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You searched for +publisher:"University of Hong Kong" +contributor:("Yao, KM"). Showing records 1 – 18 of 18 total matches.

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University of Hong Kong

1. 江家耀; Kong, Ka-yiu. Characterization of the roles of yeast nuclear exosome cofactor TRAMP complex in pre-mRNA splicing.

Degree: PhD, 2013, University of Hong Kong

In budding yeast, the Trf4/5p-Air1/2p-Mtr4p polyadenylation (TRAMP) complex recognizes unwanted RNA transcripts in the nucleus and then targets them to the nuclear exosome for rapid… (more)

Subjects/Keywords: Messenger RNA; Yeast - Molecular aspects

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APA (6th Edition):

江家耀; Kong, K. (2013). Characterization of the roles of yeast nuclear exosome cofactor TRAMP complex in pre-mRNA splicing. (Doctoral Dissertation). University of Hong Kong. Retrieved from Kong, K. [江家耀]. (2013). Characterization of the roles of yeast nuclear exosome cofactor TRAMP complex in pre-mRNA splicing. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5108671 ; http://dx.doi.org/10.5353/th_b5108671 ; http://hdl.handle.net/10722/193522

Chicago Manual of Style (16th Edition):

江家耀; Kong, Ka-yiu. “Characterization of the roles of yeast nuclear exosome cofactor TRAMP complex in pre-mRNA splicing.” 2013. Doctoral Dissertation, University of Hong Kong. Accessed August 18, 2019. Kong, K. [江家耀]. (2013). Characterization of the roles of yeast nuclear exosome cofactor TRAMP complex in pre-mRNA splicing. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5108671 ; http://dx.doi.org/10.5353/th_b5108671 ; http://hdl.handle.net/10722/193522.

MLA Handbook (7th Edition):

江家耀; Kong, Ka-yiu. “Characterization of the roles of yeast nuclear exosome cofactor TRAMP complex in pre-mRNA splicing.” 2013. Web. 18 Aug 2019.

Vancouver:

江家耀; Kong K. Characterization of the roles of yeast nuclear exosome cofactor TRAMP complex in pre-mRNA splicing. [Internet] [Doctoral dissertation]. University of Hong Kong; 2013. [cited 2019 Aug 18]. Available from: Kong, K. [江家耀]. (2013). Characterization of the roles of yeast nuclear exosome cofactor TRAMP complex in pre-mRNA splicing. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5108671 ; http://dx.doi.org/10.5353/th_b5108671 ; http://hdl.handle.net/10722/193522.

Council of Science Editors:

江家耀; Kong K. Characterization of the roles of yeast nuclear exosome cofactor TRAMP complex in pre-mRNA splicing. [Doctoral Dissertation]. University of Hong Kong; 2013. Available from: Kong, K. [江家耀]. (2013). Characterization of the roles of yeast nuclear exosome cofactor TRAMP complex in pre-mRNA splicing. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5108671 ; http://dx.doi.org/10.5353/th_b5108671 ; http://hdl.handle.net/10722/193522


University of Hong Kong

2. 郭倩婷.; Kwok, Sin-ting, Cindy. The role of SoxE transcription factors in melanoma development.

Degree: M. Phil., 2011, University of Hong Kong

Melanoma is a malignant type of skin cancer arising from the combined effects of genetic alteration and extrinsic signaling, resulting in transformation of neural crest… (more)

Subjects/Keywords: Melanoma - Genetic aspects.; Transcription factors.

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APA (6th Edition):

郭倩婷.; Kwok, Sin-ting, C. (2011). The role of SoxE transcription factors in melanoma development. (Masters Thesis). University of Hong Kong. Retrieved from Kwok, S. C. [郭倩婷]. (2011). The role of SoxE transcription factors in melanoma development. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4725107 ; http://dx.doi.org/10.5353/th_b4725107 ; http://hdl.handle.net/10722/146144

Chicago Manual of Style (16th Edition):

郭倩婷.; Kwok, Sin-ting, Cindy. “The role of SoxE transcription factors in melanoma development.” 2011. Masters Thesis, University of Hong Kong. Accessed August 18, 2019. Kwok, S. C. [郭倩婷]. (2011). The role of SoxE transcription factors in melanoma development. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4725107 ; http://dx.doi.org/10.5353/th_b4725107 ; http://hdl.handle.net/10722/146144.

MLA Handbook (7th Edition):

郭倩婷.; Kwok, Sin-ting, Cindy. “The role of SoxE transcription factors in melanoma development.” 2011. Web. 18 Aug 2019.

Vancouver:

郭倩婷.; Kwok, Sin-ting C. The role of SoxE transcription factors in melanoma development. [Internet] [Masters thesis]. University of Hong Kong; 2011. [cited 2019 Aug 18]. Available from: Kwok, S. C. [郭倩婷]. (2011). The role of SoxE transcription factors in melanoma development. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4725107 ; http://dx.doi.org/10.5353/th_b4725107 ; http://hdl.handle.net/10722/146144.

Council of Science Editors:

郭倩婷.; Kwok, Sin-ting C. The role of SoxE transcription factors in melanoma development. [Masters Thesis]. University of Hong Kong; 2011. Available from: Kwok, S. C. [郭倩婷]. (2011). The role of SoxE transcription factors in melanoma development. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4725107 ; http://dx.doi.org/10.5353/th_b4725107 ; http://hdl.handle.net/10722/146144


University of Hong Kong

3. Chong, Tsz-yat, Ian. Inducing the progressive differentiation of hESCs into pancreatic progenitor cells.

Degree: M. Phil., 2013, University of Hong Kong

 Diabetes is a chronic disorder of the pancreas, where a decline in the insulin-producing β-cell population disrupts metabolic homeostasis. Pancreatic transplantation has shown to be… (more)

Subjects/Keywords: Pancreatic beta cells; Embryonic stem cells

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APA (6th Edition):

Chong, Tsz-yat, I. (2013). Inducing the progressive differentiation of hESCs into pancreatic progenitor cells. (Masters Thesis). University of Hong Kong. Retrieved from Chong, T. I. [莊子逸]. (2013). Inducing the progressive differentiation of hESCs into pancreatic progenitor cells. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5177339 ; http://dx.doi.org/10.5353/th_b5177339 ; http://hdl.handle.net/10722/196433

Chicago Manual of Style (16th Edition):

Chong, Tsz-yat, Ian. “Inducing the progressive differentiation of hESCs into pancreatic progenitor cells.” 2013. Masters Thesis, University of Hong Kong. Accessed August 18, 2019. Chong, T. I. [莊子逸]. (2013). Inducing the progressive differentiation of hESCs into pancreatic progenitor cells. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5177339 ; http://dx.doi.org/10.5353/th_b5177339 ; http://hdl.handle.net/10722/196433.

