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You searched for subject:( Shank3). Showing records 1 – 8 of 8 total matches.

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1. Darville, Hélène. Utilisation des cellules souches pluripotentes pour la recherche et la validation de composés thérapeutiques pour les formes génétiques d'autisme liées à SHANK3 : The use of pluripotent stem cells for the study of autism and the discovery of new therapeutics.

Degree: Docteur es, Sciences de la vie et de la santé, 2015, Paris Saclay

 Objectifs : Le gène SHANK3 code pour une protéine dite d’« échafaudage » localisée dans les synapses des neurones glutamatergiques. Elle est nécessaire au bon… (more)

Subjects/Keywords: SHANK3; Neurones corticaux glutamatergiques

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APA (6th Edition):

Darville, H. (2015). Utilisation des cellules souches pluripotentes pour la recherche et la validation de composés thérapeutiques pour les formes génétiques d'autisme liées à SHANK3 : The use of pluripotent stem cells for the study of autism and the discovery of new therapeutics. (Doctoral Dissertation). Paris Saclay. Retrieved from http://www.theses.fr/2015SACLE012

Chicago Manual of Style (16th Edition):

Darville, Hélène. “Utilisation des cellules souches pluripotentes pour la recherche et la validation de composés thérapeutiques pour les formes génétiques d'autisme liées à SHANK3 : The use of pluripotent stem cells for the study of autism and the discovery of new therapeutics.” 2015. Doctoral Dissertation, Paris Saclay. Accessed February 22, 2019. http://www.theses.fr/2015SACLE012.

MLA Handbook (7th Edition):

Darville, Hélène. “Utilisation des cellules souches pluripotentes pour la recherche et la validation de composés thérapeutiques pour les formes génétiques d'autisme liées à SHANK3 : The use of pluripotent stem cells for the study of autism and the discovery of new therapeutics.” 2015. Web. 22 Feb 2019.

Vancouver:

Darville H. Utilisation des cellules souches pluripotentes pour la recherche et la validation de composés thérapeutiques pour les formes génétiques d'autisme liées à SHANK3 : The use of pluripotent stem cells for the study of autism and the discovery of new therapeutics. [Internet] [Doctoral dissertation]. Paris Saclay; 2015. [cited 2019 Feb 22]. Available from: http://www.theses.fr/2015SACLE012.

Council of Science Editors:

Darville H. Utilisation des cellules souches pluripotentes pour la recherche et la validation de composés thérapeutiques pour les formes génétiques d'autisme liées à SHANK3 : The use of pluripotent stem cells for the study of autism and the discovery of new therapeutics. [Doctoral Dissertation]. Paris Saclay; 2015. Available from: http://www.theses.fr/2015SACLE012


Duke University

2. Bey, Alexandra Lyndon. Using Shank3 Model Mice to Probe the Neuroanatomic Basis of Autism .

Degree: 2017, Duke University

  Autism spectrum disorders (ASDs) are increasingly prevalent, and the costs associated with caring for affected patients across the lifespan are immense. However, the pathophysiology… (more)

Subjects/Keywords: Neurosciences; Genetics; Mental health; autism; behavior; genetics; mouse models; Shank3

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APA (6th Edition):

Bey, A. L. (2017). Using Shank3 Model Mice to Probe the Neuroanatomic Basis of Autism . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/14354

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):

Bey, Alexandra Lyndon. “Using Shank3 Model Mice to Probe the Neuroanatomic Basis of Autism .” 2017. Thesis, Duke University. Accessed February 22, 2019. http://hdl.handle.net/10161/14354.

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

MLA Handbook (7th Edition):

Bey, Alexandra Lyndon. “Using Shank3 Model Mice to Probe the Neuroanatomic Basis of Autism .” 2017. Web. 22 Feb 2019.

Vancouver:

Bey AL. Using Shank3 Model Mice to Probe the Neuroanatomic Basis of Autism . [Internet] [Thesis]. Duke University; 2017. [cited 2019 Feb 22]. Available from: http://hdl.handle.net/10161/14354.

