Advanced search options

Advanced Search Options 🞨

Browse by author name (“Author name starts with…”).

Find ETDs with:

in
/  
in
/  
in
/  
in

Written in Published in Earliest date Latest date

Sorted by

Results per page:

Sorted by: relevance · author · university · dateNew search

You searched for subject:(Muscular Dystrophy). Showing records 1 – 30 of 398 total matches.

[1] [2] [3] [4] [5] … [14]

Search Limiters

Last 2 Years | English Only

Degrees

Levels

Languages

Country

▼ Search Limiters


University of Georgia

1. Praissman, Jeremy Lawrence. The role of [beta]-1,4-glucuronyltransferase 1 in [alpha]-dystroglycan function.

Degree: PhD, Biochemistry and Molecular Biology, 2015, University of Georgia

 Alpha-dystroglycan (α-DG) is a necessary cell-surface receptor in diverse metazoan species and is particularly important in mammalian neural development and muscular structure. However, the complex… (more)

Subjects/Keywords: Congenital muscular dystrophy

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Praissman, J. L. (2015). The role of [beta]-1,4-glucuronyltransferase 1 in [alpha]-dystroglycan function. (Doctoral Dissertation). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/praissman_jeremy_l_201505_phd

Chicago Manual of Style (16th Edition):

Praissman, Jeremy Lawrence. “The role of [beta]-1,4-glucuronyltransferase 1 in [alpha]-dystroglycan function.” 2015. Doctoral Dissertation, University of Georgia. Accessed January 24, 2020. http://purl.galileo.usg.edu/uga_etd/praissman_jeremy_l_201505_phd.

MLA Handbook (7th Edition):

Praissman, Jeremy Lawrence. “The role of [beta]-1,4-glucuronyltransferase 1 in [alpha]-dystroglycan function.” 2015. Web. 24 Jan 2020.

Vancouver:

Praissman JL. The role of [beta]-1,4-glucuronyltransferase 1 in [alpha]-dystroglycan function. [Internet] [Doctoral dissertation]. University of Georgia; 2015. [cited 2020 Jan 24]. Available from: http://purl.galileo.usg.edu/uga_etd/praissman_jeremy_l_201505_phd.

Council of Science Editors:

Praissman JL. The role of [beta]-1,4-glucuronyltransferase 1 in [alpha]-dystroglycan function. [Doctoral Dissertation]. University of Georgia; 2015. Available from: http://purl.galileo.usg.edu/uga_etd/praissman_jeremy_l_201505_phd


Oregon State University

2. Codding, Sara Jone. Functional and Structural Analyses of Three Distinct proteins by Biochemical and Biophysical Techniques.

Degree: PhD, Biochemistry & Biophysics, 2016, Oregon State University

 The focus of this dissertation was to understand protein function and structure on a molecular level. To do this successfully, a variety of biochemical and… (more)

Subjects/Keywords: dysferlin; Muscular dystrophy  – Molecular aspects

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Codding, S. J. (2016). Functional and Structural Analyses of Three Distinct proteins by Biochemical and Biophysical Techniques. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/60138

Chicago Manual of Style (16th Edition):

Codding, Sara Jone. “Functional and Structural Analyses of Three Distinct proteins by Biochemical and Biophysical Techniques.” 2016. Doctoral Dissertation, Oregon State University. Accessed January 24, 2020. http://hdl.handle.net/1957/60138.

MLA Handbook (7th Edition):

Codding, Sara Jone. “Functional and Structural Analyses of Three Distinct proteins by Biochemical and Biophysical Techniques.” 2016. Web. 24 Jan 2020.

Vancouver:

Codding SJ. Functional and Structural Analyses of Three Distinct proteins by Biochemical and Biophysical Techniques. [Internet] [Doctoral dissertation]. Oregon State University; 2016. [cited 2020 Jan 24]. Available from: http://hdl.handle.net/1957/60138.

Council of Science Editors:

Codding SJ. Functional and Structural Analyses of Three Distinct proteins by Biochemical and Biophysical Techniques. [Doctoral Dissertation]. Oregon State University; 2016. Available from: http://hdl.handle.net/1957/60138


University of Western Australia

3. Pellegrini, Kathryn. Myoblast transplantation : murine studies.

Degree: PhD, 2011, University of Western Australia

[Truncated abstract] Duchenne muscular dystrophy (DMD) is a severe X-linked recessive disorder characterised by widespread muscle fibre necrosis followed by the replacement of muscle with… (more)

Subjects/Keywords: Muscular dystrophy; Myoblasts; Cell transplantation

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Pellegrini, K. (2011). Myoblast transplantation : murine studies. (Doctoral Dissertation). University of Western Australia. Retrieved from http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=30767&local_base=GEN01-INS01

Chicago Manual of Style (16th Edition):

Pellegrini, Kathryn. “Myoblast transplantation : murine studies.” 2011. Doctoral Dissertation, University of Western Australia. Accessed January 24, 2020. http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=30767&local_base=GEN01-INS01.

MLA Handbook (7th Edition):

Pellegrini, Kathryn. “Myoblast transplantation : murine studies.” 2011. Web. 24 Jan 2020.

Vancouver:

Pellegrini K. Myoblast transplantation : murine studies. [Internet] [Doctoral dissertation]. University of Western Australia; 2011. [cited 2020 Jan 24]. Available from: http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=30767&local_base=GEN01-INS01.

Council of Science Editors:

Pellegrini K. Myoblast transplantation : murine studies. [Doctoral Dissertation]. University of Western Australia; 2011. Available from: http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=30767&local_base=GEN01-INS01


Universiteit Utrecht

4. Haastert, M.A. van. Myotonic Dystrophy type 1 and Duchenne Muscular Dystrophy: cognitive profile and behavioral functioning.

Degree: 2010, Universiteit Utrecht

 Duchenne muscular dystrophy (DMD) and myotonic dystrophy type 1 (DM1) are two neuromuscular disorders with a proven correlation between neurological deficits and cognitive deficits. These… (more)

Subjects/Keywords: Sociale Wetenschappen; Muscular Dystrophy, cognitive

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Haastert, M. A. v. (2010). Myotonic Dystrophy type 1 and Duchenne Muscular Dystrophy: cognitive profile and behavioral functioning. (Masters Thesis). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/210569

Chicago Manual of Style (16th Edition):

Haastert, M A van. “Myotonic Dystrophy type 1 and Duchenne Muscular Dystrophy: cognitive profile and behavioral functioning.” 2010. Masters Thesis, Universiteit Utrecht. Accessed January 24, 2020. http://dspace.library.uu.nl:8080/handle/1874/210569.

MLA Handbook (7th Edition):

Haastert, M A van. “Myotonic Dystrophy type 1 and Duchenne Muscular Dystrophy: cognitive profile and behavioral functioning.” 2010. Web. 24 Jan 2020.

Vancouver:

Haastert MAv. Myotonic Dystrophy type 1 and Duchenne Muscular Dystrophy: cognitive profile and behavioral functioning. [Internet] [Masters thesis]. Universiteit Utrecht; 2010. [cited 2020 Jan 24]. Available from: http://dspace.library.uu.nl:8080/handle/1874/210569.

