol. 18,6 (1976): 805-12. doi: https://doi.org/10.1002/bit.260180604
MacDonald N. Time delay in simple chemostat models. Biotechnol Bioeng. 1976 Jun;18(6):805-12. doi: 10.1002/bit.260180604. PMID: 1268333.
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Approaches to the problem of metabolic heterogeneity in the kidney.

The International journal of biochemistry

Guder WG, Ross BD.
PMID: 7399008
Int J Biochem. 1980;12(1):1-2. doi: 10.1016/0020-711x(80)90032-4.

No abstract available.

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Guder WG, Ross BD. Approaches to the problem of metabolic heterogeneity in the kidney. Int J Biochem. 1980;12(1):1-2doi: 10.1016/0020-711x(80)90032-4.
Guder, W. G., & Ross, B. D. (1980). Approaches to the problem of metabolic heterogeneity in the kidney. The International journal of biochemistry, 12(1), 1-2. https://doi.org/10.1016/0020-711x(80)90032-4
Guder, W G, and Ross, B D. "Approaches to the problem of metabolic heterogeneity in the kidney." The International journal of biochemistry vol. 12,1 (1980): 1-2. doi: https://doi.org/10.1016/0020-711x(80)90032-4
Guder WG, Ross BD. Approaches to the problem of metabolic heterogeneity in the kidney. Int J Biochem. 1980;12(1):1-2. doi: 10.1016/0020-711x(80)90032-4. PMID: 7399008.
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A potential platform for developing 3D tubular scaffolds for paediatric organ development.

Journal of materials science. Materials in medicine

de Mel A, Yap T, Cittadella G, Hale LR, Maghsoudlou P, de Coppi P, Birchall MA, Seifalian AM.
PMID: 25737129
J Mater Sci Mater Med. 2015 Mar;26(3):141. doi: 10.1007/s10856-015-5477-4. Epub 2015 Mar 04.

Children suffer from damaged or loss of hollow organs i.e. trachea, oesophagus or arteries from birth defects or diseases. Generally these organs possess an outer matrix consisting of collagen, elastin, and cells such as smooth muscle cells (SMC) and...

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de Mel A, Yap T, Cittadella G, et al. A potential platform for developing 3D tubular scaffolds for paediatric organ development. J Mater Sci Mater Med. 2015;26(3):141doi: 10.1007/s10856-015-5477-4.
de Mel, A., Yap, T., Cittadella, G., Hale, L. R., Maghsoudlou, P., de Coppi, P., Birchall, M. A., & Seifalian, A. M. (2015). A potential platform for developing 3D tubular scaffolds for paediatric organ development. Journal of materials science. Materials in medicine, 26(3), 141. https://doi.org/10.1007/s10856-015-5477-4
de Mel, Achala, et al. "A potential platform for developing 3D tubular scaffolds for paediatric organ development." Journal of materials science. Materials in medicine vol. 26,3 (2015): 141. doi: https://doi.org/10.1007/s10856-015-5477-4
de Mel A, Yap T, Cittadella G, Hale LR, Maghsoudlou P, de Coppi P, Birchall MA, Seifalian AM. A potential platform for developing 3D tubular scaffolds for paediatric organ development. J Mater Sci Mater Med. 2015 Mar;26(3):141. doi: 10.1007/s10856-015-5477-4. Epub 2015 Mar 04. PMID: 25737129.
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From Micro to Macro: The Hierarchical Design in a Micropatterned Scaffold for Cell Assembling and Transplantation.

Advanced materials (Deerfield Beach, Fla.)

Wang K, Wang X, Han C, Hou W, Wang J, Chen L, Luo Y.
PMID: 28066985
Adv Mater. 2017 Jan;29(2). doi: 10.1002/adma.201604600. Epub 2016 Nov 07.

A microwell-patterned membranous scaffold that integrates nano- and microscale topographical characteristics based on polyurethane is fabricated for transplanting syngeneic islets and allogeneic mesenchymal stem cells into diabetic rodents. The scaffold effectively allows for assembling of single cells/microtissues, enables the...

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Wang K, Wang X, Han C, et al. From Micro to Macro: The Hierarchical Design in a Micropatterned Scaffold for Cell Assembling and Transplantation. Adv Mater. 2016;29(2)doi: 10.1002/adma.201604600.
Wang, K., Wang, X., Han, C., Hou, W., Wang, J., Chen, L., & Luo, Y. (2017). From Micro to Macro: The Hierarchical Design in a Micropatterned Scaffold for Cell Assembling and Transplantation. Advanced materials (Deerfield Beach, Fla.), 29(2), . https://doi.org/10.1002/adma.201604600
Wang, Kai, et al. "From Micro to Macro: The Hierarchical Design in a Micropatterned Scaffold for Cell Assembling and Transplantation." Advanced materials (Deerfield Beach, Fla.) vol. 29,2 (2017). doi: https://doi.org/10.1002/adma.201604600
Wang K, Wang X, Han C, Hou W, Wang J, Chen L, Luo Y. From Micro to Macro: The Hierarchical Design in a Micropatterned Scaffold for Cell Assembling and Transplantation. Adv Mater. 2017 Jan;29(2). doi: 10.1002/adma.201604600. Epub 2016 Nov 07. PMID: 28066985.
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Metabolic profiling using HPLC allows classification of drugs according to their mechanisms of action in HL-1 cardiomyocytes.

