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You searched for subject:(Fragile X Syndrome). Showing records 1 – 30 of 197 total matches.

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University of Melbourne

1. Aliaga, Solange. The significance of low level mosaicism in Fragile X Syndrome.

Degree: 2017, University of Melbourne

Fragile X Syndrome (FXS) is the most common single disorder associated with intellectual disability (ID) and autism spectrum disorder (ASD). FXS is fundamentally caused by… (more)

Subjects/Keywords: Fragile X Syndrome; FMR1; methylation

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

APA (6th Edition):

Aliaga, S. (2017). The significance of low level mosaicism in Fragile X Syndrome. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/198116

Chicago Manual of Style (16th Edition):

Aliaga, Solange. “The significance of low level mosaicism in Fragile X Syndrome.” 2017. Doctoral Dissertation, University of Melbourne. Accessed April 14, 2021. http://hdl.handle.net/11343/198116.

MLA Handbook (7th Edition):

Aliaga, Solange. “The significance of low level mosaicism in Fragile X Syndrome.” 2017. Web. 14 Apr 2021.

Vancouver:

Aliaga S. The significance of low level mosaicism in Fragile X Syndrome. [Internet] [Doctoral dissertation]. University of Melbourne; 2017. [cited 2021 Apr 14]. Available from: http://hdl.handle.net/11343/198116.

Council of Science Editors:

Aliaga S. The significance of low level mosaicism in Fragile X Syndrome. [Doctoral Dissertation]. University of Melbourne; 2017. Available from: http://hdl.handle.net/11343/198116


Universiteit Utrecht

2. Legerstee, K. Cytoplasmic FMRP Interacting Protein 1 (CYFIP1) - A key player in the pathophysiology of the Fragile X Syndrome?.

Degree: 2011, Universiteit Utrecht

 This literature study investigates the role Cyfip1 could play in the pathophysiology of the Fragile X Syndrome (FXS). FXS, the most common form of mental… (more)

Subjects/Keywords: Fragile X Syndrome; Cyfip1; mGluR theory of fragile X

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APA (6th Edition):

Legerstee, K. (2011). Cytoplasmic FMRP Interacting Protein 1 (CYFIP1) - A key player in the pathophysiology of the Fragile X Syndrome?. (Masters Thesis). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/206609

Chicago Manual of Style (16th Edition):

Legerstee, K. “Cytoplasmic FMRP Interacting Protein 1 (CYFIP1) - A key player in the pathophysiology of the Fragile X Syndrome?.” 2011. Masters Thesis, Universiteit Utrecht. Accessed April 14, 2021. http://dspace.library.uu.nl:8080/handle/1874/206609.

MLA Handbook (7th Edition):

Legerstee, K. “Cytoplasmic FMRP Interacting Protein 1 (CYFIP1) - A key player in the pathophysiology of the Fragile X Syndrome?.” 2011. Web. 14 Apr 2021.

Vancouver:

Legerstee K. Cytoplasmic FMRP Interacting Protein 1 (CYFIP1) - A key player in the pathophysiology of the Fragile X Syndrome?. [Internet] [Masters thesis]. Universiteit Utrecht; 2011. [cited 2021 Apr 14]. Available from: http://dspace.library.uu.nl:8080/handle/1874/206609.

Council of Science Editors:

Legerstee K. Cytoplasmic FMRP Interacting Protein 1 (CYFIP1) - A key player in the pathophysiology of the Fragile X Syndrome?. [Masters Thesis]. Universiteit Utrecht; 2011. Available from: http://dspace.library.uu.nl:8080/handle/1874/206609


University of Illinois – Urbana-Champaign

3. 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 April 14, 2021. http://hdl.handle.net/2142/18643.

MLA Handbook (7th Edition):

Kao, Der-I. “FMRP dependent synaptic delivery of messenger RNA.” 2011. Web. 14 Apr 2021.

Vancouver:

Kao D. FMRP dependent synaptic delivery of messenger RNA. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2011. [cited 2021 Apr 14]. 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


Tulane University

4. Sawyer, Edward. The effects of BMS-204352, an activator of voltage-gated potassium channels, in the infralimbic cortex of the Fmr1 knockout mouse, an animal model of fragile X syndrome.

Degree: 2020, Tulane University

[email protected]

Autism spectrum disorders (ASD) are commonly characterized by abnormal social behaviors. Fragile X syndrome (FXS) is the most common inherited intellectual disability in humans… (more)

Subjects/Keywords: prefrontal cortex; fragile X syndrome; social behavior

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APA (6th Edition):

Sawyer, E. (2020). The effects of BMS-204352, an activator of voltage-gated potassium channels, in the infralimbic cortex of the Fmr1 knockout mouse, an animal model of fragile X syndrome. (Thesis). Tulane University. Retrieved from https://digitallibrary.tulane.edu/islandora/object/tulane:120452

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):

Sawyer, Edward. “The effects of BMS-204352, an activator of voltage-gated potassium channels, in the infralimbic cortex of the Fmr1 knockout mouse, an animal model of fragile X syndrome.” 2020. Thesis, Tulane University. Accessed April 14, 2021. https://digitallibrary.tulane.edu/islandora/object/tulane:120452.

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

MLA Handbook (7th Edition):

Sawyer, Edward. “The effects of BMS-204352, an activator of voltage-gated potassium channels, in the infralimbic cortex of the Fmr1 knockout mouse, an animal model of fragile X syndrome.” 2020. Web. 14 Apr 2021.

Vancouver:

Sawyer E. The effects of BMS-204352, an activator of voltage-gated potassium channels, in the infralimbic cortex of the Fmr1 knockout mouse, an animal model of fragile X syndrome. [Internet] [Thesis]. Tulane University; 2020. [cited 2021 Apr 14]. Available from: https://digitallibrary.tulane.edu/islandora/object/tulane:120452.

