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University: University of Cambridge

You searched for subject:(signalling). Showing records 1 – 30 of 35 total matches.

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University of Cambridge

1. Pillidge, Zoe. Transcription and chromatin dynamics in the Notch signalling response .

Degree: 2019, University of Cambridge

 During normal development, different genes are expressed in different cell types, often directed by cell signalling pathways and the pre-existing chromatin environment. The highly-conserved Notch… (more)

Subjects/Keywords: Notch; chromatin; transcription; development; signalling

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

APA (6th Edition):

Pillidge, Z. (2019). Transcription and chromatin dynamics in the Notch signalling response . (Thesis). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/290796

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):

Pillidge, Zoe. “Transcription and chromatin dynamics in the Notch signalling response .” 2019. Thesis, University of Cambridge. Accessed October 15, 2019. https://www.repository.cam.ac.uk/handle/1810/290796.

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

MLA Handbook (7th Edition):

Pillidge, Zoe. “Transcription and chromatin dynamics in the Notch signalling response .” 2019. Web. 15 Oct 2019.

Vancouver:

Pillidge Z. Transcription and chromatin dynamics in the Notch signalling response . [Internet] [Thesis]. University of Cambridge; 2019. [cited 2019 Oct 15]. Available from: https://www.repository.cam.ac.uk/handle/1810/290796.

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

Council of Science Editors:

Pillidge Z. Transcription and chromatin dynamics in the Notch signalling response . [Thesis]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/290796

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


University of Cambridge

2. Tan, Sin Lih. The physiological role of P2X4 receptors in lysosome function.

Degree: PhD, 2017, University of Cambridge

 P2X4 receptors (P2X4R) are ligand-gated ion channels activated by ATP and with a high permeability to Ca2+. They are predominantly localised to lysosomes and from… (more)

Subjects/Keywords: 615.1; P2X4; Lysosome; Calcium signalling; lysosome fusion

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

APA (6th Edition):

Tan, S. L. (2017). The physiological role of P2X4 receptors in lysosome function. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/267925 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.725602

Chicago Manual of Style (16th Edition):

Tan, Sin Lih. “The physiological role of P2X4 receptors in lysosome function.” 2017. Doctoral Dissertation, University of Cambridge. Accessed October 15, 2019. https://www.repository.cam.ac.uk/handle/1810/267925 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.725602.

MLA Handbook (7th Edition):

Tan, Sin Lih. “The physiological role of P2X4 receptors in lysosome function.” 2017. Web. 15 Oct 2019.

Vancouver:

Tan SL. The physiological role of P2X4 receptors in lysosome function. [Internet] [Doctoral dissertation]. University of Cambridge; 2017. [cited 2019 Oct 15]. Available from: https://www.repository.cam.ac.uk/handle/1810/267925 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.725602.

Council of Science Editors:

Tan SL. The physiological role of P2X4 receptors in lysosome function. [Doctoral Dissertation]. University of Cambridge; 2017. Available from: https://www.repository.cam.ac.uk/handle/1810/267925 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.725602


University of Cambridge

3. Tan, Sin Lih. The physiological role of P2X4 receptors in lysosome function .

Degree: 2017, University of Cambridge

 P2X4 receptors (P2X4R) are ligand-gated ion channels activated by ATP and with a high permeability to Ca2+. They are predominantly localised to lysosomes and from… (more)

Subjects/Keywords: P2X4; Lysosome; Calcium signalling; lysosome fusion

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

APA (6th Edition):

Tan, S. L. (2017). The physiological role of P2X4 receptors in lysosome function . (Thesis). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/267925

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):

Tan, Sin Lih. “The physiological role of P2X4 receptors in lysosome function .” 2017. Thesis, University of Cambridge. Accessed October 15, 2019. https://www.repository.cam.ac.uk/handle/1810/267925.

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

MLA Handbook (7th Edition):

Tan, Sin Lih. “The physiological role of P2X4 receptors in lysosome function .” 2017. Web. 15 Oct 2019.

Vancouver:

Tan SL. The physiological role of P2X4 receptors in lysosome function . [Internet] [Thesis]. University of Cambridge; 2017. [cited 2019 Oct 15]. Available from: https://www.repository.cam.ac.uk/handle/1810/267925.

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

Council of Science Editors:

Tan SL. The physiological role of P2X4 receptors in lysosome function . [Thesis]. University of Cambridge; 2017. Available from: https://www.repository.cam.ac.uk/handle/1810/267925

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


University of Cambridge

4. Stuart, Kate Ann. ERK1/2 signalling and protein ubiquitylation in the control of apoptosis .

Degree: 2019, University of Cambridge

 Programmed cell death, or apoptosis, is critical for normal developmental processes that involve cell turnover including embryogenesis and development and function of the immune system.… (more)

Subjects/Keywords: BIM; ERK1/2 signalling; DUB; Ubiquitin; Apoptosis

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

APA (6th Edition):

Stuart, K. A. (2019). ERK1/2 signalling and protein ubiquitylation in the control of apoptosis . (Thesis). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/293975

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):

Stuart, Kate Ann. “ERK1/2 signalling and protein ubiquitylation in the control of apoptosis .” 2019. Thesis, University of Cambridge. Accessed October 15, 2019. https://www.repository.cam.ac.uk/handle/1810/293975.

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

MLA Handbook (7th Edition):

Stuart, Kate Ann. “ERK1/2 signalling and protein ubiquitylation in the control of apoptosis .” 2019. Web. 15 Oct 2019.

Vancouver:

Stuart KA. ERK1/2 signalling and protein ubiquitylation in the control of apoptosis . [Internet] [Thesis]. University of Cambridge; 2019. [cited 2019 Oct 15]. Available from: https://www.repository.cam.ac.uk/handle/1810/293975.

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

Council of Science Editors:

Stuart KA. ERK1/2 signalling and protein ubiquitylation in the control of apoptosis . [Thesis]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/293975

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


University of Cambridge

5. Luff, Daisy Helen. Elucidating the molecular mechanisms of p110δ activation in T cell antigen receptor signalling .

Degree: 2019, University of Cambridge

 Phosphoinositide 3-kinases (PI3Ks) are activated in immune cells downstream of the antigen recognition receptors, the signals from which are crucial for the development, differentiation and… (more)

Subjects/Keywords: PI3K; TCR Signalling; Proteomics; CRISPR/Cas9; T Cells; p110δ; TCR; Interactomics; Lymphocyte Signalling; AviTag

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

APA (6th Edition):

Luff, D. H. (2019). Elucidating the molecular mechanisms of p110δ activation in T cell antigen receptor signalling . (Thesis). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/291052

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):

Luff, Daisy Helen. “Elucidating the molecular mechanisms of p110δ activation in T cell antigen receptor signalling .” 2019. Thesis, University of Cambridge. Accessed October 15, 2019. https://www.repository.cam.ac.uk/handle/1810/291052.