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

Council of Science Editors:

Bey AL. Using Shank3 Model Mice to Probe the Neuroanatomic Basis of Autism . [Thesis]. Duke University; 2017. Available from: http://hdl.handle.net/10161/14354

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

3. Gouder, Laura. Etude de l'effet de mutations du gène SHANK3 dans les TSA à partir de neurones corticaux humains dérivés de cellules souches pluripotentes induites : Analysis of the determining factors on the injury assessment of an injured pedestrian child.

Degree: Docteur es, Neurobiologie, 2016, Sorbonne Paris Cité

Les Troubles du Spectre Autistique (TSA) affectent un individu sur 100 en France et sont caractérisés par des déficits de la communication et des interactions… (more)

Subjects/Keywords: Troubles du spectre autistique; IPSC; Neurones corticaux glutamatergiques; SHANK3; Épines dendritiques; Imagerie calcique; Autism; IPSC; Cortical glutamatergic neurons; SHANK3; Dendritic spines; Calcium imaging; 616.85882

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APA (6th Edition):

Gouder, L. (2016). Etude de l'effet de mutations du gène SHANK3 dans les TSA à partir de neurones corticaux humains dérivés de cellules souches pluripotentes induites : Analysis of the determining factors on the injury assessment of an injured pedestrian child. (Doctoral Dissertation). Sorbonne Paris Cité. Retrieved from http://www.theses.fr/2016USPCB089

Chicago Manual of Style (16th Edition):

Gouder, Laura. “Etude de l'effet de mutations du gène SHANK3 dans les TSA à partir de neurones corticaux humains dérivés de cellules souches pluripotentes induites : Analysis of the determining factors on the injury assessment of an injured pedestrian child.” 2016. Doctoral Dissertation, Sorbonne Paris Cité. Accessed February 22, 2019. http://www.theses.fr/2016USPCB089.

MLA Handbook (7th Edition):

Gouder, Laura. “Etude de l'effet de mutations du gène SHANK3 dans les TSA à partir de neurones corticaux humains dérivés de cellules souches pluripotentes induites : Analysis of the determining factors on the injury assessment of an injured pedestrian child.” 2016. Web. 22 Feb 2019.

Vancouver:

Gouder L. Etude de l'effet de mutations du gène SHANK3 dans les TSA à partir de neurones corticaux humains dérivés de cellules souches pluripotentes induites : Analysis of the determining factors on the injury assessment of an injured pedestrian child. [Internet] [Doctoral dissertation]. Sorbonne Paris Cité; 2016. [cited 2019 Feb 22]. Available from: http://www.theses.fr/2016USPCB089.

Council of Science Editors:

Gouder L. Etude de l'effet de mutations du gène SHANK3 dans les TSA à partir de neurones corticaux humains dérivés de cellules souches pluripotentes induites : Analysis of the determining factors on the injury assessment of an injured pedestrian child. [Doctoral Dissertation]. Sorbonne Paris Cité; 2016. Available from: http://www.theses.fr/2016USPCB089


Clemson University

4. Sarasua, Sara. Analysis of Genotype, Phenotype, and Age Progression in Phelan-McDermid Syndrome.

Degree: PhD, Genetics, 2012, Clemson University

 Phelan-McDermid syndrome is a developmental disability syndrome associated with deletions of the terminal end of one copy of chromosome 22q13. The observed chromosomal aberrations include… (more)

Subjects/Keywords: 22q13; epidemiology; genotype-phenotype; longitudinal; Phelan-McDermid syndrome; SHANK3; Genetics and Genomics

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APA (6th Edition):

Sarasua, S. (2012). Analysis of Genotype, Phenotype, and Age Progression in Phelan-McDermid Syndrome. (Doctoral Dissertation). Clemson University. Retrieved from https://tigerprints.clemson.edu/all_dissertations/1032

Chicago Manual of Style (16th Edition):

Sarasua, Sara. “Analysis of Genotype, Phenotype, and Age Progression in Phelan-McDermid Syndrome.” 2012. Doctoral Dissertation, Clemson University. Accessed February 22, 2019. https://tigerprints.clemson.edu/all_dissertations/1032.

