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You searched for subject:(FMRP). Showing records 1 – 30 of 42 total matches.

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1. Piazzon, Nathalie. Rôle du complexe de Survie des MotoNeurones (SMN) dans la biogenèse des particules ARN/Protéines : Function of the Survival of Motor Neuron (SMN) complex in the biogenesis of RNA/protein particles.

Degree: Docteur es, Biologie Moléculaire et Cellulaire, 2008, Université Henri Poincaré – Nancy I

L’amyotrophie spinale (SMA) est causée par une réduction du taux de la protéine de Survie des MotoNeurones (SMN). Cette protéine est associée aux protéines Gemin… (more)

Subjects/Keywords: Protéine FMRP

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

APA (6th Edition):

Piazzon, N. (2008). Rôle du complexe de Survie des MotoNeurones (SMN) dans la biogenèse des particules ARN/Protéines : Function of the Survival of Motor Neuron (SMN) complex in the biogenesis of RNA/protein particles. (Doctoral Dissertation). Université Henri Poincaré – Nancy I. Retrieved from http://www.theses.fr/2008NAN10063

Chicago Manual of Style (16th Edition):

Piazzon, Nathalie. “Rôle du complexe de Survie des MotoNeurones (SMN) dans la biogenèse des particules ARN/Protéines : Function of the Survival of Motor Neuron (SMN) complex in the biogenesis of RNA/protein particles.” 2008. Doctoral Dissertation, Université Henri Poincaré – Nancy I. Accessed March 05, 2021. http://www.theses.fr/2008NAN10063.

MLA Handbook (7th Edition):

Piazzon, Nathalie. “Rôle du complexe de Survie des MotoNeurones (SMN) dans la biogenèse des particules ARN/Protéines : Function of the Survival of Motor Neuron (SMN) complex in the biogenesis of RNA/protein particles.” 2008. Web. 05 Mar 2021.

Vancouver:

Piazzon N. Rôle du complexe de Survie des MotoNeurones (SMN) dans la biogenèse des particules ARN/Protéines : Function of the Survival of Motor Neuron (SMN) complex in the biogenesis of RNA/protein particles. [Internet] [Doctoral dissertation]. Université Henri Poincaré – Nancy I; 2008. [cited 2021 Mar 05]. Available from: http://www.theses.fr/2008NAN10063.

Council of Science Editors:

Piazzon N. Rôle du complexe de Survie des MotoNeurones (SMN) dans la biogenèse des particules ARN/Protéines : Function of the Survival of Motor Neuron (SMN) complex in the biogenesis of RNA/protein particles. [Doctoral Dissertation]. Université Henri Poincaré – Nancy I; 2008. Available from: http://www.theses.fr/2008NAN10063

2. Abekhoukh-Achiou, Sabiha. Étude de la fonction de FMRP par l'analyse de ses interacteurs : Function of FMRP by analyzing its interactors.

Degree: Docteur es, Interactions moléculaires et cellulaires, 2014, Nice

Le Syndrome de l'X fragile (FXS) est la forme la plus fréquente de retard mental héréditaire. Il est causé par l’inactivation du gène FMR1 codant… (more)

Subjects/Keywords: FXS; FMRP; GRK4; CYFIP1; CYFIP2; FXS; FMRP; GRK4; CYFIP1; CYFIP2

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APA (6th Edition):

Abekhoukh-Achiou, S. (2014). Étude de la fonction de FMRP par l'analyse de ses interacteurs : Function of FMRP by analyzing its interactors. (Doctoral Dissertation). Nice. Retrieved from http://www.theses.fr/2014NICE4029

Chicago Manual of Style (16th Edition):

Abekhoukh-Achiou, Sabiha. “Étude de la fonction de FMRP par l'analyse de ses interacteurs : Function of FMRP by analyzing its interactors.” 2014. Doctoral Dissertation, Nice. Accessed March 05, 2021. http://www.theses.fr/2014NICE4029.

MLA Handbook (7th Edition):

Abekhoukh-Achiou, Sabiha. “Étude de la fonction de FMRP par l'analyse de ses interacteurs : Function of FMRP by analyzing its interactors.” 2014. Web. 05 Mar 2021.

Vancouver:

Abekhoukh-Achiou S. Étude de la fonction de FMRP par l'analyse de ses interacteurs : Function of FMRP by analyzing its interactors. [Internet] [Doctoral dissertation]. Nice; 2014. [cited 2021 Mar 05]. Available from: http://www.theses.fr/2014NICE4029.

Council of Science Editors:

Abekhoukh-Achiou S. Étude de la fonction de FMRP par l'analyse de ses interacteurs : Function of FMRP by analyzing its interactors. [Doctoral Dissertation]. Nice; 2014. Available from: http://www.theses.fr/2014NICE4029

3. Khayachi, Anouar. Rôles fonctionnels de la SUMOylation de FMRP « Fragile X Mental Retardation Protein » : Functional roles of FMRP sumoylation.

Degree: Docteur es, Interactions moléculaires et cellulaires, 2015, Nice

Le syndrome de l’X-fragile est la forme la plus fréquente de déficience intellectuelle héréditaire liée au chromosome X. Cette maladie résulte de la mutation du… (more)

Subjects/Keywords: Sumoylation; X fragile; FMRP; Sumoylation; Fragile X; FMRP

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APA (6th Edition):

Khayachi, A. (2015). Rôles fonctionnels de la SUMOylation de FMRP « Fragile X Mental Retardation Protein » : Functional roles of FMRP sumoylation. (Doctoral Dissertation). Nice. Retrieved from http://www.theses.fr/2015NICE4031

Chicago Manual of Style (16th Edition):

Khayachi, Anouar. “Rôles fonctionnels de la SUMOylation de FMRP « Fragile X Mental Retardation Protein » : Functional roles of FMRP sumoylation.” 2015. Doctoral Dissertation, Nice. Accessed March 05, 2021. http://www.theses.fr/2015NICE4031.

MLA Handbook (7th Edition):

Khayachi, Anouar. “Rôles fonctionnels de la SUMOylation de FMRP « Fragile X Mental Retardation Protein » : Functional roles of FMRP sumoylation.” 2015. Web. 05 Mar 2021.

Vancouver:

Khayachi A. Rôles fonctionnels de la SUMOylation de FMRP « Fragile X Mental Retardation Protein » : Functional roles of FMRP sumoylation. [Internet] [Doctoral dissertation]. Nice; 2015. [cited 2021 Mar 05]. Available from: http://www.theses.fr/2015NICE4031.

Council of Science Editors:

Khayachi A. Rôles fonctionnels de la SUMOylation de FMRP « Fragile X Mental Retardation Protein » : Functional roles of FMRP sumoylation. [Doctoral Dissertation]. Nice; 2015. Available from: http://www.theses.fr/2015NICE4031


Université de Sherbrooke

4. Lauzière, Véronique. Distribution subcellulaire de la protéine FMRP dans les plaquettes sanguines quiescentes et activées.

Degree: 2011, Université de Sherbrooke

FMRP est une protéine cytoplasmique possédant des domaines consensus de liaison à l'ARN. Dans tous les tissus ou types cellulaires étudiés jusqu'à présent, elle est… (more)

Subjects/Keywords: Syndrome du X fragile; Plaquette sanguine; FMRP

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APA (6th Edition):

Lauzière, V. (2011). Distribution subcellulaire de la protéine FMRP dans les plaquettes sanguines quiescentes et activées. (Masters Thesis). Université de Sherbrooke. Retrieved from http://hdl.handle.net/11143/5549

Chicago Manual of Style (16th Edition):

Lauzière, Véronique. “Distribution subcellulaire de la protéine FMRP dans les plaquettes sanguines quiescentes et activées.” 2011. Masters Thesis, Université de Sherbrooke. Accessed March 05, 2021. http://hdl.handle.net/11143/5549.