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

MLA Handbook (7th Edition):

Luff, Daisy Helen. “Elucidating the molecular mechanisms of p110δ activation in T cell antigen receptor signalling .” 2019. Web. 15 Oct 2019.

Vancouver:

Luff DH. Elucidating the molecular mechanisms of p110δ activation in T cell antigen receptor signalling . [Internet] [Thesis]. University of Cambridge; 2019. [cited 2019 Oct 15]. Available from: https://www.repository.cam.ac.uk/handle/1810/291052.

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

Council of Science Editors:

Luff DH. Elucidating the molecular mechanisms of p110δ activation in T cell antigen receptor signalling . [Thesis]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/291052

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


University of Cambridge

6. Lago Cooke, Santiago Guillermo. A novel pipeline for drug discovery in neuropsychiatric disorders using high-content single-cell screening of signalling network responses ex vivo.

Degree: PhD, 2016, University of Cambridge

 The current work entails the development of a novel high content platform for the measurement of kinetic ligand responses across cell signalling networks at the… (more)

Subjects/Keywords: drug discovery; neuropsychiatric disorders; high-content screening; single-cell; signalling network

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

APA (6th Edition):

Lago Cooke, S. G. (2016). A novel pipeline for drug discovery in neuropsychiatric disorders using high-content single-cell screening of signalling network responses ex vivo. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/270297 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744241

Chicago Manual of Style (16th Edition):

Lago Cooke, Santiago Guillermo. “A novel pipeline for drug discovery in neuropsychiatric disorders using high-content single-cell screening of signalling network responses ex vivo.” 2016. Doctoral Dissertation, University of Cambridge. Accessed October 15, 2019. https://www.repository.cam.ac.uk/handle/1810/270297 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744241.

MLA Handbook (7th Edition):

Lago Cooke, Santiago Guillermo. “A novel pipeline for drug discovery in neuropsychiatric disorders using high-content single-cell screening of signalling network responses ex vivo.” 2016. Web. 15 Oct 2019.

Vancouver:

Lago Cooke SG. A novel pipeline for drug discovery in neuropsychiatric disorders using high-content single-cell screening of signalling network responses ex vivo. [Internet] [Doctoral dissertation]. University of Cambridge; 2016. [cited 2019 Oct 15]. Available from: https://www.repository.cam.ac.uk/handle/1810/270297 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744241.

Council of Science Editors:

Lago Cooke SG. A novel pipeline for drug discovery in neuropsychiatric disorders using high-content single-cell screening of signalling network responses ex vivo. [Doctoral Dissertation]. University of Cambridge; 2016. Available from: https://www.repository.cam.ac.uk/handle/1810/270297 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744241


University of Cambridge

7. Bradley, David. The evolution of protein kinase specificity .

Degree: 2019, University of Cambridge

 Protein phosphorylation represents one of the most important post-translational modifica- tions (PTMs) for cell signalling, and is is catalysed by a group of enzymes called… (more)

Subjects/Keywords: Signalling; Protein evolution; Phylogenetics; Structural biology; Phosphoproteomics; Protein kinases

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

APA (6th Edition):

Bradley, D. (2019). The evolution of protein kinase specificity . (Thesis). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/290500

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):

Bradley, David. “The evolution of protein kinase specificity .” 2019. Thesis, University of Cambridge. Accessed October 15, 2019. https://www.repository.cam.ac.uk/handle/1810/290500.

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

MLA Handbook (7th Edition):

Bradley, David. “The evolution of protein kinase specificity .” 2019. Web. 15 Oct 2019.

Vancouver:

Bradley D. The evolution of protein kinase specificity . [Internet] [Thesis]. University of Cambridge; 2019. [cited 2019 Oct 15]. Available from: https://www.repository.cam.ac.uk/handle/1810/290500.

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

Council of Science Editors:

Bradley D. The evolution of protein kinase specificity . [Thesis]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/290500

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


University of Cambridge

8. Lago Cooke, Santiago Guillermo. A NOVEL PIPELINE FOR DRUG DISCOVERY IN NEUROPSYCHIATRIC DISORDERS USING HIGH-CONTENT SINGLE-CELL SCREENING OF SIGNALLING NETWORK RESPONSES EX VIVO .

Degree: 2016, University of Cambridge

 The current work entails the development of a novel high content platform for the measurement of kinetic ligand responses across cell signalling networks at the… (more)

Subjects/Keywords: drug discovery; neuropsychiatric disorders; high-content screening; single-cell; signalling network

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Lago Cooke, S. G. (2016). A NOVEL PIPELINE FOR DRUG DISCOVERY IN NEUROPSYCHIATRIC DISORDERS USING HIGH-CONTENT SINGLE-CELL SCREENING OF SIGNALLING NETWORK RESPONSES EX VIVO . (Thesis). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/270297

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):

Lago Cooke, Santiago Guillermo. “A NOVEL PIPELINE FOR DRUG DISCOVERY IN NEUROPSYCHIATRIC DISORDERS USING HIGH-CONTENT SINGLE-CELL SCREENING OF SIGNALLING NETWORK RESPONSES EX VIVO .” 2016. Thesis, University of Cambridge. Accessed October 15, 2019. https://www.repository.cam.ac.uk/handle/1810/270297.

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

MLA Handbook (7th Edition):

Lago Cooke, Santiago Guillermo. “A NOVEL PIPELINE FOR DRUG DISCOVERY IN NEUROPSYCHIATRIC DISORDERS USING HIGH-CONTENT SINGLE-CELL SCREENING OF SIGNALLING NETWORK RESPONSES EX VIVO .” 2016. Web. 15 Oct 2019.

Vancouver:

Lago Cooke SG. A NOVEL PIPELINE FOR DRUG DISCOVERY IN NEUROPSYCHIATRIC DISORDERS USING HIGH-CONTENT SINGLE-CELL SCREENING OF SIGNALLING NETWORK RESPONSES EX VIVO . [Internet] [Thesis]. University of Cambridge; 2016. [cited 2019 Oct 15]. Available from: https://www.repository.cam.ac.uk/handle/1810/270297.

