The generation of CYP2C9 knocked-down human hepatocyte library: a utilization of crispr/cas9 system / Ruhil Nadirah Che Omar
There is an issue of inconsistencies of working with hepatocytes obtained from different human liver donors in drug metabolism studies. CRISPR type II (Cas9) is the most recent development in biotechnology that could potentially resolve this limitation by precise and efficient alteration of genetic...
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my-uitm-ir.1072342024-12-04T08:29:45Z The generation of CYP2C9 knocked-down human hepatocyte library: a utilization of crispr/cas9 system / Ruhil Nadirah Che Omar 2024 Che Omar, Ruhil Nadirah DNA. Deoxyribonucleic acids Genetics There is an issue of inconsistencies of working with hepatocytes obtained from different human liver donors in drug metabolism studies. CRISPR type II (Cas9) is the most recent development in biotechnology that could potentially resolve this limitation by precise and efficient alteration of genetic sequences. It works in almost any kind of living cells and became possible after the recent discovery of genome editing technologies. Clustered regularly interspaced short palindromic repeats (CRISPR) – associated nucleus (Cas), allows for small changes to a known, targeted location on the DNA sequence efficiently at a faster rate, and ease of use. 2024 Thesis https://ir.uitm.edu.my/id/eprint/107234/ https://ir.uitm.edu.my/id/eprint/107234/1/107234.pdf text en public masters Universiti Teknologi MARA (UiTM) Faculty of Pharmacy |
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Universiti Teknologi MARA |
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English |
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DNA Deoxyribonucleic acids Genetics |
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DNA Deoxyribonucleic acids Genetics Che Omar, Ruhil Nadirah The generation of CYP2C9 knocked-down human hepatocyte library: a utilization of crispr/cas9 system / Ruhil Nadirah Che Omar |
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There is an issue of inconsistencies of working with hepatocytes obtained from different human liver donors in drug metabolism studies. CRISPR type II (Cas9) is the most recent development in biotechnology that could potentially resolve this limitation by precise and efficient alteration of genetic sequences. It works in almost any kind of living cells and became possible after the recent discovery of genome editing technologies. Clustered regularly interspaced short palindromic repeats (CRISPR) – associated nucleus (Cas), allows for small changes to a known, targeted location on the DNA sequence efficiently at a faster rate, and ease of use. |
format |
Thesis |
qualification_level |
Master's degree |
author |
Che Omar, Ruhil Nadirah |
author_facet |
Che Omar, Ruhil Nadirah |
author_sort |
Che Omar, Ruhil Nadirah |
title |
The generation of CYP2C9 knocked-down human hepatocyte library: a utilization of crispr/cas9 system / Ruhil Nadirah Che Omar |
title_short |
The generation of CYP2C9 knocked-down human hepatocyte library: a utilization of crispr/cas9 system / Ruhil Nadirah Che Omar |
title_full |
The generation of CYP2C9 knocked-down human hepatocyte library: a utilization of crispr/cas9 system / Ruhil Nadirah Che Omar |
title_fullStr |
The generation of CYP2C9 knocked-down human hepatocyte library: a utilization of crispr/cas9 system / Ruhil Nadirah Che Omar |
title_full_unstemmed |
The generation of CYP2C9 knocked-down human hepatocyte library: a utilization of crispr/cas9 system / Ruhil Nadirah Che Omar |
title_sort |
generation of cyp2c9 knocked-down human hepatocyte library: a utilization of crispr/cas9 system / ruhil nadirah che omar |
granting_institution |
Universiti Teknologi MARA (UiTM) |
granting_department |
Faculty of Pharmacy |
publishDate |
2024 |
url |
https://ir.uitm.edu.my/id/eprint/107234/1/107234.pdf |
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1818588217096536064 |