MLA Handbook (7th Edition):

Sarasua, Sara. “Analysis of Genotype, Phenotype, and Age Progression in Phelan-McDermid Syndrome.” 2012. Web. 22 Feb 2019.

Vancouver:

Sarasua S. Analysis of Genotype, Phenotype, and Age Progression in Phelan-McDermid Syndrome. [Internet] [Doctoral dissertation]. Clemson University; 2012. [cited 2019 Feb 22]. Available from: https://tigerprints.clemson.edu/all_dissertations/1032.

Council of Science Editors:

Sarasua S. Analysis of Genotype, Phenotype, and Age Progression in Phelan-McDermid Syndrome. [Doctoral Dissertation]. Clemson University; 2012. Available from: https://tigerprints.clemson.edu/all_dissertations/1032


Virginia Commonwealth University

5. Shah, Nikhil N. SH3 AND MULTIPLE ANKYRIN REPEAT DOMAIN 3 (SHANK3) AFFECTS THE EXPRESSION OF HYPERPOLARIZATION-ACTIVATED CYCLIC NUCLEOTIDE-GATED (HCN) CHANNELS IN MOUSE MODELS OF AUTISM.

Degree: MS, Physiology and Biophysics, 2017, Virginia Commonwealth University

  SH3 and multiple ankyrin repeat domains 3 (SHANK3) is a multidomain scaffold protein that is highly augmented in the postsynaptic density (PSD) of excitatory… (more)

Subjects/Keywords: SHANK3; HCN; Autism; Ih-Current; Channelopathy; Yeast Two-Hybridization; Biochemistry; Genetics; Molecular Biology

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APA (6th Edition):

Shah, N. N. (2017). SH3 AND MULTIPLE ANKYRIN REPEAT DOMAIN 3 (SHANK3) AFFECTS THE EXPRESSION OF HYPERPOLARIZATION-ACTIVATED CYCLIC NUCLEOTIDE-GATED (HCN) CHANNELS IN MOUSE MODELS OF AUTISM. (Thesis). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/4997

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):

Shah, Nikhil N. “SH3 AND MULTIPLE ANKYRIN REPEAT DOMAIN 3 (SHANK3) AFFECTS THE EXPRESSION OF HYPERPOLARIZATION-ACTIVATED CYCLIC NUCLEOTIDE-GATED (HCN) CHANNELS IN MOUSE MODELS OF AUTISM.” 2017. Thesis, Virginia Commonwealth University. Accessed February 22, 2019. https://scholarscompass.vcu.edu/etd/4997.

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

MLA Handbook (7th Edition):

Shah, Nikhil N. “SH3 AND MULTIPLE ANKYRIN REPEAT DOMAIN 3 (SHANK3) AFFECTS THE EXPRESSION OF HYPERPOLARIZATION-ACTIVATED CYCLIC NUCLEOTIDE-GATED (HCN) CHANNELS IN MOUSE MODELS OF AUTISM.” 2017. Web. 22 Feb 2019.

Vancouver:

Shah NN. SH3 AND MULTIPLE ANKYRIN REPEAT DOMAIN 3 (SHANK3) AFFECTS THE EXPRESSION OF HYPERPOLARIZATION-ACTIVATED CYCLIC NUCLEOTIDE-GATED (HCN) CHANNELS IN MOUSE MODELS OF AUTISM. [Internet] [Thesis]. Virginia Commonwealth University; 2017. [cited 2019 Feb 22]. Available from: https://scholarscompass.vcu.edu/etd/4997.