MLA Handbook (7th Edition):

Chong, Tsz-yat, Ian. “Inducing the progressive differentiation of hESCs into pancreatic progenitor cells.” 2013. Web. 18 Aug 2019.

Vancouver:

Chong, Tsz-yat I. Inducing the progressive differentiation of hESCs into pancreatic progenitor cells. [Internet] [Masters thesis]. University of Hong Kong; 2013. [cited 2019 Aug 18]. Available from: Chong, T. I. [莊子逸]. (2013). Inducing the progressive differentiation of hESCs into pancreatic progenitor cells. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5177339 ; http://dx.doi.org/10.5353/th_b5177339 ; http://hdl.handle.net/10722/196433.

Council of Science Editors:

Chong, Tsz-yat I. Inducing the progressive differentiation of hESCs into pancreatic progenitor cells. [Masters Thesis]. University of Hong Kong; 2013. Available from: Chong, T. I. [莊子逸]. (2013). Inducing the progressive differentiation of hESCs into pancreatic progenitor cells. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5177339 ; http://dx.doi.org/10.5353/th_b5177339 ; http://hdl.handle.net/10722/196433


University of Hong Kong

4. 楊文龍.; Yeung, Man-lung. Proteolytic cleavage of PDZD2 generates a secreted peptide containing two PDZ domains.

Degree: PhD, 2003, University of Hong Kong

published_or_final_version

Biochemistry

Doctoral

Doctor of Philosophy

Advisors/Committee Members: Yao, KM.

Subjects/Keywords: RNA-protein interactions.; Peptides.; Proteins - Analysis

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APA (6th Edition):

楊文龍.; Yeung, M. (2003). Proteolytic cleavage of PDZD2 generates a secreted peptide containing two PDZ domains. (Doctoral Dissertation). University of Hong Kong. Retrieved from Yeung, M. [楊文龍]. (2003). Proteolytic cleavage of PDZD2 generates a secreted peptide containing two PDZ domains. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3124505 ; http://dx.doi.org/10.5353/th_b3124505 ; http://hdl.handle.net/10722/35695

Chicago Manual of Style (16th Edition):

楊文龍.; Yeung, Man-lung. “Proteolytic cleavage of PDZD2 generates a secreted peptide containing two PDZ domains.” 2003. Doctoral Dissertation, University of Hong Kong. Accessed August 18, 2019. Yeung, M. [楊文龍]. (2003). Proteolytic cleavage of PDZD2 generates a secreted peptide containing two PDZ domains. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3124505 ; http://dx.doi.org/10.5353/th_b3124505 ; http://hdl.handle.net/10722/35695.

MLA Handbook (7th Edition):

楊文龍.; Yeung, Man-lung. “Proteolytic cleavage of PDZD2 generates a secreted peptide containing two PDZ domains.” 2003. Web. 18 Aug 2019.

Vancouver:

楊文龍.; Yeung M. Proteolytic cleavage of PDZD2 generates a secreted peptide containing two PDZ domains. [Internet] [Doctoral dissertation]. University of Hong Kong; 2003. [cited 2019 Aug 18]. Available from: Yeung, M. [楊文龍]. (2003). Proteolytic cleavage of PDZD2 generates a secreted peptide containing two PDZ domains. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3124505 ; http://dx.doi.org/10.5353/th_b3124505 ; http://hdl.handle.net/10722/35695.

Council of Science Editors:

楊文龍.; Yeung M. Proteolytic cleavage of PDZD2 generates a secreted peptide containing two PDZ domains. [Doctoral Dissertation]. University of Hong Kong; 2003. Available from: Yeung, M. [楊文龍]. (2003). Proteolytic cleavage of PDZD2 generates a secreted peptide containing two PDZ domains. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3124505 ; http://dx.doi.org/10.5353/th_b3124505 ; http://hdl.handle.net/10722/35695


University of Hong Kong

5. 程子忻.; Ching, Chi-yun, Johannes. Transcriptional regulation of p16INK4a expression by the forkhead box transcription factor FOXM1.

Degree: M. Phil., 2003, University of Hong Kong

abstract

toc

published_or_final_version

Biochemistry

Master

Master of Philosophy

Advisors/Committee Members: Yao, KM.

Subjects/Keywords: Transcription factors.; Cyclin-dependent kinases.; Genetic regulation.

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APA (6th Edition):

程子忻.; Ching, Chi-yun, J. (2003). Transcriptional regulation of p16INK4a expression by the forkhead box transcription factor FOXM1. (Masters Thesis). University of Hong Kong. Retrieved from Ching, C. J. [程子忻]. (2003). Transcriptional regulation of p16INK4a expression by the forkhead box transcription factor FOXM1. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b2946619 ; http://dx.doi.org/10.5353/th_b2946619 ; http://hdl.handle.net/10722/30757

Chicago Manual of Style (16th Edition):

程子忻.; Ching, Chi-yun, Johannes. “Transcriptional regulation of p16INK4a expression by the forkhead box transcription factor FOXM1.” 2003. Masters Thesis, University of Hong Kong. Accessed August 18, 2019. Ching, C. J. [程子忻]. (2003). Transcriptional regulation of p16INK4a expression by the forkhead box transcription factor FOXM1. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b2946619 ; http://dx.doi.org/10.5353/th_b2946619 ; http://hdl.handle.net/10722/30757.

