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You searched for subject:(Myopathy). Showing records 1 – 30 of 143 total matches.

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Universiteit Utrecht

1. Webb, J.K. The incidence of post anaesthetic myopathy (PAM) in horses after general anaesthesia for MRI in comparison to the incidence of PAM in horses anaesthetised for other reasons.

Degree: 2013, Universiteit Utrecht

 In a retrospective study the anaesthetic records of 1270 horses were evaluated to determine the incidence of post anaesthetic myopathy (PAM). These horses were grouped… (more)

Subjects/Keywords: post anaesthetic myopathy; MRI; anaesthesia

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

APA (6th Edition):

Webb, J. K. (2013). The incidence of post anaesthetic myopathy (PAM) in horses after general anaesthesia for MRI in comparison to the incidence of PAM in horses anaesthetised for other reasons. (Masters Thesis). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/287271

Chicago Manual of Style (16th Edition):

Webb, J K. “The incidence of post anaesthetic myopathy (PAM) in horses after general anaesthesia for MRI in comparison to the incidence of PAM in horses anaesthetised for other reasons.” 2013. Masters Thesis, Universiteit Utrecht. Accessed April 06, 2020. http://dspace.library.uu.nl:8080/handle/1874/287271.

MLA Handbook (7th Edition):

Webb, J K. “The incidence of post anaesthetic myopathy (PAM) in horses after general anaesthesia for MRI in comparison to the incidence of PAM in horses anaesthetised for other reasons.” 2013. Web. 06 Apr 2020.

Vancouver:

Webb JK. The incidence of post anaesthetic myopathy (PAM) in horses after general anaesthesia for MRI in comparison to the incidence of PAM in horses anaesthetised for other reasons. [Internet] [Masters thesis]. Universiteit Utrecht; 2013. [cited 2020 Apr 06]. Available from: http://dspace.library.uu.nl:8080/handle/1874/287271.

Council of Science Editors:

Webb JK. The incidence of post anaesthetic myopathy (PAM) in horses after general anaesthesia for MRI in comparison to the incidence of PAM in horses anaesthetised for other reasons. [Masters Thesis]. Universiteit Utrecht; 2013. Available from: http://dspace.library.uu.nl:8080/handle/1874/287271


University of Sydney

2. Summers, Matthew Amiel. Molecular Analysis of Neurofibromin Deficient Muscle .

Degree: 2017, University of Sydney

 The genetic disease neurofibromatosis type 1 (NF1) is classically associated with central nervous system and tumour manifestations. However, recent clinical and basic studies have confirmed… (more)

Subjects/Keywords: NF1; Muscle Weakness; Myopathy; Diet

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APA (6th Edition):

Summers, M. A. (2017). Molecular Analysis of Neurofibromin Deficient Muscle . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/17288

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):

Summers, Matthew Amiel. “Molecular Analysis of Neurofibromin Deficient Muscle .” 2017. Thesis, University of Sydney. Accessed April 06, 2020. http://hdl.handle.net/2123/17288.

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

MLA Handbook (7th Edition):

Summers, Matthew Amiel. “Molecular Analysis of Neurofibromin Deficient Muscle .” 2017. Web. 06 Apr 2020.

Vancouver:

Summers MA. Molecular Analysis of Neurofibromin Deficient Muscle . [Internet] [Thesis]. University of Sydney; 2017. [cited 2020 Apr 06]. Available from: http://hdl.handle.net/2123/17288.

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

Council of Science Editors:

Summers MA. Molecular Analysis of Neurofibromin Deficient Muscle . [Thesis]. University of Sydney; 2017. Available from: http://hdl.handle.net/2123/17288

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


University of Minnesota

3. Teixeira, Raffaella. Molecular bases of equine polysaccharide storage myopathies.

Degree: PhD, Veterinary Medicine, 2015, University of Minnesota

 Polysaccharide Storage Myopathy (PSSM) is a form of glycogen storage disease in horses, characterized by abnormal polysaccharide inclusions in skeletal muscle. PSSM1 is caused by… (more)

Subjects/Keywords: equine; genetics; myopathy; polysaccharide; PSSM

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APA (6th Edition):

Teixeira, R. (2015). Molecular bases of equine polysaccharide storage myopathies. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/173808

Chicago Manual of Style (16th Edition):

Teixeira, Raffaella. “Molecular bases of equine polysaccharide storage myopathies.” 2015. Doctoral Dissertation, University of Minnesota. Accessed April 06, 2020. http://hdl.handle.net/11299/173808.

MLA Handbook (7th Edition):

Teixeira, Raffaella. “Molecular bases of equine polysaccharide storage myopathies.” 2015. Web. 06 Apr 2020.

Vancouver:

Teixeira R. Molecular bases of equine polysaccharide storage myopathies. [Internet] [Doctoral dissertation]. University of Minnesota; 2015. [cited 2020 Apr 06]. Available from: http://hdl.handle.net/11299/173808.

