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You searched for subject:(O GlcNAcylation). Showing records 1 – 30 of 31 total matches.

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1. Lafont, Florian. Implication des modifications post-traductionnelles de DNA-PKcs dans la régulation de la réponse aux dommages à l'ADN. : Involvement of DNA-PKcs post-translational modifications in the regulation of DNA damage response.

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie, 2017, Nantes

Les cellules humaines sont soumises à des stress induisant des cassures double-brin de l’ADN principalement réparées par la voie NHEJ, où la kinase DNA-PKcs joue… (more)

Subjects/Keywords: O-GlcNAcylation

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APA (6th Edition):

Lafont, F. (2017). Implication des modifications post-traductionnelles de DNA-PKcs dans la régulation de la réponse aux dommages à l'ADN. : Involvement of DNA-PKcs post-translational modifications in the regulation of DNA damage response. (Doctoral Dissertation). Nantes. Retrieved from http://www.theses.fr/2017NANT1023

Chicago Manual of Style (16th Edition):

Lafont, Florian. “Implication des modifications post-traductionnelles de DNA-PKcs dans la régulation de la réponse aux dommages à l'ADN. : Involvement of DNA-PKcs post-translational modifications in the regulation of DNA damage response.” 2017. Doctoral Dissertation, Nantes. Accessed October 26, 2020. http://www.theses.fr/2017NANT1023.

MLA Handbook (7th Edition):

Lafont, Florian. “Implication des modifications post-traductionnelles de DNA-PKcs dans la régulation de la réponse aux dommages à l'ADN. : Involvement of DNA-PKcs post-translational modifications in the regulation of DNA damage response.” 2017. Web. 26 Oct 2020.

Vancouver:

Lafont F. Implication des modifications post-traductionnelles de DNA-PKcs dans la régulation de la réponse aux dommages à l'ADN. : Involvement of DNA-PKcs post-translational modifications in the regulation of DNA damage response. [Internet] [Doctoral dissertation]. Nantes; 2017. [cited 2020 Oct 26]. Available from: http://www.theses.fr/2017NANT1023.

Council of Science Editors:

Lafont F. Implication des modifications post-traductionnelles de DNA-PKcs dans la régulation de la réponse aux dommages à l'ADN. : Involvement of DNA-PKcs post-translational modifications in the regulation of DNA damage response. [Doctoral Dissertation]. Nantes; 2017. Available from: http://www.theses.fr/2017NANT1023

2. Pérez-Cervera, Yobana. Etude des relations "O-GlcNAcylation et microdomaines lipidiques" : Study of relationship "lipid microdomaines and O-GlcNAcylation".

Degree: Docteur es, Sciences de la vie et de la santé, 2012, Université Lille I – Sciences et Technologies

La O-GlcNAcylation est une modification post-traductionnelle appartenant au groupe des glycosylations. C’est une modification dynamique, analogue à la phosphorylation, dont la réversibilité est contrôlée par… (more)

Subjects/Keywords: O-GlcNAcylation; 572.68

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APA (6th Edition):

Pérez-Cervera, Y. (2012). Etude des relations "O-GlcNAcylation et microdomaines lipidiques" : Study of relationship "lipid microdomaines and O-GlcNAcylation". (Doctoral Dissertation). Université Lille I – Sciences et Technologies. Retrieved from http://www.theses.fr/2012LIL10105

Chicago Manual of Style (16th Edition):

Pérez-Cervera, Yobana. “Etude des relations "O-GlcNAcylation et microdomaines lipidiques" : Study of relationship "lipid microdomaines and O-GlcNAcylation".” 2012. Doctoral Dissertation, Université Lille I – Sciences et Technologies. Accessed October 26, 2020. http://www.theses.fr/2012LIL10105.

MLA Handbook (7th Edition):

Pérez-Cervera, Yobana. “Etude des relations "O-GlcNAcylation et microdomaines lipidiques" : Study of relationship "lipid microdomaines and O-GlcNAcylation".” 2012. Web. 26 Oct 2020.

Vancouver:

Pérez-Cervera Y. Etude des relations "O-GlcNAcylation et microdomaines lipidiques" : Study of relationship "lipid microdomaines and O-GlcNAcylation". [Internet] [Doctoral dissertation]. Université Lille I – Sciences et Technologies; 2012. [cited 2020 Oct 26]. Available from: http://www.theses.fr/2012LIL10105.

Council of Science Editors:

Pérez-Cervera Y. Etude des relations "O-GlcNAcylation et microdomaines lipidiques" : Study of relationship "lipid microdomaines and O-GlcNAcylation". [Doctoral Dissertation]. Université Lille I – Sciences et Technologies; 2012. Available from: http://www.theses.fr/2012LIL10105

3. Biwi, James Tapiwa. Nouvelles connaissances sur la régulation de la glycosylation complexe par O-GlcNAcylation dans des lignées coliques saines et cancéreuses : Novel insights on complex glycosylation regulation by O-GlcNAcylation in healthy and cancer colon cell lines.

Degree: Docteur es, Biomolécules, pharmacologie, thérapeutique, 2019, Université Lille I – Sciences et Technologies

 Le cancer colorectal (CCR) est une pathologie dont les causes tiennent en partie d’un style de vie basé sur un régime alimentaire de type occidental… (more)

Subjects/Keywords: O-GlcNAcylation; 571.978

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APA (6th Edition):

Biwi, J. T. (2019). Nouvelles connaissances sur la régulation de la glycosylation complexe par O-GlcNAcylation dans des lignées coliques saines et cancéreuses : Novel insights on complex glycosylation regulation by O-GlcNAcylation in healthy and cancer colon cell lines. (Doctoral Dissertation). Université Lille I – Sciences et Technologies. Retrieved from http://www.theses.fr/2019LIL1S104

Chicago Manual of Style (16th Edition):

Biwi, James Tapiwa. “Nouvelles connaissances sur la régulation de la glycosylation complexe par O-GlcNAcylation dans des lignées coliques saines et cancéreuses : Novel insights on complex glycosylation regulation by O-GlcNAcylation in healthy and cancer colon cell lines.” 2019. Doctoral Dissertation, Université Lille I – Sciences et Technologies. Accessed October 26, 2020. http://www.theses.fr/2019LIL1S104.

MLA Handbook (7th Edition):

Biwi, James Tapiwa. “Nouvelles connaissances sur la régulation de la glycosylation complexe par O-GlcNAcylation dans des lignées coliques saines et cancéreuses : Novel insights on complex glycosylation regulation by O-GlcNAcylation in healthy and cancer colon cell lines.” 2019. Web. 26 Oct 2020.

Vancouver:

Biwi JT. Nouvelles connaissances sur la régulation de la glycosylation complexe par O-GlcNAcylation dans des lignées coliques saines et cancéreuses : Novel insights on complex glycosylation regulation by O-GlcNAcylation in healthy and cancer colon cell lines. [Internet] [Doctoral dissertation]. Université Lille I – Sciences et Technologies; 2019. [cited 2020 Oct 26]. Available from: http://www.theses.fr/2019LIL1S104.

Council of Science Editors:

Biwi JT. Nouvelles connaissances sur la régulation de la glycosylation complexe par O-GlcNAcylation dans des lignées coliques saines et cancéreuses : Novel insights on complex glycosylation regulation by O-GlcNAcylation in healthy and cancer colon cell lines. [Doctoral Dissertation]. Université Lille I – Sciences et Technologies; 2019. Available from: http://www.theses.fr/2019LIL1S104

4. Fourneau, Julie. Conséquences d’une perturbation de l’expérience sensorimotrice sur la plasticité synaptique du cortex cérébral : implication de deux modifications post-traductionnelles, la phosphorylation et la O-GlcNAcylation : Consequences of sensorimotor perturbation on synaptic plasticity of the cerebral cortex : involvement of two post-translational modifications, phosphorylation and O-GlcNAcylation.