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

Council of Science Editors:

Lago Cooke SG. A NOVEL PIPELINE FOR DRUG DISCOVERY IN NEUROPSYCHIATRIC DISORDERS USING HIGH-CONTENT SINGLE-CELL SCREENING OF SIGNALLING NETWORK RESPONSES EX VIVO . [Thesis]. University of Cambridge; 2016. Available from: https://www.repository.cam.ac.uk/handle/1810/270297

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

9. Cama, Jehangir. Quantifying passive drug transport across lipid membranes .

Degree: 2016, University of Cambridge

 Antibiotic resistance has emerged as one of the World’s leading public health challenges. The inexorable emergence of drug resistant pathogens, combined with a steep decline… (more)

Subjects/Keywords: Antibiotic resistance; Microfluidics; Vesicles; Membrane Transport; Indole signalling; UV autofluorescence

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Cama, J. (2016). Quantifying passive drug transport across lipid membranes . (Thesis). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/254296

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):

Cama, Jehangir. “Quantifying passive drug transport across lipid membranes .” 2016. Thesis, University of Cambridge. Accessed October 15, 2019. https://www.repository.cam.ac.uk/handle/1810/254296.

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

MLA Handbook (7th Edition):

Cama, Jehangir. “Quantifying passive drug transport across lipid membranes .” 2016. Web. 15 Oct 2019.

Vancouver:

Cama J. Quantifying passive drug transport across lipid membranes . [Internet] [Thesis]. University of Cambridge; 2016. [cited 2019 Oct 15]. Available from: https://www.repository.cam.ac.uk/handle/1810/254296.

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

Council of Science Editors:

Cama J. Quantifying passive drug transport across lipid membranes . [Thesis]. University of Cambridge; 2016. Available from: https://www.repository.cam.ac.uk/handle/1810/254296

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


University of Cambridge

10. Cama, Jehangir. Quantifying passive drug transport across lipid membranes.

Degree: PhD, 2016, University of Cambridge

 Antibiotic resistance has emerged as one of the World's leading public health challenges. The inexorable emergence of drug resistant pathogens, combined with a steep decline… (more)

Subjects/Keywords: 530; Antibiotic resistance; Microfluidics; Vesicles; Membrane Transport; Indole signalling; UV autofluorescence

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Cama, J. (2016). Quantifying passive drug transport across lipid membranes. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/254296 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.681250

Chicago Manual of Style (16th Edition):

Cama, Jehangir. “Quantifying passive drug transport across lipid membranes.” 2016. Doctoral Dissertation, University of Cambridge. Accessed October 15, 2019. https://www.repository.cam.ac.uk/handle/1810/254296 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.681250.

MLA Handbook (7th Edition):

Cama, Jehangir. “Quantifying passive drug transport across lipid membranes.” 2016. Web. 15 Oct 2019.

Vancouver:

Cama J. Quantifying passive drug transport across lipid membranes. [Internet] [Doctoral dissertation]. University of Cambridge; 2016. [cited 2019 Oct 15]. Available from: https://www.repository.cam.ac.uk/handle/1810/254296 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.681250.

Council of Science Editors:

Cama J. Quantifying passive drug transport across lipid membranes. [Doctoral Dissertation]. University of Cambridge; 2016. Available from: https://www.repository.cam.ac.uk/handle/1810/254296 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.681250


University of Cambridge

11. Zhao, Mo. Towards an understanding of the role of Ca2+ signalling in neural stem cell activation .

Degree: 2019, University of Cambridge

 Regeneration of the adult human brain is a long time clinical challenge. The adult mammalian brain contains neural stem cells (NSCs) that are capable of… (more)

Subjects/Keywords: Neural stem cell; neuroblasts; quiescence; Calcium signalling; Drosophila development

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

APA (6th Edition):

Zhao, M. (2019). Towards an understanding of the role of Ca2+ signalling in neural stem cell activation . (Thesis). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/294312

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):

Zhao, Mo. “Towards an understanding of the role of Ca2+ signalling in neural stem cell activation .” 2019. Thesis, University of Cambridge. Accessed October 15, 2019. https://www.repository.cam.ac.uk/handle/1810/294312.

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

MLA Handbook (7th Edition):

Zhao, Mo. “Towards an understanding of the role of Ca2+ signalling in neural stem cell activation .” 2019. Web. 15 Oct 2019.

Vancouver:

Zhao M. Towards an understanding of the role of Ca2+ signalling in neural stem cell activation . [Internet] [Thesis]. University of Cambridge; 2019. [cited 2019 Oct 15]. Available from: https://www.repository.cam.ac.uk/handle/1810/294312.

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

Council of Science Editors:

Zhao M. Towards an understanding of the role of Ca2+ signalling in neural stem cell activation . [Thesis]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/294312

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


University of Cambridge

12. Bradley, David. The evolution of protein kinase specificity.

Degree: PhD, 2019, University of Cambridge

 Protein phosphorylation represents one of the most important post-translational modifica- tions (PTMs) for cell signalling, and is is catalysed by a group of enzymes called… (more)

Subjects/Keywords: Signalling; Protein evolution; Phylogenetics; Structural biology; Phosphoproteomics; Protein kinases

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Bradley, D. (2019). The evolution of protein kinase specificity. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/290500 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.774602

Chicago Manual of Style (16th Edition):

Bradley, David. “The evolution of protein kinase specificity.” 2019. Doctoral Dissertation, University of Cambridge. Accessed October 15, 2019. https://www.repository.cam.ac.uk/handle/1810/290500 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.774602.

MLA Handbook (7th Edition):

Bradley, David. “The evolution of protein kinase specificity.” 2019. Web. 15 Oct 2019.

Vancouver:

Bradley D. The evolution of protein kinase specificity. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2019 Oct 15]. Available from: https://www.repository.cam.ac.uk/handle/1810/290500 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.774602.