MLA Handbook (7th Edition):

程子忻.; Ching, Chi-yun, Johannes. “Transcriptional regulation of p16INK4a expression by the forkhead box transcription factor FOXM1.” 2003. Web. 18 Aug 2019.

Vancouver:

程子忻.; Ching, Chi-yun J. Transcriptional regulation of p16INK4a expression by the forkhead box transcription factor FOXM1. [Internet] [Masters thesis]. University of Hong Kong; 2003. [cited 2019 Aug 18]. Available from: Ching, C. J. [程子忻]. (2003). Transcriptional regulation of p16INK4a expression by the forkhead box transcription factor FOXM1. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b2946619 ; http://dx.doi.org/10.5353/th_b2946619 ; http://hdl.handle.net/10722/30757.

Council of Science Editors:

程子忻.; Ching, Chi-yun J. Transcriptional regulation of p16INK4a expression by the forkhead box transcription factor FOXM1. [Masters Thesis]. University of Hong Kong; 2003. Available from: Ching, C. J. [程子忻]. (2003). Transcriptional regulation of p16INK4a expression by the forkhead box transcription factor FOXM1. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b2946619 ; http://dx.doi.org/10.5353/th_b2946619 ; http://hdl.handle.net/10722/30757


University of Hong Kong

6. Cheung, Man-sze. Investigating the role of FoxM1 in cell cycle progression by inducibleRNA interference.

Degree: M. Phil., 2004, University of Hong Kong

published_or_final_version

toc

abstract

Biochemistry

Master

Master of Philosophy

Advisors/Committee Members: Yao, KM.

Subjects/Keywords: Small interfering RNA.; Cell cycle.; Transcription factors.

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APA (6th Edition):

Cheung, M. (2004). Investigating the role of FoxM1 in cell cycle progression by inducibleRNA interference. (Masters Thesis). University of Hong Kong. Retrieved from Cheung, M. [張敏思]. (2004). Investigating the role of FoxM1 in cell cycle progression by inducible RNA interference. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3039640 ; http://dx.doi.org/10.5353/th_b3039640 ; http://hdl.handle.net/10722/32059

Chicago Manual of Style (16th Edition):

Cheung, Man-sze. “Investigating the role of FoxM1 in cell cycle progression by inducibleRNA interference.” 2004. Masters Thesis, University of Hong Kong. Accessed August 18, 2019. Cheung, M. [張敏思]. (2004). Investigating the role of FoxM1 in cell cycle progression by inducible RNA interference. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3039640 ; http://dx.doi.org/10.5353/th_b3039640 ; http://hdl.handle.net/10722/32059.

MLA Handbook (7th Edition):

Cheung, Man-sze. “Investigating the role of FoxM1 in cell cycle progression by inducibleRNA interference.” 2004. Web. 18 Aug 2019.

Vancouver:

Cheung M. Investigating the role of FoxM1 in cell cycle progression by inducibleRNA interference. [Internet] [Masters thesis]. University of Hong Kong; 2004. [cited 2019 Aug 18]. Available from: Cheung, M. [張敏思]. (2004). Investigating the role of FoxM1 in cell cycle progression by inducible RNA interference. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3039640 ; http://dx.doi.org/10.5353/th_b3039640 ; http://hdl.handle.net/10722/32059.

Council of Science Editors:

Cheung M. Investigating the role of FoxM1 in cell cycle progression by inducibleRNA interference. [Masters Thesis]. University of Hong Kong; 2004. Available from: Cheung, M. [張敏思]. (2004). Investigating the role of FoxM1 in cell cycle progression by inducible RNA interference. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3039640 ; http://dx.doi.org/10.5353/th_b3039640 ; http://hdl.handle.net/10722/32059


University of Hong Kong

7. Tsang, Siu-wai. Involvement of Pdzd2 in the regulation of pancreatic beta-cell functions.

Degree: PhD, 2007, University of Hong Kong

published_or_final_version

Biochemistry

Doctoral

Doctor of Philosophy

Advisors/Committee Members: Yao, KM.

Subjects/Keywords: Proteins.; Pancreatic beta cells.

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APA (6th Edition):

Tsang, S. (2007). Involvement of Pdzd2 in the regulation of pancreatic beta-cell functions. (Doctoral Dissertation). University of Hong Kong. Retrieved from Tsang, S. [曾少慧]. (2007). Involvement of Pdzd2 in the regulation of pancreatic beta-cell functions. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3979374 ; http://dx.doi.org/10.5353/th_b3979374 ; http://hdl.handle.net/10722/54494

Chicago Manual of Style (16th Edition):

Tsang, Siu-wai. “Involvement of Pdzd2 in the regulation of pancreatic beta-cell functions.” 2007. Doctoral Dissertation, University of Hong Kong. Accessed August 18, 2019. Tsang, S. [曾少慧]. (2007). Involvement of Pdzd2 in the regulation of pancreatic beta-cell functions. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3979374 ; http://dx.doi.org/10.5353/th_b3979374 ; http://hdl.handle.net/10722/54494.

MLA Handbook (7th Edition):

Tsang, Siu-wai. “Involvement of Pdzd2 in the regulation of pancreatic beta-cell functions.” 2007. Web. 18 Aug 2019.

Vancouver:

Tsang S. Involvement of Pdzd2 in the regulation of pancreatic beta-cell functions. [Internet] [Doctoral dissertation]. University of Hong Kong; 2007. [cited 2019 Aug 18]. Available from: Tsang, S. [曾少慧]. (2007). Involvement of Pdzd2 in the regulation of pancreatic beta-cell functions. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3979374 ; http://dx.doi.org/10.5353/th_b3979374 ; http://hdl.handle.net/10722/54494.