Council of Science Editors:

Haastert MAv. Myotonic Dystrophy type 1 and Duchenne Muscular Dystrophy: cognitive profile and behavioral functioning. [Masters Thesis]. Universiteit Utrecht; 2010. Available from: http://dspace.library.uu.nl:8080/handle/1874/210569


Texas A&M University

5. Baker, Ryan Andrew. The Role of Protein O-MannosylTransferase in the Development of Drosophila Torsion Phenotypes.

Degree: PhD, Biochemistry, 2016, Texas A&M University

 Congenital muscular dystrophies (CMD’s) are serious diseases affecting muscle, brain, eye, and other tissues and often result in premature death of patients. These forms of… (more)

Subjects/Keywords: O-mannosylation; Drosophila; Muscular Dystrophy

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Baker, R. A. (2016). The Role of Protein O-MannosylTransferase in the Development of Drosophila Torsion Phenotypes. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/158608

Chicago Manual of Style (16th Edition):

Baker, Ryan Andrew. “The Role of Protein O-MannosylTransferase in the Development of Drosophila Torsion Phenotypes.” 2016. Doctoral Dissertation, Texas A&M University. Accessed January 24, 2020. http://hdl.handle.net/1969.1/158608.

MLA Handbook (7th Edition):

Baker, Ryan Andrew. “The Role of Protein O-MannosylTransferase in the Development of Drosophila Torsion Phenotypes.” 2016. Web. 24 Jan 2020.

Vancouver:

Baker RA. The Role of Protein O-MannosylTransferase in the Development of Drosophila Torsion Phenotypes. [Internet] [Doctoral dissertation]. Texas A&M University; 2016. [cited 2020 Jan 24]. Available from: http://hdl.handle.net/1969.1/158608.

Council of Science Editors:

Baker RA. The Role of Protein O-MannosylTransferase in the Development of Drosophila Torsion Phenotypes. [Doctoral Dissertation]. Texas A&M University; 2016. Available from: http://hdl.handle.net/1969.1/158608


Oregon State University

6. Roffler, Sheila Ann. Nutritional muscular dystrophy production and pectoral muscle 5'-nucleotidase activity in the chick.

Degree: MS, Chemistry, 1964, Oregon State University

 In an attempt to find a laboratory species which develops an experimental myopathy similar to white muscle disease (WMD) in lambs, comparative studies of nutritional… (more)

Subjects/Keywords: Muscular dystrophy

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Roffler, S. A. (1964). Nutritional muscular dystrophy production and pectoral muscle 5'-nucleotidase activity in the chick. (Masters Thesis). Oregon State University. Retrieved from http://hdl.handle.net/1957/49038

Chicago Manual of Style (16th Edition):

Roffler, Sheila Ann. “Nutritional muscular dystrophy production and pectoral muscle 5'-nucleotidase activity in the chick.” 1964. Masters Thesis, Oregon State University. Accessed January 24, 2020. http://hdl.handle.net/1957/49038.

MLA Handbook (7th Edition):

Roffler, Sheila Ann. “Nutritional muscular dystrophy production and pectoral muscle 5'-nucleotidase activity in the chick.” 1964. Web. 24 Jan 2020.

Vancouver:

Roffler SA. Nutritional muscular dystrophy production and pectoral muscle 5'-nucleotidase activity in the chick. [Internet] [Masters thesis]. Oregon State University; 1964. [cited 2020 Jan 24]. Available from: http://hdl.handle.net/1957/49038.

Council of Science Editors:

Roffler SA. Nutritional muscular dystrophy production and pectoral muscle 5'-nucleotidase activity in the chick. [Masters Thesis]. Oregon State University; 1964. Available from: http://hdl.handle.net/1957/49038


University of Minnesota

7. Coffman, Christian. Calorimetric Determination of Dystrophin ABD1 Unfolding Energetics.

Degree: MS, Chemistry, 2018, University of Minnesota

Muscular Dystrophy (MD) is a disease that effects the structural integrity of muscle cells. Studies have linked the Dystrophin protein to MD as the most… (more)

Subjects/Keywords: Calorimetry; Dystrophin; Muscular Dystrophy; Thermodynamics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Coffman, C. (2018). Calorimetric Determination of Dystrophin ABD1 Unfolding Energetics. (Masters Thesis). University of Minnesota. Retrieved from http://hdl.handle.net/11299/202099

Chicago Manual of Style (16th Edition):

Coffman, Christian. “Calorimetric Determination of Dystrophin ABD1 Unfolding Energetics.” 2018. Masters Thesis, University of Minnesota. Accessed January 24, 2020. http://hdl.handle.net/11299/202099.

MLA Handbook (7th Edition):

Coffman, Christian. “Calorimetric Determination of Dystrophin ABD1 Unfolding Energetics.” 2018. Web. 24 Jan 2020.

Vancouver:

Coffman C. Calorimetric Determination of Dystrophin ABD1 Unfolding Energetics. [Internet] [Masters thesis]. University of Minnesota; 2018. [cited 2020 Jan 24]. Available from: http://hdl.handle.net/11299/202099.

Council of Science Editors:

Coffman C. Calorimetric Determination of Dystrophin ABD1 Unfolding Energetics. [Masters Thesis]. University of Minnesota; 2018. Available from: http://hdl.handle.net/11299/202099


University of Melbourne

8. Roberts, Mary. Daytime predictors of sleep disordered breathing in Duchenne muscular dystrophy.

Degree: 2017, University of Melbourne

 Sleep disordered breathing (SDB) in Duchenne muscular dystrophy (DMD) progresses to respiratory failure. The gold standard for diagnosis is polysomnography (PSG) but the optimal timing… (more)

Subjects/Keywords: duchenne muscular dystrophy; daytime predictors

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Roberts, M. (2017). Daytime predictors of sleep disordered breathing in Duchenne muscular dystrophy. (Masters Thesis). University of Melbourne. Retrieved from http://hdl.handle.net/11343/194347

Chicago Manual of Style (16th Edition):

Roberts, Mary. “Daytime predictors of sleep disordered breathing in Duchenne muscular dystrophy.” 2017. Masters Thesis, University of Melbourne. Accessed January 24, 2020. http://hdl.handle.net/11343/194347.

MLA Handbook (7th Edition):

Roberts, Mary. “Daytime predictors of sleep disordered breathing in Duchenne muscular dystrophy.” 2017. Web. 24 Jan 2020.

Vancouver:

Roberts M. Daytime predictors of sleep disordered breathing in Duchenne muscular dystrophy. [Internet] [Masters thesis]. University of Melbourne; 2017. [cited 2020 Jan 24]. Available from: http://hdl.handle.net/11343/194347.

