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Biochemical and Parasitological Studies on the Effect of hUCB-Selected CD34(+) Progenitor/Stem Cells in Mice Infected with Schistosoma mansoni.

International journal of stem cells

Abou-Zied AM, Soliman RH, Hefila SM, Imam SA.
PMID: 25473447
Int J Stem Cells. 2014 Nov;7(2):98-107. doi: 10.15283/ijsc.2014.7.2.98.

BACKGROUND AND OBJECTIVES: Placenta and blood that remained in the umbilical cord is routinely available as a discarded tissue after deliveries and it is free of any legal, moral, ethical or religious objections, providing a high number of multipotent...

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Abou-Zied AM, Soliman RH, Hefila SM, et al. Biochemical and Parasitological Studies on the Effect of hUCB-Selected CD34(+) Progenitor/Stem Cells in Mice Infected with Schistosoma mansoni. Int J Stem Cells. 2014;7(2):98-107doi: 10.15283/ijsc.2014.7.2.98.
Abou-Zied, A. M., Soliman, R. H., Hefila, S. M., & Imam, S. A. (2014). Biochemical and Parasitological Studies on the Effect of hUCB-Selected CD34(+) Progenitor/Stem Cells in Mice Infected with Schistosoma mansoni. International journal of stem cells, 7(2), 98-107. https://doi.org/10.15283/ijsc.2014.7.2.98
Abou-Zied, Akram M, et al. "Biochemical and Parasitological Studies on the Effect of hUCB-Selected CD34(+) Progenitor/Stem Cells in Mice Infected with Schistosoma mansoni." International journal of stem cells vol. 7,2 (2014): 98-107. doi: https://doi.org/10.15283/ijsc.2014.7.2.98
Abou-Zied AM, Soliman RH, Hefila SM, Imam SA. Biochemical and Parasitological Studies on the Effect of hUCB-Selected CD34(+) Progenitor/Stem Cells in Mice Infected with Schistosoma mansoni. Int J Stem Cells. 2014 Nov;7(2):98-107. doi: 10.15283/ijsc.2014.7.2.98. PMID: 25473447; PMCID: PMC4249909.
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Growth Properties and Pluripotency Marker Expression of Spontaneously Formed Three-dimensional Aggregates of Human Adipose-derived Stem Cells.

International journal of stem cells

Bogdanova-Jatniece A, Berzins U, Kozlovska T.
PMID: 25473452
Int J Stem Cells. 2014 Nov;7(2):143-52. doi: 10.15283/ijsc.2014.7.2.143.

BACKGROUND AND OBJECTIVES: Recent findings suggest that therapeutic potential of mesenchymal stem cells (MSCs) could be increased through aggregation into three-dimensional (3D) bodies, and different culture methods have been employed to obtain 3D spheroids of MSCs. In the current...

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Bogdanova-Jatniece A, Berzins U, Kozlovska T. Growth Properties and Pluripotency Marker Expression of Spontaneously Formed Three-dimensional Aggregates of Human Adipose-derived Stem Cells. Int J Stem Cells. 2014;7(2):143-52doi: 10.15283/ijsc.2014.7.2.143.
Bogdanova-Jatniece, A., Berzins, U., & Kozlovska, T. (2014). Growth Properties and Pluripotency Marker Expression of Spontaneously Formed Three-dimensional Aggregates of Human Adipose-derived Stem Cells. International journal of stem cells, 7(2), 143-52. https://doi.org/10.15283/ijsc.2014.7.2.143
Bogdanova-Jatniece, Ance, et al. "Growth Properties and Pluripotency Marker Expression of Spontaneously Formed Three-dimensional Aggregates of Human Adipose-derived Stem Cells." International journal of stem cells vol. 7,2 (2014): 143-52. doi: https://doi.org/10.15283/ijsc.2014.7.2.143
Bogdanova-Jatniece A, Berzins U, Kozlovska T. Growth Properties and Pluripotency Marker Expression of Spontaneously Formed Three-dimensional Aggregates of Human Adipose-derived Stem Cells. Int J Stem Cells. 2014 Nov;7(2):143-52. doi: 10.15283/ijsc.2014.7.2.143. PMID: 25473452; PMCID: PMC4249897.
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SoxD Transcription Factors: Multifaceted Players of Neural Development.

International journal of stem cells

Ji EH, Kim J.
PMID: 27426080
Int J Stem Cells. 2016 May 30;9(1):3-8. doi: 10.15283/ijsc.2016.9.1.3.

