Applications of CRISPR technologies in transplantation
In transplantation, the ever‐increasing number of an organ's demand and long‐term graft dysfunction constitute some of the major problems. Therefore, alternative solutions to increase the quantity and quality of the organ supply for transplantation are desired. On this subject, revolutionary Cl...
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Published in | American journal of transplantation Vol. 20; no. 12; pp. 3285 - 3293 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Limited
01.12.2020
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Subjects | |
Online Access | Get full text |
ISSN | 1600-6135 1600-6143 1600-6143 |
DOI | 10.1111/ajt.16095 |
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Abstract | In transplantation, the ever‐increasing number of an organ's demand and long‐term graft dysfunction constitute some of the major problems. Therefore, alternative solutions to increase the quantity and quality of the organ supply for transplantation are desired. On this subject, revolutionary Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) technology holds enormous potential for the scientific community with its expanding toolbox. In this minireview, we summarize the history and mechanism of CRISPR/Cas9 systems and explore its potential applications in cellular‐ and organ‐level transplantation. The last part of this review includes future opportunities as well as the challenges in the transplantation field.
This minireview of CRISPR technologies, the state‐of‐the‐art approach to genome editing, focuses on current and future applications in transplantation. |
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AbstractList | In transplantation, the ever-increasing number of an organ's demand and long-term graft dysfunction constitute some of the major problems. Therefore, alternative solutions to increase the quantity and quality of the organ supply for transplantation are desired. On this subject, revolutionary Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) technology holds enormous potential for the scientific community with its expanding toolbox. In this minireview, we summarize the history and mechanism of CRISPR/Cas9 systems and explore its potential applications in cellular- and organ-level transplantation. The last part of this review includes future opportunities as well as the challenges in the transplantation field. In transplantation, the ever-increasing number of organ’s demand and long-term graft dysfunction constitute some of the major problems. Therefore, alternative solutions to increase the quantity and quality of the organ supply for transplantation are desired. On this subject, revolutionary CRISPR technology holds enormous potential for the scientific community with its expanding toolbox. In this minireview, we summarize the history and mechanism of CRISPR/Cas9 systems and explore its potential applications at cellular and organ level transplantation. The last part of this review includes future opportunities as well as the challenges in the transplantation field. In transplantation, the ever‐increasing number of an organ's demand and long‐term graft dysfunction constitute some of the major problems. Therefore, alternative solutions to increase the quantity and quality of the organ supply for transplantation are desired. On this subject, revolutionary Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) technology holds enormous potential for the scientific community with its expanding toolbox. In this minireview, we summarize the history and mechanism of CRISPR/Cas9 systems and explore its potential applications in cellular‐ and organ‐level transplantation. The last part of this review includes future opportunities as well as the challenges in the transplantation field. This minireview of CRISPR technologies, the state‐of‐the‐art approach to genome editing, focuses on current and future applications in transplantation. In transplantation, the ever-increasing number of an organ's demand and long-term graft dysfunction constitute some of the major problems. Therefore, alternative solutions to increase the quantity and quality of the organ supply for transplantation are desired. On this subject, revolutionary Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) technology holds enormous potential for the scientific community with its expanding toolbox. In this minireview, we summarize the history and mechanism of CRISPR/Cas9 systems and explore its potential applications in cellular- and organ-level transplantation. The last part of this review includes future opportunities as well as the challenges in the transplantation field.In transplantation, the ever-increasing number of an organ's demand and long-term graft dysfunction constitute some of the major problems. Therefore, alternative solutions to increase the quantity and quality of the organ supply for transplantation are desired. On this subject, revolutionary Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) technology holds enormous potential for the scientific community with its expanding toolbox. In this minireview, we summarize the history and mechanism of CRISPR/Cas9 systems and explore its potential applications in cellular- and organ-level transplantation. The last part of this review includes future opportunities as well as the challenges in the transplantation field. |
Author | Kuscu, Cem Eason, James D. Kuscu, Canan Maluf, Daniel Bajwa, Amandeep Mas, Valeria R. |
AuthorAffiliation | 1 Transplant Research Institute, James D. Eason Transplant Institute, Department of Surgery, School of Medicine, University of Tennessee Health Science Center, Memphis, TN |
AuthorAffiliation_xml | – name: 1 Transplant Research Institute, James D. Eason Transplant Institute, Department of Surgery, School of Medicine, University of Tennessee Health Science Center, Memphis, TN |
Author_xml | – sequence: 1 givenname: Cem orcidid: 0000-0001-7154-6762 surname: Kuscu fullname: Kuscu, Cem email: ckuscu1@uthsc.edu organization: University of Tennessee Health Science Center – sequence: 2 givenname: Canan surname: Kuscu fullname: Kuscu, Canan organization: University of Tennessee Health Science Center – sequence: 3 givenname: Amandeep surname: Bajwa fullname: Bajwa, Amandeep organization: University of Tennessee Health Science Center – sequence: 4 givenname: James D. surname: Eason fullname: Eason, James D. organization: University of Tennessee Health Science Center – sequence: 5 givenname: Daniel orcidid: 0000-0002-5921-4834 surname: Maluf fullname: Maluf, Daniel organization: University of Tennessee Health Science Center – sequence: 6 givenname: Valeria R. surname: Mas fullname: Mas, Valeria R. organization: University of Tennessee Health Science Center |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/32484284$$D View this record in MEDLINE/PubMed |
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Snippet | In transplantation, the ever‐increasing number of an organ's demand and long‐term graft dysfunction constitute some of the major problems. Therefore,... In transplantation, the ever-increasing number of an organ's demand and long-term graft dysfunction constitute some of the major problems. Therefore,... In transplantation, the ever-increasing number of organ’s demand and long-term graft dysfunction constitute some of the major problems. Therefore, alternative... |
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SubjectTerms | animal models: porcine basic (laboratory) research/science Blood & organ donations Clustered Regularly Interspaced Short Palindromic Repeats CRISPR genomics immunosuppression/immune modulation molecular biology Organ Transplantation tolerance: chimerism translational research/science Transplantation Transplants & implants xenoantigen xenotransplantation |
Title | Applications of CRISPR technologies in transplantation |
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