Council of Science Editors:

Roberts M. Daytime predictors of sleep disordered breathing in Duchenne muscular dystrophy. [Masters Thesis]. University of Melbourne; 2017. Available from: http://hdl.handle.net/11343/194347


University of Ottawa

9. Pryce, Benjamin. Role of the Ste20 Like Kinase in Muscle Development and Muscular Dystrophy .

Degree: 2019, University of Ottawa

 Duchenne Muscular Dystrophy (DMD) is a fatal X-linked disorder affecting 1 out of every 3500 male births. The underlying cause of DMD is mutations within… (more)

Subjects/Keywords: SLK; Skeletal Muscle; Muscular Dystrophy

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Pryce, B. (2019). Role of the Ste20 Like Kinase in Muscle Development and Muscular Dystrophy . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/38710

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):

Pryce, Benjamin. “Role of the Ste20 Like Kinase in Muscle Development and Muscular Dystrophy .” 2019. Thesis, University of Ottawa. Accessed January 24, 2020. http://hdl.handle.net/10393/38710.

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

MLA Handbook (7th Edition):

Pryce, Benjamin. “Role of the Ste20 Like Kinase in Muscle Development and Muscular Dystrophy .” 2019. Web. 24 Jan 2020.

Vancouver:

Pryce B. Role of the Ste20 Like Kinase in Muscle Development and Muscular Dystrophy . [Internet] [Thesis]. University of Ottawa; 2019. [cited 2020 Jan 24]. Available from: http://hdl.handle.net/10393/38710.

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

Council of Science Editors:

Pryce B. Role of the Ste20 Like Kinase in Muscle Development and Muscular Dystrophy . [Thesis]. University of Ottawa; 2019. Available from: http://hdl.handle.net/10393/38710

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


University of Ottawa

10. Girgis, John. A Study of the Role of the Six Family of Transcription Factors in Adult Skeletal Muscle Homeostasis .

Degree: 2018, University of Ottawa

At the author’s request, the abstract has been removed due to the confidential nature of the thesis. It will be added once the embargo period has passed.

Subjects/Keywords: Muscle; Transcription; Muscular dystrophy; Six

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Girgis, J. (2018). A Study of the Role of the Six Family of Transcription Factors in Adult Skeletal Muscle Homeostasis . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/37891

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):

Girgis, John. “A Study of the Role of the Six Family of Transcription Factors in Adult Skeletal Muscle Homeostasis .” 2018. Thesis, University of Ottawa. Accessed January 24, 2020. http://hdl.handle.net/10393/37891.

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

MLA Handbook (7th Edition):

Girgis, John. “A Study of the Role of the Six Family of Transcription Factors in Adult Skeletal Muscle Homeostasis .” 2018. Web. 24 Jan 2020.

Vancouver:

Girgis J. A Study of the Role of the Six Family of Transcription Factors in Adult Skeletal Muscle Homeostasis . [Internet] [Thesis]. University of Ottawa; 2018. [cited 2020 Jan 24]. Available from: http://hdl.handle.net/10393/37891.

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

Council of Science Editors:

Girgis J. A Study of the Role of the Six Family of Transcription Factors in Adult Skeletal Muscle Homeostasis . [Thesis]. University of Ottawa; 2018. Available from: http://hdl.handle.net/10393/37891

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


Georgia State University

11. Hill, Bailey. Characterization of Individuals with Muscular Dystrophy from the Muscular Dystrophy Surveillance, Tracking, and Research Network (MD STARnet) Pilot in the United States.

Degree: MPH, Public Health, 2018, Georgia State University

  Introduction: Because of the variability in muscular dystrophy (MD) in terms of clinical manifestations, affected demographic, and health trajectories, it is important to study… (more)

Subjects/Keywords: Population-based Surveillance; Muscular Dystrophy

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Hill, B. (2018). Characterization of Individuals with Muscular Dystrophy from the Muscular Dystrophy Surveillance, Tracking, and Research Network (MD STARnet) Pilot in the United States. (Thesis). Georgia State University. Retrieved from https://scholarworks.gsu.edu/iph_theses/599

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):

Hill, Bailey. “Characterization of Individuals with Muscular Dystrophy from the Muscular Dystrophy Surveillance, Tracking, and Research Network (MD STARnet) Pilot in the United States.” 2018. Thesis, Georgia State University. Accessed January 24, 2020. https://scholarworks.gsu.edu/iph_theses/599.

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

MLA Handbook (7th Edition):

Hill, Bailey. “Characterization of Individuals with Muscular Dystrophy from the Muscular Dystrophy Surveillance, Tracking, and Research Network (MD STARnet) Pilot in the United States.” 2018. Web. 24 Jan 2020.

Vancouver:

Hill B. Characterization of Individuals with Muscular Dystrophy from the Muscular Dystrophy Surveillance, Tracking, and Research Network (MD STARnet) Pilot in the United States. [Internet] [Thesis]. Georgia State University; 2018. [cited 2020 Jan 24]. Available from: https://scholarworks.gsu.edu/iph_theses/599.

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

Council of Science Editors:

Hill B. Characterization of Individuals with Muscular Dystrophy from the Muscular Dystrophy Surveillance, Tracking, and Research Network (MD STARnet) Pilot in the United States. [Thesis]. Georgia State University; 2018. Available from: https://scholarworks.gsu.edu/iph_theses/599

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

12. Lopes, Vanessa Ferreira. Caracterização funcional das diferentes linhagens de modelos murinos para distrofias musculares.

Degree: Mestrado, Biotecnologia, 2011, University of São Paulo

As distrofias musculares constituem um grupo heterogêneo de doenças genéticas, caracterizadas por uma degeneração progressiva e irreversível dos músculos. Modelos murinos distróficos, como o mdx,… (more)

Subjects/Keywords: Animal models; Animal strains; Distrofia muscular; Distrofia muscular animal; Linhagens animais; Modelos animais; Muscular dystrophy; Muscular dystrophy animal

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Lopes, V. F. (2011). Caracterização funcional das diferentes linhagens de modelos murinos para distrofias musculares. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/87/87131/tde-04052011-150431/ ;

Chicago Manual of Style (16th Edition):

Lopes, Vanessa Ferreira. “Caracterização funcional das diferentes linhagens de modelos murinos para distrofias musculares.” 2011. Masters Thesis, University of São Paulo. Accessed January 24, 2020. http://www.teses.usp.br/teses/disponiveis/87/87131/tde-04052011-150431/ ;.

MLA Handbook (7th Edition):

Lopes, Vanessa Ferreira. “Caracterização funcional das diferentes linhagens de modelos murinos para distrofias musculares.” 2011. Web. 24 Jan 2020.

Vancouver:

Lopes VF. Caracterização funcional das diferentes linhagens de modelos murinos para distrofias musculares. [Internet] [Masters thesis]. University of São Paulo; 2011. [cited 2020 Jan 24]. Available from: http://www.teses.usp.br/teses/disponiveis/87/87131/tde-04052011-150431/ ;.

