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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2017
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my.usm.eprints.45479 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. |
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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 |
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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. |
format |
Thesis |
author |
Phang,, Su Ling |
author_facet |
Phang,, Su Ling |
author_sort |
Phang,, Su Ling |
title |
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_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_sort |
defeciancy of puma and noxa for melanomagenesis in a mouse model of melanoma |
publishDate |
2017 |
url |
http://eprints.usm.my/45479/1/PHANG%20SU%20LING.pdf http://eprints.usm.my/45479/ |
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1646011364491132928 |
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13.211869 |