Degree: Docteur es, Neursciences, 2018, Université Lille I – Sciences et Technologies

La sédentarité ou un alitement prolongé sont des situations ayant en commun une perturbation sensorimotrice (PSM), conduisant à une dégradation de la posture et la… (more)

Subjects/Keywords: O-GlcNAcylation; 573.86

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APA (6th Edition):

Fourneau, J. (2018). Conséquences d’une perturbation de l’expérience sensorimotrice sur la plasticité synaptique du cortex cérébral : implication de deux modifications post-traductionnelles, la phosphorylation et la O-GlcNAcylation : Consequences of sensorimotor perturbation on synaptic plasticity of the cerebral cortex : involvement of two post-translational modifications, phosphorylation and O-GlcNAcylation. (Doctoral Dissertation). Université Lille I – Sciences et Technologies. Retrieved from http://www.theses.fr/2018LIL1S105

Chicago Manual of Style (16th Edition):

Fourneau, Julie. “Conséquences d’une perturbation de l’expérience sensorimotrice sur la plasticité synaptique du cortex cérébral : implication de deux modifications post-traductionnelles, la phosphorylation et la O-GlcNAcylation : Consequences of sensorimotor perturbation on synaptic plasticity of the cerebral cortex : involvement of two post-translational modifications, phosphorylation and O-GlcNAcylation.” 2018. Doctoral Dissertation, Université Lille I – Sciences et Technologies. Accessed October 26, 2020. http://www.theses.fr/2018LIL1S105.

MLA Handbook (7th Edition):

Fourneau, Julie. “Conséquences d’une perturbation de l’expérience sensorimotrice sur la plasticité synaptique du cortex cérébral : implication de deux modifications post-traductionnelles, la phosphorylation et la O-GlcNAcylation : Consequences of sensorimotor perturbation on synaptic plasticity of the cerebral cortex : involvement of two post-translational modifications, phosphorylation and O-GlcNAcylation.” 2018. Web. 26 Oct 2020.

Vancouver:

Fourneau J. Conséquences d’une perturbation de l’expérience sensorimotrice sur la plasticité synaptique du cortex cérébral : implication de deux modifications post-traductionnelles, la phosphorylation et la O-GlcNAcylation : Consequences of sensorimotor perturbation on synaptic plasticity of the cerebral cortex : involvement of two post-translational modifications, phosphorylation and O-GlcNAcylation. [Internet] [Doctoral dissertation]. Université Lille I – Sciences et Technologies; 2018. [cited 2020 Oct 26]. Available from: http://www.theses.fr/2018LIL1S105.

Council of Science Editors:

Fourneau J. Conséquences d’une perturbation de l’expérience sensorimotrice sur la plasticité synaptique du cortex cérébral : implication de deux modifications post-traductionnelles, la phosphorylation et la O-GlcNAcylation : Consequences of sensorimotor perturbation on synaptic plasticity of the cerebral cortex : involvement of two post-translational modifications, phosphorylation and O-GlcNAcylation. [Doctoral Dissertation]. Université Lille I – Sciences et Technologies; 2018. Available from: http://www.theses.fr/2018LIL1S105

5. Kamah, Amina. Identification et caractérisation des modifications post-traductionnelles de la protéine TAU : implication dans le processus d'agrégation : Identification and characterization of post-translational modification of tau : implication in aggregation process.

Degree: Docteur es, Biochimie et biologie structurale, 2015, Université Lille I – Sciences et Technologies

Les démences séniles sont caractérisées, au niveau moléculaire, par l’agrégation de quelquesprotéines-clés. On peut donner comme exemple l’α-synucléine, dans la maladie de Parkinson,ou le peptide… (more)

Subjects/Keywords: O-GlcNAcylation; Immunophilines; 572.633

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APA (6th Edition):

Kamah, A. (2015). Identification et caractérisation des modifications post-traductionnelles de la protéine TAU : implication dans le processus d'agrégation : Identification and characterization of post-translational modification of tau : implication in aggregation process. (Doctoral Dissertation). Université Lille I – Sciences et Technologies. Retrieved from http://www.theses.fr/2015LIL10049

Chicago Manual of Style (16th Edition):

Kamah, Amina. “Identification et caractérisation des modifications post-traductionnelles de la protéine TAU : implication dans le processus d'agrégation : Identification and characterization of post-translational modification of tau : implication in aggregation process.” 2015. Doctoral Dissertation, Université Lille I – Sciences et Technologies. Accessed October 26, 2020. http://www.theses.fr/2015LIL10049.

MLA Handbook (7th Edition):

Kamah, Amina. “Identification et caractérisation des modifications post-traductionnelles de la protéine TAU : implication dans le processus d'agrégation : Identification and characterization of post-translational modification of tau : implication in aggregation process.” 2015. Web. 26 Oct 2020.

Vancouver:

Kamah A. Identification et caractérisation des modifications post-traductionnelles de la protéine TAU : implication dans le processus d'agrégation : Identification and characterization of post-translational modification of tau : implication in aggregation process. [Internet] [Doctoral dissertation]. Université Lille I – Sciences et Technologies; 2015. [cited 2020 Oct 26]. Available from: http://www.theses.fr/2015LIL10049.

Council of Science Editors:

Kamah A. Identification et caractérisation des modifications post-traductionnelles de la protéine TAU : implication dans le processus d'agrégation : Identification and characterization of post-translational modification of tau : implication in aggregation process. [Doctoral Dissertation]. Université Lille I – Sciences et Technologies; 2015. Available from: http://www.theses.fr/2015LIL10049

6. Kanwal, Shahzina. Effect of O-GlcNAcylation on tamoxifen sensitivity in breast cancer derived MCF-7 cells : Effet de la O-GlcNAcylation sur la sensibilité du tamoxifène dans le cancer du sein dérivé des cellules MCF-7.

Degree: Docteur es, Biologie cellulaire, 2013, Université Paris Descartes – Paris V

Pas de résumé en français

One of the hallmarks of cancer cells is to exhibit increased uptake and consumption of glucose.3-5% of the glucose entering… (more)

Subjects/Keywords: Cancer du sein; O-GlcNAcylation

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APA (6th Edition):

Kanwal, S. (2013). Effect of O-GlcNAcylation on tamoxifen sensitivity in breast cancer derived MCF-7 cells : Effet de la O-GlcNAcylation sur la sensibilité du tamoxifène dans le cancer du sein dérivé des cellules MCF-7. (Doctoral Dissertation). Université Paris Descartes – Paris V. Retrieved from http://www.theses.fr/2013PA05T006

Chicago Manual of Style (16th Edition):

Kanwal, Shahzina. “Effect of O-GlcNAcylation on tamoxifen sensitivity in breast cancer derived MCF-7 cells : Effet de la O-GlcNAcylation sur la sensibilité du tamoxifène dans le cancer du sein dérivé des cellules MCF-7.” 2013. Doctoral Dissertation, Université Paris Descartes – Paris V. Accessed October 26, 2020. http://www.theses.fr/2013PA05T006.

MLA Handbook (7th Edition):

Kanwal, Shahzina. “Effect of O-GlcNAcylation on tamoxifen sensitivity in breast cancer derived MCF-7 cells : Effet de la O-GlcNAcylation sur la sensibilité du tamoxifène dans le cancer du sein dérivé des cellules MCF-7.” 2013. Web. 26 Oct 2020.

Vancouver:

Kanwal S. Effect of O-GlcNAcylation on tamoxifen sensitivity in breast cancer derived MCF-7 cells : Effet de la O-GlcNAcylation sur la sensibilité du tamoxifène dans le cancer du sein dérivé des cellules MCF-7. [Internet] [Doctoral dissertation]. Université Paris Descartes – Paris V; 2013. [cited 2020 Oct 26]. Available from: http://www.theses.fr/2013PA05T006.

Council of Science Editors:

Kanwal S. Effect of O-GlcNAcylation on tamoxifen sensitivity in breast cancer derived MCF-7 cells : Effet de la O-GlcNAcylation sur la sensibilité du tamoxifène dans le cancer du sein dérivé des cellules MCF-7. [Doctoral Dissertation]. Université Paris Descartes – Paris V; 2013. Available from: http://www.theses.fr/2013PA05T006

7. Leturcq, Maïté. Etude du rôle de la dynamique de O-GlcNAcylation sur les protéines du complexe Minichromosome Maintenance MCM2-7 dans les cellules somatiques humaines : Study of the role of O-GlcNAc dynamic on the Minichromosome Maintenance MCM2-7 complex in human somatic cells.

Degree: Docteur es, Sciences de la vie et de la santé, 2018, Université Lille I – Sciences et Technologies

Un des acteurs essentiels de la réplication de l’ADN est le complexe MCM2-7. Ce complexe est composé de 6 protéines (MCM2 à MCM7) organisées en… (more)

Subjects/Keywords: Complexe minichromosome maintenance; O-GlcNAcylation; 572.68

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APA (6th Edition):

Leturcq, M. (2018). Etude du rôle de la dynamique de O-GlcNAcylation sur les protéines du complexe Minichromosome Maintenance MCM2-7 dans les cellules somatiques humaines : Study of the role of O-GlcNAc dynamic on the Minichromosome Maintenance MCM2-7 complex in human somatic cells. (Doctoral Dissertation). Université Lille I – Sciences et Technologies. Retrieved from http://www.theses.fr/2018LIL1S102

Chicago Manual of Style (16th Edition):

Leturcq, Maïté. “Etude du rôle de la dynamique de O-GlcNAcylation sur les protéines du complexe Minichromosome Maintenance MCM2-7 dans les cellules somatiques humaines : Study of the role of O-GlcNAc dynamic on the Minichromosome Maintenance MCM2-7 complex in human somatic cells.” 2018. Doctoral Dissertation, Université Lille I – Sciences et Technologies. Accessed October 26, 2020. http://www.theses.fr/2018LIL1S102.

