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You searched for subject:(Spinal Muscular Atrophy). Showing records 1 – 30 of 103 total matches.

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University of Utah

1. Cutler, Hilary Lauren. Continuous blood glucose monitoring and dietary intake in a cohort of children with spinal muscular atrophy type II.

Degree: MSin Nutrition, College of Health, 2016, University of Utah

 Previous studies have documented metabolic abnormalities in individuals with spinal muscular atrophy (SMA). This study investigated the impact of diet and fasting on blood glucose… (more)

Subjects/Keywords: blood glucose; SMA; spinal muscular atrophy

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APA (6th Edition):

Cutler, H. L. (2016). Continuous blood glucose monitoring and dietary intake in a cohort of children with spinal muscular atrophy type II. (Masters Thesis). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/4094/rec/556

Chicago Manual of Style (16th Edition):

Cutler, Hilary Lauren. “Continuous blood glucose monitoring and dietary intake in a cohort of children with spinal muscular atrophy type II.” 2016. Masters Thesis, University of Utah. Accessed July 16, 2019. http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/4094/rec/556.

MLA Handbook (7th Edition):

Cutler, Hilary Lauren. “Continuous blood glucose monitoring and dietary intake in a cohort of children with spinal muscular atrophy type II.” 2016. Web. 16 Jul 2019.

Vancouver:

Cutler HL. Continuous blood glucose monitoring and dietary intake in a cohort of children with spinal muscular atrophy type II. [Internet] [Masters thesis]. University of Utah; 2016. [cited 2019 Jul 16]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/4094/rec/556.

Council of Science Editors:

Cutler HL. Continuous blood glucose monitoring and dietary intake in a cohort of children with spinal muscular atrophy type II. [Masters Thesis]. University of Utah; 2016. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/4094/rec/556

2. Xu, Xixi. IMPAIRMENT OF MOTOR AXON DEVELOPMENT IN SPINAL MUSCULAR ATROPHY.

Degree: 2014, Johns Hopkins University

Spinal muscular atrophy (SMA) is an inherited motor neuron disease caused by mutation of the survival of motor neuron 1(SMN1) gene and deficient expression of… (more)

Subjects/Keywords: Spinal Muscular Atrophy; SMA; motor axon development

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APA (6th Edition):

Xu, X. (2014). IMPAIRMENT OF MOTOR AXON DEVELOPMENT IN SPINAL MUSCULAR ATROPHY. (Thesis). Johns Hopkins University. Retrieved from http://jhir.library.jhu.edu/handle/1774.2/38102

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):

Xu, Xixi. “IMPAIRMENT OF MOTOR AXON DEVELOPMENT IN SPINAL MUSCULAR ATROPHY.” 2014. Thesis, Johns Hopkins University. Accessed July 16, 2019. http://jhir.library.jhu.edu/handle/1774.2/38102.

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

MLA Handbook (7th Edition):

Xu, Xixi. “IMPAIRMENT OF MOTOR AXON DEVELOPMENT IN SPINAL MUSCULAR ATROPHY.” 2014. Web. 16 Jul 2019.

Vancouver:

Xu X. IMPAIRMENT OF MOTOR AXON DEVELOPMENT IN SPINAL MUSCULAR ATROPHY. [Internet] [Thesis]. Johns Hopkins University; 2014. [cited 2019 Jul 16]. Available from: http://jhir.library.jhu.edu/handle/1774.2/38102.

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

Council of Science Editors:

Xu X. IMPAIRMENT OF MOTOR AXON DEVELOPMENT IN SPINAL MUSCULAR ATROPHY. [Thesis]. Johns Hopkins University; 2014. Available from: http://jhir.library.jhu.edu/handle/1774.2/38102

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


University of Utah

3. Peterson, Susan. Weight gain, dietary intake, and body composition in patients with type 2 and type 3 sma.

Degree: MSin Nutrition, College of Health, 2015, University of Utah

 Children with spinal muscular atrophy (SMA) types 2 and 3 are at risk for overweight and increased body fat. Research objectives were to determine whether… (more)

Subjects/Keywords: Dietary; Obese; Overweight; Spinal muscular atrophy

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APA (6th Edition):

Peterson, S. (2015). Weight gain, dietary intake, and body composition in patients with type 2 and type 3 sma. (Masters Thesis). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/3916/rec/2914

Chicago Manual of Style (16th Edition):

Peterson, Susan. “Weight gain, dietary intake, and body composition in patients with type 2 and type 3 sma.” 2015. Masters Thesis, University of Utah. Accessed July 16, 2019. http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/3916/rec/2914.

MLA Handbook (7th Edition):

Peterson, Susan. “Weight gain, dietary intake, and body composition in patients with type 2 and type 3 sma.” 2015. Web. 16 Jul 2019.

Vancouver:

Peterson S. Weight gain, dietary intake, and body composition in patients with type 2 and type 3 sma. [Internet] [Masters thesis]. University of Utah; 2015. [cited 2019 Jul 16]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/3916/rec/2914.

Council of Science Editors:

Peterson S. Weight gain, dietary intake, and body composition in patients with type 2 and type 3 sma. [Masters Thesis]. University of Utah; 2015. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/3916/rec/2914


University of Edinburgh

4. Aghamaleky Sarvestany, Arwin. Schwann cell pathology in spinal muscular atrophy (SMA).

Degree: PhD, 2015, University of Edinburgh

 The childhood neuromuscular disease spinal muscular atrophy (SMA) is caused by low levels of survival motor neuron (SMN) protein. Historically, SMA has been characterised as… (more)

Subjects/Keywords: 616.7; spinal muscular atrophy; Schwann cells; myelination

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APA (6th Edition):

Aghamaleky Sarvestany, A. (2015). Schwann cell pathology in spinal muscular atrophy (SMA). (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/15908

Chicago Manual of Style (16th Edition):

Aghamaleky Sarvestany, Arwin. “Schwann cell pathology in spinal muscular atrophy (SMA).” 2015. Doctoral Dissertation, University of Edinburgh. Accessed July 16, 2019. http://hdl.handle.net/1842/15908.

MLA Handbook (7th Edition):

Aghamaleky Sarvestany, Arwin. “Schwann cell pathology in spinal muscular atrophy (SMA).” 2015. Web. 16 Jul 2019.

Vancouver:

Aghamaleky Sarvestany A. Schwann cell pathology in spinal muscular atrophy (SMA). [Internet] [Doctoral dissertation]. University of Edinburgh; 2015. [cited 2019 Jul 16]. Available from: http://hdl.handle.net/1842/15908.

