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You searched for subject:(phosphorylation). Showing records 1 – 30 of 49 total matches.

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Universiteit Utrecht

1. Gorp, A.G.M. van. The identification and functional characterisation of novel targets of Protein Kinase B (PKB/c-akt) action.

Degree: 2007, Universiteit Utrecht

 Cancer is the result of a disturbed balance between cell division and growth on one hand, and programmed cell death on the other. Crucial cellular… (more)

Subjects/Keywords: Geneeskunde; cancer; translation; phosphorylation; signaltransduction; PI3K; PKB; proteomics; microarray; Foxo3a; eIF4B

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APA (6th Edition):

Gorp, A. G. M. v. (2007). The identification and functional characterisation of novel targets of Protein Kinase B (PKB/c-akt) action. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/21792

Chicago Manual of Style (16th Edition):

Gorp, A G M van. “The identification and functional characterisation of novel targets of Protein Kinase B (PKB/c-akt) action.” 2007. Doctoral Dissertation, Universiteit Utrecht. Accessed October 15, 2019. http://dspace.library.uu.nl:8080/handle/1874/21792.

MLA Handbook (7th Edition):

Gorp, A G M van. “The identification and functional characterisation of novel targets of Protein Kinase B (PKB/c-akt) action.” 2007. Web. 15 Oct 2019.

Vancouver:

Gorp AGMv. The identification and functional characterisation of novel targets of Protein Kinase B (PKB/c-akt) action. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2007. [cited 2019 Oct 15]. Available from: http://dspace.library.uu.nl:8080/handle/1874/21792.

Council of Science Editors:

Gorp AGMv. The identification and functional characterisation of novel targets of Protein Kinase B (PKB/c-akt) action. [Doctoral Dissertation]. Universiteit Utrecht; 2007. Available from: http://dspace.library.uu.nl:8080/handle/1874/21792


Universiteit Utrecht

2. D'Annibale, S. Mechanisms of crosstalk between phosphorylation and ubiquitylation in the regulation of cell proliferation.

Degree: 2014, Universiteit Utrecht

 Cell cycle progression is tightly controlled by the ubiquitin-proteasome system. Cullin-RING ubiquitin ligases are the major players responsible for the periodic proteolysis of many regulators… (more)

Subjects/Keywords: Geneeskunde; cell growth and proliferation; ubiquitin-proteasome system; phosphorylation; SCFβTrCP; cancer

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APA (6th Edition):

D'Annibale, S. (2014). Mechanisms of crosstalk between phosphorylation and ubiquitylation in the regulation of cell proliferation. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/300358

Chicago Manual of Style (16th Edition):

D'Annibale, S. “Mechanisms of crosstalk between phosphorylation and ubiquitylation in the regulation of cell proliferation.” 2014. Doctoral Dissertation, Universiteit Utrecht. Accessed October 15, 2019. http://dspace.library.uu.nl:8080/handle/1874/300358.

MLA Handbook (7th Edition):

D'Annibale, S. “Mechanisms of crosstalk between phosphorylation and ubiquitylation in the regulation of cell proliferation.” 2014. Web. 15 Oct 2019.

Vancouver:

D'Annibale S. Mechanisms of crosstalk between phosphorylation and ubiquitylation in the regulation of cell proliferation. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2014. [cited 2019 Oct 15]. Available from: http://dspace.library.uu.nl:8080/handle/1874/300358.

Council of Science Editors:

D'Annibale S. Mechanisms of crosstalk between phosphorylation and ubiquitylation in the regulation of cell proliferation. [Doctoral Dissertation]. Universiteit Utrecht; 2014. Available from: http://dspace.library.uu.nl:8080/handle/1874/300358

3. Graauw, Marjo de. Molecular and cellular responses to renal injury: a (phospho)-proteomic approach.

Degree: 2007, Department Toxicology, Leiden/Amsterdam Center for Drug Research (LACDR), Faculty of Science, Leiden University

 Our kidneys play a major role in regulating the body’s internal environment, via transportation of water, salt, potassium and waste products. As a result of… (more)

Subjects/Keywords: Cytoskeleton; Phosphorylation; Proteomics; Renal injury; Cytoskeleton; Phosphorylation; Proteomics; Renal injury

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APA (6th Edition):

Graauw, M. d. (2007). Molecular and cellular responses to renal injury: a (phospho)-proteomic approach. (Doctoral Dissertation). Department Toxicology, Leiden/Amsterdam Center for Drug Research (LACDR), Faculty of Science, Leiden University. Retrieved from http://hdl.handle.net/1887/12036

Chicago Manual of Style (16th Edition):

Graauw, Marjo de. “Molecular and cellular responses to renal injury: a (phospho)-proteomic approach.” 2007. Doctoral Dissertation, Department Toxicology, Leiden/Amsterdam Center for Drug Research (LACDR), Faculty of Science, Leiden University. Accessed October 15, 2019. http://hdl.handle.net/1887/12036.

MLA Handbook (7th Edition):

Graauw, Marjo de. “Molecular and cellular responses to renal injury: a (phospho)-proteomic approach.” 2007. Web. 15 Oct 2019.

Vancouver:

Graauw Md. Molecular and cellular responses to renal injury: a (phospho)-proteomic approach. [Internet] [Doctoral dissertation]. Department Toxicology, Leiden/Amsterdam Center for Drug Research (LACDR), Faculty of Science, Leiden University; 2007. [cited 2019 Oct 15]. Available from: http://hdl.handle.net/1887/12036.

Council of Science Editors:

Graauw Md. Molecular and cellular responses to renal injury: a (phospho)-proteomic approach. [Doctoral Dissertation]. Department Toxicology, Leiden/Amsterdam Center for Drug Research (LACDR), Faculty of Science, Leiden University; 2007. Available from: http://hdl.handle.net/1887/12036


Universiteit Utrecht

4. Dam, K. van. “Comparative sequence analysis of canine progesterone receptor-B-Upstream Segment and the relationship of this segment with the estrous cycle in Canidae".

Degree: 2008, Universiteit Utrecht

 The dog seems to have unique features concerning activation function (AF) 3 domain and putative phosphorylation sites of the progesterone receptor-B-Upstream Segment (BUS) in comparison… (more)

Subjects/Keywords: Diergeneeskunde; progesterone receptor, dog, canine, BUS, estrous cycle, AF3 domain, phosphorylation sites, luteal phase, Canidae

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APA (6th Edition):

Dam, K. v. (2008). “Comparative sequence analysis of canine progesterone receptor-B-Upstream Segment and the relationship of this segment with the estrous cycle in Canidae". (Masters Thesis). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/35787

Chicago Manual of Style (16th Edition):

Dam, K van. ““Comparative sequence analysis of canine progesterone receptor-B-Upstream Segment and the relationship of this segment with the estrous cycle in Canidae".” 2008. Masters Thesis, Universiteit Utrecht. Accessed October 15, 2019. http://dspace.library.uu.nl:8080/handle/1874/35787.

MLA Handbook (7th Edition):

Dam, K van. ““Comparative sequence analysis of canine progesterone receptor-B-Upstream Segment and the relationship of this segment with the estrous cycle in Canidae".” 2008. Web. 15 Oct 2019.

Vancouver:

Dam Kv. “Comparative sequence analysis of canine progesterone receptor-B-Upstream Segment and the relationship of this segment with the estrous cycle in Canidae". [Internet] [Masters thesis]. Universiteit Utrecht; 2008. [cited 2019 Oct 15]. Available from: http://dspace.library.uu.nl:8080/handle/1874/35787.

Council of Science Editors:

Dam Kv. “Comparative sequence analysis of canine progesterone receptor-B-Upstream Segment and the relationship of this segment with the estrous cycle in Canidae". [Masters Thesis]. Universiteit Utrecht; 2008. Available from: http://dspace.library.uu.nl:8080/handle/1874/35787


Universiteit Utrecht

5. Giansanti, Piero. Signaling network dynamics investigated by quantitative phosphoproteomics.

Degree: 2014, Universiteit Utrecht

 This thesis describes the application of proteomics technologies to get insight into several aspects of phosphorylation signaling dynamics. The core tool in all performed experiments… (more)

Subjects/Keywords: protein phosphorylation; quantitative phosphoproteomics; mass spectrometry; signaling network; kinases; tyrosine kinases inhibitors

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APA (6th Edition):

Giansanti, P. (2014). Signaling network dynamics investigated by quantitative phosphoproteomics. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/308082

Chicago Manual of Style (16th Edition):

Giansanti, Piero. “Signaling network dynamics investigated by quantitative phosphoproteomics.” 2014. Doctoral Dissertation, Universiteit Utrecht. Accessed October 15, 2019. http://dspace.library.uu.nl:8080/handle/1874/308082.