Council of Science Editors:

Bradley D. The evolution of protein kinase specificity. [Doctoral Dissertation]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/290500 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.774602


University of Cambridge

13. Matthus, Elsa. Phosphate starvation alters calcium signalling in roots of Arabidopsis thaliana .

Degree: 2019, University of Cambridge

 Low bioavailability of phosphate (P) due to low concentration and high immobility in soils is a key limiting factor in crop production. Application of excess… (more)

Subjects/Keywords: plant; root; Arabidopsis thaliana; Arabidopsis; calcium signalling; plant nutrition; phosphate nutrition; iron nutrition; reactive oxygen species; abiotic stress; extracellular nucleotide signalling; ATP; fluorescence microscopy; ratiometric imaging; GCaMP3; aequorin

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

APA (6th Edition):

Matthus, E. (2019). Phosphate starvation alters calcium signalling in roots of Arabidopsis thaliana . (Thesis). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/290260

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):

Matthus, Elsa. “Phosphate starvation alters calcium signalling in roots of Arabidopsis thaliana .” 2019. Thesis, University of Cambridge. Accessed October 15, 2019. https://www.repository.cam.ac.uk/handle/1810/290260.

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

MLA Handbook (7th Edition):

Matthus, Elsa. “Phosphate starvation alters calcium signalling in roots of Arabidopsis thaliana .” 2019. Web. 15 Oct 2019.

Vancouver:

Matthus E. Phosphate starvation alters calcium signalling in roots of Arabidopsis thaliana . [Internet] [Thesis]. University of Cambridge; 2019. [cited 2019 Oct 15]. Available from: https://www.repository.cam.ac.uk/handle/1810/290260.

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

Council of Science Editors:

Matthus E. Phosphate starvation alters calcium signalling in roots of Arabidopsis thaliana . [Thesis]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/290260

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


University of Cambridge

14. Matthus, Elsa. Phosphate starvation alters calcium signalling in roots of Arabidopsis thaliana.

Degree: PhD, 2019, University of Cambridge

 Low bioavailability of phosphate (P) due to low concentration and high immobility in soils is a key limiting factor in crop production. Application of excess… (more)

Subjects/Keywords: plant; root; Arabidopsis thaliana; Arabidopsis; calcium signalling; plant nutrition; phosphate nutrition; iron nutrition; reactive oxygen species; abiotic stress; extracellular nucleotide signalling; ATP; fluorescence microscopy; ratiometric imaging; GCaMP3; aequorin

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

APA (6th Edition):

Matthus, E. (2019). Phosphate starvation alters calcium signalling in roots of Arabidopsis thaliana. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/290260 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.767898

Chicago Manual of Style (16th Edition):

Matthus, Elsa. “Phosphate starvation alters calcium signalling in roots of Arabidopsis thaliana.” 2019. Doctoral Dissertation, University of Cambridge. Accessed October 15, 2019. https://www.repository.cam.ac.uk/handle/1810/290260 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.767898.

MLA Handbook (7th Edition):

Matthus, Elsa. “Phosphate starvation alters calcium signalling in roots of Arabidopsis thaliana.” 2019. Web. 15 Oct 2019.

Vancouver:

Matthus E. Phosphate starvation alters calcium signalling in roots of Arabidopsis thaliana. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2019 Oct 15]. Available from: https://www.repository.cam.ac.uk/handle/1810/290260 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.767898.

Council of Science Editors:

Matthus E. Phosphate starvation alters calcium signalling in roots of Arabidopsis thaliana. [Doctoral Dissertation]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/290260 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.767898


University of Cambridge

15. Hinchy, Elizabeth. How cellular ATP/ADP ratios and reactive oxygen species affect AMPK signalling.

Degree: PhD, 2017, University of Cambridge

 Mitochondria are key generators of cellular ATP, vital to complex life. Historically, mitochondrial generation of reactive oxygen species (ROS) was considered to be an unregulated… (more)

Subjects/Keywords: AMPK; AMP-activated protein kinase; mitochondria; mitochondrial ROS; ROS; H2O2; redox-signalling; thiols

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

APA (6th Edition):

Hinchy, E. (2017). How cellular ATP/ADP ratios and reactive oxygen species affect AMPK signalling. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/270029 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744361

Chicago Manual of Style (16th Edition):

Hinchy, Elizabeth. “How cellular ATP/ADP ratios and reactive oxygen species affect AMPK signalling.” 2017. Doctoral Dissertation, University of Cambridge. Accessed October 15, 2019. https://www.repository.cam.ac.uk/handle/1810/270029 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744361.

MLA Handbook (7th Edition):

Hinchy, Elizabeth. “How cellular ATP/ADP ratios and reactive oxygen species affect AMPK signalling.” 2017. Web. 15 Oct 2019.

Vancouver:

Hinchy E. How cellular ATP/ADP ratios and reactive oxygen species affect AMPK signalling. [Internet] [Doctoral dissertation]. University of Cambridge; 2017. [cited 2019 Oct 15]. Available from: https://www.repository.cam.ac.uk/handle/1810/270029 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744361.

Council of Science Editors:

Hinchy E. How cellular ATP/ADP ratios and reactive oxygen species affect AMPK signalling. [Doctoral Dissertation]. University of Cambridge; 2017. Available from: https://www.repository.cam.ac.uk/handle/1810/270029 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744361


University of Cambridge

16. Hinchy, Elizabeth. How cellular ATP/ADP ratios and reactive oxygen species affect AMPK signalling .

Degree: 2017, University of Cambridge

 Mitochondria are key generators of cellular ATP, vital to complex life. Historically, mitochondrial generation of reactive oxygen species (ROS) was considered to be an unregulated… (more)

Subjects/Keywords: AMPK; AMP-activated protein kinase; mitochondria; mitochondrial ROS; ROS; H2O2; redox-signalling; thiols

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

APA (6th Edition):

Hinchy, E. (2017). How cellular ATP/ADP ratios and reactive oxygen species affect AMPK signalling . (Thesis). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/270029

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):

Hinchy, Elizabeth. “How cellular ATP/ADP ratios and reactive oxygen species affect AMPK signalling .” 2017. Thesis, University of Cambridge. Accessed October 15, 2019. https://www.repository.cam.ac.uk/handle/1810/270029.

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

MLA Handbook (7th Edition):

Hinchy, Elizabeth. “How cellular ATP/ADP ratios and reactive oxygen species affect AMPK signalling .” 2017. Web. 15 Oct 2019.

Vancouver:

Hinchy E. How cellular ATP/ADP ratios and reactive oxygen species affect AMPK signalling . [Internet] [Thesis]. University of Cambridge; 2017. [cited 2019 Oct 15]. Available from: https://www.repository.cam.ac.uk/handle/1810/270029.