Council of Science Editors:

Aghamaleky Sarvestany A. Schwann cell pathology in spinal muscular atrophy (SMA). [Doctoral Dissertation]. University of Edinburgh; 2015. Available from: http://hdl.handle.net/1842/15908


University of Edinburgh

5. Somers, Eilidh. Novel capillary defects in spinal muscular atrophy.

Degree: PhD, 2015, University of Edinburgh

Spinal Muscular Atrophy (SMA) is an autosomal, recessive form of childhood motor neuron disease and the most common genetic cause of infant mortality in the… (more)

Subjects/Keywords: 616.7; capillaries; spinal muscular atrophy; SMA; vasculature

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APA (6th Edition):

Somers, E. (2015). Novel capillary defects in spinal muscular atrophy. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/16208

Chicago Manual of Style (16th Edition):

Somers, Eilidh. “Novel capillary defects in spinal muscular atrophy.” 2015. Doctoral Dissertation, University of Edinburgh. Accessed July 16, 2019. http://hdl.handle.net/1842/16208.

MLA Handbook (7th Edition):

Somers, Eilidh. “Novel capillary defects in spinal muscular atrophy.” 2015. Web. 16 Jul 2019.

Vancouver:

Somers E. Novel capillary defects in spinal muscular atrophy. [Internet] [Doctoral dissertation]. University of Edinburgh; 2015. [cited 2019 Jul 16]. Available from: http://hdl.handle.net/1842/16208.

Council of Science Editors:

Somers E. Novel capillary defects in spinal muscular atrophy. [Doctoral Dissertation]. University of Edinburgh; 2015. Available from: http://hdl.handle.net/1842/16208


University of Cincinnati

6. Wasserman, Halley M, M.D. Low bone mineral density and fractures are highly prevalent in pediatric patients with Spinal Muscular Atrophy regardless of disease severity.

Degree: MS, Medicine: Clinical and Translational Research, 2016, University of Cincinnati

 Purpose: Fractures and poor bone health due to limited ambulation are significant concerns for patients with Spinal Muscular Atrophy (SMA). However, the prevalence of fractures,… (more)

Subjects/Keywords: Surgery; Osteoporosis; Children; spinal muscular atrophy; Fractures

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APA (6th Edition):

Wasserman, Halley M, M. D. (2016). Low bone mineral density and fractures are highly prevalent in pediatric patients with Spinal Muscular Atrophy regardless of disease severity. (Masters Thesis). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1458299334

Chicago Manual of Style (16th Edition):

Wasserman, Halley M, M D. “Low bone mineral density and fractures are highly prevalent in pediatric patients with Spinal Muscular Atrophy regardless of disease severity.” 2016. Masters Thesis, University of Cincinnati. Accessed July 16, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1458299334.

MLA Handbook (7th Edition):

Wasserman, Halley M, M D. “Low bone mineral density and fractures are highly prevalent in pediatric patients with Spinal Muscular Atrophy regardless of disease severity.” 2016. Web. 16 Jul 2019.

Vancouver:

Wasserman, Halley M MD. Low bone mineral density and fractures are highly prevalent in pediatric patients with Spinal Muscular Atrophy regardless of disease severity. [Internet] [Masters thesis]. University of Cincinnati; 2016. [cited 2019 Jul 16]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1458299334.

Council of Science Editors:

Wasserman, Halley M MD. Low bone mineral density and fractures are highly prevalent in pediatric patients with Spinal Muscular Atrophy regardless of disease severity. [Masters Thesis]. University of Cincinnati; 2016. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1458299334

7. -3606-5757. Reliability and validity of the ACTIVE-mini for quantifying movement in infants with spinal muscular atrophy.

Degree: PhD, Physical Therapy, 2018, Texas Woman's University

 Background: Motor function assessment of individuals with SMA I is challenging due to the low level of function typically obtained and the fragility of the… (more)

Subjects/Keywords: spinal muscular atrophy; SMA; ACTIVE-mini

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APA (6th Edition):

-3606-5757. (2018). Reliability and validity of the ACTIVE-mini for quantifying movement in infants with spinal muscular atrophy. (Doctoral Dissertation). Texas Woman's University. Retrieved from http://hdl.handle.net/11274/11000

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Chicago Manual of Style (16th Edition):

-3606-5757. “Reliability and validity of the ACTIVE-mini for quantifying movement in infants with spinal muscular atrophy.” 2018. Doctoral Dissertation, Texas Woman's University. Accessed July 16, 2019. http://hdl.handle.net/11274/11000.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

MLA Handbook (7th Edition):

-3606-5757. “Reliability and validity of the ACTIVE-mini for quantifying movement in infants with spinal muscular atrophy.” 2018. Web. 16 Jul 2019.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

-3606-5757. Reliability and validity of the ACTIVE-mini for quantifying movement in infants with spinal muscular atrophy. [Internet] [Doctoral dissertation]. Texas Woman's University; 2018. [cited 2019 Jul 16]. Available from: http://hdl.handle.net/11274/11000.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Council of Science Editors:

-3606-5757. Reliability and validity of the ACTIVE-mini for quantifying movement in infants with spinal muscular atrophy. [Doctoral Dissertation]. Texas Woman's University; 2018. Available from: http://hdl.handle.net/11274/11000

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete


Universitat de Valencia

8. Konieczny, Piotr. A Spinal Muscular Atrophy Reporter System for in vivo Drug Discovery in Drosophila melanogaster .

Degree: 2018, Universitat de Valencia

 Fondo La Atrofia Muscular Espinal es un desorden neuromuscular raro y fatal causado por la pérdida o reducción en los niveles de proteína de la… (more)

Subjects/Keywords: drosophila melanogaster; drug discovery; spinal muscular atrophy

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APA (6th Edition):

Konieczny, P. (2018). A Spinal Muscular Atrophy Reporter System for in vivo Drug Discovery in Drosophila melanogaster . (Doctoral Dissertation). Universitat de Valencia. Retrieved from http://hdl.handle.net/10550/67671

Chicago Manual of Style (16th Edition):

Konieczny, Piotr. “A Spinal Muscular Atrophy Reporter System for in vivo Drug Discovery in Drosophila melanogaster .” 2018. Doctoral Dissertation, Universitat de Valencia. Accessed July 16, 2019. http://hdl.handle.net/10550/67671.

MLA Handbook (7th Edition):

Konieczny, Piotr. “A Spinal Muscular Atrophy Reporter System for in vivo Drug Discovery in Drosophila melanogaster .” 2018. Web. 16 Jul 2019.

