Defeciancy Of Puma And Noxa For Melanomagenesis In A Mouse Model Of Melanoma

It is commonly believed without sufficient evidence that the impairment of the ability to undergo apoptosis (a mode of programmed cell death) in response to conventional treatment such as cytotoxic drugs, gained melanoma its notorious resistance to therapy. Studies to determine the contribution of t...

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Main Author: Phang,, Su Ling
Format: Thesis
Language:English
Published: 2017
Subjects:
Online Access:http://eprints.usm.my/45479/
http://eprints.usm.my/45479/1/PHANG%20SU%20LING.pdf
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author Phang,, Su Ling
author_facet Phang,, Su Ling
author_sort Phang,, Su Ling
building USM Institutional Repository
collection Online Access
description It is commonly believed without sufficient evidence that the impairment of the ability to undergo apoptosis (a mode of programmed cell death) in response to conventional treatment such as cytotoxic drugs, gained melanoma its notorious resistance to therapy. Studies to determine the contribution of the intrinsic apoptosis pathway for melanomagenesis are often deterred by utilisation of in vitro cell culture models and xenograft models. An established mouse model of melanoma, the Cdkn2a -/-, Tyr-HRASG12V, was utilised in this study to obviate limitations posted by the usage of in vitro and xenograft models.
first_indexed 2025-11-15T18:01:37Z
format Thesis
id usm-45479
institution Universiti Sains Malaysia
institution_category Local University
language English
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publishDate 2017
recordtype eprints
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spelling usm-454792019-09-19T01:05:11Z http://eprints.usm.my/45479/ Defeciancy Of Puma And Noxa For Melanomagenesis In A Mouse Model Of Melanoma Phang,, Su Ling QH1 Natural history (General - Including nature conservation, geographical distribution) It is commonly believed without sufficient evidence that the impairment of the ability to undergo apoptosis (a mode of programmed cell death) in response to conventional treatment such as cytotoxic drugs, gained melanoma its notorious resistance to therapy. Studies to determine the contribution of the intrinsic apoptosis pathway for melanomagenesis are often deterred by utilisation of in vitro cell culture models and xenograft models. An established mouse model of melanoma, the Cdkn2a -/-, Tyr-HRASG12V, was utilised in this study to obviate limitations posted by the usage of in vitro and xenograft models. 2017-07 Thesis NonPeerReviewed application/pdf en http://eprints.usm.my/45479/1/PHANG%20SU%20LING.pdf Phang,, Su Ling (2017) Defeciancy Of Puma And Noxa For Melanomagenesis In A Mouse Model Of Melanoma. Masters thesis, Universiti Sains Malaysia.
spellingShingle QH1 Natural history (General - Including nature conservation, geographical distribution)
Phang,, Su Ling
Defeciancy Of Puma And Noxa For Melanomagenesis In A Mouse Model Of Melanoma
title Defeciancy Of Puma And Noxa For Melanomagenesis In A Mouse Model Of Melanoma
title_full Defeciancy Of Puma And Noxa For Melanomagenesis In A Mouse Model Of Melanoma
title_fullStr Defeciancy Of Puma And Noxa For Melanomagenesis In A Mouse Model Of Melanoma
title_full_unstemmed Defeciancy Of Puma And Noxa For Melanomagenesis In A Mouse Model Of Melanoma
title_short Defeciancy Of Puma And Noxa For Melanomagenesis In A Mouse Model Of Melanoma
title_sort defeciancy of puma and noxa for melanomagenesis in a mouse model of melanoma
topic QH1 Natural history (General - Including nature conservation, geographical distribution)
url http://eprints.usm.my/45479/
http://eprints.usm.my/45479/1/PHANG%20SU%20LING.pdf