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University: University of New South Wales

You searched for subject:(signalling). Showing records 1 – 21 of 21 total matches.

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University of New South Wales

1. Lu, Hao Kim. Mechanism of the inhibitory effects of leukocyte immunoglobulin-like receptor B4 (LILRB4) on monocytes.

Degree: Medical Sciences, 2011, University of New South Wales

 The leukocyte immunoglobulin-like receptor (LILR) B4 belongs to a family of activating and inhibitory cell surface receptors that are increasingly recognised as key regulators of… (more)

Subjects/Keywords: Monocytes; LILRB4; Signalling; Cytokines; Ligands

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APA (6th Edition):

Lu, H. K. (2011). Mechanism of the inhibitory effects of leukocyte immunoglobulin-like receptor B4 (LILRB4) on monocytes. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/51613 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10280/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Lu, Hao Kim. “Mechanism of the inhibitory effects of leukocyte immunoglobulin-like receptor B4 (LILRB4) on monocytes.” 2011. Doctoral Dissertation, University of New South Wales. Accessed October 19, 2019. http://handle.unsw.edu.au/1959.4/51613 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10280/SOURCE02?view=true.

MLA Handbook (7th Edition):

Lu, Hao Kim. “Mechanism of the inhibitory effects of leukocyte immunoglobulin-like receptor B4 (LILRB4) on monocytes.” 2011. Web. 19 Oct 2019.

Vancouver:

Lu HK. Mechanism of the inhibitory effects of leukocyte immunoglobulin-like receptor B4 (LILRB4) on monocytes. [Internet] [Doctoral dissertation]. University of New South Wales; 2011. [cited 2019 Oct 19]. Available from: http://handle.unsw.edu.au/1959.4/51613 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10280/SOURCE02?view=true.

Council of Science Editors:

Lu HK. Mechanism of the inhibitory effects of leukocyte immunoglobulin-like receptor B4 (LILRB4) on monocytes. [Doctoral Dissertation]. University of New South Wales; 2011. Available from: http://handle.unsw.edu.au/1959.4/51613 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10280/SOURCE02?view=true


University of New South Wales

2. Colvin, Emily Kate. Aberrations in embryonic signalling pathways in pancreatic cancer.

Degree: Garvan Institute of Medical Research, 2011, University of New South Wales

 Pancreatic cancer (PC) is the fourth leading cause of cancer death in western societies, with a 5-year survival rate of approximately 5%. There is an… (more)

Subjects/Keywords: Biomarker; Pancreatic Cancer; Retinoic Acid Signalling

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APA (6th Edition):

Colvin, E. K. (2011). Aberrations in embryonic signalling pathways in pancreatic cancer. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/51452 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10138/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Colvin, Emily Kate. “Aberrations in embryonic signalling pathways in pancreatic cancer.” 2011. Doctoral Dissertation, University of New South Wales. Accessed October 19, 2019. http://handle.unsw.edu.au/1959.4/51452 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10138/SOURCE02?view=true.

MLA Handbook (7th Edition):

Colvin, Emily Kate. “Aberrations in embryonic signalling pathways in pancreatic cancer.” 2011. Web. 19 Oct 2019.

Vancouver:

Colvin EK. Aberrations in embryonic signalling pathways in pancreatic cancer. [Internet] [Doctoral dissertation]. University of New South Wales; 2011. [cited 2019 Oct 19]. Available from: http://handle.unsw.edu.au/1959.4/51452 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10138/SOURCE02?view=true.

Council of Science Editors:

Colvin EK. Aberrations in embryonic signalling pathways in pancreatic cancer. [Doctoral Dissertation]. University of New South Wales; 2011. Available from: http://handle.unsw.edu.au/1959.4/51452 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10138/SOURCE02?view=true


University of New South Wales

3. Hulugalle, Dhakshinari. Computational investigation of thiol-based redox modifications in proteins: redox-active disulfides, Zn2+ sites and their associations.

Degree: Victor Chang Cardiac Research Institute, 2013, University of New South Wales

 Thiol based redox signalling is an emerging area of research in protein science. Reversible disulfide bonding and Zn2+ expulsion are two important but less explored… (more)

Subjects/Keywords: Forbidden disulfides; Redox signalling; Zn fingers; aHDD

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APA (6th Edition):

Hulugalle, D. (2013). Computational investigation of thiol-based redox modifications in proteins: redox-active disulfides, Zn2+ sites and their associations. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/52584 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:11257/SOURCE01?view=true

Chicago Manual of Style (16th Edition):

Hulugalle, Dhakshinari. “Computational investigation of thiol-based redox modifications in proteins: redox-active disulfides, Zn2+ sites and their associations.” 2013. Doctoral Dissertation, University of New South Wales. Accessed October 19, 2019. http://handle.unsw.edu.au/1959.4/52584 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:11257/SOURCE01?view=true.