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

Council of Science Editors:

Shah NN. SH3 AND MULTIPLE ANKYRIN REPEAT DOMAIN 3 (SHANK3) AFFECTS THE EXPRESSION OF HYPERPOLARIZATION-ACTIVATED CYCLIC NUCLEOTIDE-GATED (HCN) CHANNELS IN MOUSE MODELS OF AUTISM. [Thesis]. Virginia Commonwealth University; 2017. Available from: https://scholarscompass.vcu.edu/etd/4997

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

6. Wells, Michael Frederick. The Role of Dysfunctional Subcortical Circuitry in Mouse Models of Developmental Disability .

Degree: 2015, Duke University

  Developmental disabilities, including intellectual disability (ID), attention-deficit hyperactivity disorder (ADHD), and autism spectrum disorders (ASD), affect approximately 1 in 6 children in the United… (more)

Subjects/Keywords: Neurosciences; Autism Spectrum Disorders; Mouse models; Psychiatric disorders; Ptchd1; Shank3

…104 Chapter 5. Shank3 knockout mice as a model of striatal dysfunction and autism spectrum… …C57Bl/6J females and the F1 offspring were used for experiments. Generation of Shank3… …Shank3 gene with loxP sites and a NEO cassette. Chimaeric mice were crossed to C57Bl/6J females… …used for subsequent matings. Backcrossed Shank3 floxed mice were then bred with C57Bl/6J β… 

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APA (6th Edition):

Wells, M. F. (2015). The Role of Dysfunctional Subcortical Circuitry in Mouse Models of Developmental Disability . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/10483

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):

Wells, Michael Frederick. “The Role of Dysfunctional Subcortical Circuitry in Mouse Models of Developmental Disability .” 2015. Thesis, Duke University. Accessed February 22, 2019. http://hdl.handle.net/10161/10483.

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

MLA Handbook (7th Edition):

Wells, Michael Frederick. “The Role of Dysfunctional Subcortical Circuitry in Mouse Models of Developmental Disability .” 2015. Web. 22 Feb 2019.

Vancouver:

Wells MF. The Role of Dysfunctional Subcortical Circuitry in Mouse Models of Developmental Disability . [Internet] [Thesis]. Duke University; 2015. [cited 2019 Feb 22]. Available from: http://hdl.handle.net/10161/10483.

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

Council of Science Editors:

Wells MF. The Role of Dysfunctional Subcortical Circuitry in Mouse Models of Developmental Disability . [Thesis]. Duke University; 2015. Available from: http://hdl.handle.net/10161/10483

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

7. Martins, Manuella. Identification of neuronal alterations induced by Shank3 mutations using iPS cells from Phelan-McDermid Patients' Fibroblasts.

Degree: 2013, Instituto Politécnico do Porto

A família de proteínas Shank é o principal conjunto de proteinas de suporte e está localizada na densidade pós-sináptica das sinapses excitatórias. Existem 3 genes… (more)

Subjects/Keywords: Shank3; Células estaminais pluripotente induzidas (iPS); Autism Spectrum Disorder (ASD); Phelan-McDermid Sindrome (PMS); mGluR5; Induced-pluripotent stem (iPS) cells; Cellule staminali pluripotente indotte (iPS)

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APA (6th Edition):

Martins, M. (2013). Identification of neuronal alterations induced by Shank3 mutations using iPS cells from Phelan-McDermid Patients' Fibroblasts. (Thesis). Instituto Politécnico do Porto. Retrieved from https://www.rcaap.pt/detail.jsp?id=oai:recipp.ipp.pt:10400.22/2369

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):

Martins, Manuella. “Identification of neuronal alterations induced by Shank3 mutations using iPS cells from Phelan-McDermid Patients' Fibroblasts.” 2013. Thesis, Instituto Politécnico do Porto. Accessed February 22, 2019. https://www.rcaap.pt/detail.jsp?id=oai:recipp.ipp.pt:10400.22/2369.

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

MLA Handbook (7th Edition):

Martins, Manuella. “Identification of neuronal alterations induced by Shank3 mutations using iPS cells from Phelan-McDermid Patients' Fibroblasts.” 2013. Web. 22 Feb 2019.