MLA Handbook (7th Edition):

Giansanti, Piero. “Signaling network dynamics investigated by quantitative phosphoproteomics.” 2014. Web. 15 Oct 2019.

Vancouver:

Giansanti P. Signaling network dynamics investigated by quantitative phosphoproteomics. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2014. [cited 2019 Oct 15]. Available from: http://dspace.library.uu.nl:8080/handle/1874/308082.

Council of Science Editors:

Giansanti P. Signaling network dynamics investigated by quantitative phosphoproteomics. [Doctoral Dissertation]. Universiteit Utrecht; 2014. Available from: http://dspace.library.uu.nl:8080/handle/1874/308082

6. Noort, Mascha van. Non-phosphorylated b-catenin in Wnt signaling.

Degree: 2002, University Utrecht

 The Wnt signaling cascade plays an important role in development and carcinogenesis. Under non-signaling conditions, a large cytoplasmic complex, consisting of the kinase GSK-3?, the… (more)

Subjects/Keywords: b-catenin; Wnt signaling; phosphorylation; monoclonal antibody; signal transduction

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APA (6th Edition):

Noort, M. v. (2002). Non-phosphorylated b-catenin in Wnt signaling. (Doctoral Dissertation). University Utrecht. Retrieved from http://dspace.library.uu.nl/handle/1874/421 ; URN:NBN:NL:UI:10-1874-421 ; URN:NBN:NL:UI:10-1874-421 ; http://dspace.library.uu.nl/handle/1874/421

Chicago Manual of Style (16th Edition):

Noort, Mascha van. “Non-phosphorylated b-catenin in Wnt signaling.” 2002. Doctoral Dissertation, University Utrecht. Accessed October 15, 2019. http://dspace.library.uu.nl/handle/1874/421 ; URN:NBN:NL:UI:10-1874-421 ; URN:NBN:NL:UI:10-1874-421 ; http://dspace.library.uu.nl/handle/1874/421.

MLA Handbook (7th Edition):

Noort, Mascha van. “Non-phosphorylated b-catenin in Wnt signaling.” 2002. Web. 15 Oct 2019.

Vancouver:

Noort Mv. Non-phosphorylated b-catenin in Wnt signaling. [Internet] [Doctoral dissertation]. University Utrecht; 2002. [cited 2019 Oct 15]. Available from: http://dspace.library.uu.nl/handle/1874/421 ; URN:NBN:NL:UI:10-1874-421 ; URN:NBN:NL:UI:10-1874-421 ; http://dspace.library.uu.nl/handle/1874/421.

Council of Science Editors:

Noort Mv. Non-phosphorylated b-catenin in Wnt signaling. [Doctoral Dissertation]. University Utrecht; 2002. Available from: http://dspace.library.uu.nl/handle/1874/421 ; URN:NBN:NL:UI:10-1874-421 ; URN:NBN:NL:UI:10-1874-421 ; http://dspace.library.uu.nl/handle/1874/421

7. Noort, Mascha van. Non-phosphorylated b-catenin in Wnt signaling.

Degree: 2002, University Utrecht

 The Wnt signaling cascade plays an important role in development and carcinogenesis. Under non-signaling conditions, a large cytoplasmic complex, consisting of the kinase GSK-3?, the… (more)

Subjects/Keywords: b-catenin; Wnt signaling; phosphorylation; monoclonal antibody; signal transduction

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APA (6th Edition):

Noort, M. v. (2002). Non-phosphorylated b-catenin in Wnt signaling. (Doctoral Dissertation). University Utrecht. Retrieved from http://dspace.library.uu.nl/handle/1874/421 ; URN:NBN:NL:UI:10-1874-421 ; URN:NBN:NL:UI:10-1874-421 ; http://dspace.library.uu.nl/handle/1874/421

Chicago Manual of Style (16th Edition):

Noort, Mascha van. “Non-phosphorylated b-catenin in Wnt signaling.” 2002. Doctoral Dissertation, University Utrecht. Accessed October 15, 2019. http://dspace.library.uu.nl/handle/1874/421 ; URN:NBN:NL:UI:10-1874-421 ; URN:NBN:NL:UI:10-1874-421 ; http://dspace.library.uu.nl/handle/1874/421.

MLA Handbook (7th Edition):

Noort, Mascha van. “Non-phosphorylated b-catenin in Wnt signaling.” 2002. Web. 15 Oct 2019.

Vancouver:

Noort Mv. Non-phosphorylated b-catenin in Wnt signaling. [Internet] [Doctoral dissertation]. University Utrecht; 2002. [cited 2019 Oct 15]. Available from: http://dspace.library.uu.nl/handle/1874/421 ; URN:NBN:NL:UI:10-1874-421 ; URN:NBN:NL:UI:10-1874-421 ; http://dspace.library.uu.nl/handle/1874/421.

Council of Science Editors:

Noort Mv. Non-phosphorylated b-catenin in Wnt signaling. [Doctoral Dissertation]. University Utrecht; 2002. Available from: http://dspace.library.uu.nl/handle/1874/421 ; URN:NBN:NL:UI:10-1874-421 ; URN:NBN:NL:UI:10-1874-421 ; http://dspace.library.uu.nl/handle/1874/421

8. Potel, C.M. Exploring new avenues in phosphoproteomics in pursuit of the elusive histidine phosphorylation.

Degree: 2018, University Utrecht

 Protein phosphorylation is the primary mean of regulation of protein biological activity. As such, communication and signaling within cells is controlled by minute changes of… (more)

Subjects/Keywords: Histidine phosphorylation; phosphoproteomics; histidine kinase; bacterial phosphoproteomics; bacterial signaling

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APA (6th Edition):

Potel, C. M. (2018). Exploring new avenues in phosphoproteomics in pursuit of the elusive histidine phosphorylation. (Doctoral Dissertation). University Utrecht. Retrieved from http://dspace.library.uu.nl/handle/1874/370166 ; URN:NBN:NL:UI:10-1874-370166 ; urn:isbn:978-94-93019-74-4 ; URN:NBN:NL:UI:10-1874-370166 ; http://dspace.library.uu.nl/handle/1874/370166

Chicago Manual of Style (16th Edition):

Potel, C M. “Exploring new avenues in phosphoproteomics in pursuit of the elusive histidine phosphorylation.” 2018. Doctoral Dissertation, University Utrecht. Accessed October 15, 2019. http://dspace.library.uu.nl/handle/1874/370166 ; URN:NBN:NL:UI:10-1874-370166 ; urn:isbn:978-94-93019-74-4 ; URN:NBN:NL:UI:10-1874-370166 ; http://dspace.library.uu.nl/handle/1874/370166.

MLA Handbook (7th Edition):

Potel, C M. “Exploring new avenues in phosphoproteomics in pursuit of the elusive histidine phosphorylation.” 2018. Web. 15 Oct 2019.

Vancouver:

Potel CM. Exploring new avenues in phosphoproteomics in pursuit of the elusive histidine phosphorylation. [Internet] [Doctoral dissertation]. University Utrecht; 2018. [cited 2019 Oct 15]. Available from: http://dspace.library.uu.nl/handle/1874/370166 ; URN:NBN:NL:UI:10-1874-370166 ; urn:isbn:978-94-93019-74-4 ; URN:NBN:NL:UI:10-1874-370166 ; http://dspace.library.uu.nl/handle/1874/370166.

Council of Science Editors:

Potel CM. Exploring new avenues in phosphoproteomics in pursuit of the elusive histidine phosphorylation. [Doctoral Dissertation]. University Utrecht; 2018. Available from: http://dspace.library.uu.nl/handle/1874/370166 ; URN:NBN:NL:UI:10-1874-370166 ; urn:isbn:978-94-93019-74-4 ; URN:NBN:NL:UI:10-1874-370166 ; http://dspace.library.uu.nl/handle/1874/370166

9. van den Toorn, H.W.P. Computational proteomics: from numbers to biology.