Vancouver:

Konieczny P. A Spinal Muscular Atrophy Reporter System for in vivo Drug Discovery in Drosophila melanogaster . [Internet] [Doctoral dissertation]. Universitat de Valencia; 2018. [cited 2019 Jul 16]. Available from: http://hdl.handle.net/10550/67671.

Council of Science Editors:

Konieczny P. A Spinal Muscular Atrophy Reporter System for in vivo Drug Discovery in Drosophila melanogaster . [Doctoral Dissertation]. Universitat de Valencia; 2018. Available from: http://hdl.handle.net/10550/67671


University of New South Wales

9. Farrar, Michelle Anne. The pathophysiology of spinal muscular atrophy.

Degree: Women's & Children's Health, 2012, University of New South Wales

 This thesis examines the disease course and pathophysiology of motor dysfunction in spinal muscular atrophy (SMA) using clinical, epidemiological, neurophysiological and genetic studies.Natural history studies… (more)

Subjects/Keywords: Pathophysiology; Spinal Muscular Atrophy; Motor neuron; Neurodegeneration

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APA (6th Edition):

Farrar, M. A. (2012). The pathophysiology of spinal muscular atrophy. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/52032 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10702/SOURCE01?view=true

Chicago Manual of Style (16th Edition):

Farrar, Michelle Anne. “The pathophysiology of spinal muscular atrophy.” 2012. Doctoral Dissertation, University of New South Wales. Accessed July 16, 2019. http://handle.unsw.edu.au/1959.4/52032 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10702/SOURCE01?view=true.

MLA Handbook (7th Edition):

Farrar, Michelle Anne. “The pathophysiology of spinal muscular atrophy.” 2012. Web. 16 Jul 2019.

Vancouver:

Farrar MA. The pathophysiology of spinal muscular atrophy. [Internet] [Doctoral dissertation]. University of New South Wales; 2012. [cited 2019 Jul 16]. Available from: http://handle.unsw.edu.au/1959.4/52032 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10702/SOURCE01?view=true.

Council of Science Editors:

Farrar MA. The pathophysiology of spinal muscular atrophy. [Doctoral Dissertation]. University of New South Wales; 2012. Available from: http://handle.unsw.edu.au/1959.4/52032 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10702/SOURCE01?view=true


University of Pennsylvania

10. Sarachan, Kathryn Lorenz. Structural Studies of the SMN-Gemin2 Complex.

Degree: 2012, University of Pennsylvania

 The proteins SMN and Gemin2 form the conserved core of the larger eponymous SMN complex, which also contains Gemins3-8 and unrip in an unknown stoichiometry.… (more)

Subjects/Keywords: Gemin2; SMN; spinal muscular atrophy; Biochemistry; Biophysics

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APA (6th Edition):

Sarachan, K. L. (2012). Structural Studies of the SMN-Gemin2 Complex. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/482

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):

Sarachan, Kathryn Lorenz. “Structural Studies of the SMN-Gemin2 Complex.” 2012. Thesis, University of Pennsylvania. Accessed July 16, 2019. https://repository.upenn.edu/edissertations/482.

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

MLA Handbook (7th Edition):

Sarachan, Kathryn Lorenz. “Structural Studies of the SMN-Gemin2 Complex.” 2012. Web. 16 Jul 2019.

Vancouver:

Sarachan KL. Structural Studies of the SMN-Gemin2 Complex. [Internet] [Thesis]. University of Pennsylvania; 2012. [cited 2019 Jul 16]. Available from: https://repository.upenn.edu/edissertations/482.

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

Council of Science Editors:

Sarachan KL. Structural Studies of the SMN-Gemin2 Complex. [Thesis]. University of Pennsylvania; 2012. Available from: https://repository.upenn.edu/edissertations/482

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

11. Onsager, Sarah. Experiences with a Service Dog of an Adolescent with Spinal Muscular Atrophy.

Degree: MSOT, Occupational Therapy, 2011, University of Puget-Sound

  Adolescents with Spinal Muscular Atrophy (SMA) may receive occupational therapy services and may at times use service dogs. Literature suggests that service dogs can… (more)

Subjects/Keywords: Spinal Muscular Atrophy; physical disability; service dog; occupational therapy; Occupational Therapy; Spinal muscular atrophy; Service dogs; Psychiatric service dogs

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APA (6th Edition):

Onsager, S. (2011). Experiences with a Service Dog of an Adolescent with Spinal Muscular Atrophy. (Masters Thesis). University of Puget-Sound. Retrieved from http://soundideas.pugetsound.edu/ms_occ_therapy/24 ; http://soundideas.pugetsound.edu/ms_occ_therapy/24

Chicago Manual of Style (16th Edition):

Onsager, Sarah. “Experiences with a Service Dog of an Adolescent with Spinal Muscular Atrophy.” 2011. Masters Thesis, University of Puget-Sound. Accessed July 16, 2019. http://soundideas.pugetsound.edu/ms_occ_therapy/24 ; http://soundideas.pugetsound.edu/ms_occ_therapy/24.

MLA Handbook (7th Edition):

Onsager, Sarah. “Experiences with a Service Dog of an Adolescent with Spinal Muscular Atrophy.” 2011. Web. 16 Jul 2019.

Vancouver:

Onsager S. Experiences with a Service Dog of an Adolescent with Spinal Muscular Atrophy. [Internet] [Masters thesis]. University of Puget-Sound; 2011. [cited 2019 Jul 16]. Available from: http://soundideas.pugetsound.edu/ms_occ_therapy/24 ; http://soundideas.pugetsound.edu/ms_occ_therapy/24.

Council of Science Editors:

Onsager S. Experiences with a Service Dog of an Adolescent with Spinal Muscular Atrophy. [Masters Thesis]. University of Puget-Sound; 2011. Available from: http://soundideas.pugetsound.edu/ms_occ_therapy/24 ; http://soundideas.pugetsound.edu/ms_occ_therapy/24


University of Utah

12. Miller, Elizabeth Ann. Glucose load tolerance in spinal muscular atrophy type II.

Degree: MS, Nutrition, 2014, University of Utah

 Children with spinal muscular atrophy (SMA) exhibit diminished lean body mass and increased fat mass compared to healthy peers; conditions that limit mobility, aggravate orthopedic… (more)

Subjects/Keywords: Body composition; Glucose tolerance; SMA; Spinal muscular atrophy

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APA (6th Edition):

Miller, E. A. (2014). Glucose load tolerance in spinal muscular atrophy type II. (Masters Thesis). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/3192/rec/1183

Chicago Manual of Style (16th Edition):

Miller, Elizabeth Ann. “Glucose load tolerance in spinal muscular atrophy type II.” 2014. Masters Thesis, University of Utah. Accessed July 16, 2019. http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/3192/rec/1183.

