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You searched for subject:(Field of Research 06 Biological Sciences 0601 Biochemistry AND Cell Biology). Showing records 1 – 30 of 1138 total matches.

[1] [2] [3] [4] [5] … [38]

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University of Canterbury

1. Chen R. Multiple P-TEFbs cooperatively regulate the release of promoter-proximally paused RNA polymerase II.

Degree: 2016, University of Canterbury

 The association of DSIF and NELF with initiated RNA Polymerase II (Pol II) is the general mechanism for inducing promoter-proximal pausing of Pol II. However,… (more)

Subjects/Keywords: Field of Research::06 - Biological Sciences::0601 - Biochemistry and Cell Biology

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APA (6th Edition):

R, C. (2016). Multiple P-TEFbs cooperatively regulate the release of promoter-proximally paused RNA polymerase II. (Thesis). University of Canterbury. Retrieved from http://hdl.handle.net/10092/15337

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):

R, Chen. “Multiple P-TEFbs cooperatively regulate the release of promoter-proximally paused RNA polymerase II.” 2016. Thesis, University of Canterbury. Accessed May 22, 2019. http://hdl.handle.net/10092/15337.

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

MLA Handbook (7th Edition):

R, Chen. “Multiple P-TEFbs cooperatively regulate the release of promoter-proximally paused RNA polymerase II.” 2016. Web. 22 May 2019.

Vancouver:

R C. Multiple P-TEFbs cooperatively regulate the release of promoter-proximally paused RNA polymerase II. [Internet] [Thesis]. University of Canterbury; 2016. [cited 2019 May 22]. Available from: http://hdl.handle.net/10092/15337.

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

Council of Science Editors:

R C. Multiple P-TEFbs cooperatively regulate the release of promoter-proximally paused RNA polymerase II. [Thesis]. University of Canterbury; 2016. Available from: http://hdl.handle.net/10092/15337

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


University of Canterbury

2. Friemann R. Substrate-bound outward-open structure of a Na+-coupled sialic acid symporter reveals a new Na+ site.

Degree: 2018, University of Canterbury

 © 2018 The Author(s). Many pathogenic bacteria utilise sialic acids as an energy source or use them as an external coating to evade immune detection.… (more)

Subjects/Keywords: Field of Research::06 - Biological Sciences::0605 - Microbiology::060501 - Bacteriology; Field of Research::06 - Biological Sciences::0601 - Biochemistry and Cell Biology::060108 - Protein Trafficking; Field of Research::06 - Biological Sciences::0601 - Biochemistry and Cell Biology::060109 - Proteomics and Intermolecular Interactions (excl. Medical Proteomics)

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APA (6th Edition):

R, F. (2018). Substrate-bound outward-open structure of a Na+-coupled sialic acid symporter reveals a new Na+ site. (Thesis). University of Canterbury. Retrieved from http://hdl.handle.net/10092/16322

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):

R, Friemann. “Substrate-bound outward-open structure of a Na+-coupled sialic acid symporter reveals a new Na+ site.” 2018. Thesis, University of Canterbury. Accessed May 22, 2019. http://hdl.handle.net/10092/16322.

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

MLA Handbook (7th Edition):

R, Friemann. “Substrate-bound outward-open structure of a Na+-coupled sialic acid symporter reveals a new Na+ site.” 2018. Web. 22 May 2019.

Vancouver:

R F. Substrate-bound outward-open structure of a Na+-coupled sialic acid symporter reveals a new Na+ site. [Internet] [Thesis]. University of Canterbury; 2018. [cited 2019 May 22]. Available from: http://hdl.handle.net/10092/16322.

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

Council of Science Editors:

R F. Substrate-bound outward-open structure of a Na+-coupled sialic acid symporter reveals a new Na+ site. [Thesis]. University of Canterbury; 2018. Available from: http://hdl.handle.net/10092/16322

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


University of Canterbury

3. Greening C. Mixotrophy drives niche expansion of verrucomicrobial methanotrophs.

Degree: 2017, University of Canterbury

 Aerobic methanotrophic bacteria have evolved a specialist lifestyle dependent on consumption of methane and other short-chain carbon compounds. However, their apparent substrate specialism runs contrary… (more)

Subjects/Keywords: Field of Research::06 - Biological Sciences::0605 - Microbiology::060501 - Bacteriology; Field of Research::06 - Biological Sciences::0601 - Biochemistry and Cell Biology::060104 - Cell Metabolism

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APA (6th Edition):

C, G. (2017). Mixotrophy drives niche expansion of verrucomicrobial methanotrophs. (Thesis). University of Canterbury. Retrieved from http://hdl.handle.net/10092/14987

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):

C, Greening. “Mixotrophy drives niche expansion of verrucomicrobial methanotrophs.” 2017. Thesis, University of Canterbury. Accessed May 22, 2019. http://hdl.handle.net/10092/14987.

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

MLA Handbook (7th Edition):

C, Greening. “Mixotrophy drives niche expansion of verrucomicrobial methanotrophs.” 2017. Web. 22 May 2019.

Vancouver:

C G. Mixotrophy drives niche expansion of verrucomicrobial methanotrophs. [Internet] [Thesis]. University of Canterbury; 2017. [cited 2019 May 22]. Available from: http://hdl.handle.net/10092/14987.

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

Council of Science Editors:

C G. Mixotrophy drives niche expansion of verrucomicrobial methanotrophs. [Thesis]. University of Canterbury; 2017. Available from: http://hdl.handle.net/10092/14987

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


University of Canterbury

4. Nelson A. Synthesis and Demonstration of the Biological Relevance of sp(3)-rich Scaffolds Distantly Related to Natural Product Frameworks.

Degree: 2017, University of Canterbury

 The productive exploration of chemical space is an enduring challenge in chemical biology and medicinal chemistry. Natural products are biologically relevant, and their frameworks have… (more)

Subjects/Keywords: chemical biology; fragments; molecular diversity; natural products; proteins; Field of Research::06 - Biological Sciences::0601 - Biochemistry and Cell Biology

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APA (6th Edition):

A, N. (2017). Synthesis and Demonstration of the Biological Relevance of sp(3)-rich Scaffolds Distantly Related to Natural Product Frameworks. (Thesis). University of Canterbury. Retrieved from http://hdl.handle.net/10092/16259

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):

A, Nelson. “Synthesis and Demonstration of the Biological Relevance of sp(3)-rich Scaffolds Distantly Related to Natural Product Frameworks.” 2017. Thesis, University of Canterbury. Accessed May 22, 2019. http://hdl.handle.net/10092/16259.

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

MLA Handbook (7th Edition):

A, Nelson. “Synthesis and Demonstration of the Biological Relevance of sp(3)-rich Scaffolds Distantly Related to Natural Product Frameworks.” 2017. Web. 22 May 2019.

Vancouver:

A N. Synthesis and Demonstration of the Biological Relevance of sp(3)-rich Scaffolds Distantly Related to Natural Product Frameworks. [Internet] [Thesis]. University of Canterbury; 2017. [cited 2019 May 22]. Available from: http://hdl.handle.net/10092/16259.