Degree: 2017, University Utrecht

 The field of biological research is increasingly trying to understand the complex processes that are too small to observe by eye, even when using a… (more)

Subjects/Keywords: computational proteomics; bioinformatics; statistics; phosphorylation; rattus trichoplax; hypertension

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APA (6th Edition):

van den Toorn, H. W. P. (2017). Computational proteomics: from numbers to biology. (Doctoral Dissertation). University Utrecht. Retrieved from http://dspace.library.uu.nl/handle/1874/356096 ; URN:NBN:NL:UI:10-1874-356096 ; urn:isbn:978-90-393-6821-3 ; URN:NBN:NL:UI:10-1874-356096 ; http://dspace.library.uu.nl/handle/1874/356096

Chicago Manual of Style (16th Edition):

van den Toorn, H W P. “Computational proteomics: from numbers to biology.” 2017. Doctoral Dissertation, University Utrecht. Accessed October 15, 2019. http://dspace.library.uu.nl/handle/1874/356096 ; URN:NBN:NL:UI:10-1874-356096 ; urn:isbn:978-90-393-6821-3 ; URN:NBN:NL:UI:10-1874-356096 ; http://dspace.library.uu.nl/handle/1874/356096.

MLA Handbook (7th Edition):

van den Toorn, H W P. “Computational proteomics: from numbers to biology.” 2017. Web. 15 Oct 2019.

Vancouver:

van den Toorn HWP. Computational proteomics: from numbers to biology. [Internet] [Doctoral dissertation]. University Utrecht; 2017. [cited 2019 Oct 15]. Available from: http://dspace.library.uu.nl/handle/1874/356096 ; URN:NBN:NL:UI:10-1874-356096 ; urn:isbn:978-90-393-6821-3 ; URN:NBN:NL:UI:10-1874-356096 ; http://dspace.library.uu.nl/handle/1874/356096.

Council of Science Editors:

van den Toorn HWP. Computational proteomics: from numbers to biology. [Doctoral Dissertation]. University Utrecht; 2017. Available from: http://dspace.library.uu.nl/handle/1874/356096 ; URN:NBN:NL:UI:10-1874-356096 ; urn:isbn:978-90-393-6821-3 ; URN:NBN:NL:UI:10-1874-356096 ; http://dspace.library.uu.nl/handle/1874/356096

10. Bruins, Wendy. The role of p53.S389 phosphorylation in DNA damage response pathways and tumorigenesis.

Degree: 2007, Department Toxicogenetics, Medicine / Leiden University Medical Center (LUMC), Leiden University

 The results presented in this thesis provide new information on the role of the p53.S389A point mutation in chemical-induced tumorigenesis. After DNA damage, p53 protein… (more)

Subjects/Keywords: Carcinogenesis; DNA repair; Microarray; Mutant mouse model; p53; Phosphorylation; UV; Carcinogenesis; DNA repair; Microarray; Mutant mouse model; p53; Phosphorylation; UV

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APA (6th Edition):

Bruins, W. (2007). The role of p53.S389 phosphorylation in DNA damage response pathways and tumorigenesis. (Doctoral Dissertation). Department Toxicogenetics, Medicine / Leiden University Medical Center (LUMC), Leiden University. Retrieved from http://hdl.handle.net/1887/12389

Chicago Manual of Style (16th Edition):

Bruins, Wendy. “The role of p53.S389 phosphorylation in DNA damage response pathways and tumorigenesis.” 2007. Doctoral Dissertation, Department Toxicogenetics, Medicine / Leiden University Medical Center (LUMC), Leiden University. Accessed October 15, 2019. http://hdl.handle.net/1887/12389.

MLA Handbook (7th Edition):

Bruins, Wendy. “The role of p53.S389 phosphorylation in DNA damage response pathways and tumorigenesis.” 2007. Web. 15 Oct 2019.

Vancouver:

Bruins W. The role of p53.S389 phosphorylation in DNA damage response pathways and tumorigenesis. [Internet] [Doctoral dissertation]. Department Toxicogenetics, Medicine / Leiden University Medical Center (LUMC), Leiden University; 2007. [cited 2019 Oct 15]. Available from: http://hdl.handle.net/1887/12389.

Council of Science Editors:

Bruins W. The role of p53.S389 phosphorylation in DNA damage response pathways and tumorigenesis. [Doctoral Dissertation]. Department Toxicogenetics, Medicine / Leiden University Medical Center (LUMC), Leiden University; 2007. Available from: http://hdl.handle.net/1887/12389

11. Vahidnia, Ali. Studies into the mechanism of arsenic-induced neurotoxicity.

Degree: 2008, Department of Clinical Pharmacy and Toxicology, Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University

 Arsenic (As) is a notoriously poisonous metalloid with known hazardous effects to human health. The project described in this thesis was aimed at elucidating the… (more)

Subjects/Keywords: Toxicology; Arsenic metabolites; Neurotoxicity; Phosphorylation; Gene expression; Toxicology; Arsenic metabolites; Neurotoxicity; Phosphorylation; Gene expression

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APA (6th Edition):

Vahidnia, A. (2008). Studies into the mechanism of arsenic-induced neurotoxicity. (Doctoral Dissertation). Department of Clinical Pharmacy and Toxicology, Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University. Retrieved from http://hdl.handle.net/1887/12605

Chicago Manual of Style (16th Edition):

Vahidnia, Ali. “Studies into the mechanism of arsenic-induced neurotoxicity.” 2008. Doctoral Dissertation, Department of Clinical Pharmacy and Toxicology, Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University. Accessed October 15, 2019. http://hdl.handle.net/1887/12605.

MLA Handbook (7th Edition):

Vahidnia, Ali. “Studies into the mechanism of arsenic-induced neurotoxicity.” 2008. Web. 15 Oct 2019.

Vancouver:

Vahidnia A. Studies into the mechanism of arsenic-induced neurotoxicity. [Internet] [Doctoral dissertation]. Department of Clinical Pharmacy and Toxicology, Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University; 2008. [cited 2019 Oct 15]. Available from: http://hdl.handle.net/1887/12605.

Council of Science Editors:

Vahidnia A. Studies into the mechanism of arsenic-induced neurotoxicity. [Doctoral Dissertation]. Department of Clinical Pharmacy and Toxicology, Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University; 2008. Available from: http://hdl.handle.net/1887/12605


Universiteit Utrecht

12. Dirksen, Eef Hubert Cecil. Dynamics of the human nuclear proteome in response to DNA damage.

Degree: 2006, Universiteit Utrecht

 The genome is constantly challenged by factors that can induce DNA damage and thereby threaten the viability of the cell. If DNA damage remains unrepaired… (more)

Subjects/Keywords: Farmacie; proteomics; DNA damage; cancer; protein quantitation; chromatin remodeling; phosphorylation; beta-elimination

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APA (6th Edition):

Dirksen, E. H. C. (2006). Dynamics of the human nuclear proteome in response to DNA damage. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/12548

Chicago Manual of Style (16th Edition):

Dirksen, Eef Hubert Cecil. “Dynamics of the human nuclear proteome in response to DNA damage.” 2006. Doctoral Dissertation, Universiteit Utrecht. Accessed October 15, 2019. http://dspace.library.uu.nl:8080/handle/1874/12548.

MLA Handbook (7th Edition):

Dirksen, Eef Hubert Cecil. “Dynamics of the human nuclear proteome in response to DNA damage.” 2006. Web. 15 Oct 2019.

Vancouver:

Dirksen EHC. Dynamics of the human nuclear proteome in response to DNA damage. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2006. [cited 2019 Oct 15]. Available from: http://dspace.library.uu.nl:8080/handle/1874/12548.

Council of Science Editors:

Dirksen EHC. Dynamics of the human nuclear proteome in response to DNA damage. [Doctoral Dissertation]. Universiteit Utrecht; 2006. Available from: http://dspace.library.uu.nl:8080/handle/1874/12548


Universiteit Utrecht

13. Veen, Antonius Adrianus Bartholomeus van. Cardiac gap junctions and action potential propagation.

Degree: 2001, Universiteit Utrecht

 Described are the results, obtained from experiments on transfected cells to those on intact heart and new data are provided on connexin phosphorylation, expression and… (more)

Subjects/Keywords: Geneeskunde; heart; action potential; cardiomyocyte; cardiac hypertrophy; electrical activation; gap junction; protein phosphorylation

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APA (6th Edition):

Veen, A. A. B. v. (2001). Cardiac gap junctions and action potential propagation. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/399

Chicago Manual of Style (16th Edition):

Veen, Antonius Adrianus Bartholomeus van. “Cardiac gap junctions and action potential propagation.” 2001. Doctoral Dissertation, Universiteit Utrecht. Accessed October 15, 2019. http://dspace.library.uu.nl:8080/handle/1874/399.