Council of Science Editors:

Teixeira R. Molecular bases of equine polysaccharide storage myopathies. [Doctoral Dissertation]. University of Minnesota; 2015. Available from: http://hdl.handle.net/11299/173808


University of Sydney

4. Sandaradura, Sarah. Application of massively parallel sequencing approaches in Nemaline Myopathy .

Degree: 2018, University of Sydney

 Nemaline myopathy (NM) is one of the most common forms of congenital myopathy. The traditional approach to diagnosis involved skeletal muscle biopsy followed by Sanger… (more)

Subjects/Keywords: congenital myopathy; genetic; neuromuscular; nemaline myopathy; massively parallel sequencing

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APA (6th Edition):

Sandaradura, S. (2018). Application of massively parallel sequencing approaches in Nemaline Myopathy . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/18998

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):

Sandaradura, Sarah. “Application of massively parallel sequencing approaches in Nemaline Myopathy .” 2018. Thesis, University of Sydney. Accessed April 06, 2020. http://hdl.handle.net/2123/18998.

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

MLA Handbook (7th Edition):

Sandaradura, Sarah. “Application of massively parallel sequencing approaches in Nemaline Myopathy .” 2018. Web. 06 Apr 2020.

Vancouver:

Sandaradura S. Application of massively parallel sequencing approaches in Nemaline Myopathy . [Internet] [Thesis]. University of Sydney; 2018. [cited 2020 Apr 06]. Available from: http://hdl.handle.net/2123/18998.

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

Council of Science Editors:

Sandaradura S. Application of massively parallel sequencing approaches in Nemaline Myopathy . [Thesis]. University of Sydney; 2018. Available from: http://hdl.handle.net/2123/18998

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

5. Vivian de Assunção Nogueira. Intoxicações natural e experimental por salinomicina em coelhos no Estado do Rio de Janeiro.

Degree: 2008, Universidade Federal Rural do Rio de Janeiro

Relata-se, pela primeira vez, um surto de intoxicação por salinomicina em coelhos. De 2000 animais, no mínimo 27 morreram após troca do coccidiostático sulfaquinoxalina pela… (more)

Subjects/Keywords: salinomicina; miopatia; coelhos.; TOXICOLOGIA; salinomycin; myopathy; rabbits

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

APA (6th Edition):

Nogueira, V. d. A. (2008). Intoxicações natural e experimental por salinomicina em coelhos no Estado do Rio de Janeiro. (Thesis). Universidade Federal Rural do Rio de Janeiro. Retrieved from http://bdtd.ufrrj.br//tde_busca/arquivo.php?codArquivo=690

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):

Nogueira, Vivian de Assunção. “Intoxicações natural e experimental por salinomicina em coelhos no Estado do Rio de Janeiro.” 2008. Thesis, Universidade Federal Rural do Rio de Janeiro. Accessed April 06, 2020. http://bdtd.ufrrj.br//tde_busca/arquivo.php?codArquivo=690.

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

MLA Handbook (7th Edition):

Nogueira, Vivian de Assunção. “Intoxicações natural e experimental por salinomicina em coelhos no Estado do Rio de Janeiro.” 2008. Web. 06 Apr 2020.

Vancouver:

Nogueira VdA. Intoxicações natural e experimental por salinomicina em coelhos no Estado do Rio de Janeiro. [Internet] [Thesis]. Universidade Federal Rural do Rio de Janeiro; 2008. [cited 2020 Apr 06]. Available from: http://bdtd.ufrrj.br//tde_busca/arquivo.php?codArquivo=690.

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

Council of Science Editors:

Nogueira VdA. Intoxicações natural e experimental por salinomicina em coelhos no Estado do Rio de Janeiro. [Thesis]. Universidade Federal Rural do Rio de Janeiro; 2008. Available from: http://bdtd.ufrrj.br//tde_busca/arquivo.php?codArquivo=690

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


McMaster University

6. Li, Yujin. Investigating the Role of the NLRP3 Inflammasome in Statin-Induced Myopathy.

Degree: MSc, 2016, McMaster University

As a front-line treatment for cardiovascular disease, statins are among some of the most widely prescribed drugs worldwide. Statins are effective at lowering cholesterol, but… (more)

Subjects/Keywords: Inflammasome; Statins; Myopathy; Prenylation; Caspase-1; Atrogenes

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APA (6th Edition):

Li, Y. (2016). Investigating the Role of the NLRP3 Inflammasome in Statin-Induced Myopathy. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/20268

Chicago Manual of Style (16th Edition):

Li, Yujin. “Investigating the Role of the NLRP3 Inflammasome in Statin-Induced Myopathy.” 2016. Masters Thesis, McMaster University. Accessed April 06, 2020. http://hdl.handle.net/11375/20268.

MLA Handbook (7th Edition):

Li, Yujin. “Investigating the Role of the NLRP3 Inflammasome in Statin-Induced Myopathy.” 2016. Web. 06 Apr 2020.

Vancouver:

Li Y. Investigating the Role of the NLRP3 Inflammasome in Statin-Induced Myopathy. [Internet] [Masters thesis]. McMaster University; 2016. [cited 2020 Apr 06]. Available from: http://hdl.handle.net/11375/20268.