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

Council of Science Editors:

A N. Synthesis and Demonstration of the Biological Relevance of sp(3)-rich Scaffolds Distantly Related to Natural Product Frameworks. [Thesis]. University of Canterbury; 2017. Available from: http://hdl.handle.net/10092/16259

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


University of Canterbury

5. Chapman HN. Femtosecond X-ray coherent diffraction of aligned amyloid fibrils on low background grapheme.

Degree: 2018, University of Canterbury

 © 2018 The Author(s). Here we present a new approach to diffraction imaging of amyloid fibrils, combining a free-standing graphene support and single nanofocused X-ray… (more)

Subjects/Keywords: Field of Research::06 - Biological Sciences::0601 - Biochemistry and Cell Biology::060109 - Proteomics and Intermolecular Interactions (excl. Medical Proteomics); Field of Research::06 - Biological Sciences::0601 - Biochemistry and Cell Biology::060102 - Bioinformatics; Field of Research::06 - Biological Sciences::0601 - Biochemistry and Cell Biology::060112 - Structural Biology (incl. Macromolecular Modelling)

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APA (6th Edition):

HN, C. (2018). Femtosecond X-ray coherent diffraction of aligned amyloid fibrils on low background grapheme. (Thesis). University of Canterbury. Retrieved from http://hdl.handle.net/10092/16228

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):

HN, Chapman. “Femtosecond X-ray coherent diffraction of aligned amyloid fibrils on low background grapheme.” 2018. Thesis, University of Canterbury. Accessed May 22, 2019. http://hdl.handle.net/10092/16228.

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

MLA Handbook (7th Edition):

HN, Chapman. “Femtosecond X-ray coherent diffraction of aligned amyloid fibrils on low background grapheme.” 2018. Web. 22 May 2019.

Vancouver:

HN C. Femtosecond X-ray coherent diffraction of aligned amyloid fibrils on low background grapheme. [Internet] [Thesis]. University of Canterbury; 2018. [cited 2019 May 22]. Available from: http://hdl.handle.net/10092/16228.

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

Council of Science Editors:

HN C. Femtosecond X-ray coherent diffraction of aligned amyloid fibrils on low background grapheme. [Thesis]. University of Canterbury; 2018. Available from: http://hdl.handle.net/10092/16228

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


University of Canterbury

6. Alkaisi, M.M. Bioimprinted polymer platforms for cell culture using soft lithography.

Degree: Electrical and Computer Engineering; University of Canterbury. Biomolecular Interaction Centre, 2014, University of Canterbury

 It is becoming recognised that traditional methods of culture in vitro on flat substrates do not replicate physiological conditions well, and a number of studies… (more)

Subjects/Keywords: bioimprint; cell culture platform; cancer cell; soft lithography; surface topography; cell microenvironment; Field of Research::06 - Biological Sciences::0601 - Biochemistry and Cell Biology::060106 - Cellular Interactions (incl. Adhesion, Matrix, Cell Wall); Field of Research::06 - Biological Sciences::0601 - Biochemistry and Cell Biology::060105 - Cell Neurochemistry

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APA (6th Edition):

Alkaisi, M. M. (2014). Bioimprinted polymer platforms for cell culture using soft lithography. (Thesis). University of Canterbury. Retrieved from http://hdl.handle.net/10092/10095

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):

Alkaisi, M M. “Bioimprinted polymer platforms for cell culture using soft lithography.” 2014. Thesis, University of Canterbury. Accessed May 22, 2019. http://hdl.handle.net/10092/10095.

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

MLA Handbook (7th Edition):

Alkaisi, M M. “Bioimprinted polymer platforms for cell culture using soft lithography.” 2014. Web. 22 May 2019.

Vancouver:

Alkaisi MM. Bioimprinted polymer platforms for cell culture using soft lithography. [Internet] [Thesis]. University of Canterbury; 2014. [cited 2019 May 22]. Available from: http://hdl.handle.net/10092/10095.

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

Council of Science Editors:

Alkaisi MM. Bioimprinted polymer platforms for cell culture using soft lithography. [Thesis]. University of Canterbury; 2014. Available from: http://hdl.handle.net/10092/10095

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


University of Canterbury

7. Alkaisi, M.M. Bioimprinted polymer platforms for cell culture using soft lithography.

Degree: Electrical and Computer Engineering; University of Canterbury. Biomolecular Interaction Centre, 2014, University of Canterbury

 Background: It is becoming recognised that traditional methods of culture in vitro on flat substrates do not replicate physiological conditions well, and a number of… (more)

Subjects/Keywords: bioimprint; cell culture platform; cancer cell; soft lithography; surface topography; cell microenvironment; Field of Research::06 - Biological Sciences::0601 - Biochemistry and Cell Biology::060104 - Cell Metabolism; Field of Research::06 - Biological Sciences::0601 - Biochemistry and Cell Biology::060103 - Cell Development, Proliferation and Death

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APA (6th Edition):

Alkaisi, M. M. (2014). Bioimprinted polymer platforms for cell culture using soft lithography. (Thesis). University of Canterbury. Retrieved from http://hdl.handle.net/10092/10493

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):

Alkaisi, M M. “Bioimprinted polymer platforms for cell culture using soft lithography.” 2014. Thesis, University of Canterbury. Accessed May 22, 2019. http://hdl.handle.net/10092/10493.

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

MLA Handbook (7th Edition):

Alkaisi, M M. “Bioimprinted polymer platforms for cell culture using soft lithography.” 2014. Web. 22 May 2019.

Vancouver:

Alkaisi MM. Bioimprinted polymer platforms for cell culture using soft lithography. [Internet] [Thesis]. University of Canterbury; 2014. [cited 2019 May 22]. Available from: http://hdl.handle.net/10092/10493.

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

Council of Science Editors:

Alkaisi MM. Bioimprinted polymer platforms for cell culture using soft lithography. [Thesis]. University of Canterbury; 2014. Available from: http://hdl.handle.net/10092/10493

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


University of Canterbury

8. Pearce, F.G. Characterisation of the first enzymes committed to lysine biosynthesis in Arabidopsis thaliana.

Degree: Biological Sciences; University of Canterbury. Biomolecular Interaction Centre, 2012, University of Canterbury

 In plants, the lysine biosynthetic pathway is an attractive target for both the development of herbicides and increasing the nutritional value of crops given that… (more)

Subjects/Keywords: Field of Research::07 - Agricultural and Veterinary Sciences::0703 - Crop and Pasture Production::070303 - Crop and Pasture Biochemistry and Physiology; Field of Research::06 - Biological Sciences::0601 - Biochemistry and Cell Biology::060107 - Enzymes; Field of Research::06 - Biological Sciences::0601 - Biochemistry and Cell Biology::060113 - Synthetic Biology; Field of Research::06 - Biological Sciences::0607 - Plant Biology::060705 - Plant Physiology

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APA (6th Edition):

Pearce, F. G. (2012). Characterisation of the first enzymes committed to lysine biosynthesis in Arabidopsis thaliana. (Thesis). University of Canterbury. Retrieved from http://hdl.handle.net/10092/8009

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):

Pearce, F G. “Characterisation of the first enzymes committed to lysine biosynthesis in Arabidopsis thaliana.” 2012. Thesis, University of Canterbury. Accessed May 22, 2019. http://hdl.handle.net/10092/8009.