MLA Handbook (7th Edition):

Hulugalle, Dhakshinari. “Computational investigation of thiol-based redox modifications in proteins: redox-active disulfides, Zn2+ sites and their associations.” 2013. Web. 19 Oct 2019.

Vancouver:

Hulugalle D. Computational investigation of thiol-based redox modifications in proteins: redox-active disulfides, Zn2+ sites and their associations. [Internet] [Doctoral dissertation]. University of New South Wales; 2013. [cited 2019 Oct 19]. Available from: http://handle.unsw.edu.au/1959.4/52584 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:11257/SOURCE01?view=true.

Council of Science Editors:

Hulugalle D. Computational investigation of thiol-based redox modifications in proteins: redox-active disulfides, Zn2+ sites and their associations. [Doctoral Dissertation]. University of New South Wales; 2013. Available from: http://handle.unsw.edu.au/1959.4/52584 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:11257/SOURCE01?view=true


University of New South Wales

4. Pelham, Simon. STAT3 mediated regulation of human antibody responses.

Degree: Garvan Institute of Medical Research, 2019, University of New South Wales

 AbstractSignal transducer and activator of transcription 3 (STAT3) is a transcription factor activated by multiple cytokines including IL-6, IL-10 and IL-21. Loss-of-function (LOF) mutations in… (more)

Subjects/Keywords: Primary immunodeficiencies; STAT3; B cells; Cytokine signalling

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APA (6th Edition):

Pelham, S. (2019). STAT3 mediated regulation of human antibody responses. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/62451

Chicago Manual of Style (16th Edition):

Pelham, Simon. “STAT3 mediated regulation of human antibody responses.” 2019. Doctoral Dissertation, University of New South Wales. Accessed October 19, 2019. http://handle.unsw.edu.au/1959.4/62451.

MLA Handbook (7th Edition):

Pelham, Simon. “STAT3 mediated regulation of human antibody responses.” 2019. Web. 19 Oct 2019.

Vancouver:

Pelham S. STAT3 mediated regulation of human antibody responses. [Internet] [Doctoral dissertation]. University of New South Wales; 2019. [cited 2019 Oct 19]. Available from: http://handle.unsw.edu.au/1959.4/62451.

Council of Science Editors:

Pelham S. STAT3 mediated regulation of human antibody responses. [Doctoral Dissertation]. University of New South Wales; 2019. Available from: http://handle.unsw.edu.au/1959.4/62451


University of New South Wales

5. Chong, Grace Hui Ying. Intercellular bacterial signalling in activated sludge.

Degree: Biotechnology & Biomolecular Sciences, 2010, University of New South Wales

 Many bacteria use quorum sensing or cell-cell signalling to alter their behaviour in response to changes in population density. The capacity to behave collectively as… (more)

Subjects/Keywords: Activated sludge; Quorum sensing; Cell signalling

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APA (6th Edition):

Chong, G. H. Y. (2010). Intercellular bacterial signalling in activated sludge. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/45670 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:8952/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Chong, Grace Hui Ying. “Intercellular bacterial signalling in activated sludge.” 2010. Doctoral Dissertation, University of New South Wales. Accessed October 19, 2019. http://handle.unsw.edu.au/1959.4/45670 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:8952/SOURCE02?view=true.

MLA Handbook (7th Edition):

Chong, Grace Hui Ying. “Intercellular bacterial signalling in activated sludge.” 2010. Web. 19 Oct 2019.

Vancouver:

Chong GHY. Intercellular bacterial signalling in activated sludge. [Internet] [Doctoral dissertation]. University of New South Wales; 2010. [cited 2019 Oct 19]. Available from: http://handle.unsw.edu.au/1959.4/45670 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:8952/SOURCE02?view=true.

Council of Science Editors:

Chong GHY. Intercellular bacterial signalling in activated sludge. [Doctoral Dissertation]. University of New South Wales; 2010. Available from: http://handle.unsw.edu.au/1959.4/45670 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:8952/SOURCE02?view=true


University of New South Wales

6. Regalia, Raymond. Exploring Cyclic Diguanylate Signalling in Marine Roseobacters.

Degree: Biotechnology & Biomolecular Sciences, 2015, University of New South Wales

 The secondary messenger cyclic diguanosine monophosphate (cyclic diguanylate or cyclic-di-GMP) is regarded as a key regulator of traits involved in transition of bacteria from a… (more)

Subjects/Keywords: Roseobacter; cyclic-di-GMP; signalling; marine; biofilm

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APA (6th Edition):

Regalia, R. (2015). Exploring Cyclic Diguanylate Signalling in Marine Roseobacters. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/55371 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:37405/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Regalia, Raymond. “Exploring Cyclic Diguanylate Signalling in Marine Roseobacters.” 2015. Doctoral Dissertation, University of New South Wales. Accessed October 19, 2019. http://handle.unsw.edu.au/1959.4/55371 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:37405/SOURCE02?view=true.