Council of Science Editors:

Li Y. Investigating the Role of the NLRP3 Inflammasome in Statin-Induced Myopathy. [Masters Thesis]. McMaster University; 2016. Available from: http://hdl.handle.net/11375/20268


University of Oxford

7. Bareja, Akshay. Utrophin upregulation and microRNAs : two avenues of Duchenne muscular dystrophy therapy research.

Degree: PhD, 2011, University of Oxford

 Characterized by the severe progressive wastage of skeletal muscle, Duchenne muscular dystrophy (DMD) is a crippling X-linked recessive disease that is caused by the absence… (more)

Subjects/Keywords: 616.042; Biology; microRNA; miRNA; utrophin; Duchenne; myopathy

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APA (6th Edition):

Bareja, A. (2011). Utrophin upregulation and microRNAs : two avenues of Duchenne muscular dystrophy therapy research. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:6a5145e9-7abf-4f86-bb8e-a3284125d99a ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.543561

Chicago Manual of Style (16th Edition):

Bareja, Akshay. “Utrophin upregulation and microRNAs : two avenues of Duchenne muscular dystrophy therapy research.” 2011. Doctoral Dissertation, University of Oxford. Accessed April 06, 2020. http://ora.ox.ac.uk/objects/uuid:6a5145e9-7abf-4f86-bb8e-a3284125d99a ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.543561.

MLA Handbook (7th Edition):

Bareja, Akshay. “Utrophin upregulation and microRNAs : two avenues of Duchenne muscular dystrophy therapy research.” 2011. Web. 06 Apr 2020.

Vancouver:

Bareja A. Utrophin upregulation and microRNAs : two avenues of Duchenne muscular dystrophy therapy research. [Internet] [Doctoral dissertation]. University of Oxford; 2011. [cited 2020 Apr 06]. Available from: http://ora.ox.ac.uk/objects/uuid:6a5145e9-7abf-4f86-bb8e-a3284125d99a ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.543561.

Council of Science Editors:

Bareja A. Utrophin upregulation and microRNAs : two avenues of Duchenne muscular dystrophy therapy research. [Doctoral Dissertation]. University of Oxford; 2011. Available from: http://ora.ox.ac.uk/objects/uuid:6a5145e9-7abf-4f86-bb8e-a3284125d99a ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.543561


Indian Institute of Science

8. Salvi, Sheetal S. Unravelling The Mechanisms Of Myofibrillogenesis And Human Myopathies Using Drosophila Mutants.

Degree: 2011, Indian Institute of Science

 Myofibrillogenesis is a complex process, which involves assembly of hundreds of structural proteins in a highly ordered manner to form the contractile structural unit of… (more)

Subjects/Keywords: Myopathy; Myofibrillogenesis; Drosophila Melanogaster; Muscular Diseases; Muscle Diseases; Sacromeric Proteins; Actin Myopathy; Myosin Myopathy; Drosophila Melanogaster - Indirect Flight Muscle System; Myositis; Drosophila Mutants; Human Myopathies; Myopathies; Molecular Biology

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

APA (6th Edition):

Salvi, S. S. (2011). Unravelling The Mechanisms Of Myofibrillogenesis And Human Myopathies Using Drosophila Mutants. (Thesis). Indian Institute of Science. Retrieved from http://hdl.handle.net/2005/2128

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):

Salvi, Sheetal S. “Unravelling The Mechanisms Of Myofibrillogenesis And Human Myopathies Using Drosophila Mutants.” 2011. Thesis, Indian Institute of Science. Accessed April 06, 2020. http://hdl.handle.net/2005/2128.

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

MLA Handbook (7th Edition):

Salvi, Sheetal S. “Unravelling The Mechanisms Of Myofibrillogenesis And Human Myopathies Using Drosophila Mutants.” 2011. Web. 06 Apr 2020.

Vancouver:

Salvi SS. Unravelling The Mechanisms Of Myofibrillogenesis And Human Myopathies Using Drosophila Mutants. [Internet] [Thesis]. Indian Institute of Science; 2011. [cited 2020 Apr 06]. Available from: http://hdl.handle.net/2005/2128.

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

Council of Science Editors:

Salvi SS. Unravelling The Mechanisms Of Myofibrillogenesis And Human Myopathies Using Drosophila Mutants. [Thesis]. Indian Institute of Science; 2011. Available from: http://hdl.handle.net/2005/2128

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


Indian Institute of Science

9. Salvi, Sheetal S. Unravelling The Mechanisms Of Myofibrillogenesis And Human Myopathies Using Drosophila Mutants.

Degree: 2011, Indian Institute of Science

 Myofibrillogenesis is a complex process, which involves assembly of hundreds of structural proteins in a highly ordered manner to form the contractile structural unit of… (more)

Subjects/Keywords: Myopathy; Myofibrillogenesis; Drosophila Melanogaster; Muscular Diseases; Muscle Diseases; Sacromeric Proteins; Actin Myopathy; Myosin Myopathy; Drosophila Melanogaster - Indirect Flight Muscle System; Myositis; Drosophila Mutants; Human Myopathies; Myopathies; Molecular Biology

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APA (6th Edition):

Salvi, S. S. (2011). Unravelling The Mechanisms Of Myofibrillogenesis And Human Myopathies Using Drosophila Mutants. (Thesis). Indian Institute of Science. Retrieved from http://etd.iisc.ernet.in/handle/2005/2128 ; http://etd.ncsi.iisc.ernet.in/abstracts/2732/G25022-Abs.pdf

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

Chicago Manual of Style (16th Edition):

Salvi, Sheetal S. “Unravelling The Mechanisms Of Myofibrillogenesis And Human Myopathies Using Drosophila Mutants.” 2011. Thesis, Indian Institute of Science. Accessed April 06, 2020. http://etd.iisc.ernet.in/handle/2005/2128 ; http://etd.ncsi.iisc.ernet.in/abstracts/2732/G25022-Abs.pdf.