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

MLA Handbook (7th Edition):

Pearce, F G. “Characterisation of the first enzymes committed to lysine biosynthesis in Arabidopsis thaliana.” 2012. Web. 22 May 2019.

Vancouver:

Pearce FG. Characterisation of the first enzymes committed to lysine biosynthesis in Arabidopsis thaliana. [Internet] [Thesis]. University of Canterbury; 2012. [cited 2019 May 22]. Available from: http://hdl.handle.net/10092/8009.

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

Council of Science Editors:

Pearce FG. Characterisation of the first enzymes committed to lysine biosynthesis in Arabidopsis thaliana. [Thesis]. University of Canterbury; 2012. Available from: http://hdl.handle.net/10092/8009

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


University of Canterbury

9. Jackson, R.R. Widespread reliance on olfactory sex and species identification by lyssomanine and spartaeine jumping spiders.

Degree: Biological Sciences, 2012, University of Canterbury

 Jumping spiders (Salticidae) are renowned for their exceptional vision, but this does not preclude use of other senses. Here we provide evidence that olfactory pheromones… (more)

Subjects/Keywords: communication; chemoreception; olfaction; pheromones; spider; Salticidae; Field of Research::06 - Biological Sciences::0608 - Zoology::060808 - Invertebrate Biology; Field of Research::06 - Biological Sciences::0608 - Zoology::060801 - Animal Behaviour; Field of Research::06 - Biological Sciences::0601 - Biochemistry and Cell Biology::060199 - Biochemistry and Cell Biology not elsewhere classified

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APA (6th Edition):

Jackson, R. R. (2012). Widespread reliance on olfactory sex and species identification by lyssomanine and spartaeine jumping spiders. (Thesis). University of Canterbury. Retrieved from http://hdl.handle.net/10092/9734

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):

Jackson, R R. “Widespread reliance on olfactory sex and species identification by lyssomanine and spartaeine jumping spiders.” 2012. Thesis, University of Canterbury. Accessed May 22, 2019. http://hdl.handle.net/10092/9734.

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

MLA Handbook (7th Edition):

Jackson, R R. “Widespread reliance on olfactory sex and species identification by lyssomanine and spartaeine jumping spiders.” 2012. Web. 22 May 2019.

Vancouver:

Jackson RR. Widespread reliance on olfactory sex and species identification by lyssomanine and spartaeine jumping spiders. [Internet] [Thesis]. University of Canterbury; 2012. [cited 2019 May 22]. Available from: http://hdl.handle.net/10092/9734.

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

Council of Science Editors:

Jackson RR. Widespread reliance on olfactory sex and species identification by lyssomanine and spartaeine jumping spiders. [Thesis]. University of Canterbury; 2012. Available from: http://hdl.handle.net/10092/9734

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


University of Canterbury

10. Woodfield TBF. Fabrication of polymeric substrates with micro- and nanoscale topography bioimprinted at progressive cell morphologies.

Degree: 2012, University of Canterbury

 This work introduces a novel process for the fabrication of polymer cell culture substrates containing physical topography based on timepoint specific cell phenotype replicas. Bioimprinting… (more)

Subjects/Keywords: Field of Research::06 - Biological Sciences::0601 - Biochemistry and Cell Biology::060106 - Cellular Interactions (incl. Adhesion, Matrix, Cell Wall); Field of Research::06 - Biological Sciences::0601 - Biochemistry and Cell Biology::060105 - Cell Neurochemistry

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APA (6th Edition):

TBF, W. (2012). Fabrication of polymeric substrates with micro- and nanoscale topography bioimprinted at progressive cell morphologies. (Thesis). University of Canterbury. Retrieved from http://hdl.handle.net/10092/13721

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):

TBF, Woodfield. “Fabrication of polymeric substrates with micro- and nanoscale topography bioimprinted at progressive cell morphologies.” 2012. Thesis, University of Canterbury. Accessed May 22, 2019. http://hdl.handle.net/10092/13721.

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

MLA Handbook (7th Edition):

TBF, Woodfield. “Fabrication of polymeric substrates with micro- and nanoscale topography bioimprinted at progressive cell morphologies.” 2012. Web. 22 May 2019.

Vancouver:

TBF W. Fabrication of polymeric substrates with micro- and nanoscale topography bioimprinted at progressive cell morphologies. [Internet] [Thesis]. University of Canterbury; 2012. [cited 2019 May 22]. Available from: http://hdl.handle.net/10092/13721.

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

Council of Science Editors:

TBF W. Fabrication of polymeric substrates with micro- and nanoscale topography bioimprinted at progressive cell morphologies. [Thesis]. University of Canterbury; 2012. Available from: http://hdl.handle.net/10092/13721

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


University of Canterbury

11. McEwan DG. Structural and functional analysis of the GABARAP interaction motif (GIM).

Degree: 2017, University of Canterbury

 © 2017 The Authors. Published under the terms of the CC BY 4.0 license. Through the canonical LC3 interaction motif (LIR), [W/F/Y]-X 1 -X 2… (more)

Subjects/Keywords: Atg8; GABARAP; LC3; PLEKHM1; autophagy; Field of Research::06 - Biological Sciences::0601 - Biochemistry and Cell Biology::060103 - Cell Development, Proliferation and Death; Field of Research::06 - Biological Sciences::0601 - Biochemistry and Cell Biology::060112 - Structural Biology (incl. Macromolecular Modelling)

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APA (6th Edition):

DG, M. (2017). Structural and functional analysis of the GABARAP interaction motif (GIM). (Thesis). University of Canterbury. Retrieved from http://hdl.handle.net/10092/15005

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):

DG, McEwan. “Structural and functional analysis of the GABARAP interaction motif (GIM).” 2017. Thesis, University of Canterbury. Accessed May 22, 2019. http://hdl.handle.net/10092/15005.

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

MLA Handbook (7th Edition):

DG, McEwan. “Structural and functional analysis of the GABARAP interaction motif (GIM).” 2017. Web. 22 May 2019.

Vancouver:

DG M. Structural and functional analysis of the GABARAP interaction motif (GIM). [Internet] [Thesis]. University of Canterbury; 2017. [cited 2019 May 22]. Available from: http://hdl.handle.net/10092/15005.