MLA Handbook (7th Edition):

Regalia, Raymond. “Exploring Cyclic Diguanylate Signalling in Marine Roseobacters.” 2015. Web. 19 Oct 2019.

Vancouver:

Regalia R. Exploring Cyclic Diguanylate Signalling in Marine Roseobacters. [Internet] [Doctoral dissertation]. University of New South Wales; 2015. [cited 2019 Oct 19]. Available from: http://handle.unsw.edu.au/1959.4/55371 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:37405/SOURCE02?view=true.

Council of Science Editors:

Regalia R. Exploring Cyclic Diguanylate Signalling in Marine Roseobacters. [Doctoral Dissertation]. University of New South Wales; 2015. Available from: http://handle.unsw.edu.au/1959.4/55371 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:37405/SOURCE02?view=true


University of New South Wales

7. Ma, Sean. The Molecular and Functional Characterisation of ROR2 in Colorectal Neoplasia.

Degree: Clinical School - Prince of Wales Hospital, 2015, University of New South Wales

 Approximately 94% of colorectal cancers have been found with mutations in the Wnt signalling pathway. The majority of these cancers are caused by hyperactivated β-catenin… (more)

Subjects/Keywords: Wnt signalling; Colorectal Cancer; ROR2; Epigenetics

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APA (6th Edition):

Ma, S. (2015). The Molecular and Functional Characterisation of ROR2 in Colorectal Neoplasia. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/55763 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:39128/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Ma, Sean. “The Molecular and Functional Characterisation of ROR2 in Colorectal Neoplasia.” 2015. Doctoral Dissertation, University of New South Wales. Accessed October 19, 2019. http://handle.unsw.edu.au/1959.4/55763 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:39128/SOURCE02?view=true.

MLA Handbook (7th Edition):

Ma, Sean. “The Molecular and Functional Characterisation of ROR2 in Colorectal Neoplasia.” 2015. Web. 19 Oct 2019.

Vancouver:

Ma S. The Molecular and Functional Characterisation of ROR2 in Colorectal Neoplasia. [Internet] [Doctoral dissertation]. University of New South Wales; 2015. [cited 2019 Oct 19]. Available from: http://handle.unsw.edu.au/1959.4/55763 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:39128/SOURCE02?view=true.

Council of Science Editors:

Ma S. The Molecular and Functional Characterisation of ROR2 in Colorectal Neoplasia. [Doctoral Dissertation]. University of New South Wales; 2015. Available from: http://handle.unsw.edu.au/1959.4/55763 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:39128/SOURCE02?view=true


University of New South Wales

8. Williamson, David. The role of LAT clusters in early immune cell signalling.

Degree: Centre for Vascular Research, 2010, University of New South Wales

 T cell activation is an essential part of the immune response and requires segregation of signalling proteins into specialised membrane domains to transmit and sustain… (more)

Subjects/Keywords: T-cell receptor (TCR); signalling; LAT clusters; triggering

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APA (6th Edition):

Williamson, D. (2010). The role of LAT clusters in early immune cell signalling. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/51514 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10201/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Williamson, David. “The role of LAT clusters in early immune cell signalling.” 2010. Doctoral Dissertation, University of New South Wales. Accessed October 19, 2019. http://handle.unsw.edu.au/1959.4/51514 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10201/SOURCE02?view=true.

MLA Handbook (7th Edition):

Williamson, David. “The role of LAT clusters in early immune cell signalling.” 2010. Web. 19 Oct 2019.

Vancouver:

Williamson D. The role of LAT clusters in early immune cell signalling. [Internet] [Doctoral dissertation]. University of New South Wales; 2010. [cited 2019 Oct 19]. Available from: http://handle.unsw.edu.au/1959.4/51514 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10201/SOURCE02?view=true.

Council of Science Editors:

Williamson D. The role of LAT clusters in early immune cell signalling. [Doctoral Dissertation]. University of New South Wales; 2010. Available from: http://handle.unsw.edu.au/1959.4/51514 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10201/SOURCE02?view=true


University of New South Wales

9. Pedersen , David. The role of protein kinase C ε in insulin receptor trafficking and insulin action.

Degree: Clinical School - St Vincent's Hospital, 2012, University of New South Wales

 The development of type 2 diabetes is reaching epidemic proportions and identifying ways to modulate insulin levels in order to maintain euglycaemia is important in… (more)

Subjects/Keywords: Insulin Receptor; Protein Kinase C epsilon; Ceacam1; Trafficking; Signalling

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APA (6th Edition):

Pedersen , D. (2012). The role of protein kinase C ε in insulin receptor trafficking and insulin action. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/51788 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10455/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Pedersen , David. “The role of protein kinase C ε in insulin receptor trafficking and insulin action.” 2012. Doctoral Dissertation, University of New South Wales. Accessed October 19, 2019. http://handle.unsw.edu.au/1959.4/51788 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10455/SOURCE02?view=true.