SoxD transcription factor subfamily includes three members, Sox5, Sox6, and Sox13. Like other Sox genes, they contain the High-Mobility-Group (HMG) box as the DNA binding domain but in addition feature the subgroup-specific leucine zipper motif. SoxD genes are expressed...

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Ji EH, Kim J. SoxD Transcription Factors: Multifaceted Players of Neural Development. Int J Stem Cells. 2016;9(1):3-8doi: 10.15283/ijsc.2016.9.1.3.
Ji, E. H., & Kim, J. (2016). SoxD Transcription Factors: Multifaceted Players of Neural Development. International journal of stem cells, 9(1), 3-8. https://doi.org/10.15283/ijsc.2016.9.1.3
Ji, Eun Hye, and Kim, Jaesang. "SoxD Transcription Factors: Multifaceted Players of Neural Development." International journal of stem cells vol. 9,1 (2016): 3-8. doi: https://doi.org/10.15283/ijsc.2016.9.1.3
Ji EH, Kim J. SoxD Transcription Factors: Multifaceted Players of Neural Development. Int J Stem Cells. 2016 May 30;9(1):3-8. doi: 10.15283/ijsc.2016.9.1.3. PMID: 27426080; PMCID: PMC4961098.
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Genetically Engineered In Vitro Erythropoiesis.

International journal of stem cells

Geiler C, Andrade I, Clayton A, Greenwald D.
PMID: 27426086
Int J Stem Cells. 2016 May 30;9(1):53-9. doi: 10.15283/ijsc.2016.9.1.53.

BACKGROUND: Engineered blood has the greatest potential to combat a predicted future shortfall in the US blood supply for transfusion treatments. Engineered blood produced from hematopoietic stem cell (HSC) derived red blood cells in a laboratory is possible, but...

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Geiler C, Andrade I, Clayton A, et al. Genetically Engineered In Vitro Erythropoiesis. Int J Stem Cells. 2016;9(1):53-9doi: 10.15283/ijsc.2016.9.1.53.
Geiler, C., Andrade, I., Clayton, A., & Greenwald, D. (2016). Genetically Engineered In Vitro Erythropoiesis. International journal of stem cells, 9(1), 53-9. https://doi.org/10.15283/ijsc.2016.9.1.53
Geiler, Cristopher, et al. "Genetically Engineered In Vitro Erythropoiesis." International journal of stem cells vol. 9,1 (2016): 53-9. doi: https://doi.org/10.15283/ijsc.2016.9.1.53
Geiler C, Andrade I, Clayton A, Greenwald D. Genetically Engineered In Vitro Erythropoiesis. Int J Stem Cells. 2016 May 30;9(1):53-9. doi: 10.15283/ijsc.2016.9.1.53. PMID: 27426086; PMCID: PMC4961104.
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Umbilical Cord Derived Mesenchymal Stem Cells Useful in Insulin Production - Another Opportunity in Cell Therapy.

International journal of stem cells

Sarang S, Viswanathan C.
PMID: 27426087
Int J Stem Cells. 2016 May 30;9(1):60-9. doi: 10.15283/ijsc.2016.9.1.60.

BACKGROUND AND OBJECTIVES: Type 1 Diabetes Mellitus (T1DM) is an autoimmune disorder resulting out of T cell mediated destruction of pancreatic beta cells. Immunomodulatory properties of mesenchymal stem cells may help to regenerate beta cells and/or prevent further destruction...

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Sarang S, Viswanathan C. Umbilical Cord Derived Mesenchymal Stem Cells Useful in Insulin Production - Another Opportunity in Cell Therapy. Int J Stem Cells. 2016;9(1):60-9doi: 10.15283/ijsc.2016.9.1.60.
Sarang, S., & Viswanathan, C. (2016). Umbilical Cord Derived Mesenchymal Stem Cells Useful in Insulin Production - Another Opportunity in Cell Therapy. International journal of stem cells, 9(1), 60-9. https://doi.org/10.15283/ijsc.2016.9.1.60
Sarang, Shabari, and Viswanathan, Chandra. "Umbilical Cord Derived Mesenchymal Stem Cells Useful in Insulin Production - Another Opportunity in Cell Therapy." International journal of stem cells vol. 9,1 (2016): 60-9. doi: https://doi.org/10.15283/ijsc.2016.9.1.60
Sarang S, Viswanathan C. Umbilical Cord Derived Mesenchymal Stem Cells Useful in Insulin Production - Another Opportunity in Cell Therapy. Int J Stem Cells. 2016 May 30;9(1):60-9. doi: 10.15283/ijsc.2016.9.1.60. PMID: 27426087; PMCID: PMC4961105.
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Study of the Effect of Route of Administration of Mesenchymal Stem Cells on Cisplatin-Induced Acute Kidney Injury in Sprague Dawley Rats.