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

Council of Science Editors:

Sawyer E. The effects of BMS-204352, an activator of voltage-gated potassium channels, in the infralimbic cortex of the Fmr1 knockout mouse, an animal model of fragile X syndrome. [Thesis]. Tulane University; 2020. Available from: https://digitallibrary.tulane.edu/islandora/object/tulane:120452

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


University of Toronto

5. Xuan, Ingrid Cong Yang. The Maternal Immune Activation Mouse Model of Autism Spectrum Disorders.

Degree: 2013, University of Toronto

Autism spectrum disorder (ASD) is a neurodevelopmental disorder characterized by impairments in social interaction and communication as well as ritualistic repetitive behaviors. Epidemiological studies suggest… (more)

Subjects/Keywords: Autism Spectrum Disorder; Fragile X Syndrome; 0317

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APA (6th Edition):

Xuan, I. C. Y. (2013). The Maternal Immune Activation Mouse Model of Autism Spectrum Disorders. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/43346

Chicago Manual of Style (16th Edition):

Xuan, Ingrid Cong Yang. “The Maternal Immune Activation Mouse Model of Autism Spectrum Disorders.” 2013. Masters Thesis, University of Toronto. Accessed April 14, 2021. http://hdl.handle.net/1807/43346.

MLA Handbook (7th Edition):

Xuan, Ingrid Cong Yang. “The Maternal Immune Activation Mouse Model of Autism Spectrum Disorders.” 2013. Web. 14 Apr 2021.

Vancouver:

Xuan ICY. The Maternal Immune Activation Mouse Model of Autism Spectrum Disorders. [Internet] [Masters thesis]. University of Toronto; 2013. [cited 2021 Apr 14]. Available from: http://hdl.handle.net/1807/43346.

Council of Science Editors:

Xuan ICY. The Maternal Immune Activation Mouse Model of Autism Spectrum Disorders. [Masters Thesis]. University of Toronto; 2013. Available from: http://hdl.handle.net/1807/43346


Baylor University

6. Nolan, Suzanne O., 1991-. Deletion of FMR1 results in sex-specific changes in behavior.

Degree: MA, Baylor University. Dept. of Psychology & Neuroscience., 2016, Baylor University

Fragile X Syndrome (FXS) is a neurodevelopmental disorder caused by excessive trinucleotide (CGG) repeats in the FMR1 gene coding for fragile x mental retardation protein… (more)

Subjects/Keywords: Fragile X Syndrome. Autism Spectrum Disorder.

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APA (6th Edition):

Nolan, Suzanne O., 1. (2016). Deletion of FMR1 results in sex-specific changes in behavior. (Masters Thesis). Baylor University. Retrieved from http://hdl.handle.net/2104/9894

Chicago Manual of Style (16th Edition):

Nolan, Suzanne O., 1991-. “Deletion of FMR1 results in sex-specific changes in behavior.” 2016. Masters Thesis, Baylor University. Accessed April 14, 2021. http://hdl.handle.net/2104/9894.

MLA Handbook (7th Edition):

Nolan, Suzanne O., 1991-. “Deletion of FMR1 results in sex-specific changes in behavior.” 2016. Web. 14 Apr 2021.

Vancouver:

Nolan, Suzanne O. 1. Deletion of FMR1 results in sex-specific changes in behavior. [Internet] [Masters thesis]. Baylor University; 2016. [cited 2021 Apr 14]. Available from: http://hdl.handle.net/2104/9894.

Council of Science Editors:

Nolan, Suzanne O. 1. Deletion of FMR1 results in sex-specific changes in behavior. [Masters Thesis]. Baylor University; 2016. Available from: http://hdl.handle.net/2104/9894


Université de Sherbrooke

7. 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 April 14, 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. 14 Apr 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 Apr 14]. 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

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

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 April 14, 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. 14 Apr 2021.

Vancouver:

Zhang Y. The Role of G-Quadruplex RNA Motif in Fragile X Syndrome. [Internet] [Masters thesis]. Duquesne University; 2014. [cited 2021 Apr 14]. 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

9. 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 April 14, 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. 14 Apr 2021.

Vancouver:

Blice-Baum A. Fragile X Mental Retardation Protein: Self-Regulation and miRNA Pathway Involvement. [Internet] [Doctoral dissertation]. Duquesne University; 2013. [cited 2021 Apr 14]. 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


University of Pennsylvania

10. Monyak, Rachel Elisabeth. Identification And Rescue Of Misregulated Insulin Signaling In A Drosophila Model Of Fragile X Syndrome.

Degree: 2016, University of Pennsylvania

Fragile X syndrome (FXS) is an undertreated neurodevelopmental disorder characterized by low IQ and a range of symptoms including disordered sleep and autism. Although FXS… (more)

Subjects/Keywords: Drosophila; Fragile X Syndrome; Insulin Signaling; Genetics

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APA (6th Edition):

Monyak, R. E. (2016). Identification And Rescue Of Misregulated Insulin Signaling In A Drosophila Model Of Fragile X Syndrome. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/2482

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):

Monyak, Rachel Elisabeth. “Identification And Rescue Of Misregulated Insulin Signaling In A Drosophila Model Of Fragile X Syndrome.” 2016. Thesis, University of Pennsylvania. Accessed April 14, 2021. https://repository.upenn.edu/edissertations/2482.

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

MLA Handbook (7th Edition):

Monyak, Rachel Elisabeth. “Identification And Rescue Of Misregulated Insulin Signaling In A Drosophila Model Of Fragile X Syndrome.” 2016. Web. 14 Apr 2021.

Vancouver:

Monyak RE. Identification And Rescue Of Misregulated Insulin Signaling In A Drosophila Model Of Fragile X Syndrome. [Internet] [Thesis]. University of Pennsylvania; 2016. [cited 2021 Apr 14]. Available from: https://repository.upenn.edu/edissertations/2482.

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

Council of Science Editors:

Monyak RE. Identification And Rescue Of Misregulated Insulin Signaling In A Drosophila Model Of Fragile X Syndrome. [Thesis]. University of Pennsylvania; 2016. Available from: https://repository.upenn.edu/edissertations/2482

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

11. Haberl, Matthias. Studying Neuronal Connectivity in the Mouse Brain in Normal Condition and Fragile X Syndrome : Neuronale connectivité dans le cerveau de souris en condition normale et en syndrome du X fragile.