MLA Handbook (7th Edition):

Miller, Elizabeth Ann. “Glucose load tolerance in spinal muscular atrophy type II.” 2014. Web. 16 Jul 2019.

Vancouver:

Miller EA. Glucose load tolerance in spinal muscular atrophy type II. [Internet] [Masters thesis]. University of Utah; 2014. [cited 2019 Jul 16]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/3192/rec/1183.

Council of Science Editors:

Miller EA. Glucose load tolerance in spinal muscular atrophy type II. [Masters Thesis]. University of Utah; 2014. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/3192/rec/1183


University of Ottawa

13. Didillon, Andréanne. RNA-Binding Protein HuD as a Potential Therapeutic Target for Spinal Muscular Atrophy .

Degree: 2018, University of Ottawa

Spinal muscular atrophy is caused by mutation of the SMN1 gene resulting in the selective loss of spinal cord motor neurons. HuD has been shown… (more)

Subjects/Keywords: Spinal muscular atrophy; HuD; Bryostatin; self-complementary adeno-associated virus

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APA (6th Edition):

Didillon, A. (2018). RNA-Binding Protein HuD as a Potential Therapeutic Target for Spinal Muscular Atrophy . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/37117

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):

Didillon, Andréanne. “RNA-Binding Protein HuD as a Potential Therapeutic Target for Spinal Muscular Atrophy .” 2018. Thesis, University of Ottawa. Accessed July 16, 2019. http://hdl.handle.net/10393/37117.

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

MLA Handbook (7th Edition):

Didillon, Andréanne. “RNA-Binding Protein HuD as a Potential Therapeutic Target for Spinal Muscular Atrophy .” 2018. Web. 16 Jul 2019.

Vancouver:

Didillon A. RNA-Binding Protein HuD as a Potential Therapeutic Target for Spinal Muscular Atrophy . [Internet] [Thesis]. University of Ottawa; 2018. [cited 2019 Jul 16]. Available from: http://hdl.handle.net/10393/37117.

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

Council of Science Editors:

Didillon A. RNA-Binding Protein HuD as a Potential Therapeutic Target for Spinal Muscular Atrophy . [Thesis]. University of Ottawa; 2018. Available from: http://hdl.handle.net/10393/37117

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


University of Edinburgh

14. Murray, Lyndsay M. Synaptic vulnerability in spinal muscular atrophy.

Degree: PhD, 2010, University of Edinburgh

 Mounting evidence suggests that synaptic connections are early pathological targets in many neurodegenerative diseases, including motor neuron disease. A better understanding of synaptic pathology is… (more)

Subjects/Keywords: 616.8; spinal muscular atrophy; neuromuscular junction; NMJ; synaptic vulnerability; synapse

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APA (6th Edition):

Murray, L. M. (2010). Synaptic vulnerability in spinal muscular atrophy. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/4419

Chicago Manual of Style (16th Edition):

Murray, Lyndsay M. “Synaptic vulnerability in spinal muscular atrophy.” 2010. Doctoral Dissertation, University of Edinburgh. Accessed July 16, 2019. http://hdl.handle.net/1842/4419.

MLA Handbook (7th Edition):

Murray, Lyndsay M. “Synaptic vulnerability in spinal muscular atrophy.” 2010. Web. 16 Jul 2019.

Vancouver:

Murray LM. Synaptic vulnerability in spinal muscular atrophy. [Internet] [Doctoral dissertation]. University of Edinburgh; 2010. [cited 2019 Jul 16]. Available from: http://hdl.handle.net/1842/4419.

Council of Science Editors:

Murray LM. Synaptic vulnerability in spinal muscular atrophy. [Doctoral Dissertation]. University of Edinburgh; 2010. Available from: http://hdl.handle.net/1842/4419


University of Aberdeen

15. Szunyogová, Eva. Understanding the pathogenesis of spinal muscular atrophy by determining the role of survival motor neuron protein in early development.

Degree: PhD, 2017, University of Aberdeen

Spinal Muscular Atrophy (SMA) is caused by mutation or deletion of the Survival Motor Neuron 1 (SMN1), which encodes cell-ubiquitous SMN protein. Although classified as… (more)

Subjects/Keywords: Spinal muscular atrophy; Motor neurons; Mitochondrial pathology; Blood coagulation disorders; Hematopoiesis

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APA (6th Edition):

Szunyogová, E. (2017). Understanding the pathogenesis of spinal muscular atrophy by determining the role of survival motor neuron protein in early development. (Doctoral Dissertation). University of Aberdeen. Retrieved from http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=237002 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.742378

Chicago Manual of Style (16th Edition):

Szunyogová, Eva. “Understanding the pathogenesis of spinal muscular atrophy by determining the role of survival motor neuron protein in early development.” 2017. Doctoral Dissertation, University of Aberdeen. Accessed July 16, 2019. http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=237002 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.742378.

MLA Handbook (7th Edition):

Szunyogová, Eva. “Understanding the pathogenesis of spinal muscular atrophy by determining the role of survival motor neuron protein in early development.” 2017. Web. 16 Jul 2019.

Vancouver:

Szunyogová E. Understanding the pathogenesis of spinal muscular atrophy by determining the role of survival motor neuron protein in early development. [Internet] [Doctoral dissertation]. University of Aberdeen; 2017. [cited 2019 Jul 16]. Available from: http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=237002 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.742378.

Council of Science Editors:

Szunyogová E. Understanding the pathogenesis of spinal muscular atrophy by determining the role of survival motor neuron protein in early development. [Doctoral Dissertation]. University of Aberdeen; 2017. Available from: http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=237002 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.742378


University of Ottawa

16. Eshraghi, Mehdi. Characterization of Synaptic Alterations and the Effect of Genetic Background in a Mouse Model of Spinal Muscular Atrophy .

Degree: 2017, University of Ottawa

Spinal muscular atrophy (SMA) is a genetic disorder characterized by muscle weakness and atrophy and death of motor neurons in humans. Although almost all cases… (more)

Subjects/Keywords: Spinal Muscular Atrophy; Genetic Background; Proteomics; Motor Neuron

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

APA (6th Edition):

Eshraghi, M. (2017). Characterization of Synaptic Alterations and the Effect of Genetic Background in a Mouse Model of Spinal Muscular Atrophy . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/36466

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):

Eshraghi, Mehdi. “Characterization of Synaptic Alterations and the Effect of Genetic Background in a Mouse Model of Spinal Muscular Atrophy .” 2017. Thesis, University of Ottawa. Accessed July 16, 2019. http://hdl.handle.net/10393/36466.