MLA Handbook (7th Edition):

Pedersen , David. “The role of protein kinase C ε in insulin receptor trafficking and insulin action.” 2012. Web. 19 Oct 2019.

Vancouver:

Pedersen D. The role of protein kinase C ε in insulin receptor trafficking and insulin action. [Internet] [Doctoral dissertation]. University of New South Wales; 2012. [cited 2019 Oct 19]. Available from: http://handle.unsw.edu.au/1959.4/51788 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10455/SOURCE02?view=true.

Council of Science Editors:

Pedersen D. The role of protein kinase C ε in insulin receptor trafficking and insulin action. [Doctoral Dissertation]. University of New South Wales; 2012. Available from: http://handle.unsw.edu.au/1959.4/51788 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10455/SOURCE02?view=true


University of New South Wales

10. Gardam, Sandra. Regulation of lymphocyte development and function by TRAF2 and TRAF3.

Degree: Clinical School - St Vincent's Hospital, 2008, University of New South Wales

 Tumour necrosis factor receptor (TNFR) family members are widely expressed in cells of the immune system and are essential for the development and function of… (more)

Subjects/Keywords: B lymphocyte; Immunology; Signalling; TRAF

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APA (6th Edition):

Gardam, S. (2008). Regulation of lymphocyte development and function by TRAF2 and TRAF3. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/42104 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:3686/SOURCE2?view=true

Chicago Manual of Style (16th Edition):

Gardam, Sandra. “Regulation of lymphocyte development and function by TRAF2 and TRAF3.” 2008. Doctoral Dissertation, University of New South Wales. Accessed October 19, 2019. http://handle.unsw.edu.au/1959.4/42104 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:3686/SOURCE2?view=true.

MLA Handbook (7th Edition):

Gardam, Sandra. “Regulation of lymphocyte development and function by TRAF2 and TRAF3.” 2008. Web. 19 Oct 2019.

Vancouver:

Gardam S. Regulation of lymphocyte development and function by TRAF2 and TRAF3. [Internet] [Doctoral dissertation]. University of New South Wales; 2008. [cited 2019 Oct 19]. Available from: http://handle.unsw.edu.au/1959.4/42104 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:3686/SOURCE2?view=true.

Council of Science Editors:

Gardam S. Regulation of lymphocyte development and function by TRAF2 and TRAF3. [Doctoral Dissertation]. University of New South Wales; 2008. Available from: http://handle.unsw.edu.au/1959.4/42104 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:3686/SOURCE2?view=true


University of New South Wales

11. Lazenby, James John. The role of N-(3-oxododecanoyl)-L-homoserine lactone in the pathogenesis of Pseudomonas aeruginosa.

Degree: Biotechnology & Biomolecular Sciences, 2011, University of New South Wales

 Pseudomonas aeruginosa lung infections are associated with significant morbidity and mortality in immunocompromised individuals and those with cystic fibrosis (CF). P. aeruginosa regulates its virulence… (more)

Subjects/Keywords: Quorurm Sensing Signalling Molecules; Pseudomonas; OdDHL; Cystic Fibrosis

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APA (6th Edition):

Lazenby, J. J. (2011). The role of N-(3-oxododecanoyl)-L-homoserine lactone in the pathogenesis of Pseudomonas aeruginosa. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/50427 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9319/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Lazenby, James John. “The role of N-(3-oxododecanoyl)-L-homoserine lactone in the pathogenesis of Pseudomonas aeruginosa.” 2011. Doctoral Dissertation, University of New South Wales. Accessed October 19, 2019. http://handle.unsw.edu.au/1959.4/50427 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9319/SOURCE02?view=true.

MLA Handbook (7th Edition):

Lazenby, James John. “The role of N-(3-oxododecanoyl)-L-homoserine lactone in the pathogenesis of Pseudomonas aeruginosa.” 2011. Web. 19 Oct 2019.

Vancouver:

Lazenby JJ. The role of N-(3-oxododecanoyl)-L-homoserine lactone in the pathogenesis of Pseudomonas aeruginosa. [Internet] [Doctoral dissertation]. University of New South Wales; 2011. [cited 2019 Oct 19]. Available from: http://handle.unsw.edu.au/1959.4/50427 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9319/SOURCE02?view=true.