Council of Science Editors:

Tsang S. Involvement of Pdzd2 in the regulation of pancreatic beta-cell functions. [Doctoral Dissertation]. University of Hong Kong; 2007. Available from: Tsang, S. [曾少慧]. (2007). Involvement of Pdzd2 in the regulation of pancreatic beta-cell functions. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3979374 ; http://dx.doi.org/10.5353/th_b3979374 ; http://hdl.handle.net/10722/54494


University of Hong Kong

8. Ma, Yam-man, Richard. The mitogen-activated protein kinase pathway regulates the subcellularlocalization and function of FOXM1.

Degree: M. Phil., 2003, University of Hong Kong

published_or_final_version

toc

abstract

Biochemistry

Master

Master of Philosophy

Advisors/Committee Members: Yao, KM, Wong, NS.

Subjects/Keywords: Genetic regulation.; Transcription factors.; Cellular signal transduction.; Protein kinases.

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APA (6th Edition):

Ma, Yam-man, R. (2003). The mitogen-activated protein kinase pathway regulates the subcellularlocalization and function of FOXM1. (Masters Thesis). University of Hong Kong. Retrieved from Ma, Y. R. [馬蔭民]. (2003). The mitogen-activated protein kinase pathway regulates the subcellular localization and function of FOXM1. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b2930537 ; http://dx.doi.org/10.5353/th_b2930537 ; http://hdl.handle.net/10722/30556

Chicago Manual of Style (16th Edition):

Ma, Yam-man, Richard. “The mitogen-activated protein kinase pathway regulates the subcellularlocalization and function of FOXM1.” 2003. Masters Thesis, University of Hong Kong. Accessed August 18, 2019. Ma, Y. R. [馬蔭民]. (2003). The mitogen-activated protein kinase pathway regulates the subcellular localization and function of FOXM1. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b2930537 ; http://dx.doi.org/10.5353/th_b2930537 ; http://hdl.handle.net/10722/30556.

MLA Handbook (7th Edition):

Ma, Yam-man, Richard. “The mitogen-activated protein kinase pathway regulates the subcellularlocalization and function of FOXM1.” 2003. Web. 18 Aug 2019.

Vancouver:

Ma, Yam-man R. The mitogen-activated protein kinase pathway regulates the subcellularlocalization and function of FOXM1. [Internet] [Masters thesis]. University of Hong Kong; 2003. [cited 2019 Aug 18]. Available from: Ma, Y. R. [馬蔭民]. (2003). The mitogen-activated protein kinase pathway regulates the subcellular localization and function of FOXM1. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b2930537 ; http://dx.doi.org/10.5353/th_b2930537 ; http://hdl.handle.net/10722/30556.

Council of Science Editors:

Ma, Yam-man R. The mitogen-activated protein kinase pathway regulates the subcellularlocalization and function of FOXM1. [Masters Thesis]. University of Hong Kong; 2003. Available from: Ma, Y. R. [馬蔭民]. (2003). The mitogen-activated protein kinase pathway regulates the subcellular localization and function of FOXM1. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b2930537 ; http://dx.doi.org/10.5353/th_b2930537 ; http://hdl.handle.net/10722/30556


University of Hong Kong

9. Tam, Siu-man, Tammy. Study of sPDZD2 function using in vitro and in vivo approaches.

Degree: M. Phil., 2004, University of Hong Kong

toc

abstract

published_or_final_version

Biochemistry

Master

Master of Philosophy

Advisors/Committee Members: Yao, KM, Chung, SK.

Subjects/Keywords: Carrier proteins.

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APA (6th Edition):

Tam, Siu-man, T. (2004). Study of sPDZD2 function using in vitro and in vivo approaches. (Masters Thesis). University of Hong Kong. Retrieved from Tam, S. T. [談少雯]. (2004). Study of sPDZD2 function using in vitro and in vivo approaches. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3039669 ; http://dx.doi.org/10.5353/th_b3039669 ; http://hdl.handle.net/10722/31726

Chicago Manual of Style (16th Edition):

Tam, Siu-man, Tammy. “Study of sPDZD2 function using in vitro and in vivo approaches.” 2004. Masters Thesis, University of Hong Kong. Accessed August 18, 2019. Tam, S. T. [談少雯]. (2004). Study of sPDZD2 function using in vitro and in vivo approaches. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3039669 ; http://dx.doi.org/10.5353/th_b3039669 ; http://hdl.handle.net/10722/31726.

MLA Handbook (7th Edition):

Tam, Siu-man, Tammy. “Study of sPDZD2 function using in vitro and in vivo approaches.” 2004. Web. 18 Aug 2019.

Vancouver:

Tam, Siu-man T. Study of sPDZD2 function using in vitro and in vivo approaches. [Internet] [Masters thesis]. University of Hong Kong; 2004. [cited 2019 Aug 18]. Available from: Tam, S. T. [談少雯]. (2004). Study of sPDZD2 function using in vitro and in vivo approaches. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3039669 ; http://dx.doi.org/10.5353/th_b3039669 ; http://hdl.handle.net/10722/31726.

Council of Science Editors:

Tam, Siu-man T. Study of sPDZD2 function using in vitro and in vivo approaches. [Masters Thesis]. University of Hong Kong; 2004. Available from: Tam, S. T. [談少雯]. (2004). Study of sPDZD2 function using in vitro and in vivo approaches. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3039669 ; http://dx.doi.org/10.5353/th_b3039669 ; http://hdl.handle.net/10722/31726


University of Hong Kong

10. 錢景彤.; Chin, King-tung, Tony. Functional characterization of the liver-enriched transcription factorCREB-H.

Degree: PhD, 2005, University of Hong Kong

published_or_final_version

abstract

Biochemistry

Doctoral

Doctor of Philosophy

Advisors/Committee Members: Yao, KM, Jin, D.

Subjects/Keywords: Genetic regulation.; Albumins.; Transcription factors.; DNA-binding proteins.