MLA Handbook (7th Edition):

Leturcq, Maïté. “Etude du rôle de la dynamique de O-GlcNAcylation sur les protéines du complexe Minichromosome Maintenance MCM2-7 dans les cellules somatiques humaines : Study of the role of O-GlcNAc dynamic on the Minichromosome Maintenance MCM2-7 complex in human somatic cells.” 2018. Web. 26 Oct 2020.

Vancouver:

Leturcq M. Etude du rôle de la dynamique de O-GlcNAcylation sur les protéines du complexe Minichromosome Maintenance MCM2-7 dans les cellules somatiques humaines : Study of the role of O-GlcNAc dynamic on the Minichromosome Maintenance MCM2-7 complex in human somatic cells. [Internet] [Doctoral dissertation]. Université Lille I – Sciences et Technologies; 2018. [cited 2020 Oct 26]. Available from: http://www.theses.fr/2018LIL1S102.

Council of Science Editors:

Leturcq M. Etude du rôle de la dynamique de O-GlcNAcylation sur les protéines du complexe Minichromosome Maintenance MCM2-7 dans les cellules somatiques humaines : Study of the role of O-GlcNAc dynamic on the Minichromosome Maintenance MCM2-7 complex in human somatic cells. [Doctoral Dissertation]. Université Lille I – Sciences et Technologies; 2018. Available from: http://www.theses.fr/2018LIL1S102

8. Baldini, Steffi. Régulation des propriétés de deux enzymes clefs du métabolisme glucido-lipidique hépatique, la GlucoKinase et la Fatty Acid Synthase par O-GlcNAcylation au cours de la lipogenèse et de la prolifération cellulaire : Regulation of two key enzymes properties in glucido-lipidic metabolism hepatic, GlucoKinase and Fatty Acid Synthase by O-GlcNAcylation in lipogenesis and cell proliferation.

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie, 2016, Université Lille I – Sciences et Technologies

Après un repas, la glycolyse, la lipogenèse et particulièrement 2 enzymes sont sollicitées : la GlucoKinase (GK) et la Fatty Acid Synthase (FAS) augmentant la… (more)

Subjects/Keywords: O-GlcNAcylation; Acide gras synthase; 572.68

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APA (6th Edition):

Baldini, S. (2016). Régulation des propriétés de deux enzymes clefs du métabolisme glucido-lipidique hépatique, la GlucoKinase et la Fatty Acid Synthase par O-GlcNAcylation au cours de la lipogenèse et de la prolifération cellulaire : Regulation of two key enzymes properties in glucido-lipidic metabolism hepatic, GlucoKinase and Fatty Acid Synthase by O-GlcNAcylation in lipogenesis and cell proliferation. (Doctoral Dissertation). Université Lille I – Sciences et Technologies. Retrieved from http://www.theses.fr/2016LIL10118

Chicago Manual of Style (16th Edition):

Baldini, Steffi. “Régulation des propriétés de deux enzymes clefs du métabolisme glucido-lipidique hépatique, la GlucoKinase et la Fatty Acid Synthase par O-GlcNAcylation au cours de la lipogenèse et de la prolifération cellulaire : Regulation of two key enzymes properties in glucido-lipidic metabolism hepatic, GlucoKinase and Fatty Acid Synthase by O-GlcNAcylation in lipogenesis and cell proliferation.” 2016. Doctoral Dissertation, Université Lille I – Sciences et Technologies. Accessed October 26, 2020. http://www.theses.fr/2016LIL10118.

MLA Handbook (7th Edition):

Baldini, Steffi. “Régulation des propriétés de deux enzymes clefs du métabolisme glucido-lipidique hépatique, la GlucoKinase et la Fatty Acid Synthase par O-GlcNAcylation au cours de la lipogenèse et de la prolifération cellulaire : Regulation of two key enzymes properties in glucido-lipidic metabolism hepatic, GlucoKinase and Fatty Acid Synthase by O-GlcNAcylation in lipogenesis and cell proliferation.” 2016. Web. 26 Oct 2020.

Vancouver:

Baldini S. Régulation des propriétés de deux enzymes clefs du métabolisme glucido-lipidique hépatique, la GlucoKinase et la Fatty Acid Synthase par O-GlcNAcylation au cours de la lipogenèse et de la prolifération cellulaire : Regulation of two key enzymes properties in glucido-lipidic metabolism hepatic, GlucoKinase and Fatty Acid Synthase by O-GlcNAcylation in lipogenesis and cell proliferation. [Internet] [Doctoral dissertation]. Université Lille I – Sciences et Technologies; 2016. [cited 2020 Oct 26]. Available from: http://www.theses.fr/2016LIL10118.

Council of Science Editors:

Baldini S. Régulation des propriétés de deux enzymes clefs du métabolisme glucido-lipidique hépatique, la GlucoKinase et la Fatty Acid Synthase par O-GlcNAcylation au cours de la lipogenèse et de la prolifération cellulaire : Regulation of two key enzymes properties in glucido-lipidic metabolism hepatic, GlucoKinase and Fatty Acid Synthase by O-GlcNAcylation in lipogenesis and cell proliferation. [Doctoral Dissertation]. Université Lille I – Sciences et Technologies; 2016. Available from: http://www.theses.fr/2016LIL10118

9. Olivier, Stéphanie. Etude de l’O-GlcNAcylation de la β-caténine : des désordres métaboliques à la cancérisation : Study of β-catenin O-GlcNAcylation : from metabolic disorders to cancerization processes.

Degree: Docteur es, Biochimie et biologie cellulaire, 2012, Université Lille I – Sciences et Technologies

Une mauvaise hygiène alimentaire et certains désordres métaboliques sont décrits depuis plusieurs années comme des facteurs de risque majeurs du cancer colorectal. Néanmoins, les mécanismes… (more)

Subjects/Keywords: O-GlcNAcylation; Béta-caténine; Dégradation protéasomale; 572.68

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APA (6th Edition):

Olivier, S. (2012). Etude de l’O-GlcNAcylation de la β-caténine : des désordres métaboliques à la cancérisation : Study of β-catenin O-GlcNAcylation : from metabolic disorders to cancerization processes. (Doctoral Dissertation). Université Lille I – Sciences et Technologies. Retrieved from http://www.theses.fr/2012LIL10193

Chicago Manual of Style (16th Edition):

Olivier, Stéphanie. “Etude de l’O-GlcNAcylation de la β-caténine : des désordres métaboliques à la cancérisation : Study of β-catenin O-GlcNAcylation : from metabolic disorders to cancerization processes.” 2012. Doctoral Dissertation, Université Lille I – Sciences et Technologies. Accessed October 26, 2020. http://www.theses.fr/2012LIL10193.

MLA Handbook (7th Edition):

Olivier, Stéphanie. “Etude de l’O-GlcNAcylation de la β-caténine : des désordres métaboliques à la cancérisation : Study of β-catenin O-GlcNAcylation : from metabolic disorders to cancerization processes.” 2012. Web. 26 Oct 2020.

Vancouver:

Olivier S. Etude de l’O-GlcNAcylation de la β-caténine : des désordres métaboliques à la cancérisation : Study of β-catenin O-GlcNAcylation : from metabolic disorders to cancerization processes. [Internet] [Doctoral dissertation]. Université Lille I – Sciences et Technologies; 2012. [cited 2020 Oct 26]. Available from: http://www.theses.fr/2012LIL10193.

Council of Science Editors:

Olivier S. Etude de l’O-GlcNAcylation de la β-caténine : des désordres métaboliques à la cancérisation : Study of β-catenin O-GlcNAcylation : from metabolic disorders to cancerization processes. [Doctoral Dissertation]. Université Lille I – Sciences et Technologies; 2012. Available from: http://www.theses.fr/2012LIL10193

10. Drougat, Ludivine. Etude de la dynamique de O-GlcNAcylation et identification de protéines différentiellement O-GlcNAcylées au cours de la transition G1/S du cycle cellulaire de cellules épithéliales humaines : Characterization of O-GlcNAc cycling and proteomic identification of differentially O-GlcNAcylated proteins during G1/S transition in human epithelial cells.