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

Council of Science Editors:

Hinchy E. How cellular ATP/ADP ratios and reactive oxygen species affect AMPK signalling . [Thesis]. University of Cambridge; 2017. Available from: https://www.repository.cam.ac.uk/handle/1810/270029

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


University of Cambridge

17. Macleod, Charlotte Victoria. Investigating TLR-4 signalling in response to protein ligands .

Degree: 2018, University of Cambridge

 Toll-like receptor (TLR)-4 is a pattern recognition receptor (PRR) that recognises the pathogen-associated molecular pattern (PAMP) lipopolysaccharide (LPS) produced by Gram-negative bacteria. LPS binds to… (more)

Subjects/Keywords: TLR-4; Mal; TIRAP; TIRF; Fibronectin; Tenascin-C; Stoichiometry; Microscopy; Innate signalling; Photobleaching

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APA (6th Edition):

Macleod, C. V. (2018). Investigating TLR-4 signalling in response to protein ligands . (Thesis). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/274540

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):

Macleod, Charlotte Victoria. “Investigating TLR-4 signalling in response to protein ligands .” 2018. Thesis, University of Cambridge. Accessed October 15, 2019. https://www.repository.cam.ac.uk/handle/1810/274540.

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

MLA Handbook (7th Edition):

Macleod, Charlotte Victoria. “Investigating TLR-4 signalling in response to protein ligands .” 2018. Web. 15 Oct 2019.

Vancouver:

Macleod CV. Investigating TLR-4 signalling in response to protein ligands . [Internet] [Thesis]. University of Cambridge; 2018. [cited 2019 Oct 15]. Available from: https://www.repository.cam.ac.uk/handle/1810/274540.

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

Council of Science Editors:

Macleod CV. Investigating TLR-4 signalling in response to protein ligands . [Thesis]. University of Cambridge; 2018. Available from: https://www.repository.cam.ac.uk/handle/1810/274540

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


University of Cambridge

18. de Almeida Pereira, Milton César. Inflammasome signalling during Salmonella Typhimurium infection.

Degree: PhD, 2018, University of Cambridge

 The innate immune system is the first line of defence against infection. It is comprised of physicochemical barriers and a variety of cell types including… (more)

Subjects/Keywords: Salmonella; Inflammasome; Cell Signalling; Cytokines; CARD9; NLRP3; Nigericin; Infection; Immunity; Innate Immunity

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

APA (6th Edition):

de Almeida Pereira, M. C. (2018). Inflammasome signalling during Salmonella Typhimurium infection. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/283642 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.763626

Chicago Manual of Style (16th Edition):

de Almeida Pereira, Milton César. “Inflammasome signalling during Salmonella Typhimurium infection.” 2018. Doctoral Dissertation, University of Cambridge. Accessed October 15, 2019. https://www.repository.cam.ac.uk/handle/1810/283642 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.763626.

MLA Handbook (7th Edition):

de Almeida Pereira, Milton César. “Inflammasome signalling during Salmonella Typhimurium infection.” 2018. Web. 15 Oct 2019.

Vancouver:

de Almeida Pereira MC. Inflammasome signalling during Salmonella Typhimurium infection. [Internet] [Doctoral dissertation]. University of Cambridge; 2018. [cited 2019 Oct 15]. Available from: https://www.repository.cam.ac.uk/handle/1810/283642 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.763626.

Council of Science Editors:

de Almeida Pereira MC. Inflammasome signalling during Salmonella Typhimurium infection. [Doctoral Dissertation]. University of Cambridge; 2018. Available from: https://www.repository.cam.ac.uk/handle/1810/283642 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.763626


University of Cambridge

19. Macleod, Charlotte Victoria. Investigating TLR-4 signalling in response to protein ligands.

Degree: PhD, 2018, University of Cambridge

 Toll-like receptor (TLR)-4 is a pattern recognition receptor (PRR) that recognises the pathogen-associated molecular pattern (PAMP) lipopolysaccharide (LPS) produced by Gram-negative bacteria. LPS binds to… (more)

Subjects/Keywords: TLR-4; Mal; TIRAP; TIRF; Fibronectin; Tenascin-C; Stoichiometry; Microscopy; Innate signalling; Photobleaching

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

APA (6th Edition):

Macleod, C. V. (2018). Investigating TLR-4 signalling in response to protein ligands. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/274540 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744655

Chicago Manual of Style (16th Edition):

Macleod, Charlotte Victoria. “Investigating TLR-4 signalling in response to protein ligands.” 2018. Doctoral Dissertation, University of Cambridge. Accessed October 15, 2019. https://www.repository.cam.ac.uk/handle/1810/274540 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744655.

MLA Handbook (7th Edition):

Macleod, Charlotte Victoria. “Investigating TLR-4 signalling in response to protein ligands.” 2018. Web. 15 Oct 2019.

Vancouver:

Macleod CV. Investigating TLR-4 signalling in response to protein ligands. [Internet] [Doctoral dissertation]. University of Cambridge; 2018. [cited 2019 Oct 15]. Available from: https://www.repository.cam.ac.uk/handle/1810/274540 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744655.

Council of Science Editors:

Macleod CV. Investigating TLR-4 signalling in response to protein ligands. [Doctoral Dissertation]. University of Cambridge; 2018. Available from: https://www.repository.cam.ac.uk/handle/1810/274540 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744655


University of Cambridge

20. Inouye, Michiko O. Role of P2Y12 receptor-mediated ADP signalling at microglia in the phagocytosis of neurons .

Degree: 2018, University of Cambridge

 Despite the prevalence of neurodegenerative disorders such as Parkinson’s and Alzheimer’s diseases, surprisingly little is known about the molecular mechanisms governing widespread neuronal loss observed… (more)

Subjects/Keywords: microglia; P2Y12; ADP; phagocytosis; calcium signalling; BV2; PC12; RT-qPCR; Flexstation; gene expression; LPS

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APA (6th Edition):

Inouye, M. O. (2018). Role of P2Y12 receptor-mediated ADP signalling at microglia in the phagocytosis of neurons . (Thesis). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/284409

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):

Inouye, Michiko O. “Role of P2Y12 receptor-mediated ADP signalling at microglia in the phagocytosis of neurons .” 2018. Thesis, University of Cambridge. Accessed October 15, 2019. https://www.repository.cam.ac.uk/handle/1810/284409.

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

MLA Handbook (7th Edition):

Inouye, Michiko O. “Role of P2Y12 receptor-mediated ADP signalling at microglia in the phagocytosis of neurons .” 2018. Web. 15 Oct 2019.

