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Showing 1 to 12 of 790 entries
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Thermo-responsive cell culture carrier: Effects on macrophage functionality and detachment efficiency.

Journal of tissue engineering

Rennert K, Nitschke M, Wallert M, Keune N, Raasch M, Lorkowski S, Mosig AS.
PMID: 28890781
J Tissue Eng. 2017 Aug 25;8:2041731417726428. doi: 10.1177/2041731417726428. eCollection 2017.

Harvesting cultivated macrophages for tissue engineering purposes by enzymatic digestion of cell adhesion molecules can potentially result in unintended activation, altered function, or behavior of these cells. Thermo-responsive polymer is a promising tool that allows for gentle macrophage detachment...

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Rennert K, Nitschke M, Wallert M, et al. Thermo-responsive cell culture carrier: Effects on macrophage functionality and detachment efficiency. J Tissue Eng. 2017;8:2041731417726428doi: 10.1177/2041731417726428.
Rennert, K., Nitschke, M., Wallert, M., Keune, N., Raasch, M., Lorkowski, S., & Mosig, A. S. (2017). Thermo-responsive cell culture carrier: Effects on macrophage functionality and detachment efficiency. Journal of tissue engineering, 82041731417726428. https://doi.org/10.1177/2041731417726428
Rennert, Knut, et al. "Thermo-responsive cell culture carrier: Effects on macrophage functionality and detachment efficiency." Journal of tissue engineering vol. 8 (2017): 2041731417726428. doi: https://doi.org/10.1177/2041731417726428
Rennert K, Nitschke M, Wallert M, Keune N, Raasch M, Lorkowski S, Mosig AS. Thermo-responsive cell culture carrier: Effects on macrophage functionality and detachment efficiency. J Tissue Eng. 2017 Aug 25;8:2041731417726428. doi: 10.1177/2041731417726428. eCollection 2017. PMID: 28890781; PMCID: PMC5574476.
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Cell collectivity regulation within migrating cell cluster during Kupffer's vesicle formation in zebrafish.

Frontiers in cell and developmental biology

Matsui T, Ishikawa H, Bessho Y.
PMID: 26000276
Front Cell Dev Biol. 2015 May 07;3:27. doi: 10.3389/fcell.2015.00027. eCollection 2015.

Although cell adhesion is thought to fasten cells tightly, cells that adhere to each other can migrate directionally. This group behavior, called "collective cell migration," is observed during normal development, wound healing, and cancer invasion. Loss-of-function of cell adhesion...

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Matsui T, Ishikawa H, Bessho Y. Cell collectivity regulation within migrating cell cluster during Kupffer's vesicle formation in zebrafish. Front Cell Dev Biol. 2015;3:27doi: 10.3389/fcell.2015.00027.
Matsui, T., Ishikawa, H., & Bessho, Y. (2015). Cell collectivity regulation within migrating cell cluster during Kupffer's vesicle formation in zebrafish. Frontiers in cell and developmental biology, 327. https://doi.org/10.3389/fcell.2015.00027
Matsui, Takaaki, et al. "Cell collectivity regulation within migrating cell cluster during Kupffer's vesicle formation in zebrafish." Frontiers in cell and developmental biology vol. 3 (2015): 27. doi: https://doi.org/10.3389/fcell.2015.00027
Matsui T, Ishikawa H, Bessho Y. Cell collectivity regulation within migrating cell cluster during Kupffer's vesicle formation in zebrafish. Front Cell Dev Biol. 2015 May 07;3:27. doi: 10.3389/fcell.2015.00027. eCollection 2015. PMID: 26000276; PMCID: PMC4423447.
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Notch-Mediated Cell Adhesion.

Biology

Murata A, Hayashi S.
PMID: 26784245
Biology (Basel). 2016 Jan 16;5(1). doi: 10.3390/biology5010005.

Notch family members are generally recognized as signaling molecules that control various cellular responses in metazoan organisms. Early fly studies and our mammalian studies demonstrated that Notch family members are also cell adhesion molecules; however, information on the physiological...

