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Defect model in rabbits. The major merit of this study was that, this implant has been tested in vivo so that with a welldesigned pilot and experimental study we were able to explain the mechanism of action of this implant on tendon healing. In addition, we followed the immune activity of the body in response to the implanted collagen prosthesis from the early stages to four months after injury by
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Oscience. Trends Neurosci. 1999;22(4):167-173. PubMed Silverman ES, Collins T. Pathways of Egr-1-mediated gene transcription in vascular biology. Am J Pathol. 1999;154(3):665-70. doi:10.1016/S00029440(10)65312-6. PubMed PMID: 10079243; PMCID: PMC1866415. Thiel G, Cibelli G. Regulation of life and death by the zinc finger transcription factor Egr-1. J Cell Physiol. 2002;193(3):287-292. doi:10.1002/
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Oscience. Trends Neurosci. 1999;22(4):167-173. PubMed Silverman ES, Collins T. Pathways of Egr-1-mediated gene transcription in vascular biology. Am J Pathol. 1999;154(3):665-70. doi:10.1016/S00029440(10)65312-6. PubMed PMID: 10079243; PMCID: PMC1866415. Thiel G, Cibelli G. Regulation of life and death by the zinc finger transcription factor Egr-1. J Cell Physiol. 2002;193(3):287-292. doi:10.1002/
1
Oscience. Trends Neurosci. 1999;22(4):167-173. PubMed Silverman ES, Collins T. Pathways of Egr-1-mediated gene transcription in vascular biology. Am J Pathol. 1999;154(3):665-70. doi:10.1016/S00029440(10)65312-6. PubMed PMID: 10079243; PMCID: PMC1866415. Thiel G, Cibelli G. Regulation of life and death by the zinc finger transcription factor Egr-1. J Cell Physiol. 2002;193(3):287-292. doi:10.1002/
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Described experiments. SM performed real-time PCR analysis of EGR2, CD163, and HLA-DRA in human mammary explant tissue and performed data analysis. SS participated in the study design, edited the manuscript, and gave final approval of the version to be published. All authors read and approved the final manuscript. Competing interests The authors do not have any financial or personal relationships
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Described experiments. SM performed real-time PCR analysis of EGR2, CD163, and HLA-DRA in human mammary explant tissue and performed data analysis. SS participated in the study design, edited the manuscript, and gave final approval of the version to be published. All authors read and approved the final manuscript. Competing interests The authors do not have any financial or personal relationships
1
Described experiments. SM performed real-time PCR analysis of EGR2, CD163, and HLA-DRA in human mammary explant tissue and performed data analysis. SS participated in the study design, edited the manuscript, and gave final approval of the version to be published. All authors read and approved the final manuscript. Competing interests The authors do not have any financial or personal relationships
1
Defect model in rabbits. The major merit of this study was that, this implant has been tested in vivo so that with a welldesigned pilot and experimental study we were able to explain the mechanism of action of this implant on tendon healing. In addition, we followed the immune activity of the body in response to the implanted collagen prosthesis from the early stages to four months after injury by