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You searched for subject:(Protein binding). Showing records 1 – 30 of 1563 total matches.

[1] [2] [3] [4] [5] … [53]

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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 March 01, 2021. 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. 01 Mar 2021.

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 2021 Mar 01]. 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


Brandeis University

2. 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 March 01, 2021. 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. 01 Mar 2021.

Vancouver:

Shen C. Mechanism of Mot1-mediated TBP dissociation from DNA studied using single-molecule fluorescence microscopy. [Internet] [Thesis]. Brandeis University; 2016. [cited 2021 Mar 01]. 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

3. 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 March 01, 2021. 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. 01 Mar 2021.

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 2021 Mar 01]. 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

4. 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 March 01, 2021. 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. 01 Mar 2021.

Vancouver:

Wang C. Biochemical and structural characterization of ankyrins. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2014. [cited 2021 Mar 01]. 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

5. 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 March 01, 2021. 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. 01 Mar 2021.

Vancouver:

Chen J. PDZ domain containing proteins in cell polarity. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2011. [cited 2021 Mar 01]. 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

6. 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 March 01, 2021. 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. 01 Mar 2021.

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 2021 Mar 01]. 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

7. 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 March 01, 2021. 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. 01 Mar 2021.

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 2021 Mar 01]. 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

8. 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 March 01, 2021. 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. 01 Mar 2021.

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 2021 Mar 01]. 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


Hong Kong University of Science and Technology

9. Yang, Zhou LIFS. Decoding WW domain tandem-mediated target recognitions in tissue growth and cell polarity.

Degree: 2019, Hong Kong University of Science and Technology

 WW domain tandem-containing proteins such as KIBRA, YAP, and MAGI play critical roles in cell growth and cell polarity via binding to and positioning target… (more)

Subjects/Keywords: Protein-protein interactions ; Protein binding ; Cells ; Growth

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APA (6th Edition):

Yang, Z. L. (2019). Decoding WW domain tandem-mediated target recognitions in tissue growth and cell polarity. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-101511 ; https://doi.org/10.14711/thesis-991012753260503412 ; http://repository.ust.hk/ir/bitstream/1783.1-101511/1/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):

Yang, Zhou LIFS. “Decoding WW domain tandem-mediated target recognitions in tissue growth and cell polarity.” 2019. Thesis, Hong Kong University of Science and Technology. Accessed March 01, 2021. http://repository.ust.hk/ir/Record/1783.1-101511 ; https://doi.org/10.14711/thesis-991012753260503412 ; http://repository.ust.hk/ir/bitstream/1783.1-101511/1/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):

Yang, Zhou LIFS. “Decoding WW domain tandem-mediated target recognitions in tissue growth and cell polarity.” 2019. Web. 01 Mar 2021.

Vancouver:

Yang ZL. Decoding WW domain tandem-mediated target recognitions in tissue growth and cell polarity. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2019. [cited 2021 Mar 01]. Available from: http://repository.ust.hk/ir/Record/1783.1-101511 ; https://doi.org/10.14711/thesis-991012753260503412 ; http://repository.ust.hk/ir/bitstream/1783.1-101511/1/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:

Yang ZL. Decoding WW domain tandem-mediated target recognitions in tissue growth and cell polarity. [Thesis]. Hong Kong University of Science and Technology; 2019. Available from: http://repository.ust.hk/ir/Record/1783.1-101511 ; https://doi.org/10.14711/thesis-991012753260503412 ; http://repository.ust.hk/ir/bitstream/1783.1-101511/1/th_redirect.html

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


University of Alberta

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

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 March 01, 2021. 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. 01 Mar 2021.

Vancouver:

Simpson DJ. The Discovery and Application of Bacteriophage Receptor Binding Proteins. [Internet] [Doctoral dissertation]. University of Alberta; 2016. [cited 2021 Mar 01]. 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 Manchester

11. 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 March 01, 2021. 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. 01 Mar 2021.

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 2021 Mar 01]. 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

12. 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 March 01, 2021. 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. 01 Mar 2021.

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 2021 Mar 01]. 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


Penn State University

13. Bastidas, Monique. Structural and functional characterization of the transcription factor Pdx1 and its interactions with DNA and proteins.

Degree: 2015, Penn State University

 Homeobox proteins are vital DNA-binding transcription factors that control the spatial and temporal expression of cells and tissue during early development. These proteins are necessary… (more)

Subjects/Keywords: protein binding; NMR; biophysical; homeodomain

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APA (6th Edition):

Bastidas, M. (2015). Structural and functional characterization of the transcription factor Pdx1 and its interactions with DNA and proteins. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/26176

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):

Bastidas, Monique. “Structural and functional characterization of the transcription factor Pdx1 and its interactions with DNA and proteins.” 2015. Thesis, Penn State University. Accessed March 01, 2021. https://submit-etda.libraries.psu.edu/catalog/26176.