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

Council of Science Editors:

DG M. Structural and functional analysis of the GABARAP interaction motif (GIM). [Thesis]. University of Canterbury; 2017. Available from: http://hdl.handle.net/10092/15005

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


University of Canterbury

12. Stadler, T. Analyzing and reconstructing reticulation networks under timing constraints.

Degree: Dept. of Mathematics and Statistics., 2009, University of Canterbury

 Reticulation networks are now frequently used to model the history of life for various groups of organisms whose evolutionary past is likely to include reticulation… (more)

Subjects/Keywords: Field of Research::01 - Mathematical Sciences::0102 - Applied Mathematics::010202 - Biological Mathematics; Field of Research::06 - Biological Sciences::0601 - Biochemistry and Cell Biology::060102 - Bioinformatics

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APA (6th Edition):

Stadler, T. (2009). Analyzing and reconstructing reticulation networks under timing constraints. (Thesis). University of Canterbury. Retrieved from http://hdl.handle.net/10092/11498

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):

Stadler, T. “Analyzing and reconstructing reticulation networks under timing constraints.” 2009. Thesis, University of Canterbury. Accessed May 22, 2019. http://hdl.handle.net/10092/11498.

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

MLA Handbook (7th Edition):

Stadler, T. “Analyzing and reconstructing reticulation networks under timing constraints.” 2009. Web. 22 May 2019.

Vancouver:

Stadler T. Analyzing and reconstructing reticulation networks under timing constraints. [Internet] [Thesis]. University of Canterbury; 2009. [cited 2019 May 22]. Available from: http://hdl.handle.net/10092/11498.

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

Council of Science Editors:

Stadler T. Analyzing and reconstructing reticulation networks under timing constraints. [Thesis]. University of Canterbury; 2009. Available from: http://hdl.handle.net/10092/11498

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


University of Canterbury

13. Zhu H. Prediction of Sphingosine protein-coding regions with a self adaptive spectral rotation method.

Degree: 2019, University of Canterbury

 © 2019 Li et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use,… (more)

Subjects/Keywords: Field of Research::01 - Mathematical Sciences::0102 - Applied Mathematics::010202 - Biological Mathematics; Field of Research::06 - Biological Sciences::0601 - Biochemistry and Cell Biology::060102 - Bioinformatics

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APA (6th Edition):

H, Z. (2019). Prediction of Sphingosine protein-coding regions with a self adaptive spectral rotation method. (Thesis). University of Canterbury. Retrieved from http://hdl.handle.net/10092/16720

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):

H, Zhu. “Prediction of Sphingosine protein-coding regions with a self adaptive spectral rotation method.” 2019. Thesis, University of Canterbury. Accessed May 22, 2019. http://hdl.handle.net/10092/16720.

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

MLA Handbook (7th Edition):

H, Zhu. “Prediction of Sphingosine protein-coding regions with a self adaptive spectral rotation method.” 2019. Web. 22 May 2019.

Vancouver:

H Z. Prediction of Sphingosine protein-coding regions with a self adaptive spectral rotation method. [Internet] [Thesis]. University of Canterbury; 2019. [cited 2019 May 22]. Available from: http://hdl.handle.net/10092/16720.

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

Council of Science Editors:

H Z. Prediction of Sphingosine protein-coding regions with a self adaptive spectral rotation method. [Thesis]. University of Canterbury; 2019. Available from: http://hdl.handle.net/10092/16720

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


University of Canterbury

14. Brimble MA. Genome mining, isolation, chemical synthesis and biological evaluation of a novel lanthipeptide, tikitericin, from the extremophilic microorganism: Thermogemmatispora strain T81.

Degree: 2018, University of Canterbury

 © The Royal Society of Chemistry 2018. Genome mining of the New Zealand extremophilic microorganism Thermogemmatispora strain T81 indicated the presence of biosynthetic machinery to… (more)

Subjects/Keywords: Field of Research::06 - Biological Sciences::0604 - Genetics::060408 - Genomics; Field of Research::06 - Biological Sciences::0605 - Microbiology::060503 - Microbial Genetics; Field of Research::06 - Biological Sciences::0601 - Biochemistry and Cell Biology::060101 - Analytical Biochemistry

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APA (6th Edition):

MA, B. (2018). Genome mining, isolation, chemical synthesis and biological evaluation of a novel lanthipeptide, tikitericin, from the extremophilic microorganism: Thermogemmatispora strain T81. (Thesis). University of Canterbury. Retrieved from http://hdl.handle.net/10092/16230

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):

MA, Brimble. “Genome mining, isolation, chemical synthesis and biological evaluation of a novel lanthipeptide, tikitericin, from the extremophilic microorganism: Thermogemmatispora strain T81.” 2018. Thesis, University of Canterbury. Accessed May 22, 2019. http://hdl.handle.net/10092/16230.

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

MLA Handbook (7th Edition):

MA, Brimble. “Genome mining, isolation, chemical synthesis and biological evaluation of a novel lanthipeptide, tikitericin, from the extremophilic microorganism: Thermogemmatispora strain T81.” 2018. Web. 22 May 2019.

Vancouver:

MA B. Genome mining, isolation, chemical synthesis and biological evaluation of a novel lanthipeptide, tikitericin, from the extremophilic microorganism: Thermogemmatispora strain T81. [Internet] [Thesis]. University of Canterbury; 2018. [cited 2019 May 22]. Available from: http://hdl.handle.net/10092/16230.

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

Council of Science Editors:

MA B. Genome mining, isolation, chemical synthesis and biological evaluation of a novel lanthipeptide, tikitericin, from the extremophilic microorganism: Thermogemmatispora strain T81. [Thesis]. University of Canterbury; 2018. Available from: http://hdl.handle.net/10092/16230

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


University of Canterbury

15. Gerrard JA. Immobilisation of tobacco etch virus (TEV) protease on a high surface area protein nanofibril scaffold.

Degree: 2018, University of Canterbury

 Tobacco etch virus (TEV) protease is widely used for the removal of poly-histidine affinity tags from proteins. In solution, it is a one-time use enzyme… (more)

Subjects/Keywords: Field of Research::06 - Biological Sciences::0601 - Biochemistry and Cell Biology::060107 - Enzymes; Field of Research::06 - Biological Sciences::0601 - Biochemistry and Cell Biology::060109 - Proteomics and Intermolecular Interactions (excl. Medical Proteomics)

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APA (6th Edition):

JA, G. (2018). Immobilisation of tobacco etch virus (TEV) protease on a high surface area protein nanofibril scaffold. (Thesis). University of Canterbury. Retrieved from http://hdl.handle.net/10092/15775

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):

JA, Gerrard. “Immobilisation of tobacco etch virus (TEV) protease on a high surface area protein nanofibril scaffold.” 2018. Thesis, University of Canterbury. Accessed May 22, 2019. http://hdl.handle.net/10092/15775.

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

MLA Handbook (7th Edition):

JA, Gerrard. “Immobilisation of tobacco etch virus (TEV) protease on a high surface area protein nanofibril scaffold.” 2018. Web. 22 May 2019.

Vancouver:

JA G. Immobilisation of tobacco etch virus (TEV) protease on a high surface area protein nanofibril scaffold. [Internet] [Thesis]. University of Canterbury; 2018. [cited 2019 May 22]. Available from: http://hdl.handle.net/10092/15775.