MLA Handbook (7th Edition):

Veen, Antonius Adrianus Bartholomeus van. “Cardiac gap junctions and action potential propagation.” 2001. Web. 15 Oct 2019.

Vancouver:

Veen AABv. Cardiac gap junctions and action potential propagation. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2001. [cited 2019 Oct 15]. Available from: http://dspace.library.uu.nl:8080/handle/1874/399.

Council of Science Editors:

Veen AABv. Cardiac gap junctions and action potential propagation. [Doctoral Dissertation]. Universiteit Utrecht; 2001. Available from: http://dspace.library.uu.nl:8080/handle/1874/399


Universiteit Utrecht

14. Noort, Mascha van. Non-phosphorylated b-catenin in Wnt signaling.

Degree: 2002, Universiteit Utrecht

 The Wnt signaling cascade plays an important role in development and carcinogenesis. Under non-signaling conditions, a large cytoplasmic complex, consisting of the kinase GSK-3?, the… (more)

Subjects/Keywords: Geneeskunde; b-catenin; Wnt signaling; phosphorylation; monoclonal antibody; signal transduction

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APA (6th Edition):

Noort, M. v. (2002). Non-phosphorylated b-catenin in Wnt signaling. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/421

Chicago Manual of Style (16th Edition):

Noort, Mascha van. “Non-phosphorylated b-catenin in Wnt signaling.” 2002. Doctoral Dissertation, Universiteit Utrecht. Accessed October 15, 2019. http://dspace.library.uu.nl:8080/handle/1874/421.

MLA Handbook (7th Edition):

Noort, Mascha van. “Non-phosphorylated b-catenin in Wnt signaling.” 2002. Web. 15 Oct 2019.

Vancouver:

Noort Mv. Non-phosphorylated b-catenin in Wnt signaling. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2002. [cited 2019 Oct 15]. Available from: http://dspace.library.uu.nl:8080/handle/1874/421.

Council of Science Editors:

Noort Mv. Non-phosphorylated b-catenin in Wnt signaling. [Doctoral Dissertation]. Universiteit Utrecht; 2002. Available from: http://dspace.library.uu.nl:8080/handle/1874/421

15. D'Annibale, S. Mechanisms of crosstalk between phosphorylation and ubiquitylation in the regulation of cell proliferation.

Degree: 2014, University Utrecht

 Cell cycle progression is tightly controlled by the ubiquitin-proteasome system. Cullin-RING ubiquitin ligases are the major players responsible for the periodic proteolysis of many regulators… (more)

Subjects/Keywords: cell growth and proliferation; ubiquitin-proteasome system; phosphorylation; SCFβTrCP; cancer

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APA (6th Edition):

D'Annibale, S. (2014). Mechanisms of crosstalk between phosphorylation and ubiquitylation in the regulation of cell proliferation. (Doctoral Dissertation). University Utrecht. Retrieved from http://dspace.library.uu.nl/handle/1874/300358 ; URN:NBN:NL:UI:10-1874-300358 ; urn:isbn:978-90-393-6223-5 ; URN:NBN:NL:UI:10-1874-300358 ; http://dspace.library.uu.nl/handle/1874/300358

Chicago Manual of Style (16th Edition):

D'Annibale, S. “Mechanisms of crosstalk between phosphorylation and ubiquitylation in the regulation of cell proliferation.” 2014. Doctoral Dissertation, University Utrecht. Accessed October 15, 2019. http://dspace.library.uu.nl/handle/1874/300358 ; URN:NBN:NL:UI:10-1874-300358 ; urn:isbn:978-90-393-6223-5 ; URN:NBN:NL:UI:10-1874-300358 ; http://dspace.library.uu.nl/handle/1874/300358.

MLA Handbook (7th Edition):

D'Annibale, S. “Mechanisms of crosstalk between phosphorylation and ubiquitylation in the regulation of cell proliferation.” 2014. Web. 15 Oct 2019.

Vancouver:

D'Annibale S. Mechanisms of crosstalk between phosphorylation and ubiquitylation in the regulation of cell proliferation. [Internet] [Doctoral dissertation]. University Utrecht; 2014. [cited 2019 Oct 15]. Available from: http://dspace.library.uu.nl/handle/1874/300358 ; URN:NBN:NL:UI:10-1874-300358 ; urn:isbn:978-90-393-6223-5 ; URN:NBN:NL:UI:10-1874-300358 ; http://dspace.library.uu.nl/handle/1874/300358.

Council of Science Editors:

D'Annibale S. Mechanisms of crosstalk between phosphorylation and ubiquitylation in the regulation of cell proliferation. [Doctoral Dissertation]. University Utrecht; 2014. Available from: http://dspace.library.uu.nl/handle/1874/300358 ; URN:NBN:NL:UI:10-1874-300358 ; urn:isbn:978-90-393-6223-5 ; URN:NBN:NL:UI:10-1874-300358 ; http://dspace.library.uu.nl/handle/1874/300358

16. D'Annibale, S. Mechanisms of crosstalk between phosphorylation and ubiquitylation in the regulation of cell proliferation.

Degree: 2014, University Utrecht

 Cell cycle progression is tightly controlled by the ubiquitin-proteasome system. Cullin-RING ubiquitin ligases are the major players responsible for the periodic proteolysis of many regulators… (more)

Subjects/Keywords: cell growth and proliferation; ubiquitin-proteasome system; phosphorylation; SCFβTrCP; cancer

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APA (6th Edition):

D'Annibale, S. (2014). Mechanisms of crosstalk between phosphorylation and ubiquitylation in the regulation of cell proliferation. (Doctoral Dissertation). University Utrecht. Retrieved from http://dspace.library.uu.nl/handle/1874/300358 ; URN:NBN:NL:UI:10-1874-300358 ; urn:isbn:978-90-393-6223-5 ; URN:NBN:NL:UI:10-1874-300358 ; http://dspace.library.uu.nl/handle/1874/300358

Chicago Manual of Style (16th Edition):

D'Annibale, S. “Mechanisms of crosstalk between phosphorylation and ubiquitylation in the regulation of cell proliferation.” 2014. Doctoral Dissertation, University Utrecht. Accessed October 15, 2019. http://dspace.library.uu.nl/handle/1874/300358 ; URN:NBN:NL:UI:10-1874-300358 ; urn:isbn:978-90-393-6223-5 ; URN:NBN:NL:UI:10-1874-300358 ; http://dspace.library.uu.nl/handle/1874/300358.

MLA Handbook (7th Edition):

D'Annibale, S. “Mechanisms of crosstalk between phosphorylation and ubiquitylation in the regulation of cell proliferation.” 2014. Web. 15 Oct 2019.

Vancouver:

D'Annibale S. Mechanisms of crosstalk between phosphorylation and ubiquitylation in the regulation of cell proliferation. [Internet] [Doctoral dissertation]. University Utrecht; 2014. [cited 2019 Oct 15]. Available from: http://dspace.library.uu.nl/handle/1874/300358 ; URN:NBN:NL:UI:10-1874-300358 ; urn:isbn:978-90-393-6223-5 ; URN:NBN:NL:UI:10-1874-300358 ; http://dspace.library.uu.nl/handle/1874/300358.