Council of Science Editors:

Lazenby JJ. The role of N-(3-oxododecanoyl)-L-homoserine lactone in the pathogenesis of Pseudomonas aeruginosa. [Doctoral Dissertation]. University of New South Wales; 2011. Available from: http://handle.unsw.edu.au/1959.4/50427 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9319/SOURCE02?view=true


University of New South Wales

12. Porta Cubas, Ana. Lyn kinase in Basal breast cancers.

Degree: Clinical School - St Vincent's Hospital, 2011, University of New South Wales

 Breast cancer is extremely heterogeneous, to the extent that some consider it to be composed of distinct diseases. Over the last 10 years, research has… (more)

Subjects/Keywords: Lyn; Breast cancer; Basal breast cancer; Tyrosine kinase; Cell signalling

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APA (6th Edition):

Porta Cubas, A. (2011). Lyn kinase in Basal breast cancers. (Masters Thesis). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/50809 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9704/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Porta Cubas, Ana. “Lyn kinase in Basal breast cancers.” 2011. Masters Thesis, University of New South Wales. Accessed October 19, 2019. http://handle.unsw.edu.au/1959.4/50809 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9704/SOURCE02?view=true.

MLA Handbook (7th Edition):

Porta Cubas, Ana. “Lyn kinase in Basal breast cancers.” 2011. Web. 19 Oct 2019.

Vancouver:

Porta Cubas A. Lyn kinase in Basal breast cancers. [Internet] [Masters thesis]. University of New South Wales; 2011. [cited 2019 Oct 19]. Available from: http://handle.unsw.edu.au/1959.4/50809 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9704/SOURCE02?view=true.

Council of Science Editors:

Porta Cubas A. Lyn kinase in Basal breast cancers. [Masters Thesis]. University of New South Wales; 2011. Available from: http://handle.unsw.edu.au/1959.4/50809 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9704/SOURCE02?view=true


University of New South Wales

13. Gray, Catheryn. Sensitivity analysis of the insulin signalling pathway for glucose transport.

Degree: Mathematics & Statistics, 2013, University of New South Wales

 There has been a dramatic global increase in the incidence of type 2 diabetes.As type 2 diabetes results from dysregulation of the control mechanism ofglucose… (more)

Subjects/Keywords: Signal transduction pathways; Insulin; Insuling signalling; Mathematiccal modelling

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APA (6th Edition):

Gray, C. (2013). Sensitivity analysis of the insulin signalling pathway for glucose transport. (Masters Thesis). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/52889 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:11567/SOURCE01?view=true

Chicago Manual of Style (16th Edition):

Gray, Catheryn. “Sensitivity analysis of the insulin signalling pathway for glucose transport.” 2013. Masters Thesis, University of New South Wales. Accessed October 19, 2019. http://handle.unsw.edu.au/1959.4/52889 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:11567/SOURCE01?view=true.

MLA Handbook (7th Edition):

Gray, Catheryn. “Sensitivity analysis of the insulin signalling pathway for glucose transport.” 2013. Web. 19 Oct 2019.

Vancouver:

Gray C. Sensitivity analysis of the insulin signalling pathway for glucose transport. [Internet] [Masters thesis]. University of New South Wales; 2013. [cited 2019 Oct 19]. Available from: http://handle.unsw.edu.au/1959.4/52889 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:11567/SOURCE01?view=true.

Council of Science Editors:

Gray C. Sensitivity analysis of the insulin signalling pathway for glucose transport. [Masters Thesis]. University of New South Wales; 2013. Available from: http://handle.unsw.edu.au/1959.4/52889 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:11567/SOURCE01?view=true


University of New South Wales

14. M Rajan, Sandhya Nair. Mechanisms of Enterovirus Induced Rat Insulinoma Cell Line Destruction: Role of Cytokines and Signalling Pathways.

Degree: Biotechnology & Biomolecular Sciences, 2014, University of New South Wales

 There is considerable evidence supporting an association between enterovirus (EV), infection, particularly Coxsackievirus B (CVB), and the development of type 1 diabetes. However, the mechanisms… (more)

Subjects/Keywords: Cytokines; Enterovirus; Type 1 diabetes; Signalling pathways; Apoptosis; Beta cells; Chemokines

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APA (6th Edition):

M Rajan, S. N. (2014). Mechanisms of Enterovirus Induced Rat Insulinoma Cell Line Destruction: Role of Cytokines and Signalling Pathways. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/54612 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:35355/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

M Rajan, Sandhya Nair. “Mechanisms of Enterovirus Induced Rat Insulinoma Cell Line Destruction: Role of Cytokines and Signalling Pathways.” 2014. Doctoral Dissertation, University of New South Wales. Accessed October 19, 2019. http://handle.unsw.edu.au/1959.4/54612 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:35355/SOURCE02?view=true.

MLA Handbook (7th Edition):

M Rajan, Sandhya Nair. “Mechanisms of Enterovirus Induced Rat Insulinoma Cell Line Destruction: Role of Cytokines and Signalling Pathways.” 2014. Web. 19 Oct 2019.