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

Council of Science Editors:

JA G. Immobilisation of tobacco etch virus (TEV) protease on a high surface area protein nanofibril scaffold. [Thesis]. University of Canterbury; 2018. Available from: http://hdl.handle.net/10092/15775

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


University of Canterbury

16. Yip CK. Bio-mimicking TiO2 Architectures for Enhanced Photocatalytic Activity under UV and Visible Light.

Degree: 2017, University of Canterbury

 Green leaves are responsible for natural photosynthesis in plants and their unique structures offer the most efficient blueprint for artificial materials in terms of solar… (more)

Subjects/Keywords: Field of Research::03 - Chemical Sciences::0306 - Physical Chemistry (incl. Structural)::030601 - Catalysis and Mechanisms of Reactions; Field of Research::06 - Biological Sciences::0601 - Biochemistry and Cell Biology

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APA (6th Edition):

CK, Y. (2017). Bio-mimicking TiO2 Architectures for Enhanced Photocatalytic Activity under UV and Visible Light. (Thesis). University of Canterbury. Retrieved from http://hdl.handle.net/10092/14990

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):

CK, Yip. “Bio-mimicking TiO2 Architectures for Enhanced Photocatalytic Activity under UV and Visible Light.” 2017. Thesis, University of Canterbury. Accessed May 22, 2019. http://hdl.handle.net/10092/14990.

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

MLA Handbook (7th Edition):

CK, Yip. “Bio-mimicking TiO2 Architectures for Enhanced Photocatalytic Activity under UV and Visible Light.” 2017. Web. 22 May 2019.

Vancouver:

CK Y. Bio-mimicking TiO2 Architectures for Enhanced Photocatalytic Activity under UV and Visible Light. [Internet] [Thesis]. University of Canterbury; 2017. [cited 2019 May 22]. Available from: http://hdl.handle.net/10092/14990.

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

Council of Science Editors:

CK Y. Bio-mimicking TiO2 Architectures for Enhanced Photocatalytic Activity under UV and Visible Light. [Thesis]. University of Canterbury; 2017. Available from: http://hdl.handle.net/10092/14990

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


University of Canterbury

17. Wang, W. An integrated platform enabling optogenetic illumination of Caenorhabditis elegans neurons and muscular force measurement in microstructured environments.

Degree: Electrical and Computer Engineering; University of Canterbury. Biomolecular Interaction Centre, 2015, University of Canterbury

 Optogenetics has been recently applied to manipulate the neural circuits of Caenorhabditis elegans (C. elegans) to investigate its mechanosensation and locomotive behavior, which is a… (more)

Subjects/Keywords: Field of Research::09 - Engineering::0906 - Electrical and Electronic Engineering; Field of Research::06 - Biological Sciences::0601 - Biochemistry and Cell Biology::060112 - Structural Biology (incl. Macromolecular Modelling)

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APA (6th Edition):

Wang, W. (2015). An integrated platform enabling optogenetic illumination of Caenorhabditis elegans neurons and muscular force measurement in microstructured environments. (Thesis). University of Canterbury. Retrieved from http://hdl.handle.net/10092/12302

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, W. “An integrated platform enabling optogenetic illumination of Caenorhabditis elegans neurons and muscular force measurement in microstructured environments.” 2015. Thesis, University of Canterbury. Accessed May 22, 2019. http://hdl.handle.net/10092/12302.

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

MLA Handbook (7th Edition):

Wang, W. “An integrated platform enabling optogenetic illumination of Caenorhabditis elegans neurons and muscular force measurement in microstructured environments.” 2015. Web. 22 May 2019.

Vancouver:

Wang W. An integrated platform enabling optogenetic illumination of Caenorhabditis elegans neurons and muscular force measurement in microstructured environments. [Internet] [Thesis]. University of Canterbury; 2015. [cited 2019 May 22]. Available from: http://hdl.handle.net/10092/12302.

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

Council of Science Editors:

Wang W. An integrated platform enabling optogenetic illumination of Caenorhabditis elegans neurons and muscular force measurement in microstructured environments. [Thesis]. University of Canterbury; 2015. Available from: http://hdl.handle.net/10092/12302

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


University of Canterbury

18. Parker EJ. Quaternary structure is an essential component that contributes to the sophisticated allosteric regulation mechanism in a key enzyme from Mycobacterium tuberculosis.

Degree: 2017, University of Canterbury

 The first enzyme of the shikimate pathway, 3-deoxy-D-arabino-heptulosonate 7-phosphate synthase (DAH7PS), adopts a range of distinct allosteric regulation mechanisms in different organisms, related to different… (more)

Subjects/Keywords: Field of Research::06 - Biological Sciences::0601 - Biochemistry and Cell Biology::060107 - Enzymes; Field of Research::03 - Chemical Sciences::0304 - Medicinal and Biomolecular Chemistry

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APA (6th Edition):

EJ, P. (2017). Quaternary structure is an essential component that contributes to the sophisticated allosteric regulation mechanism in a key enzyme from Mycobacterium tuberculosis. (Thesis). University of Canterbury. Retrieved from http://hdl.handle.net/10092/14686

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):

EJ, Parker. “Quaternary structure is an essential component that contributes to the sophisticated allosteric regulation mechanism in a key enzyme from Mycobacterium tuberculosis.” 2017. Thesis, University of Canterbury. Accessed May 22, 2019. http://hdl.handle.net/10092/14686.

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

MLA Handbook (7th Edition):

EJ, Parker. “Quaternary structure is an essential component that contributes to the sophisticated allosteric regulation mechanism in a key enzyme from Mycobacterium tuberculosis.” 2017. Web. 22 May 2019.

Vancouver:

EJ P. Quaternary structure is an essential component that contributes to the sophisticated allosteric regulation mechanism in a key enzyme from Mycobacterium tuberculosis. [Internet] [Thesis]. University of Canterbury; 2017. [cited 2019 May 22]. Available from: http://hdl.handle.net/10092/14686.

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

Council of Science Editors:

EJ P. Quaternary structure is an essential component that contributes to the sophisticated allosteric regulation mechanism in a key enzyme from Mycobacterium tuberculosis. [Thesis]. University of Canterbury; 2017. Available from: http://hdl.handle.net/10092/14686

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


University of Canterbury

19. Blaikie, R.J. Spatially-Resolved Measurement of Dissolved Oxygen in Multi-Stream Microfluidic Devices.

Degree: Electrical and Computer Engineering, 2010, University of Canterbury

 Dissolved oxygen (DO) is an important parameter with significant effect on cellular development and function. Micron-scale laminar flow and hydrodynamic focusing provide ideal tools for… (more)

Subjects/Keywords: microfluidics; hydrodynamic focusing; optical oxygen sensor; PtOEPK/PS; spatial measurement; Fields of Research; Field of Research::06 - Biological Sciences::0601 - Biochemistry and Cell Biology

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APA (6th Edition):

Blaikie, R. J. (2010). Spatially-Resolved Measurement of Dissolved Oxygen in Multi-Stream Microfluidic Devices. (Thesis). University of Canterbury. Retrieved from http://hdl.handle.net/10092/4717

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):

Blaikie, R J. “Spatially-Resolved Measurement of Dissolved Oxygen in Multi-Stream Microfluidic Devices.” 2010. Thesis, University of Canterbury. Accessed May 22, 2019. http://hdl.handle.net/10092/4717.