Vancouver:

Inouye MO. Role of P2Y12 receptor-mediated ADP signalling at microglia in the phagocytosis of neurons . [Internet] [Thesis]. University of Cambridge; 2018. [cited 2019 Oct 15]. Available from: https://www.repository.cam.ac.uk/handle/1810/284409.

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

Council of Science Editors:

Inouye MO. Role of P2Y12 receptor-mediated ADP signalling at microglia in the phagocytosis of neurons . [Thesis]. University of Cambridge; 2018. Available from: https://www.repository.cam.ac.uk/handle/1810/284409

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


University of Cambridge

21. Norwood, Stephanie Alix. Investigating the Morphology and Behaviour of Quiescent Neural Stem Cells in Drosophila Melanogaster .

Degree: 2019, University of Cambridge

 Understanding stem cell behaviour and the mechanisms that govern stem cell proliferation is a key question in developmental biology. Stem cell divisions must be carefully… (more)

Subjects/Keywords: Drosophila; stem cell; quiescence; neurons; glia; signalling; interactions; niche; neural; stem; cell; morphology; structure

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APA (6th Edition):

Norwood, S. A. (2019). Investigating the Morphology and Behaviour of Quiescent Neural Stem Cells in Drosophila Melanogaster . (Thesis). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/296279

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):

Norwood, Stephanie Alix. “Investigating the Morphology and Behaviour of Quiescent Neural Stem Cells in Drosophila Melanogaster .” 2019. Thesis, University of Cambridge. Accessed October 15, 2019. https://www.repository.cam.ac.uk/handle/1810/296279.

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

MLA Handbook (7th Edition):

Norwood, Stephanie Alix. “Investigating the Morphology and Behaviour of Quiescent Neural Stem Cells in Drosophila Melanogaster .” 2019. Web. 15 Oct 2019.

Vancouver:

Norwood SA. Investigating the Morphology and Behaviour of Quiescent Neural Stem Cells in Drosophila Melanogaster . [Internet] [Thesis]. University of Cambridge; 2019. [cited 2019 Oct 15]. Available from: https://www.repository.cam.ac.uk/handle/1810/296279.

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

Council of Science Editors:

Norwood SA. Investigating the Morphology and Behaviour of Quiescent Neural Stem Cells in Drosophila Melanogaster . [Thesis]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/296279

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


University of Cambridge

22. Sadiq, Barzan A. A dissection of class I phosphoinositide 3-kinase signalling in mouse embryonic fibroblasts and prostate organoids.

Degree: PhD, 2018, University of Cambridge

 Class I PI3Ks are a family (α, β, δ and γ) of ubiquitous lipid kinases that can be activated by cell surface receptors to 3-phosphorylate… (more)

Subjects/Keywords: Class I PI3K; PI(45)P2; PI(34)P2; PI(345)P3; phosphoinositide 3-kinase; phosphoinositide 3-kinase signalling; mouse embryonic fibroblasts; MEF; Prostate cancer; prostate organoids; PI3K/Akt signalling pathway; PI3K/PKB signalling pathway; Tumour microenvironment; Lipidomics; Microscopy; Confocal; TIRF; Widefield; MS Lipidomics; A dissection of class I phosphoinositide 3-kinase signalling in mouse embryonic fibroblasts and prostate organoids; Lipid signalling; Phospholipid signalling; pH and Tumour microenvironment; Acidic extracellular microenvironment and cancer; PI3K nuclear localisation; AviTag; Avi-Tag; Streptavidin; Biotinylation; PTEN-null; PTEN; PI3Ka; PI3Kß; PI3Kd; PI3K?; Imaris; Bitplane Imaris; Therapeutic interventions; Effects of pH on class I PI3K signalling

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

APA (6th Edition):

Sadiq, B. A. (2018). A dissection of class I phosphoinositide 3-kinase signalling in mouse embryonic fibroblasts and prostate organoids. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/278056 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.753373

Chicago Manual of Style (16th Edition):

Sadiq, Barzan A. “A dissection of class I phosphoinositide 3-kinase signalling in mouse embryonic fibroblasts and prostate organoids.” 2018. Doctoral Dissertation, University of Cambridge. Accessed October 15, 2019. https://www.repository.cam.ac.uk/handle/1810/278056 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.753373.

MLA Handbook (7th Edition):

Sadiq, Barzan A. “A dissection of class I phosphoinositide 3-kinase signalling in mouse embryonic fibroblasts and prostate organoids.” 2018. Web. 15 Oct 2019.

Vancouver:

Sadiq BA. A dissection of class I phosphoinositide 3-kinase signalling in mouse embryonic fibroblasts and prostate organoids. [Internet] [Doctoral dissertation]. University of Cambridge; 2018. [cited 2019 Oct 15]. Available from: https://www.repository.cam.ac.uk/handle/1810/278056 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.753373.

Council of Science Editors:

Sadiq BA. A dissection of class I phosphoinositide 3-kinase signalling in mouse embryonic fibroblasts and prostate organoids. [Doctoral Dissertation]. University of Cambridge; 2018. Available from: https://www.repository.cam.ac.uk/handle/1810/278056 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.753373


University of Cambridge

23. Davenport, Peter William. A metabolomics-based analysis of acyl-homoserine lactone quorum sensing in Pseudomonas aeruginosa.

Degree: PhD, 2018, University of Cambridge

 Pseudomonas aeruginosa is a metabolically versatile environmental bacterium that grows in extremely diverse habitats—from sea water to jet fuel—and is able to infect a large… (more)

Subjects/Keywords: Pseudomonas aeruginosa; quorum sensing; metabolomics; intercellular signalling; bacterial physiology; functional genomics; mass spectrometry; nuclear magnetic resonance spectroscopy; bacterial metabolism

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APA (6th Edition):

Davenport, P. W. (2018). A metabolomics-based analysis of acyl-homoserine lactone quorum sensing in Pseudomonas aeruginosa. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/274674 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744675

Chicago Manual of Style (16th Edition):

Davenport, Peter William. “A metabolomics-based analysis of acyl-homoserine lactone quorum sensing in Pseudomonas aeruginosa.” 2018. Doctoral Dissertation, University of Cambridge. Accessed October 15, 2019. https://www.repository.cam.ac.uk/handle/1810/274674 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744675.

MLA Handbook (7th Edition):

Davenport, Peter William. “A metabolomics-based analysis of acyl-homoserine lactone quorum sensing in Pseudomonas aeruginosa.” 2018. Web. 15 Oct 2019.

