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You searched for subject:(Protein binding). Showing records 1 – 30 of 1419 total matches.

[1] [2] [3] [4] [5] … [48]

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Hong Kong University of Science and Technology

1. Zhu, Jiawei. The novel role of SLY1 in golgi-ER retrograde protein secretory pathway in budding yeast.

Degree: 2015, Hong Kong University of Science and Technology

 Bi-directional trafficking in the early protein secretary protein pathway is a universal phenomenon within eukaryotic cells. In yeast, the retrograde trafficking based on COPI coated… (more)

Subjects/Keywords: Protein binding ; Protein-protein interactions

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APA (6th Edition):

Zhu, J. (2015). The novel role of SLY1 in golgi-ER retrograde protein secretory pathway in budding yeast. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-86332 ; https://doi.org/10.14711/thesis-b1514822 ; http://repository.ust.hk/ir/bitstream/1783.1-86332/1/th_redirect.html

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Zhu, Jiawei. “The novel role of SLY1 in golgi-ER retrograde protein secretory pathway in budding yeast.” 2015. Thesis, Hong Kong University of Science and Technology. Accessed February 19, 2020. http://repository.ust.hk/ir/Record/1783.1-86332 ; https://doi.org/10.14711/thesis-b1514822 ; http://repository.ust.hk/ir/bitstream/1783.1-86332/1/th_redirect.html.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Zhu, Jiawei. “The novel role of SLY1 in golgi-ER retrograde protein secretory pathway in budding yeast.” 2015. Web. 19 Feb 2020.

Vancouver:

Zhu J. The novel role of SLY1 in golgi-ER retrograde protein secretory pathway in budding yeast. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2015. [cited 2020 Feb 19]. Available from: http://repository.ust.hk/ir/Record/1783.1-86332 ; https://doi.org/10.14711/thesis-b1514822 ; http://repository.ust.hk/ir/bitstream/1783.1-86332/1/th_redirect.html.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Zhu J. The novel role of SLY1 in golgi-ER retrograde protein secretory pathway in budding yeast. [Thesis]. Hong Kong University of Science and Technology; 2015. Available from: http://repository.ust.hk/ir/Record/1783.1-86332 ; https://doi.org/10.14711/thesis-b1514822 ; http://repository.ust.hk/ir/bitstream/1783.1-86332/1/th_redirect.html

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Hong Kong

2. Lo, Ka-ching. Case studies on protein-interaction of LSD1 SWIRM-ARDED and Afmp4p/Mp1p : pro-inflammatory mediators.

Degree: PhD, 2012, University of Hong Kong

Protein-ligand and protein-protein interactions play important roles in almost all cellular processes therefore it is a general belief that understanding protein-ligand/protein interaction is essential for… (more)

Subjects/Keywords: Protein binding; Ligand binding (Biochemistry)

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APA (6th Edition):

Lo, K. (2012). Case studies on protein-interaction of LSD1 SWIRM-ARDED and Afmp4p/Mp1p : pro-inflammatory mediators. (Doctoral Dissertation). University of Hong Kong. Retrieved from Lo, K. [羅嘉澄]. (2012). Case studies on protein-interaction of LSD1 SWIRM-ARDED and Afmp4p/Mp1p : pro-inflammatory mediators. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4961748 ; http://dx.doi.org/10.5353/th_b4961748 ; http://hdl.handle.net/10722/221525

Chicago Manual of Style (16th Edition):

Lo, Ka-ching. “Case studies on protein-interaction of LSD1 SWIRM-ARDED and Afmp4p/Mp1p : pro-inflammatory mediators.” 2012. Doctoral Dissertation, University of Hong Kong. Accessed February 19, 2020. Lo, K. [羅嘉澄]. (2012). Case studies on protein-interaction of LSD1 SWIRM-ARDED and Afmp4p/Mp1p : pro-inflammatory mediators. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4961748 ; http://dx.doi.org/10.5353/th_b4961748 ; http://hdl.handle.net/10722/221525.

MLA Handbook (7th Edition):

Lo, Ka-ching. “Case studies on protein-interaction of LSD1 SWIRM-ARDED and Afmp4p/Mp1p : pro-inflammatory mediators.” 2012. Web. 19 Feb 2020.

Vancouver:

Lo K. Case studies on protein-interaction of LSD1 SWIRM-ARDED and Afmp4p/Mp1p : pro-inflammatory mediators. [Internet] [Doctoral dissertation]. University of Hong Kong; 2012. [cited 2020 Feb 19]. Available from: Lo, K. [羅嘉澄]. (2012). Case studies on protein-interaction of LSD1 SWIRM-ARDED and Afmp4p/Mp1p : pro-inflammatory mediators. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4961748 ; http://dx.doi.org/10.5353/th_b4961748 ; http://hdl.handle.net/10722/221525.

Council of Science Editors:

Lo K. Case studies on protein-interaction of LSD1 SWIRM-ARDED and Afmp4p/Mp1p : pro-inflammatory mediators. [Doctoral Dissertation]. University of Hong Kong; 2012. Available from: Lo, K. [羅嘉澄]. (2012). Case studies on protein-interaction of LSD1 SWIRM-ARDED and Afmp4p/Mp1p : pro-inflammatory mediators. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4961748 ; http://dx.doi.org/10.5353/th_b4961748 ; http://hdl.handle.net/10722/221525


University of Hong Kong

3. 赵倩; Zhao, Qian. Identification of a binding target of triptolide and related studies.

Degree: PhD, 2012, University of Hong Kong

Triptolide, a diterpene triepoxide extracted from traditional Chinese medicinal herb Tripterygium wilfordii Hook. F has been shown to have profound inhibitory effects against tumor progression,… (more)

Subjects/Keywords: Protein binding.; Triptolide.

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APA (6th Edition):

赵倩; Zhao, Q. (2012). Identification of a binding target of triptolide and related studies. (Doctoral Dissertation). University of Hong Kong. Retrieved from Zhao, Q. [赵倩]. (2012). Identification of a binding target of triptolide and related studies. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4819916 ; http://dx.doi.org/10.5353/th_b4819916 ; http://hdl.handle.net/10722/185517

Chicago Manual of Style (16th Edition):

赵倩; Zhao, Qian. “Identification of a binding target of triptolide and related studies.” 2012. Doctoral Dissertation, University of Hong Kong. Accessed February 19, 2020. Zhao, Q. [赵倩]. (2012). Identification of a binding target of triptolide and related studies. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4819916 ; http://dx.doi.org/10.5353/th_b4819916 ; http://hdl.handle.net/10722/185517.

MLA Handbook (7th Edition):

赵倩; Zhao, Qian. “Identification of a binding target of triptolide and related studies.” 2012. Web. 19 Feb 2020.

Vancouver:

赵倩; Zhao Q. Identification of a binding target of triptolide and related studies. [Internet] [Doctoral dissertation]. University of Hong Kong; 2012. [cited 2020 Feb 19]. Available from: Zhao, Q. [赵倩]. (2012). Identification of a binding target of triptolide and related studies. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4819916 ; http://dx.doi.org/10.5353/th_b4819916 ; http://hdl.handle.net/10722/185517.