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Murata A, Hayashi S. Notch-Mediated Cell Adhesion. Biology (Basel). 2016;5(1)doi: 10.3390/biology5010005.
Murata, A., & Hayashi, S. (2016). Notch-Mediated Cell Adhesion. Biology, 5(1), . https://doi.org/10.3390/biology5010005
Murata, Akihiko, and Hayashi, Shin-Ichi. "Notch-Mediated Cell Adhesion." Biology vol. 5,1 (2016). doi: https://doi.org/10.3390/biology5010005
Murata A, Hayashi S. Notch-Mediated Cell Adhesion. Biology (Basel). 2016 Jan 16;5(1). doi: 10.3390/biology5010005. PMID: 26784245; PMCID: PMC4810162.
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Axonal Membranes and Their Domains: Assembly and Function of the Axon Initial Segment and Node of Ranvier.

Frontiers in cellular neuroscience

Nelson AD, Jenkins PM.
PMID: 28536506
Front Cell Neurosci. 2017 May 09;11:136. doi: 10.3389/fncel.2017.00136. eCollection 2017.

Neurons are highly specialized cells of the nervous system that receive, process and transmit electrical signals critical for normal brain function. Here, we review the intricate organization of axonal membrane domains that facilitate rapid action potential conduction underlying communication...

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Nelson AD, Jenkins PM. Axonal Membranes and Their Domains: Assembly and Function of the Axon Initial Segment and Node of Ranvier. Front Cell Neurosci. 2017;11:136doi: 10.3389/fncel.2017.00136.
Nelson, A. D., & Jenkins, P. M. (2017). Axonal Membranes and Their Domains: Assembly and Function of the Axon Initial Segment and Node of Ranvier. Frontiers in cellular neuroscience, 11136. https://doi.org/10.3389/fncel.2017.00136
Nelson, Andrew D, and Jenkins, Paul M. "Axonal Membranes and Their Domains: Assembly and Function of the Axon Initial Segment and Node of Ranvier." Frontiers in cellular neuroscience vol. 11 (2017): 136. doi: https://doi.org/10.3389/fncel.2017.00136
Nelson AD, Jenkins PM. Axonal Membranes and Their Domains: Assembly and Function of the Axon Initial Segment and Node of Ranvier. Front Cell Neurosci. 2017 May 09;11:136. doi: 10.3389/fncel.2017.00136. eCollection 2017. PMID: 28536506; PMCID: PMC5422562.
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Vitamin C blocks TNF-α-induced NF-kB activation and ICAM-1 expression in human neuroblastoma cells.

Archives of pharmacal research

Son EW, Mo SJ, Rhee DK, Pyo S.
PMID: 27518391
Arch Pharm Res. 2004 Oct;27(10):1073. doi: 10.1007/BF02975434.

Interactions of the cell adhesion molecules are known to play important roles in mediating inflammation. The proinflammatory cytokine, tumor necrosis factor-α (TNF-α), activates the NF-kB signaling pathway, which induces the expression of various genes, such as intercellular adhesion molecule-1...

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Son EW, Mo SJ, Rhee DK, et al. Vitamin C blocks TNF-α-induced NF-kB activation and ICAM-1 expression in human neuroblastoma cells. Arch Pharm Res. 2004;27(10):1073doi: 10.1007/BF02975434.
Son, E. W., Mo, S. J., Rhee, D. K., & Pyo, S. (2004). Vitamin C blocks TNF-α-induced NF-kB activation and ICAM-1 expression in human neuroblastoma cells. Archives of pharmacal research, 27(10), 1073. https://doi.org/10.1007/BF02975434
Son, Eun-Wha, et al. "Vitamin C blocks TNF-α-induced NF-kB activation and ICAM-1 expression in human neuroblastoma cells." Archives of pharmacal research vol. 27,10 (2004): 1073. doi: https://doi.org/10.1007/BF02975434
Son EW, Mo SJ, Rhee DK, Pyo S. Vitamin C blocks TNF-α-induced NF-kB activation and ICAM-1 expression in human neuroblastoma cells. Arch Pharm Res. 2004 Oct;27(10):1073. doi: 10.1007/BF02975434. PMID: 27518391.
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Alterations in cell adhesion proteins and cardiomyopathy.

World journal of cardiology

Li J.
PMID: 24944760
World J Cardiol. 2014 May 26;6(5):304-13. doi: 10.4330/wjc.v6.i5.304.