Council of Science Editors:

D'Annibale S. Mechanisms of crosstalk between phosphorylation and ubiquitylation in the regulation of cell proliferation. [Doctoral Dissertation]. University Utrecht; 2014. Available from: http://dspace.library.uu.nl/handle/1874/300358 ; URN:NBN:NL:UI:10-1874-300358 ; urn:isbn:978-90-393-6223-5 ; URN:NBN:NL:UI:10-1874-300358 ; http://dspace.library.uu.nl/handle/1874/300358

17. Dirksen, Eef Hubert Cecil. Dynamics of the human nuclear proteome in response to DNA damage.

Degree: 2006, University Utrecht

 The genome is constantly challenged by factors that can induce DNA damage and thereby threaten the viability of the cell. If DNA damage remains unrepaired… (more)

Subjects/Keywords: proteomics; DNA damage; cancer; protein quantitation; chromatin remodeling; phosphorylation; beta-elimination

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APA (6th Edition):

Dirksen, E. H. C. (2006). Dynamics of the human nuclear proteome in response to DNA damage. (Doctoral Dissertation). University Utrecht. Retrieved from http://dspace.library.uu.nl/handle/1874/12548 ; URN:NBN:NL:UI:10-1874-12548 ; urn:isbn:90-393-4297-0 ; URN:NBN:NL:UI:10-1874-12548 ; http://dspace.library.uu.nl/handle/1874/12548

Chicago Manual of Style (16th Edition):

Dirksen, Eef Hubert Cecil. “Dynamics of the human nuclear proteome in response to DNA damage.” 2006. Doctoral Dissertation, University Utrecht. Accessed October 15, 2019. http://dspace.library.uu.nl/handle/1874/12548 ; URN:NBN:NL:UI:10-1874-12548 ; urn:isbn:90-393-4297-0 ; URN:NBN:NL:UI:10-1874-12548 ; http://dspace.library.uu.nl/handle/1874/12548.

MLA Handbook (7th Edition):

Dirksen, Eef Hubert Cecil. “Dynamics of the human nuclear proteome in response to DNA damage.” 2006. Web. 15 Oct 2019.

Vancouver:

Dirksen EHC. Dynamics of the human nuclear proteome in response to DNA damage. [Internet] [Doctoral dissertation]. University Utrecht; 2006. [cited 2019 Oct 15]. Available from: http://dspace.library.uu.nl/handle/1874/12548 ; URN:NBN:NL:UI:10-1874-12548 ; urn:isbn:90-393-4297-0 ; URN:NBN:NL:UI:10-1874-12548 ; http://dspace.library.uu.nl/handle/1874/12548.

Council of Science Editors:

Dirksen EHC. Dynamics of the human nuclear proteome in response to DNA damage. [Doctoral Dissertation]. University Utrecht; 2006. Available from: http://dspace.library.uu.nl/handle/1874/12548 ; URN:NBN:NL:UI:10-1874-12548 ; urn:isbn:90-393-4297-0 ; URN:NBN:NL:UI:10-1874-12548 ; http://dspace.library.uu.nl/handle/1874/12548

18. Gorp, A.G.M. van. The identification and functional characterisation of novel targets of Protein Kinase B (PKB/c-akt) action.

Degree: 2007, University Utrecht

 Cancer is the result of a disturbed balance between cell division and growth on one hand, and programmed cell death on the other. Crucial cellular… (more)

Subjects/Keywords: cancer; translation; phosphorylation; signaltransduction; PI3K; PKB; proteomics; microarray; Foxo3a; eIF4B

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

APA (6th Edition):

Gorp, A. G. M. v. (2007). The identification and functional characterisation of novel targets of Protein Kinase B (PKB/c-akt) action. (Doctoral Dissertation). University Utrecht. Retrieved from http://dspace.library.uu.nl/handle/1874/21792 ; URN:NBN:NL:UI:10-1874-21792 ; urn:isbn:978-90-393-4537-5 ; URN:NBN:NL:UI:10-1874-21792 ; http://dspace.library.uu.nl/handle/1874/21792

Chicago Manual of Style (16th Edition):

Gorp, A G M van. “The identification and functional characterisation of novel targets of Protein Kinase B (PKB/c-akt) action.” 2007. Doctoral Dissertation, University Utrecht. Accessed October 15, 2019. http://dspace.library.uu.nl/handle/1874/21792 ; URN:NBN:NL:UI:10-1874-21792 ; urn:isbn:978-90-393-4537-5 ; URN:NBN:NL:UI:10-1874-21792 ; http://dspace.library.uu.nl/handle/1874/21792.

MLA Handbook (7th Edition):

Gorp, A G M van. “The identification and functional characterisation of novel targets of Protein Kinase B (PKB/c-akt) action.” 2007. Web. 15 Oct 2019.

Vancouver:

Gorp AGMv. The identification and functional characterisation of novel targets of Protein Kinase B (PKB/c-akt) action. [Internet] [Doctoral dissertation]. University Utrecht; 2007. [cited 2019 Oct 15]. Available from: http://dspace.library.uu.nl/handle/1874/21792 ; URN:NBN:NL:UI:10-1874-21792 ; urn:isbn:978-90-393-4537-5 ; URN:NBN:NL:UI:10-1874-21792 ; http://dspace.library.uu.nl/handle/1874/21792.

Council of Science Editors:

Gorp AGMv. The identification and functional characterisation of novel targets of Protein Kinase B (PKB/c-akt) action. [Doctoral Dissertation]. University Utrecht; 2007. Available from: http://dspace.library.uu.nl/handle/1874/21792 ; URN:NBN:NL:UI:10-1874-21792 ; urn:isbn:978-90-393-4537-5 ; URN:NBN:NL:UI:10-1874-21792 ; http://dspace.library.uu.nl/handle/1874/21792

19. Flesch, F.M. Capacitation dependent changes in the sperm plasma membrane influence porcine gamete interaction.

Degree: 2000, University Utrecht

 Although the sperm cell was first seen through Van Leeuwenhoek’s microscope in the late seventieth century and despite much effort in the last 40 years… (more)

Subjects/Keywords: sperm cell; plasma membrane; acrosome; lectin; oocyte; interaction; capacitation; cholesterol distribution; tyrosine phosphorylation

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APA (6th Edition):

Flesch, F. M. (2000). Capacitation dependent changes in the sperm plasma membrane influence porcine gamete interaction. (Doctoral Dissertation). University Utrecht. Retrieved from http://dspace.library.uu.nl/handle/1874/3229 ; URN:NBN:NL:UI:10-1874-3229 ; urn:isbn:90-393-2465-4 ; URN:NBN:NL:UI:10-1874-3229 ; http://dspace.library.uu.nl/handle/1874/3229

Chicago Manual of Style (16th Edition):

Flesch, F M. “Capacitation dependent changes in the sperm plasma membrane influence porcine gamete interaction.” 2000. Doctoral Dissertation, University Utrecht. Accessed October 15, 2019. http://dspace.library.uu.nl/handle/1874/3229 ; URN:NBN:NL:UI:10-1874-3229 ; urn:isbn:90-393-2465-4 ; URN:NBN:NL:UI:10-1874-3229 ; http://dspace.library.uu.nl/handle/1874/3229.

MLA Handbook (7th Edition):

Flesch, F M. “Capacitation dependent changes in the sperm plasma membrane influence porcine gamete interaction.” 2000. Web. 15 Oct 2019.

Vancouver:

Flesch FM. Capacitation dependent changes in the sperm plasma membrane influence porcine gamete interaction. [Internet] [Doctoral dissertation]. University Utrecht; 2000. [cited 2019 Oct 15]. Available from: http://dspace.library.uu.nl/handle/1874/3229 ; URN:NBN:NL:UI:10-1874-3229 ; urn:isbn:90-393-2465-4 ; URN:NBN:NL:UI:10-1874-3229 ; http://dspace.library.uu.nl/handle/1874/3229.

Council of Science Editors:

Flesch FM. Capacitation dependent changes in the sperm plasma membrane influence porcine gamete interaction. [Doctoral Dissertation]. University Utrecht; 2000. Available from: http://dspace.library.uu.nl/handle/1874/3229 ; URN:NBN:NL:UI:10-1874-3229 ; urn:isbn:90-393-2465-4 ; URN:NBN:NL:UI:10-1874-3229 ; http://dspace.library.uu.nl/handle/1874/3229

20. Gorp, A.G.M. van. The identification and functional characterisation of novel targets of Protein Kinase B (PKB/c-akt) action.

Degree: 2007, University Utrecht

 Cancer is the result of a disturbed balance between cell division and growth on one hand, and programmed cell death on the other. Crucial cellular… (more)

Subjects/Keywords: cancer; translation; phosphorylation; signaltransduction; PI3K; PKB; proteomics; microarray; Foxo3a; eIF4B

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

APA (6th Edition):

Gorp, A. G. M. v. (2007). The identification and functional characterisation of novel targets of Protein Kinase B (PKB/c-akt) action. (Doctoral Dissertation). University Utrecht. Retrieved from http://dspace.library.uu.nl/handle/1874/21792 ; URN:NBN:NL:UI:10-1874-21792 ; urn:isbn:978-90-393-4537-5 ; URN:NBN:NL:UI:10-1874-21792 ; http://dspace.library.uu.nl/handle/1874/21792

Chicago Manual of Style (16th Edition):

Gorp, A G M van. “The identification and functional characterisation of novel targets of Protein Kinase B (PKB/c-akt) action.” 2007. Doctoral Dissertation, University Utrecht. Accessed October 15, 2019. http://dspace.library.uu.nl/handle/1874/21792 ; URN:NBN:NL:UI:10-1874-21792 ; urn:isbn:978-90-393-4537-5 ; URN:NBN:NL:UI:10-1874-21792 ; http://dspace.library.uu.nl/handle/1874/21792.

