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You searched for +publisher:"University of Hong Kong" +contributor:("Huang, J"). Showing records 1 – 26 of 26 total matches.

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University of Hong Kong

1. 石蕾; Shi, Lei. Development of an inter-kingdom delivery and expression system for therapeutic molecules against cancer.

Degree: PhD, 2013, University of Hong Kong

 Background: Several bacterial species such as Clostridium, E.coli and Salmonella can colonize within solid tumors and potentially be used as anticancer agents. The naturally occurring… (more)

Subjects/Keywords: Antineoplastic agents; Salmonella - Genetics

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APA (6th Edition):

石蕾; Shi, L. (2013). Development of an inter-kingdom delivery and expression system for therapeutic molecules against cancer. (Doctoral Dissertation). University of Hong Kong. Retrieved from Shi, L. [石蕾]. (2013). Development of an inter-kingdom delivery and expression system for therapeutic molecules against cancer. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5060568 ; http://dx.doi.org/10.5353/th_b5060568 ; http://hdl.handle.net/10722/227052

Chicago Manual of Style (16th Edition):

石蕾; Shi, Lei. “Development of an inter-kingdom delivery and expression system for therapeutic molecules against cancer.” 2013. Doctoral Dissertation, University of Hong Kong. Accessed August 19, 2019. Shi, L. [石蕾]. (2013). Development of an inter-kingdom delivery and expression system for therapeutic molecules against cancer. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5060568 ; http://dx.doi.org/10.5353/th_b5060568 ; http://hdl.handle.net/10722/227052.

MLA Handbook (7th Edition):

石蕾; Shi, Lei. “Development of an inter-kingdom delivery and expression system for therapeutic molecules against cancer.” 2013. Web. 19 Aug 2019.

Vancouver:

石蕾; Shi L. Development of an inter-kingdom delivery and expression system for therapeutic molecules against cancer. [Internet] [Doctoral dissertation]. University of Hong Kong; 2013. [cited 2019 Aug 19]. Available from: Shi, L. [石蕾]. (2013). Development of an inter-kingdom delivery and expression system for therapeutic molecules against cancer. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5060568 ; http://dx.doi.org/10.5353/th_b5060568 ; http://hdl.handle.net/10722/227052.

Council of Science Editors:

石蕾; Shi L. Development of an inter-kingdom delivery and expression system for therapeutic molecules against cancer. [Doctoral Dissertation]. University of Hong Kong; 2013. Available from: Shi, L. [石蕾]. (2013). Development of an inter-kingdom delivery and expression system for therapeutic molecules against cancer. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5060568 ; http://dx.doi.org/10.5353/th_b5060568 ; http://hdl.handle.net/10722/227052


University of Hong Kong

2. Zheng, Songyue. Comparative immunological evaluation of recombinant Salmonella typhimurium strains expressing model antigens as live oral vaccines.

Degree: PhD, 2012, University of Hong Kong

Despite the development of various systems to generate live recombinant Salmonella Typhimurium vaccine strains, little work has been performed to systematically evaluate and compare their… (more)

Subjects/Keywords: Salmonella infections - Immunological aspects.; Oral vaccines.

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APA (6th Edition):

Zheng, S. (2012). Comparative immunological evaluation of recombinant Salmonella typhimurium strains expressing model antigens as live oral vaccines. (Doctoral Dissertation). University of Hong Kong. Retrieved from Zheng, S. [郑嵩岳]. (2012). Comparative immunological evaluation of recombinant Salmonella typhimurium strains expressing model antigens as live oral vaccines. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4961773 ; http://dx.doi.org/10.5353/th_b4961773 ; http://hdl.handle.net/10722/180953

Chicago Manual of Style (16th Edition):

Zheng, Songyue. “Comparative immunological evaluation of recombinant Salmonella typhimurium strains expressing model antigens as live oral vaccines.” 2012. Doctoral Dissertation, University of Hong Kong. Accessed August 19, 2019. Zheng, S. [郑嵩岳]. (2012). Comparative immunological evaluation of recombinant Salmonella typhimurium strains expressing model antigens as live oral vaccines. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4961773 ; http://dx.doi.org/10.5353/th_b4961773 ; http://hdl.handle.net/10722/180953.

MLA Handbook (7th Edition):

Zheng, Songyue. “Comparative immunological evaluation of recombinant Salmonella typhimurium strains expressing model antigens as live oral vaccines.” 2012. Web. 19 Aug 2019.

Vancouver:

Zheng S. Comparative immunological evaluation of recombinant Salmonella typhimurium strains expressing model antigens as live oral vaccines. [Internet] [Doctoral dissertation]. University of Hong Kong; 2012. [cited 2019 Aug 19]. Available from: Zheng, S. [郑嵩岳]. (2012). Comparative immunological evaluation of recombinant Salmonella typhimurium strains expressing model antigens as live oral vaccines. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4961773 ; http://dx.doi.org/10.5353/th_b4961773 ; http://hdl.handle.net/10722/180953.

Council of Science Editors:

Zheng S. Comparative immunological evaluation of recombinant Salmonella typhimurium strains expressing model antigens as live oral vaccines. [Doctoral Dissertation]. University of Hong Kong; 2012. Available from: Zheng, S. [郑嵩岳]. (2012). Comparative immunological evaluation of recombinant Salmonella typhimurium strains expressing model antigens as live oral vaccines. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4961773 ; http://dx.doi.org/10.5353/th_b4961773 ; http://hdl.handle.net/10722/180953


University of Hong Kong

3. 刘陈立.; Liu, Chenli. Formation of novel biological patterns by controlling cell motility.

Degree: PhD, 2011, University of Hong Kong

The Best PhD Thesis in the Faculties of Dentistry, Engineering, Medicine and Science (University of Hong Kong), Li Ka Shing Prize,2010-11

published_or_final_version

Biochemistry

Doctoral

Doctor of Philosophy

Advisors/Committee Members: Zhou, Z, Huang, J.

Subjects/Keywords: Cells - Motility.; Pattern formation (Biology)

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APA (6th Edition):

刘陈立.; Liu, C. (2011). Formation of novel biological patterns by controlling cell motility. (Doctoral Dissertation). University of Hong Kong. Retrieved from Liu, C. [刘陈立]. (2011). Formation of novel biological patterns by controlling cell motility. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4654191 ; http://dx.doi.org/10.5353/th_b4654191 ; http://hdl.handle.net/10722/142016

Chicago Manual of Style (16th Edition):

刘陈立.; Liu, Chenli. “Formation of novel biological patterns by controlling cell motility.” 2011. Doctoral Dissertation, University of Hong Kong. Accessed August 19, 2019. Liu, C. [刘陈立]. (2011). Formation of novel biological patterns by controlling cell motility. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4654191 ; http://dx.doi.org/10.5353/th_b4654191 ; http://hdl.handle.net/10722/142016.

MLA Handbook (7th Edition):

刘陈立.; Liu, Chenli. “Formation of novel biological patterns by controlling cell motility.” 2011. Web. 19 Aug 2019.

Vancouver:

刘陈立.; Liu C. Formation of novel biological patterns by controlling cell motility. [Internet] [Doctoral dissertation]. University of Hong Kong; 2011. [cited 2019 Aug 19]. Available from: Liu, C. [刘陈立]. (2011). Formation of novel biological patterns by controlling cell motility. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4654191 ; http://dx.doi.org/10.5353/th_b4654191 ; http://hdl.handle.net/10722/142016.

Council of Science Editors:

刘陈立.; Liu C. Formation of novel biological patterns by controlling cell motility. [Doctoral Dissertation]. University of Hong Kong; 2011. Available from: Liu, C. [刘陈立]. (2011). Formation of novel biological patterns by controlling cell motility. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4654191 ; http://dx.doi.org/10.5353/th_b4654191 ; http://hdl.handle.net/10722/142016


University of Hong Kong

4. Kimura, Mari. Towards intracellular aptamers: delivery of anti-SCV helicase aptamers and development of aptamers againstSATB1.

Degree: M. Phil., 2012, University of Hong Kong

 Aptamers are small RNAs or DNAs that specifically bind to targets through complementary three-dimensional structure with high affinity. Aptamers are screened by an in… (more)

Subjects/Keywords: Oligonucleotides.