Vancouver:

M Rajan SN. Mechanisms of Enterovirus Induced Rat Insulinoma Cell Line Destruction: Role of Cytokines and Signalling Pathways. [Internet] [Doctoral dissertation]. University of New South Wales; 2014. [cited 2019 Oct 19]. Available from: http://handle.unsw.edu.au/1959.4/54612 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:35355/SOURCE02?view=true.

Council of Science Editors:

M Rajan SN. Mechanisms of Enterovirus Induced Rat Insulinoma Cell Line Destruction: Role of Cytokines and Signalling Pathways. [Doctoral Dissertation]. University of New South Wales; 2014. Available from: http://handle.unsw.edu.au/1959.4/54612 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:35355/SOURCE02?view=true


University of New South Wales

15. Chowdhury, Md.Kamrul. Glucagon regulation of β-catenin/TCF7L2 signalling in the liver: a potential new target for the treatment of type 2 diabetes.

Degree: Medical Sciences, 2017, University of New South Wales

 Type 2 diabetes (T2D) is a chronic metabolic disease that has become a major global health problem. It is well known that high blood glucose,… (more)

Subjects/Keywords: PKA, PKB, Wnt; Type 2 Diabetes; Glucagon, β-catenin/TCF7L2 signalling

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APA (6th Edition):

Chowdhury, M. K. (2017). Glucagon regulation of β-catenin/TCF7L2 signalling in the liver: a potential new target for the treatment of type 2 diabetes. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/58021 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:45309/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Chowdhury, Md Kamrul. “Glucagon regulation of β-catenin/TCF7L2 signalling in the liver: a potential new target for the treatment of type 2 diabetes.” 2017. Doctoral Dissertation, University of New South Wales. Accessed October 19, 2019. http://handle.unsw.edu.au/1959.4/58021 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:45309/SOURCE02?view=true.

MLA Handbook (7th Edition):

Chowdhury, Md Kamrul. “Glucagon regulation of β-catenin/TCF7L2 signalling in the liver: a potential new target for the treatment of type 2 diabetes.” 2017. Web. 19 Oct 2019.

Vancouver:

Chowdhury MK. Glucagon regulation of β-catenin/TCF7L2 signalling in the liver: a potential new target for the treatment of type 2 diabetes. [Internet] [Doctoral dissertation]. University of New South Wales; 2017. [cited 2019 Oct 19]. Available from: http://handle.unsw.edu.au/1959.4/58021 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:45309/SOURCE02?view=true.

Council of Science Editors:

Chowdhury MK. Glucagon regulation of β-catenin/TCF7L2 signalling in the liver: a potential new target for the treatment of type 2 diabetes. [Doctoral Dissertation]. University of New South Wales; 2017. Available from: http://handle.unsw.edu.au/1959.4/58021 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:45309/SOURCE02?view=true


University of New South Wales

16. Humphrey, Sean James. The Insulin-regulated Phosphoproteome.

Degree: Clinical School - St Vincent's Hospital, 2014, University of New South Wales

 A major challenge of the post-genomics era is to define the connectivity of protein phosphorylation networks. In this thesis, I describe and quantitatively delineate the… (more)

Subjects/Keywords: mTORC2; Akt; mTOR; SIN1; Insulin; Phosphoproteome; Phosphoproteomics; Signalling; Network; Mass spectrometry; Proteomics; Kinases

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APA (6th Edition):

Humphrey, S. J. (2014). The Insulin-regulated Phosphoproteome. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/53474 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:12169/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Humphrey, Sean James. “The Insulin-regulated Phosphoproteome.” 2014. Doctoral Dissertation, University of New South Wales. Accessed October 19, 2019. http://handle.unsw.edu.au/1959.4/53474 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:12169/SOURCE02?view=true.

MLA Handbook (7th Edition):

Humphrey, Sean James. “The Insulin-regulated Phosphoproteome.” 2014. Web. 19 Oct 2019.

Vancouver:

Humphrey SJ. The Insulin-regulated Phosphoproteome. [Internet] [Doctoral dissertation]. University of New South Wales; 2014. [cited 2019 Oct 19]. Available from: http://handle.unsw.edu.au/1959.4/53474 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:12169/SOURCE02?view=true.

Council of Science Editors:

Humphrey SJ. The Insulin-regulated Phosphoproteome. [Doctoral Dissertation]. University of New South Wales; 2014. Available from: http://handle.unsw.edu.au/1959.4/53474 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:12169/SOURCE02?view=true


University of New South Wales

17. Alhag Amhmad, Moftah. Discovering the mechanism of action of nutritional therapy and evolving an innovative formula for the treatment of Crohn's disease.