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

MLA Handbook (7th Edition):

Blaikie, R J. “Spatially-Resolved Measurement of Dissolved Oxygen in Multi-Stream Microfluidic Devices.” 2010. Web. 22 May 2019.

Vancouver:

Blaikie RJ. Spatially-Resolved Measurement of Dissolved Oxygen in Multi-Stream Microfluidic Devices. [Internet] [Thesis]. University of Canterbury; 2010. [cited 2019 May 22]. Available from: http://hdl.handle.net/10092/4717.

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

Council of Science Editors:

Blaikie RJ. Spatially-Resolved Measurement of Dissolved Oxygen in Multi-Stream Microfluidic Devices. [Thesis]. University of Canterbury; 2010. Available from: http://hdl.handle.net/10092/4717

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


University of Canterbury

20. Ribeiro SG. Passion fruit chlorotic mottle virus: Molecular characterization of a new divergent geminivirus in Brazil.

Degree: 2018, University of Canterbury

 © 2018 by the authors. Licensee MDPI, Basel, Switzerland. Brazil is one of the major passion fruit producers worldwide. Viral diseases are among the most… (more)

Subjects/Keywords: geminivirus; passion fruit; Passiflora sp.; Field of Research::06 - Biological Sciences::0601 - Biochemistry and Cell Biology::060103 - Cell Development, Proliferation and Death

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APA (6th Edition):

SG, R. (2018). Passion fruit chlorotic mottle virus: Molecular characterization of a new divergent geminivirus in Brazil. (Thesis). University of Canterbury. Retrieved from http://hdl.handle.net/10092/16371

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):

SG, Ribeiro. “Passion fruit chlorotic mottle virus: Molecular characterization of a new divergent geminivirus in Brazil.” 2018. Thesis, University of Canterbury. Accessed May 22, 2019. http://hdl.handle.net/10092/16371.

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

MLA Handbook (7th Edition):

SG, Ribeiro. “Passion fruit chlorotic mottle virus: Molecular characterization of a new divergent geminivirus in Brazil.” 2018. Web. 22 May 2019.

Vancouver:

SG R. Passion fruit chlorotic mottle virus: Molecular characterization of a new divergent geminivirus in Brazil. [Internet] [Thesis]. University of Canterbury; 2018. [cited 2019 May 22]. Available from: http://hdl.handle.net/10092/16371.

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

Council of Science Editors:

SG R. Passion fruit chlorotic mottle virus: Molecular characterization of a new divergent geminivirus in Brazil. [Thesis]. University of Canterbury; 2018. Available from: http://hdl.handle.net/10092/16371

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


University of Canterbury

21. Kasim A. IsoGeneGUI: Multiple Approaches for Dose-Response Analysis of Microarray Data Using R.

Degree: 2017, University of Canterbury

 The analysis of transcriptomic experiments with ordered covariates, such as dose-response data, has become a central topic in bioinformatics, in particular in omics studies. Consequently,… (more)

Subjects/Keywords: Field of Research::06 - Biological Sciences::0604 - Genetics::060405 - Gene Expression (incl. Microarray and other genome-wide approaches); Field of Research::06 - Biological Sciences::0601 - Biochemistry and Cell Biology::060102 - Bioinformatics; Field of Research::08 - Information and Computing Sciences::0803 - Computer Software::080301 - Bioinformatics Software

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APA (6th Edition):

A, K. (2017). IsoGeneGUI: Multiple Approaches for Dose-Response Analysis of Microarray Data Using R. (Thesis). University of Canterbury. Retrieved from http://hdl.handle.net/10092/13520

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):

A, Kasim. “IsoGeneGUI: Multiple Approaches for Dose-Response Analysis of Microarray Data Using R.” 2017. Thesis, University of Canterbury. Accessed May 22, 2019. http://hdl.handle.net/10092/13520.

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

MLA Handbook (7th Edition):

A, Kasim. “IsoGeneGUI: Multiple Approaches for Dose-Response Analysis of Microarray Data Using R.” 2017. Web. 22 May 2019.

Vancouver:

A K. IsoGeneGUI: Multiple Approaches for Dose-Response Analysis of Microarray Data Using R. [Internet] [Thesis]. University of Canterbury; 2017. [cited 2019 May 22]. Available from: http://hdl.handle.net/10092/13520.

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

Council of Science Editors:

A K. IsoGeneGUI: Multiple Approaches for Dose-Response Analysis of Microarray Data Using R. [Thesis]. University of Canterbury; 2017. Available from: http://hdl.handle.net/10092/13520

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


University of Canterbury

22. Jackson, R.R. Mediation of a plant-spider association by specific volatile compounds.

Degree: Biological Sciences; University of Canterbury. Chemistry, 2012, University of Canterbury

 Evarcha culicivora, an East African jumping spider (Salticidae), is the only spider for which there is evidence of innate olfactory affinity for particular plant species.… (more)

Subjects/Keywords: plant-arthropod interactions; Evarcha culicivora; Lantana camara; Salticidae; sensory ecology; plant volatiles; Field of Research::06 - Biological Sciences::0608 - Zoology::060808 - Invertebrate Biology; Field of Research::06 - Biological Sciences::0601 - Biochemistry and Cell Biology::060101 - Analytical Biochemistry; Field of Research::06 - Biological Sciences::0608 - Zoology::060801 - Animal Behaviour

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APA (6th Edition):

Jackson, R. R. (2012). Mediation of a plant-spider association by specific volatile compounds. (Thesis). University of Canterbury. Retrieved from http://hdl.handle.net/10092/9735

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):

Jackson, R R. “Mediation of a plant-spider association by specific volatile compounds.” 2012. Thesis, University of Canterbury. Accessed May 22, 2019. http://hdl.handle.net/10092/9735.

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

MLA Handbook (7th Edition):

Jackson, R R. “Mediation of a plant-spider association by specific volatile compounds.” 2012. Web. 22 May 2019.

Vancouver:

Jackson RR. Mediation of a plant-spider association by specific volatile compounds. [Internet] [Thesis]. University of Canterbury; 2012. [cited 2019 May 22]. Available from: http://hdl.handle.net/10092/9735.

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

Council of Science Editors:

Jackson RR. Mediation of a plant-spider association by specific volatile compounds. [Thesis]. University of Canterbury; 2012. Available from: http://hdl.handle.net/10092/9735

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


University of Canterbury

23. Steel, M. A. General time reversible distances with unequal rates across sites.

Degree: Dept. of Mathematics, 1996, University of Canterbury

 A series of new results, with proofs, useful to the study of DNA sequences using Markov models of substitution are presented. General time-reversible distances can… (more)

Subjects/Keywords: Field of Research::06 - Biological Sciences::0601 - Biochemistry and Cell Biology::060102 - Bioinformatics

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APA (6th Edition):

Steel, M. A. (1996). General time reversible distances with unequal rates across sites. (Thesis). University of Canterbury. Retrieved from http://hdl.handle.net/10092/10780

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):

Steel, M A. “General time reversible distances with unequal rates across sites.” 1996. Thesis, University of Canterbury. Accessed May 22, 2019. http://hdl.handle.net/10092/10780.