Toxicology and applied pharmacology

Strigun A, Wahrheit J, Beckers S, Heinzle E, Noor F.
PMID: 21320520
Toxicol Appl Pharmacol. 2011 Apr 15;252(2):183-91. doi: 10.1016/j.taap.2011.02.008. Epub 2011 Feb 12.

Along with hepatotoxicity, cardiotoxic side effects remain one of the major reasons for drug withdrawals and boxed warnings. Prediction methods for cardiotoxicity are insufficient. High content screening comprising of not only electrophysiological characterization but also cellular molecular alterations are...

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Strigun A, Wahrheit J, Beckers S, et al. Metabolic profiling using HPLC allows classification of drugs according to their mechanisms of action in HL-1 cardiomyocytes. Toxicol Appl Pharmacol. 2011;252(2):183-91doi: 10.1016/j.taap.2011.02.008.
Strigun, A., Wahrheit, J., Beckers, S., Heinzle, E., & Noor, F. (2011). Metabolic profiling using HPLC allows classification of drugs according to their mechanisms of action in HL-1 cardiomyocytes. Toxicology and applied pharmacology, 252(2), 183-91. https://doi.org/10.1016/j.taap.2011.02.008
Strigun, Alexander, et al. "Metabolic profiling using HPLC allows classification of drugs according to their mechanisms of action in HL-1 cardiomyocytes." Toxicology and applied pharmacology vol. 252,2 (2011): 183-91. doi: https://doi.org/10.1016/j.taap.2011.02.008
Strigun A, Wahrheit J, Beckers S, Heinzle E, Noor F. Metabolic profiling using HPLC allows classification of drugs according to their mechanisms of action in HL-1 cardiomyocytes. Toxicol Appl Pharmacol. 2011 Apr 15;252(2):183-91. doi: 10.1016/j.taap.2011.02.008. Epub 2011 Feb 12. PMID: 21320520.
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Gradient generation platforms: new directions for an established microfluidic technology.

Lab on a chip

Berthier E, Beebe DJ.
PMID: 25008971
Lab Chip. 2014 Sep 07;14(17):3241-7. doi: 10.1039/c4lc00448e.

Microscale platforms are enabling for cell-based studies as they allow the recapitulation of physiological conditions such as extracellular matrix (ECM) configurations and soluble factors interactions. Gradient generation platforms have been one of the few applications of microfluidics that have...

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Berthier E, Beebe DJ. Gradient generation platforms: new directions for an established microfluidic technology. Lab Chip. 2014;14(17):3241-7doi: 10.1039/c4lc00448e.
Berthier, E., & Beebe, D. J. (2014). Gradient generation platforms: new directions for an established microfluidic technology. Lab on a chip, 14(17), 3241-7. https://doi.org/10.1039/c4lc00448e
Berthier, E, and Beebe, D J. "Gradient generation platforms: new directions for an established microfluidic technology." Lab on a chip vol. 14,17 (2014): 3241-7. doi: https://doi.org/10.1039/c4lc00448e
Berthier E, Beebe DJ. Gradient generation platforms: new directions for an established microfluidic technology. Lab Chip. 2014 Sep 07;14(17):3241-7. doi: 10.1039/c4lc00448e. PMID: 25008971; PMCID: PMC4134926.
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Analysis of protein changes using two-dimensional difference gel electrophoresis.

Methods in molecular biology (Clifton, N.J.)

Gao W.
PMID: 24623216
Methods Mol Biol. 2014;1105:17-30. doi: 10.1007/978-1-62703-739-6_2.

A protocol for protein analysis using two-dimensional difference gel electrophoresis (2D-DIGE) is described. 2D-DIGE is one of the most popular and versatile methods of protein separation among rapidly increasing proteomics technologies. Similar to traditional two-dimensional polyacrylamide gel electrophoresis (2D-PAGE),...

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Gao W. Analysis of protein changes using two-dimensional difference gel electrophoresis. Methods Mol Biol. 2014;1105:17-30doi: 10.1007/978-1-62703-739-6_2.
Gao, W. (2014). Analysis of protein changes using two-dimensional difference gel electrophoresis. Methods in molecular biology (Clifton, N.J.), 110517-30. https://doi.org/10.1007/978-1-62703-739-6_2
Gao, Weimin. "Analysis of protein changes using two-dimensional difference gel electrophoresis." Methods in molecular biology (Clifton, N.J.) vol. 1105 (2014): 17-30. doi: https://doi.org/10.1007/978-1-62703-739-6_2
Gao W. Analysis of protein changes using two-dimensional difference gel electrophoresis. Methods Mol Biol. 2014;1105:17-30. doi: 10.1007/978-1-62703-739-6_2. PMID: 24623216.
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Human Genetic Mutant Cell Repository.

Cytogenetics and cell genetics

[No authors listed]
PMID: 4780771
Cytogenet Cell Genet. 1973;12(5):367-73. doi: 10.1159/000130475.
Free Article

No abstract available.

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Human Genetic Mutant Cell Repository. Cytogenet Cell Genet. 1973;12(5):367-73doi: 10.1159/000130475.
(1973). Human Genetic Mutant Cell Repository. Cytogenetics and cell genetics, 12(5), 367-73. https://doi.org/10.1159/000130475
"Human Genetic Mutant Cell Repository." Cytogenetics and cell genetics vol. 12,5 (1973): 367-73. doi: https://doi.org/10.1159/000130475
Human Genetic Mutant Cell Repository. Cytogenet Cell Genet. 1973;12(5):367-73. doi: 10.1159/000130475. PMID: 4780771.
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Showing 13 to 24 of 28 entries