Vancouver:

Martins M. Identification of neuronal alterations induced by Shank3 mutations using iPS cells from Phelan-McDermid Patients' Fibroblasts. [Internet] [Thesis]. Instituto Politécnico do Porto; 2013. [cited 2019 Feb 22]. Available from: https://www.rcaap.pt/detail.jsp?id=oai:recipp.ipp.pt:10400.22/2369.

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

Council of Science Editors:

Martins M. Identification of neuronal alterations induced by Shank3 mutations using iPS cells from Phelan-McDermid Patients' Fibroblasts. [Thesis]. Instituto Politécnico do Porto; 2013. Available from: https://www.rcaap.pt/detail.jsp?id=oai:recipp.ipp.pt:10400.22/2369

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

8. Munera Salazar , Lina Maria. VARIACIONES DEL GEN SHANK3 EN INDIVIDUOS COLOMBIANOS CON TRASTORNOS DEL ESPECTRO AUTISTA .

Degree: 2013, Universidad de los Andes

 Los trastornos del espectro autista (TEAs) son un grupo de desordenes del neurodesarrollo comunes y altamente heredables. Se ha demostrado que muchos genes asociados con… (more)

Subjects/Keywords: Trastorno del espectro autista; SH3 and multiple ankyrin repeat domains 3 SHANK3; tamizaje; variaciones; población colombiana.

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APA (6th Edition):

Munera Salazar , L. M. (2013). VARIACIONES DEL GEN SHANK3 EN INDIVIDUOS COLOMBIANOS CON TRASTORNOS DEL ESPECTRO AUTISTA . (Thesis). Universidad de los Andes. Retrieved from http://documentodegrado.uniandes.edu.co/documentos/200623627_fecha_2013_09_23_hora_17_07_05_parte_1.pdf;http://documentodegrado.uniandes.edu.co/documentos/200623627_fecha_2013_09_23_hora_17_07_05_parte_2.pdf

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):

Munera Salazar , Lina Maria. “VARIACIONES DEL GEN SHANK3 EN INDIVIDUOS COLOMBIANOS CON TRASTORNOS DEL ESPECTRO AUTISTA .” 2013. Thesis, Universidad de los Andes. Accessed February 22, 2019. http://documentodegrado.uniandes.edu.co/documentos/200623627_fecha_2013_09_23_hora_17_07_05_parte_1.pdf;http://documentodegrado.uniandes.edu.co/documentos/200623627_fecha_2013_09_23_hora_17_07_05_parte_2.pdf.

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

MLA Handbook (7th Edition):

Munera Salazar , Lina Maria. “VARIACIONES DEL GEN SHANK3 EN INDIVIDUOS COLOMBIANOS CON TRASTORNOS DEL ESPECTRO AUTISTA .” 2013. Web. 22 Feb 2019.

Vancouver:

Munera Salazar LM. VARIACIONES DEL GEN SHANK3 EN INDIVIDUOS COLOMBIANOS CON TRASTORNOS DEL ESPECTRO AUTISTA . [Internet] [Thesis]. Universidad de los Andes; 2013. [cited 2019 Feb 22]. Available from: http://documentodegrado.uniandes.edu.co/documentos/200623627_fecha_2013_09_23_hora_17_07_05_parte_1.pdf;http://documentodegrado.uniandes.edu.co/documentos/200623627_fecha_2013_09_23_hora_17_07_05_parte_2.pdf.

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

Council of Science Editors:

Munera Salazar LM. VARIACIONES DEL GEN SHANK3 EN INDIVIDUOS COLOMBIANOS CON TRASTORNOS DEL ESPECTRO AUTISTA . [Thesis]. Universidad de los Andes; 2013. Available from: http://documentodegrado.uniandes.edu.co/documentos/200623627_fecha_2013_09_23_hora_17_07_05_parte_1.pdf;http://documentodegrado.uniandes.edu.co/documentos/200623627_fecha_2013_09_23_hora_17_07_05_parte_2.pdf

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

.