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

MLA Handbook (7th Edition):

Steel, M A. “General time reversible distances with unequal rates across sites.” 1996. Web. 22 May 2019.

Vancouver:

Steel MA. General time reversible distances with unequal rates across sites. [Internet] [Thesis]. University of Canterbury; 1996. [cited 2019 May 22]. Available from: http://hdl.handle.net/10092/10780.

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

Council of Science Editors:

Steel MA. General time reversible distances with unequal rates across sites. [Thesis]. University of Canterbury; 1996. Available from: http://hdl.handle.net/10092/10780

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


University of Canterbury

24. Chen R. P-TEFb: finding its ways to release promoter-proximally paused RNA Polymerase II.

Degree: 2017, University of Canterbury

The release of a paused Pol II depends on the recruitment of P-TEFb. Recent studies showed that both active P-TEFb and inactive P-TEFb (7SK snRNP) can be recruited to the promoter regions of global genes by different mechanisms. Here, we summarize the recent advances on these distinct recruitment mechanisms.

Subjects/Keywords: P-TEFb; 7SK snRNP; Brd4; SEC; KAP1; RNA Pol II; promoter-proximal pausing; transcription elongation; Field of Research::06 - Biological Sciences::0601 - Biochemistry and Cell Biology

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APA (6th Edition):

R, C. (2017). P-TEFb: finding its ways to release promoter-proximally paused RNA Polymerase II. (Thesis). University of Canterbury. Retrieved from http://hdl.handle.net/10092/15360

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):

R, Chen. “P-TEFb: finding its ways to release promoter-proximally paused RNA Polymerase II.” 2017. Thesis, University of Canterbury. Accessed May 22, 2019. http://hdl.handle.net/10092/15360.

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

MLA Handbook (7th Edition):

R, Chen. “P-TEFb: finding its ways to release promoter-proximally paused RNA Polymerase II.” 2017. Web. 22 May 2019.

Vancouver:

R C. P-TEFb: finding its ways to release promoter-proximally paused RNA Polymerase II. [Internet] [Thesis]. University of Canterbury; 2017. [cited 2019 May 22]. Available from: http://hdl.handle.net/10092/15360.

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

Council of Science Editors:

R C. P-TEFb: finding its ways to release promoter-proximally paused RNA Polymerase II. [Thesis]. University of Canterbury; 2017. Available from: http://hdl.handle.net/10092/15360

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


University of Canterbury

25. Robinson CV. Lipid binding attenuates channel closure of the outer membrane protein OmpF.

Degree: 2018, University of Canterbury

 © 2018 National Academy of Sciences. All Rights Reserved. Strong interactions between lipids and proteins occur primarily through association of charged headgroups and amino acid… (more)

Subjects/Keywords: mass spectrometry; lipids; OmpF; Field of Research::06 - Biological Sciences::0601 - Biochemistry and Cell Biology::060109 - Proteomics and Intermolecular Interactions (excl. Medical Proteomics); Field of Research::03 - Chemical Sciences::0304 - Medicinal and Biomolecular Chemistry::030406 - Proteins and Peptides; Field of Research::11 - Medical and Health Sciences::1101 - Medical Biochemistry and Metabolomics::110104 - Medical Biochemistry: Lipids; Field of Research::06 - Biological Sciences::0601 - Biochemistry and Cell Biology::060101 - Analytical Biochemistry

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APA (6th Edition):

CV, R. (2018). Lipid binding attenuates channel closure of the outer membrane protein OmpF. (Thesis). University of Canterbury. Retrieved from http://hdl.handle.net/10092/16236

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):

CV, Robinson. “Lipid binding attenuates channel closure of the outer membrane protein OmpF.” 2018. Thesis, University of Canterbury. Accessed May 22, 2019. http://hdl.handle.net/10092/16236.

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

MLA Handbook (7th Edition):

CV, Robinson. “Lipid binding attenuates channel closure of the outer membrane protein OmpF.” 2018. Web. 22 May 2019.

Vancouver:

CV R. Lipid binding attenuates channel closure of the outer membrane protein OmpF. [Internet] [Thesis]. University of Canterbury; 2018. [cited 2019 May 22]. Available from: http://hdl.handle.net/10092/16236.

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

Council of Science Editors:

CV R. Lipid binding attenuates channel closure of the outer membrane protein OmpF. [Thesis]. University of Canterbury; 2018. Available from: http://hdl.handle.net/10092/16236

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


University of Canterbury

26. Robinson CV. Ligand binding to a G protein–coupled receptor captured in a mass spectrometer.

Degree: 2017, University of Canterbury

 Copyright © 2017 The Authors, some rights reserved. G protein (heterotrimeric guanine nucleotide–binding protein)–coupled receptors belong to the largest family of membrane-embedded cell surface proteins… (more)

Subjects/Keywords: G-protein coupled receptors; ligand binding; mass spectrometry; Field of Research::06 - Biological Sciences::0601 - Biochemistry and Cell Biology::060109 - Proteomics and Intermolecular Interactions (excl. Medical Proteomics); Field of Research::06 - Biological Sciences::0601 - Biochemistry and Cell Biology::060101 - Analytical Biochemistry; Field of Research::11 - Medical and Health Sciences::1101 - Medical Biochemistry and Metabolomics::110106 - Medical Biochemistry: Proteins and Peptides (incl. Medical Proteomics); Field of Research::03 - Chemical Sciences::0304 - Medicinal and Biomolecular Chemistry::030406 - Proteins and Peptides

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

APA (6th Edition):

CV, R. (2017). Ligand binding to a G protein–coupled receptor captured in a mass spectrometer. (Thesis). University of Canterbury. Retrieved from http://hdl.handle.net/10092/16237

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):

CV, Robinson. “Ligand binding to a G protein–coupled receptor captured in a mass spectrometer.” 2017. Thesis, University of Canterbury. Accessed May 22, 2019. http://hdl.handle.net/10092/16237.

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

MLA Handbook (7th Edition):

CV, Robinson. “Ligand binding to a G protein–coupled receptor captured in a mass spectrometer.” 2017. Web. 22 May 2019.

Vancouver:

CV R. Ligand binding to a G protein–coupled receptor captured in a mass spectrometer. [Internet] [Thesis]. University of Canterbury; 2017. [cited 2019 May 22]. Available from: http://hdl.handle.net/10092/16237.