Degree: Women's & Children's Health, 2015, University of New South Wales

 Exclusive Enteral Nutrition (EEN), utilizing a nutritionally complete polymeric formula (PF), can suppress gut inflammation and induce remission in active Crohn disease (CD). However, PF’s… (more)

Subjects/Keywords: experimental colitis, signalling pathways; Crohn's disease, Enteral Nutrition, Polymeric formula; Glutamine, Arginine, Curcumin

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APA (6th Edition):

Alhag Amhmad, M. (2015). Discovering the mechanism of action of nutritional therapy and evolving an innovative formula for the treatment of Crohn's disease. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/54918 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:36179/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Alhag Amhmad, Moftah. “Discovering the mechanism of action of nutritional therapy and evolving an innovative formula for the treatment of Crohn's disease.” 2015. Doctoral Dissertation, University of New South Wales. Accessed October 19, 2019. http://handle.unsw.edu.au/1959.4/54918 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:36179/SOURCE02?view=true.

MLA Handbook (7th Edition):

Alhag Amhmad, Moftah. “Discovering the mechanism of action of nutritional therapy and evolving an innovative formula for the treatment of Crohn's disease.” 2015. Web. 19 Oct 2019.

Vancouver:

Alhag Amhmad M. Discovering the mechanism of action of nutritional therapy and evolving an innovative formula for the treatment of Crohn's disease. [Internet] [Doctoral dissertation]. University of New South Wales; 2015. [cited 2019 Oct 19]. Available from: http://handle.unsw.edu.au/1959.4/54918 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:36179/SOURCE02?view=true.

Council of Science Editors:

Alhag Amhmad M. Discovering the mechanism of action of nutritional therapy and evolving an innovative formula for the treatment of Crohn's disease. [Doctoral Dissertation]. University of New South Wales; 2015. Available from: http://handle.unsw.edu.au/1959.4/54918 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:36179/SOURCE02?view=true


University of New South Wales

18. Johnson, Jacque-Lynne Francine Annette. The role of the zebrafish scube gene family in Hedgehog signalling and slow muscle development.

Degree: Victor Chang Cardiac Research Institute, 2009, University of New South Wales

 Hedgehog (Hh) signalling from the notochord induces the slow muscle cell fate in the adaxial cells of the developing zebrafish embryo. Slow muscle formation is… (more)

Subjects/Keywords: zebrafish; muscle development; Hedgehog signalling; scube gene family

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APA (6th Edition):

Johnson, J. F. A. (2009). The role of the zebrafish scube gene family in Hedgehog signalling and slow muscle development. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/43316 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:4404/SOURCE1?view=true

Chicago Manual of Style (16th Edition):

Johnson, Jacque-Lynne Francine Annette. “The role of the zebrafish scube gene family in Hedgehog signalling and slow muscle development.” 2009. Doctoral Dissertation, University of New South Wales. Accessed October 19, 2019. http://handle.unsw.edu.au/1959.4/43316 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:4404/SOURCE1?view=true.

MLA Handbook (7th Edition):

Johnson, Jacque-Lynne Francine Annette. “The role of the zebrafish scube gene family in Hedgehog signalling and slow muscle development.” 2009. Web. 19 Oct 2019.

Vancouver:

Johnson JFA. The role of the zebrafish scube gene family in Hedgehog signalling and slow muscle development. [Internet] [Doctoral dissertation]. University of New South Wales; 2009. [cited 2019 Oct 19]. Available from: http://handle.unsw.edu.au/1959.4/43316 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:4404/SOURCE1?view=true.

Council of Science Editors:

Johnson JFA. The role of the zebrafish scube gene family in Hedgehog signalling and slow muscle development. [Doctoral Dissertation]. University of New South Wales; 2009. Available from: http://handle.unsw.edu.au/1959.4/43316 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:4404/SOURCE1?view=true


University of New South Wales

19. Murrow, Beverley. Role of guanine nucleotide exchange factors for Rab10 in insulin-regulated GLUT4 trafficking.

Degree: Clinical School - St Vincent's Hospital, 2017, University of New South Wales

 The insulin regulation of glucose uptake via translocation of the glucose transporter, GLUT4, is essential for maintenance of whole-body glucose homeostasis. GLUT4 traffic is a… (more)

Subjects/Keywords: DENND4C; DENN; DENND4A; GLUT4; Signalling; Mass spectrometry; Adipocyte; Rab GTPase; Rab10; AS160; GEF; Insulin; 14-3-3; Phosphorylation; Phosphoproteomics

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APA (6th Edition):

Murrow, B. (2017). Role of guanine nucleotide exchange factors for Rab10 in insulin-regulated GLUT4 trafficking. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/57311 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:43275/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Murrow, Beverley. “Role of guanine nucleotide exchange factors for Rab10 in insulin-regulated GLUT4 trafficking.” 2017. Doctoral Dissertation, University of New South Wales. Accessed October 19, 2019. http://handle.unsw.edu.au/1959.4/57311 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:43275/SOURCE02?view=true.