Cell adhesive junction is specialized intercellular structure composed of cell adhesion proteins. They are essential to connect adjacent heart muscle cell and make heart contraction effectively and properly. Clinical and genetic studies have revealed close relationship between cell adhesive...

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Li J. Alterations in cell adhesion proteins and cardiomyopathy. World J Cardiol. 2014;6(5):304-13doi: 10.4330/wjc.v6.i5.304.
Li, J. (2014). Alterations in cell adhesion proteins and cardiomyopathy. World journal of cardiology, 6(5), 304-13. https://doi.org/10.4330/wjc.v6.i5.304
Li, Jifen. "Alterations in cell adhesion proteins and cardiomyopathy." World journal of cardiology vol. 6,5 (2014): 304-13. doi: https://doi.org/10.4330/wjc.v6.i5.304
Li J. Alterations in cell adhesion proteins and cardiomyopathy. World J Cardiol. 2014 May 26;6(5):304-13. doi: 10.4330/wjc.v6.i5.304. PMID: 24944760; PMCID: PMC4062122.
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Diet-induced changes in brain structure and behavior in old gerbils.

Nutrition & diabetes

Goncharova K, Skibo G, Kovalenko T, Osadchenko I, Ushakova G, Vovchanskii M, Pierzynowski SG.
PMID: 26075640
Nutr Diabetes. 2015 Jun 15;5:e163. doi: 10.1038/nutd.2015.13.

BACKGROUND/OBJECTIVES: Aging is associated with many physiological alterations such as changes in metabolism, food intake and brain dysfunction. Possible ways to correct age-related brain dysfunction using dietary treatments still remains undeveloped. The aim of our research was to investigate...

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Goncharova K, Skibo G, Kovalenko T, et al. Diet-induced changes in brain structure and behavior in old gerbils. Nutr Diabetes. 2015;5:e163doi: 10.1038/nutd.2015.13.
Goncharova, K., Skibo, G., Kovalenko, T., Osadchenko, I., Ushakova, G., Vovchanskii, M., & Pierzynowski, S. G. (2015). Diet-induced changes in brain structure and behavior in old gerbils. Nutrition & diabetes, 5e163. https://doi.org/10.1038/nutd.2015.13
Goncharova, K, et al. "Diet-induced changes in brain structure and behavior in old gerbils." Nutrition & diabetes vol. 5 (2015): e163. doi: https://doi.org/10.1038/nutd.2015.13
Goncharova K, Skibo G, Kovalenko T, Osadchenko I, Ushakova G, Vovchanskii M, Pierzynowski SG. Diet-induced changes in brain structure and behavior in old gerbils. Nutr Diabetes. 2015 Jun 15;5:e163. doi: 10.1038/nutd.2015.13. PMID: 26075640; PMCID: PMC4491854.
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Expression analysis of CD44 isoforms S and V3, in patients with esophageal squamous cell carcinoma.

Iranian journal of basic medical sciences

Mansouri A, Foroughmand AM, Abbaszadegan MR, Memar B, Mahmoudian RA, Gholamin M.
PMID: 26019801
Iran J Basic Med Sci. 2015 Apr;18(4):380-4.

OBJECTIVES: CD44 is a member of the cell adhesion molecules family. Naturally, CD44S, along with CD44V3 influence the cell motility, migration, and adhesion, while in tumor cells they lead to tumor invasion, progression, and metastasis. The purpose of this...

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Mansouri A, Foroughmand AM, Abbaszadegan MR, et al. Expression analysis of CD44 isoforms S and V3, in patients with esophageal squamous cell carcinoma. Iran J Basic Med Sci. 2015;18(4):380-4
Mansouri, A., Foroughmand, A. M., Abbaszadegan, M. R., Memar, B., Mahmoudian, R. A., & Gholamin, M. (2015). Expression analysis of CD44 isoforms S and V3, in patients with esophageal squamous cell carcinoma. Iranian journal of basic medical sciences, 18(4), 380-4.
Mansouri, Atena, et al. "Expression analysis of CD44 isoforms S and V3, in patients with esophageal squamous cell carcinoma." Iranian journal of basic medical sciences vol. 18,4 (2015): 380-4.
Mansouri A, Foroughmand AM, Abbaszadegan MR, Memar B, Mahmoudian RA, Gholamin M. Expression analysis of CD44 isoforms S and V3, in patients with esophageal squamous cell carcinoma. Iran J Basic Med Sci. 2015 Apr;18(4):380-4. PMID: 26019801; PMCID: PMC4439453.
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Selective Localization of Shanks to VGLUT1-Positive Excitatory Synapses in the Mouse Hippocampus.