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

Council of Science Editors:

CV R. Ligand binding to a G protein–coupled receptor captured in a mass spectrometer. [Thesis]. University of Canterbury; 2017. Available from: http://hdl.handle.net/10092/16237

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


University of Canterbury

27. Greening C. Cofactor Tail Length Modulates Catalysis of Bacterial F420-Dependent Oxidoreductases.

Degree: 2017, University of Canterbury

 F420 is a microbial cofactor that mediates a wide range of physiologically important and industrially relevant redox reactions, including in methanogenesis and tetracycline biosynthesis. This… (more)

Subjects/Keywords: F420; redox; biocatalysis; biodegradation; mycobacterium; actinobacteria; cofactor; Field of Research::06 - Biological Sciences::0601 - Biochemistry and Cell Biology::060101 - Analytical Biochemistry; Field of Research::03 - Chemical Sciences::0304 - Medicinal and Biomolecular Chemistry::030401 - Biologically Active Molecules; Field of Research::10 - Technology::1003 - Industrial Biotechnology::100301 - Biocatalysis and Enzyme Technology; Field of Research::06 - Biological Sciences::0605 - Microbiology::060501 - Bacteriology

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

APA (6th Edition):

C, G. (2017). Cofactor Tail Length Modulates Catalysis of Bacterial F420-Dependent Oxidoreductases. (Thesis). University of Canterbury. Retrieved from http://hdl.handle.net/10092/15164

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):

C, Greening. “Cofactor Tail Length Modulates Catalysis of Bacterial F420-Dependent Oxidoreductases.” 2017. Thesis, University of Canterbury. Accessed May 22, 2019. http://hdl.handle.net/10092/15164.

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

MLA Handbook (7th Edition):

C, Greening. “Cofactor Tail Length Modulates Catalysis of Bacterial F420-Dependent Oxidoreductases.” 2017. Web. 22 May 2019.

Vancouver:

C G. Cofactor Tail Length Modulates Catalysis of Bacterial F420-Dependent Oxidoreductases. [Internet] [Thesis]. University of Canterbury; 2017. [cited 2019 May 22]. Available from: http://hdl.handle.net/10092/15164.

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

Council of Science Editors:

C G. Cofactor Tail Length Modulates Catalysis of Bacterial F420-Dependent Oxidoreductases. [Thesis]. University of Canterbury; 2017. Available from: http://hdl.handle.net/10092/15164

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


University of Canterbury

28. Dobson RCJ. The Sodium Sialic acid symporter from Staphylococcus aureus has altered substrate specificity.

Degree: 2018, University of Canterbury

 © 2018 North, Wahlgren, Remus, Scalise, Kessans, Dunevall, Claesson, Soares da Costa, Perugini, Ramaswamy, Allison, Indiveri, Friemann and Dobson. Mammalian cell surfaces are decorated with… (more)

Subjects/Keywords: antibiotic resistance; sialic acids; SiaT; sodium solute symporter; Staphylococcus aureus; Field of Research::06 - Biological Sciences::0605 - Microbiology::060501 - Bacteriology; Field of Research::06 - Biological Sciences::0601 - Biochemistry and Cell Biology

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

APA (6th Edition):

RCJ, D. (2018). The Sodium Sialic acid symporter from Staphylococcus aureus has altered substrate specificity. (Thesis). University of Canterbury. Retrieved from http://hdl.handle.net/10092/16172

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):

RCJ, Dobson. “The Sodium Sialic acid symporter from Staphylococcus aureus has altered substrate specificity.” 2018. Thesis, University of Canterbury. Accessed May 22, 2019. http://hdl.handle.net/10092/16172.

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

MLA Handbook (7th Edition):

RCJ, Dobson. “The Sodium Sialic acid symporter from Staphylococcus aureus has altered substrate specificity.” 2018. Web. 22 May 2019.

Vancouver:

RCJ D. The Sodium Sialic acid symporter from Staphylococcus aureus has altered substrate specificity. [Internet] [Thesis]. University of Canterbury; 2018. [cited 2019 May 22]. Available from: http://hdl.handle.net/10092/16172.

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

Council of Science Editors:

RCJ D. The Sodium Sialic acid symporter from Staphylococcus aureus has altered substrate specificity. [Thesis]. University of Canterbury; 2018. Available from: http://hdl.handle.net/10092/16172

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


University of Canterbury

29. Barbar EJ. Multivalency regulates activity in an intrinsically disordered transcription factor.

Degree: 2018, University of Canterbury

 © Clark et al. The transcription factor ASCIZ (ATMIN, ZNF822) has an unusually high number of recognition motifs for the product of its main target… (more)

Subjects/Keywords: Intrinsically disordered proteins; NMR; dynamic complexes; electron microscopy; human; molecular biophysics; multivalency; structural biology; transcription factors; Field of Research::02 - Physical Sciences::0299 - Other Physical Sciences::029901 - Biological Physics; Field of Research::06 - Biological Sciences::0601 - Biochemistry and Cell Biology::060112 - Structural Biology (incl. Macromolecular Modelling)

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

APA (6th Edition):

EJ, B. (2018). Multivalency regulates activity in an intrinsically disordered transcription factor. (Thesis). University of Canterbury. Retrieved from http://hdl.handle.net/10092/16205

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):

EJ, Barbar. “Multivalency regulates activity in an intrinsically disordered transcription factor.” 2018. Thesis, University of Canterbury. Accessed May 22, 2019. http://hdl.handle.net/10092/16205.

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

MLA Handbook (7th Edition):

EJ, Barbar. “Multivalency regulates activity in an intrinsically disordered transcription factor.” 2018. Web. 22 May 2019.

Vancouver:

EJ B. Multivalency regulates activity in an intrinsically disordered transcription factor. [Internet] [Thesis]. University of Canterbury; 2018. [cited 2019 May 22]. Available from: http://hdl.handle.net/10092/16205.

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

Council of Science Editors:

EJ B. Multivalency regulates activity in an intrinsically disordered transcription factor. [Thesis]. University of Canterbury; 2018. Available from: http://hdl.handle.net/10092/16205

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


University of Canterbury

30. John, S. Anaerobic biodegradability of wood: a preliminary review.

Degree: Civil and Natural Resources Engineering, 2010, University of Canterbury

 The literature shows that wood is relatively non-biodegradable in anaerobic environments, though there is a wide variety of results ranging from <2% to 40% of… (more)

Subjects/Keywords: Field of Research::09 - Engineering::0912 - Materials Engineering::091210 - Timber, Pulp and Paper; Field of Research::06 - Biological Sciences::0601 - Biochemistry and Cell Biology::060199 - Biochemistry and Cell Biology not elsewhere classified

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

APA (6th Edition):

John, S. (2010). Anaerobic biodegradability of wood: a preliminary review. (Thesis). University of Canterbury. Retrieved from http://hdl.handle.net/10092/5088

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):

John, S. “Anaerobic biodegradability of wood: a preliminary review.” 2010. Thesis, University of Canterbury. Accessed May 22, 2019. http://hdl.handle.net/10092/5088.

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

MLA Handbook (7th Edition):

John, S. “Anaerobic biodegradability of wood: a preliminary review.” 2010. Web. 22 May 2019.

Vancouver:

John S. Anaerobic biodegradability of wood: a preliminary review. [Internet] [Thesis]. University of Canterbury; 2010. [cited 2019 May 22]. Available from: http://hdl.handle.net/10092/5088.

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

Council of Science Editors:

John S. Anaerobic biodegradability of wood: a preliminary review. [Thesis]. University of Canterbury; 2010. Available from: http://hdl.handle.net/10092/5088

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

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