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You searched for subject:(O GlcNAcylation). Showing records 1 – 25 of 25 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 September 17, 2019. 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. 17 Sep 2019.

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 2019 Sep 17]. 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 September 17, 2019. 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. 17 Sep 2019.

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 2019 Sep 17]. 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. 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 September 17, 2019. 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. 17 Sep 2019.

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 2019 Sep 17]. 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

4. 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 September 17, 2019. 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. 17 Sep 2019.

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 2019 Sep 17]. 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

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 September 17, 2019. 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. 17 Sep 2019.

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 2019 Sep 17]. 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. 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 September 17, 2019. 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. 17 Sep 2019.

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 2019 Sep 17]. 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

7. 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 September 17, 2019. 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. 17 Sep 2019.

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 2019 Sep 17]. 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

8. 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 September 17, 2019. 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. 17 Sep 2019.

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 2019 Sep 17]. 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

9. 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 September 17, 2019. 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. 17 Sep 2019.

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 2019 Sep 17]. 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

10. 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 (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 September 17, 2019. 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. 17 Sep 2019.

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 2019 Sep 17]. 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


Duke University

11. 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 September 17, 2019. 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. 17 Sep 2019.

Vancouver:

Sui N. DELLA is O-Fucosylated by SPINDLY . [Internet] [Thesis]. Duke University; 2016. [cited 2019 Sep 17]. 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

12. 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 (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 September 17, 2019. 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. 17 Sep 2019.

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 2019 Sep 17]. 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 California – San Diego

13. 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 September 17, 2019. 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. 17 Sep 2019.

Vancouver:

Bracha T. The Topography of Neuronal Metabolism. [Internet] [Thesis]. University of California – San Diego; 2019. [cited 2019 Sep 17]. 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 Alberta

14. 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 September 17, 2019. 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. 17 Sep 2019.

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 2019 Sep 17]. 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


Université de Montréal

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

Degree: 2016, Université de Montréal

 Les modifications post-traductionnelles telles que la phosphorylation, l’OGlcNAcylation et l’ubiquitination jouent des rôles critiques dans la coordination des fonctions protéiques et par conséquent influencent grandement… (more)

Subjects/Keywords: FOXK1; FOXK2; BAP1; OGT; Ubiquitination; O-GlcNAcylation; Adipogenèse; Cancer; Métabolisme; Polycomb; Adipogenesis; Metabolism

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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 September 17, 2019. 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. 17 Sep 2019.

Vancouver:

Iannantuono N. Régulation du facteur de transcription FOXK1 par O-GlcNAcylation : implications dans la différenciation adipocytaire . [Internet] [Thesis]. Université de Montréal; 2016. [cited 2019 Sep 17]. 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

16. 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

 L’O-GlcNAcylation est une modification post-traductionnelle qui consiste en l’ajout covalent du N-acetylglucosamine au groupement hydroxyle des sérines et thréonines des protéines nucléaires et cytoplasmiques. Ce… (more)

Subjects/Keywords: OGT; O-GlcNAcylation; Histones; H2BS112; BAP1; FOXK1; Transcription; Épigénétique; Chromatine; Adipogenèse; Epigenetic; Chromatin; Adipogenesis

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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 September 17, 2019. 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. 17 Sep 2019.

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 2019 Sep 17]. 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


University of Delaware

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

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

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 September 17, 2019. 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. 17 Sep 2019.

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 2019 Sep 17]. 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

18. 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 September 17, 2019. 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. 17 Sep 2019.

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 2019 Sep 17]. 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/ ;

19. 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 September 17, 2019. 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. 17 Sep 2019.

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 2019 Sep 17]. 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

20. 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 September 17, 2019. 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. 17 Sep 2019.

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 2019 Sep 17]. 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/ ;

21. 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 September 17, 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. 17 Sep 2019.

Vancouver:

Shi J. Peptide substrate-assisted study of O-GlcNAc transferase and O-GlcNAcylation. [Internet] [Doctoral dissertation]. University Utrecht; 2018. [cited 2019 Sep 17]. 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


Université de Montréal

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

Degree: 2014, Université de Montréal

 Le régulateur transcriptionnel BAP1 est une déubiquitinase nucléaire (DUB) dont le substrat est l’histone H2A modifiée par monoubiquitination au niveau des residus lysines 118 et… (more)

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

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

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 September 17, 2019. 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. 17 Sep 2019.

Vancouver:

Mashtalir N. Regulation of BAP1 tumor suppressor complex by post-translational modifications . [Internet] [Thesis]. Université de Montréal; 2014. [cited 2019 Sep 17]. 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

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

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 September 17, 2019. 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. 17 Sep 2019.

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 2019 Sep 17]. 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

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

Degree: 2016, Université de Montréal

 L’ubiquitination, une modification post-traductionnelle importante pour le contrôle de nombreux processus cellulaires, est une réaction réversible. La réaction inverse, nommée déubiquitination est catalysée par les… (more)

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

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

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 September 17, 2019. 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. 17 Sep 2019.

Vancouver:

Daou S. Étude fonctionnelle d’un nouveau complexe multi-enzymatique régulant l’épigénome . [Internet] [Thesis]. Université de Montréal; 2016. [cited 2019 Sep 17]. 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


University of Queensland

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

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 September 17, 2019. 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. 17 Sep 2019.

Vancouver:

Ahmad W. Metabolic study of Alzheimer’s disease using mutant C. elegans. [Internet] [Thesis]. University of Queensland; 2017. [cited 2019 Sep 17]. 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

.