Council of Science Editors:

赵倩; Zhao Q. Identification of a binding target of triptolide and related studies. [Doctoral Dissertation]. University of Hong Kong; 2012. Available from: Zhao, Q. [赵倩]. (2012). Identification of a binding target of triptolide and related studies. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4819916 ; http://dx.doi.org/10.5353/th_b4819916 ; http://hdl.handle.net/10722/185517


Brandeis University

4. Shen, Ciyue. Mechanism of Mot1-mediated TBP dissociation from DNA studied using single-molecule fluorescence microscopy.

Degree: 2016, Brandeis University

 TATA-binding protein (TBP) is a required factor in eukaryotic transcription. It specifically binds to an A-T-rich sequence of the promoter known as the TATA-box, and… (more)

Subjects/Keywords: TATA-binding protein

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APA (6th Edition):

Shen, C. (2016). Mechanism of Mot1-mediated TBP dissociation from DNA studied using single-molecule fluorescence microscopy. (Thesis). Brandeis University. Retrieved from http://hdl.handle.net/10192/32290

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Shen, Ciyue. “Mechanism of Mot1-mediated TBP dissociation from DNA studied using single-molecule fluorescence microscopy.” 2016. Thesis, Brandeis University. Accessed February 19, 2020. http://hdl.handle.net/10192/32290.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Shen, Ciyue. “Mechanism of Mot1-mediated TBP dissociation from DNA studied using single-molecule fluorescence microscopy.” 2016. Web. 19 Feb 2020.

Vancouver:

Shen C. Mechanism of Mot1-mediated TBP dissociation from DNA studied using single-molecule fluorescence microscopy. [Internet] [Thesis]. Brandeis University; 2016. [cited 2020 Feb 19]. Available from: http://hdl.handle.net/10192/32290.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Shen C. Mechanism of Mot1-mediated TBP dissociation from DNA studied using single-molecule fluorescence microscopy. [Thesis]. Brandeis University; 2016. Available from: http://hdl.handle.net/10192/32290

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Alberta

5. Peng, Zhenling. Large-scale Characterization Of Intrinsic Disorder And High-throughput Prediction Of RNA, DNA and Protein Binding Mediated By Intrinsic Disorder.

Degree: PhD, Department of Electrical and Computer Engineering, 2014, University of Alberta

 Intrinsically disordered proteins lack stable 3D structures in vivo, are functionally important, and are very common in nature. In the past three decades, many studies… (more)

Subjects/Keywords: protein-DNA binding; protein-RNA binding; protein-protein interaction; Intrinsic disorder

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APA (6th Edition):

Peng, Z. (2014). Large-scale Characterization Of Intrinsic Disorder And High-throughput Prediction Of RNA, DNA and Protein Binding Mediated By Intrinsic Disorder. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/dv13zt305

Chicago Manual of Style (16th Edition):

Peng, Zhenling. “Large-scale Characterization Of Intrinsic Disorder And High-throughput Prediction Of RNA, DNA and Protein Binding Mediated By Intrinsic Disorder.” 2014. Doctoral Dissertation, University of Alberta. Accessed February 19, 2020. https://era.library.ualberta.ca/files/dv13zt305.

MLA Handbook (7th Edition):

Peng, Zhenling. “Large-scale Characterization Of Intrinsic Disorder And High-throughput Prediction Of RNA, DNA and Protein Binding Mediated By Intrinsic Disorder.” 2014. Web. 19 Feb 2020.

Vancouver:

Peng Z. Large-scale Characterization Of Intrinsic Disorder And High-throughput Prediction Of RNA, DNA and Protein Binding Mediated By Intrinsic Disorder. [Internet] [Doctoral dissertation]. University of Alberta; 2014. [cited 2020 Feb 19]. Available from: https://era.library.ualberta.ca/files/dv13zt305.

Council of Science Editors:

Peng Z. Large-scale Characterization Of Intrinsic Disorder And High-throughput Prediction Of RNA, DNA and Protein Binding Mediated By Intrinsic Disorder. [Doctoral Dissertation]. University of Alberta; 2014. Available from: https://era.library.ualberta.ca/files/dv13zt305


Hong Kong University of Science and Technology

6. Wang, Chao. Biochemical and structural characterization of ankyrins.

Degree: 2014, Hong Kong University of Science and Technology

 Ankyrin adaptors together with their spectrin partners coordinate diverse ion channels and cell adhesion molecules within plasma membrane domains and thereby promote physiological activities including… (more)

Subjects/Keywords: Proteins ; Protein binding ; Protein-protein interactions

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APA (6th Edition):

Wang, C. (2014). Biochemical and structural characterization of ankyrins. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-71766 ; https://doi.org/10.14711/thesis-b1302214 ; http://repository.ust.hk/ir/bitstream/1783.1-71766/1/th_redirect.html

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Wang, Chao. “Biochemical and structural characterization of ankyrins.” 2014. Thesis, Hong Kong University of Science and Technology. Accessed February 19, 2020. http://repository.ust.hk/ir/Record/1783.1-71766 ; https://doi.org/10.14711/thesis-b1302214 ; http://repository.ust.hk/ir/bitstream/1783.1-71766/1/th_redirect.html.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Wang, Chao. “Biochemical and structural characterization of ankyrins.” 2014. Web. 19 Feb 2020.

Vancouver:

Wang C. Biochemical and structural characterization of ankyrins. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2014. [cited 2020 Feb 19]. Available from: http://repository.ust.hk/ir/Record/1783.1-71766 ; https://doi.org/10.14711/thesis-b1302214 ; http://repository.ust.hk/ir/bitstream/1783.1-71766/1/th_redirect.html.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Wang C. Biochemical and structural characterization of ankyrins. [Thesis]. Hong Kong University of Science and Technology; 2014. Available from: http://repository.ust.hk/ir/Record/1783.1-71766 ; https://doi.org/10.14711/thesis-b1302214 ; http://repository.ust.hk/ir/bitstream/1783.1-71766/1/th_redirect.html

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Hong Kong University of Science and Technology

7. Chen, Jia. PDZ domain containing proteins in cell polarity.

Degree: 2011, Hong Kong University of Science and Technology

 In my thesis, I’ll use PDZ domain as an example to illustrate how could a small modular domain achieves its specific and diverse binding property… (more)

Subjects/Keywords: Carrier proteins ; Protein binding ; Protein-protein interactions

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APA (6th Edition):

Chen, J. (2011). PDZ domain containing proteins in cell polarity. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-7617 ; https://doi.org/10.14711/thesis-b1160526 ; http://repository.ust.hk/ir/bitstream/1783.1-7617/1/th_redirect.html

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Chen, Jia. “PDZ domain containing proteins in cell polarity.” 2011. Thesis, Hong Kong University of Science and Technology. Accessed February 19, 2020. http://repository.ust.hk/ir/Record/1783.1-7617 ; https://doi.org/10.14711/thesis-b1160526 ; http://repository.ust.hk/ir/bitstream/1783.1-7617/1/th_redirect.html.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Chen, Jia. “PDZ domain containing proteins in cell polarity.” 2011. Web. 19 Feb 2020.