Vancouver:

Davenport PW. A metabolomics-based analysis of acyl-homoserine lactone quorum sensing in Pseudomonas aeruginosa. [Internet] [Doctoral dissertation]. University of Cambridge; 2018. [cited 2019 Oct 15]. Available from: https://www.repository.cam.ac.uk/handle/1810/274674 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744675.

Council of Science Editors:

Davenport PW. A metabolomics-based analysis of acyl-homoserine lactone quorum sensing in Pseudomonas aeruginosa. [Doctoral Dissertation]. University of Cambridge; 2018. Available from: https://www.repository.cam.ac.uk/handle/1810/274674 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744675


University of Cambridge

24. Cotton, Thomas Richard. The structure of human pro-myostatin and molecular basis of latency.

Degree: PhD, 2019, University of Cambridge

 Myostatin is a secreted growth factor of the transforming growth-factor β (TGFβ) superfamily, and a powerful negative regulator of muscle mass in vertebrates. As such,… (more)

Subjects/Keywords: Myostatin; TGF-beta; Muscle; X-ray crystallography; prodomain; latency; activation; extracellular matrix; Crystal structure; pro-myostatin; growth factor; signalling

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

APA (6th Edition):

Cotton, T. R. (2019). The structure of human pro-myostatin and molecular basis of latency. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/288560 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.767763

Chicago Manual of Style (16th Edition):

Cotton, Thomas Richard. “The structure of human pro-myostatin and molecular basis of latency.” 2019. Doctoral Dissertation, University of Cambridge. Accessed October 15, 2019. https://www.repository.cam.ac.uk/handle/1810/288560 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.767763.

MLA Handbook (7th Edition):

Cotton, Thomas Richard. “The structure of human pro-myostatin and molecular basis of latency.” 2019. Web. 15 Oct 2019.

Vancouver:

Cotton TR. The structure of human pro-myostatin and molecular basis of latency. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2019 Oct 15]. Available from: https://www.repository.cam.ac.uk/handle/1810/288560 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.767763.

Council of Science Editors:

Cotton TR. The structure of human pro-myostatin and molecular basis of latency. [Doctoral Dissertation]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/288560 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.767763


University of Cambridge

25. Merenda, Alessandra. Development of a new screening system for the identification of RNF43-related genes and characterisation of other PA-RING family members.

Degree: PhD, 2017, University of Cambridge

 The E3 ubiquitin ligase RNF43 (RING finger protein 43) is an important negative modulator of the WNT signalling pathway that acts at the plasma membrane… (more)

Subjects/Keywords: 572; Wnt signalling; RNF43; E3 ubiquitin ligase; PA-RING family; CRISPR; Genetic screen; Frizzled interenalisation; Transmembrane protein regulation

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

APA (6th Edition):

Merenda, A. (2017). Development of a new screening system for the identification of RNF43-related genes and characterisation of other PA-RING family members. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/267982 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.725613

Chicago Manual of Style (16th Edition):

Merenda, Alessandra. “Development of a new screening system for the identification of RNF43-related genes and characterisation of other PA-RING family members.” 2017. Doctoral Dissertation, University of Cambridge. Accessed October 15, 2019. https://www.repository.cam.ac.uk/handle/1810/267982 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.725613.

MLA Handbook (7th Edition):

Merenda, Alessandra. “Development of a new screening system for the identification of RNF43-related genes and characterisation of other PA-RING family members.” 2017. Web. 15 Oct 2019.

Vancouver:

Merenda A. Development of a new screening system for the identification of RNF43-related genes and characterisation of other PA-RING family members. [Internet] [Doctoral dissertation]. University of Cambridge; 2017. [cited 2019 Oct 15]. Available from: https://www.repository.cam.ac.uk/handle/1810/267982 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.725613.

Council of Science Editors:

Merenda A. Development of a new screening system for the identification of RNF43-related genes and characterisation of other PA-RING family members. [Doctoral Dissertation]. University of Cambridge; 2017. Available from: https://www.repository.cam.ac.uk/handle/1810/267982 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.725613


University of Cambridge

26. Merenda, Alessandra. Development of a new screening system for the identification of RNF43-related genes and characterisation of other PA-RING family members.

Degree: 2017, University of Cambridge

 The E3 ubiquitin ligase RNF43 (RING finger protein 43) is an important negative modulator of the WNT signalling pathway that acts at the plasma membrane… (more)

Subjects/Keywords: Wnt signalling; RNF43; E3 ubiquitin ligase; PA-RING family; CRISPR; Genetic screen; Frizzled interenalisation; Transmembrane protein regulation

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

APA (6th Edition):

Merenda, A. (2017). Development of a new screening system for the identification of RNF43-related genes and characterisation of other PA-RING family members. (Thesis). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/267982

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):

Merenda, Alessandra. “Development of a new screening system for the identification of RNF43-related genes and characterisation of other PA-RING family members. ” 2017. Thesis, University of Cambridge. Accessed October 15, 2019. https://www.repository.cam.ac.uk/handle/1810/267982.

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

MLA Handbook (7th Edition):

Merenda, Alessandra. “Development of a new screening system for the identification of RNF43-related genes and characterisation of other PA-RING family members. ” 2017. Web. 15 Oct 2019.

Vancouver:

Merenda A. Development of a new screening system for the identification of RNF43-related genes and characterisation of other PA-RING family members. [Internet] [Thesis]. University of Cambridge; 2017. [cited 2019 Oct 15]. Available from: https://www.repository.cam.ac.uk/handle/1810/267982.

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

Council of Science Editors:

Merenda A. Development of a new screening system for the identification of RNF43-related genes and characterisation of other PA-RING family members. [Thesis]. University of Cambridge; 2017. Available from: https://www.repository.cam.ac.uk/handle/1810/267982

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


University of Cambridge

27. Watson, Joanna. Structural and biochemical insight into the interactions of Cdc42 with TOCA1 and N-WASP .

Degree: 2017, University of Cambridge

 Cdc42 is a member of the Rho family of small GTPases, which, together with its homologues RhoA and Rac1, controls a multitude of cellular functions… (more)

Subjects/Keywords: Cdc42; NMR; TOCA1; NWASP; WASL; N-WASP; GTPase; G protein; HR1 domain; Filopodia; Endocytosis; Cell signalling; Protein protein interaction

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

APA (6th Edition):

Watson, J. (2017). Structural and biochemical insight into the interactions of Cdc42 with TOCA1 and N-WASP . (Thesis). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/268520

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):

Watson, Joanna. “Structural and biochemical insight into the interactions of Cdc42 with TOCA1 and N-WASP .” 2017. Thesis, University of Cambridge. Accessed October 15, 2019. https://www.repository.cam.ac.uk/handle/1810/268520.