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APA (6th Edition):

錢景彤.; Chin, King-tung, T. (2005). Functional characterization of the liver-enriched transcription factorCREB-H. (Doctoral Dissertation). University of Hong Kong. Retrieved from Chin, K. T. [錢景彤]. (2005). Functional characterization of the liver-enriched transcription factor CREB-H. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3167323 ; http://dx.doi.org/10.5353/th_b3167323 ; http://hdl.handle.net/10722/40281

Chicago Manual of Style (16th Edition):

錢景彤.; Chin, King-tung, Tony. “Functional characterization of the liver-enriched transcription factorCREB-H.” 2005. Doctoral Dissertation, University of Hong Kong. Accessed August 18, 2019. Chin, K. T. [錢景彤]. (2005). Functional characterization of the liver-enriched transcription factor CREB-H. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3167323 ; http://dx.doi.org/10.5353/th_b3167323 ; http://hdl.handle.net/10722/40281.

MLA Handbook (7th Edition):

錢景彤.; Chin, King-tung, Tony. “Functional characterization of the liver-enriched transcription factorCREB-H.” 2005. Web. 18 Aug 2019.

Vancouver:

錢景彤.; Chin, King-tung T. Functional characterization of the liver-enriched transcription factorCREB-H. [Internet] [Doctoral dissertation]. University of Hong Kong; 2005. [cited 2019 Aug 18]. Available from: Chin, K. T. [錢景彤]. (2005). Functional characterization of the liver-enriched transcription factor CREB-H. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3167323 ; http://dx.doi.org/10.5353/th_b3167323 ; http://hdl.handle.net/10722/40281.

Council of Science Editors:

錢景彤.; Chin, King-tung T. Functional characterization of the liver-enriched transcription factorCREB-H. [Doctoral Dissertation]. University of Hong Kong; 2005. Available from: Chin, K. T. [錢景彤]. (2005). Functional characterization of the liver-enriched transcription factor CREB-H. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3167323 ; http://dx.doi.org/10.5353/th_b3167323 ; http://hdl.handle.net/10722/40281


University of Hong Kong

11. Tong, Ho-kwan. Functional regulation of the forkhead box M1 transcription factor by Raf/MEK/MAPK signaling.

Degree: M. Phil., 2006, University of Hong Kong

abstract

published_or_final_version

Biochemistry

Master

Master of Philosophy

Advisors/Committee Members: Wong, NS, Yao, KM.

Subjects/Keywords: Mitogen-activated protein kinases.; Cellular signal transduction.; Cell proliferation.; Transcription factors.

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APA (6th Edition):

Tong, H. (2006). Functional regulation of the forkhead box M1 transcription factor by Raf/MEK/MAPK signaling. (Masters Thesis). University of Hong Kong. Retrieved from Tong, H. [湯皓鈞]. (2006). Functional regulation of the forkhead box M1 transcription factor by Raf/MEK/MAPK signaling. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3765459 ; http://dx.doi.org/10.5353/th_b3765459 ; http://hdl.handle.net/10722/50186

Chicago Manual of Style (16th Edition):

Tong, Ho-kwan. “Functional regulation of the forkhead box M1 transcription factor by Raf/MEK/MAPK signaling.” 2006. Masters Thesis, University of Hong Kong. Accessed August 18, 2019. Tong, H. [湯皓鈞]. (2006). Functional regulation of the forkhead box M1 transcription factor by Raf/MEK/MAPK signaling. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3765459 ; http://dx.doi.org/10.5353/th_b3765459 ; http://hdl.handle.net/10722/50186.

MLA Handbook (7th Edition):

Tong, Ho-kwan. “Functional regulation of the forkhead box M1 transcription factor by Raf/MEK/MAPK signaling.” 2006. Web. 18 Aug 2019.

Vancouver:

Tong H. Functional regulation of the forkhead box M1 transcription factor by Raf/MEK/MAPK signaling. [Internet] [Masters thesis]. University of Hong Kong; 2006. [cited 2019 Aug 18]. Available from: Tong, H. [湯皓鈞]. (2006). Functional regulation of the forkhead box M1 transcription factor by Raf/MEK/MAPK signaling. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3765459 ; http://dx.doi.org/10.5353/th_b3765459 ; http://hdl.handle.net/10722/50186.

Council of Science Editors:

Tong H. Functional regulation of the forkhead box M1 transcription factor by Raf/MEK/MAPK signaling. [Masters Thesis]. University of Hong Kong; 2006. Available from: Tong, H. [湯皓鈞]. (2006). Functional regulation of the forkhead box M1 transcription factor by Raf/MEK/MAPK signaling. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3765459 ; http://dx.doi.org/10.5353/th_b3765459 ; http://hdl.handle.net/10722/50186


University of Hong Kong

12. Kok, Kin-hang. Roles of human double-stranded RNA binding proteins TRBP and PACT in RNA interference.

Degree: PhD, 2006, University of Hong Kong

published_or_final_version

abstract

Biochemistry

Doctoral

Doctor of Philosophy

Advisors/Committee Members: Yao, KM, Jin, D.

Subjects/Keywords: Carrier proteins.; Gene silencing.; Nucleoproteins.; RNA-protein interactions.

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APA (6th Edition):

Kok, K. (2006). Roles of human double-stranded RNA binding proteins TRBP and PACT in RNA interference. (Doctoral Dissertation). University of Hong Kong. Retrieved from Kok, K. [郭健恆]. (2006). Roles of human double-stranded RNA binding proteins TRBP and PACT in RNA interference. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3852321 ; http://dx.doi.org/10.5353/th_b3852321 ; http://hdl.handle.net/10722/50196

Chicago Manual of Style (16th Edition):

Kok, Kin-hang. “Roles of human double-stranded RNA binding proteins TRBP and PACT in RNA interference.” 2006. Doctoral Dissertation, University of Hong Kong. Accessed August 18, 2019. Kok, K. [郭健恆]. (2006). Roles of human double-stranded RNA binding proteins TRBP and PACT in RNA interference. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3852321 ; http://dx.doi.org/10.5353/th_b3852321 ; http://hdl.handle.net/10722/50196.