MLA Handbook (7th Edition):

Lauzière, Véronique. “Distribution subcellulaire de la protéine FMRP dans les plaquettes sanguines quiescentes et activées.” 2011. Web. 05 Mar 2021.

Vancouver:

Lauzière V. Distribution subcellulaire de la protéine FMRP dans les plaquettes sanguines quiescentes et activées. [Internet] [Masters thesis]. Université de Sherbrooke; 2011. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/11143/5549.

Council of Science Editors:

Lauzière V. Distribution subcellulaire de la protéine FMRP dans les plaquettes sanguines quiescentes et activées. [Masters Thesis]. Université de Sherbrooke; 2011. Available from: http://hdl.handle.net/11143/5549


Duquesne University

5. Zhang, Yang. The Role of G-Quadruplex RNA Motif in Fragile X Syndrome.

Degree: MS, Pharmaceutics, 2014, Duquesne University

 Fragile X syndrome (FXS), the most common cause of inherited mental impairment, is caused by the loss of expression of the fragile X mental retardation… (more)

Subjects/Keywords: FMRP; Fragile X syndrome; G-quadruplex; RNA

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APA (6th Edition):

Zhang, Y. (2014). The Role of G-Quadruplex RNA Motif in Fragile X Syndrome. (Masters Thesis). Duquesne University. Retrieved from https://dsc.duq.edu/etd/1411

Chicago Manual of Style (16th Edition):

Zhang, Yang. “The Role of G-Quadruplex RNA Motif in Fragile X Syndrome.” 2014. Masters Thesis, Duquesne University. Accessed March 05, 2021. https://dsc.duq.edu/etd/1411.

MLA Handbook (7th Edition):

Zhang, Yang. “The Role of G-Quadruplex RNA Motif in Fragile X Syndrome.” 2014. Web. 05 Mar 2021.

Vancouver:

Zhang Y. The Role of G-Quadruplex RNA Motif in Fragile X Syndrome. [Internet] [Masters thesis]. Duquesne University; 2014. [cited 2021 Mar 05]. Available from: https://dsc.duq.edu/etd/1411.

Council of Science Editors:

Zhang Y. The Role of G-Quadruplex RNA Motif in Fragile X Syndrome. [Masters Thesis]. Duquesne University; 2014. Available from: https://dsc.duq.edu/etd/1411


Duquesne University

6. Blice-Baum, Anna. Fragile X Mental Retardation Protein: Self-Regulation and miRNA Pathway Involvement.

Degree: PhD, Chemistry and Biochemistry, 2013, Duquesne University

 Fragile X syndrome, the most common form of inherited mental impairment in humans, affects 1 of 4000 males and 1 of 8000 females. It is… (more)

Subjects/Keywords: FMRP; Fragile X syndrome; G-quadruplex; mRNA

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APA (6th Edition):

Blice-Baum, A. (2013). Fragile X Mental Retardation Protein: Self-Regulation and miRNA Pathway Involvement. (Doctoral Dissertation). Duquesne University. Retrieved from https://dsc.duq.edu/etd/330

Chicago Manual of Style (16th Edition):

Blice-Baum, Anna. “Fragile X Mental Retardation Protein: Self-Regulation and miRNA Pathway Involvement.” 2013. Doctoral Dissertation, Duquesne University. Accessed March 05, 2021. https://dsc.duq.edu/etd/330.

MLA Handbook (7th Edition):

Blice-Baum, Anna. “Fragile X Mental Retardation Protein: Self-Regulation and miRNA Pathway Involvement.” 2013. Web. 05 Mar 2021.

Vancouver:

Blice-Baum A. Fragile X Mental Retardation Protein: Self-Regulation and miRNA Pathway Involvement. [Internet] [Doctoral dissertation]. Duquesne University; 2013. [cited 2021 Mar 05]. Available from: https://dsc.duq.edu/etd/330.

Council of Science Editors:

Blice-Baum A. Fragile X Mental Retardation Protein: Self-Regulation and miRNA Pathway Involvement. [Doctoral Dissertation]. Duquesne University; 2013. Available from: https://dsc.duq.edu/etd/330

7. Daroles, Laura. Le rôle de la Fragile X Mental Retardation Protein et de alpha CamKII dans la plasticité des cellules granulaires du bulbe olfactif en réponse à l'apprentissage : The role of the Fragile X Mental retardation Protein in granules cells of the olfactory bulb in response to learning.

Degree: Docteur es, Neurosciences, 2016, Université Pierre et Marie Curie – Paris VI

La Fragile X Mental Retardation Protein (FMRP) est une protéine régulant la traduction locale de nombreux ARNm dans le cerveau. Elle est absente dans le… (more)

Subjects/Keywords: FMRP; ΑCamKII; Apprentissage; Plasticité structurelle; Traduction locale; Bulbe olfactif; FMRP; ΑCamKII; Structural plasticity; 573.8

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APA (6th Edition):

Daroles, L. (2016). Le rôle de la Fragile X Mental Retardation Protein et de alpha CamKII dans la plasticité des cellules granulaires du bulbe olfactif en réponse à l'apprentissage : The role of the Fragile X Mental retardation Protein in granules cells of the olfactory bulb in response to learning. (Doctoral Dissertation). Université Pierre et Marie Curie – Paris VI. Retrieved from http://www.theses.fr/2016PA066037

Chicago Manual of Style (16th Edition):

Daroles, Laura. “Le rôle de la Fragile X Mental Retardation Protein et de alpha CamKII dans la plasticité des cellules granulaires du bulbe olfactif en réponse à l'apprentissage : The role of the Fragile X Mental retardation Protein in granules cells of the olfactory bulb in response to learning.” 2016. Doctoral Dissertation, Université Pierre et Marie Curie – Paris VI. Accessed March 05, 2021. http://www.theses.fr/2016PA066037.

MLA Handbook (7th Edition):

Daroles, Laura. “Le rôle de la Fragile X Mental Retardation Protein et de alpha CamKII dans la plasticité des cellules granulaires du bulbe olfactif en réponse à l'apprentissage : The role of the Fragile X Mental retardation Protein in granules cells of the olfactory bulb in response to learning.” 2016. Web. 05 Mar 2021.

Vancouver:

Daroles L. Le rôle de la Fragile X Mental Retardation Protein et de alpha CamKII dans la plasticité des cellules granulaires du bulbe olfactif en réponse à l'apprentissage : The role of the Fragile X Mental retardation Protein in granules cells of the olfactory bulb in response to learning. [Internet] [Doctoral dissertation]. Université Pierre et Marie Curie – Paris VI; 2016. [cited 2021 Mar 05]. Available from: http://www.theses.fr/2016PA066037.

Council of Science Editors:

Daroles L. Le rôle de la Fragile X Mental Retardation Protein et de alpha CamKII dans la plasticité des cellules granulaires du bulbe olfactif en réponse à l'apprentissage : The role of the Fragile X Mental retardation Protein in granules cells of the olfactory bulb in response to learning. [Doctoral Dissertation]. Université Pierre et Marie Curie – Paris VI; 2016. Available from: http://www.theses.fr/2016PA066037

8. Prieto Garcia, Marta. Conséquences physiopathologiques d’une mutation faux sens X-fragile : Pathophysiological consequences of a Fragile X missense mutation.