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

MLA Handbook (7th Edition):

Salvi, Sheetal S. “Unravelling The Mechanisms Of Myofibrillogenesis And Human Myopathies Using Drosophila Mutants.” 2011. Web. 06 Apr 2020.

Vancouver:

Salvi SS. Unravelling The Mechanisms Of Myofibrillogenesis And Human Myopathies Using Drosophila Mutants. [Internet] [Thesis]. Indian Institute of Science; 2011. [cited 2020 Apr 06]. Available from: http://etd.iisc.ernet.in/handle/2005/2128 ; http://etd.ncsi.iisc.ernet.in/abstracts/2732/G25022-Abs.pdf.

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

Council of Science Editors:

Salvi SS. Unravelling The Mechanisms Of Myofibrillogenesis And Human Myopathies Using Drosophila Mutants. [Thesis]. Indian Institute of Science; 2011. Available from: http://etd.iisc.ernet.in/handle/2005/2128 ; http://etd.ncsi.iisc.ernet.in/abstracts/2732/G25022-Abs.pdf

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


University of Western Australia

10. Rojana-udomsart, Arada. Clinical, immunological and immunogenetic studies on sporadic inclusion body myositis and other inflammatory myopathies.

Degree: PhD, 2013, University of Western Australia

[Truncated abstract] The pathogenesis of sporadic inclusion body myositis (sIBM), the most common myopathy in individuals over 50 years of age, is still poorly understood.… (more)

Subjects/Keywords: Sporadic inclusion body myositis; Inflammatory myopathies; Necrotising myopathy; HLA-DRB1; HLA-DRB3; Autoantibody in sIBM; Paraspinal myopathy; Sjogren's syndrome

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APA (6th Edition):

Rojana-udomsart, A. (2013). Clinical, immunological and immunogenetic studies on sporadic inclusion body myositis and other inflammatory myopathies. (Doctoral Dissertation). University of Western Australia. Retrieved from http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=40117&local_base=GEN01-INS01

Chicago Manual of Style (16th Edition):

Rojana-udomsart, Arada. “Clinical, immunological and immunogenetic studies on sporadic inclusion body myositis and other inflammatory myopathies.” 2013. Doctoral Dissertation, University of Western Australia. Accessed April 06, 2020. http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=40117&local_base=GEN01-INS01.

MLA Handbook (7th Edition):

Rojana-udomsart, Arada. “Clinical, immunological and immunogenetic studies on sporadic inclusion body myositis and other inflammatory myopathies.” 2013. Web. 06 Apr 2020.

Vancouver:

Rojana-udomsart A. Clinical, immunological and immunogenetic studies on sporadic inclusion body myositis and other inflammatory myopathies. [Internet] [Doctoral dissertation]. University of Western Australia; 2013. [cited 2020 Apr 06]. Available from: http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=40117&local_base=GEN01-INS01.

Council of Science Editors:

Rojana-udomsart A. Clinical, immunological and immunogenetic studies on sporadic inclusion body myositis and other inflammatory myopathies. [Doctoral Dissertation]. University of Western Australia; 2013. Available from: http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=40117&local_base=GEN01-INS01


University of Gothenburg / Göteborgs Universitet

11. Dahl Halvarsson, Martin. Study the role of patient-specific mutations by genetic disease modeling.

Degree: 2019, University of Gothenburg / Göteborgs Universitet

 Many genetic diseases inherited in a dominant fashion have a complex pathological pattern. TOR1A mediated Dystonia-1 (DYT1) is an example of incomplete penetrance, affecting only… (more)

Subjects/Keywords: Muscles; Myosin; MYH7; Myosin storage myopathy; Laing early-onset myopathy; Drosophila; TOR1A; DYT1; HCM; heart disease

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APA (6th Edition):

Dahl Halvarsson, M. (2019). Study the role of patient-specific mutations by genetic disease modeling. (Thesis). University of Gothenburg / Göteborgs Universitet. Retrieved from http://hdl.handle.net/2077/58487

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):

Dahl Halvarsson, Martin. “Study the role of patient-specific mutations by genetic disease modeling.” 2019. Thesis, University of Gothenburg / Göteborgs Universitet. Accessed April 06, 2020. http://hdl.handle.net/2077/58487.

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

MLA Handbook (7th Edition):

Dahl Halvarsson, Martin. “Study the role of patient-specific mutations by genetic disease modeling.” 2019. Web. 06 Apr 2020.

Vancouver:

Dahl Halvarsson M. Study the role of patient-specific mutations by genetic disease modeling. [Internet] [Thesis]. University of Gothenburg / Göteborgs Universitet; 2019. [cited 2020 Apr 06]. Available from: http://hdl.handle.net/2077/58487.

