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-ep.454792019-09-19T01:05:11Z Defeciancy Of Puma And Noxa For Melanomagenesis In A Mouse Model Of Melanoma 2017-07 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 http://eprints.usm.my/45479/ http://eprints.usm.my/45479/1/PHANG%20SU%20LING.pdf application/pdf en public masters Universiti Sains Malaysia Pusat Pengajian Sains Kajihayat |
| institution |
Universiti Sains Malaysia |
| collection |
USM Institutional Repository |
| language |
English |
| topic |
QH1 Natural history (General - Including nature conservation geographical distribution) |
| 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 |
| 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. |
| format |
Thesis |
| qualification_level |
Master's degree |
| 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 |
| granting_institution |
Universiti Sains Malaysia |
| granting_department |
Pusat Pengajian Sains Kajihayat |
| publishDate |
2017 |
| url |
http://eprints.usm.my/45479/1/PHANG%20SU%20LING.pdf |
| _version_ |
1747821518884175872 |