Council of Science Editors:

Lopes VF. Caracterização funcional das diferentes linhagens de modelos murinos para distrofias musculares. [Masters Thesis]. University of São Paulo; 2011. Available from: http://www.teses.usp.br/teses/disponiveis/87/87131/tde-04052011-150431/ ;


University of Aberdeen

13. Evans, Darrell John Rhys. The behaviour and commitment of myoblasts during mammalian skeletal muscle formation.

Degree: PhD, 1994, University of Aberdeen

 During mammalian skeletal muscle development, muscle fibres form in a biphasic manner from the fusion of myoblasts. Primary fibres form first, which subsequently provide a… (more)

Subjects/Keywords: 572.8; Muscular dystrophy

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Evans, D. J. R. (1994). The behaviour and commitment of myoblasts during mammalian skeletal muscle formation. (Doctoral Dissertation). University of Aberdeen. Retrieved from http://digitool.abdn.ac.uk/R?func=search-advanced-go&find_code1=WSN&request1=AAIU603173 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.387256

Chicago Manual of Style (16th Edition):

Evans, Darrell John Rhys. “The behaviour and commitment of myoblasts during mammalian skeletal muscle formation.” 1994. Doctoral Dissertation, University of Aberdeen. Accessed January 24, 2020. http://digitool.abdn.ac.uk/R?func=search-advanced-go&find_code1=WSN&request1=AAIU603173 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.387256.

MLA Handbook (7th Edition):

Evans, Darrell John Rhys. “The behaviour and commitment of myoblasts during mammalian skeletal muscle formation.” 1994. Web. 24 Jan 2020.

Vancouver:

Evans DJR. The behaviour and commitment of myoblasts during mammalian skeletal muscle formation. [Internet] [Doctoral dissertation]. University of Aberdeen; 1994. [cited 2020 Jan 24]. Available from: http://digitool.abdn.ac.uk/R?func=search-advanced-go&find_code1=WSN&request1=AAIU603173 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.387256.

Council of Science Editors:

Evans DJR. The behaviour and commitment of myoblasts during mammalian skeletal muscle formation. [Doctoral Dissertation]. University of Aberdeen; 1994. Available from: http://digitool.abdn.ac.uk/R?func=search-advanced-go&find_code1=WSN&request1=AAIU603173 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.387256


Texas A&M University

14. Stoughton, William Benjamin. Skeletal Muscle Homeostasis in Golden Retriever Muscular Dystrophy: The Role of Apoptosis & Autophagy in GRMD Pathogenesis.

Degree: PhD, Biomedical Sciences, 2016, Texas A&M University

 Duchenne muscular dystrophy (DMD) is an X-linked recessive genetic disorder caused by mutations in the DMD gene, which results in loss of the dystrophin protein… (more)

Subjects/Keywords: Golden retriever muscular dystrophy; autophagy; apoptosis; APIP

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Stoughton, W. B. (2016). Skeletal Muscle Homeostasis in Golden Retriever Muscular Dystrophy: The Role of Apoptosis & Autophagy in GRMD Pathogenesis. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/159037

Chicago Manual of Style (16th Edition):

Stoughton, William Benjamin. “Skeletal Muscle Homeostasis in Golden Retriever Muscular Dystrophy: The Role of Apoptosis & Autophagy in GRMD Pathogenesis.” 2016. Doctoral Dissertation, Texas A&M University. Accessed January 24, 2020. http://hdl.handle.net/1969.1/159037.

MLA Handbook (7th Edition):

Stoughton, William Benjamin. “Skeletal Muscle Homeostasis in Golden Retriever Muscular Dystrophy: The Role of Apoptosis & Autophagy in GRMD Pathogenesis.” 2016. Web. 24 Jan 2020.

Vancouver:

Stoughton WB. Skeletal Muscle Homeostasis in Golden Retriever Muscular Dystrophy: The Role of Apoptosis & Autophagy in GRMD Pathogenesis. [Internet] [Doctoral dissertation]. Texas A&M University; 2016. [cited 2020 Jan 24]. Available from: http://hdl.handle.net/1969.1/159037.

Council of Science Editors:

Stoughton WB. Skeletal Muscle Homeostasis in Golden Retriever Muscular Dystrophy: The Role of Apoptosis & Autophagy in GRMD Pathogenesis. [Doctoral Dissertation]. Texas A&M University; 2016. Available from: http://hdl.handle.net/1969.1/159037


University of Houston

15. Gold, Alanna 1984-. DUCHENNE MUSCULAR DYSTROPHY: ACADEMIC ACHIEVEMENT AND COGNITIVE CORRELATES.

Degree: Psychology, Department of, 2016, University of Houston

 The purpose of this study is to further explore the neuropsychological profile of children with Duchenne muscular dystrophy (DMD), and how core cognitive deficits relate… (more)

Subjects/Keywords: Duchenne muscular dystrophy; academic achievement; cognition

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Gold, A. 1. (2016). DUCHENNE MUSCULAR DYSTROPHY: ACADEMIC ACHIEVEMENT AND COGNITIVE CORRELATES. (Thesis). University of Houston. Retrieved from http://hdl.handle.net/10657/1299

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):

Gold, Alanna 1984-. “DUCHENNE MUSCULAR DYSTROPHY: ACADEMIC ACHIEVEMENT AND COGNITIVE CORRELATES.” 2016. Thesis, University of Houston. Accessed January 24, 2020. http://hdl.handle.net/10657/1299.

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

MLA Handbook (7th Edition):

Gold, Alanna 1984-. “DUCHENNE MUSCULAR DYSTROPHY: ACADEMIC ACHIEVEMENT AND COGNITIVE CORRELATES.” 2016. Web. 24 Jan 2020.

Vancouver:

Gold A1. DUCHENNE MUSCULAR DYSTROPHY: ACADEMIC ACHIEVEMENT AND COGNITIVE CORRELATES. [Internet] [Thesis]. University of Houston; 2016. [cited 2020 Jan 24]. Available from: http://hdl.handle.net/10657/1299.

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

Council of Science Editors:

Gold A1. DUCHENNE MUSCULAR DYSTROPHY: ACADEMIC ACHIEVEMENT AND COGNITIVE CORRELATES. [Thesis]. University of Houston; 2016. Available from: http://hdl.handle.net/10657/1299

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


Massey University

16. Muthu, Muralidharan. Structural and biochemical characterisation of utrophin and dystrophin spectrin repeat domains : submitted in partial fulfilment of the requirements for the degree of Doctor of Philosophy in Biochemistry, Massey University, Palmerston North, NZ .

Degree: 2012, Massey University

 Duchenne and Becker muscular dystrophies are muscle-wasting disorders caused by mutations in the X-linked dystrophin gene. Dystrophin is a large cytoskeletal protein belonging to the… (more)

Subjects/Keywords: Duchenne muscular dystrophy; Genetic aspects; Dystrophin; Spectrin

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Muthu, M. (2012). Structural and biochemical characterisation of utrophin and dystrophin spectrin repeat domains : submitted in partial fulfilment of the requirements for the degree of Doctor of Philosophy in Biochemistry, Massey University, Palmerston North, NZ . (Thesis). Massey University. Retrieved from http://hdl.handle.net/10179/4949

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):

Muthu, Muralidharan. “Structural and biochemical characterisation of utrophin and dystrophin spectrin repeat domains : submitted in partial fulfilment of the requirements for the degree of Doctor of Philosophy in Biochemistry, Massey University, Palmerston North, NZ .” 2012. Thesis, Massey University. Accessed January 24, 2020. http://hdl.handle.net/10179/4949.