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

Council of Science Editors:

Dahl Halvarsson M. Study the role of patient-specific mutations by genetic disease modeling. [Thesis]. University of Gothenburg / Göteborgs Universitet; 2019. Available from: http://hdl.handle.net/2077/58487

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


University of Rochester

12. Loy, Ryan Eric. Altered Type 1 Ryanodine Receptor Activity and Functional Rescue In a Mouse Model of Central Core Disease.

Degree: PhD, 2011, University of Rochester

 The type 1 isoform of the ryanodine receptor (RyR1) controls the release of Ca2+ from the sarcoplasmic reticulum (SR) during skeletal muscle excitation-contraction (EC) coupling.… (more)

Subjects/Keywords: Ryanodine Receptor; Myopathy; Central Core Disease; Malignant Hyperthermia; Ca2+

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APA (6th Edition):

Loy, R. E. (2011). Altered Type 1 Ryanodine Receptor Activity and Functional Rescue In a Mouse Model of Central Core Disease. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/13950

Chicago Manual of Style (16th Edition):

Loy, Ryan Eric. “Altered Type 1 Ryanodine Receptor Activity and Functional Rescue In a Mouse Model of Central Core Disease.” 2011. Doctoral Dissertation, University of Rochester. Accessed April 06, 2020. http://hdl.handle.net/1802/13950.

MLA Handbook (7th Edition):

Loy, Ryan Eric. “Altered Type 1 Ryanodine Receptor Activity and Functional Rescue In a Mouse Model of Central Core Disease.” 2011. Web. 06 Apr 2020.

Vancouver:

Loy RE. Altered Type 1 Ryanodine Receptor Activity and Functional Rescue In a Mouse Model of Central Core Disease. [Internet] [Doctoral dissertation]. University of Rochester; 2011. [cited 2020 Apr 06]. Available from: http://hdl.handle.net/1802/13950.

Council of Science Editors:

Loy RE. Altered Type 1 Ryanodine Receptor Activity and Functional Rescue In a Mouse Model of Central Core Disease. [Doctoral Dissertation]. University of Rochester; 2011. Available from: http://hdl.handle.net/1802/13950


Université de Montréal

13. Zetler, Rosa Zea. Genetic association study of plasma creatine kinase levels in the Montreal Heart Institute Hospital Cohort .

Degree: 2015, Université de Montréal

 Il a déjà été démontré que les statines (ou inhibiteurs de la HMG-CoA réductase) sont efficaces pour réduire le LDL-cholestérol et elles se sont depuis… (more)

Subjects/Keywords: statin; creatine kinase; myopathy; statine; créatine kinase; myopathie

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APA (6th Edition):

Zetler, R. Z. (2015). Genetic association study of plasma creatine kinase levels in the Montreal Heart Institute Hospital Cohort . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/11554

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):

Zetler, Rosa Zea. “Genetic association study of plasma creatine kinase levels in the Montreal Heart Institute Hospital Cohort .” 2015. Thesis, Université de Montréal. Accessed April 06, 2020. http://hdl.handle.net/1866/11554.

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

MLA Handbook (7th Edition):

Zetler, Rosa Zea. “Genetic association study of plasma creatine kinase levels in the Montreal Heart Institute Hospital Cohort .” 2015. Web. 06 Apr 2020.

Vancouver:

Zetler RZ. Genetic association study of plasma creatine kinase levels in the Montreal Heart Institute Hospital Cohort . [Internet] [Thesis]. Université de Montréal; 2015. [cited 2020 Apr 06]. Available from: http://hdl.handle.net/1866/11554.

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

Council of Science Editors:

Zetler RZ. Genetic association study of plasma creatine kinase levels in the Montreal Heart Institute Hospital Cohort . [Thesis]. Université de Montréal; 2015. Available from: http://hdl.handle.net/1866/11554

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

14. 森本, 陽介. Heat treatment inhibits skeletal muscle atrophy of glucocorticoid-induced myopathy in rats : 温熱療法はステロイド筋症ラットの骨格筋萎縮を抑制する.

Degree: 博士(医学), 2015, Nagasaki University / 長崎大学

 The purpose of this study was to investigate the influence of heat treatment on glucocorticoid (GC)-induced myopathy. Eight-week-old Wistar rats were randomly assigned to the… (more)

Subjects/Keywords: GC-induced myopathy; heat treatment; muscle fiber; Hsp72; capillary

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APA (6th Edition):

森本, . (2015). Heat treatment inhibits skeletal muscle atrophy of glucocorticoid-induced myopathy in rats : 温熱療法はステロイド筋症ラットの骨格筋萎縮を抑制する. (Thesis). Nagasaki University / 長崎大学. Retrieved from http://hdl.handle.net/10069/36058

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):

森本, 陽介. “Heat treatment inhibits skeletal muscle atrophy of glucocorticoid-induced myopathy in rats : 温熱療法はステロイド筋症ラットの骨格筋萎縮を抑制する.” 2015. Thesis, Nagasaki University / 長崎大学. Accessed April 06, 2020. http://hdl.handle.net/10069/36058.

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

MLA Handbook (7th Edition):

森本, 陽介. “Heat treatment inhibits skeletal muscle atrophy of glucocorticoid-induced myopathy in rats : 温熱療法はステロイド筋症ラットの骨格筋萎縮を抑制する.” 2015. Web. 06 Apr 2020.