Vancouver:

Chen J. PDZ domain containing proteins in cell polarity. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2011. [cited 2020 Feb 19]. Available from: http://repository.ust.hk/ir/Record/1783.1-7617 ; https://doi.org/10.14711/thesis-b1160526 ; http://repository.ust.hk/ir/bitstream/1783.1-7617/1/th_redirect.html.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Chen J. PDZ domain containing proteins in cell polarity. [Thesis]. Hong Kong University of Science and Technology; 2011. Available from: http://repository.ust.hk/ir/Record/1783.1-7617 ; https://doi.org/10.14711/thesis-b1160526 ; http://repository.ust.hk/ir/bitstream/1783.1-7617/1/th_redirect.html

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Hong Kong University of Science and Technology

8. Zheng, Zhaorong. Structure determination and property characterization of MAGI-3 PDZ4 domain and BDNF prodomain.

Degree: 2012, Hong Kong University of Science and Technology

 As one of the most abundant protein-protein interaction module in the eukaryotic genomes, PDZ domain participates in a variety of cellular activities including neuronal signal… (more)

Subjects/Keywords: Protein binding ; Neurotrophic functions ; Protein-protein interactions

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APA (6th Edition):

Zheng, Z. (2012). Structure determination and property characterization of MAGI-3 PDZ4 domain and BDNF prodomain. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-7855 ; https://doi.org/10.14711/thesis-b1180093 ; http://repository.ust.hk/ir/bitstream/1783.1-7855/1/th_redirect.html

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Zheng, Zhaorong. “Structure determination and property characterization of MAGI-3 PDZ4 domain and BDNF prodomain.” 2012. Thesis, Hong Kong University of Science and Technology. Accessed February 19, 2020. http://repository.ust.hk/ir/Record/1783.1-7855 ; https://doi.org/10.14711/thesis-b1180093 ; http://repository.ust.hk/ir/bitstream/1783.1-7855/1/th_redirect.html.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Zheng, Zhaorong. “Structure determination and property characterization of MAGI-3 PDZ4 domain and BDNF prodomain.” 2012. Web. 19 Feb 2020.

Vancouver:

Zheng Z. Structure determination and property characterization of MAGI-3 PDZ4 domain and BDNF prodomain. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2012. [cited 2020 Feb 19]. Available from: http://repository.ust.hk/ir/Record/1783.1-7855 ; https://doi.org/10.14711/thesis-b1180093 ; http://repository.ust.hk/ir/bitstream/1783.1-7855/1/th_redirect.html.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Zheng Z. Structure determination and property characterization of MAGI-3 PDZ4 domain and BDNF prodomain. [Thesis]. Hong Kong University of Science and Technology; 2012. Available from: http://repository.ust.hk/ir/Record/1783.1-7855 ; https://doi.org/10.14711/thesis-b1180093 ; http://repository.ust.hk/ir/bitstream/1783.1-7855/1/th_redirect.html

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Hong Kong University of Science and Technology

9. Ye, Fei. Structures and target recognition properties of a multi-PDZ domain scaffold protein INAD.

Degree: 2013, Hong Kong University of Science and Technology

 PDZ domains are highly abundant protein-protein interaction modules and often found in multi-domain scaffold proteins. PDZ-domain-containing scaffold proteins regulate multiple biological processes, including trafficking and… (more)

Subjects/Keywords: Protein-protein interactions ; Protein binding ; Carrier proteins

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APA (6th Edition):

Ye, F. (2013). Structures and target recognition properties of a multi-PDZ domain scaffold protein INAD. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-80943 ; https://doi.org/10.14711/thesis-b1250978 ; http://repository.ust.hk/ir/bitstream/1783.1-80943/1/th_redirect.html

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Ye, Fei. “Structures and target recognition properties of a multi-PDZ domain scaffold protein INAD.” 2013. Thesis, Hong Kong University of Science and Technology. Accessed February 19, 2020. http://repository.ust.hk/ir/Record/1783.1-80943 ; https://doi.org/10.14711/thesis-b1250978 ; http://repository.ust.hk/ir/bitstream/1783.1-80943/1/th_redirect.html.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Ye, Fei. “Structures and target recognition properties of a multi-PDZ domain scaffold protein INAD.” 2013. Web. 19 Feb 2020.

Vancouver:

Ye F. Structures and target recognition properties of a multi-PDZ domain scaffold protein INAD. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2013. [cited 2020 Feb 19]. Available from: http://repository.ust.hk/ir/Record/1783.1-80943 ; https://doi.org/10.14711/thesis-b1250978 ; http://repository.ust.hk/ir/bitstream/1783.1-80943/1/th_redirect.html.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Ye F. Structures and target recognition properties of a multi-PDZ domain scaffold protein INAD. [Thesis]. Hong Kong University of Science and Technology; 2013. Available from: http://repository.ust.hk/ir/Record/1783.1-80943 ; https://doi.org/10.14711/thesis-b1250978 ; http://repository.ust.hk/ir/bitstream/1783.1-80943/1/th_redirect.html

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Hong Kong University of Science and Technology

10. Xia, Yitian. Characterization of the interaction between PSD-95 GK domain and MAP1A.

Degree: 2014, Hong Kong University of Science and Technology

 Nervous system, mainly composed of large numbers of neurons and glia cells, plays central roles in controlling various physiological functions in the metazoan. The normal… (more)

Subjects/Keywords: Synapses ; Tubulins ; Protein binding ; Protein-protein interactions

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APA (6th Edition):

Xia, Y. (2014). Characterization of the interaction between PSD-95 GK domain and MAP1A. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-87481 ; https://doi.org/10.14711/thesis-b1334216 ; http://repository.ust.hk/ir/bitstream/1783.1-87481/1/th_redirect.html

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Xia, Yitian. “Characterization of the interaction between PSD-95 GK domain and MAP1A.” 2014. Thesis, Hong Kong University of Science and Technology. Accessed February 19, 2020. http://repository.ust.hk/ir/Record/1783.1-87481 ; https://doi.org/10.14711/thesis-b1334216 ; http://repository.ust.hk/ir/bitstream/1783.1-87481/1/th_redirect.html.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Xia, Yitian. “Characterization of the interaction between PSD-95 GK domain and MAP1A.” 2014. Web. 19 Feb 2020.

Vancouver:

Xia Y. Characterization of the interaction between PSD-95 GK domain and MAP1A. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2014. [cited 2020 Feb 19]. Available from: http://repository.ust.hk/ir/Record/1783.1-87481 ; https://doi.org/10.14711/thesis-b1334216 ; http://repository.ust.hk/ir/bitstream/1783.1-87481/1/th_redirect.html.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Xia Y. Characterization of the interaction between PSD-95 GK domain and MAP1A. [Thesis]. Hong Kong University of Science and Technology; 2014. Available from: http://repository.ust.hk/ir/Record/1783.1-87481 ; https://doi.org/10.14711/thesis-b1334216 ; http://repository.ust.hk/ir/bitstream/1783.1-87481/1/th_redirect.html

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Indian Institute of Science

11. Prajapati, Ravindra Singh. Thermodynamic Characterization Of Wild Type And Mutants Of The E.coli Periplasmic Binding Proteins LBP, LIVBP, MBP And RBP.