Degree: Docteur es, Sciences de la vie et de la santé, 2020, Université Côte d'Azur

Mon projet de thèse vise à élucider les conséquences physiopathologiques d'une mutation faux sens sur le gène FMR1 identifiée chez des patients atteints du syndrome… (more)

Subjects/Keywords: Syndrome du X fragile (SFX); FMRP; R138Q; Synapse; Sumoylation; FXS; FMRP; R138Q; Synapse; Sumoylation

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APA (6th Edition):

Prieto Garcia, M. (2020). Conséquences physiopathologiques d’une mutation faux sens X-fragile : Pathophysiological consequences of a Fragile X missense mutation. (Doctoral Dissertation). Université Côte d'Azur. Retrieved from http://www.theses.fr/2020COAZ6003

Chicago Manual of Style (16th Edition):

Prieto Garcia, Marta. “Conséquences physiopathologiques d’une mutation faux sens X-fragile : Pathophysiological consequences of a Fragile X missense mutation.” 2020. Doctoral Dissertation, Université Côte d'Azur. Accessed March 05, 2021. http://www.theses.fr/2020COAZ6003.

MLA Handbook (7th Edition):

Prieto Garcia, Marta. “Conséquences physiopathologiques d’une mutation faux sens X-fragile : Pathophysiological consequences of a Fragile X missense mutation.” 2020. Web. 05 Mar 2021.

Vancouver:

Prieto Garcia M. Conséquences physiopathologiques d’une mutation faux sens X-fragile : Pathophysiological consequences of a Fragile X missense mutation. [Internet] [Doctoral dissertation]. Université Côte d'Azur; 2020. [cited 2021 Mar 05]. Available from: http://www.theses.fr/2020COAZ6003.

Council of Science Editors:

Prieto Garcia M. Conséquences physiopathologiques d’une mutation faux sens X-fragile : Pathophysiological consequences of a Fragile X missense mutation. [Doctoral Dissertation]. Université Côte d'Azur; 2020. Available from: http://www.theses.fr/2020COAZ6003

9. Velloso, Fernando Janczur. Variabilidade do domínio KH-2 da proteína do retardo mental do X frágil (FMRP).

Degree: PhD, Biologia (Genética), 2013, University of São Paulo

 A proteína do retardo mental do X frágil (FMRP), codificada pelo gene do Retardo Mental do X Frágil (do inglês, Fragile Mental Retardation 1, FMR1)… (more)

Subjects/Keywords: Alternative splicing KH-2 protein; Domínio KH-Z; FMR1; FMR1; FMRP; FMRP; Frágil X syndrome; Síndrome do X Frágil; Splicing alternativo

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APA (6th Edition):

Velloso, F. J. (2013). Variabilidade do domínio KH-2 da proteína do retardo mental do X frágil (FMRP). (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/41/41131/tde-21032014-090729/ ;

Chicago Manual of Style (16th Edition):

Velloso, Fernando Janczur. “Variabilidade do domínio KH-2 da proteína do retardo mental do X frágil (FMRP).” 2013. Doctoral Dissertation, University of São Paulo. Accessed March 05, 2021. http://www.teses.usp.br/teses/disponiveis/41/41131/tde-21032014-090729/ ;.

MLA Handbook (7th Edition):

Velloso, Fernando Janczur. “Variabilidade do domínio KH-2 da proteína do retardo mental do X frágil (FMRP).” 2013. Web. 05 Mar 2021.

Vancouver:

Velloso FJ. Variabilidade do domínio KH-2 da proteína do retardo mental do X frágil (FMRP). [Internet] [Doctoral dissertation]. University of São Paulo; 2013. [cited 2021 Mar 05]. Available from: http://www.teses.usp.br/teses/disponiveis/41/41131/tde-21032014-090729/ ;.

Council of Science Editors:

Velloso FJ. Variabilidade do domínio KH-2 da proteína do retardo mental do X frágil (FMRP). [Doctoral Dissertation]. University of São Paulo; 2013. Available from: http://www.teses.usp.br/teses/disponiveis/41/41131/tde-21032014-090729/ ;


University of California – Riverside

10. Sidhu, Harpreet Kaur. Genetic Removal of Matrix Metalloproteinase 9 Rescues the Symptoms of Fragile X Syndrome in a Mouse Model.

Degree: Neuroscience, 2013, University of California – Riverside

 Fragile X syndrome (FXS), the most common single gene cause of inherited intellectual disability, is caused by a trinucleotide CGG repeat expansion in the 5'… (more)

Subjects/Keywords: Neurosciences; Fmr1 ko; FMRP; Fragile X syndrome; MMP9

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APA (6th Edition):

Sidhu, H. K. (2013). Genetic Removal of Matrix Metalloproteinase 9 Rescues the Symptoms of Fragile X Syndrome in a Mouse Model. (Thesis). University of California – Riverside. Retrieved from http://www.escholarship.org/uc/item/13d3w6t7

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):

Sidhu, Harpreet Kaur. “Genetic Removal of Matrix Metalloproteinase 9 Rescues the Symptoms of Fragile X Syndrome in a Mouse Model.” 2013. Thesis, University of California – Riverside. Accessed March 05, 2021. http://www.escholarship.org/uc/item/13d3w6t7.

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

MLA Handbook (7th Edition):

Sidhu, Harpreet Kaur. “Genetic Removal of Matrix Metalloproteinase 9 Rescues the Symptoms of Fragile X Syndrome in a Mouse Model.” 2013. Web. 05 Mar 2021.

Vancouver:

Sidhu HK. Genetic Removal of Matrix Metalloproteinase 9 Rescues the Symptoms of Fragile X Syndrome in a Mouse Model. [Internet] [Thesis]. University of California – Riverside; 2013. [cited 2021 Mar 05]. Available from: http://www.escholarship.org/uc/item/13d3w6t7.

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

Council of Science Editors:

Sidhu HK. Genetic Removal of Matrix Metalloproteinase 9 Rescues the Symptoms of Fragile X Syndrome in a Mouse Model. [Thesis]. University of California – Riverside; 2013. Available from: http://www.escholarship.org/uc/item/13d3w6t7

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


University of California – San Diego

11. Athar, Youssi Momen. Dissecting the RNA Binding Specificity of Fragile X Mental Retardation Protein.

Degree: Chemistry, 2016, University of California – San Diego

FMRP binds and regulates translation of neuronal mRNAs. Loss of FMRP causes aberrant expression of proteins, which results in Fragile X syndrome. Three promising RNA… (more)

Subjects/Keywords: Biochemistry; Molecular biology; FMRP; G-quadruplex; Ribosome; RNA

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APA (6th Edition):

Athar, Y. M. (2016). Dissecting the RNA Binding Specificity of Fragile X Mental Retardation Protein. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/2sx2h4cb

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):

Athar, Youssi Momen. “Dissecting the RNA Binding Specificity of Fragile X Mental Retardation Protein.” 2016. Thesis, University of California – San Diego. Accessed March 05, 2021. http://www.escholarship.org/uc/item/2sx2h4cb.

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

MLA Handbook (7th Edition):

Athar, Youssi Momen. “Dissecting the RNA Binding Specificity of Fragile X Mental Retardation Protein.” 2016. Web. 05 Mar 2021.

Vancouver:

Athar YM. Dissecting the RNA Binding Specificity of Fragile X Mental Retardation Protein. [Internet] [Thesis]. University of California – San Diego; 2016. [cited 2021 Mar 05]. Available from: http://www.escholarship.org/uc/item/2sx2h4cb.