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APA (6th Edition):

Kimura, M. (2012). Towards intracellular aptamers: delivery of anti-SCV helicase aptamers and development of aptamers againstSATB1. (Masters Thesis). University of Hong Kong. Retrieved from Kimura, M. [木村摩利]. (2012). Towards intracellular aptamers : delivery of anti-SCV helicase aptamers and development of aptamers against SATB1. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4807989 ; http://dx.doi.org/10.5353/th_b4807989 ; http://hdl.handle.net/10722/161584

Chicago Manual of Style (16th Edition):

Kimura, Mari. “Towards intracellular aptamers: delivery of anti-SCV helicase aptamers and development of aptamers againstSATB1.” 2012. Masters Thesis, University of Hong Kong. Accessed August 19, 2019. Kimura, M. [木村摩利]. (2012). Towards intracellular aptamers : delivery of anti-SCV helicase aptamers and development of aptamers against SATB1. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4807989 ; http://dx.doi.org/10.5353/th_b4807989 ; http://hdl.handle.net/10722/161584.

MLA Handbook (7th Edition):

Kimura, Mari. “Towards intracellular aptamers: delivery of anti-SCV helicase aptamers and development of aptamers againstSATB1.” 2012. Web. 19 Aug 2019.

Vancouver:

Kimura M. Towards intracellular aptamers: delivery of anti-SCV helicase aptamers and development of aptamers againstSATB1. [Internet] [Masters thesis]. University of Hong Kong; 2012. [cited 2019 Aug 19]. Available from: Kimura, M. [木村摩利]. (2012). Towards intracellular aptamers : delivery of anti-SCV helicase aptamers and development of aptamers against SATB1. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4807989 ; http://dx.doi.org/10.5353/th_b4807989 ; http://hdl.handle.net/10722/161584.

Council of Science Editors:

Kimura M. Towards intracellular aptamers: delivery of anti-SCV helicase aptamers and development of aptamers againstSATB1. [Masters Thesis]. University of Hong Kong; 2012. Available from: Kimura, M. [木村摩利]. (2012). Towards intracellular aptamers : delivery of anti-SCV helicase aptamers and development of aptamers against SATB1. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4807989 ; http://dx.doi.org/10.5353/th_b4807989 ; http://hdl.handle.net/10722/161584


University of Hong Kong

5. Fu, Xiongfei. Quantitative study of pattern formation on a density-dependent motility biological system.

Degree: PhD, 2012, University of Hong Kong

Quantitative biology is an emerging field that attracts intensive research interests. Pattern formation is a widely studied topic both in biology and physics. Scientists have… (more)

Subjects/Keywords: Pattern formation (Biology); Cells - Motility.

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APA (6th Edition):

Fu, X. (2012). Quantitative study of pattern formation on a density-dependent motility biological system. (Doctoral Dissertation). University of Hong Kong. Retrieved from Fu, X. [傅雄飞]. (2012). Quantitative study of pattern formation on a density-dependent motility biological system. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4819942 ; http://dx.doi.org/10.5353/th_b4819942 ; http://hdl.handle.net/10722/167218

Chicago Manual of Style (16th Edition):

Fu, Xiongfei. “Quantitative study of pattern formation on a density-dependent motility biological system.” 2012. Doctoral Dissertation, University of Hong Kong. Accessed August 19, 2019. Fu, X. [傅雄飞]. (2012). Quantitative study of pattern formation on a density-dependent motility biological system. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4819942 ; http://dx.doi.org/10.5353/th_b4819942 ; http://hdl.handle.net/10722/167218.

MLA Handbook (7th Edition):

Fu, Xiongfei. “Quantitative study of pattern formation on a density-dependent motility biological system.” 2012. Web. 19 Aug 2019.

Vancouver:

Fu X. Quantitative study of pattern formation on a density-dependent motility biological system. [Internet] [Doctoral dissertation]. University of Hong Kong; 2012. [cited 2019 Aug 19]. Available from: Fu, X. [傅雄飞]. (2012). Quantitative study of pattern formation on a density-dependent motility biological system. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4819942 ; http://dx.doi.org/10.5353/th_b4819942 ; http://hdl.handle.net/10722/167218.

Council of Science Editors:

Fu X. Quantitative study of pattern formation on a density-dependent motility biological system. [Doctoral Dissertation]. University of Hong Kong; 2012. Available from: Fu, X. [傅雄飞]. (2012). Quantitative study of pattern formation on a density-dependent motility biological system. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4819942 ; http://dx.doi.org/10.5353/th_b4819942 ; http://hdl.handle.net/10722/167218


University of Hong Kong

6. 黃雅誼; Wong, Nga-yi, Queenie. DNA engineering utilizing thymidylate synthase A (thyA) selection system in Escherichia coli.

Degree: M. Phil., 2001, University of Hong Kong

published_or_final_version

Molecular Biology

Master

Master of Philosophy

Advisors/Committee Members: Huang, J.

Subjects/Keywords: Escherichia coli - Genetics.; Recombinant DNA.; Genetic engineering.

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APA (6th Edition):

黃雅誼; Wong, Nga-yi, Q. (2001). DNA engineering utilizing thymidylate synthase A (thyA) selection system in Escherichia coli. (Masters Thesis). University of Hong Kong. Retrieved from Wong, N. Q. [黃雅誼]. (2001). DNA engineering utilizing thymidylate synthase A (thyA) selection system in Escherichia coli. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3122685 ; http://dx.doi.org/10.5353/th_b3122685 ; http://hdl.handle.net/10722/33635

Chicago Manual of Style (16th Edition):

黃雅誼; Wong, Nga-yi, Queenie. “DNA engineering utilizing thymidylate synthase A (thyA) selection system in Escherichia coli.” 2001. Masters Thesis, University of Hong Kong. Accessed August 19, 2019. Wong, N. Q. [黃雅誼]. (2001). DNA engineering utilizing thymidylate synthase A (thyA) selection system in Escherichia coli. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3122685 ; http://dx.doi.org/10.5353/th_b3122685 ; http://hdl.handle.net/10722/33635.

MLA Handbook (7th Edition):

黃雅誼; Wong, Nga-yi, Queenie. “DNA engineering utilizing thymidylate synthase A (thyA) selection system in Escherichia coli.” 2001. Web. 19 Aug 2019.

Vancouver:

黃雅誼; Wong, Nga-yi Q. DNA engineering utilizing thymidylate synthase A (thyA) selection system in Escherichia coli. [Internet] [Masters thesis]. University of Hong Kong; 2001. [cited 2019 Aug 19]. Available from: Wong, N. Q. [黃雅誼]. (2001). DNA engineering utilizing thymidylate synthase A (thyA) selection system in Escherichia coli. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3122685 ; http://dx.doi.org/10.5353/th_b3122685 ; http://hdl.handle.net/10722/33635.

Council of Science Editors:

黃雅誼; Wong, Nga-yi Q. DNA engineering utilizing thymidylate synthase A (thyA) selection system in Escherichia coli. [Masters Thesis]. University of Hong Kong; 2001. Available from: Wong, N. Q. [黃雅誼]. (2001). DNA engineering utilizing thymidylate synthase A (thyA) selection system in Escherichia coli. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3122685 ; http://dx.doi.org/10.5353/th_b3122685 ; http://hdl.handle.net/10722/33635


University of Hong Kong

7. 吳凱琳.; Ng, Hoi-lam, Alam. Characterization of cre expression in BAC-Pcp2-IRES-Cre transgenic mice.

Degree: M. Phil., 2005, University of Hong Kong

published_or_final_version

abstract

Biochemistry

Master

Master of Philosophy

Advisors/Committee Members: Huang, J.

Subjects/Keywords: Biological transport.; Transgenic mice.; Gene expression.; Kinesin.; Genetic recombination

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APA (6th Edition):

吳凱琳.; Ng, Hoi-lam, A. (2005). Characterization of cre expression in BAC-Pcp2-IRES-Cre transgenic mice. (Masters Thesis). University of Hong Kong. Retrieved from Ng, H. A. [吳凱琳]. (2005). Characterization of cre expression in BAC-Pcp2-IRES-Cre transgenic mice. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3627824 ; http://dx.doi.org/10.5353/th_b3627824 ; http://hdl.handle.net/10722/41355

Chicago Manual of Style (16th Edition):

吳凱琳.; Ng, Hoi-lam, Alam. “Characterization of cre expression in BAC-Pcp2-IRES-Cre transgenic mice.” 2005. Masters Thesis, University of Hong Kong. Accessed August 19, 2019. Ng, H. A. [吳凱琳]. (2005). Characterization of cre expression in BAC-Pcp2-IRES-Cre transgenic mice. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3627824 ; http://dx.doi.org/10.5353/th_b3627824 ; http://hdl.handle.net/10722/41355.