Degree: Docteur es, Sciences de la Vie et de la Santé, 2012, Université Lille I – Sciences et Technologies

La O-GlcNAcylation est une glycosylation dynamique et réversible sous le contrôle de la O-GlcNAc Transférase (OGT) qui transfère un résidu de GlcNAc sur les Ser/Thr… (more)

Subjects/Keywords: O-GlcNAcylation; Transition G1/S; 572.68

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APA (6th Edition):

Drougat, L. (2012). Etude de la dynamique de O-GlcNAcylation et identification de protéines différentiellement O-GlcNAcylées au cours de la transition G1/S du cycle cellulaire de cellules épithéliales humaines : Characterization of O-GlcNAc cycling and proteomic identification of differentially O-GlcNAcylated proteins during G1/S transition in human epithelial cells. (Doctoral Dissertation). Université Lille I – Sciences et Technologies. Retrieved from http://www.theses.fr/2012LIL10086

Chicago Manual of Style (16th Edition):

Drougat, Ludivine. “Etude de la dynamique de O-GlcNAcylation et identification de protéines différentiellement O-GlcNAcylées au cours de la transition G1/S du cycle cellulaire de cellules épithéliales humaines : Characterization of O-GlcNAc cycling and proteomic identification of differentially O-GlcNAcylated proteins during G1/S transition in human epithelial cells.” 2012. Doctoral Dissertation, Université Lille I – Sciences et Technologies. Accessed October 26, 2020. http://www.theses.fr/2012LIL10086.

MLA Handbook (7th Edition):

Drougat, Ludivine. “Etude de la dynamique de O-GlcNAcylation et identification de protéines différentiellement O-GlcNAcylées au cours de la transition G1/S du cycle cellulaire de cellules épithéliales humaines : Characterization of O-GlcNAc cycling and proteomic identification of differentially O-GlcNAcylated proteins during G1/S transition in human epithelial cells.” 2012. Web. 26 Oct 2020.

Vancouver:

Drougat L. Etude de la dynamique de O-GlcNAcylation et identification de protéines différentiellement O-GlcNAcylées au cours de la transition G1/S du cycle cellulaire de cellules épithéliales humaines : Characterization of O-GlcNAc cycling and proteomic identification of differentially O-GlcNAcylated proteins during G1/S transition in human epithelial cells. [Internet] [Doctoral dissertation]. Université Lille I – Sciences et Technologies; 2012. [cited 2020 Oct 26]. Available from: http://www.theses.fr/2012LIL10086.

Council of Science Editors:

Drougat L. Etude de la dynamique de O-GlcNAcylation et identification de protéines différentiellement O-GlcNAcylées au cours de la transition G1/S du cycle cellulaire de cellules épithéliales humaines : Characterization of O-GlcNAc cycling and proteomic identification of differentially O-GlcNAcylated proteins during G1/S transition in human epithelial cells. [Doctoral Dissertation]. Université Lille I – Sciences et Technologies; 2012. Available from: http://www.theses.fr/2012LIL10086

11. Baudoin, Léa. Rôle de la O-GlcNAcylation dans les effets pro-inflammatoires du LPS dans le macrophage : Role of O-GlcNAcylation on the pro-inflammatory effects of LPS in macrophages.

Degree: Docteur es, Physiologie, 2017, Sorbonne Paris Cité

 Au cours des dernières décennies, les modifications comportementales ont conduit à une forte augmentation de la prévalence des maladies métaboliques comme l’obésité et le diabète… (more)

Subjects/Keywords: O-GlcNAcylation; Macrophages; Maladies métaboliques; Inflammation; LPS; O-GlcNAcylation; Macrophages; Metabolic diseases; Inflammation; LPS; 616.4

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

APA (6th Edition):

Baudoin, L. (2017). Rôle de la O-GlcNAcylation dans les effets pro-inflammatoires du LPS dans le macrophage : Role of O-GlcNAcylation on the pro-inflammatory effects of LPS in macrophages. (Doctoral Dissertation). Sorbonne Paris Cité. Retrieved from http://www.theses.fr/2017USPCB098

Chicago Manual of Style (16th Edition):

Baudoin, Léa. “Rôle de la O-GlcNAcylation dans les effets pro-inflammatoires du LPS dans le macrophage : Role of O-GlcNAcylation on the pro-inflammatory effects of LPS in macrophages.” 2017. Doctoral Dissertation, Sorbonne Paris Cité. Accessed October 26, 2020. http://www.theses.fr/2017USPCB098.

MLA Handbook (7th Edition):

Baudoin, Léa. “Rôle de la O-GlcNAcylation dans les effets pro-inflammatoires du LPS dans le macrophage : Role of O-GlcNAcylation on the pro-inflammatory effects of LPS in macrophages.” 2017. Web. 26 Oct 2020.

Vancouver:

Baudoin L. Rôle de la O-GlcNAcylation dans les effets pro-inflammatoires du LPS dans le macrophage : Role of O-GlcNAcylation on the pro-inflammatory effects of LPS in macrophages. [Internet] [Doctoral dissertation]. Sorbonne Paris Cité; 2017. [cited 2020 Oct 26]. Available from: http://www.theses.fr/2017USPCB098.

Council of Science Editors:

Baudoin L. Rôle de la O-GlcNAcylation dans les effets pro-inflammatoires du LPS dans le macrophage : Role of O-GlcNAcylation on the pro-inflammatory effects of LPS in macrophages. [Doctoral Dissertation]. Sorbonne Paris Cité; 2017. Available from: http://www.theses.fr/2017USPCB098

12. Maffei, Benoit. Investigation of the role of tissue transglutaminase (TG2) in the infection by Chlamydia trachomatis : a key player in the metabolic rewiring of the host cell : Étude du rôle de la transglutaminase tissulaire (TG2) dans l'infection par Chlamydia trachomatis : un effecteur clé dans le détournement du métabolisme de la cellule hôte.

Degree: Docteur es, Microbiologie cellulaire, 2018, Sorbonne université

Chlamydia trachomatis est une bactérie pathogène intracellulaire obligatoire infectant l'Homme causant des infections sexuellement transmissibles et des infections oculaires. Au cours de son cycle infectieux… (more)

Subjects/Keywords: Chlamydia; Infection; TG2; O-GlcNAcylation; Métabolisme; GFPT; Chlamydia; Infection; TG2; O-GlcNAcylation; Metabolism; GFPT; 571.6

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APA (6th Edition):

Maffei, B. (2018). Investigation of the role of tissue transglutaminase (TG2) in the infection by Chlamydia trachomatis : a key player in the metabolic rewiring of the host cell : Étude du rôle de la transglutaminase tissulaire (TG2) dans l'infection par Chlamydia trachomatis : un effecteur clé dans le détournement du métabolisme de la cellule hôte. (Doctoral Dissertation). Sorbonne université. Retrieved from http://www.theses.fr/2018SORUS532

Chicago Manual of Style (16th Edition):

Maffei, Benoit. “Investigation of the role of tissue transglutaminase (TG2) in the infection by Chlamydia trachomatis : a key player in the metabolic rewiring of the host cell : Étude du rôle de la transglutaminase tissulaire (TG2) dans l'infection par Chlamydia trachomatis : un effecteur clé dans le détournement du métabolisme de la cellule hôte.” 2018. Doctoral Dissertation, Sorbonne université. Accessed October 26, 2020. http://www.theses.fr/2018SORUS532.

MLA Handbook (7th Edition):

Maffei, Benoit. “Investigation of the role of tissue transglutaminase (TG2) in the infection by Chlamydia trachomatis : a key player in the metabolic rewiring of the host cell : Étude du rôle de la transglutaminase tissulaire (TG2) dans l'infection par Chlamydia trachomatis : un effecteur clé dans le détournement du métabolisme de la cellule hôte.” 2018. Web. 26 Oct 2020.

Vancouver:

Maffei B. Investigation of the role of tissue transglutaminase (TG2) in the infection by Chlamydia trachomatis : a key player in the metabolic rewiring of the host cell : Étude du rôle de la transglutaminase tissulaire (TG2) dans l'infection par Chlamydia trachomatis : un effecteur clé dans le détournement du métabolisme de la cellule hôte. [Internet] [Doctoral dissertation]. Sorbonne université; 2018. [cited 2020 Oct 26]. Available from: http://www.theses.fr/2018SORUS532.