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

MLA Handbook (7th Edition):

Muthu, Muralidharan. “Structural and biochemical characterisation of utrophin and dystrophin spectrin repeat domains : submitted in partial fulfilment of the requirements for the degree of Doctor of Philosophy in Biochemistry, Massey University, Palmerston North, NZ .” 2012. Web. 24 Jan 2020.

Vancouver:

Muthu M. Structural and biochemical characterisation of utrophin and dystrophin spectrin repeat domains : submitted in partial fulfilment of the requirements for the degree of Doctor of Philosophy in Biochemistry, Massey University, Palmerston North, NZ . [Internet] [Thesis]. Massey University; 2012. [cited 2020 Jan 24]. Available from: http://hdl.handle.net/10179/4949.

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

Council of Science Editors:

Muthu M. Structural and biochemical characterisation of utrophin and dystrophin spectrin repeat domains : submitted in partial fulfilment of the requirements for the degree of Doctor of Philosophy in Biochemistry, Massey University, Palmerston North, NZ . [Thesis]. Massey University; 2012. Available from: http://hdl.handle.net/10179/4949

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


University of Debrecen

17. Umar, Muhammad Azeem Jalil. Pharmacotherapy of Duchenne Muscular Dystrophy .

Degree: DE – Általános Orvostudományi Kar, University of Debrecen

 Duchenne muscular dystrophy is a myopathic disease caused by mutations in the dystrophin gene. It is inherited in an X-linked recessive manner from mothers to… (more)

Subjects/Keywords: Duchenne Muscular Dystrophy

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Umar, M. A. J. (n.d.). Pharmacotherapy of Duchenne Muscular Dystrophy . (Thesis). University of Debrecen. Retrieved from http://hdl.handle.net/2437/257231

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Umar, Muhammad Azeem Jalil. “Pharmacotherapy of Duchenne Muscular Dystrophy .” Thesis, University of Debrecen. Accessed January 24, 2020. http://hdl.handle.net/2437/257231.

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Umar, Muhammad Azeem Jalil. “Pharmacotherapy of Duchenne Muscular Dystrophy .” Web. 24 Jan 2020.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Vancouver:

Umar MAJ. Pharmacotherapy of Duchenne Muscular Dystrophy . [Internet] [Thesis]. University of Debrecen; [cited 2020 Jan 24]. Available from: http://hdl.handle.net/2437/257231.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

Council of Science Editors:

Umar MAJ. Pharmacotherapy of Duchenne Muscular Dystrophy . [Thesis]. University of Debrecen; Available from: http://hdl.handle.net/2437/257231

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.


Columbia University

18. Garcia, Enrique Jose. ER stress and lipid droplet-dependent proteostasis in response to lipid stress in yeast and a novel congenital muscular dystrophy.

Degree: 2019, Columbia University

 Phospholipids are the major components of cell membranes and have a wide variety of structures, shapes and properties. Different ratios of phospholipid species confer different… (more)

Subjects/Keywords: Molecular biology; Cytology; Lecithin; Muscular dystrophy; Lipids

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Garcia, E. J. (2019). ER stress and lipid droplet-dependent proteostasis in response to lipid stress in yeast and a novel congenital muscular dystrophy. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/d8-a0av-xs61

Chicago Manual of Style (16th Edition):

Garcia, Enrique Jose. “ER stress and lipid droplet-dependent proteostasis in response to lipid stress in yeast and a novel congenital muscular dystrophy.” 2019. Doctoral Dissertation, Columbia University. Accessed January 24, 2020. https://doi.org/10.7916/d8-a0av-xs61.

MLA Handbook (7th Edition):

Garcia, Enrique Jose. “ER stress and lipid droplet-dependent proteostasis in response to lipid stress in yeast and a novel congenital muscular dystrophy.” 2019. Web. 24 Jan 2020.

Vancouver:

Garcia EJ. ER stress and lipid droplet-dependent proteostasis in response to lipid stress in yeast and a novel congenital muscular dystrophy. [Internet] [Doctoral dissertation]. Columbia University; 2019. [cited 2020 Jan 24]. Available from: https://doi.org/10.7916/d8-a0av-xs61.

Council of Science Editors:

Garcia EJ. ER stress and lipid droplet-dependent proteostasis in response to lipid stress in yeast and a novel congenital muscular dystrophy. [Doctoral Dissertation]. Columbia University; 2019. Available from: https://doi.org/10.7916/d8-a0av-xs61


University of Ottawa

19. Al-Rewashdy, Hasanen. Determining the Contribution of Utrophin A Versus Other Components of the Slow, Oxidative Phenotype in the Beneficial Adaptations of Dystrophic Muscle Fibers Following AMPK Activation .

Degree: 2014, University of Ottawa

 Duchenne Muscular Dystrophy (DMD) results from the absence of a functional dystrophin protein. Among its possible therapeutic options is the upregulation of dystrophin’s autosomal analogue,… (more)

Subjects/Keywords: Utrophin; Duchenne Muscular Dystrophy; Dystrophin; AMPK; AICAR

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Al-Rewashdy, H. (2014). Determining the Contribution of Utrophin A Versus Other Components of the Slow, Oxidative Phenotype in the Beneficial Adaptations of Dystrophic Muscle Fibers Following AMPK Activation . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/31470

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):

Al-Rewashdy, Hasanen. “Determining the Contribution of Utrophin A Versus Other Components of the Slow, Oxidative Phenotype in the Beneficial Adaptations of Dystrophic Muscle Fibers Following AMPK Activation .” 2014. Thesis, University of Ottawa. Accessed January 24, 2020. http://hdl.handle.net/10393/31470.

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

MLA Handbook (7th Edition):

Al-Rewashdy, Hasanen. “Determining the Contribution of Utrophin A Versus Other Components of the Slow, Oxidative Phenotype in the Beneficial Adaptations of Dystrophic Muscle Fibers Following AMPK Activation .” 2014. Web. 24 Jan 2020.

Vancouver:

Al-Rewashdy H. Determining the Contribution of Utrophin A Versus Other Components of the Slow, Oxidative Phenotype in the Beneficial Adaptations of Dystrophic Muscle Fibers Following AMPK Activation . [Internet] [Thesis]. University of Ottawa; 2014. [cited 2020 Jan 24]. Available from: http://hdl.handle.net/10393/31470.