Degree: Docteur es, Neurosciences, 2014, Bordeaux; Universität Zürich

Le but de ce travail est l'étude de la connectivité anatomique et fonctionnelle desréseaux neuronaux et le développement des nouveaux outils à cet effet. Car… (more)

Subjects/Keywords: Traçage Virale; Syndrome du X Fragile; Connectivité; Viral tracing; Fragile X Syndrome; Connectivity

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APA (6th Edition):

Haberl, M. (2014). Studying Neuronal Connectivity in the Mouse Brain in Normal Condition and Fragile X Syndrome : Neuronale connectivité dans le cerveau de souris en condition normale et en syndrome du X fragile. (Doctoral Dissertation). Bordeaux; Universität Zürich. Retrieved from http://www.theses.fr/2014BORD0480

Chicago Manual of Style (16th Edition):

Haberl, Matthias. “Studying Neuronal Connectivity in the Mouse Brain in Normal Condition and Fragile X Syndrome : Neuronale connectivité dans le cerveau de souris en condition normale et en syndrome du X fragile.” 2014. Doctoral Dissertation, Bordeaux; Universität Zürich. Accessed April 14, 2021. http://www.theses.fr/2014BORD0480.

MLA Handbook (7th Edition):

Haberl, Matthias. “Studying Neuronal Connectivity in the Mouse Brain in Normal Condition and Fragile X Syndrome : Neuronale connectivité dans le cerveau de souris en condition normale et en syndrome du X fragile.” 2014. Web. 14 Apr 2021.

Vancouver:

Haberl M. Studying Neuronal Connectivity in the Mouse Brain in Normal Condition and Fragile X Syndrome : Neuronale connectivité dans le cerveau de souris en condition normale et en syndrome du X fragile. [Internet] [Doctoral dissertation]. Bordeaux; Universität Zürich; 2014. [cited 2021 Apr 14]. Available from: http://www.theses.fr/2014BORD0480.

Council of Science Editors:

Haberl M. Studying Neuronal Connectivity in the Mouse Brain in Normal Condition and Fragile X Syndrome : Neuronale connectivité dans le cerveau de souris en condition normale et en syndrome du X fragile. [Doctoral Dissertation]. Bordeaux; Universität Zürich; 2014. Available from: http://www.theses.fr/2014BORD0480


University of New South Wales

12. Birch, Rachael. Evidence for specific neurobehavioural signatures in male carriers of the FMR1 premutation.

Degree: Psychiatry, 2015, University of New South Wales

 Premutation (PM) expansions (55–200 CGG repeats) of the Fragile X Mental Retardation 1 (FMR1) gene confer risk for the development of fragile X-associated tremor ataxia… (more)

Subjects/Keywords: Fragile X-associated disorders; Fragile X Mental Retardation 1 (FMR1) gene; Fragile X-associated tremor ataxia syndrome (FXTAS)

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APA (6th Edition):

Birch, R. (2015). Evidence for specific neurobehavioural signatures in male carriers of the FMR1 premutation. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/54868 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:36072/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Birch, Rachael. “Evidence for specific neurobehavioural signatures in male carriers of the FMR1 premutation.” 2015. Doctoral Dissertation, University of New South Wales. Accessed April 14, 2021. http://handle.unsw.edu.au/1959.4/54868 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:36072/SOURCE02?view=true.

MLA Handbook (7th Edition):

Birch, Rachael. “Evidence for specific neurobehavioural signatures in male carriers of the FMR1 premutation.” 2015. Web. 14 Apr 2021.

Vancouver:

Birch R. Evidence for specific neurobehavioural signatures in male carriers of the FMR1 premutation. [Internet] [Doctoral dissertation]. University of New South Wales; 2015. [cited 2021 Apr 14]. Available from: http://handle.unsw.edu.au/1959.4/54868 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:36072/SOURCE02?view=true.

Council of Science Editors:

Birch R. Evidence for specific neurobehavioural signatures in male carriers of the FMR1 premutation. [Doctoral Dissertation]. University of New South Wales; 2015. Available from: http://handle.unsw.edu.au/1959.4/54868 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:36072/SOURCE02?view=true


Drexel University

13. Zimmer, Stephanie Elaine. Structure-Function Analysis of Axonal Fragile X Mental Retardation Protein.

Degree: 2015, Drexel University

 Silencing of the Fragile X Mental Retardation Protein (FMRP)-encoding gene Fmr1 causes Fragile X Syndrome, the leading known cause of autism. FMRP is an alternatively… (more)

Subjects/Keywords: Biology; Fragile X syndrome; X-linked mental retardation

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APA (6th Edition):

Zimmer, S. E. (2015). Structure-Function Analysis of Axonal Fragile X Mental Retardation Protein. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/idea:6495

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):

Zimmer, Stephanie Elaine. “Structure-Function Analysis of Axonal Fragile X Mental Retardation Protein.” 2015. Thesis, Drexel University. Accessed April 14, 2021. http://hdl.handle.net/1860/idea:6495.

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

MLA Handbook (7th Edition):

Zimmer, Stephanie Elaine. “Structure-Function Analysis of Axonal Fragile X Mental Retardation Protein.” 2015. Web. 14 Apr 2021.

Vancouver:

Zimmer SE. Structure-Function Analysis of Axonal Fragile X Mental Retardation Protein. [Internet] [Thesis]. Drexel University; 2015. [cited 2021 Apr 14]. Available from: http://hdl.handle.net/1860/idea:6495.

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

Council of Science Editors:

Zimmer SE. Structure-Function Analysis of Axonal Fragile X Mental Retardation Protein. [Thesis]. Drexel University; 2015. Available from: http://hdl.handle.net/1860/idea:6495

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

14. Aloisi, Elisabetta. Involvement of mGluR5/Homer crosstalk disruption in the pathophysiology of Fragile X Syndrome : Participation de la perturbation de l'interaction entre mGluR5 et Homer dans la physiopathologie du Syndrome de l'X Fragile.

