Reprogramming foreskin fibroblast cells from haemophilia type-a patients into induced pluripotent stem cells
Induced Pluripotent Stem Cells (iPS cells) has an enormous potential in clinical application for example in the modelling of haemophilia. Studies on human pluripotent stem cells give hope to formulate potential cellular therapies for disease modelling. This study was designed to reprogram fibroblast...
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Main Author: | |
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Format: | Thesis Book |
Language: | English |
Published: |
Sungai Buloh, Selangor
Universiti Teknologi MARA. Faculty of Medicine
2017
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Online Access: | Click Here to View Status and Holdings. |
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Summary: | Induced Pluripotent Stem Cells (iPS cells) has an enormous potential in clinical application for example in the modelling of haemophilia. Studies on human pluripotent stem cells give hope to formulate potential cellular therapies for disease modelling. This study was designed to reprogram fibroblast cells from haemophilia type-A patients into iPS cells using four different techniques. Enzyme dissociation and explant culture technique were used to isolate primary cell fibroblast from haemophilia type-A patient. The enzymatic dissociation technique required three days to develop into fibroblast cells. compared to explant culture which required 10 days in culture. Properties of the iPS cells depended on the reprogramming method. Morphological characteristics of iPS cells were observed only in Stemgent mRNA and Neon® Reprogramming techniques. Expressions of pluripotency were verified using pluripotency markers. Downregulated and upregulated gene expression were analysed using qRT-PCR. This study provides new information on the development of haemophilia modelling, based on patient specific iPS cells using integration-free methods |
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Item Description: | UiTM Digitized |
Physical Description: | xvi, 168 pages illustrations, charts (some colour) 30 cm 1 computer optical disc (4 ¾ in.) |
Format: | System requirements for CD-ROM: Intel Pentium II or faster processor with 450 MHz (or equivalent), browser Internet Explorer 5.5 or higher (6.0 or higher recommended), Firefox 1.0.2 or higher, Acrobat |
Bibliography: | Includes bibliographical references (page 148-158) |