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

Council of Science Editors:

Al-Rewashdy H. Determining the Contribution of Utrophin A Versus Other Components of the Slow, Oxidative Phenotype in the Beneficial Adaptations of Dystrophic Muscle Fibers Following AMPK Activation . [Thesis]. University of Ottawa; 2014. Available from: http://hdl.handle.net/10393/31470

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


Brandeis University

20. Konakondla, Jacob Vinay Vikas. Molecular Interaction of circMbl and MBL in vivo.

Degree: 2019, Brandeis University

 CircRNAs are an evolutionarily conserved class of RNAs produced by a process named back-splicing to form covalently closed loop structures lacking 3’ & 5’ ends.… (more)

Subjects/Keywords: circRNAs; circMbl; mbl; muscleblind; Muscular Dystrophy

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Konakondla, J. V. V. (2019). Molecular Interaction of circMbl and MBL in vivo. (Thesis). Brandeis University. Retrieved from http://hdl.handle.net/10192/36532

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):

Konakondla, Jacob Vinay Vikas. “Molecular Interaction of circMbl and MBL in vivo.” 2019. Thesis, Brandeis University. Accessed January 24, 2020. http://hdl.handle.net/10192/36532.

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

MLA Handbook (7th Edition):

Konakondla, Jacob Vinay Vikas. “Molecular Interaction of circMbl and MBL in vivo.” 2019. Web. 24 Jan 2020.

Vancouver:

Konakondla JVV. Molecular Interaction of circMbl and MBL in vivo. [Internet] [Thesis]. Brandeis University; 2019. [cited 2020 Jan 24]. Available from: http://hdl.handle.net/10192/36532.

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

Council of Science Editors:

Konakondla JVV. Molecular Interaction of circMbl and MBL in vivo. [Thesis]. Brandeis University; 2019. Available from: http://hdl.handle.net/10192/36532

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

21. Guiraud, Simon. Evaluation de régulateurs positifs de la croissance musculaire chez un modèle dystrophique murin : Evaluation of positive regulators of muscle growth in a murine dystrophic model.

Degree: Docteur es, Biologie cellulaire et moléculaire, 2011, Evry-Val d'Essonne

En 1997, le caractère culard, un phénotype hypermusclé chez le bovin, est attribué à des mutations dans le gène de la myostatine (MSTN). Depuis, il… (more)

Subjects/Keywords: Myostatine; Décorine; Myostatin; Skeletal muscle; Muscular dystrophy

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Guiraud, S. (2011). Evaluation de régulateurs positifs de la croissance musculaire chez un modèle dystrophique murin : Evaluation of positive regulators of muscle growth in a murine dystrophic model. (Doctoral Dissertation). Evry-Val d'Essonne. Retrieved from http://www.theses.fr/2011EVRY0014

Chicago Manual of Style (16th Edition):

Guiraud, Simon. “Evaluation de régulateurs positifs de la croissance musculaire chez un modèle dystrophique murin : Evaluation of positive regulators of muscle growth in a murine dystrophic model.” 2011. Doctoral Dissertation, Evry-Val d'Essonne. Accessed January 24, 2020. http://www.theses.fr/2011EVRY0014.

MLA Handbook (7th Edition):

Guiraud, Simon. “Evaluation de régulateurs positifs de la croissance musculaire chez un modèle dystrophique murin : Evaluation of positive regulators of muscle growth in a murine dystrophic model.” 2011. Web. 24 Jan 2020.

Vancouver:

Guiraud S. Evaluation de régulateurs positifs de la croissance musculaire chez un modèle dystrophique murin : Evaluation of positive regulators of muscle growth in a murine dystrophic model. [Internet] [Doctoral dissertation]. Evry-Val d'Essonne; 2011. [cited 2020 Jan 24]. Available from: http://www.theses.fr/2011EVRY0014.

Council of Science Editors:

Guiraud S. Evaluation de régulateurs positifs de la croissance musculaire chez un modèle dystrophique murin : Evaluation of positive regulators of muscle growth in a murine dystrophic model. [Doctoral Dissertation]. Evry-Val d'Essonne; 2011. Available from: http://www.theses.fr/2011EVRY0014


University of Arizona

22. Babaria, Arati. Molecular Mechanisms that Underlie Duchenne Muscular Dystrophy .

Degree: 2016, University of Arizona

 Duchenne muscular dystrophy is an inherited, X-linked recessive skeletal muscle disorder that is characterized by mutations in the dystrophin gene [1]. Therefore, the disease affects… (more)

Subjects/Keywords: Muscular Dystrophy; Cellular and Molecular Medicine; Duchenne

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Babaria, A. (2016). Molecular Mechanisms that Underlie Duchenne Muscular Dystrophy . (Masters Thesis). University of Arizona. Retrieved from http://hdl.handle.net/10150/612573

Chicago Manual of Style (16th Edition):

Babaria, Arati. “Molecular Mechanisms that Underlie Duchenne Muscular Dystrophy .” 2016. Masters Thesis, University of Arizona. Accessed January 24, 2020. http://hdl.handle.net/10150/612573.

MLA Handbook (7th Edition):

Babaria, Arati. “Molecular Mechanisms that Underlie Duchenne Muscular Dystrophy .” 2016. Web. 24 Jan 2020.

Vancouver:

Babaria A. Molecular Mechanisms that Underlie Duchenne Muscular Dystrophy . [Internet] [Masters thesis]. University of Arizona; 2016. [cited 2020 Jan 24]. Available from: http://hdl.handle.net/10150/612573.

Council of Science Editors:

Babaria A. Molecular Mechanisms that Underlie Duchenne Muscular Dystrophy . [Masters Thesis]. University of Arizona; 2016. Available from: http://hdl.handle.net/10150/612573


University of Sydney

23. Ban, Joanne. Novel Effects of the MuSK System in Muscles of Wild-Type and mdx Mice .

Degree: 2018, University of Sydney

 The agrin/Muscle specific kinase (MuSK)/Rapsyn is the most established signalling pathway promoting the development of the neuromuscular junction. Duchenne muscular dystrophy (DMD) is an X-linked… (more)

Subjects/Keywords: Duchenne muscular dystrophy; mdx; NMJ; Neuromuscular transmission

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Ban, J. (2018). Novel Effects of the MuSK System in Muscles of Wild-Type and mdx Mice . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/18704

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):

Ban, Joanne. “Novel Effects of the MuSK System in Muscles of Wild-Type and mdx Mice .” 2018. Thesis, University of Sydney. Accessed January 24, 2020. http://hdl.handle.net/2123/18704.

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

MLA Handbook (7th Edition):

Ban, Joanne. “Novel Effects of the MuSK System in Muscles of Wild-Type and mdx Mice .” 2018. Web. 24 Jan 2020.

Vancouver:

Ban J. Novel Effects of the MuSK System in Muscles of Wild-Type and mdx Mice . [Internet] [Thesis]. University of Sydney; 2018. [cited 2020 Jan 24]. Available from: http://hdl.handle.net/2123/18704.