Degree: 2006, Indian Institute of Science

 Native states of globular proteins typically show stabilization in the range of 5 to 15 kcal/mol with respect to their unfolded states. There has been… (more)

Subjects/Keywords: Proteins; Escherechia Coli; Leucine Binding Protein; Maltose Binding Protein; Ribose Binding Protein; Leucine Valine Binding Protein; Protein Folding; Protein Stability; Periplasmic Binding Protein; Thioredoxin (Trx); Biochemistry

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APA (6th Edition):

Prajapati, R. S. (2006). Thermodynamic Characterization Of Wild Type And Mutants Of The E.coli Periplasmic Binding Proteins LBP, LIVBP, MBP And RBP. (Thesis). Indian Institute of Science. Retrieved from http://hdl.handle.net/2005/428

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Prajapati, Ravindra Singh. “Thermodynamic Characterization Of Wild Type And Mutants Of The E.coli Periplasmic Binding Proteins LBP, LIVBP, MBP And RBP.” 2006. Thesis, Indian Institute of Science. Accessed February 19, 2020. http://hdl.handle.net/2005/428.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Prajapati, Ravindra Singh. “Thermodynamic Characterization Of Wild Type And Mutants Of The E.coli Periplasmic Binding Proteins LBP, LIVBP, MBP And RBP.” 2006. Web. 19 Feb 2020.

Vancouver:

Prajapati RS. Thermodynamic Characterization Of Wild Type And Mutants Of The E.coli Periplasmic Binding Proteins LBP, LIVBP, MBP And RBP. [Internet] [Thesis]. Indian Institute of Science; 2006. [cited 2020 Feb 19]. Available from: http://hdl.handle.net/2005/428.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Prajapati RS. Thermodynamic Characterization Of Wild Type And Mutants Of The E.coli Periplasmic Binding Proteins LBP, LIVBP, MBP And RBP. [Thesis]. Indian Institute of Science; 2006. Available from: http://hdl.handle.net/2005/428

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Alberta

12. Simpson, David James. The Discovery and Application of Bacteriophage Receptor Binding Proteins.

Degree: PhD, Department of Biological Sciences, 2016, University of Alberta

 Bacteriophages are considered to be the most abundant and potentially the most diverse form of life on earth. Phage receptor binding proteins (RBPs), which allow… (more)

Subjects/Keywords: Bacteriophage; Receptor Binding Protein; Salmonella

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APA (6th Edition):

Simpson, D. J. (2016). The Discovery and Application of Bacteriophage Receptor Binding Proteins. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/csj1392172

Chicago Manual of Style (16th Edition):

Simpson, David James. “The Discovery and Application of Bacteriophage Receptor Binding Proteins.” 2016. Doctoral Dissertation, University of Alberta. Accessed February 19, 2020. https://era.library.ualberta.ca/files/csj1392172.

MLA Handbook (7th Edition):

Simpson, David James. “The Discovery and Application of Bacteriophage Receptor Binding Proteins.” 2016. Web. 19 Feb 2020.

Vancouver:

Simpson DJ. The Discovery and Application of Bacteriophage Receptor Binding Proteins. [Internet] [Doctoral dissertation]. University of Alberta; 2016. [cited 2020 Feb 19]. Available from: https://era.library.ualberta.ca/files/csj1392172.

Council of Science Editors:

Simpson DJ. The Discovery and Application of Bacteriophage Receptor Binding Proteins. [Doctoral Dissertation]. University of Alberta; 2016. Available from: https://era.library.ualberta.ca/files/csj1392172


University of New Mexico

13. Okello, Grace. COLD INDUCIBLE RNA BINDING PROTEIN IS DISRUPTED IN ER+PR+HER2- TUMORS.

Degree: Biomedical Sciences Graduate Program, 2014, University of New Mexico

 RNA binding proteins (RBPs) and microRNAs (miRNAs) control gene expression post-transcriptionally by targeting mRNAs for translational activation, repression, or degradation. To date, aberrant expression of… (more)

Subjects/Keywords: Cold inducible RNA Binding Protein

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APA (6th Edition):

Okello, G. (2014). COLD INDUCIBLE RNA BINDING PROTEIN IS DISRUPTED IN ER+PR+HER2- TUMORS. (Masters Thesis). University of New Mexico. Retrieved from https://digitalrepository.unm.edu/biom_etds/83

Chicago Manual of Style (16th Edition):

Okello, Grace. “COLD INDUCIBLE RNA BINDING PROTEIN IS DISRUPTED IN ER+PR+HER2- TUMORS.” 2014. Masters Thesis, University of New Mexico. Accessed February 19, 2020. https://digitalrepository.unm.edu/biom_etds/83.

MLA Handbook (7th Edition):

Okello, Grace. “COLD INDUCIBLE RNA BINDING PROTEIN IS DISRUPTED IN ER+PR+HER2- TUMORS.” 2014. Web. 19 Feb 2020.

Vancouver:

Okello G. COLD INDUCIBLE RNA BINDING PROTEIN IS DISRUPTED IN ER+PR+HER2- TUMORS. [Internet] [Masters thesis]. University of New Mexico; 2014. [cited 2020 Feb 19]. Available from: https://digitalrepository.unm.edu/biom_etds/83.

Council of Science Editors:

Okello G. COLD INDUCIBLE RNA BINDING PROTEIN IS DISRUPTED IN ER+PR+HER2- TUMORS. [Masters Thesis]. University of New Mexico; 2014. Available from: https://digitalrepository.unm.edu/biom_etds/83


Brock University

14. Baptist, Matilda. The effect of lysobisphosphatidic acid (LBPA) on α-tocopherol transfer protein (α-TTP) binding to lipid membranes .

Degree: Department of Biological Sciences, 2010, Brock University

 The a-tocopherol transfer protein (a-TTP) is responsible for the retention of the atocopherol form of vitamin E in living organisms. The detailed ligand transfer mechanism… (more)

Subjects/Keywords: Vitamin E; Protein binding.

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APA (6th Edition):

Baptist, M. (2010). The effect of lysobisphosphatidic acid (LBPA) on α-tocopherol transfer protein (α-TTP) binding to lipid membranes . (Thesis). Brock University. Retrieved from http://hdl.handle.net/10464/2956

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Baptist, Matilda. “The effect of lysobisphosphatidic acid (LBPA) on α-tocopherol transfer protein (α-TTP) binding to lipid membranes .” 2010. Thesis, Brock University. Accessed February 19, 2020. http://hdl.handle.net/10464/2956.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Baptist, Matilda. “The effect of lysobisphosphatidic acid (LBPA) on α-tocopherol transfer protein (α-TTP) binding to lipid membranes .” 2010. Web. 19 Feb 2020.