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

MLA Handbook (7th Edition):

Eshraghi, Mehdi. “Characterization of Synaptic Alterations and the Effect of Genetic Background in a Mouse Model of Spinal Muscular Atrophy .” 2017. Web. 16 Jul 2019.

Vancouver:

Eshraghi M. Characterization of Synaptic Alterations and the Effect of Genetic Background in a Mouse Model of Spinal Muscular Atrophy . [Internet] [Thesis]. University of Ottawa; 2017. [cited 2019 Jul 16]. Available from: http://hdl.handle.net/10393/36466.

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

Council of Science Editors:

Eshraghi M. Characterization of Synaptic Alterations and the Effect of Genetic Background in a Mouse Model of Spinal Muscular Atrophy . [Thesis]. University of Ottawa; 2017. Available from: http://hdl.handle.net/10393/36466

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


University of Ottawa

17. Haghandish, Amir. Characterizing the Role of HuR in Skeletal Muscle of Mice with Spinal Muscular Atrophy .

Degree: 2017, University of Ottawa

Spinal muscular atrophy (SMA) is a debilitating neuromuscular disorder characterized by insufficient SMN protein, resulting in motoneuron death. Initially, it was thought that motoneuronal death… (more)

Subjects/Keywords: Spinal Muscular Atrophy; HuR; CARM1; SMA; Skeletal Muscle; Differentiation

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

APA (6th Edition):

Haghandish, A. (2017). Characterizing the Role of HuR in Skeletal Muscle of Mice with Spinal Muscular Atrophy . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/36746

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):

Haghandish, Amir. “Characterizing the Role of HuR in Skeletal Muscle of Mice with Spinal Muscular Atrophy .” 2017. Thesis, University of Ottawa. Accessed July 16, 2019. http://hdl.handle.net/10393/36746.

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

MLA Handbook (7th Edition):

Haghandish, Amir. “Characterizing the Role of HuR in Skeletal Muscle of Mice with Spinal Muscular Atrophy .” 2017. Web. 16 Jul 2019.

Vancouver:

Haghandish A. Characterizing the Role of HuR in Skeletal Muscle of Mice with Spinal Muscular Atrophy . [Internet] [Thesis]. University of Ottawa; 2017. [cited 2019 Jul 16]. Available from: http://hdl.handle.net/10393/36746.

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

Council of Science Editors:

Haghandish A. Characterizing the Role of HuR in Skeletal Muscle of Mice with Spinal Muscular Atrophy . [Thesis]. University of Ottawa; 2017. Available from: http://hdl.handle.net/10393/36746

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


University of Edinburgh

18. Powis, Rachael Anita. Targeting the ubiquitin proteasome system to develop novel therapeutic approaches for spinal muscular atrophy.

Degree: PhD, 2016, University of Edinburgh

Spinal muscular atrophy (SMA) is a severe genetic neuromuscular disorder characterised by lower motor neuron degeneration and paralysis. Although it is a leading genetic cause… (more)

Subjects/Keywords: SMA; spinal muscular atrophy; ubiquitin; Uba1; gene therapy

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APA (6th Edition):

Powis, R. A. (2016). Targeting the ubiquitin proteasome system to develop novel therapeutic approaches for spinal muscular atrophy. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/25854

Chicago Manual of Style (16th Edition):

Powis, Rachael Anita. “Targeting the ubiquitin proteasome system to develop novel therapeutic approaches for spinal muscular atrophy.” 2016. Doctoral Dissertation, University of Edinburgh. Accessed July 16, 2019. http://hdl.handle.net/1842/25854.

MLA Handbook (7th Edition):

Powis, Rachael Anita. “Targeting the ubiquitin proteasome system to develop novel therapeutic approaches for spinal muscular atrophy.” 2016. Web. 16 Jul 2019.

Vancouver:

Powis RA. Targeting the ubiquitin proteasome system to develop novel therapeutic approaches for spinal muscular atrophy. [Internet] [Doctoral dissertation]. University of Edinburgh; 2016. [cited 2019 Jul 16]. Available from: http://hdl.handle.net/1842/25854.

Council of Science Editors:

Powis RA. Targeting the ubiquitin proteasome system to develop novel therapeutic approaches for spinal muscular atrophy. [Doctoral Dissertation]. University of Edinburgh; 2016. Available from: http://hdl.handle.net/1842/25854


University of Aberdeen

19. Thomson, Alison Kathryn. Organ developmental and maturational defects in Spinal Muscular Atrophy.

Degree: PhD, 2016, University of Aberdeen

Spinal Muscular Atrophy (SMA), traditionally described as a predominantly childhood form of motor neuron disease, is a leading genetic cause of infant mortality. Although motor… (more)

Subjects/Keywords: 616.7; Spinal muscular atrophy; Organs (Anatomy); Abnormalities; Human

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

APA (6th Edition):

Thomson, A. K. (2016). Organ developmental and maturational defects in Spinal Muscular Atrophy. (Doctoral Dissertation). University of Aberdeen. Retrieved from http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=231849 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.715448

Chicago Manual of Style (16th Edition):

Thomson, Alison Kathryn. “Organ developmental and maturational defects in Spinal Muscular Atrophy.” 2016. Doctoral Dissertation, University of Aberdeen. Accessed July 16, 2019. http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=231849 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.715448.

MLA Handbook (7th Edition):

Thomson, Alison Kathryn. “Organ developmental and maturational defects in Spinal Muscular Atrophy.” 2016. Web. 16 Jul 2019.

Vancouver:

Thomson AK. Organ developmental and maturational defects in Spinal Muscular Atrophy. [Internet] [Doctoral dissertation]. University of Aberdeen; 2016. [cited 2019 Jul 16]. Available from: http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=231849 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.715448.

Council of Science Editors:

Thomson AK. Organ developmental and maturational defects in Spinal Muscular Atrophy. [Doctoral Dissertation]. University of Aberdeen; 2016. Available from: http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=231849 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.715448


Columbia University

20. Janas, Anna. A Stem Cell Model of the Motor Circuit Reveals Distinct Requirements for SMN in Motor Neuron Survival and Function.