MLA Handbook (7th Edition):

Kok, Kin-hang. “Roles of human double-stranded RNA binding proteins TRBP and PACT in RNA interference.” 2006. Web. 18 Aug 2019.

Vancouver:

Kok K. Roles of human double-stranded RNA binding proteins TRBP and PACT in RNA interference. [Internet] [Doctoral dissertation]. University of Hong Kong; 2006. [cited 2019 Aug 18]. Available from: Kok, K. [郭健恆]. (2006). Roles of human double-stranded RNA binding proteins TRBP and PACT in RNA interference. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3852321 ; http://dx.doi.org/10.5353/th_b3852321 ; http://hdl.handle.net/10722/50196.

Council of Science Editors:

Kok K. Roles of human double-stranded RNA binding proteins TRBP and PACT in RNA interference. [Doctoral Dissertation]. University of Hong Kong; 2006. Available from: Kok, K. [郭健恆]. (2006). Roles of human double-stranded RNA binding proteins TRBP and PACT in RNA interference. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3852321 ; http://dx.doi.org/10.5353/th_b3852321 ; http://hdl.handle.net/10722/50196


University of Hong Kong

13. Tam, Chun-wai. Secreted PDZ domain-containing protein 2 (sPDZD2): a potential autocrine tumor suppressor.

Degree: PhD, 2007, University of Hong Kong

abstract

published_or_final_version

Physiology

Doctoral

Doctor of Philosophy

Advisors/Committee Members: Yao, KM, Shiu, SYW.

Subjects/Keywords: Cancer cells - Growth.; Prostate - Cancer - Genetic aspects.; Apoptosis.; Antioncogenes

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APA (6th Edition):

Tam, C. (2007). Secreted PDZ domain-containing protein 2 (sPDZD2): a potential autocrine tumor suppressor. (Doctoral Dissertation). University of Hong Kong. Retrieved from Tam, C. [談振偉]. (2007). Secreted PDZ domain-containing protein 2 (sPDZD2) : a potential autocrine tumor suppressor. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3955737 ; http://dx.doi.org/10.5353/th_b3955737 ; http://hdl.handle.net/10722/52400

Chicago Manual of Style (16th Edition):

Tam, Chun-wai. “Secreted PDZ domain-containing protein 2 (sPDZD2): a potential autocrine tumor suppressor.” 2007. Doctoral Dissertation, University of Hong Kong. Accessed August 18, 2019. Tam, C. [談振偉]. (2007). Secreted PDZ domain-containing protein 2 (sPDZD2) : a potential autocrine tumor suppressor. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3955737 ; http://dx.doi.org/10.5353/th_b3955737 ; http://hdl.handle.net/10722/52400.

MLA Handbook (7th Edition):

Tam, Chun-wai. “Secreted PDZ domain-containing protein 2 (sPDZD2): a potential autocrine tumor suppressor.” 2007. Web. 18 Aug 2019.

Vancouver:

Tam C. Secreted PDZ domain-containing protein 2 (sPDZD2): a potential autocrine tumor suppressor. [Internet] [Doctoral dissertation]. University of Hong Kong; 2007. [cited 2019 Aug 18]. Available from: Tam, C. [談振偉]. (2007). Secreted PDZ domain-containing protein 2 (sPDZD2) : a potential autocrine tumor suppressor. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3955737 ; http://dx.doi.org/10.5353/th_b3955737 ; http://hdl.handle.net/10722/52400.

Council of Science Editors:

Tam C. Secreted PDZ domain-containing protein 2 (sPDZD2): a potential autocrine tumor suppressor. [Doctoral Dissertation]. University of Hong Kong; 2007. Available from: Tam, C. [談振偉]. (2007). Secreted PDZ domain-containing protein 2 (sPDZD2) : a potential autocrine tumor suppressor. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3955737 ; http://dx.doi.org/10.5353/th_b3955737 ; http://hdl.handle.net/10722/52400


University of Hong Kong

14. Cheng, Shan, Amy. Structure-function studies of secreted PDZ domain-containing protein 2(sPDZD2).

Degree: M. Phil., 2007, University of Hong Kong

abstract

published_or_final_version

Physiology

Master

Master of Philosophy

Advisors/Committee Members: Shiu, SYW, Yao, KM.

Subjects/Keywords: Recombinant proteins.; Cancer cells - Proliferation.; Prostate - Cancer.

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APA (6th Edition):

Cheng, Shan, A. (2007). Structure-function studies of secreted PDZ domain-containing protein 2(sPDZD2). (Masters Thesis). University of Hong Kong. Retrieved from Cheng, S. A. [鄭珊]. (2007). Structure-function studies of secreted PDZ domain-containing protein 2 (sPDZD2). (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3955810 ; http://dx.doi.org/10.5353/th_b3955810 ; http://hdl.handle.net/10722/52405

Chicago Manual of Style (16th Edition):

Cheng, Shan, Amy. “Structure-function studies of secreted PDZ domain-containing protein 2(sPDZD2).” 2007. Masters Thesis, University of Hong Kong. Accessed August 18, 2019. Cheng, S. A. [鄭珊]. (2007). Structure-function studies of secreted PDZ domain-containing protein 2 (sPDZD2). (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3955810 ; http://dx.doi.org/10.5353/th_b3955810 ; http://hdl.handle.net/10722/52405.

MLA Handbook (7th Edition):

Cheng, Shan, Amy. “Structure-function studies of secreted PDZ domain-containing protein 2(sPDZD2).” 2007. Web. 18 Aug 2019.