Vancouver:

森本 . Heat treatment inhibits skeletal muscle atrophy of glucocorticoid-induced myopathy in rats : 温熱療法はステロイド筋症ラットの骨格筋萎縮を抑制する. [Internet] [Thesis]. Nagasaki University / 長崎大学; 2015. [cited 2020 Apr 06]. Available from: http://hdl.handle.net/10069/36058.

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

Council of Science Editors:

森本 . Heat treatment inhibits skeletal muscle atrophy of glucocorticoid-induced myopathy in rats : 温熱療法はステロイド筋症ラットの骨格筋萎縮を抑制する. [Thesis]. Nagasaki University / 長崎大学; 2015. Available from: http://hdl.handle.net/10069/36058

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


Louisiana State University

15. Thompson, Jessica. Effects of clenbuterol on skeletal and cardiac muscle in horses.

Degree: MS, Veterinary Medicine, 2009, Louisiana State University

 Clenbuterol is a commonly prescribed β2-adrenergic agonist approved for veterinary use as a bronchodilator in horses with reactive and obstructive airway disease. Potential for abuse… (more)

Subjects/Keywords: cardiac troponin I; echocardiogram; apoptosis; beta-adrenergic agonist; myopathy; horse; clenbuterol

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APA (6th Edition):

Thompson, J. (2009). Effects of clenbuterol on skeletal and cardiac muscle in horses. (Masters Thesis). Louisiana State University. Retrieved from etd-07092009-163446 ; https://digitalcommons.lsu.edu/gradschool_theses/359

Chicago Manual of Style (16th Edition):

Thompson, Jessica. “Effects of clenbuterol on skeletal and cardiac muscle in horses.” 2009. Masters Thesis, Louisiana State University. Accessed April 06, 2020. etd-07092009-163446 ; https://digitalcommons.lsu.edu/gradschool_theses/359.

MLA Handbook (7th Edition):

Thompson, Jessica. “Effects of clenbuterol on skeletal and cardiac muscle in horses.” 2009. Web. 06 Apr 2020.

Vancouver:

Thompson J. Effects of clenbuterol on skeletal and cardiac muscle in horses. [Internet] [Masters thesis]. Louisiana State University; 2009. [cited 2020 Apr 06]. Available from: etd-07092009-163446 ; https://digitalcommons.lsu.edu/gradschool_theses/359.

Council of Science Editors:

Thompson J. Effects of clenbuterol on skeletal and cardiac muscle in horses. [Masters Thesis]. Louisiana State University; 2009. Available from: etd-07092009-163446 ; https://digitalcommons.lsu.edu/gradschool_theses/359


University of California – Irvine

16. Simon, Mariella T. Mitochondrial Metabolism and Morphology in Mitochondrial Disease States.

Degree: Biological Sciences, 2016, University of California – Irvine

 ABSTRACT OF THE DISSERTATIONMitochondrial Metabolism and Morphologyin Mitochondrial Disease StatesByMariella Theresa SimonDoctor of Philosophy in Biological SciencesUniversity of California, Irvine, 2016Professor Susanne Rafelski, ChairMitochondria are… (more)

Subjects/Keywords: Cellular biology; Genetics; Leigh Syndrome; LonP1; Mitochondrial Disease; Mitochondrial Myopathy; Nars2

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APA (6th Edition):

Simon, M. T. (2016). Mitochondrial Metabolism and Morphology in Mitochondrial Disease States. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/7ss5250z

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):

Simon, Mariella T. “Mitochondrial Metabolism and Morphology in Mitochondrial Disease States.” 2016. Thesis, University of California – Irvine. Accessed April 06, 2020. http://www.escholarship.org/uc/item/7ss5250z.

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

MLA Handbook (7th Edition):

Simon, Mariella T. “Mitochondrial Metabolism and Morphology in Mitochondrial Disease States.” 2016. Web. 06 Apr 2020.

Vancouver:

Simon MT. Mitochondrial Metabolism and Morphology in Mitochondrial Disease States. [Internet] [Thesis]. University of California – Irvine; 2016. [cited 2020 Apr 06]. Available from: http://www.escholarship.org/uc/item/7ss5250z.

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

Council of Science Editors:

Simon MT. Mitochondrial Metabolism and Morphology in Mitochondrial Disease States. [Thesis]. University of California – Irvine; 2016. Available from: http://www.escholarship.org/uc/item/7ss5250z

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

17. Dionnet, Eugénie. Exploration de l'hétérogénéité mutationnelle et de ses conséquences pathologiques dans les myopathies : analyses des mécanismes et développement d'outils thérapeutiques : Exploration of mutational heterogeneity and its pathological consequences in myopathies : analysis of mechanisms and therapeutic tools development.