MLA Handbook (7th Edition):

吳凱琳.; Ng, Hoi-lam, Alam. “Characterization of cre expression in BAC-Pcp2-IRES-Cre transgenic mice.” 2005. Web. 19 Aug 2019.

Vancouver:

吳凱琳.; Ng, Hoi-lam A. Characterization of cre expression in BAC-Pcp2-IRES-Cre transgenic mice. [Internet] [Masters thesis]. University of Hong Kong; 2005. [cited 2019 Aug 19]. Available from: Ng, H. A. [吳凱琳]. (2005). Characterization of cre expression in BAC-Pcp2-IRES-Cre transgenic mice. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3627824 ; http://dx.doi.org/10.5353/th_b3627824 ; http://hdl.handle.net/10722/41355.

Council of Science Editors:

吳凱琳.; Ng, Hoi-lam A. Characterization of cre expression in BAC-Pcp2-IRES-Cre transgenic mice. [Masters Thesis]. University of Hong Kong; 2005. Available from: Ng, H. A. [吳凱琳]. (2005). Characterization of cre expression in BAC-Pcp2-IRES-Cre transgenic mice. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3627824 ; http://dx.doi.org/10.5353/th_b3627824 ; http://hdl.handle.net/10722/41355


University of Hong Kong

8. 禤承恩.; Huen, Shing-yan, Michael. A mechanistic study of lambdaphage-mediated recombination in E. coli.

Degree: PhD, 2006, University of Hong Kong

published_or_final_version

abstract

Biochemistry

Doctoral

Doctor of Philosophy

Advisors/Committee Members: Huang, J.

Subjects/Keywords: Genetic recombination.; Escherichia coli.; Bacteriophages - Genetics.; Recombinant DNA.; Bacterial genetics.

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APA (6th Edition):

禤承恩.; Huen, Shing-yan, M. (2006). A mechanistic study of lambdaphage-mediated recombination in E. coli. (Doctoral Dissertation). University of Hong Kong. Retrieved from Huen, S. M. [禤承恩]. (2006). A mechanistic study of lambdaphage-mediated recombination in E. coli. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3532185 ; http://dx.doi.org/10.5353/th_b3532185 ; http://hdl.handle.net/10722/26889

Chicago Manual of Style (16th Edition):

禤承恩.; Huen, Shing-yan, Michael. “A mechanistic study of lambdaphage-mediated recombination in E. coli.” 2006. Doctoral Dissertation, University of Hong Kong. Accessed August 19, 2019. Huen, S. M. [禤承恩]. (2006). A mechanistic study of lambdaphage-mediated recombination in E. coli. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3532185 ; http://dx.doi.org/10.5353/th_b3532185 ; http://hdl.handle.net/10722/26889.

MLA Handbook (7th Edition):

禤承恩.; Huen, Shing-yan, Michael. “A mechanistic study of lambdaphage-mediated recombination in E. coli.” 2006. Web. 19 Aug 2019.

Vancouver:

禤承恩.; Huen, Shing-yan M. A mechanistic study of lambdaphage-mediated recombination in E. coli. [Internet] [Doctoral dissertation]. University of Hong Kong; 2006. [cited 2019 Aug 19]. Available from: Huen, S. M. [禤承恩]. (2006). A mechanistic study of lambdaphage-mediated recombination in E. coli. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3532185 ; http://dx.doi.org/10.5353/th_b3532185 ; http://hdl.handle.net/10722/26889.

Council of Science Editors:

禤承恩.; Huen, Shing-yan M. A mechanistic study of lambdaphage-mediated recombination in E. coli. [Doctoral Dissertation]. University of Hong Kong; 2006. Available from: Huen, S. M. [禤承恩]. (2006). A mechanistic study of lambdaphage-mediated recombination in E. coli. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3532185 ; http://dx.doi.org/10.5353/th_b3532185 ; http://hdl.handle.net/10722/26889


University of Hong Kong

9. 陸林宇.; Lu, Linyu. Investigations into the feasibility of single-strandedoligonucleotide-mediated targeted gene repair in mammalian cells.

Degree: PhD, 2006, University of Hong Kong

abstract

published_or_final_version

Biochemistry

Doctoral

Doctor of Philosophy

Advisors/Committee Members: Huang, J.

Subjects/Keywords: DNA repair.; Mice - Cytogenetics.; Gene targeting

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APA (6th Edition):

陸林宇.; Lu, L. (2006). Investigations into the feasibility of single-strandedoligonucleotide-mediated targeted gene repair in mammalian cells. (Doctoral Dissertation). University of Hong Kong. Retrieved from Lu, L. [陸林宇]. (2006). Investigations into the feasibility of single-stranded oligonucleotide-mediated targeted gene repair in mammalian cells. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3872279 ; http://dx.doi.org/10.5353/th_b3872279 ; http://hdl.handle.net/10722/50195

Chicago Manual of Style (16th Edition):

陸林宇.; Lu, Linyu. “Investigations into the feasibility of single-strandedoligonucleotide-mediated targeted gene repair in mammalian cells.” 2006. Doctoral Dissertation, University of Hong Kong. Accessed August 19, 2019. Lu, L. [陸林宇]. (2006). Investigations into the feasibility of single-stranded oligonucleotide-mediated targeted gene repair in mammalian cells. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3872279 ; http://dx.doi.org/10.5353/th_b3872279 ; http://hdl.handle.net/10722/50195.

MLA Handbook (7th Edition):

陸林宇.; Lu, Linyu. “Investigations into the feasibility of single-strandedoligonucleotide-mediated targeted gene repair in mammalian cells.” 2006. Web. 19 Aug 2019.

Vancouver:

陸林宇.; Lu L. Investigations into the feasibility of single-strandedoligonucleotide-mediated targeted gene repair in mammalian cells. [Internet] [Doctoral dissertation]. University of Hong Kong; 2006. [cited 2019 Aug 19]. Available from: Lu, L. [陸林宇]. (2006). Investigations into the feasibility of single-stranded oligonucleotide-mediated targeted gene repair in mammalian cells. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3872279 ; http://dx.doi.org/10.5353/th_b3872279 ; http://hdl.handle.net/10722/50195.

Council of Science Editors:

陸林宇.; Lu L. Investigations into the feasibility of single-strandedoligonucleotide-mediated targeted gene repair in mammalian cells. [Doctoral Dissertation]. University of Hong Kong; 2006. Available from: Lu, L. [陸林宇]. (2006). Investigations into the feasibility of single-stranded oligonucleotide-mediated targeted gene repair in mammalian cells. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3872279 ; http://dx.doi.org/10.5353/th_b3872279 ; http://hdl.handle.net/10722/50195


University of Hong Kong

10. Hui, Wing-sum. Molecular and mutation analysis of hereditary multiple exostoses.

Degree: M. Phil., 2002, University of Hong Kong

published_or_final_version

Biochemistry

Master

Master of Philosophy

Advisors/Committee Members: Huang, J.

Subjects/Keywords: Mutation (Biology); Cartilage cells - Genetics.; Exostosis - Molecular aspects.; Genetic disorders.

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APA (6th Edition):

Hui, W. (2002). Molecular and mutation analysis of hereditary multiple exostoses. (Masters Thesis). University of Hong Kong. Retrieved from Hui, W. [許永森]. (2002). Molecular and mutation analysis of hereditary multiple exostoses. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4257708 ; http://dx.doi.org/10.5353/th_b4257708 ; http://hdl.handle.net/10722/55961

Chicago Manual of Style (16th Edition):

Hui, Wing-sum. “Molecular and mutation analysis of hereditary multiple exostoses.” 2002. Masters Thesis, University of Hong Kong. Accessed August 19, 2019. Hui, W. [許永森]. (2002). Molecular and mutation analysis of hereditary multiple exostoses. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4257708 ; http://dx.doi.org/10.5353/th_b4257708 ; http://hdl.handle.net/10722/55961.