Vancouver:

Cheng, Shan A. Structure-function studies of secreted PDZ domain-containing protein 2(sPDZD2). [Internet] [Masters thesis]. University of Hong Kong; 2007. [cited 2019 Aug 18]. Available from: Cheng, S. A. [鄭珊]. (2007). Structure-function studies of secreted PDZ domain-containing protein 2 (sPDZD2). (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3955810 ; http://dx.doi.org/10.5353/th_b3955810 ; http://hdl.handle.net/10722/52405.

Council of Science Editors:

Cheng, Shan A. Structure-function studies of secreted PDZ domain-containing protein 2(sPDZD2). [Masters Thesis]. University of Hong Kong; 2007. Available from: Cheng, S. A. [鄭珊]. (2007). Structure-function studies of secreted PDZ domain-containing protein 2 (sPDZD2). (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3955810 ; http://dx.doi.org/10.5353/th_b3955810 ; http://hdl.handle.net/10722/52405


University of Hong Kong

15. 黎威龍.; Lai, Wai-lung. The role of unfolded protein response in the cytotoxicity mechanism ofN-(4-hydroxyphenyl)retinamide.

Degree: PhD, 2008, University of Hong Kong

published_or_final_version

Biochemistry

Doctoral

Doctor of Philosophy

Advisors/Committee Members: Yao, KM, Wong, NS.

Subjects/Keywords: Protein folding.; Eukaryotic cells.; Retinoids.

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APA (6th Edition):

黎威龍.; Lai, W. (2008). The role of unfolded protein response in the cytotoxicity mechanism ofN-(4-hydroxyphenyl)retinamide. (Doctoral Dissertation). University of Hong Kong. Retrieved from Lai, W. [黎威龍]. (2008). The role of unfolded protein response in the cytotoxicity mechanism of N-(4-hydroxyphenyl)retinamide. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3979392 ; http://dx.doi.org/10.5353/th_b3979392 ; http://hdl.handle.net/10722/54495

Chicago Manual of Style (16th Edition):

黎威龍.; Lai, Wai-lung. “The role of unfolded protein response in the cytotoxicity mechanism ofN-(4-hydroxyphenyl)retinamide.” 2008. Doctoral Dissertation, University of Hong Kong. Accessed August 18, 2019. Lai, W. [黎威龍]. (2008). The role of unfolded protein response in the cytotoxicity mechanism of N-(4-hydroxyphenyl)retinamide. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3979392 ; http://dx.doi.org/10.5353/th_b3979392 ; http://hdl.handle.net/10722/54495.

MLA Handbook (7th Edition):

黎威龍.; Lai, Wai-lung. “The role of unfolded protein response in the cytotoxicity mechanism ofN-(4-hydroxyphenyl)retinamide.” 2008. Web. 18 Aug 2019.

Vancouver:

黎威龍.; Lai W. The role of unfolded protein response in the cytotoxicity mechanism ofN-(4-hydroxyphenyl)retinamide. [Internet] [Doctoral dissertation]. University of Hong Kong; 2008. [cited 2019 Aug 18]. Available from: Lai, W. [黎威龍]. (2008). The role of unfolded protein response in the cytotoxicity mechanism of N-(4-hydroxyphenyl)retinamide. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3979392 ; http://dx.doi.org/10.5353/th_b3979392 ; http://hdl.handle.net/10722/54495.

Council of Science Editors:

黎威龍.; Lai W. The role of unfolded protein response in the cytotoxicity mechanism ofN-(4-hydroxyphenyl)retinamide. [Doctoral Dissertation]. University of Hong Kong; 2008. Available from: Lai, W. [黎威龍]. (2008). The role of unfolded protein response in the cytotoxicity mechanism of N-(4-hydroxyphenyl)retinamide. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3979392 ; http://dx.doi.org/10.5353/th_b3979392 ; http://hdl.handle.net/10722/54495


University of Hong Kong

16. Pang, Bo. Antiproliferative actions of melatonin and secreted PDZ domain-containing protein 2 (sPDZD2) on tumor cells.

Degree: M. Phil., 2009, University of Hong Kong

published_or_final_version

Physiology

Master

Master of Philosophy

Advisors/Committee Members: Yao, KM, Shiu, SYW.

Subjects/Keywords: Prostate - Cancer - Molecular aspects.; Antioncogenes.; Melatonin.; Cancer cells - Growth - Regulation.

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APA (6th Edition):

Pang, B. (2009). Antiproliferative actions of melatonin and secreted PDZ domain-containing protein 2 (sPDZD2) on tumor cells. (Masters Thesis). University of Hong Kong. Retrieved from Pang, B. [龐博]. (2009). Antiproliferative actions of melatonin and secreted PDZ domain-containing protein 2 (sPDZD2) on tumor cells. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4322406 ; http://dx.doi.org/10.5353/th_b4322406 ; http://hdl.handle.net/10722/56785

Chicago Manual of Style (16th Edition):

Pang, Bo. “Antiproliferative actions of melatonin and secreted PDZ domain-containing protein 2 (sPDZD2) on tumor cells.” 2009. Masters Thesis, University of Hong Kong. Accessed August 18, 2019. Pang, B. [龐博]. (2009). Antiproliferative actions of melatonin and secreted PDZ domain-containing protein 2 (sPDZD2) on tumor cells. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4322406 ; http://dx.doi.org/10.5353/th_b4322406 ; http://hdl.handle.net/10722/56785.

MLA Handbook (7th Edition):

Pang, Bo. “Antiproliferative actions of melatonin and secreted PDZ domain-containing protein 2 (sPDZD2) on tumor cells.” 2009. Web. 18 Aug 2019.

Vancouver:

Pang B. Antiproliferative actions of melatonin and secreted PDZ domain-containing protein 2 (sPDZD2) on tumor cells. [Internet] [Masters thesis]. University of Hong Kong; 2009. [cited 2019 Aug 18]. Available from: Pang, B. [龐博]. (2009). Antiproliferative actions of melatonin and secreted PDZ domain-containing protein 2 (sPDZD2) on tumor cells. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4322406 ; http://dx.doi.org/10.5353/th_b4322406 ; http://hdl.handle.net/10722/56785.