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

Council of Science Editors:

Athar YM. Dissecting the RNA Binding Specificity of Fragile X Mental Retardation Protein. [Thesis]. University of California – San Diego; 2016. Available from: http://www.escholarship.org/uc/item/2sx2h4cb

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


University of California – Santa Cruz

12. Aharon, Adam. Dendritic Spine Abnormalities In A Mouse Model Of Fragile X Syndrome.

Degree: Molecular Cell and Developmental Biology, 2015, University of California – Santa Cruz

 Fragile X syndrome (FXS) is the most common form of genetically inherited mental retardation and although it has been investigated for over 20 years, how… (more)

Subjects/Keywords: Neurosciences; Molecular biology; Dendritic spines; Fmr1; FMRP; Fragile X Syndrome

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APA (6th Edition):

Aharon, A. (2015). Dendritic Spine Abnormalities In A Mouse Model Of Fragile X Syndrome. (Thesis). University of California – Santa Cruz. Retrieved from http://www.escholarship.org/uc/item/4z72f1hw

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):

Aharon, Adam. “Dendritic Spine Abnormalities In A Mouse Model Of Fragile X Syndrome.” 2015. Thesis, University of California – Santa Cruz. Accessed March 05, 2021. http://www.escholarship.org/uc/item/4z72f1hw.

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

MLA Handbook (7th Edition):

Aharon, Adam. “Dendritic Spine Abnormalities In A Mouse Model Of Fragile X Syndrome.” 2015. Web. 05 Mar 2021.

Vancouver:

Aharon A. Dendritic Spine Abnormalities In A Mouse Model Of Fragile X Syndrome. [Internet] [Thesis]. University of California – Santa Cruz; 2015. [cited 2021 Mar 05]. Available from: http://www.escholarship.org/uc/item/4z72f1hw.

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

Council of Science Editors:

Aharon A. Dendritic Spine Abnormalities In A Mouse Model Of Fragile X Syndrome. [Thesis]. University of California – Santa Cruz; 2015. Available from: http://www.escholarship.org/uc/item/4z72f1hw

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


Université de Sherbrooke

13. Meunier, Alexandre J. Étude de l'interaction entre FMRP et le cytosquelette lors de l'activation plaquettaire: Study of the interaction between FMRP and the cytoskeleton upon platelet activation.

Degree: 2012, Université de Sherbrooke

 Résumé: Le syndrome du X fragile, première cause monogénique de déficience intellectuelle héréditaire, découle de l'expansion du nombre de répétitions CGG dans le gène FMR1… (more)

Subjects/Keywords: Polyribosome; Cytosquelette; Plaquette sanguine; FMRP; Syndrome du X fragile

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APA (6th Edition):

Meunier, A. J. (2012). Étude de l'interaction entre FMRP et le cytosquelette lors de l'activation plaquettaire: Study of the interaction between FMRP and the cytoskeleton upon platelet activation. (Masters Thesis). Université de Sherbrooke. Retrieved from http://hdl.handle.net/11143/6342

Chicago Manual of Style (16th Edition):

Meunier, Alexandre J. “Étude de l'interaction entre FMRP et le cytosquelette lors de l'activation plaquettaire: Study of the interaction between FMRP and the cytoskeleton upon platelet activation.” 2012. Masters Thesis, Université de Sherbrooke. Accessed March 05, 2021. http://hdl.handle.net/11143/6342.

MLA Handbook (7th Edition):

Meunier, Alexandre J. “Étude de l'interaction entre FMRP et le cytosquelette lors de l'activation plaquettaire: Study of the interaction between FMRP and the cytoskeleton upon platelet activation.” 2012. Web. 05 Mar 2021.

Vancouver:

Meunier AJ. Étude de l'interaction entre FMRP et le cytosquelette lors de l'activation plaquettaire: Study of the interaction between FMRP and the cytoskeleton upon platelet activation. [Internet] [Masters thesis]. Université de Sherbrooke; 2012. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/11143/6342.

Council of Science Editors:

Meunier AJ. Étude de l'interaction entre FMRP et le cytosquelette lors de l'activation plaquettaire: Study of the interaction between FMRP and the cytoskeleton upon platelet activation. [Masters Thesis]. Université de Sherbrooke; 2012. Available from: http://hdl.handle.net/11143/6342


Université de Sherbrooke

14. Lessard, Mandy. Dosage quantitatif de la protéine FMRP : développement d'un nouvel outil diagnostique pour le syndrome du X fragile.

Degree: 2011, Université de Sherbrooke

 Le syndrome du X fragile est la première cause monogénique de déficience intellectuelle héréditaire affectant un garçon sur 5161 et une fille sur 6000. La… (more)

Subjects/Keywords: Syndrome du X fragile; Plaquettes sanguines; Immunobuvardage quantitatif; Fonctions cognitives; FMRP

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APA (6th Edition):

Lessard, M. (2011). Dosage quantitatif de la protéine FMRP : développement d'un nouvel outil diagnostique pour le syndrome du X fragile. (Masters Thesis). Université de Sherbrooke. Retrieved from http://hdl.handle.net/11143/5560

Chicago Manual of Style (16th Edition):

Lessard, Mandy. “Dosage quantitatif de la protéine FMRP : développement d'un nouvel outil diagnostique pour le syndrome du X fragile.” 2011. Masters Thesis, Université de Sherbrooke. Accessed March 05, 2021. http://hdl.handle.net/11143/5560.

MLA Handbook (7th Edition):

Lessard, Mandy. “Dosage quantitatif de la protéine FMRP : développement d'un nouvel outil diagnostique pour le syndrome du X fragile.” 2011. Web. 05 Mar 2021.

Vancouver:

Lessard M. Dosage quantitatif de la protéine FMRP : développement d'un nouvel outil diagnostique pour le syndrome du X fragile. [Internet] [Masters thesis]. Université de Sherbrooke; 2011. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/11143/5560.

Council of Science Editors:

Lessard M. Dosage quantitatif de la protéine FMRP : développement d'un nouvel outil diagnostique pour le syndrome du X fragile. [Masters Thesis]. Université de Sherbrooke; 2011. Available from: http://hdl.handle.net/11143/5560


University of Illinois – Urbana-Champaign

15. Kao, Der-I. FMRP dependent synaptic delivery of messenger RNA.

Degree: PhD, 4094, 2011, University of Illinois – Urbana-Champaign

 Fragile X mental retardation is the most common inherited form of mental retardation. The loss of FMRP function results in Fragile X Mental Retardation. In… (more)

Subjects/Keywords: Fragile X Syndrome; Fragile X Mental Retardation Protein (FMRP); mRNA targeting

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APA (6th Edition):

Kao, D. (2011). FMRP dependent synaptic delivery of messenger RNA. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/18643

Chicago Manual of Style (16th Edition):

Kao, Der-I. “FMRP dependent synaptic delivery of messenger RNA.” 2011. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed March 05, 2021. http://hdl.handle.net/2142/18643.

MLA Handbook (7th Edition):

Kao, Der-I. “FMRP dependent synaptic delivery of messenger RNA.” 2011. Web. 05 Mar 2021.

Vancouver:

Kao D. FMRP dependent synaptic delivery of messenger RNA. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2011. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/2142/18643.

Council of Science Editors:

Kao D. FMRP dependent synaptic delivery of messenger RNA. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2011. Available from: http://hdl.handle.net/2142/18643


Duquesne University

16. Stefanovic, Snezana. G Quadruplex RNA Structures in PSD-95 Mrna: Potential Regulators of Mir-125a Seed Binding Site Accessibility.