MLA Handbook (7th Edition):

Hui, Wing-sum. “Molecular and mutation analysis of hereditary multiple exostoses.” 2002. Web. 19 Aug 2019.

Vancouver:

Hui W. Molecular and mutation analysis of hereditary multiple exostoses. [Internet] [Masters thesis]. University of Hong Kong; 2002. [cited 2019 Aug 19]. Available from: Hui, W. [許永森]. (2002). Molecular and mutation analysis of hereditary multiple exostoses. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4257708 ; http://dx.doi.org/10.5353/th_b4257708 ; http://hdl.handle.net/10722/55961.

Council of Science Editors:

Hui W. Molecular and mutation analysis of hereditary multiple exostoses. [Masters Thesis]. University of Hong Kong; 2002. Available from: Hui, W. [許永森]. (2002). Molecular and mutation analysis of hereditary multiple exostoses. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4257708 ; http://dx.doi.org/10.5353/th_b4257708 ; http://hdl.handle.net/10722/55961


University of Hong Kong

11. Wang, Jing. The study of KIF5B-mediated intracellular transport in neurons.

Degree: PhD, 2008, University of Hong Kong

published_or_final_version

Biochemistry

Doctoral

Doctor of Philosophy

Advisors/Committee Members: Huang, J.

Subjects/Keywords: Biological transport.; Neurons.; Kinesin.

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APA (6th Edition):

Wang, J. (2008). The study of KIF5B-mediated intracellular transport in neurons. (Doctoral Dissertation). University of Hong Kong. Retrieved from Wang, J. [王景]. (2008). The study of KIF5B-mediated intracellular transport in neurons. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4163376 ; http://dx.doi.org/10.5353/th_b4163376 ; http://hdl.handle.net/10722/57035

Chicago Manual of Style (16th Edition):

Wang, Jing. “The study of KIF5B-mediated intracellular transport in neurons.” 2008. Doctoral Dissertation, University of Hong Kong. Accessed August 19, 2019. Wang, J. [王景]. (2008). The study of KIF5B-mediated intracellular transport in neurons. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4163376 ; http://dx.doi.org/10.5353/th_b4163376 ; http://hdl.handle.net/10722/57035.

MLA Handbook (7th Edition):

Wang, Jing. “The study of KIF5B-mediated intracellular transport in neurons.” 2008. Web. 19 Aug 2019.

Vancouver:

Wang J. The study of KIF5B-mediated intracellular transport in neurons. [Internet] [Doctoral dissertation]. University of Hong Kong; 2008. [cited 2019 Aug 19]. Available from: Wang, J. [王景]. (2008). The study of KIF5B-mediated intracellular transport in neurons. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4163376 ; http://dx.doi.org/10.5353/th_b4163376 ; http://hdl.handle.net/10722/57035.

Council of Science Editors:

Wang J. The study of KIF5B-mediated intracellular transport in neurons. [Doctoral Dissertation]. University of Hong Kong; 2008. Available from: Wang, J. [王景]. (2008). The study of KIF5B-mediated intracellular transport in neurons. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4163376 ; http://dx.doi.org/10.5353/th_b4163376 ; http://hdl.handle.net/10722/57035


University of Hong Kong

12. 葛瑞光.; Ge, Ruiguang. A biochemical and proteomic view of nickel homeostasis and bismuth treatment: identification of bismuth-targetedproteins in Helicobacter pylori and characterization of a nickel-storage protein hpn.

Degree: PhD, 2006, University of Hong Kong

abstract

published_or_final_version

Chemistry

Doctoral

Doctor of Philosophy

Advisors/Committee Members: Huang, J, Sun, H.

Subjects/Keywords: Proteomics.; Helicobacter pylori infections - Treatment.; Molecular biology.; Peptic ulcer - Treatment.; Bismuth - Therapeutic use.

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APA (6th Edition):

葛瑞光.; Ge, R. (2006). A biochemical and proteomic view of nickel homeostasis and bismuth treatment: identification of bismuth-targetedproteins in Helicobacter pylori and characterization of a nickel-storage protein hpn. (Doctoral Dissertation). University of Hong Kong. Retrieved from Ge, R. [葛瑞光]. (2006). A biochemical and proteomic view of nickel homeostasis and bismuth treatment : identification of bismuth-targeted proteins in Helicobacter pylori and characterization of a nickel-storage protein hpn. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3794724 ; http://dx.doi.org/10.5353/th_b3794724 ; http://hdl.handle.net/10722/50398

Chicago Manual of Style (16th Edition):

葛瑞光.; Ge, Ruiguang. “A biochemical and proteomic view of nickel homeostasis and bismuth treatment: identification of bismuth-targetedproteins in Helicobacter pylori and characterization of a nickel-storage protein hpn.” 2006. Doctoral Dissertation, University of Hong Kong. Accessed August 19, 2019. Ge, R. [葛瑞光]. (2006). A biochemical and proteomic view of nickel homeostasis and bismuth treatment : identification of bismuth-targeted proteins in Helicobacter pylori and characterization of a nickel-storage protein hpn. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3794724 ; http://dx.doi.org/10.5353/th_b3794724 ; http://hdl.handle.net/10722/50398.

MLA Handbook (7th Edition):

葛瑞光.; Ge, Ruiguang. “A biochemical and proteomic view of nickel homeostasis and bismuth treatment: identification of bismuth-targetedproteins in Helicobacter pylori and characterization of a nickel-storage protein hpn.” 2006. Web. 19 Aug 2019.

Vancouver:

葛瑞光.; Ge R. A biochemical and proteomic view of nickel homeostasis and bismuth treatment: identification of bismuth-targetedproteins in Helicobacter pylori and characterization of a nickel-storage protein hpn. [Internet] [Doctoral dissertation]. University of Hong Kong; 2006. [cited 2019 Aug 19]. Available from: Ge, R. [葛瑞光]. (2006). A biochemical and proteomic view of nickel homeostasis and bismuth treatment : identification of bismuth-targeted proteins in Helicobacter pylori and characterization of a nickel-storage protein hpn. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3794724 ; http://dx.doi.org/10.5353/th_b3794724 ; http://hdl.handle.net/10722/50398.

Council of Science Editors:

葛瑞光.; Ge R. A biochemical and proteomic view of nickel homeostasis and bismuth treatment: identification of bismuth-targetedproteins in Helicobacter pylori and characterization of a nickel-storage protein hpn. [Doctoral Dissertation]. University of Hong Kong; 2006. Available from: Ge, R. [葛瑞光]. (2006). A biochemical and proteomic view of nickel homeostasis and bismuth treatment : identification of bismuth-targeted proteins in Helicobacter pylori and characterization of a nickel-storage protein hpn. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3794724 ; http://dx.doi.org/10.5353/th_b3794724 ; http://hdl.handle.net/10722/50398


University of Hong Kong

13. 陳牧唅.; Chen, Muhan. Application of transgenic mice models in functional study of two putative oncogenes: ALC-1 and EIF5A2.

Degree: PhD, 2007, University of Hong Kong

abstract

published_or_final_version

Clinical Oncology

Doctoral

Doctor of Philosophy

Advisors/Committee Members: Huang, J, Guan, X.

Subjects/Keywords: Gene expression.; Transgenic mice - Genetics.; Oncogenes.

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APA (6th Edition):

陳牧唅.; Chen, M. (2007). Application of transgenic mice models in functional study of two putative oncogenes: ALC-1 and EIF5A2. (Doctoral Dissertation). University of Hong Kong. Retrieved from Chen, M. [陳牧唅]. (2007). Application of transgenic mice models in functional study of two putative oncogenes : ALC-1 and EIF5A2. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3859346 ; http://dx.doi.org/10.5353/th_b3859346 ; http://hdl.handle.net/10722/50696

Chicago Manual of Style (16th Edition):

陳牧唅.; Chen, Muhan. “Application of transgenic mice models in functional study of two putative oncogenes: ALC-1 and EIF5A2.” 2007. Doctoral Dissertation, University of Hong Kong. Accessed August 19, 2019. Chen, M. [陳牧唅]. (2007). Application of transgenic mice models in functional study of two putative oncogenes : ALC-1 and EIF5A2. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3859346 ; http://dx.doi.org/10.5353/th_b3859346 ; http://hdl.handle.net/10722/50696.