Council of Science Editors:

Maffei B. Investigation of the role of tissue transglutaminase (TG2) in the infection by Chlamydia trachomatis : a key player in the metabolic rewiring of the host cell : Étude du rôle de la transglutaminase tissulaire (TG2) dans l'infection par Chlamydia trachomatis : un effecteur clé dans le détournement du métabolisme de la cellule hôte. [Doctoral Dissertation]. Sorbonne université; 2018. Available from: http://www.theses.fr/2018SORUS532


Duke University

13. Sui, Ning. DELLA is O-Fucosylated by SPINDLY .

Degree: 2016, Duke University

  Plant growth and development are strictly regulated by internal hormonal signaling networks, which integrate and coordinate to promote plants’ adaptation and survival in the… (more)

Subjects/Keywords: Biology; Biochemistry; DELLA; GRAS; O-fucosylation; O-GlcNAcylation; SPINDLY (SPY)

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APA (6th Edition):

Sui, N. (2016). DELLA is O-Fucosylated by SPINDLY . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/13413

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):

Sui, Ning. “DELLA is O-Fucosylated by SPINDLY .” 2016. Thesis, Duke University. Accessed October 26, 2020. http://hdl.handle.net/10161/13413.

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

MLA Handbook (7th Edition):

Sui, Ning. “DELLA is O-Fucosylated by SPINDLY .” 2016. Web. 26 Oct 2020.

Vancouver:

Sui N. DELLA is O-Fucosylated by SPINDLY . [Internet] [Thesis]. Duke University; 2016. [cited 2020 Oct 26]. Available from: http://hdl.handle.net/10161/13413.

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

Council of Science Editors:

Sui N. DELLA is O-Fucosylated by SPINDLY . [Thesis]. Duke University; 2016. Available from: http://hdl.handle.net/10161/13413

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


University of California – San Diego

14. Bracha, Teva. The Topography of Neuronal Metabolism.

Degree: Biology, 2019, University of California – San Diego

 Maintaining homeostasis through energy metabolism is a crucial function all cells must perform. This is especially true in the context of the brain, where even… (more)

Subjects/Keywords: Biology; Metabolic Coupling; Metabolic Flux Assay; Mitochondria; Normalization; O-GlcNAcylation; Phosphofructokinase

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APA (6th Edition):

Bracha, T. (2019). The Topography of Neuronal Metabolism. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/79h9f6sd

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):

Bracha, Teva. “The Topography of Neuronal Metabolism.” 2019. Thesis, University of California – San Diego. Accessed October 26, 2020. http://www.escholarship.org/uc/item/79h9f6sd.

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

MLA Handbook (7th Edition):

Bracha, Teva. “The Topography of Neuronal Metabolism.” 2019. Web. 26 Oct 2020.

Vancouver:

Bracha T. The Topography of Neuronal Metabolism. [Internet] [Thesis]. University of California – San Diego; 2019. [cited 2020 Oct 26]. Available from: http://www.escholarship.org/uc/item/79h9f6sd.

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

Council of Science Editors:

Bracha T. The Topography of Neuronal Metabolism. [Thesis]. University of California – San Diego; 2019. Available from: http://www.escholarship.org/uc/item/79h9f6sd

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


University of Otago

15. Okolo, Chidinma. The role of O-GlcNAcylation in regulating the function and structure of cardiac ryanodine receptors .

Degree: University of Otago

 Diabetes mellitus is projected to be the leading cause of death worldwide by the year 2030 and has been linked to many cardiovascular disorders, which… (more)

Subjects/Keywords: O-GlcNAcylation; RyR2; CaMKII

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APA (6th Edition):

Okolo, C. (n.d.). The role of O-GlcNAcylation in regulating the function and structure of cardiac ryanodine receptors . (Doctoral Dissertation). University of Otago. Retrieved from http://hdl.handle.net/10523/9784

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Chicago Manual of Style (16th Edition):

Okolo, Chidinma. “The role of O-GlcNAcylation in regulating the function and structure of cardiac ryanodine receptors .” Doctoral Dissertation, University of Otago. Accessed October 26, 2020. http://hdl.handle.net/10523/9784.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

MLA Handbook (7th Edition):

Okolo, Chidinma. “The role of O-GlcNAcylation in regulating the function and structure of cardiac ryanodine receptors .” Web. 26 Oct 2020.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Vancouver:

Okolo C. The role of O-GlcNAcylation in regulating the function and structure of cardiac ryanodine receptors . [Internet] [Doctoral dissertation]. University of Otago; [cited 2020 Oct 26]. Available from: http://hdl.handle.net/10523/9784.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Council of Science Editors:

Okolo C. The role of O-GlcNAcylation in regulating the function and structure of cardiac ryanodine receptors . [Doctoral Dissertation]. University of Otago; Available from: http://hdl.handle.net/10523/9784

Note: this citation may be lacking information needed for this citation format:
No year of publication.

16. Berrabah, Wahiba. Régulation du récepteur nucléaire Farnesoid X Receptor par la voie de biosynthèse des hexosamines : Regulation of nuclear receptor Farnesoid X Receptor through the hexosamine biosynthesis pathway.

Degree: Docteur es, Biochimie et biologie moléculaire, 2013, Université Lille II – Droit et Santé

Chez les patients diabétiques, le flux hépatique du glucose est perturbé affectant les voies qui lui sont associées telle que la voie de biosynthèse des… (more)

Subjects/Keywords: FXR; O-GlcNAcylation; Récepteurs nucléaires; Farnesoid X Receptor; Nuclear receptor

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

APA (6th Edition):

Berrabah, W. (2013). Régulation du récepteur nucléaire Farnesoid X Receptor par la voie de biosynthèse des hexosamines : Regulation of nuclear receptor Farnesoid X Receptor through the hexosamine biosynthesis pathway. (Doctoral Dissertation). Université Lille II – Droit et Santé. Retrieved from http://www.theses.fr/2013LIL2S020

Chicago Manual of Style (16th Edition):

Berrabah, Wahiba. “Régulation du récepteur nucléaire Farnesoid X Receptor par la voie de biosynthèse des hexosamines : Regulation of nuclear receptor Farnesoid X Receptor through the hexosamine biosynthesis pathway.” 2013. Doctoral Dissertation, Université Lille II – Droit et Santé. Accessed October 26, 2020. http://www.theses.fr/2013LIL2S020.

MLA Handbook (7th Edition):

Berrabah, Wahiba. “Régulation du récepteur nucléaire Farnesoid X Receptor par la voie de biosynthèse des hexosamines : Regulation of nuclear receptor Farnesoid X Receptor through the hexosamine biosynthesis pathway.” 2013. Web. 26 Oct 2020.

Vancouver:

Berrabah W. Régulation du récepteur nucléaire Farnesoid X Receptor par la voie de biosynthèse des hexosamines : Regulation of nuclear receptor Farnesoid X Receptor through the hexosamine biosynthesis pathway. [Internet] [Doctoral dissertation]. Université Lille II – Droit et Santé 2013. [cited 2020 Oct 26]. Available from: http://www.theses.fr/2013LIL2S020.

Council of Science Editors:

Berrabah W. Régulation du récepteur nucléaire Farnesoid X Receptor par la voie de biosynthèse des hexosamines : Regulation of nuclear receptor Farnesoid X Receptor through the hexosamine biosynthesis pathway. [Doctoral Dissertation]. Université Lille II – Droit et Santé 2013. Available from: http://www.theses.fr/2013LIL2S020


University of Alberta

17. Ha, Jacqueline R. β-catenin is O-GlcNAc modified at Serine 23: Implications for β-catenin’s Subcellular Distribution and Transcriptional Activity.

Degree: MS, Medical Sciences-Paediatrics, 2012, University of Alberta

 β-catenin is a potent oncoprotein that serves as a structural anchor at the adherens junctions and as a transcriptional co-activator of the Wnt Signaling pathway.… (more)

Subjects/Keywords: β-catenin; β-catenin is O-GlcNAc modified at Serine 23; O-GlcNAcylation

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APA (6th Edition):

Ha, J. R. (2012). β-catenin is O-GlcNAc modified at Serine 23: Implications for β-catenin’s Subcellular Distribution and Transcriptional Activity. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/jd472x88t

Chicago Manual of Style (16th Edition):

Ha, Jacqueline R. “β-catenin is O-GlcNAc modified at Serine 23: Implications for β-catenin’s Subcellular Distribution and Transcriptional Activity.” 2012. Masters Thesis, University of Alberta. Accessed October 26, 2020. https://era.library.ualberta.ca/files/jd472x88t.

MLA Handbook (7th Edition):

Ha, Jacqueline R. “β-catenin is O-GlcNAc modified at Serine 23: Implications for β-catenin’s Subcellular Distribution and Transcriptional Activity.” 2012. Web. 26 Oct 2020.