Vancouver:

Baptist M. The effect of lysobisphosphatidic acid (LBPA) on α-tocopherol transfer protein (α-TTP) binding to lipid membranes . [Internet] [Thesis]. Brock University; 2010. [cited 2020 Feb 19]. Available from: http://hdl.handle.net/10464/2956.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Baptist M. The effect of lysobisphosphatidic acid (LBPA) on α-tocopherol transfer protein (α-TTP) binding to lipid membranes . [Thesis]. Brock University; 2010. Available from: http://hdl.handle.net/10464/2956

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Brock University

15. Zhang, Wen Xiao. Mechanism of tocopherol transfer by human α-tocopherol transfer protein (α-hTTP) .

Degree: Centre for Biotechnology, 2010, Brock University

 Vitamin E is a well known fat soluble chain breaking antioxidant. It is a general tenn used to describe a family of eight stereoisomers of… (more)

Subjects/Keywords: Protein binding; Vitamin E

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APA (6th Edition):

Zhang, W. X. (2010). Mechanism of tocopherol transfer by human α-tocopherol transfer protein (α-hTTP) . (Thesis). Brock University. Retrieved from http://hdl.handle.net/10464/3044

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Zhang, Wen Xiao. “Mechanism of tocopherol transfer by human α-tocopherol transfer protein (α-hTTP) .” 2010. Thesis, Brock University. Accessed February 19, 2020. http://hdl.handle.net/10464/3044.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Zhang, Wen Xiao. “Mechanism of tocopherol transfer by human α-tocopherol transfer protein (α-hTTP) .” 2010. Web. 19 Feb 2020.

Vancouver:

Zhang WX. Mechanism of tocopherol transfer by human α-tocopherol transfer protein (α-hTTP) . [Internet] [Thesis]. Brock University; 2010. [cited 2020 Feb 19]. Available from: http://hdl.handle.net/10464/3044.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Zhang WX. Mechanism of tocopherol transfer by human α-tocopherol transfer protein (α-hTTP) . [Thesis]. Brock University; 2010. Available from: http://hdl.handle.net/10464/3044

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Montana State University

16. Cousin, Jonathan Martin. Glycodendrimers : tools to study multivalent galectin-1 interactions.

Degree: College of Letters & Science, 2015, Montana State University

 Galectin-1 is a carbohydrate binding protein that mediates cancer processes through multivalent interactions with glycoproteins expressed on the surface of cancer cells and in the… (more)

Subjects/Keywords: Protein binding.; Dendrimers.; Cancer.

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APA (6th Edition):

Cousin, J. M. (2015). Glycodendrimers : tools to study multivalent galectin-1 interactions. (Thesis). Montana State University. Retrieved from https://scholarworks.montana.edu/xmlui/handle/1/10154

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Cousin, Jonathan Martin. “Glycodendrimers : tools to study multivalent galectin-1 interactions.” 2015. Thesis, Montana State University. Accessed February 19, 2020. https://scholarworks.montana.edu/xmlui/handle/1/10154.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Cousin, Jonathan Martin. “Glycodendrimers : tools to study multivalent galectin-1 interactions.” 2015. Web. 19 Feb 2020.

Vancouver:

Cousin JM. Glycodendrimers : tools to study multivalent galectin-1 interactions. [Internet] [Thesis]. Montana State University; 2015. [cited 2020 Feb 19]. Available from: https://scholarworks.montana.edu/xmlui/handle/1/10154.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Cousin JM. Glycodendrimers : tools to study multivalent galectin-1 interactions. [Thesis]. Montana State University; 2015. Available from: https://scholarworks.montana.edu/xmlui/handle/1/10154

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Western Australia

17. Mohamad Razif, Muhammad Fazril. Engineering RNA-binding proteins.

Degree: PhD, 2012, University of Western Australia

RNA-protein interactions have key roles in the regulation of gene expression and are vital for many cellular processes and complex developmental programs in eukaryotes. Proteins… (more)

Subjects/Keywords: Protein engineering; RNA binding proteins

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APA (6th Edition):

Mohamad Razif, M. F. (2012). Engineering RNA-binding proteins. (Doctoral Dissertation). University of Western Australia. Retrieved from http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=34900&local_base=GEN01-INS01

Chicago Manual of Style (16th Edition):

Mohamad Razif, Muhammad Fazril. “Engineering RNA-binding proteins.” 2012. Doctoral Dissertation, University of Western Australia. Accessed February 19, 2020. http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=34900&local_base=GEN01-INS01.

MLA Handbook (7th Edition):

Mohamad Razif, Muhammad Fazril. “Engineering RNA-binding proteins.” 2012. Web. 19 Feb 2020.

Vancouver:

Mohamad Razif MF. Engineering RNA-binding proteins. [Internet] [Doctoral dissertation]. University of Western Australia; 2012. [cited 2020 Feb 19]. Available from: http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=34900&local_base=GEN01-INS01.

Council of Science Editors:

Mohamad Razif MF. Engineering RNA-binding proteins. [Doctoral Dissertation]. University of Western Australia; 2012. Available from: http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=34900&local_base=GEN01-INS01


University of Manchester

18. Saeed, Sadia. Uncovering the molecular mechanism of ParG dimerization and its role in segrosome assembly of multidrug resistance plasmid TP228.

Degree: PhD, 2012, University of Manchester

 The multidrug resistance plasmid TP228 replicates at low copy number in Escherichia coli. Stable partitioning of this plasmid is mediated by three essential components: a… (more)

Subjects/Keywords: 572.8; ParG DNA binding protein

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Saeed, S. (2012). Uncovering the molecular mechanism of ParG dimerization and its role in segrosome assembly of multidrug resistance plasmid TP228. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/uncovering-the-molecular-mechanism-of-parg-dimerization-and-its-role-in-segrosome-assembly-of-multidrug-resistance-plasmid-tp228(76dda7e1-a14c-4d85-9b10-6524e1fb9281).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.647355

Chicago Manual of Style (16th Edition):

Saeed, Sadia. “Uncovering the molecular mechanism of ParG dimerization and its role in segrosome assembly of multidrug resistance plasmid TP228.” 2012. Doctoral Dissertation, University of Manchester. Accessed February 19, 2020. https://www.research.manchester.ac.uk/portal/en/theses/uncovering-the-molecular-mechanism-of-parg-dimerization-and-its-role-in-segrosome-assembly-of-multidrug-resistance-plasmid-tp228(76dda7e1-a14c-4d85-9b10-6524e1fb9281).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.647355.

MLA Handbook (7th Edition):

Saeed, Sadia. “Uncovering the molecular mechanism of ParG dimerization and its role in segrosome assembly of multidrug resistance plasmid TP228.” 2012. Web. 19 Feb 2020.

Vancouver:

Saeed S. Uncovering the molecular mechanism of ParG dimerization and its role in segrosome assembly of multidrug resistance plasmid TP228. [Internet] [Doctoral dissertation]. University of Manchester; 2012. [cited 2020 Feb 19]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/uncovering-the-molecular-mechanism-of-parg-dimerization-and-its-role-in-segrosome-assembly-of-multidrug-resistance-plasmid-tp228(76dda7e1-a14c-4d85-9b10-6524e1fb9281).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.647355.