International journal of stem cells

Moustafa FE, Sobh MA, Abouelkheir M, Khater Y, Mahmoud K, Saad MA, Sobh MA.
PMID: 27426089
Int J Stem Cells. 2016 May 30;9(1):79-89. doi: 10.15283/ijsc.2016.9.1.79.

BACKGROUND AND OBJECTIVES: Mesenchymal stem cells (MSCs) have been shown to ameliorate cisplatin-induced acute kidney injury (AKI). The present study compares the efficacy of different routes of MSCs administration on kidney damage and regeneration after cisplatin-induced AKI.METHODS: A single...

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Moustafa FE, Sobh MA, Abouelkheir M, et al. Study of the Effect of Route of Administration of Mesenchymal Stem Cells on Cisplatin-Induced Acute Kidney Injury in Sprague Dawley Rats. Int J Stem Cells. 2016;9(1):79-89doi: 10.15283/ijsc.2016.9.1.79.
Moustafa, F. E., Sobh, M. A., Abouelkheir, M., Khater, Y., Mahmoud, K., Saad, M. A., & Sobh, M. A. (2016). Study of the Effect of Route of Administration of Mesenchymal Stem Cells on Cisplatin-Induced Acute Kidney Injury in Sprague Dawley Rats. International journal of stem cells, 9(1), 79-89. https://doi.org/10.15283/ijsc.2016.9.1.79
Moustafa, Fatma E, et al. "Study of the Effect of Route of Administration of Mesenchymal Stem Cells on Cisplatin-Induced Acute Kidney Injury in Sprague Dawley Rats." International journal of stem cells vol. 9,1 (2016): 79-89. doi: https://doi.org/10.15283/ijsc.2016.9.1.79
Moustafa FE, Sobh MA, Abouelkheir M, Khater Y, Mahmoud K, Saad MA, Sobh MA. Study of the Effect of Route of Administration of Mesenchymal Stem Cells on Cisplatin-Induced Acute Kidney Injury in Sprague Dawley Rats. Int J Stem Cells. 2016 May 30;9(1):79-89. doi: 10.15283/ijsc.2016.9.1.79. PMID: 27426089; PMCID: PMC4961107.
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Therapeutic Potential of Bone Marrow-Derived Mesenchymal Stem Cells on Experimental Liver Injury Induced by Schistosoma mansoni: A Histological Study.

International journal of stem cells

Fikry H, Gawad SA, Baher W.
PMID: 27426091
Int J Stem Cells. 2016 May 30;9(1):96-106. doi: 10.15283/ijsc.2016.9.1.96.

BACKGROUND AND OBJECTIVES: Bone marrow derived mesenchymal stem cells (BM-MSCs) have been proposed as effective treatment of many diseases owing to their unique ability to differentiate into other cell types in vivo. Schistosoma mansoni (S. mansoni) infection is characterized...

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Fikry H, Gawad SA, Baher W. Therapeutic Potential of Bone Marrow-Derived Mesenchymal Stem Cells on Experimental Liver Injury Induced by Schistosoma mansoni: A Histological Study. Int J Stem Cells. 2016;9(1):96-106doi: 10.15283/ijsc.2016.9.1.96.
Fikry, H., Gawad, S. A., & Baher, W. (2016). Therapeutic Potential of Bone Marrow-Derived Mesenchymal Stem Cells on Experimental Liver Injury Induced by Schistosoma mansoni: A Histological Study. International journal of stem cells, 9(1), 96-106. https://doi.org/10.15283/ijsc.2016.9.1.96
Fikry, Heba, et al. "Therapeutic Potential of Bone Marrow-Derived Mesenchymal Stem Cells on Experimental Liver Injury Induced by Schistosoma mansoni: A Histological Study." International journal of stem cells vol. 9,1 (2016): 96-106. doi: https://doi.org/10.15283/ijsc.2016.9.1.96
Fikry H, Gawad SA, Baher W. Therapeutic Potential of Bone Marrow-Derived Mesenchymal Stem Cells on Experimental Liver Injury Induced by Schistosoma mansoni: A Histological Study. Int J Stem Cells. 2016 May 30;9(1):96-106. doi: 10.15283/ijsc.2016.9.1.96. PMID: 27426091; PMCID: PMC4961109.
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Severe Type 2 Diabetes Induces Reversible Modifications of Endothelial Progenitor Cells Which are Ameliorate by Glycemic Control.