Vancouver:

Ha JR. β-catenin is O-GlcNAc modified at Serine 23: Implications for β-catenin’s Subcellular Distribution and Transcriptional Activity. [Internet] [Masters thesis]. University of Alberta; 2012. [cited 2020 Oct 26]. Available from: https://era.library.ualberta.ca/files/jd472x88t.

Council of Science Editors:

Ha JR. β-catenin is O-GlcNAc modified at Serine 23: Implications for β-catenin’s Subcellular Distribution and Transcriptional Activity. [Masters Thesis]. University of Alberta; 2012. Available from: https://era.library.ualberta.ca/files/jd472x88t


University of Delaware

18. Hou, Ching-Wen. The sweet modification of Nod2, an innate immune receptor involved in Crohn's disease.

Degree: PhD, University of Delaware, Department of Chemistry and Biochemistry, 2017, University of Delaware

 The innate immune system, the first line of defense against pathogens, utilizes a series of receptors, including Toll-like receptors and Nod-like receptors, to generate the… (more)

Subjects/Keywords: Pure sciences; Crohn's disease; NF-kB activity; Nod2; O-GlcNAcylation; Protein stability

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APA (6th Edition):

Hou, C. (2017). The sweet modification of Nod2, an innate immune receptor involved in Crohn's disease. (Doctoral Dissertation). University of Delaware. Retrieved from http://udspace.udel.edu/handle/19716/23031

Chicago Manual of Style (16th Edition):

Hou, Ching-Wen. “The sweet modification of Nod2, an innate immune receptor involved in Crohn's disease.” 2017. Doctoral Dissertation, University of Delaware. Accessed October 26, 2020. http://udspace.udel.edu/handle/19716/23031.

MLA Handbook (7th Edition):

Hou, Ching-Wen. “The sweet modification of Nod2, an innate immune receptor involved in Crohn's disease.” 2017. Web. 26 Oct 2020.

Vancouver:

Hou C. The sweet modification of Nod2, an innate immune receptor involved in Crohn's disease. [Internet] [Doctoral dissertation]. University of Delaware; 2017. [cited 2020 Oct 26]. Available from: http://udspace.udel.edu/handle/19716/23031.

Council of Science Editors:

Hou C. The sweet modification of Nod2, an innate immune receptor involved in Crohn's disease. [Doctoral Dissertation]. University of Delaware; 2017. Available from: http://udspace.udel.edu/handle/19716/23031


University of Cambridge

19. Mason, Bethany Jane. Functional Analysis of the F-box protein Fbxl17.

Degree: PhD, 2020, University of Cambridge

 Advances in DNA sequencing technology have allowed detailed characterisation of cancer genomes and has highlighted the contribution of somatic structural variations to the mutational landscape… (more)

Subjects/Keywords: Breast cancer; FBXL17; Genome rearrangements; O-GlcNAcylation; Uap1; DNA damage; 53BP1; Ubiquitin; E3 ligase

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APA (6th Edition):

Mason, B. J. (2020). Functional Analysis of the F-box protein Fbxl17. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/304874

Chicago Manual of Style (16th Edition):

Mason, Bethany Jane. “Functional Analysis of the F-box protein Fbxl17.” 2020. Doctoral Dissertation, University of Cambridge. Accessed October 26, 2020. https://www.repository.cam.ac.uk/handle/1810/304874.

MLA Handbook (7th Edition):

Mason, Bethany Jane. “Functional Analysis of the F-box protein Fbxl17.” 2020. Web. 26 Oct 2020.

Vancouver:

Mason BJ. Functional Analysis of the F-box protein Fbxl17. [Internet] [Doctoral dissertation]. University of Cambridge; 2020. [cited 2020 Oct 26]. Available from: https://www.repository.cam.ac.uk/handle/1810/304874.

Council of Science Editors:

Mason BJ. Functional Analysis of the F-box protein Fbxl17. [Doctoral Dissertation]. University of Cambridge; 2020. Available from: https://www.repository.cam.ac.uk/handle/1810/304874

20. Nunes, Paulo Sergio Gonçalves. Desenvolvimento de método de preparação de biomarcadores moleculares relacionados a N-acetilglicosaminas para estudos de sinalização celular.

Degree: Mestrado, Produtos Naturais e Sintéticos, 2014, University of São Paulo

Os carboidratos apresentam-se envolvidos em diversos eventos celulares, tais como geração de energia, sustentação celular, reconhecimento celular, processos de sinalização, etc. A OGlcNAcilação, uma das… (more)

Subjects/Keywords: Carboidratos fluorados; Cell signaling; Fluorinated carbohydrates; Fluorinated gluco-aminoacids; Glicoaminoácidos fluorados; O-GlcNAcilação; O-GlcNAcylation; Sinalização celular.

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APA (6th Edition):

Nunes, P. S. G. (2014). Desenvolvimento de método de preparação de biomarcadores moleculares relacionados a N-acetilglicosaminas para estudos de sinalização celular. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/60/60138/tde-21052014-153215/ ;

Chicago Manual of Style (16th Edition):

Nunes, Paulo Sergio Gonçalves. “Desenvolvimento de método de preparação de biomarcadores moleculares relacionados a N-acetilglicosaminas para estudos de sinalização celular.” 2014. Masters Thesis, University of São Paulo. Accessed October 26, 2020. http://www.teses.usp.br/teses/disponiveis/60/60138/tde-21052014-153215/ ;.

MLA Handbook (7th Edition):

Nunes, Paulo Sergio Gonçalves. “Desenvolvimento de método de preparação de biomarcadores moleculares relacionados a N-acetilglicosaminas para estudos de sinalização celular.” 2014. Web. 26 Oct 2020.

Vancouver:

Nunes PSG. Desenvolvimento de método de preparação de biomarcadores moleculares relacionados a N-acetilglicosaminas para estudos de sinalização celular. [Internet] [Masters thesis]. University of São Paulo; 2014. [cited 2020 Oct 26]. Available from: http://www.teses.usp.br/teses/disponiveis/60/60138/tde-21052014-153215/ ;.

Council of Science Editors:

Nunes PSG. Desenvolvimento de método de preparação de biomarcadores moleculares relacionados a N-acetilglicosaminas para estudos de sinalização celular. [Masters Thesis]. University of São Paulo; 2014. Available from: http://www.teses.usp.br/teses/disponiveis/60/60138/tde-21052014-153215/ ;

21. Lima, Victor Vitorino. Papel da O-glicosilação com N-acetil-glucosamina (O-GlcNAc) nas alterações vasculares associadas a altos níveis de endotelina-1.

Degree: PhD, Farmacologia, 2012, University of São Paulo

 LIMA, V.V. Papel da O-glicosilação com N-acetil-glucosamina (O-GlcNAc) nas alterações vasculares associadas a altos níveis de endotelina-1. 2012. 106 f. Tese (Doutorado) - Faculdade de… (more)

Subjects/Keywords: Endotelina-1; Endothelin-1; O-GlcNAcylation (O-GlcNAc); O-Glicosilação-NAc; Reatividade Vascular; RhoA/Rho-kinase pathway.; Vascular reactivity; Via de sinalização RhoA/Rho-cinase.

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APA (6th Edition):

Lima, V. V. (2012). Papel da O-glicosilação com N-acetil-glucosamina (O-GlcNAc) nas alterações vasculares associadas a altos níveis de endotelina-1. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/17/17133/tde-15082013-114532/ ;

Chicago Manual of Style (16th Edition):

Lima, Victor Vitorino. “Papel da O-glicosilação com N-acetil-glucosamina (O-GlcNAc) nas alterações vasculares associadas a altos níveis de endotelina-1.” 2012. Doctoral Dissertation, University of São Paulo. Accessed October 26, 2020. http://www.teses.usp.br/teses/disponiveis/17/17133/tde-15082013-114532/ ;.

MLA Handbook (7th Edition):

Lima, Victor Vitorino. “Papel da O-glicosilação com N-acetil-glucosamina (O-GlcNAc) nas alterações vasculares associadas a altos níveis de endotelina-1.” 2012. Web. 26 Oct 2020.

Vancouver:

Lima VV. Papel da O-glicosilação com N-acetil-glucosamina (O-GlcNAc) nas alterações vasculares associadas a altos níveis de endotelina-1. [Internet] [Doctoral dissertation]. University of São Paulo; 2012. [cited 2020 Oct 26]. Available from: http://www.teses.usp.br/teses/disponiveis/17/17133/tde-15082013-114532/ ;.