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

MLA Handbook (7th Edition):

Bastidas, Monique. “Structural and functional characterization of the transcription factor Pdx1 and its interactions with DNA and proteins.” 2015. Web. 01 Mar 2021.

Vancouver:

Bastidas M. Structural and functional characterization of the transcription factor Pdx1 and its interactions with DNA and proteins. [Internet] [Thesis]. Penn State University; 2015. [cited 2021 Mar 01]. Available from: https://submit-etda.libraries.psu.edu/catalog/26176.

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

Council of Science Editors:

Bastidas M. Structural and functional characterization of the transcription factor Pdx1 and its interactions with DNA and proteins. [Thesis]. Penn State University; 2015. Available from: https://submit-etda.libraries.psu.edu/catalog/26176

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


Queens University

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

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 March 01, 2021. 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. 01 Mar 2021.

Vancouver:

Sun T. Structural Basis of Antifreeze Proteins Binding to Ice . [Internet] [Thesis]. Queens University; 2015. [cited 2021 Mar 01]. 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


University of Manchester

15. 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 (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 March 01, 2021. 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. 01 Mar 2021.

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 2021 Mar 01]. 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


Hong Kong University of Science and Technology

16. 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 March 01, 2021. 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. 01 Mar 2021.

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 2021 Mar 01]. 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

17. 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 March 01, 2021. 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. 01 Mar 2021.

Vancouver:

Chen K. Mechanistic studies of ankyrin-B/ankyrin-G autoinhibition and regulation. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2014. [cited 2021 Mar 01]. 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

18. 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 March 01, 2021. 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. 01 Mar 2021.

Vancouver:

Ranganathan A. Protein – Ligand Binding: Estimation of Binding Free Energies. [Internet] [Thesis]. KTH; 2012. [cited 2021 Mar 01]. 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


Montana State University

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

Degree: PhD, 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. (Doctoral Dissertation). Montana State University. Retrieved from https://scholarworks.montana.edu/xmlui/handle/1/10154

Chicago Manual of Style (16th Edition):

Cousin, Jonathan Martin. “Glycodendrimers : tools to study multivalent galectin-1 interactions.” 2015. Doctoral Dissertation, Montana State University. Accessed March 01, 2021. https://scholarworks.montana.edu/xmlui/handle/1/10154.

MLA Handbook (7th Edition):

Cousin, Jonathan Martin. “Glycodendrimers : tools to study multivalent galectin-1 interactions.” 2015. Web. 01 Mar 2021.

Vancouver:

Cousin JM. Glycodendrimers : tools to study multivalent galectin-1 interactions. [Internet] [Doctoral dissertation]. Montana State University; 2015. [cited 2021 Mar 01]. Available from: https://scholarworks.montana.edu/xmlui/handle/1/10154.

Council of Science Editors:

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


University of New Mexico

20. 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 March 01, 2021. 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. 01 Mar 2021.

Vancouver:

Okello G. COLD INDUCIBLE RNA BINDING PROTEIN IS DISRUPTED IN ER+PR+HER2- TUMORS. [Internet] [Masters thesis]. University of New Mexico; 2014. [cited 2021 Mar 01]. 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

21. 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 March 01, 2021. 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. 01 Mar 2021.

Vancouver:

Aldridge MJ. Functional analysis of a novel DNA binding protein of Streptomyces coelicolor. [Internet] [Doctoral dissertation]. Swansea University; 2012. [cited 2021 Mar 01]. 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


University of Texas Southwestern Medical Center

22. 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 March 01, 2021. 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. 01 Mar 2021.

Vancouver:

Soniat, Michael Maurice I. Structural and Biochemical Studies of Multiple Importin-Histone Interactions. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2016. [cited 2021 Mar 01]. 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


University of Missouri – Columbia

23. Cummings, Andrea Hicks. Toward selective inactivation of protein tyrosine phosphatase 1B via exo-affinity labeling agents.