International journal of stem cells

De Pascale MR, Bruzzese G, Crimi E, Grimaldi V, Liguori A, Brongo S, Barbieri M, Picascia A, Schiano C, Sommese L, Ferrara N, Paolisso G, Napoli C.
PMID: 27426095
Int J Stem Cells. 2016 May 30;9(1):137-44. doi: 10.15283/ijsc.2016.9.1.137.

BACKGROUND: Circulating endothelial progenitors cells (EPCs) play a critical role in neovascularization and endothelial repair. There is a growing evidence that hyperglycemia related to Diabetes Mellitus (DM) decreases EPC number and function so promoting vascular complications.AIM OF THE STUDY:...

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De Pascale MR, Bruzzese G, Crimi E, et al. Severe Type 2 Diabetes Induces Reversible Modifications of Endothelial Progenitor Cells Which are Ameliorate by Glycemic Control. Int J Stem Cells. 2016;9(1):137-44doi: 10.15283/ijsc.2016.9.1.137.
De Pascale, M. R., Bruzzese, G., Crimi, E., Grimaldi, V., Liguori, A., Brongo, S., Barbieri, M., Picascia, A., Schiano, C., Sommese, L., Ferrara, N., Paolisso, G., & Napoli, C. (2016). Severe Type 2 Diabetes Induces Reversible Modifications of Endothelial Progenitor Cells Which are Ameliorate by Glycemic Control. International journal of stem cells, 9(1), 137-44. https://doi.org/10.15283/ijsc.2016.9.1.137
De Pascale, Maria Rosaria, et al. "Severe Type 2 Diabetes Induces Reversible Modifications of Endothelial Progenitor Cells Which are Ameliorate by Glycemic Control." International journal of stem cells vol. 9,1 (2016): 137-44. doi: https://doi.org/10.15283/ijsc.2016.9.1.137
De Pascale MR, Bruzzese G, Crimi E, Grimaldi V, Liguori A, Brongo S, Barbieri M, Picascia A, Schiano C, Sommese L, Ferrara N, Paolisso G, Napoli C. Severe Type 2 Diabetes Induces Reversible Modifications of Endothelial Progenitor Cells Which are Ameliorate by Glycemic Control. Int J Stem Cells. 2016 May 30;9(1):137-44. doi: 10.15283/ijsc.2016.9.1.137. PMID: 27426095; PMCID: PMC4961113.
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Moderate Hypoxia Exhibits Increased Endothelial Progenitor Vessel-forming Ability However Gestational Diabetes Caused to Impede Compensatory Defense Reaction.

International journal of stem cells

Dincer UD.
PMID: 27426097
Int J Stem Cells. 2016 May 30;9(1):152-62. doi: 10.15283/ijsc.2016.9.1.152.

Endothelium represents a defense barrier and responds and integrates neuro humoral stimulus which describes as a compensatory mechanism. Endothelium formed with endothelial cells (ECs) and their progenitors. Endothelial progenitor cells (EPCs) represent minor subpopulation of mononuclear cells in the...

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Dincer UD. Moderate Hypoxia Exhibits Increased Endothelial Progenitor Vessel-forming Ability However Gestational Diabetes Caused to Impede Compensatory Defense Reaction. Int J Stem Cells. 2016;9(1):152-62doi: 10.15283/ijsc.2016.9.1.152.
Dincer, U. D. (2016). Moderate Hypoxia Exhibits Increased Endothelial Progenitor Vessel-forming Ability However Gestational Diabetes Caused to Impede Compensatory Defense Reaction. International journal of stem cells, 9(1), 152-62. https://doi.org/10.15283/ijsc.2016.9.1.152
Dincer, U Deniz. "Moderate Hypoxia Exhibits Increased Endothelial Progenitor Vessel-forming Ability However Gestational Diabetes Caused to Impede Compensatory Defense Reaction." International journal of stem cells vol. 9,1 (2016): 152-62. doi: https://doi.org/10.15283/ijsc.2016.9.1.152
Dincer UD. Moderate Hypoxia Exhibits Increased Endothelial Progenitor Vessel-forming Ability However Gestational Diabetes Caused to Impede Compensatory Defense Reaction. Int J Stem Cells. 2016 May 30;9(1):152-62. doi: 10.15283/ijsc.2016.9.1.152. PMID: 27426097; PMCID: PMC4961115.
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Science and ethics: bridge to the future for regenerative medicine.

International journal of stem cells

Patricio VJ.
PMID: 24298338
Int J Stem Cells. 2011 Nov;4(2):79-84. doi: 10.15283/ijsc.2011.4.2.79.