Council of Science Editors:

Lima VV. Papel da O-glicosilação com N-acetil-glucosamina (O-GlcNAc) nas alterações vasculares associadas a altos níveis de endotelina-1. [Doctoral Dissertation]. University of São Paulo; 2012. Available from: http://www.teses.usp.br/teses/disponiveis/17/17133/tde-15082013-114532/ ;

22. Porez, Geoffrey. Nouvelles propriétés hépatiques des récepteurs nucléaires FXR et Rev-Erb Alpha : New liver function of nuclear receptors FXR and Rev-Erb Alpha.

Degree: Docteur es, Biochimie et biologie moléculaire, 2014, Université Lille II – Droit et Santé

Les orosomucoïdes, membres de la superfamille des lipocalines, sont parmi les protéinesplasmatiques les plus abondantes. Ce sont des protéines de la phase aiguë de l’inflammationsecrétées… (more)

Subjects/Keywords: FXR; Récepteurs nucléaires; Rev-Erbx; Orosomucoïdes; O-GlcNAcylation; Foie; Récepteurs nucléaires; Nuclear bile acid receptor; Farnesoid x Receptor (FXR); ORMs

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APA (6th Edition):

Porez, G. (2014). Nouvelles propriétés hépatiques des récepteurs nucléaires FXR et Rev-Erb Alpha : New liver function of nuclear receptors FXR and Rev-Erb Alpha. (Doctoral Dissertation). Université Lille II – Droit et Santé. Retrieved from http://www.theses.fr/2014LIL2S015

Chicago Manual of Style (16th Edition):

Porez, Geoffrey. “Nouvelles propriétés hépatiques des récepteurs nucléaires FXR et Rev-Erb Alpha : New liver function of nuclear receptors FXR and Rev-Erb Alpha.” 2014. Doctoral Dissertation, Université Lille II – Droit et Santé. Accessed October 26, 2020. http://www.theses.fr/2014LIL2S015.

MLA Handbook (7th Edition):

Porez, Geoffrey. “Nouvelles propriétés hépatiques des récepteurs nucléaires FXR et Rev-Erb Alpha : New liver function of nuclear receptors FXR and Rev-Erb Alpha.” 2014. Web. 26 Oct 2020.

Vancouver:

Porez G. Nouvelles propriétés hépatiques des récepteurs nucléaires FXR et Rev-Erb Alpha : New liver function of nuclear receptors FXR and Rev-Erb Alpha. [Internet] [Doctoral dissertation]. Université Lille II – Droit et Santé 2014. [cited 2020 Oct 26]. Available from: http://www.theses.fr/2014LIL2S015.

Council of Science Editors:

Porez G. Nouvelles propriétés hépatiques des récepteurs nucléaires FXR et Rev-Erb Alpha : New liver function of nuclear receptors FXR and Rev-Erb Alpha. [Doctoral Dissertation]. Université Lille II – Droit et Santé 2014. Available from: http://www.theses.fr/2014LIL2S015


Wayne State University

23. Ndombera, Fidelis. Carbohydrate-Based Inducers Of Cellular Stress For Targeting Cancer Cell Metabolism.

Degree: PhD, Chemistry, 2018, Wayne State University

  ABSTRACT CARBOHYDRATE-BASED INDUCERS OF CELLULAR STRESS FOR TARGETING CANCER CELL METABOLISM by FIDELIS TOLOYI NDOMBERA May 2018 Advisor: Dr. Young-Hoon Ahn Major: Chemistry (Biochemistry)… (more)

Subjects/Keywords: 2-DEOXY-D-GLUCOSE; AMPK; p53; Anticancer agent; ER stress/N-glycosylation inhibitor; Metabolomics/O-GlcNAcylation; Reactive oxygen species inducer; Biochemistry; Cell Biology; Chemistry

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APA (6th Edition):

Ndombera, F. (2018). Carbohydrate-Based Inducers Of Cellular Stress For Targeting Cancer Cell Metabolism. (Doctoral Dissertation). Wayne State University. Retrieved from https://digitalcommons.wayne.edu/oa_dissertations/1951

Chicago Manual of Style (16th Edition):

Ndombera, Fidelis. “Carbohydrate-Based Inducers Of Cellular Stress For Targeting Cancer Cell Metabolism.” 2018. Doctoral Dissertation, Wayne State University. Accessed October 26, 2020. https://digitalcommons.wayne.edu/oa_dissertations/1951.

MLA Handbook (7th Edition):

Ndombera, Fidelis. “Carbohydrate-Based Inducers Of Cellular Stress For Targeting Cancer Cell Metabolism.” 2018. Web. 26 Oct 2020.

Vancouver:

Ndombera F. Carbohydrate-Based Inducers Of Cellular Stress For Targeting Cancer Cell Metabolism. [Internet] [Doctoral dissertation]. Wayne State University; 2018. [cited 2020 Oct 26]. Available from: https://digitalcommons.wayne.edu/oa_dissertations/1951.

Council of Science Editors:

Ndombera F. Carbohydrate-Based Inducers Of Cellular Stress For Targeting Cancer Cell Metabolism. [Doctoral Dissertation]. Wayne State University; 2018. Available from: https://digitalcommons.wayne.edu/oa_dissertations/1951

24. 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 https://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 ; https://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 26, 2020. https://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 ; https://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. 26 Oct 2020.

Vancouver:

Shi J. Peptide substrate-assisted study of O-GlcNAc transferase and O-GlcNAcylation. [Internet] [Doctoral dissertation]. University Utrecht; 2018. [cited 2020 Oct 26]. Available from: https://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 ; https://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: https://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 ; https://dspace.library.uu.nl/handle/1874/363526


Université de Montréal

25. Iannantuono, Nicholas. Régulation du facteur de transcription FOXK1 par O-GlcNAcylation : implications dans la différenciation adipocytaire.

Degree: 2016, Université de Montréal

Subjects/Keywords: FOXK1; FOXK2; BAP1; OGT; Ubiquitination; O-GlcNAcylation; Adipogenèse; Cancer; Métabolisme; Polycomb; Adipogenesis; Metabolism; Biology - Cell / Biologie - Cellule (UMI : 0379)

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

APA (6th Edition):

Iannantuono, N. (2016). Régulation du facteur de transcription FOXK1 par O-GlcNAcylation : implications dans la différenciation adipocytaire. (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/13646

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):

Iannantuono, Nicholas. “Régulation du facteur de transcription FOXK1 par O-GlcNAcylation : implications dans la différenciation adipocytaire.” 2016. Thesis, Université de Montréal. Accessed October 26, 2020. http://hdl.handle.net/1866/13646.

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

MLA Handbook (7th Edition):

Iannantuono, Nicholas. “Régulation du facteur de transcription FOXK1 par O-GlcNAcylation : implications dans la différenciation adipocytaire.” 2016. Web. 26 Oct 2020.

Vancouver:

Iannantuono N. Régulation du facteur de transcription FOXK1 par O-GlcNAcylation : implications dans la différenciation adipocytaire. [Internet] [Thesis]. Université de Montréal; 2016. [cited 2020 Oct 26]. Available from: http://hdl.handle.net/1866/13646.

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

Council of Science Editors:

Iannantuono N. Régulation du facteur de transcription FOXK1 par O-GlcNAcylation : implications dans la différenciation adipocytaire. [Thesis]. Université de Montréal; 2016. Available from: http://hdl.handle.net/1866/13646

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


Université de Montréal

26. Gagnon, Jessica. Caractérisation du rôle transcriptionnel et épigénétique de l’O-GlcNAcylation des histones et du facteur de transcription FOXK1.

Degree: 2016, Université de Montréal

Subjects/Keywords: OGT; O-GlcNAcylation; Histones; H2BS112; BAP1; FOXK1; Transcription; Épigénétique; Chromatine; Adipogenèse; Epigenetic; Chromatin; Adipogenesis; Biology - Cell / Biologie - Cellule (UMI : 0379)

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APA (6th Edition):

Gagnon, J. (2016). Caractérisation du rôle transcriptionnel et épigénétique de l’O-GlcNAcylation des histones et du facteur de transcription FOXK1. (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/13659

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):

Gagnon, Jessica. “Caractérisation du rôle transcriptionnel et épigénétique de l’O-GlcNAcylation des histones et du facteur de transcription FOXK1.” 2016. Thesis, Université de Montréal. Accessed October 26, 2020. http://hdl.handle.net/1866/13659.

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

MLA Handbook (7th Edition):

Gagnon, Jessica. “Caractérisation du rôle transcriptionnel et épigénétique de l’O-GlcNAcylation des histones et du facteur de transcription FOXK1.” 2016. Web. 26 Oct 2020.

