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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Main Author: Che Omar, Ruhil Nadirah
Format: Thesis
Language:English
Published: 2024
Subjects:
DNA
Online Access:https://ir.uitm.edu.my/id/eprint/107234/1/107234.pdf
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spelling 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
institution Universiti Teknologi MARA
collection UiTM Institutional Repository
language English
topic DNA
Deoxyribonucleic acids
Genetics
spellingShingle 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
description 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
_version_ 1818588217096536064