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

Council of Science Editors:

Ban J. Novel Effects of the MuSK System in Muscles of Wild-Type and mdx Mice . [Thesis]. University of Sydney; 2018. Available from: http://hdl.handle.net/2123/18704

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


University of Sydney

24. Woolger, Natalie Marian. The cellular and molecular characterisation of the Muscular Dystrophy protein dysferlin .

Degree: 2018, University of Sydney

 Mutations in the dysferlin gene cause a group of inherited muscular dystrophies, collectively known as dysferlinopathies. Dysferlinopathies are disabling muscle diseases caused by the absence… (more)

Subjects/Keywords: Dysperlin; protien; muscular dystrophy; membrane repair

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Woolger, N. M. (2018). The cellular and molecular characterisation of the Muscular Dystrophy protein dysferlin . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/18656

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):

Woolger, Natalie Marian. “The cellular and molecular characterisation of the Muscular Dystrophy protein dysferlin .” 2018. Thesis, University of Sydney. Accessed January 24, 2020. http://hdl.handle.net/2123/18656.

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

MLA Handbook (7th Edition):

Woolger, Natalie Marian. “The cellular and molecular characterisation of the Muscular Dystrophy protein dysferlin .” 2018. Web. 24 Jan 2020.

Vancouver:

Woolger NM. The cellular and molecular characterisation of the Muscular Dystrophy protein dysferlin . [Internet] [Thesis]. University of Sydney; 2018. [cited 2020 Jan 24]. Available from: http://hdl.handle.net/2123/18656.

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

Council of Science Editors:

Woolger NM. The cellular and molecular characterisation of the Muscular Dystrophy protein dysferlin . [Thesis]. University of Sydney; 2018. Available from: http://hdl.handle.net/2123/18656

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


University College Cork

25. Manning, Jennifer. Immune and stress factors in the pathophysiology of the mdx mouse model of Duchenne Muscular Dystrophy.

Degree: 2014, University College Cork

 Duchenne Muscular Dystrophy (DMD) is a fatal multi-system neuromuscular disease caused by loss of dystrophin. The loss of dystrophin from membranes of contractile muscle cells… (more)

Subjects/Keywords: Muscle; Muscular Dystrophy; Stress; Inflammation; Interleukin - 6

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Manning, J. (2014). Immune and stress factors in the pathophysiology of the mdx mouse model of Duchenne Muscular Dystrophy. (Thesis). University College Cork. Retrieved from http://hdl.handle.net/10468/1902

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):

Manning, Jennifer. “Immune and stress factors in the pathophysiology of the mdx mouse model of Duchenne Muscular Dystrophy.” 2014. Thesis, University College Cork. Accessed January 24, 2020. http://hdl.handle.net/10468/1902.

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

MLA Handbook (7th Edition):

Manning, Jennifer. “Immune and stress factors in the pathophysiology of the mdx mouse model of Duchenne Muscular Dystrophy.” 2014. Web. 24 Jan 2020.

Vancouver:

Manning J. Immune and stress factors in the pathophysiology of the mdx mouse model of Duchenne Muscular Dystrophy. [Internet] [Thesis]. University College Cork; 2014. [cited 2020 Jan 24]. Available from: http://hdl.handle.net/10468/1902.

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

Council of Science Editors:

Manning J. Immune and stress factors in the pathophysiology of the mdx mouse model of Duchenne Muscular Dystrophy. [Thesis]. University College Cork; 2014. Available from: http://hdl.handle.net/10468/1902

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


University of Cincinnati

26. Gladstone, Amy R. Assessing the Genetic Counseling Needs of Parents who have Adopted a Child with Duchenne or Becker Muscular Dystrophy.

Degree: MS, Medicine: Genetic Counseling, 2013, University of Cincinnati

 Introduction: Duchenne / Becker muscular dystrophy (DBMD) is an x-linked condition with a wide variation of clinical presentation due to specific gene mutations and the… (more)

Subjects/Keywords: Surgery; Adoption; Genetic Counseling; Duchenne Muscular Dystrophy; Becker Muscular Dystrophy; Qualitative Research; Special-Needs Adoption

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Gladstone, A. R. (2013). Assessing the Genetic Counseling Needs of Parents who have Adopted a Child with Duchenne or Becker Muscular Dystrophy. (Masters Thesis). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1367924226

Chicago Manual of Style (16th Edition):

Gladstone, Amy R. “Assessing the Genetic Counseling Needs of Parents who have Adopted a Child with Duchenne or Becker Muscular Dystrophy.” 2013. Masters Thesis, University of Cincinnati. Accessed January 24, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1367924226.

MLA Handbook (7th Edition):

Gladstone, Amy R. “Assessing the Genetic Counseling Needs of Parents who have Adopted a Child with Duchenne or Becker Muscular Dystrophy.” 2013. Web. 24 Jan 2020.

Vancouver:

Gladstone AR. Assessing the Genetic Counseling Needs of Parents who have Adopted a Child with Duchenne or Becker Muscular Dystrophy. [Internet] [Masters thesis]. University of Cincinnati; 2013. [cited 2020 Jan 24]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1367924226.

Council of Science Editors:

Gladstone AR. Assessing the Genetic Counseling Needs of Parents who have Adopted a Child with Duchenne or Becker Muscular Dystrophy. [Masters Thesis]. University of Cincinnati; 2013. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1367924226


Universiteit Utrecht

27. Bartels, B. Cardiopulmonary exercise testing in ambulatory children with Duchenne and Becker Muscular Dystrophy: a pilot study.

Degree: 2012, Universiteit Utrecht

 Introduction The cardiopulmonary exercise test (CPET) is the gold-standard for exercise capacity and could be of additional value to the physical evaluation of children with… (more)

Subjects/Keywords: Duchenne muscular dystrophy; Becker muscular dystrophy; cardiopulmonary exercise test; feasibility; outcome parameter

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Bartels, B. (2012). Cardiopulmonary exercise testing in ambulatory children with Duchenne and Becker Muscular Dystrophy: a pilot study. (Masters Thesis). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/253738

Chicago Manual of Style (16th Edition):

Bartels, B. “Cardiopulmonary exercise testing in ambulatory children with Duchenne and Becker Muscular Dystrophy: a pilot study.” 2012. Masters Thesis, Universiteit Utrecht. Accessed January 24, 2020. http://dspace.library.uu.nl:8080/handle/1874/253738.

MLA Handbook (7th Edition):

Bartels, B. “Cardiopulmonary exercise testing in ambulatory children with Duchenne and Becker Muscular Dystrophy: a pilot study.” 2012. Web. 24 Jan 2020.

Vancouver:

Bartels B. Cardiopulmonary exercise testing in ambulatory children with Duchenne and Becker Muscular Dystrophy: a pilot study. [Internet] [Masters thesis]. Universiteit Utrecht; 2012. [cited 2020 Jan 24]. Available from: http://dspace.library.uu.nl:8080/handle/1874/253738.

Council of Science Editors:

Bartels B. Cardiopulmonary exercise testing in ambulatory children with Duchenne and Becker Muscular Dystrophy: a pilot study. [Masters Thesis]. Universiteit Utrecht; 2012. Available from: http://dspace.library.uu.nl:8080/handle/1874/253738

28. Hollinger, Katrin. Evaluating the PGC-1 alpha pathway and a new preclinical model to advance treatment options for dystrophinopathies.