Degree: Docteur es, Neurosciences, 2015, Bordeaux; Università degli studi (Catane, Italie)

 Le Syndrome de l'X Fragile (FXS) est la forme héréditaire majoritaire de déficience intellectuelle et la cause monogénique de l'autisme. Le FXS est causé par… (more)

Subjects/Keywords: Syndrome de l'X Fragile; Protéines Homer; MGluR5; Fragile X Syndrom; Homer proteins; MGluR5

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APA (6th Edition):

Aloisi, E. (2015). Involvement of mGluR5/Homer crosstalk disruption in the pathophysiology of Fragile X Syndrome : Participation de la perturbation de l'interaction entre mGluR5 et Homer dans la physiopathologie du Syndrome de l'X Fragile. (Doctoral Dissertation). Bordeaux; Università degli studi (Catane, Italie). Retrieved from http://www.theses.fr/2015BORD0006

Chicago Manual of Style (16th Edition):

Aloisi, Elisabetta. “Involvement of mGluR5/Homer crosstalk disruption in the pathophysiology of Fragile X Syndrome : Participation de la perturbation de l'interaction entre mGluR5 et Homer dans la physiopathologie du Syndrome de l'X Fragile.” 2015. Doctoral Dissertation, Bordeaux; Università degli studi (Catane, Italie). Accessed April 14, 2021. http://www.theses.fr/2015BORD0006.

MLA Handbook (7th Edition):

Aloisi, Elisabetta. “Involvement of mGluR5/Homer crosstalk disruption in the pathophysiology of Fragile X Syndrome : Participation de la perturbation de l'interaction entre mGluR5 et Homer dans la physiopathologie du Syndrome de l'X Fragile.” 2015. Web. 14 Apr 2021.

Vancouver:

Aloisi E. Involvement of mGluR5/Homer crosstalk disruption in the pathophysiology of Fragile X Syndrome : Participation de la perturbation de l'interaction entre mGluR5 et Homer dans la physiopathologie du Syndrome de l'X Fragile. [Internet] [Doctoral dissertation]. Bordeaux; Università degli studi (Catane, Italie); 2015. [cited 2021 Apr 14]. Available from: http://www.theses.fr/2015BORD0006.

Council of Science Editors:

Aloisi E. Involvement of mGluR5/Homer crosstalk disruption in the pathophysiology of Fragile X Syndrome : Participation de la perturbation de l'interaction entre mGluR5 et Homer dans la physiopathologie du Syndrome de l'X Fragile. [Doctoral Dissertation]. Bordeaux; Università degli studi (Catane, Italie); 2015. Available from: http://www.theses.fr/2015BORD0006

15. 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 · 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. (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 April 14, 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. 14 Apr 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 Apr 14]. 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

16. Caku, Artuela. Étude ouverte pour évaluer l'efficacité et l'innocuité de la lovastatine chez les individus atteints du syndrome du X fragile.

Degree: M. Sc., Sciences cliniques, 2015, Université de Sherbrooke

 Résumé : Le syndrome du X fragile (SXF) est la première cause de déficience intellectuelle héréditaire et résulte de mutations dans le gène FMR1 menant… (more)

Subjects/Keywords: Syndrome de X Fragile; Traitement; Lovastatin; Voie de signalisation ERK; Comportement adaptif; Fragile X Syndrome; Treatment; Lovastatin; ERK; Adaptive behaviour

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APA (6th Edition):

Caku, A. (2015). Étude ouverte pour évaluer l'efficacité et l'innocuité de la lovastatine chez les individus atteints du syndrome du X fragile. (Masters Thesis). Université de Sherbrooke. Retrieved from http://www.collectionscanada.gc.ca/obj/thesescanada/vol2/QSHERU/TC-QSHERU-11143_6862.pdf ; http://savoirs.usherbrooke.ca/bitstream/11143/6862/9/Caku_Artuela_MSc_2015.pdf

Chicago Manual of Style (16th Edition):

Caku, Artuela. “Étude ouverte pour évaluer l'efficacité et l'innocuité de la lovastatine chez les individus atteints du syndrome du X fragile.” 2015. Masters Thesis, Université de Sherbrooke. Accessed April 14, 2021. http://www.collectionscanada.gc.ca/obj/thesescanada/vol2/QSHERU/TC-QSHERU-11143_6862.pdf ; http://savoirs.usherbrooke.ca/bitstream/11143/6862/9/Caku_Artuela_MSc_2015.pdf.

MLA Handbook (7th Edition):

Caku, Artuela. “Étude ouverte pour évaluer l'efficacité et l'innocuité de la lovastatine chez les individus atteints du syndrome du X fragile.” 2015. Web. 14 Apr 2021.

Vancouver:

Caku A. Étude ouverte pour évaluer l'efficacité et l'innocuité de la lovastatine chez les individus atteints du syndrome du X fragile. [Internet] [Masters thesis]. Université de Sherbrooke; 2015. [cited 2021 Apr 14]. Available from: http://www.collectionscanada.gc.ca/obj/thesescanada/vol2/QSHERU/TC-QSHERU-11143_6862.pdf ; http://savoirs.usherbrooke.ca/bitstream/11143/6862/9/Caku_Artuela_MSc_2015.pdf.

Council of Science Editors:

Caku A. Étude ouverte pour évaluer l'efficacité et l'innocuité de la lovastatine chez les individus atteints du syndrome du X fragile. [Masters Thesis]. Université de Sherbrooke; 2015. Available from: http://www.collectionscanada.gc.ca/obj/thesescanada/vol2/QSHERU/TC-QSHERU-11143_6862.pdf ; http://savoirs.usherbrooke.ca/bitstream/11143/6862/9/Caku_Artuela_MSc_2015.pdf

17. Shorb, JoAnne E. Raising fragile : the experiences & perspectives of the families of male Fragile X individuals.

Degree: MS, Education, 2013, Oregon State University

 The purpose of this qualitative research study was to address the experiences and perspectives of those who have grown up with and raised males who… (more)

Subjects/Keywords: Fragile X Syndrome; Fragile X syndrome

…27 LIST OF TABLES Table Page Table 1: General Information about Fragile X Syndrome… …Individuals afflicted with Fragile X syndrome and their families are such uncategorizable social… …groups and individuals. Fragile X syndrome is a condition, a form of mental retardation that… …condition (Fragile X syndrome) exists. Parents with experiences such as these have… …sorry to tell you that he has been diagnosed with FragileX Syndrome,” she said. My eyes… 

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APA (6th Edition):

Shorb, J. E. (2013). Raising fragile : the experiences & perspectives of the families of male Fragile X individuals. (Masters Thesis). Oregon State University. Retrieved from http://hdl.handle.net/1957/38603

Chicago Manual of Style (16th Edition):

Shorb, JoAnne E. “Raising fragile : the experiences & perspectives of the families of male Fragile X individuals.” 2013. Masters Thesis, Oregon State University. Accessed April 14, 2021. http://hdl.handle.net/1957/38603.