Degree: PhD, Chemistry and Biochemistry, 2015, Duquesne University

 Fragile X syndrome (FXS) is the most common inherited form of intellectual disability caused by the CGG trinucleotide expansion in the 5'-untranslated region of the… (more)

Subjects/Keywords: Pure sciences; Fmrp; Fragile x syndrome; Mir-125a; Psd-95

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APA (6th Edition):

Stefanovic, S. (2015). G Quadruplex RNA Structures in PSD-95 Mrna: Potential Regulators of Mir-125a Seed Binding Site Accessibility. (Doctoral Dissertation). Duquesne University. Retrieved from https://dsc.duq.edu/etd/1518

Chicago Manual of Style (16th Edition):

Stefanovic, Snezana. “G Quadruplex RNA Structures in PSD-95 Mrna: Potential Regulators of Mir-125a Seed Binding Site Accessibility.” 2015. Doctoral Dissertation, Duquesne University. Accessed March 05, 2021. https://dsc.duq.edu/etd/1518.

MLA Handbook (7th Edition):

Stefanovic, Snezana. “G Quadruplex RNA Structures in PSD-95 Mrna: Potential Regulators of Mir-125a Seed Binding Site Accessibility.” 2015. Web. 05 Mar 2021.

Vancouver:

Stefanovic S. G Quadruplex RNA Structures in PSD-95 Mrna: Potential Regulators of Mir-125a Seed Binding Site Accessibility. [Internet] [Doctoral dissertation]. Duquesne University; 2015. [cited 2021 Mar 05]. Available from: https://dsc.duq.edu/etd/1518.

Council of Science Editors:

Stefanovic S. G Quadruplex RNA Structures in PSD-95 Mrna: Potential Regulators of Mir-125a Seed Binding Site Accessibility. [Doctoral Dissertation]. Duquesne University; 2015. Available from: https://dsc.duq.edu/etd/1518


University of Edinburgh

17. Chiang, Chih-Yuan. Cortical development & plasticity in the FMRP KO mouse.

Degree: PhD, 2016, University of Edinburgh

 Autism is one of the leading causes of human intellectual disability (ID). More than 1% of the human population has autism spectrum disorders (ASDs), and… (more)

Subjects/Keywords: 573.8; FXS; FMRP; autism; dendritic spine; myelination; gamma; SRP

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APA (6th Edition):

Chiang, C. (2016). Cortical development & plasticity in the FMRP KO mouse. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/22055

Chicago Manual of Style (16th Edition):

Chiang, Chih-Yuan. “Cortical development & plasticity in the FMRP KO mouse.” 2016. Doctoral Dissertation, University of Edinburgh. Accessed March 05, 2021. http://hdl.handle.net/1842/22055.

MLA Handbook (7th Edition):

Chiang, Chih-Yuan. “Cortical development & plasticity in the FMRP KO mouse.” 2016. Web. 05 Mar 2021.

Vancouver:

Chiang C. Cortical development & plasticity in the FMRP KO mouse. [Internet] [Doctoral dissertation]. University of Edinburgh; 2016. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/1842/22055.

Council of Science Editors:

Chiang C. Cortical development & plasticity in the FMRP KO mouse. [Doctoral Dissertation]. University of Edinburgh; 2016. Available from: http://hdl.handle.net/1842/22055

18. Tabet, Ricardos. Bases moléculaires de la physiopathologie du syndrome de l'X fragile : Understanding the molecular basis of fragile X syndrome.

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie, 2013, Université de Strasbourg

Le syndrome de l’X fragile représente la première cause de déficience intellectuelle héréditaire. Ce syndrome résulte de l’absence de la protéine FMRP. FMRP est proposée… (more)

Subjects/Keywords: Syndrome de l’X fragile; FMRP; Protéine de liaison aux ARN; CLIP; Neurone; Déficience intellectuelle; Fragile X syndrome; FMRP; RNA binding protein; CLIP; Neuron; Intellectual disability; 572.8

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APA (6th Edition):

Tabet, R. (2013). Bases moléculaires de la physiopathologie du syndrome de l'X fragile : Understanding the molecular basis of fragile X syndrome. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2013STRAJ090

Chicago Manual of Style (16th Edition):

Tabet, Ricardos. “Bases moléculaires de la physiopathologie du syndrome de l'X fragile : Understanding the molecular basis of fragile X syndrome.” 2013. Doctoral Dissertation, Université de Strasbourg. Accessed March 05, 2021. http://www.theses.fr/2013STRAJ090.

MLA Handbook (7th Edition):

Tabet, Ricardos. “Bases moléculaires de la physiopathologie du syndrome de l'X fragile : Understanding the molecular basis of fragile X syndrome.” 2013. Web. 05 Mar 2021.

Vancouver:

Tabet R. Bases moléculaires de la physiopathologie du syndrome de l'X fragile : Understanding the molecular basis of fragile X syndrome. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2013. [cited 2021 Mar 05]. Available from: http://www.theses.fr/2013STRAJ090.

Council of Science Editors:

Tabet R. Bases moléculaires de la physiopathologie du syndrome de l'X fragile : Understanding the molecular basis of fragile X syndrome. [Doctoral Dissertation]. Université de Strasbourg; 2013. Available from: http://www.theses.fr/2013STRAJ090

19. Κανελλόπουλος, Αλέξανδρος. Η διελεύκανση των μοριακών μηχανισμών μάθησης και μνήμης με την χρήση μοντέλων γνωσιακών δυσλειτουργιών στην drosophila melanogaster.

Degree: 2012, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ)

 This doctoral thesis is titled "Elucidating the molecular mechanisms of learning and memory using models of cognitive dysfunction in Drosophila melanogaster".The reason it was chosen… (more)

Subjects/Keywords: Μάθηση; Μνήμη; Δροσόφιλα; Σύνδρομο εύθραυστου χ; Κυκλικό AMP; Μεταβοτροπικοί γλουταμινεργικοί υποδοχείς; Πρωτείνη FMRP; Γονίδιο FMR1; FMRP protein; FMR1 gene; Learning; Memory; Drosophila; Fragile X syndrome; CAMP; Metabotropic glutaminergic receptors

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APA (6th Edition):

Κανελλόπουλος, . . (2012). Η διελεύκανση των μοριακών μηχανισμών μάθησης και μνήμης με την χρήση μοντέλων γνωσιακών δυσλειτουργιών στην drosophila melanogaster. (Thesis). National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Retrieved from http://hdl.handle.net/10442/hedi/29553

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):

Κανελλόπουλος, Αλέξανδρος. “Η διελεύκανση των μοριακών μηχανισμών μάθησης και μνήμης με την χρήση μοντέλων γνωσιακών δυσλειτουργιών στην drosophila melanogaster.” 2012. Thesis, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Accessed March 05, 2021. http://hdl.handle.net/10442/hedi/29553.

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

MLA Handbook (7th Edition):

Κανελλόπουλος, Αλέξανδρος. “Η διελεύκανση των μοριακών μηχανισμών μάθησης και μνήμης με την χρήση μοντέλων γνωσιακών δυσλειτουργιών στην drosophila melanogaster.” 2012. Web. 05 Mar 2021.

Vancouver:

Κανελλόπουλος . Η διελεύκανση των μοριακών μηχανισμών μάθησης και μνήμης με την χρήση μοντέλων γνωσιακών δυσλειτουργιών στην drosophila melanogaster. [Internet] [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2012. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/10442/hedi/29553.