Degree: Docteur es, Pathologie humaine. Génétique humaine, 2016, Aix Marseille Université

Aujourd’hui encore, le diagnostic des maladies génétiques et la compréhension des mécanismes pathologiques qui en découlent demeurent difficile. On dénombre à ce jour plus de… (more)

Subjects/Keywords: Myopathie; Calcium; Muscle squelettique; Arn; Myopathy; Calcium; Skeletal muscle; Rna

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APA (6th Edition):

Dionnet, E. (2016). Exploration de l'hétérogénéité mutationnelle et de ses conséquences pathologiques dans les myopathies : analyses des mécanismes et développement d'outils thérapeutiques : Exploration of mutational heterogeneity and its pathological consequences in myopathies : analysis of mechanisms and therapeutic tools development. (Doctoral Dissertation). Aix Marseille Université. Retrieved from http://www.theses.fr/2016AIXM5046

Chicago Manual of Style (16th Edition):

Dionnet, Eugénie. “Exploration de l'hétérogénéité mutationnelle et de ses conséquences pathologiques dans les myopathies : analyses des mécanismes et développement d'outils thérapeutiques : Exploration of mutational heterogeneity and its pathological consequences in myopathies : analysis of mechanisms and therapeutic tools development.” 2016. Doctoral Dissertation, Aix Marseille Université. Accessed April 06, 2020. http://www.theses.fr/2016AIXM5046.

MLA Handbook (7th Edition):

Dionnet, Eugénie. “Exploration de l'hétérogénéité mutationnelle et de ses conséquences pathologiques dans les myopathies : analyses des mécanismes et développement d'outils thérapeutiques : Exploration of mutational heterogeneity and its pathological consequences in myopathies : analysis of mechanisms and therapeutic tools development.” 2016. Web. 06 Apr 2020.

Vancouver:

Dionnet E. Exploration de l'hétérogénéité mutationnelle et de ses conséquences pathologiques dans les myopathies : analyses des mécanismes et développement d'outils thérapeutiques : Exploration of mutational heterogeneity and its pathological consequences in myopathies : analysis of mechanisms and therapeutic tools development. [Internet] [Doctoral dissertation]. Aix Marseille Université 2016. [cited 2020 Apr 06]. Available from: http://www.theses.fr/2016AIXM5046.

Council of Science Editors:

Dionnet E. Exploration de l'hétérogénéité mutationnelle et de ses conséquences pathologiques dans les myopathies : analyses des mécanismes et développement d'outils thérapeutiques : Exploration of mutational heterogeneity and its pathological consequences in myopathies : analysis of mechanisms and therapeutic tools development. [Doctoral Dissertation]. Aix Marseille Université 2016. Available from: http://www.theses.fr/2016AIXM5046

18. 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

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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 April 06, 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. 06 Apr 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 Apr 06]. 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


University of Arkansas

19. Solo, Jessica. Meat Quality and Sensory Analysis of Broiler Breast Fillets with Woody Breast Muscle Myopathy.

Degree: MS, 2016, University of Arkansas

  Recently, the poultry industry has encountered an emerging muscle myopathy known as woody breast (WB), which is characterized by hardness throughout the Pectoralis major… (more)

Subjects/Keywords: Biological sciences; Broiler; Myopathy; Sensory; Agricultural Education; Poultry or Avian Science

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APA (6th Edition):

Solo, J. (2016). Meat Quality and Sensory Analysis of Broiler Breast Fillets with Woody Breast Muscle Myopathy. (Masters Thesis). University of Arkansas. Retrieved from https://scholarworks.uark.edu/etd/1603

Chicago Manual of Style (16th Edition):

Solo, Jessica. “Meat Quality and Sensory Analysis of Broiler Breast Fillets with Woody Breast Muscle Myopathy.” 2016. Masters Thesis, University of Arkansas. Accessed April 06, 2020. https://scholarworks.uark.edu/etd/1603.

MLA Handbook (7th Edition):

Solo, Jessica. “Meat Quality and Sensory Analysis of Broiler Breast Fillets with Woody Breast Muscle Myopathy.” 2016. Web. 06 Apr 2020.

Vancouver:

Solo J. Meat Quality and Sensory Analysis of Broiler Breast Fillets with Woody Breast Muscle Myopathy. [Internet] [Masters thesis]. University of Arkansas; 2016. [cited 2020 Apr 06]. Available from: https://scholarworks.uark.edu/etd/1603.

Council of Science Editors:

Solo J. Meat Quality and Sensory Analysis of Broiler Breast Fillets with Woody Breast Muscle Myopathy. [Masters Thesis]. University of Arkansas; 2016. Available from: https://scholarworks.uark.edu/etd/1603


University of Waterloo

20. Chambers, Paige. The Effects of a Calcineurin Inhibitor on Muscle Fibre Type and the Pathology of Centronuclear Myopathy in PlnOE Mice.

Degree: 2017, University of Waterloo

 The sarco(endo)plasmic reticulum Ca2+ ATPase (SERCA) pump is responsible for pumping calcium from the cytosol back into the lumen of the sarcoplasmic reticulum post contraction.… (more)

Subjects/Keywords: Calcineurin; Calcium; Centronuclear Myopathy; Muscle Disease; SERCA; Phospholamban

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APA (6th Edition):

Chambers, P. (2017). The Effects of a Calcineurin Inhibitor on Muscle Fibre Type and the Pathology of Centronuclear Myopathy in PlnOE Mice. (Thesis). University of Waterloo. Retrieved from http://hdl.handle.net/10012/11281

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):

Chambers, Paige. “The Effects of a Calcineurin Inhibitor on Muscle Fibre Type and the Pathology of Centronuclear Myopathy in PlnOE Mice.” 2017. Thesis, University of Waterloo. Accessed April 06, 2020. http://hdl.handle.net/10012/11281.