Degree: 2014, University of Missouri – Columbia

 Exo-affinity labeling agents are compounds that achieve selectivity by modifying non-catalytic residues in a protein. They have been utilized as tools in molecular biology and… (more)

Subjects/Keywords: Protein binding; Protein-tyrosine phosphatase; Thiols  – Analysis

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APA (6th Edition):

Cummings, A. H. (2014). Toward selective inactivation of protein tyrosine phosphatase 1B via exo-affinity labeling agents. (Thesis). University of Missouri – Columbia. Retrieved from http://hdl.handle.net/10355/48205

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):

Cummings, Andrea Hicks. “Toward selective inactivation of protein tyrosine phosphatase 1B via exo-affinity labeling agents.” 2014. Thesis, University of Missouri – Columbia. Accessed March 01, 2021. http://hdl.handle.net/10355/48205.

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

MLA Handbook (7th Edition):

Cummings, Andrea Hicks. “Toward selective inactivation of protein tyrosine phosphatase 1B via exo-affinity labeling agents.” 2014. Web. 01 Mar 2021.

Vancouver:

Cummings AH. Toward selective inactivation of protein tyrosine phosphatase 1B via exo-affinity labeling agents. [Internet] [Thesis]. University of Missouri – Columbia; 2014. [cited 2021 Mar 01]. Available from: http://hdl.handle.net/10355/48205.

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

Council of Science Editors:

Cummings AH. Toward selective inactivation of protein tyrosine phosphatase 1B via exo-affinity labeling agents. [Thesis]. University of Missouri – Columbia; 2014. Available from: http://hdl.handle.net/10355/48205

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


Rhodes University

24. Matereke, Lavious Tapiwa. Analysis of predictive power of binding affinity of PBM-derived sequences.

Degree: Faculty of Science, Biochemistry and Microbiology, 2015, Rhodes University

 A transcription factor (TF) is a protein that binds to specific DNA sequences as part of the initiation stage of transcription. Various methods of finding… (more)

Subjects/Keywords: Transcription factors; Protein binding; DNA-binding proteins; Chromatin; Protein microarrays

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APA (6th Edition):

Matereke, L. T. (2015). Analysis of predictive power of binding affinity of PBM-derived sequences. (Thesis). Rhodes University. Retrieved from http://hdl.handle.net/10962/d1018666

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):

Matereke, Lavious Tapiwa. “Analysis of predictive power of binding affinity of PBM-derived sequences.” 2015. Thesis, Rhodes University. Accessed March 01, 2021. http://hdl.handle.net/10962/d1018666.

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

MLA Handbook (7th Edition):

Matereke, Lavious Tapiwa. “Analysis of predictive power of binding affinity of PBM-derived sequences.” 2015. Web. 01 Mar 2021.

Vancouver:

Matereke LT. Analysis of predictive power of binding affinity of PBM-derived sequences. [Internet] [Thesis]. Rhodes University; 2015. [cited 2021 Mar 01]. Available from: http://hdl.handle.net/10962/d1018666.

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

Council of Science Editors:

Matereke LT. Analysis of predictive power of binding affinity of PBM-derived sequences. [Thesis]. Rhodes University; 2015. Available from: http://hdl.handle.net/10962/d1018666

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

25. Cooney, David. Possible Interacting Proteins for Retinol Binding Protein and Cellular Retinol Binding Protein.

Degree: 2011, RIAN

 Retinol or vitamin A is crucial for many biological processes in the body such as proliferation, differentiation and reproduction. It is mainly stored in the… (more)

Subjects/Keywords: Biology; Interacting Proteins; Retinol Binding Protein; Cellular Retinol Binding Protein

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

APA (6th Edition):

Cooney, D. (2011). Possible Interacting Proteins for Retinol Binding Protein and Cellular Retinol Binding Protein. (Thesis). RIAN. Retrieved from http://eprints.maynoothuniversity.ie/4001/

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):

Cooney, David. “Possible Interacting Proteins for Retinol Binding Protein and Cellular Retinol Binding Protein.” 2011. Thesis, RIAN. Accessed March 01, 2021. http://eprints.maynoothuniversity.ie/4001/.

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

MLA Handbook (7th Edition):

Cooney, David. “Possible Interacting Proteins for Retinol Binding Protein and Cellular Retinol Binding Protein.” 2011. Web. 01 Mar 2021.

Vancouver:

Cooney D. Possible Interacting Proteins for Retinol Binding Protein and Cellular Retinol Binding Protein. [Internet] [Thesis]. RIAN; 2011. [cited 2021 Mar 01]. Available from: http://eprints.maynoothuniversity.ie/4001/.