Degree: 2015, Columbia University

 Neuronal circuit perturbations are emerging as important determinants in the pathogenesis of neurodegenerative diseases, including Alzheimer’s disease, Huntington’s disease, and spinal muscular atrophy (SMA). SMA… (more)

Subjects/Keywords: Neural circuitry; Nervous system – Degeneration; Spinal muscular atrophy; Motor neurons; Neurosciences

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

APA (6th Edition):

Janas, A. (2015). A Stem Cell Model of the Motor Circuit Reveals Distinct Requirements for SMN in Motor Neuron Survival and Function. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8FX78KZ

Chicago Manual of Style (16th Edition):

Janas, Anna. “A Stem Cell Model of the Motor Circuit Reveals Distinct Requirements for SMN in Motor Neuron Survival and Function.” 2015. Doctoral Dissertation, Columbia University. Accessed July 16, 2019. https://doi.org/10.7916/D8FX78KZ.

MLA Handbook (7th Edition):

Janas, Anna. “A Stem Cell Model of the Motor Circuit Reveals Distinct Requirements for SMN in Motor Neuron Survival and Function.” 2015. Web. 16 Jul 2019.

Vancouver:

Janas A. A Stem Cell Model of the Motor Circuit Reveals Distinct Requirements for SMN in Motor Neuron Survival and Function. [Internet] [Doctoral dissertation]. Columbia University; 2015. [cited 2019 Jul 16]. Available from: https://doi.org/10.7916/D8FX78KZ.

Council of Science Editors:

Janas A. A Stem Cell Model of the Motor Circuit Reveals Distinct Requirements for SMN in Motor Neuron Survival and Function. [Doctoral Dissertation]. Columbia University; 2015. Available from: https://doi.org/10.7916/D8FX78KZ


Columbia University

21. Lee, Justin. Characterization of motor pool selectivity of neuromuscular degeneration and identification of molecular correlates of disease resistance in Type I spinal muscular atrophy.

Degree: 2015, Columbia University

 Selective neuronal loss in response to loss or dysfunction of a ubiquitously expressed protein is a hallmark of neurodegenerative disease. Proximal spinal muscular atrophy (SMA)… (more)

Subjects/Keywords: Spinal muscular atrophy; Nervous system – Degeneration; Neuromuscular diseases; Neurosciences; Pathology; Biology

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

APA (6th Edition):

Lee, J. (2015). Characterization of motor pool selectivity of neuromuscular degeneration and identification of molecular correlates of disease resistance in Type I spinal muscular atrophy. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8513XBQ

Chicago Manual of Style (16th Edition):

Lee, Justin. “Characterization of motor pool selectivity of neuromuscular degeneration and identification of molecular correlates of disease resistance in Type I spinal muscular atrophy.” 2015. Doctoral Dissertation, Columbia University. Accessed July 16, 2019. https://doi.org/10.7916/D8513XBQ.

MLA Handbook (7th Edition):

Lee, Justin. “Characterization of motor pool selectivity of neuromuscular degeneration and identification of molecular correlates of disease resistance in Type I spinal muscular atrophy.” 2015. Web. 16 Jul 2019.

Vancouver:

Lee J. Characterization of motor pool selectivity of neuromuscular degeneration and identification of molecular correlates of disease resistance in Type I spinal muscular atrophy. [Internet] [Doctoral dissertation]. Columbia University; 2015. [cited 2019 Jul 16]. Available from: https://doi.org/10.7916/D8513XBQ.

Council of Science Editors:

Lee J. Characterization of motor pool selectivity of neuromuscular degeneration and identification of molecular correlates of disease resistance in Type I spinal muscular atrophy. [Doctoral Dissertation]. Columbia University; 2015. Available from: https://doi.org/10.7916/D8513XBQ


Brandeis University

22. Steeves, Marcie. Perinatal Loss Manifested Through the Lens of the Extended Family Unit.

Degree: 2012, Brandeis University

 Perinatal loss secondary to a genetic disorder is a complex and multidimensional experience, often felt across the extended family unit, including parents, relatives, friends, and… (more)

Subjects/Keywords: Perinatal loss; narrative analysis; genetic counseling; spinal muscular atrophy

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APA (6th Edition):

Steeves, M. (2012). Perinatal Loss Manifested Through the Lens of the Extended Family Unit. (Thesis). Brandeis University. Retrieved from http://hdl.handle.net/10192/83

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):

Steeves, Marcie. “Perinatal Loss Manifested Through the Lens of the Extended Family Unit.” 2012. Thesis, Brandeis University. Accessed July 16, 2019. http://hdl.handle.net/10192/83.

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

MLA Handbook (7th Edition):

Steeves, Marcie. “Perinatal Loss Manifested Through the Lens of the Extended Family Unit.” 2012. Web. 16 Jul 2019.

Vancouver:

Steeves M. Perinatal Loss Manifested Through the Lens of the Extended Family Unit. [Internet] [Thesis]. Brandeis University; 2012. [cited 2019 Jul 16]. Available from: http://hdl.handle.net/10192/83.

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

Council of Science Editors:

Steeves M. Perinatal Loss Manifested Through the Lens of the Extended Family Unit. [Thesis]. Brandeis University; 2012. Available from: http://hdl.handle.net/10192/83

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


Brandeis University

23. Zettler, Bethany. Prenatal Genetic Counselors’ Current Attitudes and Practices Regarding Discussion of Disease-Modulating Treatment for Spinal Muscular Atrophy.

Degree: 2019, Brandeis University

Spinal muscular atrophy (SMA) is an autosomal recessive genetic disease characterized by muscle weakness and atrophy with typical cognition. The first disease-modulating therapy for SMA,… (more)

Subjects/Keywords: Spinal muscular atrophy; neurogenetics; nusinersen; prenatal; genetic counseling; carrier screening; treatment

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

APA (6th Edition):

Zettler, B. (2019). Prenatal Genetic Counselors’ Current Attitudes and Practices Regarding Discussion of Disease-Modulating Treatment for Spinal Muscular Atrophy. (Thesis). Brandeis University. Retrieved from http://hdl.handle.net/10192/36760

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):

Zettler, Bethany. “Prenatal Genetic Counselors’ Current Attitudes and Practices Regarding Discussion of Disease-Modulating Treatment for Spinal Muscular Atrophy.” 2019. Thesis, Brandeis University. Accessed July 16, 2019. http://hdl.handle.net/10192/36760.

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

MLA Handbook (7th Edition):

Zettler, Bethany. “Prenatal Genetic Counselors’ Current Attitudes and Practices Regarding Discussion of Disease-Modulating Treatment for Spinal Muscular Atrophy.” 2019. Web. 16 Jul 2019.

Vancouver:

Zettler B. Prenatal Genetic Counselors’ Current Attitudes and Practices Regarding Discussion of Disease-Modulating Treatment for Spinal Muscular Atrophy. [Internet] [Thesis]. Brandeis University; 2019. [cited 2019 Jul 16]. Available from: http://hdl.handle.net/10192/36760.