MLA Handbook (7th Edition):

陳牧唅.; Chen, Muhan. “Application of transgenic mice models in functional study of two putative oncogenes: ALC-1 and EIF5A2.” 2007. Web. 19 Aug 2019.

Vancouver:

陳牧唅.; Chen M. Application of transgenic mice models in functional study of two putative oncogenes: ALC-1 and EIF5A2. [Internet] [Doctoral dissertation]. University of Hong Kong; 2007. [cited 2019 Aug 19]. Available from: Chen, M. [陳牧唅]. (2007). Application of transgenic mice models in functional study of two putative oncogenes : ALC-1 and EIF5A2. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3859346 ; http://dx.doi.org/10.5353/th_b3859346 ; http://hdl.handle.net/10722/50696.

Council of Science Editors:

陳牧唅.; Chen M. Application of transgenic mice models in functional study of two putative oncogenes: ALC-1 and EIF5A2. [Doctoral Dissertation]. University of Hong Kong; 2007. Available from: Chen, M. [陳牧唅]. (2007). Application of transgenic mice models in functional study of two putative oncogenes : ALC-1 and EIF5A2. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3859346 ; http://dx.doi.org/10.5353/th_b3859346 ; http://hdl.handle.net/10722/50696


University of Hong Kong

14. Wang, Zai. Kinesin-1 in skeletal muscle.

Degree: PhD, 2008, University of Hong Kong

published_or_final_version

Biochemistry

Doctoral

Doctor of Philosophy

Advisors/Committee Members: Zheng, B, Huang, J.

Subjects/Keywords: Striated muscle.; Kinesin.

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APA (6th Edition):

Wang, Z. (2008). Kinesin-1 in skeletal muscle. (Doctoral Dissertation). University of Hong Kong. Retrieved from Wang, Z. [王在]. (2008). Kinesin-1 in skeletal muscle. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4175787 ; http://dx.doi.org/10.5353/th_b4175787 ; http://hdl.handle.net/10722/56794

Chicago Manual of Style (16th Edition):

Wang, Zai. “Kinesin-1 in skeletal muscle.” 2008. Doctoral Dissertation, University of Hong Kong. Accessed August 19, 2019. Wang, Z. [王在]. (2008). Kinesin-1 in skeletal muscle. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4175787 ; http://dx.doi.org/10.5353/th_b4175787 ; http://hdl.handle.net/10722/56794.

MLA Handbook (7th Edition):

Wang, Zai. “Kinesin-1 in skeletal muscle.” 2008. Web. 19 Aug 2019.

Vancouver:

Wang Z. Kinesin-1 in skeletal muscle. [Internet] [Doctoral dissertation]. University of Hong Kong; 2008. [cited 2019 Aug 19]. Available from: Wang, Z. [王在]. (2008). Kinesin-1 in skeletal muscle. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4175787 ; http://dx.doi.org/10.5353/th_b4175787 ; http://hdl.handle.net/10722/56794.

Council of Science Editors:

Wang Z. Kinesin-1 in skeletal muscle. [Doctoral Dissertation]. University of Hong Kong; 2008. Available from: Wang, Z. [王在]. (2008). Kinesin-1 in skeletal muscle. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4175787 ; http://dx.doi.org/10.5353/th_b4175787 ; http://hdl.handle.net/10722/56794


University of Hong Kong

15. Zeng, Yong. Mechanistic studies on the polymorphism at -77GT repeats regions of IFNAR1 and its correlation to the susceptibility to chronic HBVinfection.

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

published_or_final_version

Microbiology

Master

Master of Philosophy

Advisors/Committee Members: Huang, J, Zheng, B.

Subjects/Keywords: Hepatitis B - Genetic aspects.; Genetic polymorphisms.

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APA (6th Edition):

Zeng, Y. (2009). Mechanistic studies on the polymorphism at -77GT repeats regions of IFNAR1 and its correlation to the susceptibility to chronic HBVinfection. (Masters Thesis). University of Hong Kong. Retrieved from Zeng, Y. [曾咏]. (2009). Mechanistic studies on the polymorphism at -77GT repeats regions of IFNAR1 and its correlation to the susceptibility to chronic HBV infection. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4327864 ; http://dx.doi.org/10.5353/th_b4327864 ; http://hdl.handle.net/10722/57026

Chicago Manual of Style (16th Edition):

Zeng, Yong. “Mechanistic studies on the polymorphism at -77GT repeats regions of IFNAR1 and its correlation to the susceptibility to chronic HBVinfection.” 2009. Masters Thesis, University of Hong Kong. Accessed August 19, 2019. Zeng, Y. [曾咏]. (2009). Mechanistic studies on the polymorphism at -77GT repeats regions of IFNAR1 and its correlation to the susceptibility to chronic HBV infection. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4327864 ; http://dx.doi.org/10.5353/th_b4327864 ; http://hdl.handle.net/10722/57026.

MLA Handbook (7th Edition):

Zeng, Yong. “Mechanistic studies on the polymorphism at -77GT repeats regions of IFNAR1 and its correlation to the susceptibility to chronic HBVinfection.” 2009. Web. 19 Aug 2019.

Vancouver:

Zeng Y. Mechanistic studies on the polymorphism at -77GT repeats regions of IFNAR1 and its correlation to the susceptibility to chronic HBVinfection. [Internet] [Masters thesis]. University of Hong Kong; 2009. [cited 2019 Aug 19]. Available from: Zeng, Y. [曾咏]. (2009). Mechanistic studies on the polymorphism at -77GT repeats regions of IFNAR1 and its correlation to the susceptibility to chronic HBV infection. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4327864 ; http://dx.doi.org/10.5353/th_b4327864 ; http://hdl.handle.net/10722/57026.

Council of Science Editors:

Zeng Y. Mechanistic studies on the polymorphism at -77GT repeats regions of IFNAR1 and its correlation to the susceptibility to chronic HBVinfection. [Masters Thesis]. University of Hong Kong; 2009. Available from: Zeng, Y. [曾咏]. (2009). Mechanistic studies on the polymorphism at -77GT repeats regions of IFNAR1 and its correlation to the susceptibility to chronic HBV infection. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4327864 ; http://dx.doi.org/10.5353/th_b4327864 ; http://hdl.handle.net/10722/57026


University of Hong Kong

16. 朱貴霞.; Zhu, Guixia. Study of the function of Kinesin-1 (KIF5B) in long bone development.

Degree: PhD, 2009, University of Hong Kong

published_or_final_version

Biochemistry

Doctoral

Doctor of Philosophy

Advisors/Committee Members: Cheah, KSE, Huang, J.

Subjects/Keywords: Cartilage cells; Biological transport.; Kinesin.; Bones - Growth.

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APA (6th Edition):

朱貴霞.; Zhu, G. (2009). Study of the function of Kinesin-1 (KIF5B) in long bone development. (Doctoral Dissertation). University of Hong Kong. Retrieved from Zhu, G. [朱貴霞]. (2009). Study of the function of Kinesin-1 (KIF5B) in long bone development. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4175791 ; http://dx.doi.org/10.5353/th_b4175791 ; http://hdl.handle.net/10722/57036

Chicago Manual of Style (16th Edition):

朱貴霞.; Zhu, Guixia. “Study of the function of Kinesin-1 (KIF5B) in long bone development.” 2009. Doctoral Dissertation, University of Hong Kong. Accessed August 19, 2019. Zhu, G. [朱貴霞]. (2009). Study of the function of Kinesin-1 (KIF5B) in long bone development. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4175791 ; http://dx.doi.org/10.5353/th_b4175791 ; http://hdl.handle.net/10722/57036.

MLA Handbook (7th Edition):

朱貴霞.; Zhu, Guixia. “Study of the function of Kinesin-1 (KIF5B) in long bone development.” 2009. Web. 19 Aug 2019.