MLA Handbook (7th Edition):

Shorb, JoAnne E. “Raising fragile : the experiences & perspectives of the families of male Fragile X individuals.” 2013. Web. 14 Apr 2021.

Vancouver:

Shorb JE. Raising fragile : the experiences & perspectives of the families of male Fragile X individuals. [Internet] [Masters thesis]. Oregon State University; 2013. [cited 2021 Apr 14]. Available from: http://hdl.handle.net/1957/38603.

Council of Science Editors:

Shorb JE. Raising fragile : the experiences & perspectives of the families of male Fragile X individuals. [Masters Thesis]. Oregon State University; 2013. Available from: http://hdl.handle.net/1957/38603


Université de Sherbrooke

18. Caku, Artuela. Étude ouverte pour évaluer l'efficacité et l'innocuité de la lovastatine chez les individus atteints du syndrome du X fragile: Lovastatine as a behavior treatment in children and adults with Fragile X Syndrome : Phase I study.

Degree: 2015, Université de Sherbrooke

 Abstract : Background: Fragile X Syndrome (FXS) results from dynamic mutations leading ultimately to the absence of expression of the Fragile X Mental Retardation Protein… (more)

Subjects/Keywords: Syndrome de X Fragile; Traitement; Lovastatin; Voie de signalisation ERK; Comportement adaptif; Fragile X Syndrome; Treatment; Lovastatin; ERK; Adaptive behaviour

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

APA (6th Edition):

Caku, A. (2015). Étude ouverte pour évaluer l'efficacité et l'innocuité de la lovastatine chez les individus atteints du syndrome du X fragile: Lovastatine as a behavior treatment in children and adults with Fragile X Syndrome : Phase I study. (Masters Thesis). Université de Sherbrooke. Retrieved from http://hdl.handle.net/11143/6862

Chicago Manual of Style (16th Edition):

Caku, Artuela. “Étude ouverte pour évaluer l'efficacité et l'innocuité de la lovastatine chez les individus atteints du syndrome du X fragile: Lovastatine as a behavior treatment in children and adults with Fragile X Syndrome : Phase I study.” 2015. Masters Thesis, Université de Sherbrooke. Accessed April 14, 2021. http://hdl.handle.net/11143/6862.

MLA Handbook (7th Edition):

Caku, Artuela. “Étude ouverte pour évaluer l'efficacité et l'innocuité de la lovastatine chez les individus atteints du syndrome du X fragile: Lovastatine as a behavior treatment in children and adults with Fragile X Syndrome : Phase I study.” 2015. Web. 14 Apr 2021.

Vancouver:

Caku A. Étude ouverte pour évaluer l'efficacité et l'innocuité de la lovastatine chez les individus atteints du syndrome du X fragile: Lovastatine as a behavior treatment in children and adults with Fragile X Syndrome : Phase I study. [Internet] [Masters thesis]. Université de Sherbrooke; 2015. [cited 2021 Apr 14]. Available from: http://hdl.handle.net/11143/6862.

Council of Science Editors:

Caku A. Étude ouverte pour évaluer l'efficacité et l'innocuité de la lovastatine chez les individus atteints du syndrome du X fragile: Lovastatine as a behavior treatment in children and adults with Fragile X Syndrome : Phase I study. [Masters Thesis]. Université de Sherbrooke; 2015. Available from: http://hdl.handle.net/11143/6862


Université de Sherbrooke

19. 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 April 14, 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. 14 Apr 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 Apr 14]. 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


Université de Sherbrooke

20. Pellerin, David. Correction de l’hyperactivité de la voie ERK par la lovastatine chez des individus avec syndrome du X fragile : potentiel des cascades signalétiques plaquettaires comme nouvelles mesures de la réponse clinique dans les essais thérapeutiques: Lovastatin corrects ERK pathway hyperactivation in fragile X syndrome: potential of platelet’s signaling cascades as new outcome measures in clinical trials.

Degree: 2017, Université de Sherbrooke

 Abstract: Background: Fragile X syndrome (FXS) results from loss of FMRP expression, which causes several signaling dysregulations, including the hyperactivation of the Mitogen-activated protein kinase… (more)

Subjects/Keywords: Syndrome du X fragile; ERK; Akt; Lovastatine; Biomarqueurs; Plaquettes; Fragile X syndrome; Lovastatin; Biomarkers; Blood platelets

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

APA (6th Edition):

Pellerin, D. (2017). Correction de l’hyperactivité de la voie ERK par la lovastatine chez des individus avec syndrome du X fragile : potentiel des cascades signalétiques plaquettaires comme nouvelles mesures de la réponse clinique dans les essais thérapeutiques: Lovastatin corrects ERK pathway hyperactivation in fragile X syndrome: potential of platelet’s signaling cascades as new outcome measures in clinical trials. (Masters Thesis). Université de Sherbrooke. Retrieved from http://hdl.handle.net/11143/11082

Chicago Manual of Style (16th Edition):

Pellerin, David. “Correction de l’hyperactivité de la voie ERK par la lovastatine chez des individus avec syndrome du X fragile : potentiel des cascades signalétiques plaquettaires comme nouvelles mesures de la réponse clinique dans les essais thérapeutiques: Lovastatin corrects ERK pathway hyperactivation in fragile X syndrome: potential of platelet’s signaling cascades as new outcome measures in clinical trials.” 2017. Masters Thesis, Université de Sherbrooke. Accessed April 14, 2021. http://hdl.handle.net/11143/11082.