MLA Handbook (7th Edition):

Gorp, A G M van. “The identification and functional characterisation of novel targets of Protein Kinase B (PKB/c-akt) action.” 2007. Web. 15 Oct 2019.

Vancouver:

Gorp AGMv. The identification and functional characterisation of novel targets of Protein Kinase B (PKB/c-akt) action. [Internet] [Doctoral dissertation]. University Utrecht; 2007. [cited 2019 Oct 15]. Available from: http://dspace.library.uu.nl/handle/1874/21792 ; URN:NBN:NL:UI:10-1874-21792 ; urn:isbn:978-90-393-4537-5 ; URN:NBN:NL:UI:10-1874-21792 ; http://dspace.library.uu.nl/handle/1874/21792.

Council of Science Editors:

Gorp AGMv. The identification and functional characterisation of novel targets of Protein Kinase B (PKB/c-akt) action. [Doctoral Dissertation]. University Utrecht; 2007. Available from: http://dspace.library.uu.nl/handle/1874/21792 ; URN:NBN:NL:UI:10-1874-21792 ; urn:isbn:978-90-393-4537-5 ; URN:NBN:NL:UI:10-1874-21792 ; http://dspace.library.uu.nl/handle/1874/21792

21. Veen, Antonius Adrianus Bartholomeus van. Cardiac gap junctions and action potential propagation.

Degree: 2001, University Utrecht

 Described are the results, obtained from experiments on transfected cells to those on intact heart and new data are provided on connexin phosphorylation, expression and… (more)

Subjects/Keywords: heart; action potential; cardiomyocyte; cardiac hypertrophy; electrical activation; gap junction; protein phosphorylation

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APA (6th Edition):

Veen, A. A. B. v. (2001). Cardiac gap junctions and action potential propagation. (Doctoral Dissertation). University Utrecht. Retrieved from http://dspace.library.uu.nl/handle/1874/399 ; URN:NBN:NL:UI:10-1874-399 ; URN:NBN:NL:UI:10-1874-399 ; http://dspace.library.uu.nl/handle/1874/399

Chicago Manual of Style (16th Edition):

Veen, Antonius Adrianus Bartholomeus van. “Cardiac gap junctions and action potential propagation.” 2001. Doctoral Dissertation, University Utrecht. Accessed October 15, 2019. http://dspace.library.uu.nl/handle/1874/399 ; URN:NBN:NL:UI:10-1874-399 ; URN:NBN:NL:UI:10-1874-399 ; http://dspace.library.uu.nl/handle/1874/399.

MLA Handbook (7th Edition):

Veen, Antonius Adrianus Bartholomeus van. “Cardiac gap junctions and action potential propagation.” 2001. Web. 15 Oct 2019.

Vancouver:

Veen AABv. Cardiac gap junctions and action potential propagation. [Internet] [Doctoral dissertation]. University Utrecht; 2001. [cited 2019 Oct 15]. Available from: http://dspace.library.uu.nl/handle/1874/399 ; URN:NBN:NL:UI:10-1874-399 ; URN:NBN:NL:UI:10-1874-399 ; http://dspace.library.uu.nl/handle/1874/399.

Council of Science Editors:

Veen AABv. Cardiac gap junctions and action potential propagation. [Doctoral Dissertation]. University Utrecht; 2001. Available from: http://dspace.library.uu.nl/handle/1874/399 ; URN:NBN:NL:UI:10-1874-399 ; URN:NBN:NL:UI:10-1874-399 ; http://dspace.library.uu.nl/handle/1874/399

22. Veen, Antonius Adrianus Bartholomeus van. Cardiac gap junctions and action potential propagation.

Degree: 2001, University Utrecht

 Described are the results, obtained from experiments on transfected cells to those on intact heart and new data are provided on connexin phosphorylation, expression and… (more)

Subjects/Keywords: heart; action potential; cardiomyocyte; cardiac hypertrophy; electrical activation; gap junction; protein phosphorylation

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

APA (6th Edition):

Veen, A. A. B. v. (2001). Cardiac gap junctions and action potential propagation. (Doctoral Dissertation). University Utrecht. Retrieved from http://dspace.library.uu.nl/handle/1874/399 ; URN:NBN:NL:UI:10-1874-399 ; URN:NBN:NL:UI:10-1874-399 ; http://dspace.library.uu.nl/handle/1874/399

Chicago Manual of Style (16th Edition):

Veen, Antonius Adrianus Bartholomeus van. “Cardiac gap junctions and action potential propagation.” 2001. Doctoral Dissertation, University Utrecht. Accessed October 15, 2019. http://dspace.library.uu.nl/handle/1874/399 ; URN:NBN:NL:UI:10-1874-399 ; URN:NBN:NL:UI:10-1874-399 ; http://dspace.library.uu.nl/handle/1874/399.

MLA Handbook (7th Edition):

Veen, Antonius Adrianus Bartholomeus van. “Cardiac gap junctions and action potential propagation.” 2001. Web. 15 Oct 2019.

Vancouver:

Veen AABv. Cardiac gap junctions and action potential propagation. [Internet] [Doctoral dissertation]. University Utrecht; 2001. [cited 2019 Oct 15]. Available from: http://dspace.library.uu.nl/handle/1874/399 ; URN:NBN:NL:UI:10-1874-399 ; URN:NBN:NL:UI:10-1874-399 ; http://dspace.library.uu.nl/handle/1874/399.

Council of Science Editors:

Veen AABv. Cardiac gap junctions and action potential propagation. [Doctoral Dissertation]. University Utrecht; 2001. Available from: http://dspace.library.uu.nl/handle/1874/399 ; URN:NBN:NL:UI:10-1874-399 ; URN:NBN:NL:UI:10-1874-399 ; http://dspace.library.uu.nl/handle/1874/399

23. Shi, J. Peptide substrate-assisted study of O-GlcNAc transferase and O-GlcNAcylation.

Degree: 2018, University Utrecht

 O-GlcNAcylation is a post translational modification (PTM) that corresponds to the addition of a single β-linked N-Acetyl-D-glucosamine (GlcNAc) sugar moiety onto the hydroxyl group of… (more)

Subjects/Keywords: O-GlcNAcylation; tyrosine phosphorylation; OGT; peptide microarray; cross-talk; mRNA display; peptide substrates

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APA (6th Edition):

Shi, J. (2018). Peptide substrate-assisted study of O-GlcNAc transferase and O-GlcNAcylation. (Doctoral Dissertation). University Utrecht. Retrieved from http://dspace.library.uu.nl/handle/1874/363526 ; URN:NBN:NL:UI:10-1874-363526 ; urn:isbn:978-90-393-6956-2 ; URN:NBN:NL:UI:10-1874-363526 ; http://dspace.library.uu.nl/handle/1874/363526

Chicago Manual of Style (16th Edition):

Shi, J. “Peptide substrate-assisted study of O-GlcNAc transferase and O-GlcNAcylation.” 2018. Doctoral Dissertation, University Utrecht. Accessed October 15, 2019. http://dspace.library.uu.nl/handle/1874/363526 ; URN:NBN:NL:UI:10-1874-363526 ; urn:isbn:978-90-393-6956-2 ; URN:NBN:NL:UI:10-1874-363526 ; http://dspace.library.uu.nl/handle/1874/363526.

MLA Handbook (7th Edition):

Shi, J. “Peptide substrate-assisted study of O-GlcNAc transferase and O-GlcNAcylation.” 2018. Web. 15 Oct 2019.

Vancouver:

Shi J. Peptide substrate-assisted study of O-GlcNAc transferase and O-GlcNAcylation. [Internet] [Doctoral dissertation]. University Utrecht; 2018. [cited 2019 Oct 15]. Available from: http://dspace.library.uu.nl/handle/1874/363526 ; URN:NBN:NL:UI:10-1874-363526 ; urn:isbn:978-90-393-6956-2 ; URN:NBN:NL:UI:10-1874-363526 ; http://dspace.library.uu.nl/handle/1874/363526.