Vancouver:

朱貴霞.; Zhu G. Study of the function of Kinesin-1 (KIF5B) in long bone development. [Internet] [Doctoral dissertation]. University of Hong Kong; 2009. [cited 2019 Aug 19]. Available from: Zhu, G. [朱貴霞]. (2009). Study of the function of Kinesin-1 (KIF5B) in long bone development. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4175791 ; http://dx.doi.org/10.5353/th_b4175791 ; http://hdl.handle.net/10722/57036.

Council of Science Editors:

朱貴霞.; Zhu G. Study of the function of Kinesin-1 (KIF5B) in long bone development. [Doctoral Dissertation]. University of Hong Kong; 2009. Available from: Zhu, G. [朱貴霞]. (2009). Study of the function of Kinesin-1 (KIF5B) in long bone development. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4175791 ; http://dx.doi.org/10.5353/th_b4175791 ; http://hdl.handle.net/10722/57036


University of Hong Kong

17. Chan, Che-man. Functional study of spike protein of a novel human coronavirus HKU1.

Degree: PhD, 2008, University of Hong Kong

published_or_final_version

Microbiology

Doctoral

Doctor of Philosophy

Advisors/Committee Members: Huang, J, Yuen, KY.

Subjects/Keywords: Coronaviruses - China - Hong Kong.; Viral proteins.

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APA (6th Edition):

Chan, C. (2008). Functional study of spike protein of a novel human coronavirus HKU1. (Doctoral Dissertation). University of Hong Kong. Retrieved from Chan, C. [陳志敏]. (2008). Functional study of spike protein of a novel human coronavirus HKU1. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4189693 ; http://dx.doi.org/10.5353/th_b4189693 ; http://hdl.handle.net/10722/57045

Chicago Manual of Style (16th Edition):

Chan, Che-man. “Functional study of spike protein of a novel human coronavirus HKU1.” 2008. Doctoral Dissertation, University of Hong Kong. Accessed August 19, 2019. Chan, C. [陳志敏]. (2008). Functional study of spike protein of a novel human coronavirus HKU1. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4189693 ; http://dx.doi.org/10.5353/th_b4189693 ; http://hdl.handle.net/10722/57045.

MLA Handbook (7th Edition):

Chan, Che-man. “Functional study of spike protein of a novel human coronavirus HKU1.” 2008. Web. 19 Aug 2019.

Vancouver:

Chan C. Functional study of spike protein of a novel human coronavirus HKU1. [Internet] [Doctoral dissertation]. University of Hong Kong; 2008. [cited 2019 Aug 19]. Available from: Chan, C. [陳志敏]. (2008). Functional study of spike protein of a novel human coronavirus HKU1. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4189693 ; http://dx.doi.org/10.5353/th_b4189693 ; http://hdl.handle.net/10722/57045.

Council of Science Editors:

Chan C. Functional study of spike protein of a novel human coronavirus HKU1. [Doctoral Dissertation]. University of Hong Kong; 2008. Available from: Chan, C. [陳志敏]. (2008). Functional study of spike protein of a novel human coronavirus HKU1. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4189693 ; http://dx.doi.org/10.5353/th_b4189693 ; http://hdl.handle.net/10722/57045


University of Hong Kong

18. Wu, Xuewei. Isthmin, a novel extracellular regulator in nodal signaling pathway.

Degree: PhD, 2011, University of Hong Kong

published_or_final_version

Biochemistry

Doctoral

Doctor of Philosophy

Advisors/Committee Members: Zhou, Z, Huang, J.

Subjects/Keywords: Transforming growth factors-beta.; Mice - Development.

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APA (6th Edition):

Wu, X. (2011). Isthmin, a novel extracellular regulator in nodal signaling pathway. (Doctoral Dissertation). University of Hong Kong. Retrieved from Wu, X. [吴雪伟]. (2010). Isthmin, a novel extracellular regulator in nodal signaling pathway. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4558657 ; http://dx.doi.org/10.5353/th_b4558657 ; http://hdl.handle.net/10722/133183

Chicago Manual of Style (16th Edition):

Wu, Xuewei. “Isthmin, a novel extracellular regulator in nodal signaling pathway.” 2011. Doctoral Dissertation, University of Hong Kong. Accessed August 19, 2019. Wu, X. [吴雪伟]. (2010). Isthmin, a novel extracellular regulator in nodal signaling pathway. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4558657 ; http://dx.doi.org/10.5353/th_b4558657 ; http://hdl.handle.net/10722/133183.

MLA Handbook (7th Edition):

Wu, Xuewei. “Isthmin, a novel extracellular regulator in nodal signaling pathway.” 2011. Web. 19 Aug 2019.

Vancouver:

Wu X. Isthmin, a novel extracellular regulator in nodal signaling pathway. [Internet] [Doctoral dissertation]. University of Hong Kong; 2011. [cited 2019 Aug 19]. Available from: Wu, X. [吴雪伟]. (2010). Isthmin, a novel extracellular regulator in nodal signaling pathway. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4558657 ; http://dx.doi.org/10.5353/th_b4558657 ; http://hdl.handle.net/10722/133183.

Council of Science Editors:

Wu X. Isthmin, a novel extracellular regulator in nodal signaling pathway. [Doctoral Dissertation]. University of Hong Kong; 2011. Available from: Wu, X. [吴雪伟]. (2010). Isthmin, a novel extracellular regulator in nodal signaling pathway. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4558657 ; http://dx.doi.org/10.5353/th_b4558657 ; http://hdl.handle.net/10722/133183


University of Hong Kong

19. 沈家滔.; Shum, Ka-to. A comparative study of G-quadruplex aptamers against multiple protein targets.

Degree: PhD, 2010, University of Hong Kong

published_or_final_version

Biochemistry

Doctoral

Doctor of Philosophy

Advisors/Committee Members: Huang, J, Tanner, JA.

Subjects/Keywords: Protein kinases.; Oligonucleotides.; DNA helicases.; Polyphosphates.; Glycoproteins.

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APA (6th Edition):

沈家滔.; Shum, K. (2010). A comparative study of G-quadruplex aptamers against multiple protein targets. (Doctoral Dissertation). University of Hong Kong. Retrieved from Shum, K. [沈家滔]. (2010). A comparative study of G-quadruplex aptamers against multiple protein targets. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4581623 ; http://dx.doi.org/10.5353/th_b4581623 ; http://hdl.handle.net/10722/133291

Chicago Manual of Style (16th Edition):

沈家滔.; Shum, Ka-to. “A comparative study of G-quadruplex aptamers against multiple protein targets.” 2010. Doctoral Dissertation, University of Hong Kong. Accessed August 19, 2019. Shum, K. [沈家滔]. (2010). A comparative study of G-quadruplex aptamers against multiple protein targets. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4581623 ; http://dx.doi.org/10.5353/th_b4581623 ; http://hdl.handle.net/10722/133291.

MLA Handbook (7th Edition):

沈家滔.; Shum, Ka-to. “A comparative study of G-quadruplex aptamers against multiple protein targets.” 2010. Web. 19 Aug 2019.

Vancouver:

沈家滔.; Shum K. A comparative study of G-quadruplex aptamers against multiple protein targets. [Internet] [Doctoral dissertation]. University of Hong Kong; 2010. [cited 2019 Aug 19]. Available from: Shum, K. [沈家滔]. (2010). A comparative study of G-quadruplex aptamers against multiple protein targets. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4581623 ; http://dx.doi.org/10.5353/th_b4581623 ; http://hdl.handle.net/10722/133291.

Council of Science Editors:

沈家滔.; Shum K. A comparative study of G-quadruplex aptamers against multiple protein targets. [Doctoral Dissertation]. University of Hong Kong; 2010. Available from: Shum, K. [沈家滔]. (2010). A comparative study of G-quadruplex aptamers against multiple protein targets. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4581623 ; http://dx.doi.org/10.5353/th_b4581623 ; http://hdl.handle.net/10722/133291


University of Hong Kong

20. Qi, Shuang. UreE-Hpn/Hpnl interaction in H. pylori, and the role of cysteines in Hpn.

Degree: PhD, 2010, University of Hong Kong

published_or_final_version

Biochemistry

Doctoral

Doctor of Philosophy

Advisors/Committee Members: Tanner, JA, Huang, J.

Subjects/Keywords: Helicobacter pylori.; Protein-protein interactions.