MLA Handbook (7th Edition):

Pellerin, David. “Correction de l’hyperactivité de la voie ERK par la lovastatine chez des individus avec syndrome du X fragile : potentiel des cascades signalétiques plaquettaires comme nouvelles mesures de la réponse clinique dans les essais thérapeutiques: Lovastatin corrects ERK pathway hyperactivation in fragile X syndrome: potential of platelet’s signaling cascades as new outcome measures in clinical trials.” 2017. Web. 14 Apr 2021.

Vancouver:

Pellerin D. Correction de l’hyperactivité de la voie ERK par la lovastatine chez des individus avec syndrome du X fragile : potentiel des cascades signalétiques plaquettaires comme nouvelles mesures de la réponse clinique dans les essais thérapeutiques: Lovastatin corrects ERK pathway hyperactivation in fragile X syndrome: potential of platelet’s signaling cascades as new outcome measures in clinical trials. [Internet] [Masters thesis]. Université de Sherbrooke; 2017. [cited 2021 Apr 14]. Available from: http://hdl.handle.net/11143/11082.

Council of Science Editors:

Pellerin D. Correction de l’hyperactivité de la voie ERK par la lovastatine chez des individus avec syndrome du X fragile : potentiel des cascades signalétiques plaquettaires comme nouvelles mesures de la réponse clinique dans les essais thérapeutiques: Lovastatin corrects ERK pathway hyperactivation in fragile X syndrome: potential of platelet’s signaling cascades as new outcome measures in clinical trials. [Masters Thesis]. Université de Sherbrooke; 2017. Available from: http://hdl.handle.net/11143/11082


Université de Sherbrooke

21. Fradet, Mathieu. Modulation du protéome plaquettaire suivant un traitement à la lovastatine; comparaison entre cohortes d’individus sains ou avec syndrome du X fragile.

Degree: 2020, Université de Sherbrooke

 Le SXF est la première cause héréditaire de déficience intellectuelle. Des études suggèrent que la lovastatine permettrait de corriger des anomalies signalétiques importantes dans la… (more)

Subjects/Keywords: Syndrome du X fragile; Lovastatine; Protéomique; Spectrométrie de masse; Biomarqueurs; Plaquettes; Fragile X syndrome; Lovastatin; Proteomics; Mass spectrometry; Biomarkers; Platelets

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APA (6th Edition):

Fradet, M. (2020). Modulation du protéome plaquettaire suivant un traitement à la lovastatine; comparaison entre cohortes d’individus sains ou avec syndrome du X fragile. (Masters Thesis). Université de Sherbrooke. Retrieved from http://hdl.handle.net/11143/17674

Chicago Manual of Style (16th Edition):

Fradet, Mathieu. “Modulation du protéome plaquettaire suivant un traitement à la lovastatine; comparaison entre cohortes d’individus sains ou avec syndrome du X fragile.” 2020. Masters Thesis, Université de Sherbrooke. Accessed April 14, 2021. http://hdl.handle.net/11143/17674.

MLA Handbook (7th Edition):

Fradet, Mathieu. “Modulation du protéome plaquettaire suivant un traitement à la lovastatine; comparaison entre cohortes d’individus sains ou avec syndrome du X fragile.” 2020. Web. 14 Apr 2021.

Vancouver:

Fradet M. Modulation du protéome plaquettaire suivant un traitement à la lovastatine; comparaison entre cohortes d’individus sains ou avec syndrome du X fragile. [Internet] [Masters thesis]. Université de Sherbrooke; 2020. [cited 2021 Apr 14]. Available from: http://hdl.handle.net/11143/17674.

Council of Science Editors:

Fradet M. Modulation du protéome plaquettaire suivant un traitement à la lovastatine; comparaison entre cohortes d’individus sains ou avec syndrome du X fragile. [Masters Thesis]. Université de Sherbrooke; 2020. Available from: http://hdl.handle.net/11143/17674

22. De Sa, Rafael. The role of intrinsic neuronal excitability for Prelimbic network function : Le role de l’excitabilité neuronale intrinsèque pour les fonctions du réseau pré-limbique.

Degree: Docteur es, Neurosciences, 2019, Bordeaux

 Le but de ce travail était de caractériser l’identité cellulaire des neurones de la couche 5 de l’aire prélimbique (PL) du cortex préfrontal médial (mPFC)… (more)

Subjects/Keywords: Cortex prefrontal; Dopamine; Canaux ioniques; Syndrome du X fragile; Mémoire; Prefrontal cortex; Dopamine; Ion channels; Fragile X syndrome; Memory

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APA (6th Edition):

De Sa, R. (2019). The role of intrinsic neuronal excitability for Prelimbic network function : Le role de l’excitabilité neuronale intrinsèque pour les fonctions du réseau pré-limbique. (Doctoral Dissertation). Bordeaux. Retrieved from http://www.theses.fr/2019BORD0150

Chicago Manual of Style (16th Edition):

De Sa, Rafael. “The role of intrinsic neuronal excitability for Prelimbic network function : Le role de l’excitabilité neuronale intrinsèque pour les fonctions du réseau pré-limbique.” 2019. Doctoral Dissertation, Bordeaux. Accessed April 14, 2021. http://www.theses.fr/2019BORD0150.

MLA Handbook (7th Edition):

De Sa, Rafael. “The role of intrinsic neuronal excitability for Prelimbic network function : Le role de l’excitabilité neuronale intrinsèque pour les fonctions du réseau pré-limbique.” 2019. Web. 14 Apr 2021.

Vancouver:

De Sa R. The role of intrinsic neuronal excitability for Prelimbic network function : Le role de l’excitabilité neuronale intrinsèque pour les fonctions du réseau pré-limbique. [Internet] [Doctoral dissertation]. Bordeaux; 2019. [cited 2021 Apr 14]. Available from: http://www.theses.fr/2019BORD0150.

Council of Science Editors:

De Sa R. The role of intrinsic neuronal excitability for Prelimbic network function : Le role de l’excitabilité neuronale intrinsèque pour les fonctions du réseau pré-limbique. [Doctoral Dissertation]. Bordeaux; 2019. Available from: http://www.theses.fr/2019BORD0150

23. Carreno-Muñoz, Maria Isabel. Etude expérimentale des dynamiques temporelles du comportement normal et pathologique chez le rat et la souris : Supervised and unsupervised investigation of the temporal dynamics of normal and pathological behaviour in the mouse and rat.