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

Council of Science Editors:

Cooney D. Possible Interacting Proteins for Retinol Binding Protein and Cellular Retinol Binding Protein. [Thesis]. RIAN; 2011. Available from: http://eprints.maynoothuniversity.ie/4001/

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

26. Cooney, David. Possible Interacting Proteins for Retinol Binding Protein and Cellular Retinol Binding Protein.

Degree: 2011, RIAN

 Retinol or vitamin A is crucial for many biological processes in the body such as proliferation, differentiation and reproduction. It is mainly stored in the… (more)

Subjects/Keywords: Biology; Interacting Proteins; Retinol Binding Protein; Cellular Retinol Binding Protein

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Cooney, D. (2011). Possible Interacting Proteins for Retinol Binding Protein and Cellular Retinol Binding Protein. (Thesis). RIAN. Retrieved from http://mural.maynoothuniversity.ie/4001/

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):

Cooney, David. “Possible Interacting Proteins for Retinol Binding Protein and Cellular Retinol Binding Protein.” 2011. Thesis, RIAN. Accessed March 01, 2021. http://mural.maynoothuniversity.ie/4001/.

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

MLA Handbook (7th Edition):

Cooney, David. “Possible Interacting Proteins for Retinol Binding Protein and Cellular Retinol Binding Protein.” 2011. Web. 01 Mar 2021.

Vancouver:

Cooney D. Possible Interacting Proteins for Retinol Binding Protein and Cellular Retinol Binding Protein. [Internet] [Thesis]. RIAN; 2011. [cited 2021 Mar 01]. Available from: http://mural.maynoothuniversity.ie/4001/.

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

Council of Science Editors:

Cooney D. Possible Interacting Proteins for Retinol Binding Protein and Cellular Retinol Binding Protein. [Thesis]. RIAN; 2011. Available from: http://mural.maynoothuniversity.ie/4001/

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


Texas State University – San Marcos

27. Schaub, Leasha J. Quantifying the Energetics of Binding Between p53 and DNA Using Electrophoretic Mobility Shift Assays.

Degree: MS, Biochemistry, 2012, Texas State University – San Marcos

 A new class of proteins has been termed “intrinsically disordered” or “ID” for short. The proteins within this class appear to lack tertiary stability, though… (more)

Subjects/Keywords: p53; Intrinsically disordered protein; Binding; p53 protein; DNA; DNA-protein interactions; DNA-binding proteins; Electrophoresis

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

APA (6th Edition):

Schaub, L. J. (2012). Quantifying the Energetics of Binding Between p53 and DNA Using Electrophoretic Mobility Shift Assays. (Masters Thesis). Texas State University – San Marcos. Retrieved from https://digital.library.txstate.edu/handle/10877/4371

Chicago Manual of Style (16th Edition):

Schaub, Leasha J. “Quantifying the Energetics of Binding Between p53 and DNA Using Electrophoretic Mobility Shift Assays.” 2012. Masters Thesis, Texas State University – San Marcos. Accessed March 01, 2021. https://digital.library.txstate.edu/handle/10877/4371.

MLA Handbook (7th Edition):

Schaub, Leasha J. “Quantifying the Energetics of Binding Between p53 and DNA Using Electrophoretic Mobility Shift Assays.” 2012. Web. 01 Mar 2021.

Vancouver:

Schaub LJ. Quantifying the Energetics of Binding Between p53 and DNA Using Electrophoretic Mobility Shift Assays. [Internet] [Masters thesis]. Texas State University – San Marcos; 2012. [cited 2021 Mar 01]. Available from: https://digital.library.txstate.edu/handle/10877/4371.

Council of Science Editors:

Schaub LJ. Quantifying the Energetics of Binding Between p53 and DNA Using Electrophoretic Mobility Shift Assays. [Masters Thesis]. Texas State University – San Marcos; 2012. Available from: https://digital.library.txstate.edu/handle/10877/4371


University of Michigan

28. Clark, Jordan. Structural Investigation of Binding Events in Proteins.

Degree: PhD, Medicinal Chemistry, 2018, University of Michigan

 Understanding the biophysical properties that describe protein binding events has allowed for the advancement of drug discovery through structure-based drug design and in silico methodology.… (more)

Subjects/Keywords: Protein flexibility; Protein structure database; Protein-ligand binding; Protein-protein interaction (PPI); Biological Chemistry; Science

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

APA (6th Edition):

Clark, J. (2018). Structural Investigation of Binding Events in Proteins. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/145943

Chicago Manual of Style (16th Edition):

Clark, Jordan. “Structural Investigation of Binding Events in Proteins.” 2018. Doctoral Dissertation, University of Michigan. Accessed March 01, 2021. http://hdl.handle.net/2027.42/145943.

MLA Handbook (7th Edition):

Clark, Jordan. “Structural Investigation of Binding Events in Proteins.” 2018. Web. 01 Mar 2021.