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APA (6th Edition):

Qi, S. (2010). UreE-Hpn/Hpnl interaction in H. pylori, and the role of cysteines in Hpn. (Doctoral Dissertation). University of Hong Kong. Retrieved from Qi, S. [亓爽]. (2010). UreE-Hpn/Hpnl interaction in H. pylori, and the role of cysteines in Hpn. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4596275 ; http://dx.doi.org/10.5353/th_b4596275 ; http://hdl.handle.net/10722/134074

Chicago Manual of Style (16th Edition):

Qi, Shuang. “UreE-Hpn/Hpnl interaction in H. pylori, and the role of cysteines in Hpn.” 2010. Doctoral Dissertation, University of Hong Kong. Accessed August 19, 2019. Qi, S. [亓爽]. (2010). UreE-Hpn/Hpnl interaction in H. pylori, and the role of cysteines in Hpn. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4596275 ; http://dx.doi.org/10.5353/th_b4596275 ; http://hdl.handle.net/10722/134074.

MLA Handbook (7th Edition):

Qi, Shuang. “UreE-Hpn/Hpnl interaction in H. pylori, and the role of cysteines in Hpn.” 2010. Web. 19 Aug 2019.

Vancouver:

Qi S. UreE-Hpn/Hpnl interaction in H. pylori, and the role of cysteines in Hpn. [Internet] [Doctoral dissertation]. University of Hong Kong; 2010. [cited 2019 Aug 19]. Available from: Qi, S. [亓爽]. (2010). UreE-Hpn/Hpnl interaction in H. pylori, and the role of cysteines in Hpn. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4596275 ; http://dx.doi.org/10.5353/th_b4596275 ; http://hdl.handle.net/10722/134074.

Council of Science Editors:

Qi S. UreE-Hpn/Hpnl interaction in H. pylori, and the role of cysteines in Hpn. [Doctoral Dissertation]. University of Hong Kong; 2010. Available from: Qi, S. [亓爽]. (2010). UreE-Hpn/Hpnl interaction in H. pylori, and the role of cysteines in Hpn. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4596275 ; http://dx.doi.org/10.5353/th_b4596275 ; http://hdl.handle.net/10722/134074


University of Hong Kong

21. 崔菊; Cui, Ju. Kinesin-1 in pancreatic beta cell and renal epithelial cell.

Degree: PhD, 2011, University of Hong Kong

published_or_final_version

Biochemistry

Doctoral

Doctor of Philosophy

Advisors/Committee Members: Zheng, B, Huang, J.

Subjects/Keywords: Pancreatic beta cells; Kinesin; Epithelial cells

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APA (6th Edition):

崔菊; Cui, J. (2011). Kinesin-1 in pancreatic beta cell and renal epithelial cell. (Doctoral Dissertation). University of Hong Kong. Retrieved from Cui, J. [崔菊]. (2011). Kinesin-1 in pancreatic beta cell and renal epithelial cell. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4608397 ; http://dx.doi.org/10.5353/th_b4608397 ; http://hdl.handle.net/10722/197835

Chicago Manual of Style (16th Edition):

崔菊; Cui, Ju. “Kinesin-1 in pancreatic beta cell and renal epithelial cell.” 2011. Doctoral Dissertation, University of Hong Kong. Accessed August 19, 2019. Cui, J. [崔菊]. (2011). Kinesin-1 in pancreatic beta cell and renal epithelial cell. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4608397 ; http://dx.doi.org/10.5353/th_b4608397 ; http://hdl.handle.net/10722/197835.

MLA Handbook (7th Edition):

崔菊; Cui, Ju. “Kinesin-1 in pancreatic beta cell and renal epithelial cell.” 2011. Web. 19 Aug 2019.

Vancouver:

崔菊; Cui J. Kinesin-1 in pancreatic beta cell and renal epithelial cell. [Internet] [Doctoral dissertation]. University of Hong Kong; 2011. [cited 2019 Aug 19]. Available from: Cui, J. [崔菊]. (2011). Kinesin-1 in pancreatic beta cell and renal epithelial cell. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4608397 ; http://dx.doi.org/10.5353/th_b4608397 ; http://hdl.handle.net/10722/197835.

Council of Science Editors:

崔菊; Cui J. Kinesin-1 in pancreatic beta cell and renal epithelial cell. [Doctoral Dissertation]. University of Hong Kong; 2011. Available from: Cui, J. [崔菊]. (2011). Kinesin-1 in pancreatic beta cell and renal epithelial cell. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4608397 ; http://dx.doi.org/10.5353/th_b4608397 ; http://hdl.handle.net/10722/197835


University of Hong Kong

22. 麥志昕; Mak, Chi-yan, Angel. Bioinformatic and functional approaches to identify potential SOX9 target genes in inner ear development.

Degree: PhD, 2010, University of Hong Kong

published_or_final_version

Biochemistry

Doctoral

Doctor of Philosophy

Advisors/Committee Members: Huang, J, Cheah, KSE.

Subjects/Keywords: Labyrinth (Ear) - Growth; Transcription factors

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APA (6th Edition):

麥志昕; Mak, Chi-yan, A. (2010). Bioinformatic and functional approaches to identify potential SOX9 target genes in inner ear development. (Doctoral Dissertation). University of Hong Kong. Retrieved from Mak, C. A. [麥志昕]. (2010). Bioinformatic and functional approaches to identify potential SOX9 target genes in inner ear development. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4560861 ; http://dx.doi.org/10.5353/th_b4560861 ; http://hdl.handle.net/10722/193405

Chicago Manual of Style (16th Edition):

麥志昕; Mak, Chi-yan, Angel. “Bioinformatic and functional approaches to identify potential SOX9 target genes in inner ear development.” 2010. Doctoral Dissertation, University of Hong Kong. Accessed August 19, 2019. Mak, C. A. [麥志昕]. (2010). Bioinformatic and functional approaches to identify potential SOX9 target genes in inner ear development. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4560861 ; http://dx.doi.org/10.5353/th_b4560861 ; http://hdl.handle.net/10722/193405.

MLA Handbook (7th Edition):

麥志昕; Mak, Chi-yan, Angel. “Bioinformatic and functional approaches to identify potential SOX9 target genes in inner ear development.” 2010. Web. 19 Aug 2019.

Vancouver:

麥志昕; Mak, Chi-yan A. Bioinformatic and functional approaches to identify potential SOX9 target genes in inner ear development. [Internet] [Doctoral dissertation]. University of Hong Kong; 2010. [cited 2019 Aug 19]. Available from: Mak, C. A. [麥志昕]. (2010). Bioinformatic and functional approaches to identify potential SOX9 target genes in inner ear development. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4560861 ; http://dx.doi.org/10.5353/th_b4560861 ; http://hdl.handle.net/10722/193405.

Council of Science Editors:

麥志昕; Mak, Chi-yan A. Bioinformatic and functional approaches to identify potential SOX9 target genes in inner ear development. [Doctoral Dissertation]. University of Hong Kong; 2010. Available from: Mak, C. A. [麥志昕]. (2010). Bioinformatic and functional approaches to identify potential SOX9 target genes in inner ear development. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4560861 ; http://dx.doi.org/10.5353/th_b4560861 ; http://hdl.handle.net/10722/193405


University of Hong Kong

23. Wu, Hao. Identification of drug resistant mutations in HIV-1 latently infected patients under successful HAART and in CRF_BC variants selected invitro.

Degree: PhD, 2011, University of Hong Kong

published_or_final_version

Microbiology

Doctoral

Doctor of Philosophy

Advisors/Committee Members: Zheng, B, Huang, J.

Subjects/Keywords: Drug resistance.; HIV (Viruses)

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APA (6th Edition):

Wu, H. (2011). Identification of drug resistant mutations in HIV-1 latently infected patients under successful HAART and in CRF_BC variants selected invitro. (Doctoral Dissertation). University of Hong Kong. Retrieved from Wu, H. [吴昊]. (2011). Identification of drug resistant mutations in HIV-1 latently infected patients under successful HAART and in CRF_BC variants selected in vitro. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4714982 ; http://dx.doi.org/10.5353/th_b4714982 ; http://hdl.handle.net/10722/145690

Chicago Manual of Style (16th Edition):

Wu, Hao. “Identification of drug resistant mutations in HIV-1 latently infected patients under successful HAART and in CRF_BC variants selected invitro.” 2011. Doctoral Dissertation, University of Hong Kong. Accessed August 19, 2019. Wu, H. [吴昊]. (2011). Identification of drug resistant mutations in HIV-1 latently infected patients under successful HAART and in CRF_BC variants selected in vitro. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4714982 ; http://dx.doi.org/10.5353/th_b4714982 ; http://hdl.handle.net/10722/145690.