Degree: 2014, Iowa State University

 Duchenne muscular dystrophy (DMD) is caused by a mutation in the dystrophin gene leading to the production of a nonfunctional protein and a dystrophin deficiency.… (more)

Subjects/Keywords: Becker muscular dystrophy; BMD; DMD; Duchenne muscular dystrophy; mdx; utrophin; Genetics; Physiology

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Hollinger, K. (2014). Evaluating the PGC-1 alpha pathway and a new preclinical model to advance treatment options for dystrophinopathies. (Thesis). Iowa State University. Retrieved from https://lib.dr.iastate.edu/etd/13794

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):

Hollinger, Katrin. “Evaluating the PGC-1 alpha pathway and a new preclinical model to advance treatment options for dystrophinopathies.” 2014. Thesis, Iowa State University. Accessed January 24, 2020. https://lib.dr.iastate.edu/etd/13794.

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

MLA Handbook (7th Edition):

Hollinger, Katrin. “Evaluating the PGC-1 alpha pathway and a new preclinical model to advance treatment options for dystrophinopathies.” 2014. Web. 24 Jan 2020.

Vancouver:

Hollinger K. Evaluating the PGC-1 alpha pathway and a new preclinical model to advance treatment options for dystrophinopathies. [Internet] [Thesis]. Iowa State University; 2014. [cited 2020 Jan 24]. Available from: https://lib.dr.iastate.edu/etd/13794.

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

Council of Science Editors:

Hollinger K. Evaluating the PGC-1 alpha pathway and a new preclinical model to advance treatment options for dystrophinopathies. [Thesis]. Iowa State University; 2014. Available from: https://lib.dr.iastate.edu/etd/13794

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


University of Rochester

29. Carrell, Samuel T. Testing the Limits of Antisense Oligonucleotide Treatment for Myotonic Dystrophy Type 1.

Degree: PhD, 2016, University of Rochester

 Myotonic dystrophy type 1 (DM1) is a dominantly-inherited muscular dystrophy that leads to progressive disease of skeletal muscle, the cardiac conduction system (CCS), and the… (more)

Subjects/Keywords: Muscular dystrophy; Antisense oligonucleotide; Myotonic dystrophy; Experimental therapeutic

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Carrell, S. T. (2016). Testing the Limits of Antisense Oligonucleotide Treatment for Myotonic Dystrophy Type 1. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/31618

Chicago Manual of Style (16th Edition):

Carrell, Samuel T. “Testing the Limits of Antisense Oligonucleotide Treatment for Myotonic Dystrophy Type 1.” 2016. Doctoral Dissertation, University of Rochester. Accessed January 24, 2020. http://hdl.handle.net/1802/31618.

MLA Handbook (7th Edition):

Carrell, Samuel T. “Testing the Limits of Antisense Oligonucleotide Treatment for Myotonic Dystrophy Type 1.” 2016. Web. 24 Jan 2020.

Vancouver:

Carrell ST. Testing the Limits of Antisense Oligonucleotide Treatment for Myotonic Dystrophy Type 1. [Internet] [Doctoral dissertation]. University of Rochester; 2016. [cited 2020 Jan 24]. Available from: http://hdl.handle.net/1802/31618.

Council of Science Editors:

Carrell ST. Testing the Limits of Antisense Oligonucleotide Treatment for Myotonic Dystrophy Type 1. [Doctoral Dissertation]. University of Rochester; 2016. Available from: http://hdl.handle.net/1802/31618

30. Sugie, Miho; Sugie, Kazuma; Eura, Nobuyuki; Iwasa, Naoki; Shiota, Tomo; Nanaura, Hitoki; Izumi, Tesseki. Characteristics of Risk-Factor Profiles Associated with Stroke in Patients with Myotonic Dystrophy Type 1. : 筋強直性ジストロフィー1型における脳卒中に関する危険因子の臨床的特徴.

Degree: 博士(医学), 2017, Nara Medical University / 奈良県立医科大学

Objective: Myotonic dystrophy type 1 (DM1) is a rare autosomal dominant disorder with highly variable phenotypic expression. Some patients have diabetes mellitus, dyslipidemia, and/or arrhythmias,… (more)

Subjects/Keywords: Myotonic dystrophy; Muscular dystrophy; Myopathy; Stroke; Arrhythmias; Atrial fibrillation; Dyslipidemia

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Sugie, Miho; Sugie, Kazuma; Eura, Nobuyuki; Iwasa, Naoki; Shiota, Tomo; Nanaura, Hitoki; Izumi, T. (2017). Characteristics of Risk-Factor Profiles Associated with Stroke in Patients with Myotonic Dystrophy Type 1. : 筋強直性ジストロフィー1型における脳卒中に関する危険因子の臨床的特徴. (Thesis). Nara Medical University / 奈良県立医科大学. Retrieved from http://hdl.handle.net/10564/3325

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):

Sugie, Miho; Sugie, Kazuma; Eura, Nobuyuki; Iwasa, Naoki; Shiota, Tomo; Nanaura, Hitoki; Izumi, Tesseki. “Characteristics of Risk-Factor Profiles Associated with Stroke in Patients with Myotonic Dystrophy Type 1. : 筋強直性ジストロフィー1型における脳卒中に関する危険因子の臨床的特徴.” 2017. Thesis, Nara Medical University / 奈良県立医科大学. Accessed January 24, 2020. http://hdl.handle.net/10564/3325.

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

MLA Handbook (7th Edition):

Sugie, Miho; Sugie, Kazuma; Eura, Nobuyuki; Iwasa, Naoki; Shiota, Tomo; Nanaura, Hitoki; Izumi, Tesseki. “Characteristics of Risk-Factor Profiles Associated with Stroke in Patients with Myotonic Dystrophy Type 1. : 筋強直性ジストロフィー1型における脳卒中に関する危険因子の臨床的特徴.” 2017. Web. 24 Jan 2020.

Vancouver:

Sugie, Miho; Sugie, Kazuma; Eura, Nobuyuki; Iwasa, Naoki; Shiota, Tomo; Nanaura, Hitoki; Izumi T. Characteristics of Risk-Factor Profiles Associated with Stroke in Patients with Myotonic Dystrophy Type 1. : 筋強直性ジストロフィー1型における脳卒中に関する危険因子の臨床的特徴. [Internet] [Thesis]. Nara Medical University / 奈良県立医科大学; 2017. [cited 2020 Jan 24]. Available from: http://hdl.handle.net/10564/3325.

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

Council of Science Editors:

Sugie, Miho; Sugie, Kazuma; Eura, Nobuyuki; Iwasa, Naoki; Shiota, Tomo; Nanaura, Hitoki; Izumi T. Characteristics of Risk-Factor Profiles Associated with Stroke in Patients with Myotonic Dystrophy Type 1. : 筋強直性ジストロフィー1型における脳卒中に関する危険因子の臨床的特徴. [Thesis]. Nara Medical University / 奈良県立医科大学; 2017. Available from: http://hdl.handle.net/10564/3325

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

[1] [2] [3] [4] [5] … [14]

.