Degree: Docteur es, Neurosciences, 2017, Bordeaux; Universidad del País Vasco

Le développement d'outils de phénotypage comportemental sophistiqués est indispensable pour comprendre le fonctionnement cognitif. A partir d'une analyse élaborée de tests comportementaux classiques, mes résultats… (more)

Subjects/Keywords: Comportement; Ethologie; Computation; Syndrome de l'X fragile; Alzheimer; Parkinson; Behavior; Ethlogy; Computation; Fragile X Syndrome; Alzheimer; Parkinson

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APA (6th Edition):

Carreno-Muñoz, M. I. (2017). Etude expérimentale des dynamiques temporelles du comportement normal et pathologique chez le rat et la souris : Supervised and unsupervised investigation of the temporal dynamics of normal and pathological behaviour in the mouse and rat. (Doctoral Dissertation). Bordeaux; Universidad del País Vasco. Retrieved from http://www.theses.fr/2017BORD0676

Chicago Manual of Style (16th Edition):

Carreno-Muñoz, Maria Isabel. “Etude expérimentale des dynamiques temporelles du comportement normal et pathologique chez le rat et la souris : Supervised and unsupervised investigation of the temporal dynamics of normal and pathological behaviour in the mouse and rat.” 2017. Doctoral Dissertation, Bordeaux; Universidad del País Vasco. Accessed April 14, 2021. http://www.theses.fr/2017BORD0676.

MLA Handbook (7th Edition):

Carreno-Muñoz, Maria Isabel. “Etude expérimentale des dynamiques temporelles du comportement normal et pathologique chez le rat et la souris : Supervised and unsupervised investigation of the temporal dynamics of normal and pathological behaviour in the mouse and rat.” 2017. Web. 14 Apr 2021.

Vancouver:

Carreno-Muñoz MI. Etude expérimentale des dynamiques temporelles du comportement normal et pathologique chez le rat et la souris : Supervised and unsupervised investigation of the temporal dynamics of normal and pathological behaviour in the mouse and rat. [Internet] [Doctoral dissertation]. Bordeaux; Universidad del País Vasco; 2017. [cited 2021 Apr 14]. Available from: http://www.theses.fr/2017BORD0676.

Council of Science Editors:

Carreno-Muñoz MI. Etude expérimentale des dynamiques temporelles du comportement normal et pathologique chez le rat et la souris : Supervised and unsupervised investigation of the temporal dynamics of normal and pathological behaviour in the mouse and rat. [Doctoral Dissertation]. Bordeaux; Universidad del País Vasco; 2017. Available from: http://www.theses.fr/2017BORD0676

24. Andrea Sousa Varela. Psychanalyse et génétique médicale : une rencontre possible à partir du syndrome du chromosome X fragile.

Degree: 2017, University of São Paulo

Cette thèse part de la proposition d\'une rencontre possible entre psychanalyse et génétique médicale par le biais des soins offerts aux enfants porteurs de syndromes… (more)

Subjects/Keywords: Clinique psychanalytique; Enfance; Épigénétique; Génétique Médicale; Psychanalyse; Syndrome de l'X fragile; Childwood; Epigenetics; Fragile X syndrome; Psychoanalysis medical genetics; Psychoanalytic clinic

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APA (6th Edition):

Varela, A. S. (2017). Psychanalyse et génétique médicale : une rencontre possible à partir du syndrome du chromosome X fragile. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/47/47133/tde-23042018-152543/

Chicago Manual of Style (16th Edition):

Varela, Andrea Sousa. “Psychanalyse et génétique médicale : une rencontre possible à partir du syndrome du chromosome X fragile.” 2017. Doctoral Dissertation, University of São Paulo. Accessed April 14, 2021. http://www.teses.usp.br/teses/disponiveis/47/47133/tde-23042018-152543/.

MLA Handbook (7th Edition):

Varela, Andrea Sousa. “Psychanalyse et génétique médicale : une rencontre possible à partir du syndrome du chromosome X fragile.” 2017. Web. 14 Apr 2021.

Vancouver:

Varela AS. Psychanalyse et génétique médicale : une rencontre possible à partir du syndrome du chromosome X fragile. [Internet] [Doctoral dissertation]. University of São Paulo; 2017. [cited 2021 Apr 14]. Available from: http://www.teses.usp.br/teses/disponiveis/47/47133/tde-23042018-152543/.

Council of Science Editors:

Varela AS. Psychanalyse et génétique médicale : une rencontre possible à partir du syndrome du chromosome X fragile. [Doctoral Dissertation]. University of São Paulo; 2017. Available from: http://www.teses.usp.br/teses/disponiveis/47/47133/tde-23042018-152543/


University of California – Riverside

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

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 April 14, 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. 14 Apr 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 Apr 14]. 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


UCLA

26. Berg, Jamee Mae. Elucidation of the Developmental Role of Janus Kinase and Microtubule-Interacting Protein 1, JAKMIP1, an Autism Candidate Gene.

Degree: Neuroscience, 2013, UCLA

 Autism Spectrum Disorders (ASD) are heritable neurodevelopmental disorders, affecting one in 88 children and involving hundreds of genes. The study of convergent biological pathways and… (more)

Subjects/Keywords: Neurosciences; Developmental biology; Animal behavior; Autism; Fragile X Syndrome; Translation

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APA (6th Edition):

Berg, J. M. (2013). Elucidation of the Developmental Role of Janus Kinase and Microtubule-Interacting Protein 1, JAKMIP1, an Autism Candidate Gene. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/1711c5zk

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):

Berg, Jamee Mae. “Elucidation of the Developmental Role of Janus Kinase and Microtubule-Interacting Protein 1, JAKMIP1, an Autism Candidate Gene.” 2013. Thesis, UCLA. Accessed April 14, 2021. http://www.escholarship.org/uc/item/1711c5zk.