Council of Science Editors:

Saeed S. Uncovering the molecular mechanism of ParG dimerization and its role in segrosome assembly of multidrug resistance plasmid TP228. [Doctoral Dissertation]. University of Manchester; 2012. Available from: https://www.research.manchester.ac.uk/portal/en/theses/uncovering-the-molecular-mechanism-of-parg-dimerization-and-its-role-in-segrosome-assembly-of-multidrug-resistance-plasmid-tp228(76dda7e1-a14c-4d85-9b10-6524e1fb9281).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.647355


University of Florida

19. Leclerc, Jenna. Lysozyme transport in p-HEMA hydrogel contact lenses.

Degree: 2010, University of Florida

 The objective of this paper is to understand and provide a model for the transport mechanism by which lysozyme deposits on poly-hydroxy ethyl methacrylate (p-HEMA)… (more)

Subjects/Keywords: Lysozyme; Protein binding; Biochemistry

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APA (6th Edition):

Leclerc, J. (2010). Lysozyme transport in p-HEMA hydrogel contact lenses. (Thesis). University of Florida. Retrieved from http://ufdc.ufl.edu/AA00061327

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Leclerc, Jenna. “Lysozyme transport in p-HEMA hydrogel contact lenses.” 2010. Thesis, University of Florida. Accessed February 19, 2020. http://ufdc.ufl.edu/AA00061327.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Leclerc, Jenna. “Lysozyme transport in p-HEMA hydrogel contact lenses.” 2010. Web. 19 Feb 2020.

Vancouver:

Leclerc J. Lysozyme transport in p-HEMA hydrogel contact lenses. [Internet] [Thesis]. University of Florida; 2010. [cited 2020 Feb 19]. Available from: http://ufdc.ufl.edu/AA00061327.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Leclerc J. Lysozyme transport in p-HEMA hydrogel contact lenses. [Thesis]. University of Florida; 2010. Available from: http://ufdc.ufl.edu/AA00061327

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Manchester

20. Saeed, Sadia. Uncovering the molecular mechanism of ParG dimerization and its role in segrosome assembly of multidrug resistance plasmid TP228.

Degree: 2012, University of Manchester

 The multidrug resistance plasmid TP228 replicates at low copy number in Escherichia coli. Stable partitioning of this plasmid is mediated by three essential components: a… (more)

Subjects/Keywords: ParG DNA binding protein

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APA (6th Edition):

Saeed, S. (2012). Uncovering the molecular mechanism of ParG dimerization and its role in segrosome assembly of multidrug resistance plasmid TP228. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:183543

Chicago Manual of Style (16th Edition):

Saeed, Sadia. “Uncovering the molecular mechanism of ParG dimerization and its role in segrosome assembly of multidrug resistance plasmid TP228.” 2012. Doctoral Dissertation, University of Manchester. Accessed February 19, 2020. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:183543.

MLA Handbook (7th Edition):

Saeed, Sadia. “Uncovering the molecular mechanism of ParG dimerization and its role in segrosome assembly of multidrug resistance plasmid TP228.” 2012. Web. 19 Feb 2020.

Vancouver:

Saeed S. Uncovering the molecular mechanism of ParG dimerization and its role in segrosome assembly of multidrug resistance plasmid TP228. [Internet] [Doctoral dissertation]. University of Manchester; 2012. [cited 2020 Feb 19]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:183543.

Council of Science Editors:

Saeed S. Uncovering the molecular mechanism of ParG dimerization and its role in segrosome assembly of multidrug resistance plasmid TP228. [Doctoral Dissertation]. University of Manchester; 2012. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:183543


McMaster University

21. Holzapfel, Nicholas. Investigating the Role of the RNA-Binding Protein MUSASHI-2 (MSI2) in Normal Hematopoiesis and Leukemia.

Degree: PhD, 2016, McMaster University

Musashi-2 (MSI2), a member of the Musashi family of RNA-binding proteins, is thought to play a critical role in the maintenance of stem cell populations… (more)

Subjects/Keywords: RNA-Binding Protein; Musashi; Hematopoiesis

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APA (6th Edition):

Holzapfel, N. (2016). Investigating the Role of the RNA-Binding Protein MUSASHI-2 (MSI2) in Normal Hematopoiesis and Leukemia. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/20628

Chicago Manual of Style (16th Edition):

Holzapfel, Nicholas. “Investigating the Role of the RNA-Binding Protein MUSASHI-2 (MSI2) in Normal Hematopoiesis and Leukemia.” 2016. Doctoral Dissertation, McMaster University. Accessed February 19, 2020. http://hdl.handle.net/11375/20628.

MLA Handbook (7th Edition):

Holzapfel, Nicholas. “Investigating the Role of the RNA-Binding Protein MUSASHI-2 (MSI2) in Normal Hematopoiesis and Leukemia.” 2016. Web. 19 Feb 2020.

Vancouver:

Holzapfel N. Investigating the Role of the RNA-Binding Protein MUSASHI-2 (MSI2) in Normal Hematopoiesis and Leukemia. [Internet] [Doctoral dissertation]. McMaster University; 2016. [cited 2020 Feb 19]. Available from: http://hdl.handle.net/11375/20628.

Council of Science Editors:

Holzapfel N. Investigating the Role of the RNA-Binding Protein MUSASHI-2 (MSI2) in Normal Hematopoiesis and Leukemia. [Doctoral Dissertation]. McMaster University; 2016. Available from: http://hdl.handle.net/11375/20628


Massey University

22. Schwalbe, Martin. Intrinsic disorder and coiled coil formation in prostate apoptosis response factor-4 (Par-4) : submitted in fulfilment of the requirements of the degree of Doctor of Philosphy, Institute of Fundamental Sciences, Massey University, New Zealand .

Degree: 2010, Massey University

 Prostate apoptosis response factor-4 (Par-4) is a ubiquitously expressed pro-apoptotic and tumour suppressive protein. Par-4 contains a highly conserved coiled coil (CC) region at the… (more)

Subjects/Keywords: Binding proteins; Protein NMR

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APA (6th Edition):

Schwalbe, M. (2010). Intrinsic disorder and coiled coil formation in prostate apoptosis response factor-4 (Par-4) : submitted in fulfilment of the requirements of the degree of Doctor of Philosphy, Institute of Fundamental Sciences, Massey University, New Zealand . (Thesis). Massey University. Retrieved from http://hdl.handle.net/10179/1688

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Schwalbe, Martin. “Intrinsic disorder and coiled coil formation in prostate apoptosis response factor-4 (Par-4) : submitted in fulfilment of the requirements of the degree of Doctor of Philosphy, Institute of Fundamental Sciences, Massey University, New Zealand .” 2010. Thesis, Massey University. Accessed February 19, 2020. http://hdl.handle.net/10179/1688.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Schwalbe, Martin. “Intrinsic disorder and coiled coil formation in prostate apoptosis response factor-4 (Par-4) : submitted in fulfilment of the requirements of the degree of Doctor of Philosphy, Institute of Fundamental Sciences, Massey University, New Zealand .” 2010. Web. 19 Feb 2020.