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

Council of Science Editors:

Zettler B. Prenatal Genetic Counselors’ Current Attitudes and Practices Regarding Discussion of Disease-Modulating Treatment for Spinal Muscular Atrophy. [Thesis]. Brandeis University; 2019. Available from: http://hdl.handle.net/10192/36760

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


University of Missouri – Columbia

24. Terryberry, Melissa S. A study of readthrough therapy for spinal muscular atrophy in a transgenic mouse model.

Degree: 2009, University of Missouri – Columbia

 [ACCESS RESTRICTED TO THE UNIVERSITY OF MISSOURI AT AUTHOR'S REQUEST.] Spinal Muscular Atrophy (SMA) is due to the loss of the telomeric survival motor neuron… (more)

Subjects/Keywords: Spinal muscular atrophy  – Treatment; Aminoglycosides; Ribosomes; Mice as laboratory animals

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APA (6th Edition):

Terryberry, M. S. (2009). A study of readthrough therapy for spinal muscular atrophy in a transgenic mouse model. (Thesis). University of Missouri – Columbia. Retrieved from http://hdl.handle.net/10355/6600

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):

Terryberry, Melissa S. “A study of readthrough therapy for spinal muscular atrophy in a transgenic mouse model.” 2009. Thesis, University of Missouri – Columbia. Accessed July 16, 2019. http://hdl.handle.net/10355/6600.

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

MLA Handbook (7th Edition):

Terryberry, Melissa S. “A study of readthrough therapy for spinal muscular atrophy in a transgenic mouse model.” 2009. Web. 16 Jul 2019.

Vancouver:

Terryberry MS. A study of readthrough therapy for spinal muscular atrophy in a transgenic mouse model. [Internet] [Thesis]. University of Missouri – Columbia; 2009. [cited 2019 Jul 16]. Available from: http://hdl.handle.net/10355/6600.

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

Council of Science Editors:

Terryberry MS. A study of readthrough therapy for spinal muscular atrophy in a transgenic mouse model. [Thesis]. University of Missouri – Columbia; 2009. Available from: http://hdl.handle.net/10355/6600

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


University of California – San Francisco

25. Huynh, Walter. Disease-Associated Mutations in Human BICD2 Hyperactivate Motility of Dynein-Dynactin.

Degree: Biochemistry and Molecular Biology, 2017, University of California – San Francisco

 Mammalian cytoplasmic dynein is a microtubule-based motor that is involved in many cellular functions, one of which includes the retrograde transport of cargo. In contrast… (more)

Subjects/Keywords: Biochemistry; Bicaudal D; dynein; motor; spinal muscular atrophy; transport

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APA (6th Edition):

Huynh, W. (2017). Disease-Associated Mutations in Human BICD2 Hyperactivate Motility of Dynein-Dynactin. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/9p33d5tj

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):

Huynh, Walter. “Disease-Associated Mutations in Human BICD2 Hyperactivate Motility of Dynein-Dynactin.” 2017. Thesis, University of California – San Francisco. Accessed July 16, 2019. http://www.escholarship.org/uc/item/9p33d5tj.

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

MLA Handbook (7th Edition):

Huynh, Walter. “Disease-Associated Mutations in Human BICD2 Hyperactivate Motility of Dynein-Dynactin.” 2017. Web. 16 Jul 2019.

Vancouver:

Huynh W. Disease-Associated Mutations in Human BICD2 Hyperactivate Motility of Dynein-Dynactin. [Internet] [Thesis]. University of California – San Francisco; 2017. [cited 2019 Jul 16]. Available from: http://www.escholarship.org/uc/item/9p33d5tj.

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

Council of Science Editors:

Huynh W. Disease-Associated Mutations in Human BICD2 Hyperactivate Motility of Dynein-Dynactin. [Thesis]. University of California – San Francisco; 2017. Available from: http://www.escholarship.org/uc/item/9p33d5tj

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


Cal Poly

26. Brose, Richard Sterling. DEVELOPMENT AND EXTRAPOLATION OF AN UNDERGRADUATE LABORATORY EXPERIMENT TO AN ELASTOMERIC SPINAL MUSCULAR ATROPHY BRACE.

Degree: MS, Chemistry & Biochemistry, 2011, Cal Poly

  Ever since the advent of polymer science, polyurethanes have played a huge role in the industrial world. They have been used in endless applications… (more)

Subjects/Keywords: polyurethane; elastomer; spinal muscular atrophy; polymer; Materials Chemistry; Polymer Chemistry

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APA (6th Edition):

Brose, R. S. (2011). DEVELOPMENT AND EXTRAPOLATION OF AN UNDERGRADUATE LABORATORY EXPERIMENT TO AN ELASTOMERIC SPINAL MUSCULAR ATROPHY BRACE. (Masters Thesis). Cal Poly. Retrieved from https://digitalcommons.calpoly.edu/theses/525 ; 10.15368/theses.2011.82

Chicago Manual of Style (16th Edition):

Brose, Richard Sterling. “DEVELOPMENT AND EXTRAPOLATION OF AN UNDERGRADUATE LABORATORY EXPERIMENT TO AN ELASTOMERIC SPINAL MUSCULAR ATROPHY BRACE.” 2011. Masters Thesis, Cal Poly. Accessed July 16, 2019. https://digitalcommons.calpoly.edu/theses/525 ; 10.15368/theses.2011.82.

MLA Handbook (7th Edition):

Brose, Richard Sterling. “DEVELOPMENT AND EXTRAPOLATION OF AN UNDERGRADUATE LABORATORY EXPERIMENT TO AN ELASTOMERIC SPINAL MUSCULAR ATROPHY BRACE.” 2011. Web. 16 Jul 2019.

Vancouver:

Brose RS. DEVELOPMENT AND EXTRAPOLATION OF AN UNDERGRADUATE LABORATORY EXPERIMENT TO AN ELASTOMERIC SPINAL MUSCULAR ATROPHY BRACE. [Internet] [Masters thesis]. Cal Poly; 2011. [cited 2019 Jul 16]. Available from: https://digitalcommons.calpoly.edu/theses/525 ; 10.15368/theses.2011.82.