Council of Science Editors:

Shi J. Peptide substrate-assisted study of O-GlcNAc transferase and O-GlcNAcylation. [Doctoral Dissertation]. University Utrecht; 2018. Available from: http://dspace.library.uu.nl/handle/1874/363526 ; URN:NBN:NL:UI:10-1874-363526 ; urn:isbn:978-90-393-6956-2 ; URN:NBN:NL:UI:10-1874-363526 ; http://dspace.library.uu.nl/handle/1874/363526

24. Schmidlin, T.T. Novel Methods and Applications of Data-independent and Targeted Mass Spectrometry : Towards Robust Quantification of Molecular Signaling Events.

Degree: 2018, University Utrecht

 Biological signaling is often relying on molecules of high similarity. Key examples are neuropeptides and phosphorylated proteins. Neuropeptides undergo a variety of enzymatic processing steps… (more)

Subjects/Keywords: Protein Phosphorylation; Neuropeptides; Molecular Assay; Targeted Mass Spectrometry; Cancer; Obesity

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APA (6th Edition):

Schmidlin, T. T. (2018). Novel Methods and Applications of Data-independent and Targeted Mass Spectrometry : Towards Robust Quantification of Molecular Signaling Events. (Doctoral Dissertation). University Utrecht. Retrieved from http://dspace.library.uu.nl/handle/1874/364779 ; URN:NBN:NL:UI:10-1874-364779 ; urn:isbn:978-94-6295-952-1 ; URN:NBN:NL:UI:10-1874-364779 ; http://dspace.library.uu.nl/handle/1874/364779

Chicago Manual of Style (16th Edition):

Schmidlin, T T. “Novel Methods and Applications of Data-independent and Targeted Mass Spectrometry : Towards Robust Quantification of Molecular Signaling Events.” 2018. Doctoral Dissertation, University Utrecht. Accessed October 15, 2019. http://dspace.library.uu.nl/handle/1874/364779 ; URN:NBN:NL:UI:10-1874-364779 ; urn:isbn:978-94-6295-952-1 ; URN:NBN:NL:UI:10-1874-364779 ; http://dspace.library.uu.nl/handle/1874/364779.

MLA Handbook (7th Edition):

Schmidlin, T T. “Novel Methods and Applications of Data-independent and Targeted Mass Spectrometry : Towards Robust Quantification of Molecular Signaling Events.” 2018. Web. 15 Oct 2019.

Vancouver:

Schmidlin TT. Novel Methods and Applications of Data-independent and Targeted Mass Spectrometry : Towards Robust Quantification of Molecular Signaling Events. [Internet] [Doctoral dissertation]. University Utrecht; 2018. [cited 2019 Oct 15]. Available from: http://dspace.library.uu.nl/handle/1874/364779 ; URN:NBN:NL:UI:10-1874-364779 ; urn:isbn:978-94-6295-952-1 ; URN:NBN:NL:UI:10-1874-364779 ; http://dspace.library.uu.nl/handle/1874/364779.

Council of Science Editors:

Schmidlin TT. Novel Methods and Applications of Data-independent and Targeted Mass Spectrometry : Towards Robust Quantification of Molecular Signaling Events. [Doctoral Dissertation]. University Utrecht; 2018. Available from: http://dspace.library.uu.nl/handle/1874/364779 ; URN:NBN:NL:UI:10-1874-364779 ; urn:isbn:978-94-6295-952-1 ; URN:NBN:NL:UI:10-1874-364779 ; http://dspace.library.uu.nl/handle/1874/364779

25. Giansanti, Piero. Signaling network dynamics investigated by quantitative phosphoproteomics.

Degree: 2014, University Utrecht

 This thesis describes the application of proteomics technologies to get insight into several aspects of phosphorylation signaling dynamics. The core tool in all performed experiments… (more)

Subjects/Keywords: protein phosphorylation; quantitative phosphoproteomics; mass spectrometry; signaling network; kinases; tyrosine kinases inhibitors

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APA (6th Edition):

Giansanti, P. (2014). Signaling network dynamics investigated by quantitative phosphoproteomics. (Doctoral Dissertation). University Utrecht. Retrieved from http://dspace.library.uu.nl/handle/1874/308082 ; URN:NBN:NL:UI:10-1874-308082 ; urn:isbn:978-90-8891-982-4 ; URN:NBN:NL:UI:10-1874-308082 ; http://dspace.library.uu.nl/handle/1874/308082

Chicago Manual of Style (16th Edition):

Giansanti, Piero. “Signaling network dynamics investigated by quantitative phosphoproteomics.” 2014. Doctoral Dissertation, University Utrecht. Accessed October 15, 2019. http://dspace.library.uu.nl/handle/1874/308082 ; URN:NBN:NL:UI:10-1874-308082 ; urn:isbn:978-90-8891-982-4 ; URN:NBN:NL:UI:10-1874-308082 ; http://dspace.library.uu.nl/handle/1874/308082.

MLA Handbook (7th Edition):

Giansanti, Piero. “Signaling network dynamics investigated by quantitative phosphoproteomics.” 2014. Web. 15 Oct 2019.

Vancouver:

Giansanti P. Signaling network dynamics investigated by quantitative phosphoproteomics. [Internet] [Doctoral dissertation]. University Utrecht; 2014. [cited 2019 Oct 15]. Available from: http://dspace.library.uu.nl/handle/1874/308082 ; URN:NBN:NL:UI:10-1874-308082 ; urn:isbn:978-90-8891-982-4 ; URN:NBN:NL:UI:10-1874-308082 ; http://dspace.library.uu.nl/handle/1874/308082.

Council of Science Editors:

Giansanti P. Signaling network dynamics investigated by quantitative phosphoproteomics. [Doctoral Dissertation]. University Utrecht; 2014. Available from: http://dspace.library.uu.nl/handle/1874/308082 ; URN:NBN:NL:UI:10-1874-308082 ; urn:isbn:978-90-8891-982-4 ; URN:NBN:NL:UI:10-1874-308082 ; http://dspace.library.uu.nl/handle/1874/308082

26. Marino, F. Extending the boundaries of MS-based proteomics: towards comprehensive analysis of the proteome and the HLA ligandome.

Degree: 2016, University Utrecht

 The work, described in this thesis, has been aimed at the improvement of proteomic workflows; from the sample preparation, to the optimization of state-of-art chromatographical… (more)

Subjects/Keywords: Alternative fragmentations; HLA class I; HLA class II; phosphorylation; methylation; glycosylation

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APA (6th Edition):

Marino, F. (2016). Extending the boundaries of MS-based proteomics: towards comprehensive analysis of the proteome and the HLA ligandome. (Doctoral Dissertation). University Utrecht. Retrieved from http://dspace.library.uu.nl/handle/1874/338044 ; URN:NBN:NL:UI:10-1874-338044 ; URN:NBN:NL:UI:10-1874-338044 ; http://dspace.library.uu.nl/handle/1874/338044

Chicago Manual of Style (16th Edition):

Marino, F. “Extending the boundaries of MS-based proteomics: towards comprehensive analysis of the proteome and the HLA ligandome.” 2016. Doctoral Dissertation, University Utrecht. Accessed October 15, 2019. http://dspace.library.uu.nl/handle/1874/338044 ; URN:NBN:NL:UI:10-1874-338044 ; URN:NBN:NL:UI:10-1874-338044 ; http://dspace.library.uu.nl/handle/1874/338044.

MLA Handbook (7th Edition):

Marino, F. “Extending the boundaries of MS-based proteomics: towards comprehensive analysis of the proteome and the HLA ligandome.” 2016. Web. 15 Oct 2019.

Vancouver:

Marino F. Extending the boundaries of MS-based proteomics: towards comprehensive analysis of the proteome and the HLA ligandome. [Internet] [Doctoral dissertation]. University Utrecht; 2016. [cited 2019 Oct 15]. Available from: http://dspace.library.uu.nl/handle/1874/338044 ; URN:NBN:NL:UI:10-1874-338044 ; URN:NBN:NL:UI:10-1874-338044 ; http://dspace.library.uu.nl/handle/1874/338044.