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

Council of Science Editors:

Κανελλόπουλος . Η διελεύκανση των μοριακών μηχανισμών μάθησης και μνήμης με την χρήση μοντέλων γνωσιακών δυσλειτουργιών στην drosophila melanogaster. [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2012. Available from: http://hdl.handle.net/10442/hedi/29553

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

20. Mostefai, Fatima. Characterization of the Molecular Mechanism by which SMN Regulates mRNA Translation .

Degree: 2017, University of Ottawa

 Despite our understanding of the role of the survival motor neuron protein (SMN) in cytoplasmic small ribonucleoproteins (snRNP) assembly, it is unclear how loss of… (more)

Subjects/Keywords: SMN; Translation regulation; DDX5; FMRP

…the RNA-binding Protein Fragile X Mental Retardation Protein (FMRP) (Piazzon… …Darnell group when they observed that the RNAbinding protein FMRP can reversibly stall ribosomes… …regulators. The RNA-binding protein FMRP is an established protein in the translational mechanism… …x28;Darnell et al. 2011; Mazroui et al. 2002). FMRP is also known to interact with SMN… …x28;Piazzon et al. 2008), however not through its Tudor domain. But FMRP would still… 

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APA (6th Edition):

Mostefai, F. (2017). Characterization of the Molecular Mechanism by which SMN Regulates mRNA Translation . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/37057

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):

Mostefai, Fatima. “Characterization of the Molecular Mechanism by which SMN Regulates mRNA Translation .” 2017. Thesis, University of Ottawa. Accessed March 05, 2021. http://hdl.handle.net/10393/37057.

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

MLA Handbook (7th Edition):

Mostefai, Fatima. “Characterization of the Molecular Mechanism by which SMN Regulates mRNA Translation .” 2017. Web. 05 Mar 2021.

Vancouver:

Mostefai F. Characterization of the Molecular Mechanism by which SMN Regulates mRNA Translation . [Internet] [Thesis]. University of Ottawa; 2017. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/10393/37057.

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

Council of Science Editors:

Mostefai F. Characterization of the Molecular Mechanism by which SMN Regulates mRNA Translation . [Thesis]. University of Ottawa; 2017. Available from: http://hdl.handle.net/10393/37057

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

21. Kenny, Phillip J. Molecular requirements for FMRP and RNA helicase MOV10 in the translational regulation of co-bound mRNAs.

Degree: PhD, Cell and Developmental Biology, 2019, University of Illinois – Urbana-Champaign

 The fragile X mental retardation protein (FMRP), regulates translation of its bound mRNAs through an incompletely defined mechanism. Historically, FMRP has been known to directly… (more)

Subjects/Keywords: RNA; FMRP; MOV10; Translational Regulation

…Retardation Protein (FMRP) is known as Fragile X Syndrome (FXS), the most common… …x29; (3) (4). FMRP is an RNA-binding protein (5), binding… …Such individuals highlight the importance of the FMRP domains in which these mutations are… …located and will be discussed in more detail later. The evidence that FMRP is a translational… …The bi-functional role of FMRP to 2 suppress or de-repress its target transcripts through… 

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APA (6th Edition):

Kenny, P. J. (2019). Molecular requirements for FMRP and RNA helicase MOV10 in the translational regulation of co-bound mRNAs. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/106194

Chicago Manual of Style (16th Edition):

Kenny, Phillip J. “Molecular requirements for FMRP and RNA helicase MOV10 in the translational regulation of co-bound mRNAs.” 2019. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed March 05, 2021. http://hdl.handle.net/2142/106194.

MLA Handbook (7th Edition):

Kenny, Phillip J. “Molecular requirements for FMRP and RNA helicase MOV10 in the translational regulation of co-bound mRNAs.” 2019. Web. 05 Mar 2021.

Vancouver:

Kenny PJ. Molecular requirements for FMRP and RNA helicase MOV10 in the translational regulation of co-bound mRNAs. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2019. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/2142/106194.

Council of Science Editors:

Kenny PJ. Molecular requirements for FMRP and RNA helicase MOV10 in the translational regulation of co-bound mRNAs. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2019. Available from: http://hdl.handle.net/2142/106194

22. Di Marco, Barbara. Modulation of Stress Granules formation: Role of mGlu5 receptor and FMRP and implications for pathophysiology of Fragile X Syndrome.

Degree: 2015, Università degli Studi di Catania

 Fragile X syndrome (FXS) is the most common form of inherited intellectual disability and autism. The genetic defect in FXS is a CGG trinucleotide repeat… (more)

Subjects/Keywords: Area 06 - Scienze mediche; Fragile X, FMRP, FXR1P, FXR2P, Stress Granules, mGlu5 receptor, astrocytes

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APA (6th Edition):

Di Marco, B. (2015). Modulation of Stress Granules formation: Role of mGlu5 receptor and FMRP and implications for pathophysiology of Fragile X Syndrome. (Thesis). Università degli Studi di Catania. Retrieved from http://hdl.handle.net/10761/3838

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):

Di Marco, Barbara. “Modulation of Stress Granules formation: Role of mGlu5 receptor and FMRP and implications for pathophysiology of Fragile X Syndrome.” 2015. Thesis, Università degli Studi di Catania. Accessed March 05, 2021. http://hdl.handle.net/10761/3838.

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

MLA Handbook (7th Edition):

Di Marco, Barbara. “Modulation of Stress Granules formation: Role of mGlu5 receptor and FMRP and implications for pathophysiology of Fragile X Syndrome.” 2015. Web. 05 Mar 2021.

Vancouver:

Di Marco B. Modulation of Stress Granules formation: Role of mGlu5 receptor and FMRP and implications for pathophysiology of Fragile X Syndrome. [Internet] [Thesis]. Università degli Studi di Catania; 2015. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/10761/3838.

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

Council of Science Editors:

Di Marco B. Modulation of Stress Granules formation: Role of mGlu5 receptor and FMRP and implications for pathophysiology of Fragile X Syndrome. [Thesis]. Università degli Studi di Catania; 2015. Available from: http://hdl.handle.net/10761/3838

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

23. Elsbernd, Joseph L. Investigation of the role of Fragile X mental retardation protein in the embryonic neocortex using RNA interference.

Degree: MA, Biological Science (Stem Cell, 2012, California State University – Sacramento

 Fragile X-associated tremor/ataxia syndrome (FXTAS) is a genetic disease characterized by impaired movement coordination, peripheral nervous system damage, limb tremors, cognitive decline, behavioral changes, autonomic… (more)

Subjects/Keywords: Stem cell; Glial; Neuron; FMRP

…ventricular (VZ) or subventricular zone (SVZ) after FMRP knockdown… …while FMRP was decreased 74% relative to wild-type (Chen et al. 2010). Previously we… …determined that FMRP is decreased by 40% in the embryonic forebrain (Cunningham et al. 2010… …x29;. There are consequences associated with premutation because FMRP is reportedly involved… …in the regulation of cell cycle regulation pathways. The decreased FMRP, toxic FMR1 mRNA… 

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APA (6th Edition):

Elsbernd, J. L. (2012). Investigation of the role of Fragile X mental retardation protein in the embryonic neocortex using RNA interference. (Masters Thesis). California State University – Sacramento. Retrieved from http://hdl.handle.net/10211.9/1768

Chicago Manual of Style (16th Edition):

Elsbernd, Joseph L. “Investigation of the role of Fragile X mental retardation protein in the embryonic neocortex using RNA interference.” 2012. Masters Thesis, California State University – Sacramento. Accessed March 05, 2021. http://hdl.handle.net/10211.9/1768.