Council of Science Editors:

Brose RS. DEVELOPMENT AND EXTRAPOLATION OF AN UNDERGRADUATE LABORATORY EXPERIMENT TO AN ELASTOMERIC SPINAL MUSCULAR ATROPHY BRACE. [Masters Thesis]. Cal Poly; 2011. Available from: https://digitalcommons.calpoly.edu/theses/525 ; 10.15368/theses.2011.82


University of Southern California

27. Gustavo, Gutierrez. Rare diseases.

Degree: MA, Journalism (Broadcast Journalism), 2012, University of Southern California

 Rare diseases or also commonly known as orphan diseases are devastating for the person dealing with them, but also for the entire family. They are… (more)

Subjects/Keywords: spinal muscular atrophy; cystic fibrosis; type II; diseases; rare; U.S. Congress; funding; Madison'; s Foundation; Children'; s Hospital; Spinal Muscular Atrophy research.

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APA (6th Edition):

Gustavo, G. (2012). Rare diseases. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/37380/rec/5399

Chicago Manual of Style (16th Edition):

Gustavo, Gutierrez. “Rare diseases.” 2012. Masters Thesis, University of Southern California. Accessed July 16, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/37380/rec/5399.

MLA Handbook (7th Edition):

Gustavo, Gutierrez. “Rare diseases.” 2012. Web. 16 Jul 2019.

Vancouver:

Gustavo G. Rare diseases. [Internet] [Masters thesis]. University of Southern California; 2012. [cited 2019 Jul 16]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/37380/rec/5399.

Council of Science Editors:

Gustavo G. Rare diseases. [Masters Thesis]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/37380/rec/5399


Northeastern University

28. Miller, Eliza Hope. Optimization of dihydroquinazolinone for treatment of spinal muscular atrophy.

Degree: MS, Department of Chemistry and Chemical Biology, 2016, Northeastern University

Spinal muscular atrophy (SMA) is an inherited neurodegenerative disease characterized by progressive muscle weakness and eventual muscle loss. It is the leading heritable cause of… (more)

Subjects/Keywords: survival motor neuron gene; dihydroquinazolinone; Spinal muscular atrophy; Genetic aspects; Spinal muscular atrophy; Treatment; Genetic transcription; Motor neurons; Heterocyclic compounds; Proteins; Analysis

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APA (6th Edition):

Miller, E. H. (2016). Optimization of dihydroquinazolinone for treatment of spinal muscular atrophy. (Masters Thesis). Northeastern University. Retrieved from http://hdl.handle.net/2047/D20213404

Chicago Manual of Style (16th Edition):

Miller, Eliza Hope. “Optimization of dihydroquinazolinone for treatment of spinal muscular atrophy.” 2016. Masters Thesis, Northeastern University. Accessed July 16, 2019. http://hdl.handle.net/2047/D20213404.

MLA Handbook (7th Edition):

Miller, Eliza Hope. “Optimization of dihydroquinazolinone for treatment of spinal muscular atrophy.” 2016. Web. 16 Jul 2019.

Vancouver:

Miller EH. Optimization of dihydroquinazolinone for treatment of spinal muscular atrophy. [Internet] [Masters thesis]. Northeastern University; 2016. [cited 2019 Jul 16]. Available from: http://hdl.handle.net/2047/D20213404.

Council of Science Editors:

Miller EH. Optimization of dihydroquinazolinone for treatment of spinal muscular atrophy. [Masters Thesis]. Northeastern University; 2016. Available from: http://hdl.handle.net/2047/D20213404


The Ohio State University

29. Murtha, Matthew J., III. Transcriptional Programming of Spinal Motor Neurons from Stem Cells.

Degree: PhD, Molecular, Cellular, and Developmental Biology, 2010, The Ohio State University

  Motor neurons are the cholinergic cells of the spinal ventral horns responsible for mediating the central nervous system’s control of voluntary muscle movement. Selective… (more)

Subjects/Keywords: Molecular Biology; Motor neuron; stem cell; amyotrophic lateral sclerosis; spinal muscular atrophy

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

APA (6th Edition):

Murtha, Matthew J., I. (2010). Transcriptional Programming of Spinal Motor Neurons from Stem Cells. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1261416295

Chicago Manual of Style (16th Edition):

Murtha, Matthew J., III. “Transcriptional Programming of Spinal Motor Neurons from Stem Cells.” 2010. Doctoral Dissertation, The Ohio State University. Accessed July 16, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1261416295.

MLA Handbook (7th Edition):

Murtha, Matthew J., III. “Transcriptional Programming of Spinal Motor Neurons from Stem Cells.” 2010. Web. 16 Jul 2019.

Vancouver:

Murtha, Matthew J. I. Transcriptional Programming of Spinal Motor Neurons from Stem Cells. [Internet] [Doctoral dissertation]. The Ohio State University; 2010. [cited 2019 Jul 16]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1261416295.

Council of Science Editors:

Murtha, Matthew J. I. Transcriptional Programming of Spinal Motor Neurons from Stem Cells. [Doctoral Dissertation]. The Ohio State University; 2010. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1261416295


The Ohio State University

30. Gladman, Jordan Tanin. Investigating the pre-mRNA splicing of the Survival Motor Neuron genes to model the Spinal Muscular Atrophy disease phenotype.

Degree: PhD, Integrated Biomedical Science Graduate Program, 2010, The Ohio State University

 Proximal spinal muscular atrophy (SMA) is a neurodegenerative disease caused by low levels of the Survival Motor Neuron (SMN) protein. In humans SMN1 and SMN2… (more)

Subjects/Keywords: Molecular Biology; Spinal Muscular Atrophy; Survival Motor Neuron; pre-mRNA, RNA splicing

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

APA (6th Edition):

Gladman, J. T. (2010). Investigating the pre-mRNA splicing of the Survival Motor Neuron genes to model the Spinal Muscular Atrophy disease phenotype. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1281365393

Chicago Manual of Style (16th Edition):

Gladman, Jordan Tanin. “Investigating the pre-mRNA splicing of the Survival Motor Neuron genes to model the Spinal Muscular Atrophy disease phenotype.” 2010. Doctoral Dissertation, The Ohio State University. Accessed July 16, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1281365393.

MLA Handbook (7th Edition):

Gladman, Jordan Tanin. “Investigating the pre-mRNA splicing of the Survival Motor Neuron genes to model the Spinal Muscular Atrophy disease phenotype.” 2010. Web. 16 Jul 2019.

Vancouver:

Gladman JT. Investigating the pre-mRNA splicing of the Survival Motor Neuron genes to model the Spinal Muscular Atrophy disease phenotype. [Internet] [Doctoral dissertation]. The Ohio State University; 2010. [cited 2019 Jul 16]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1281365393.

Council of Science Editors:

Gladman JT. Investigating the pre-mRNA splicing of the Survival Motor Neuron genes to model the Spinal Muscular Atrophy disease phenotype. [Doctoral Dissertation]. The Ohio State University; 2010. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1281365393

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