Vancouver:

Schwalbe M. Intrinsic disorder and coiled coil formation in prostate apoptosis response factor-4 (Par-4) : submitted in fulfilment of the requirements of the degree of Doctor of Philosphy, Institute of Fundamental Sciences, Massey University, New Zealand . [Internet] [Thesis]. Massey University; 2010. [cited 2020 Feb 19]. Available from: http://hdl.handle.net/10179/1688.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Schwalbe M. Intrinsic disorder and coiled coil formation in prostate apoptosis response factor-4 (Par-4) : submitted in fulfilment of the requirements of the degree of Doctor of Philosphy, Institute of Fundamental Sciences, Massey University, New Zealand . [Thesis]. Massey University; 2010. Available from: http://hdl.handle.net/10179/1688

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

23. Aldridge, Matthew J. Functional analysis of a novel DNA binding protein of Streptomyces coelicolor.

Degree: PhD, 2012, Swansea University

 Secondary metabolism occurs after the main growth phase in Streptomyces. A 'transition phase' occurs to remodel global patterns of gene expression at the onset of… (more)

Subjects/Keywords: 572.8; DNA binding protein; DNA

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APA (6th Edition):

Aldridge, M. J. (2012). Functional analysis of a novel DNA binding protein of Streptomyces coelicolor. (Doctoral Dissertation). Swansea University. Retrieved from https://cronfa.swan.ac.uk/Record/cronfa42406 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.678565

Chicago Manual of Style (16th Edition):

Aldridge, Matthew J. “Functional analysis of a novel DNA binding protein of Streptomyces coelicolor.” 2012. Doctoral Dissertation, Swansea University. Accessed February 19, 2020. https://cronfa.swan.ac.uk/Record/cronfa42406 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.678565.

MLA Handbook (7th Edition):

Aldridge, Matthew J. “Functional analysis of a novel DNA binding protein of Streptomyces coelicolor.” 2012. Web. 19 Feb 2020.

Vancouver:

Aldridge MJ. Functional analysis of a novel DNA binding protein of Streptomyces coelicolor. [Internet] [Doctoral dissertation]. Swansea University; 2012. [cited 2020 Feb 19]. Available from: https://cronfa.swan.ac.uk/Record/cronfa42406 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.678565.

Council of Science Editors:

Aldridge MJ. Functional analysis of a novel DNA binding protein of Streptomyces coelicolor. [Doctoral Dissertation]. Swansea University; 2012. Available from: https://cronfa.swan.ac.uk/Record/cronfa42406 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.678565


Queens University

24. Sun, Tianjun. Structural Basis of Antifreeze Proteins Binding to Ice .

Degree: Biomedical and Molecular Sciences, 2015, Queens University

 Antifreeze proteins (AFPs) are a class of proteins that adsorb to the surface of ice crystals to prevent their growth. Recent structural work has shown… (more)

Subjects/Keywords: Ice-Binding Mechanism; Antifreeze Protein

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APA (6th Edition):

Sun, T. (2015). Structural Basis of Antifreeze Proteins Binding to Ice . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/13546

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Sun, Tianjun. “Structural Basis of Antifreeze Proteins Binding to Ice .” 2015. Thesis, Queens University. Accessed February 19, 2020. http://hdl.handle.net/1974/13546.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Sun, Tianjun. “Structural Basis of Antifreeze Proteins Binding to Ice .” 2015. Web. 19 Feb 2020.

Vancouver:

Sun T. Structural Basis of Antifreeze Proteins Binding to Ice . [Internet] [Thesis]. Queens University; 2015. [cited 2020 Feb 19]. Available from: http://hdl.handle.net/1974/13546.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Sun T. Structural Basis of Antifreeze Proteins Binding to Ice . [Thesis]. Queens University; 2015. Available from: http://hdl.handle.net/1974/13546

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Hong Kong University of Science and Technology

25. Li, Youjun. Complex structure of crumbs cytoplasmic tail with moesin FERM domain reveals a novel FERM-binding mode.

Degree: 2012, Hong Kong University of Science and Technology

 The apical transmembrane protein Crumbs is a determinant of apical-basal cell polarity. The short cytoplasmic domain of Crumbs, containing two highly conserved motifs, a PSD95/Discs-large/ZO1… (more)

Subjects/Keywords: Membrane proteins ; Structure ; Protein binding

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APA (6th Edition):

Li, Y. (2012). Complex structure of crumbs cytoplasmic tail with moesin FERM domain reveals a novel FERM-binding mode. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-73408 ; https://doi.org/10.14711/thesis-b1190245 ; http://repository.ust.hk/ir/bitstream/1783.1-73408/1/th_redirect.html

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Li, Youjun. “Complex structure of crumbs cytoplasmic tail with moesin FERM domain reveals a novel FERM-binding mode.” 2012. Thesis, Hong Kong University of Science and Technology. Accessed February 19, 2020. http://repository.ust.hk/ir/Record/1783.1-73408 ; https://doi.org/10.14711/thesis-b1190245 ; http://repository.ust.hk/ir/bitstream/1783.1-73408/1/th_redirect.html.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Li, Youjun. “Complex structure of crumbs cytoplasmic tail with moesin FERM domain reveals a novel FERM-binding mode.” 2012. Web. 19 Feb 2020.

Vancouver:

Li Y. Complex structure of crumbs cytoplasmic tail with moesin FERM domain reveals a novel FERM-binding mode. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2012. [cited 2020 Feb 19]. Available from: http://repository.ust.hk/ir/Record/1783.1-73408 ; https://doi.org/10.14711/thesis-b1190245 ; http://repository.ust.hk/ir/bitstream/1783.1-73408/1/th_redirect.html.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Li Y. Complex structure of crumbs cytoplasmic tail with moesin FERM domain reveals a novel FERM-binding mode. [Thesis]. Hong Kong University of Science and Technology; 2012. Available from: http://repository.ust.hk/ir/Record/1783.1-73408 ; https://doi.org/10.14711/thesis-b1190245 ; http://repository.ust.hk/ir/bitstream/1783.1-73408/1/th_redirect.html

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Hong Kong University of Science and Technology

26. Chen, Keyu. Mechanistic studies of ankyrin-B/ankyrin-G autoinhibition and regulation.

Degree: 2014, Hong Kong University of Science and Technology

 Ankyrins are a family of scaffold proteins, which serves to link great varieties of functional related but structurally diverse integral membrane proteins to the spectrin-based… (more)

Subjects/Keywords: Scaffold proteins ; Protein binding

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APA (6th Edition):

Chen, K. (2014). Mechanistic studies of ankyrin-B/ankyrin-G autoinhibition and regulation. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-86331 ; https://doi.org/10.14711/thesis-b1334213 ; http://repository.ust.hk/ir/bitstream/1783.1-86331/1/th_redirect.html

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Chen, Keyu. “Mechanistic studies of ankyrin-B/ankyrin-G autoinhibition and regulation.” 2014. Thesis, Hong Kong University of Science and Technology. Accessed February 19, 2020. http://repository.ust.hk/ir/Record/1783.1-86331 ; https://doi.org/10.14711/thesis-b1334213 ; http://repository.ust.hk/ir/bitstream/1783.1-86331/1/th_redirect.html.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Chen, Keyu. “Mechanistic studies of ankyrin-B/ankyrin-G autoinhibition and regulation.” 2014. Web. 19 Feb 2020.