The objective of this article is to reflect on the relationship between regenerative medicine and ethics, using as references the Aristotelian concept of what is ethical and that of Raessler Van Potter about bioethics. To do this, I will...

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Patricio VJ. Science and ethics: bridge to the future for regenerative medicine. Int J Stem Cells. 2011;4(2):79-84doi: 10.15283/ijsc.2011.4.2.79.
Patricio, V. J. (2011). Science and ethics: bridge to the future for regenerative medicine. International journal of stem cells, 4(2), 79-84. https://doi.org/10.15283/ijsc.2011.4.2.79
Patricio, Ventura-Juncá. "Science and ethics: bridge to the future for regenerative medicine." International journal of stem cells vol. 4,2 (2011): 79-84. doi: https://doi.org/10.15283/ijsc.2011.4.2.79
Patricio VJ. Science and ethics: bridge to the future for regenerative medicine. Int J Stem Cells. 2011 Nov;4(2):79-84. doi: 10.15283/ijsc.2011.4.2.79. PMID: 24298338; PMCID: PMC3840959.
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Dopamine neuron generation from human embryonic stem cells.

International journal of stem cells

Kim YS, Park CH.
PMID: 24298339
Int J Stem Cells. 2011 Nov;4(2):85-7. doi: 10.15283/ijsc.2011.4.2.85.

The capacity of pluripotency and self-renewal of human embryonic stem (hES) cells may provide unlimited cell source for cell replacement therapy. In this manuscript we summarize hES differentiation protocols coculture with PA6 or MS5 stromal cells. After 7∼ 9...

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Kim YS, Park CH. Dopamine neuron generation from human embryonic stem cells. Int J Stem Cells. 2011;4(2):85-7doi: 10.15283/ijsc.2011.4.2.85.
Kim, Y. S., & Park, C. H. (2011). Dopamine neuron generation from human embryonic stem cells. International journal of stem cells, 4(2), 85-7. https://doi.org/10.15283/ijsc.2011.4.2.85
Kim, Yong-Sik, and Park, Chang-Hwan. "Dopamine neuron generation from human embryonic stem cells." International journal of stem cells vol. 4,2 (2011): 85-7. doi: https://doi.org/10.15283/ijsc.2011.4.2.85
Kim YS, Park CH. Dopamine neuron generation from human embryonic stem cells. Int J Stem Cells. 2011 Nov;4(2):85-7. doi: 10.15283/ijsc.2011.4.2.85. PMID: 24298339; PMCID: PMC3840963.
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The Porcine Aortic Tissue Culture System in vitro for Stem Cell Research.

International journal of stem cells

Kim DE, Oh KH, Yang JH, Kwon SK, Cho TJ, Lee SB, Nam H, Lee DS, Lee JR, Lee G, Cho J.
PMID: 24298344
Int J Stem Cells. 2011 Nov;4(2):116-22. doi: 10.15283/ijsc.2011.4.2.116.

BACKGROUND AND OBJECTIVES: Due to the shortage of human donors for transplantation, the use of animal organs for xenotransplantation has come into great interest. Xeno-derived vessels and cardiac valves would be possible alternatives for the patient suffering from cardiovascular...

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Kim DE, Oh KH, Yang JH, et al. The Porcine Aortic Tissue Culture System in vitro for Stem Cell Research. Int J Stem Cells. 2011;4(2):116-22doi: 10.15283/ijsc.2011.4.2.116.
Kim, D. E., Oh, K. H., Yang, J. H., Kwon, S. K., Cho, T. J., Lee, S. B., Nam, H., Lee, D. S., Lee, J. R., Lee, G., & Cho, J. (2011). The Porcine Aortic Tissue Culture System in vitro for Stem Cell Research. International journal of stem cells, 4(2), 116-22. https://doi.org/10.15283/ijsc.2011.4.2.116
Kim, Dong-Eun, et al. "The Porcine Aortic Tissue Culture System in vitro for Stem Cell Research." International journal of stem cells vol. 4,2 (2011): 116-22. doi: https://doi.org/10.15283/ijsc.2011.4.2.116
Kim DE, Oh KH, Yang JH, Kwon SK, Cho TJ, Lee SB, Nam H, Lee DS, Lee JR, Lee G, Cho J. The Porcine Aortic Tissue Culture System in vitro for Stem Cell Research. Int J Stem Cells. 2011 Nov;4(2):116-22. doi: 10.15283/ijsc.2011.4.2.116. PMID: 24298344; PMCID: PMC3840957.
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Showing 1 to 12 of 383 entries