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

MLA Handbook (7th Edition):

Berg, Jamee Mae. “Elucidation of the Developmental Role of Janus Kinase and Microtubule-Interacting Protein 1, JAKMIP1, an Autism Candidate Gene.” 2013. Web. 14 Apr 2021.

Vancouver:

Berg JM. Elucidation of the Developmental Role of Janus Kinase and Microtubule-Interacting Protein 1, JAKMIP1, an Autism Candidate Gene. [Internet] [Thesis]. UCLA; 2013. [cited 2021 Apr 14]. Available from: http://www.escholarship.org/uc/item/1711c5zk.

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

Council of Science Editors:

Berg JM. Elucidation of the Developmental Role of Janus Kinase and Microtubule-Interacting Protein 1, JAKMIP1, an Autism Candidate Gene. [Thesis]. UCLA; 2013. Available from: http://www.escholarship.org/uc/item/1711c5zk

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


University of California – Santa Cruz

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

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 April 14, 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. 14 Apr 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 Apr 14]. 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


University of Alberta

28. Chambers, Daniel B. Understanding the Molecular Basis of Memory Defects in Fragile X Syndrome.

Degree: MS, Centre for Neuroscience, 2014, University of Alberta

Fragile X Syndrome (FXS) is the most common genetic cause of Intellectual Disability, affecting 1 in 4000 boys and 1 in 6000 girls. Work in… (more)

Subjects/Keywords: Fragile X Syndrome; Neuroscience; Drosophila; Intellectual Disability; Learning and Memory

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

APA (6th Edition):

Chambers, D. B. (2014). Understanding the Molecular Basis of Memory Defects in Fragile X Syndrome. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/czp38wc83b

Chicago Manual of Style (16th Edition):

Chambers, Daniel B. “Understanding the Molecular Basis of Memory Defects in Fragile X Syndrome.” 2014. Masters Thesis, University of Alberta. Accessed April 14, 2021. https://era.library.ualberta.ca/files/czp38wc83b.

MLA Handbook (7th Edition):

Chambers, Daniel B. “Understanding the Molecular Basis of Memory Defects in Fragile X Syndrome.” 2014. Web. 14 Apr 2021.

Vancouver:

Chambers DB. Understanding the Molecular Basis of Memory Defects in Fragile X Syndrome. [Internet] [Masters thesis]. University of Alberta; 2014. [cited 2021 Apr 14]. Available from: https://era.library.ualberta.ca/files/czp38wc83b.

Council of Science Editors:

Chambers DB. Understanding the Molecular Basis of Memory Defects in Fragile X Syndrome. [Masters Thesis]. University of Alberta; 2014. Available from: https://era.library.ualberta.ca/files/czp38wc83b


University of Texas Southwestern Medical Center

29. Collins, Katie Anne. The Role of Homer Scaffolding to Metabotropic Glutamate Receptor 5 in the Mouse Models of Neurodevelopement Disorders.

Degree: 2014, University of Texas Southwestern Medical Center

 Autism is a neurological disorder characterized by repetetive behaviors, social anxiety and verbal and non-verbal communication. Fragile X Syndrome (FXS) is the most common genetic… (more)

Subjects/Keywords: Carrier Proteins; Fragile X Syndrome; Gene Expression Regulation; Receptors, Metabotropic Glutamate

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

APA (6th Edition):

Collins, K. A. (2014). The Role of Homer Scaffolding to Metabotropic Glutamate Receptor 5 in the Mouse Models of Neurodevelopement Disorders. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/3308

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):

Collins, Katie Anne. “The Role of Homer Scaffolding to Metabotropic Glutamate Receptor 5 in the Mouse Models of Neurodevelopement Disorders.” 2014. Thesis, University of Texas Southwestern Medical Center. Accessed April 14, 2021. http://hdl.handle.net/2152.5/3308.

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

MLA Handbook (7th Edition):

Collins, Katie Anne. “The Role of Homer Scaffolding to Metabotropic Glutamate Receptor 5 in the Mouse Models of Neurodevelopement Disorders.” 2014. Web. 14 Apr 2021.

Vancouver:

Collins KA. The Role of Homer Scaffolding to Metabotropic Glutamate Receptor 5 in the Mouse Models of Neurodevelopement Disorders. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2014. [cited 2021 Apr 14]. Available from: http://hdl.handle.net/2152.5/3308.

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

Council of Science Editors:

Collins KA. The Role of Homer Scaffolding to Metabotropic Glutamate Receptor 5 in the Mouse Models of Neurodevelopement Disorders. [Thesis]. University of Texas Southwestern Medical Center; 2014. Available from: http://hdl.handle.net/2152.5/3308

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


Boston University

30. Penz, Craig Christopher. Baseline characteristics influencing placebo response in clinical trials of treatments for fragile X syndrome.

Degree: 2014, Boston University

Fragile X Syndrome (FXS) is a disorder caused by a congenital mutation of the FMR1 gene on the X chromosome. FXS is associated with moderate… (more)

Subjects/Keywords: Pharmaceutical sciences; Placebo effect; Placebo response; Fragile X syndrome

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

APA (6th Edition):

Penz, C. C. (2014). Baseline characteristics influencing placebo response in clinical trials of treatments for fragile X syndrome. (Thesis). Boston University. Retrieved from http://hdl.handle.net/2144/15220

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):

Penz, Craig Christopher. “Baseline characteristics influencing placebo response in clinical trials of treatments for fragile X syndrome.” 2014. Thesis, Boston University. Accessed April 14, 2021. http://hdl.handle.net/2144/15220.

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

MLA Handbook (7th Edition):

Penz, Craig Christopher. “Baseline characteristics influencing placebo response in clinical trials of treatments for fragile X syndrome.” 2014. Web. 14 Apr 2021.

Vancouver:

Penz CC. Baseline characteristics influencing placebo response in clinical trials of treatments for fragile X syndrome. [Internet] [Thesis]. Boston University; 2014. [cited 2021 Apr 14]. Available from: http://hdl.handle.net/2144/15220.

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

Council of Science Editors:

Penz CC. Baseline characteristics influencing placebo response in clinical trials of treatments for fragile X syndrome. [Thesis]. Boston University; 2014. Available from: http://hdl.handle.net/2144/15220

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

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