MLA Handbook (7th Edition):

Elsbernd, Joseph L. “Investigation of the role of Fragile X mental retardation protein in the embryonic neocortex using RNA interference.” 2012. Web. 05 Mar 2021.

Vancouver:

Elsbernd JL. Investigation of the role of Fragile X mental retardation protein in the embryonic neocortex using RNA interference. [Internet] [Masters thesis]. California State University – Sacramento; 2012. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/10211.9/1768.

Council of Science Editors:

Elsbernd JL. Investigation of the role of Fragile X mental retardation protein in the embryonic neocortex using RNA interference. [Masters Thesis]. California State University – Sacramento; 2012. Available from: http://hdl.handle.net/10211.9/1768

24. Mc Coy, Marie. Fonctions globales de FMRP dans la différenciation cellulaire dans un modèle non-neuronal: le MEG-01.

Degree: M. Sc., Biochimie, 2015, Université de Sherbrooke

 Résumé: Mémoire présenté à la Faculté de médecine et des sciences de la santé en vue de l’obtention du diplôme de maître sciences (M.Sc.) en… (more)

Subjects/Keywords: Syndrome du X fragile; FMRP; FMR1; MEG-01; Différentiation; Ribonucléoprotéine; Développement; MRNP; Fragile X Syndrome; Differentiation

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APA (6th Edition):

Mc Coy, M. (2015). Fonctions globales de FMRP dans la différenciation cellulaire dans un modèle non-neuronal: le MEG-01. (Masters Thesis). Université de Sherbrooke. Retrieved from http://www.collectionscanada.gc.ca/obj/thesescanada/vol2/QSHERU/TC-QSHERU-11143_7713.pdf ; http://savoirs.usherbrooke.ca/bitstream/11143/7713/5/Mccoy_Marie_MSc_2015.pdf

Chicago Manual of Style (16th Edition):

Mc Coy, Marie. “Fonctions globales de FMRP dans la différenciation cellulaire dans un modèle non-neuronal: le MEG-01.” 2015. Masters Thesis, Université de Sherbrooke. Accessed March 05, 2021. http://www.collectionscanada.gc.ca/obj/thesescanada/vol2/QSHERU/TC-QSHERU-11143_7713.pdf ; http://savoirs.usherbrooke.ca/bitstream/11143/7713/5/Mccoy_Marie_MSc_2015.pdf.

MLA Handbook (7th Edition):

Mc Coy, Marie. “Fonctions globales de FMRP dans la différenciation cellulaire dans un modèle non-neuronal: le MEG-01.” 2015. Web. 05 Mar 2021.

Vancouver:

Mc Coy M. Fonctions globales de FMRP dans la différenciation cellulaire dans un modèle non-neuronal: le MEG-01. [Internet] [Masters thesis]. Université de Sherbrooke; 2015. [cited 2021 Mar 05]. Available from: http://www.collectionscanada.gc.ca/obj/thesescanada/vol2/QSHERU/TC-QSHERU-11143_7713.pdf ; http://savoirs.usherbrooke.ca/bitstream/11143/7713/5/Mccoy_Marie_MSc_2015.pdf.

Council of Science Editors:

Mc Coy M. Fonctions globales de FMRP dans la différenciation cellulaire dans un modèle non-neuronal: le MEG-01. [Masters Thesis]. Université de Sherbrooke; 2015. Available from: http://www.collectionscanada.gc.ca/obj/thesescanada/vol2/QSHERU/TC-QSHERU-11143_7713.pdf ; http://savoirs.usherbrooke.ca/bitstream/11143/7713/5/Mccoy_Marie_MSc_2015.pdf


University of Toronto

25. Shang, Yuze. Fragile X Mental Retardation Protein is Required for Chemically-induced Long-term Potentiation of the Hippocampus in Adult Mice.

Degree: 2009, University of Toronto

Fragile X syndrome (FXS) is caused by the lack of fragile X mental retardation protein (FMRP). The animal model of FXS, Fmr1 knockout (KO) mice,… (more)

Subjects/Keywords: FMRP; glycine; LTP; synaptic plasticity; ERK1/2; hippocampus; 0317

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APA (6th Edition):

Shang, Y. (2009). Fragile X Mental Retardation Protein is Required for Chemically-induced Long-term Potentiation of the Hippocampus in Adult Mice. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/18857

Chicago Manual of Style (16th Edition):

Shang, Yuze. “Fragile X Mental Retardation Protein is Required for Chemically-induced Long-term Potentiation of the Hippocampus in Adult Mice.” 2009. Masters Thesis, University of Toronto. Accessed March 05, 2021. http://hdl.handle.net/1807/18857.

MLA Handbook (7th Edition):

Shang, Yuze. “Fragile X Mental Retardation Protein is Required for Chemically-induced Long-term Potentiation of the Hippocampus in Adult Mice.” 2009. Web. 05 Mar 2021.

Vancouver:

Shang Y. Fragile X Mental Retardation Protein is Required for Chemically-induced Long-term Potentiation of the Hippocampus in Adult Mice. [Internet] [Masters thesis]. University of Toronto; 2009. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/1807/18857.

Council of Science Editors:

Shang Y. Fragile X Mental Retardation Protein is Required for Chemically-induced Long-term Potentiation of the Hippocampus in Adult Mice. [Masters Thesis]. University of Toronto; 2009. Available from: http://hdl.handle.net/1807/18857


Université de Sherbrooke

26. Mc Coy, Marie. Fonctions globales de FMRP dans la différenciation cellulaire dans un modèle non-neuronal: le MEG-01: Global functions of FMRP in the cellular differentiation of a non-neuronal model: the MEG-01.

Degree: 2015, Université de Sherbrooke

 Abstract: The present article-based memoire will explore the involvement of an important RNA-binding protein, FMRP, in cellular differentiation. This protein is well-known for the developmental… (more)

Subjects/Keywords: Syndrome du X fragile; FMRP; FMR1; MEG-01; Différentiation; Ribonucléoprotéine; Développement; MRNP; Fragile X Syndrome; Differentiation

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

APA (6th Edition):

Mc Coy, M. (2015). Fonctions globales de FMRP dans la différenciation cellulaire dans un modèle non-neuronal: le MEG-01: Global functions of FMRP in the cellular differentiation of a non-neuronal model: the MEG-01. (Masters Thesis). Université de Sherbrooke. Retrieved from http://hdl.handle.net/11143/7713

Chicago Manual of Style (16th Edition):

Mc Coy, Marie. “Fonctions globales de FMRP dans la différenciation cellulaire dans un modèle non-neuronal: le MEG-01: Global functions of FMRP in the cellular differentiation of a non-neuronal model: the MEG-01.” 2015. Masters Thesis, Université de Sherbrooke. Accessed March 05, 2021. http://hdl.handle.net/11143/7713.

MLA Handbook (7th Edition):

Mc Coy, Marie. “Fonctions globales de FMRP dans la différenciation cellulaire dans un modèle non-neuronal: le MEG-01: Global functions of FMRP in the cellular differentiation of a non-neuronal model: the MEG-01.” 2015. Web. 05 Mar 2021.

Vancouver:

Mc Coy M. Fonctions globales de FMRP dans la différenciation cellulaire dans un modèle non-neuronal: le MEG-01: Global functions of FMRP in the cellular differentiation of a non-neuronal model: the MEG-01. [Internet] [Masters thesis]. Université de Sherbrooke; 2015. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/11143/7713.