Frontiers in cellular neuroscience

Heise C, Schroeder JC, Schoen M, Halbedl S, Reim D, Woelfle S, Kreutz MR, Schmeisser MJ, Boeckers TM.
PMID: 27199660
Front Cell Neurosci. 2016 Apr 26;10:106. doi: 10.3389/fncel.2016.00106. eCollection 2016.

Members of the Shank family of multidomain proteins (Shank1, Shank2, and Shank3) are core components of the postsynaptic density (PSD) of excitatory synapses. At synaptic sites Shanks serve as scaffolding molecules that cluster neurotransmitter receptors as well as cell...

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Heise C, Schroeder JC, Schoen M, et al. Selective Localization of Shanks to VGLUT1-Positive Excitatory Synapses in the Mouse Hippocampus. Front Cell Neurosci. 2016;10:106doi: 10.3389/fncel.2016.00106.
Heise, C., Schroeder, J. C., Schoen, M., Halbedl, S., Reim, D., Woelfle, S., Kreutz, M. R., Schmeisser, M. J., & Boeckers, T. M. (2016). Selective Localization of Shanks to VGLUT1-Positive Excitatory Synapses in the Mouse Hippocampus. Frontiers in cellular neuroscience, 10106. https://doi.org/10.3389/fncel.2016.00106
Heise, Christopher, et al. "Selective Localization of Shanks to VGLUT1-Positive Excitatory Synapses in the Mouse Hippocampus." Frontiers in cellular neuroscience vol. 10 (2016): 106. doi: https://doi.org/10.3389/fncel.2016.00106
Heise C, Schroeder JC, Schoen M, Halbedl S, Reim D, Woelfle S, Kreutz MR, Schmeisser MJ, Boeckers TM. Selective Localization of Shanks to VGLUT1-Positive Excitatory Synapses in the Mouse Hippocampus. Front Cell Neurosci. 2016 Apr 26;10:106. doi: 10.3389/fncel.2016.00106. eCollection 2016. PMID: 27199660; PMCID: PMC4844616.
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Transcriptome analysis of mammary epithelial cell gene expression reveals novel roles of the extracellular matrix.

Biochemistry and biophysics reports

Wanyonyi SS, Kumar A, Du Preez R, Lefevre C, Nicholas KR.
PMID: 28955800
Biochem Biophys Rep. 2017 Sep 05;12:120-128. doi: 10.1016/j.bbrep.2017.08.013. eCollection 2017 Dec.

BACKGROUND: The unique lactation strategy of the tammar wallaby METHODS: WallMEC from MID lactation mammary glands were cultured on ECM from MID or LATE lactation and treated for 5 days with 1 μg/ml cortisol, 1 μg/ml insulin, 0.2 µg/ml...

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Wanyonyi SS, Kumar A, Du Preez R, et al. Transcriptome analysis of mammary epithelial cell gene expression reveals novel roles of the extracellular matrix. Biochem Biophys Rep. 2017;12:120-128doi: 10.1016/j.bbrep.2017.08.013.
Wanyonyi, S. S., Kumar, A., Du Preez, R., Lefevre, C., & Nicholas, K. R. (2017). Transcriptome analysis of mammary epithelial cell gene expression reveals novel roles of the extracellular matrix. Biochemistry and biophysics reports, 12120-128. https://doi.org/10.1016/j.bbrep.2017.08.013
Wanyonyi, Stephen S, et al. "Transcriptome analysis of mammary epithelial cell gene expression reveals novel roles of the extracellular matrix." Biochemistry and biophysics reports vol. 12 (2017): 120-128. doi: https://doi.org/10.1016/j.bbrep.2017.08.013
Wanyonyi SS, Kumar A, Du Preez R, Lefevre C, Nicholas KR. Transcriptome analysis of mammary epithelial cell gene expression reveals novel roles of the extracellular matrix. Biochem Biophys Rep. 2017 Sep 05;12:120-128. doi: 10.1016/j.bbrep.2017.08.013. eCollection 2017 Dec. PMID: 28955800; PMCID: PMC5613237.
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Microarray analysis of differentially expressed genes and their functions in omental visceral adipose tissues of pregnant women with vs. without gestational diabetes mellitus.