Council of Science Editors:

Pang B. Antiproliferative actions of melatonin and secreted PDZ domain-containing protein 2 (sPDZD2) on tumor cells. [Masters Thesis]. University of Hong Kong; 2009. Available from: Pang, B. [龐博]. (2009). Antiproliferative actions of melatonin and secreted PDZ domain-containing protein 2 (sPDZD2) on tumor cells. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4322406 ; http://dx.doi.org/10.5353/th_b4322406 ; http://hdl.handle.net/10722/56785


University of Hong Kong

17. Lam, King-yin, Andy. Differential regulation of FOXM1 isoforms by RaF/MEK/ERK signaling.

Degree: M. Phil., 2010, University of Hong Kong

published_or_final_version

Biochemistry

Master

Master of Philosophy

Advisors/Committee Members: Shiu, SYW, Yao, KM.

Subjects/Keywords: Transcription factors.; Cellular signal transduction.; Mitogen-activated protein kinases.

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APA (6th Edition):

Lam, King-yin, A. (2010). Differential regulation of FOXM1 isoforms by RaF/MEK/ERK signaling. (Masters Thesis). University of Hong Kong. Retrieved from Lam, K. A. [林敬賢]. (2010). Differential regulation of FOXM1 isoforms by RaF/MEK/ERK signaling. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4425101 ; http://dx.doi.org/10.5353/th_b4425101 ; http://hdl.handle.net/10722/65109

Chicago Manual of Style (16th Edition):

Lam, King-yin, Andy. “Differential regulation of FOXM1 isoforms by RaF/MEK/ERK signaling.” 2010. Masters Thesis, University of Hong Kong. Accessed August 18, 2019. Lam, K. A. [林敬賢]. (2010). Differential regulation of FOXM1 isoforms by RaF/MEK/ERK signaling. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4425101 ; http://dx.doi.org/10.5353/th_b4425101 ; http://hdl.handle.net/10722/65109.

MLA Handbook (7th Edition):

Lam, King-yin, Andy. “Differential regulation of FOXM1 isoforms by RaF/MEK/ERK signaling.” 2010. Web. 18 Aug 2019.

Vancouver:

Lam, King-yin A. Differential regulation of FOXM1 isoforms by RaF/MEK/ERK signaling. [Internet] [Masters thesis]. University of Hong Kong; 2010. [cited 2019 Aug 18]. Available from: Lam, K. A. [林敬賢]. (2010). Differential regulation of FOXM1 isoforms by RaF/MEK/ERK signaling. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4425101 ; http://dx.doi.org/10.5353/th_b4425101 ; http://hdl.handle.net/10722/65109.

Council of Science Editors:

Lam, King-yin A. Differential regulation of FOXM1 isoforms by RaF/MEK/ERK signaling. [Masters Thesis]. University of Hong Kong; 2010. Available from: Lam, K. A. [林敬賢]. (2010). Differential regulation of FOXM1 isoforms by RaF/MEK/ERK signaling. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4425101 ; http://dx.doi.org/10.5353/th_b4425101 ; http://hdl.handle.net/10722/65109


University of Hong Kong

18. 蔡美儀.; Choi, Mei-yee. Functional studies on sedlin and its involvement in spondyloepiphysealdysplasia tarda.

Degree: PhD, 2008, University of Hong Kong

published_or_final_version

Biochemistry

Doctoral

Doctor of Philosophy

Advisors/Committee Members: Yao, KM, Chan, D, Tanner, JA.

Subjects/Keywords: Bones - Abnormalities - Genetic aspects.; Dwarfism - Genetic aspects.; Mutation (Biology)

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APA (6th Edition):

蔡美儀.; Choi, M. (2008). Functional studies on sedlin and its involvement in spondyloepiphysealdysplasia tarda. (Doctoral Dissertation). University of Hong Kong. Retrieved from Choi, M. [蔡美儀]. (2008). Functional studies on sedlin and its involvement in spondyloepiphyseal dysplasia tarda. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4129054 ; http://dx.doi.org/10.5353/th_b4129054 ; http://hdl.handle.net/10722/50191

Chicago Manual of Style (16th Edition):

蔡美儀.; Choi, Mei-yee. “Functional studies on sedlin and its involvement in spondyloepiphysealdysplasia tarda.” 2008. Doctoral Dissertation, University of Hong Kong. Accessed August 18, 2019. Choi, M. [蔡美儀]. (2008). Functional studies on sedlin and its involvement in spondyloepiphyseal dysplasia tarda. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4129054 ; http://dx.doi.org/10.5353/th_b4129054 ; http://hdl.handle.net/10722/50191.

MLA Handbook (7th Edition):

蔡美儀.; Choi, Mei-yee. “Functional studies on sedlin and its involvement in spondyloepiphysealdysplasia tarda.” 2008. Web. 18 Aug 2019.

Vancouver:

蔡美儀.; Choi M. Functional studies on sedlin and its involvement in spondyloepiphysealdysplasia tarda. [Internet] [Doctoral dissertation]. University of Hong Kong; 2008. [cited 2019 Aug 18]. Available from: Choi, M. [蔡美儀]. (2008). Functional studies on sedlin and its involvement in spondyloepiphyseal dysplasia tarda. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4129054 ; http://dx.doi.org/10.5353/th_b4129054 ; http://hdl.handle.net/10722/50191.

Council of Science Editors:

蔡美儀.; Choi M. Functional studies on sedlin and its involvement in spondyloepiphysealdysplasia tarda. [Doctoral Dissertation]. University of Hong Kong; 2008. Available from: Choi, M. [蔡美儀]. (2008). Functional studies on sedlin and its involvement in spondyloepiphyseal dysplasia tarda. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4129054 ; http://dx.doi.org/10.5353/th_b4129054 ; http://hdl.handle.net/10722/50191

.