Vancouver:

Gagnon J. Caractérisation du rôle transcriptionnel et épigénétique de l’O-GlcNAcylation des histones et du facteur de transcription FOXK1. [Internet] [Thesis]. Université de Montréal; 2016. [cited 2020 Oct 26]. Available from: http://hdl.handle.net/1866/13659.

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

Council of Science Editors:

Gagnon J. Caractérisation du rôle transcriptionnel et épigénétique de l’O-GlcNAcylation des histones et du facteur de transcription FOXK1. [Thesis]. Université de Montréal; 2016. Available from: http://hdl.handle.net/1866/13659

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

27. Gao, Xiaofei. MODULATION OF THE NF-KAPPA B SIGNALING PATHWAY BY THE BACTERIAL TYPE III SECRETION SYSTEM EFFECTORS.

Degree: PhD, Microbiology, Molecular Genetics & Immunology, 2012, University of Kansas

 The type III secretion system (T3SS) is a bacterial injection system expressed by many Gram-negative bacteria. During the last two decades, the repertoire of T3SS… (more)

Subjects/Keywords: Microbiology; Immunology; Nf-kb; O-glcnacylation; Rps3; Type three secretion system

…169
 NleB is a glycosyltransferase and O-GlcNAcylates GAPDH… …177
 NleB disrupts the interaction between GAPDH and TRAF2 through its O-GlcNAc transferase… …185
 The O-GlcNAc transferase activity is required for the function of NleB on NF-κB… …182 Fig. 45. NleB O-GlcNAcylates GAPDH… …187 Fig. 46. The The O-GlcNAc transferase activity is essential for the function of NleB on… 

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APA (6th Edition):

Gao, X. (2012). MODULATION OF THE NF-KAPPA B SIGNALING PATHWAY BY THE BACTERIAL TYPE III SECRETION SYSTEM EFFECTORS. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/10239

Chicago Manual of Style (16th Edition):

Gao, Xiaofei. “MODULATION OF THE NF-KAPPA B SIGNALING PATHWAY BY THE BACTERIAL TYPE III SECRETION SYSTEM EFFECTORS.” 2012. Doctoral Dissertation, University of Kansas. Accessed October 26, 2020. http://hdl.handle.net/1808/10239.

MLA Handbook (7th Edition):

Gao, Xiaofei. “MODULATION OF THE NF-KAPPA B SIGNALING PATHWAY BY THE BACTERIAL TYPE III SECRETION SYSTEM EFFECTORS.” 2012. Web. 26 Oct 2020.

Vancouver:

Gao X. MODULATION OF THE NF-KAPPA B SIGNALING PATHWAY BY THE BACTERIAL TYPE III SECRETION SYSTEM EFFECTORS. [Internet] [Doctoral dissertation]. University of Kansas; 2012. [cited 2020 Oct 26]. Available from: http://hdl.handle.net/1808/10239.

Council of Science Editors:

Gao X. MODULATION OF THE NF-KAPPA B SIGNALING PATHWAY BY THE BACTERIAL TYPE III SECRETION SYSTEM EFFECTORS. [Doctoral Dissertation]. University of Kansas; 2012. Available from: http://hdl.handle.net/1808/10239


University of Queensland

28. Ahmad, Waqar. Metabolic study of Alzheimer’s disease using mutant C. elegans.

Degree: School of Biological Sciences, 2017, University of Queensland

Subjects/Keywords: Alzheimers-Disease; glucose energy metabolism; Dihydrolipoamide dehydrogenase; beta-amyloid; Tau protein (Tau); Oligomerization; phosphorylation; O-GlcNAcylation; neurotoxicity; phosphine; 0304 Medicinal and Biomolecular Chemistry; 0601 Biochemistry and Cell Biology; 1109 Neurosciences

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APA (6th Edition):

Ahmad, W. (2017). Metabolic study of Alzheimer’s disease using mutant C. elegans. (Thesis). University of Queensland. Retrieved from http://espace.library.uq.edu.au/view/UQ:535405

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):

Ahmad, Waqar. “Metabolic study of Alzheimer’s disease using mutant C. elegans.” 2017. Thesis, University of Queensland. Accessed October 26, 2020. http://espace.library.uq.edu.au/view/UQ:535405.

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

MLA Handbook (7th Edition):

Ahmad, Waqar. “Metabolic study of Alzheimer’s disease using mutant C. elegans.” 2017. Web. 26 Oct 2020.

Vancouver:

Ahmad W. Metabolic study of Alzheimer’s disease using mutant C. elegans. [Internet] [Thesis]. University of Queensland; 2017. [cited 2020 Oct 26]. Available from: http://espace.library.uq.edu.au/view/UQ:535405.

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

Council of Science Editors:

Ahmad W. Metabolic study of Alzheimer’s disease using mutant C. elegans. [Thesis]. University of Queensland; 2017. Available from: http://espace.library.uq.edu.au/view/UQ:535405

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


Université de Montréal

29. Mashtalir, Nazar. Regulation of BAP1 tumor suppressor complex by post-translational modifications.

Degree: 2014, Université de Montréal

Subjects/Keywords: Chromatine; Marque épigénctique; O-GlcNAcylation; Régulation protéolytique; Ubiquitination; Déubiquitinase; Ubiquitine ligase atypique; Activité auto-catalytique; Cancer; O-linked beta-N-acetylglucosamine transferase; Chromatin; Epigenetic mark; Proteolytic processing; Ubiquitination; Deubiquitinase; Atypical ubiquitin ligase; Autocatalytic activity; Host cell factor 1; BRCA1-associated protein 1; UBE2O; Biology - Molecular / Biologie - Biologie moléculaire (UMI : 0307)

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APA (6th Edition):

Mashtalir, N. (2014). Regulation of BAP1 tumor suppressor complex by post-translational modifications. (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/12772

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):

Mashtalir, Nazar. “Regulation of BAP1 tumor suppressor complex by post-translational modifications.” 2014. Thesis, Université de Montréal. Accessed October 26, 2020. http://hdl.handle.net/1866/12772.

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

MLA Handbook (7th Edition):

Mashtalir, Nazar. “Regulation of BAP1 tumor suppressor complex by post-translational modifications.” 2014. Web. 26 Oct 2020.

Vancouver:

Mashtalir N. Regulation of BAP1 tumor suppressor complex by post-translational modifications. [Internet] [Thesis]. Université de Montréal; 2014. [cited 2020 Oct 26]. Available from: http://hdl.handle.net/1866/12772.

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

Council of Science Editors:

Mashtalir N. Regulation of BAP1 tumor suppressor complex by post-translational modifications. [Thesis]. Université de Montréal; 2014. Available from: http://hdl.handle.net/1866/12772

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

30. Daou, Salima. Étude fonctionnelle d’un nouveau complexe multi-enzymatique régulant l’épigénome.

Degree: 2016, Université de Montréal

Subjects/Keywords: Chromatine; Modifications post-traductionnelles des histones; Histone H2A K118/K119 monoubiquitination; Protéines Polycombes; Complexe PR-DUB; Ubiquitination; Déubiquitination; BAP1; HCF-1; OGT; O-GlcNAcylation; Clivage protéolytique; ASXL1; ASXL2; Prolifération cellulaire; Chromatin; Histones post-translational modifications; Polycomb proteins; Proteolytic cleavage; Cell proliferation; Deubiquitination; PR-DUB complex; Biology - Molecular / Biologie - Biologie moléculaire (UMI : 0307)

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APA (6th Edition):

Daou, S. (2016). Étude fonctionnelle d’un nouveau complexe multi-enzymatique régulant l’épigénome. (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/15975

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):

Daou, Salima. “Étude fonctionnelle d’un nouveau complexe multi-enzymatique régulant l’épigénome.” 2016. Thesis, Université de Montréal. Accessed October 26, 2020. http://hdl.handle.net/1866/15975.

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

MLA Handbook (7th Edition):

Daou, Salima. “Étude fonctionnelle d’un nouveau complexe multi-enzymatique régulant l’épigénome.” 2016. Web. 26 Oct 2020.

Vancouver:

Daou S. Étude fonctionnelle d’un nouveau complexe multi-enzymatique régulant l’épigénome. [Internet] [Thesis]. Université de Montréal; 2016. [cited 2020 Oct 26]. Available from: http://hdl.handle.net/1866/15975.

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

Council of Science Editors:

Daou S. Étude fonctionnelle d’un nouveau complexe multi-enzymatique régulant l’épigénome. [Thesis]. Université de Montréal; 2016. Available from: http://hdl.handle.net/1866/15975

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

[1] [2]

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