MLA Handbook (7th Edition):

Wu, Hao. “Identification of drug resistant mutations in HIV-1 latently infected patients under successful HAART and in CRF_BC variants selected invitro.” 2011. Web. 19 Aug 2019.

Vancouver:

Wu H. Identification of drug resistant mutations in HIV-1 latently infected patients under successful HAART and in CRF_BC variants selected invitro. [Internet] [Doctoral dissertation]. University of Hong Kong; 2011. [cited 2019 Aug 19]. Available from: Wu, H. [吴昊]. (2011). Identification of drug resistant mutations in HIV-1 latently infected patients under successful HAART and in CRF_BC variants selected in vitro. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4714982 ; http://dx.doi.org/10.5353/th_b4714982 ; http://hdl.handle.net/10722/145690.

Council of Science Editors:

Wu H. Identification of drug resistant mutations in HIV-1 latently infected patients under successful HAART and in CRF_BC variants selected invitro. [Doctoral Dissertation]. University of Hong Kong; 2011. Available from: Wu, H. [吴昊]. (2011). Identification of drug resistant mutations in HIV-1 latently infected patients under successful HAART and in CRF_BC variants selected in vitro. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4714982 ; http://dx.doi.org/10.5353/th_b4714982 ; http://hdl.handle.net/10722/145690


University of Hong Kong

24. Zhang, Le. Epigenetic regulation in laminopathy-based premature aging.

Degree: PhD, 2011, University of Hong Kong

published_or_final_version

Biochemistry

Doctoral

Doctor of Philosophy

Advisors/Committee Members: Huang, J, Zhou, Z.

Subjects/Keywords: Aging - Genetic aspects.; Chromosome abnormalities.; Epigenesis.; Cells - Aging.

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APA (6th Edition):

Zhang, L. (2011). Epigenetic regulation in laminopathy-based premature aging. (Doctoral Dissertation). University of Hong Kong. Retrieved from Zhang, L. [张乐]. (2011). Epigenetic regulation in laminopathy-based premature aging. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4633767 ; http://dx.doi.org/10.5353/th_b4633767 ; http://hdl.handle.net/10722/141938

Chicago Manual of Style (16th Edition):

Zhang, Le. “Epigenetic regulation in laminopathy-based premature aging.” 2011. Doctoral Dissertation, University of Hong Kong. Accessed August 19, 2019. Zhang, L. [张乐]. (2011). Epigenetic regulation in laminopathy-based premature aging. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4633767 ; http://dx.doi.org/10.5353/th_b4633767 ; http://hdl.handle.net/10722/141938.

MLA Handbook (7th Edition):

Zhang, Le. “Epigenetic regulation in laminopathy-based premature aging.” 2011. Web. 19 Aug 2019.

Vancouver:

Zhang L. Epigenetic regulation in laminopathy-based premature aging. [Internet] [Doctoral dissertation]. University of Hong Kong; 2011. [cited 2019 Aug 19]. Available from: Zhang, L. [张乐]. (2011). Epigenetic regulation in laminopathy-based premature aging. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4633767 ; http://dx.doi.org/10.5353/th_b4633767 ; http://hdl.handle.net/10722/141938.

Council of Science Editors:

Zhang L. Epigenetic regulation in laminopathy-based premature aging. [Doctoral Dissertation]. University of Hong Kong; 2011. Available from: Zhang, L. [张乐]. (2011). Epigenetic regulation in laminopathy-based premature aging. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4633767 ; http://dx.doi.org/10.5353/th_b4633767 ; http://hdl.handle.net/10722/141938


University of Hong Kong

25. Lu, Song. Phenotype analysis of Pdss2 conditional knockout mouse.

Degree: PhD, 2010, University of Hong Kong

published_or_final_version

Biochemistry

Doctoral

Doctor of Philosophy

Advisors/Committee Members: Huang, J, Zhou, Z.

Subjects/Keywords: Cerebellum - Diseases - Animal models.; Transgenic mice - Genetics.; Cerebellum - Diseases - Genetic aspects.; Ubiquinones.

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APA (6th Edition):

Lu, S. (2010). Phenotype analysis of Pdss2 conditional knockout mouse. (Doctoral Dissertation). University of Hong Kong. Retrieved from Lu, S. [鲁嵩]. (2010). Phenotype analysis of Pdss2 conditional knockout mouse. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4555238 ; http://dx.doi.org/10.5353/th_b4555238 ; http://hdl.handle.net/10722/143995

Chicago Manual of Style (16th Edition):

Lu, Song. “Phenotype analysis of Pdss2 conditional knockout mouse.” 2010. Doctoral Dissertation, University of Hong Kong. Accessed August 19, 2019. Lu, S. [鲁嵩]. (2010). Phenotype analysis of Pdss2 conditional knockout mouse. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4555238 ; http://dx.doi.org/10.5353/th_b4555238 ; http://hdl.handle.net/10722/143995.

MLA Handbook (7th Edition):

Lu, Song. “Phenotype analysis of Pdss2 conditional knockout mouse.” 2010. Web. 19 Aug 2019.

Vancouver:

Lu S. Phenotype analysis of Pdss2 conditional knockout mouse. [Internet] [Doctoral dissertation]. University of Hong Kong; 2010. [cited 2019 Aug 19]. Available from: Lu, S. [鲁嵩]. (2010). Phenotype analysis of Pdss2 conditional knockout mouse. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4555238 ; http://dx.doi.org/10.5353/th_b4555238 ; http://hdl.handle.net/10722/143995.

Council of Science Editors:

Lu S. Phenotype analysis of Pdss2 conditional knockout mouse. [Doctoral Dissertation]. University of Hong Kong; 2010. Available from: Lu, S. [鲁嵩]. (2010). Phenotype analysis of Pdss2 conditional knockout mouse. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4555238 ; http://dx.doi.org/10.5353/th_b4555238 ; http://hdl.handle.net/10722/143995


University of Hong Kong

26. Miao, Yuanying. The localization of E. coli persistent gene products.

Degree: PhD, 2010, University of Hong Kong

published_or_final_version

Biochemistry

Doctoral

Doctor of Philosophy

Advisors/Committee Members: Huang, J, Zhou, Z.

Subjects/Keywords: Escherichia coli - Genetics.

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APA (6th Edition):

Miao, Y. (2010). The localization of E. coli persistent gene products. (Doctoral Dissertation). University of Hong Kong. Retrieved from Miao, Y. [缪元颖]. (2010). The localization of E. coli persistent gene products. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4555479 ; http://dx.doi.org/10.5353/th_b4555479 ; http://hdl.handle.net/10722/143999

Chicago Manual of Style (16th Edition):

Miao, Yuanying. “The localization of E. coli persistent gene products.” 2010. Doctoral Dissertation, University of Hong Kong. Accessed August 19, 2019. Miao, Y. [缪元颖]. (2010). The localization of E. coli persistent gene products. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4555479 ; http://dx.doi.org/10.5353/th_b4555479 ; http://hdl.handle.net/10722/143999.

MLA Handbook (7th Edition):

Miao, Yuanying. “The localization of E. coli persistent gene products.” 2010. Web. 19 Aug 2019.

Vancouver:

Miao Y. The localization of E. coli persistent gene products. [Internet] [Doctoral dissertation]. University of Hong Kong; 2010. [cited 2019 Aug 19]. Available from: Miao, Y. [缪元颖]. (2010). The localization of E. coli persistent gene products. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4555479 ; http://dx.doi.org/10.5353/th_b4555479 ; http://hdl.handle.net/10722/143999.

Council of Science Editors:

Miao Y. The localization of E. coli persistent gene products. [Doctoral Dissertation]. University of Hong Kong; 2010. Available from: Miao, Y. [缪元颖]. (2010). The localization of E. coli persistent gene products. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4555479 ; http://dx.doi.org/10.5353/th_b4555479 ; http://hdl.handle.net/10722/143999

.