Council of Science Editors:

Marino F. Extending the boundaries of MS-based proteomics: towards comprehensive analysis of the proteome and the HLA ligandome. [Doctoral Dissertation]. University Utrecht; 2016. Available from: http://dspace.library.uu.nl/handle/1874/338044 ; URN:NBN:NL:UI:10-1874-338044 ; URN:NBN:NL:UI:10-1874-338044 ; http://dspace.library.uu.nl/handle/1874/338044

27. Shadid, B. Studies on the synthesis of phosphorylated and alanylated cytokinins.

Degree: 1990, Agricultural University

  New approaches are described in this thesis towards the syntheses of phosphorylated and alanylated cytokinins. In chapter 1 a general picture of the stucture… (more)

Subjects/Keywords: cytokininen; synthese; fosforylering; Organische chemie; cytokinins; synthesis; phosphorylation; Organic Chemistry

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APA (6th Edition):

Shadid, B. (1990). Studies on the synthesis of phosphorylated and alanylated cytokinins. (Doctoral Dissertation). Agricultural University. Retrieved from http://library.wur.nl/WebQuery/wurpubs/10916 ; urn:nbn:nl:ui:32-10916 ; urn:nbn:nl:ui:32-10916 ; http://library.wur.nl/WebQuery/wurpubs/10916

Chicago Manual of Style (16th Edition):

Shadid, B. “Studies on the synthesis of phosphorylated and alanylated cytokinins.” 1990. Doctoral Dissertation, Agricultural University. Accessed October 15, 2019. http://library.wur.nl/WebQuery/wurpubs/10916 ; urn:nbn:nl:ui:32-10916 ; urn:nbn:nl:ui:32-10916 ; http://library.wur.nl/WebQuery/wurpubs/10916.

MLA Handbook (7th Edition):

Shadid, B. “Studies on the synthesis of phosphorylated and alanylated cytokinins.” 1990. Web. 15 Oct 2019.

Vancouver:

Shadid B. Studies on the synthesis of phosphorylated and alanylated cytokinins. [Internet] [Doctoral dissertation]. Agricultural University; 1990. [cited 2019 Oct 15]. Available from: http://library.wur.nl/WebQuery/wurpubs/10916 ; urn:nbn:nl:ui:32-10916 ; urn:nbn:nl:ui:32-10916 ; http://library.wur.nl/WebQuery/wurpubs/10916.

Council of Science Editors:

Shadid B. Studies on the synthesis of phosphorylated and alanylated cytokinins. [Doctoral Dissertation]. Agricultural University; 1990. Available from: http://library.wur.nl/WebQuery/wurpubs/10916 ; urn:nbn:nl:ui:32-10916 ; urn:nbn:nl:ui:32-10916 ; http://library.wur.nl/WebQuery/wurpubs/10916


Leiden University

28. Kistemaker, H.A.V. Synthesis of well-defined ADP-Ribosylated biomolecules.

Degree: 2017, Leiden University

 The post-translational modification of proteins known as adenosine diphosphate ribosylation (ADPr) is involved in a wide variety of important biological processes and is also associated… (more)

Subjects/Keywords: poly-ADPr; PARP; ADP-ribose; Ribose; Pyrophosphate; Phosphorylation; Ribosylation; Glycosylation; MARylation; PARylation; poly-ADPr; PARP; ADP-ribose; Ribose; Pyrophosphate; Phosphorylation; Ribosylation; Glycosylation; MARylation; PARylation

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APA (6th Edition):

Kistemaker, H. A. V. (2017). Synthesis of well-defined ADP-Ribosylated biomolecules. (Doctoral Dissertation). Leiden University. Retrieved from http://hdl.handle.net/1887/49075

Chicago Manual of Style (16th Edition):

Kistemaker, H A V. “Synthesis of well-defined ADP-Ribosylated biomolecules.” 2017. Doctoral Dissertation, Leiden University. Accessed October 15, 2019. http://hdl.handle.net/1887/49075.

MLA Handbook (7th Edition):

Kistemaker, H A V. “Synthesis of well-defined ADP-Ribosylated biomolecules.” 2017. Web. 15 Oct 2019.

Vancouver:

Kistemaker HAV. Synthesis of well-defined ADP-Ribosylated biomolecules. [Internet] [Doctoral dissertation]. Leiden University; 2017. [cited 2019 Oct 15]. Available from: http://hdl.handle.net/1887/49075.

Council of Science Editors:

Kistemaker HAV. Synthesis of well-defined ADP-Ribosylated biomolecules. [Doctoral Dissertation]. Leiden University; 2017. Available from: http://hdl.handle.net/1887/49075


Leiden University

29. Gelderen, van, K. Arabidopsis AGC3 kinases and PIN plasma membrane abundance.

Degree: 2017, Leiden University

 The plant hormone auxin plays a central role in the growth and development of plants. Auxin acts in a concentration dependent manner and polar cell-to-cell… (more)

Subjects/Keywords: AGC3 kinases; PIN plasma membrane; Arabidopsis; D6 kinases; PIN phosphorylation; PINOID; AGC3 kinases; PIN plasma membrane; Arabidopsis; D6 kinases; PIN phosphorylation; PINOID

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APA (6th Edition):

Gelderen, van, K. (2017). Arabidopsis AGC3 kinases and PIN plasma membrane abundance. (Doctoral Dissertation). Leiden University. Retrieved from http://hdl.handle.net/1887/50504

Chicago Manual of Style (16th Edition):

Gelderen, van, K. “Arabidopsis AGC3 kinases and PIN plasma membrane abundance.” 2017. Doctoral Dissertation, Leiden University. Accessed October 15, 2019. http://hdl.handle.net/1887/50504.

MLA Handbook (7th Edition):

Gelderen, van, K. “Arabidopsis AGC3 kinases and PIN plasma membrane abundance.” 2017. Web. 15 Oct 2019.

Vancouver:

Gelderen, van K. Arabidopsis AGC3 kinases and PIN plasma membrane abundance. [Internet] [Doctoral dissertation]. Leiden University; 2017. [cited 2019 Oct 15]. Available from: http://hdl.handle.net/1887/50504.

Council of Science Editors:

Gelderen, van K. Arabidopsis AGC3 kinases and PIN plasma membrane abundance. [Doctoral Dissertation]. Leiden University; 2017. Available from: http://hdl.handle.net/1887/50504

30. Huang, Fang. PIN protein phosphorylation by plant AGC3 kinases and its role in polar auxin transport.

Degree: 2010, Molecular Developmental Genetics Department, Institute of Biology (IBL), Leiden University

 Polar cell-to-cell transport of plant hormone auxin mediated by plasma membrane (PM)-localized PIN-FORMED (PIN) auxin efflux carriers generates auxin gradients that provide positional information for… (more)

Subjects/Keywords: Phosphorylation; PID serine/threonine kinase protein; PIN auxin efflux carriers; Polar auxin transport; Polarity; Trafficking; Phosphorylation; PID serine/threonine kinase protein; PIN auxin efflux carriers; Polar auxin transport; Polarity; Trafficking

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APA (6th Edition):

Huang, F. (2010). PIN protein phosphorylation by plant AGC3 kinases and its role in polar auxin transport. (Doctoral Dissertation). Molecular Developmental Genetics Department, Institute of Biology (IBL), Leiden University. Retrieved from http://hdl.handle.net/1887/15916

Chicago Manual of Style (16th Edition):

Huang, Fang. “PIN protein phosphorylation by plant AGC3 kinases and its role in polar auxin transport.” 2010. Doctoral Dissertation, Molecular Developmental Genetics Department, Institute of Biology (IBL), Leiden University. Accessed October 15, 2019. http://hdl.handle.net/1887/15916.

MLA Handbook (7th Edition):

Huang, Fang. “PIN protein phosphorylation by plant AGC3 kinases and its role in polar auxin transport.” 2010. Web. 15 Oct 2019.

Vancouver:

Huang F. PIN protein phosphorylation by plant AGC3 kinases and its role in polar auxin transport. [Internet] [Doctoral dissertation]. Molecular Developmental Genetics Department, Institute of Biology (IBL), Leiden University; 2010. [cited 2019 Oct 15]. Available from: http://hdl.handle.net/1887/15916.

Council of Science Editors:

Huang F. PIN protein phosphorylation by plant AGC3 kinases and its role in polar auxin transport. [Doctoral Dissertation]. Molecular Developmental Genetics Department, Institute of Biology (IBL), Leiden University; 2010. Available from: http://hdl.handle.net/1887/15916

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