MLA Handbook (7th Edition):

Murrow, Beverley. “Role of guanine nucleotide exchange factors for Rab10 in insulin-regulated GLUT4 trafficking.” 2017. Web. 19 Oct 2019.

Vancouver:

Murrow B. Role of guanine nucleotide exchange factors for Rab10 in insulin-regulated GLUT4 trafficking. [Internet] [Doctoral dissertation]. University of New South Wales; 2017. [cited 2019 Oct 19]. Available from: http://handle.unsw.edu.au/1959.4/57311 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:43275/SOURCE02?view=true.

Council of Science Editors:

Murrow B. Role of guanine nucleotide exchange factors for Rab10 in insulin-regulated GLUT4 trafficking. [Doctoral Dissertation]. University of New South Wales; 2017. Available from: http://handle.unsw.edu.au/1959.4/57311 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:43275/SOURCE02?view=true


University of New South Wales

20. Cazzolli, Rosanna. The effects of linoleate on insulin action in skeletal muscle cells.

Degree: Clinical School - St Vincent's Hospital, 2005, University of New South Wales

 Emerging evidence suggests that an important mechanism for the negative feedback control of insulin signalling involves the inhibition of tyrosine phosphorylation of IRS-1 by its… (more)

Subjects/Keywords: insulin signalling; type 2 diabetes; linoleate; IRS-1; phosphatidic acid

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APA (6th Edition):

Cazzolli, R. (2005). The effects of linoleate on insulin action in skeletal muscle cells. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/22925 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:802/SOURCE01?view=true

Chicago Manual of Style (16th Edition):

Cazzolli, Rosanna. “The effects of linoleate on insulin action in skeletal muscle cells.” 2005. Doctoral Dissertation, University of New South Wales. Accessed October 19, 2019. http://handle.unsw.edu.au/1959.4/22925 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:802/SOURCE01?view=true.

MLA Handbook (7th Edition):

Cazzolli, Rosanna. “The effects of linoleate on insulin action in skeletal muscle cells.” 2005. Web. 19 Oct 2019.

Vancouver:

Cazzolli R. The effects of linoleate on insulin action in skeletal muscle cells. [Internet] [Doctoral dissertation]. University of New South Wales; 2005. [cited 2019 Oct 19]. Available from: http://handle.unsw.edu.au/1959.4/22925 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:802/SOURCE01?view=true.

Council of Science Editors:

Cazzolli R. The effects of linoleate on insulin action in skeletal muscle cells. [Doctoral Dissertation]. University of New South Wales; 2005. Available from: http://handle.unsw.edu.au/1959.4/22925 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:802/SOURCE01?view=true


University of New South Wales

21. McDougald, S. Diane. Regulation of starvation and nonculturability in the marine pathogen, Vibrio vulnificus.

Degree: Microbiology and Immunology, 2000, University of New South Wales

 Vibrio vulnificus is a model environmental organism exhibiting a classical starvation response during nutrient limitation as well as a non-culturable state when exposed to low… (more)

Subjects/Keywords: Starvation; nonculturability; VBNC; quorum sensing; signalling; AI-2; Vibrio. luxR; Vibrio vulnificus; starvation; cold adaptation

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APA (6th Edition):

McDougald, S. D. (2000). Regulation of starvation and nonculturability in the marine pathogen, Vibrio vulnificus. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/19118 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:551/SOURCE01?view=true

Chicago Manual of Style (16th Edition):

McDougald, S Diane. “Regulation of starvation and nonculturability in the marine pathogen, Vibrio vulnificus.” 2000. Doctoral Dissertation, University of New South Wales. Accessed October 19, 2019. http://handle.unsw.edu.au/1959.4/19118 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:551/SOURCE01?view=true.

MLA Handbook (7th Edition):

McDougald, S Diane. “Regulation of starvation and nonculturability in the marine pathogen, Vibrio vulnificus.” 2000. Web. 19 Oct 2019.

Vancouver:

McDougald SD. Regulation of starvation and nonculturability in the marine pathogen, Vibrio vulnificus. [Internet] [Doctoral dissertation]. University of New South Wales; 2000. [cited 2019 Oct 19]. Available from: http://handle.unsw.edu.au/1959.4/19118 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:551/SOURCE01?view=true.

Council of Science Editors:

McDougald SD. Regulation of starvation and nonculturability in the marine pathogen, Vibrio vulnificus. [Doctoral Dissertation]. University of New South Wales; 2000. Available from: http://handle.unsw.edu.au/1959.4/19118 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:551/SOURCE01?view=true

.