Vancouver:

Chen K. Mechanistic studies of ankyrin-B/ankyrin-G autoinhibition and regulation. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2014. [cited 2020 Feb 19]. Available from: http://repository.ust.hk/ir/Record/1783.1-86331 ; https://doi.org/10.14711/thesis-b1334213 ; http://repository.ust.hk/ir/bitstream/1783.1-86331/1/th_redirect.html.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Chen K. Mechanistic studies of ankyrin-B/ankyrin-G autoinhibition and regulation. [Thesis]. Hong Kong University of Science and Technology; 2014. Available from: http://repository.ust.hk/ir/Record/1783.1-86331 ; https://doi.org/10.14711/thesis-b1334213 ; http://repository.ust.hk/ir/bitstream/1783.1-86331/1/th_redirect.html

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


KTH

27. Ranganathan, Anirudh. Protein – Ligand Binding: Estimation of Binding Free Energies.

Degree: Chemical Science and Engineering (CHE), 2012, KTH

  Accurate prediction of binding free energies of protein-ligand system has long been a focus area for theoretical and computational studies; with important implications in… (more)

Subjects/Keywords: Protein+ligand+binding+free+energy

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Ranganathan, A. (2012). Protein – Ligand Binding: Estimation of Binding Free Energies. (Thesis). KTH. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-147527

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Ranganathan, Anirudh. “Protein – Ligand Binding: Estimation of Binding Free Energies.” 2012. Thesis, KTH. Accessed February 19, 2020. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-147527.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Ranganathan, Anirudh. “Protein – Ligand Binding: Estimation of Binding Free Energies.” 2012. Web. 19 Feb 2020.

Vancouver:

Ranganathan A. Protein – Ligand Binding: Estimation of Binding Free Energies. [Internet] [Thesis]. KTH; 2012. [cited 2020 Feb 19]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-147527.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Ranganathan A. Protein – Ligand Binding: Estimation of Binding Free Energies. [Thesis]. KTH; 2012. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-147527

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

28. Johnson, Rachel Anne. Utilizing Isothermal Titration Calorimetry to Quantify the Thermodynamics of Cadmium Mimicry: A Comparison to Calcium.

Degree: 2016, NC Docks

 Isothermal titration calorimetry (ITC) is a powerful calorimetric method which can determine all thermodynamic parameters (K, [Delta]H, [Delta]G, and [Delta]S) for a binding event in… (more)

Subjects/Keywords: Calorimetry; Protein binding; Thermodynamics

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APA (6th Edition):

Johnson, R. A. (2016). Utilizing Isothermal Titration Calorimetry to Quantify the Thermodynamics of Cadmium Mimicry: A Comparison to Calcium. (Thesis). NC Docks. Retrieved from http://libres.uncg.edu/ir/ecu/f/0000-embargo-holder.txt

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Johnson, Rachel Anne. “Utilizing Isothermal Titration Calorimetry to Quantify the Thermodynamics of Cadmium Mimicry: A Comparison to Calcium.” 2016. Thesis, NC Docks. Accessed February 19, 2020. http://libres.uncg.edu/ir/ecu/f/0000-embargo-holder.txt.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Johnson, Rachel Anne. “Utilizing Isothermal Titration Calorimetry to Quantify the Thermodynamics of Cadmium Mimicry: A Comparison to Calcium.” 2016. Web. 19 Feb 2020.

Vancouver:

Johnson RA. Utilizing Isothermal Titration Calorimetry to Quantify the Thermodynamics of Cadmium Mimicry: A Comparison to Calcium. [Internet] [Thesis]. NC Docks; 2016. [cited 2020 Feb 19]. Available from: http://libres.uncg.edu/ir/ecu/f/0000-embargo-holder.txt.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Johnson RA. Utilizing Isothermal Titration Calorimetry to Quantify the Thermodynamics of Cadmium Mimicry: A Comparison to Calcium. [Thesis]. NC Docks; 2016. Available from: http://libres.uncg.edu/ir/ecu/f/0000-embargo-holder.txt

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Texas Southwestern Medical Center

29. Soniat, Michael Maurice, II. Structural and Biochemical Studies of Multiple Importin-Histone Interactions.

Degree: 2016, University of Texas Southwestern Medical Center

 Multiple Importins can bind the N-terminal tails of histones H3 and H4, and import them into the nucleus to be assembled into the nucleosomes. However,… (more)

Subjects/Keywords: Histones; Karyopherins; Protein Binding; Protein Domains

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APA (6th Edition):

Soniat, Michael Maurice, I. (2016). Structural and Biochemical Studies of Multiple Importin-Histone Interactions. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/5306

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Soniat, Michael Maurice, II. “Structural and Biochemical Studies of Multiple Importin-Histone Interactions.” 2016. Thesis, University of Texas Southwestern Medical Center. Accessed February 19, 2020. http://hdl.handle.net/2152.5/5306.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Soniat, Michael Maurice, II. “Structural and Biochemical Studies of Multiple Importin-Histone Interactions.” 2016. Web. 19 Feb 2020.

Vancouver:

Soniat, Michael Maurice I. Structural and Biochemical Studies of Multiple Importin-Histone Interactions. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2016. [cited 2020 Feb 19]. Available from: http://hdl.handle.net/2152.5/5306.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Soniat, Michael Maurice I. Structural and Biochemical Studies of Multiple Importin-Histone Interactions. [Thesis]. University of Texas Southwestern Medical Center; 2016. Available from: http://hdl.handle.net/2152.5/5306

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Texas A&M University

30. Zeng, Bin. Functional characterization of acyl-CoA binding protein (ACBP) and oxysterol binding protein-related proteins (ORPS) from Cryptosporidium parvum.

Degree: 2009, Texas A&M University

 From opportunistic protist Cryptosporidium parvum we identified and functionally assayed a fatty acyl-CoA-binding protein (ACBP) gene. The CpACBP1 gene encodes a protein of 268 aa… (more)

Subjects/Keywords: acyl-CoA binding protein; oxysterol binding protein-related proteins

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APA (6th Edition):

Zeng, B. (2009). Functional characterization of acyl-CoA binding protein (ACBP) and oxysterol binding protein-related proteins (ORPS) from Cryptosporidium parvum. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-1211

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Zeng, Bin. “Functional characterization of acyl-CoA binding protein (ACBP) and oxysterol binding protein-related proteins (ORPS) from Cryptosporidium parvum.” 2009. Thesis, Texas A&M University. Accessed February 19, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-1211.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Zeng, Bin. “Functional characterization of acyl-CoA binding protein (ACBP) and oxysterol binding protein-related proteins (ORPS) from Cryptosporidium parvum.” 2009. Web. 19 Feb 2020.

Vancouver:

Zeng B. Functional characterization of acyl-CoA binding protein (ACBP) and oxysterol binding protein-related proteins (ORPS) from Cryptosporidium parvum. [Internet] [Thesis]. Texas A&M University; 2009. [cited 2020 Feb 19]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-1211.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Zeng B. Functional characterization of acyl-CoA binding protein (ACBP) and oxysterol binding protein-related proteins (ORPS) from Cryptosporidium parvum. [Thesis]. Texas A&M University; 2009. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-1211

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

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