Biomedical reports

Qian Y, Sun H, Xiao H, Ma M, Xiao X, Qu Q.
PMID: 28529732
Biomed Rep. 2017 May;6(5):503-512. doi: 10.3892/br.2017.878. Epub 2017 Mar 22.

Increasing evidence has shown that insulin resistance in omental visceral adipose tissue (OVAT) is a characteristic of gestational diabetes mellitus (GDM). The present study aimed to identify differentially expressed genes (DEGs) and their associated functions and pathways involved in...

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Qian Y, Sun H, Xiao H, et al. Microarray analysis of differentially expressed genes and their functions in omental visceral adipose tissues of pregnant women with vs. without gestational diabetes mellitus. Biomed Rep. 2017;6(5):503-512doi: 10.3892/br.2017.878.
Qian, Y., Sun, H., Xiao, H., Ma, M., Xiao, X., & Qu, Q. (2017). Microarray analysis of differentially expressed genes and their functions in omental visceral adipose tissues of pregnant women with vs. without gestational diabetes mellitus. Biomedical reports, 6(5), 503-512. https://doi.org/10.3892/br.2017.878
Qian, Yuan, et al. "Microarray analysis of differentially expressed genes and their functions in omental visceral adipose tissues of pregnant women with vs. without gestational diabetes mellitus." Biomedical reports vol. 6,5 (2017): 503-512. doi: https://doi.org/10.3892/br.2017.878
Qian Y, Sun H, Xiao H, Ma M, Xiao X, Qu Q. Microarray analysis of differentially expressed genes and their functions in omental visceral adipose tissues of pregnant women with vs. without gestational diabetes mellitus. Biomed Rep. 2017 May;6(5):503-512. doi: 10.3892/br.2017.878. Epub 2017 Mar 22. PMID: 28529732; PMCID: PMC5431681.
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Adhesion molecules from the diatom Phaeodactylum tricornutum (Bacillariophyceae): genomic identification by amino-acid profiling and in vivo analysis.

Journal of phycology

Willis A, Eason-Hubbard M, Hodson O, Maheswari U, Bowler C, Wetherbee R.
PMID: 26988639
J Phycol. 2014 Oct;50(5):837-49. doi: 10.1111/jpy.12214. Epub 2014 Aug 04.

Cell adhesion molecules (CAMs) are important in prokaryotes and eukaryotes for cell-cell and cell-substratum interactions. The characteristics of adhesive proteins in the model diatom Phaeodactylum tricornutum were investigated by bioinformatic analysis and in vivo characterization. Bioinformatic analysis of the...

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Willis A, Eason-Hubbard M, Hodson O, et al. Adhesion molecules from the diatom Phaeodactylum tricornutum (Bacillariophyceae): genomic identification by amino-acid profiling and in vivo analysis. J Phycol. 2014;50(5):837-49doi: 10.1111/jpy.12214.
Willis, A., Eason-Hubbard, M., Hodson, O., Maheswari, U., Bowler, C., & Wetherbee, R. (2014). Adhesion molecules from the diatom Phaeodactylum tricornutum (Bacillariophyceae): genomic identification by amino-acid profiling and in vivo analysis. Journal of phycology, 50(5), 837-49. https://doi.org/10.1111/jpy.12214
Willis, Anusuya, et al. "Adhesion molecules from the diatom Phaeodactylum tricornutum (Bacillariophyceae): genomic identification by amino-acid profiling and in vivo analysis." Journal of phycology vol. 50,5 (2014): 837-49. doi: https://doi.org/10.1111/jpy.12214
Willis A, Eason-Hubbard M, Hodson O, Maheswari U, Bowler C, Wetherbee R. Adhesion molecules from the diatom Phaeodactylum tricornutum (Bacillariophyceae): genomic identification by amino-acid profiling and in vivo analysis. J Phycol. 2014 Oct;50(5):837-49. doi: 10.1111/jpy.12214. Epub 2014 Aug 04. PMID: 26988639.
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Showing 1 to 12 of 790 entries