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

MLA Handbook (7th Edition):

Watson, Joanna. “Structural and biochemical insight into the interactions of Cdc42 with TOCA1 and N-WASP .” 2017. Web. 15 Oct 2019.

Vancouver:

Watson J. Structural and biochemical insight into the interactions of Cdc42 with TOCA1 and N-WASP . [Internet] [Thesis]. University of Cambridge; 2017. [cited 2019 Oct 15]. Available from: https://www.repository.cam.ac.uk/handle/1810/268520.

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

Council of Science Editors:

Watson J. Structural and biochemical insight into the interactions of Cdc42 with TOCA1 and N-WASP . [Thesis]. University of Cambridge; 2017. Available from: https://www.repository.cam.ac.uk/handle/1810/268520

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


University of Cambridge

28. Sharma, Sumana. Genome-scale identification of cellular pathways required for cell surface recognition .

Degree: 2018, University of Cambridge

 A range of biochemically diverse molecules located in the plasma membrane— such as proteins, glycans, and lipids—mediate cellular recognition events, initiation of signalling pathways, and… (more)

Subjects/Keywords: CRISPR-Cas9; Low-affinity interaction; Cellular-signalling; Loss-of-function genetic screens; Glycoseaminoglycans; Receptor-ligand interactions; GABA receptor

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

APA (6th Edition):

Sharma, S. (2018). Genome-scale identification of cellular pathways required for cell surface recognition . (Thesis). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/271825

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):

Sharma, Sumana. “Genome-scale identification of cellular pathways required for cell surface recognition .” 2018. Thesis, University of Cambridge. Accessed October 15, 2019. https://www.repository.cam.ac.uk/handle/1810/271825.

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

MLA Handbook (7th Edition):

Sharma, Sumana. “Genome-scale identification of cellular pathways required for cell surface recognition .” 2018. Web. 15 Oct 2019.

Vancouver:

Sharma S. Genome-scale identification of cellular pathways required for cell surface recognition . [Internet] [Thesis]. University of Cambridge; 2018. [cited 2019 Oct 15]. Available from: https://www.repository.cam.ac.uk/handle/1810/271825.

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

Council of Science Editors:

Sharma S. Genome-scale identification of cellular pathways required for cell surface recognition . [Thesis]. University of Cambridge; 2018. Available from: https://www.repository.cam.ac.uk/handle/1810/271825

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


University of Cambridge

29. Harris, Michael James. Development of an Optogenetic Toolkit for the Interrogation of T cell Signalling Dynamics .

Degree: 2018, University of Cambridge

 T cells are a cornerstone of the mammalian adaptive immune system. A range of T-cell subsets exist that can orchestrate the overall immune response to… (more)

Subjects/Keywords: T cell; Optogenetic; LOVTRAP; LOV2; Signalling; Adaptive Immunity; Bispecific Antibodies; FcRH5; Linker for Activation of T cells (LAT); CAR T cell

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

APA (6th Edition):

Harris, M. J. (2018). Development of an Optogenetic Toolkit for the Interrogation of T cell Signalling Dynamics . (Thesis). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/274251

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):

Harris, Michael James. “Development of an Optogenetic Toolkit for the Interrogation of T cell Signalling Dynamics .” 2018. Thesis, University of Cambridge. Accessed October 15, 2019. https://www.repository.cam.ac.uk/handle/1810/274251.

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

MLA Handbook (7th Edition):

Harris, Michael James. “Development of an Optogenetic Toolkit for the Interrogation of T cell Signalling Dynamics .” 2018. Web. 15 Oct 2019.

Vancouver:

Harris MJ. Development of an Optogenetic Toolkit for the Interrogation of T cell Signalling Dynamics . [Internet] [Thesis]. University of Cambridge; 2018. [cited 2019 Oct 15]. Available from: https://www.repository.cam.ac.uk/handle/1810/274251.

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

Council of Science Editors:

Harris MJ. Development of an Optogenetic Toolkit for the Interrogation of T cell Signalling Dynamics . [Thesis]. University of Cambridge; 2018. Available from: https://www.repository.cam.ac.uk/handle/1810/274251

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


University of Cambridge

30. Davenport, Peter William. A Metabolomics-Based Analysis of Acyl-Homoserine Lactone Quorum Sensing in Pseudomonas aeruginosa .

Degree: 2018, University of Cambridge

 Pseudomonas aeruginosa is a metabolically versatile environmental bacterium that grows in extremely diverse habitats—from sea water to jet fuel—and is able to infect a large… (more)

Subjects/Keywords: Pseudomonas aeruginosa; quorum sensing; metabolomics; intercellular signalling; bacterial physiology; functional genomics; mass spectrometry; nuclear magnetic resonance spectroscopy; bacterial metabolism

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

APA (6th Edition):

Davenport, P. W. (2018). A Metabolomics-Based Analysis of Acyl-Homoserine Lactone Quorum Sensing in Pseudomonas aeruginosa . (Thesis). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/274674

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):

Davenport, Peter William. “A Metabolomics-Based Analysis of Acyl-Homoserine Lactone Quorum Sensing in Pseudomonas aeruginosa .” 2018. Thesis, University of Cambridge. Accessed October 15, 2019. https://www.repository.cam.ac.uk/handle/1810/274674.

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

MLA Handbook (7th Edition):

Davenport, Peter William. “A Metabolomics-Based Analysis of Acyl-Homoserine Lactone Quorum Sensing in Pseudomonas aeruginosa .” 2018. Web. 15 Oct 2019.

Vancouver:

Davenport PW. A Metabolomics-Based Analysis of Acyl-Homoserine Lactone Quorum Sensing in Pseudomonas aeruginosa . [Internet] [Thesis]. University of Cambridge; 2018. [cited 2019 Oct 15]. Available from: https://www.repository.cam.ac.uk/handle/1810/274674.

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

Council of Science Editors:

Davenport PW. A Metabolomics-Based Analysis of Acyl-Homoserine Lactone Quorum Sensing in Pseudomonas aeruginosa . [Thesis]. University of Cambridge; 2018. Available from: https://www.repository.cam.ac.uk/handle/1810/274674

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

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