Council of Science Editors:

Mc Coy M. Fonctions globales de FMRP dans la différenciation cellulaire dans un modèle non-neuronal: le MEG-01: Global functions of FMRP in the cellular differentiation of a non-neuronal model: the MEG-01. [Masters Thesis]. Université de Sherbrooke; 2015. Available from: http://hdl.handle.net/11143/7713


University of Illinois – Urbana-Champaign

27. Belagodu, Amogh P. Analysis of the expression and effects of vascular endothelial growth factor family of molecules on Fragile X Syndrome abnormalities in a mouse model.

Degree: PhD, Neuroscience, 2017, University of Illinois – Urbana-Champaign

 Fragile X Syndrome (FXS) is the most common form of inherited mental retardation affecting 1:3600 males and 1:8000 females (Cornish et al., 2008). The primary… (more)

Subjects/Keywords: Fragile X Syndrome (FXS); Fragile X Mental Retardation Protein (FMRP); Vascular endothelial growth factor (VEGF); Autism

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APA (6th Edition):

Belagodu, A. P. (2017). Analysis of the expression and effects of vascular endothelial growth factor family of molecules on Fragile X Syndrome abnormalities in a mouse model. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/97769

Chicago Manual of Style (16th Edition):

Belagodu, Amogh P. “Analysis of the expression and effects of vascular endothelial growth factor family of molecules on Fragile X Syndrome abnormalities in a mouse model.” 2017. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed March 05, 2021. http://hdl.handle.net/2142/97769.

MLA Handbook (7th Edition):

Belagodu, Amogh P. “Analysis of the expression and effects of vascular endothelial growth factor family of molecules on Fragile X Syndrome abnormalities in a mouse model.” 2017. Web. 05 Mar 2021.

Vancouver:

Belagodu AP. Analysis of the expression and effects of vascular endothelial growth factor family of molecules on Fragile X Syndrome abnormalities in a mouse model. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2017. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/2142/97769.

Council of Science Editors:

Belagodu AP. Analysis of the expression and effects of vascular endothelial growth factor family of molecules on Fragile X Syndrome abnormalities in a mouse model. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2017. Available from: http://hdl.handle.net/2142/97769

28. Furlong, Jacqueline Rochelle. Regulation of Synaptogenesis by the miRNA Pathway and FMR/P Bodies.

Degree: MS, Biological Sciences, 2015, U of Denver

  Post-transcriptional regulation of mRNA is facilitated by different mechanisms, such as microRNA (miRNA) induced gene silencing or fragile X mental retardation protein (FMRP) mediated… (more)

Subjects/Keywords: Drosophila melanogaster; FMRP; Fragile X mental retardation protein; miRNA; P bodies; Post-transcriptional regulation; RNA; Biology; Cell Biology; Molecular Biology

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APA (6th Edition):

Furlong, J. R. (2015). Regulation of Synaptogenesis by the miRNA Pathway and FMR/P Bodies. (Thesis). U of Denver. Retrieved from https://digitalcommons.du.edu/etd/1025

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):

Furlong, Jacqueline Rochelle. “Regulation of Synaptogenesis by the miRNA Pathway and FMR/P Bodies.” 2015. Thesis, U of Denver. Accessed March 05, 2021. https://digitalcommons.du.edu/etd/1025.

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

MLA Handbook (7th Edition):

Furlong, Jacqueline Rochelle. “Regulation of Synaptogenesis by the miRNA Pathway and FMR/P Bodies.” 2015. Web. 05 Mar 2021.

Vancouver:

Furlong JR. Regulation of Synaptogenesis by the miRNA Pathway and FMR/P Bodies. [Internet] [Thesis]. U of Denver; 2015. [cited 2021 Mar 05]. Available from: https://digitalcommons.du.edu/etd/1025.

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

Council of Science Editors:

Furlong JR. Regulation of Synaptogenesis by the miRNA Pathway and FMR/P Bodies. [Thesis]. U of Denver; 2015. Available from: https://digitalcommons.du.edu/etd/1025

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


University of Edinburgh

29. Muscas, Melania. Investigating potential treatment strategies and underlying mechanisms in the Fragile X Syndrome mouse and rat models.

Degree: PhD, 2019, University of Edinburgh

 Fragile X syndrome (FXS) is the most common heritable monogenic cause of intellectual disability (ID) and autism. Along with physical dysmorphic features, it is characterized… (more)

Subjects/Keywords: Fragile X syndrome; protein synthesis regulatory pathways; signalling cascades; FXS; elevated translation; FMRP protein; ERK1/2; VU0152100; M4 PAM

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

APA (6th Edition):

Muscas, M. (2019). Investigating potential treatment strategies and underlying mechanisms in the Fragile X Syndrome mouse and rat models. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/36928

Chicago Manual of Style (16th Edition):

Muscas, Melania. “Investigating potential treatment strategies and underlying mechanisms in the Fragile X Syndrome mouse and rat models.” 2019. Doctoral Dissertation, University of Edinburgh. Accessed March 05, 2021. http://hdl.handle.net/1842/36928.

MLA Handbook (7th Edition):

Muscas, Melania. “Investigating potential treatment strategies and underlying mechanisms in the Fragile X Syndrome mouse and rat models.” 2019. Web. 05 Mar 2021.

Vancouver:

Muscas M. Investigating potential treatment strategies and underlying mechanisms in the Fragile X Syndrome mouse and rat models. [Internet] [Doctoral dissertation]. University of Edinburgh; 2019. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/1842/36928.

Council of Science Editors:

Muscas M. Investigating potential treatment strategies and underlying mechanisms in the Fragile X Syndrome mouse and rat models. [Doctoral Dissertation]. University of Edinburgh; 2019. Available from: http://hdl.handle.net/1842/36928


University of Edinburgh

30. Muscas, Melania. Investigating potential treatment strategies and underlying mechanisms in the Fragile X Syndrome mouse and rat models.

Degree: PhD, 2019, University of Edinburgh

 Fragile X syndrome (FXS) is the most common heritable monogenic cause of intellectual disability (ID) and autism. Along with physical dysmorphic features, it is characterized… (more)

Subjects/Keywords: Fragile X syndrome; protein synthesis regulatory pathways; signalling cascades; FXS; elevated translation; FMRP protein; ERK1/2; VU0152100; M4 PAM

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

APA (6th Edition):

Muscas, M. (2019). Investigating potential treatment strategies and underlying mechanisms in the Fragile X Syndrome mouse and rat models. (Doctoral Dissertation). University of Edinburgh. Retrieved from https://doi.org/10.7488/era/229 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.802263

Chicago Manual of Style (16th Edition):

Muscas, Melania. “Investigating potential treatment strategies and underlying mechanisms in the Fragile X Syndrome mouse and rat models.” 2019. Doctoral Dissertation, University of Edinburgh. Accessed March 05, 2021. https://doi.org/10.7488/era/229 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.802263.

MLA Handbook (7th Edition):

Muscas, Melania. “Investigating potential treatment strategies and underlying mechanisms in the Fragile X Syndrome mouse and rat models.” 2019. Web. 05 Mar 2021.

Vancouver:

Muscas M. Investigating potential treatment strategies and underlying mechanisms in the Fragile X Syndrome mouse and rat models. [Internet] [Doctoral dissertation]. University of Edinburgh; 2019. [cited 2021 Mar 05]. Available from: https://doi.org/10.7488/era/229 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.802263.

Council of Science Editors:

Muscas M. Investigating potential treatment strategies and underlying mechanisms in the Fragile X Syndrome mouse and rat models. [Doctoral Dissertation]. University of Edinburgh; 2019. Available from: https://doi.org/10.7488/era/229 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.802263

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