Vancouver:

Clark J. Structural Investigation of Binding Events in Proteins. [Internet] [Doctoral dissertation]. University of Michigan; 2018. [cited 2021 Mar 01]. Available from: http://hdl.handle.net/2027.42/145943.

Council of Science Editors:

Clark J. Structural Investigation of Binding Events in Proteins. [Doctoral Dissertation]. University of Michigan; 2018. Available from: http://hdl.handle.net/2027.42/145943


University of Wollongong

29. Bogema, Daniel Ross. Genomic and proteomic analyses of Mycoplasma hyopneumoniae.

Degree: PhD, 2012, University of Wollongong

  Mycoplasma hyopneumoniae is the aetiological agent of mycoplasmal enzootic pneumonia (MEP), a chronic respiratory disease affecting pigs that inflicts significant economic damage on the… (more)

Subjects/Keywords: mycoplasma hyopneumoniae; adhesion; protein processing; heparin-binding protein; cilium-binding proteins; protein motifs; plasminogen-binding proteins; antigenic variation

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

APA (6th Edition):

Bogema, D. R. (2012). Genomic and proteomic analyses of Mycoplasma hyopneumoniae. (Doctoral Dissertation). University of Wollongong. Retrieved from 060109 Proteomics and Intermolecular Interactions (excl. Medical Proteomics), 060501 Bacteriology, 070205 Animal Protection (Pests and Pathogens) ; https://ro.uow.edu.au/theses/3485

Chicago Manual of Style (16th Edition):

Bogema, Daniel Ross. “Genomic and proteomic analyses of Mycoplasma hyopneumoniae.” 2012. Doctoral Dissertation, University of Wollongong. Accessed March 01, 2021. 060109 Proteomics and Intermolecular Interactions (excl. Medical Proteomics), 060501 Bacteriology, 070205 Animal Protection (Pests and Pathogens) ; https://ro.uow.edu.au/theses/3485.

MLA Handbook (7th Edition):

Bogema, Daniel Ross. “Genomic and proteomic analyses of Mycoplasma hyopneumoniae.” 2012. Web. 01 Mar 2021.

Vancouver:

Bogema DR. Genomic and proteomic analyses of Mycoplasma hyopneumoniae. [Internet] [Doctoral dissertation]. University of Wollongong; 2012. [cited 2021 Mar 01]. Available from: 060109 Proteomics and Intermolecular Interactions (excl. Medical Proteomics), 060501 Bacteriology, 070205 Animal Protection (Pests and Pathogens) ; https://ro.uow.edu.au/theses/3485.

Council of Science Editors:

Bogema DR. Genomic and proteomic analyses of Mycoplasma hyopneumoniae. [Doctoral Dissertation]. University of Wollongong; 2012. Available from: 060109 Proteomics and Intermolecular Interactions (excl. Medical Proteomics), 060501 Bacteriology, 070205 Animal Protection (Pests and Pathogens) ; https://ro.uow.edu.au/theses/3485


Boston University

30. Frame, Nicholas. The structural basis for lipid interactions of serum amyloid A.

Degree: PhD, Biophysics, 2019, Boston University

 Serum amyloid A (SAA) is a small, evolutionarily well-conserved, acute-phase protein best known as the protein precursor for amyloid A amyloidosis. During acute injury, infection,… (more)

Subjects/Keywords: Biophysics; Intrinsically disordered protein; Lipoprotein nanoparticle; Protein-lipid binding; Protein structure

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

APA (6th Edition):

Frame, N. (2019). The structural basis for lipid interactions of serum amyloid A. (Doctoral Dissertation). Boston University. Retrieved from http://hdl.handle.net/2144/38578

Chicago Manual of Style (16th Edition):

Frame, Nicholas. “The structural basis for lipid interactions of serum amyloid A.” 2019. Doctoral Dissertation, Boston University. Accessed March 01, 2021. http://hdl.handle.net/2144/38578.

MLA Handbook (7th Edition):

Frame, Nicholas. “The structural basis for lipid interactions of serum amyloid A.” 2019. Web. 01 Mar 2021.

Vancouver:

Frame N. The structural basis for lipid interactions of serum amyloid A. [Internet] [Doctoral dissertation]. Boston University; 2019. [cited 2021 Mar 01]. Available from: http://hdl.handle.net/2144/38578.

Council of Science Editors:

Frame N. The structural basis for lipid interactions of serum amyloid A. [Doctoral Dissertation]. Boston University; 2019. Available from: http://hdl.handle.net/2144/38578

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