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

MLA Handbook (7th Edition):

Chambers, Paige. “The Effects of a Calcineurin Inhibitor on Muscle Fibre Type and the Pathology of Centronuclear Myopathy in PlnOE Mice.” 2017. Web. 06 Apr 2020.

Vancouver:

Chambers P. The Effects of a Calcineurin Inhibitor on Muscle Fibre Type and the Pathology of Centronuclear Myopathy in PlnOE Mice. [Internet] [Thesis]. University of Waterloo; 2017. [cited 2020 Apr 06]. Available from: http://hdl.handle.net/10012/11281.

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

Council of Science Editors:

Chambers P. The Effects of a Calcineurin Inhibitor on Muscle Fibre Type and the Pathology of Centronuclear Myopathy in PlnOE Mice. [Thesis]. University of Waterloo; 2017. Available from: http://hdl.handle.net/10012/11281

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


University of Waterloo

21. Fajardo, Val Andrew. The Role of Phospholamban and Sarcolipin in Skeletal Muscle Disease.

Degree: 2016, University of Waterloo

 Sarcolipin (SLN) and phospholamban (PLN) are two small proteins that physically interact with and inhibit the sarco(endo)plasmic reticulum Ca2+-ATPase (SERCA) pump. Results from our laboratory… (more)

Subjects/Keywords: SERCA; muscle atrophy; muscle weakness; myopathy; dystrophy; calcineurin

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APA (6th Edition):

Fajardo, V. A. (2016). The Role of Phospholamban and Sarcolipin in Skeletal Muscle Disease. (Thesis). University of Waterloo. Retrieved from http://hdl.handle.net/10012/10162

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):

Fajardo, Val Andrew. “The Role of Phospholamban and Sarcolipin in Skeletal Muscle Disease.” 2016. Thesis, University of Waterloo. Accessed April 06, 2020. http://hdl.handle.net/10012/10162.

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

MLA Handbook (7th Edition):

Fajardo, Val Andrew. “The Role of Phospholamban and Sarcolipin in Skeletal Muscle Disease.” 2016. Web. 06 Apr 2020.

Vancouver:

Fajardo VA. The Role of Phospholamban and Sarcolipin in Skeletal Muscle Disease. [Internet] [Thesis]. University of Waterloo; 2016. [cited 2020 Apr 06]. Available from: http://hdl.handle.net/10012/10162.

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

Council of Science Editors:

Fajardo VA. The Role of Phospholamban and Sarcolipin in Skeletal Muscle Disease. [Thesis]. University of Waterloo; 2016. Available from: http://hdl.handle.net/10012/10162

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


University of Toronto

22. Maani, Nika. Tamoxifen Therapy in a Murine Model of Myotubular Myopathy.

Degree: 2018, University of Toronto

X-linked myotubular myopathy (XLMTM), also known as myotubular myopathy (MTM), is a fatal pediatric congenital myopathy caused by loss-of-function mutations in MTM1 that is without… (more)

Subjects/Keywords: Medical Genetics; Myotubular Myopathy; Neuromusuclar Disease; Paediatric Neurology; Therapy; 0369

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APA (6th Edition):

Maani, N. (2018). Tamoxifen Therapy in a Murine Model of Myotubular Myopathy. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/91399

Chicago Manual of Style (16th Edition):

Maani, Nika. “Tamoxifen Therapy in a Murine Model of Myotubular Myopathy.” 2018. Masters Thesis, University of Toronto. Accessed April 06, 2020. http://hdl.handle.net/1807/91399.

MLA Handbook (7th Edition):

Maani, Nika. “Tamoxifen Therapy in a Murine Model of Myotubular Myopathy.” 2018. Web. 06 Apr 2020.

Vancouver:

Maani N. Tamoxifen Therapy in a Murine Model of Myotubular Myopathy. [Internet] [Masters thesis]. University of Toronto; 2018. [cited 2020 Apr 06]. Available from: http://hdl.handle.net/1807/91399.

Council of Science Editors:

Maani N. Tamoxifen Therapy in a Murine Model of Myotubular Myopathy. [Masters Thesis]. University of Toronto; 2018. Available from: http://hdl.handle.net/1807/91399


University of Toronto

23. Qiu, Boyang. Screening for Suppressors of Nemaline Myopathy in Zebrafish and Mouse Models of the Disease.

Degree: 2019, University of Toronto

Nemaline myopathy is a rare neuromuscular disorder that affects 1 in 50,000 live births, with prevalence as high as 1 in 20,000 in certain populations.… (more)

Subjects/Keywords: Drug screening; Mouse; Muscle; Nebulin; Nemaline myopathy; Zebrafish; 0307

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APA (6th Edition):

Qiu, B. (2019). Screening for Suppressors of Nemaline Myopathy in Zebrafish and Mouse Models of the Disease. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/98318

Chicago Manual of Style (16th Edition):

Qiu, Boyang. “Screening for Suppressors of Nemaline Myopathy in Zebrafish and Mouse Models of the Disease.” 2019. Masters Thesis, University of Toronto. Accessed April 06, 2020. http://hdl.handle.net/1807/98318.

MLA Handbook (7th Edition):

Qiu, Boyang. “Screening for Suppressors of Nemaline Myopathy in Zebrafish and Mouse Models of the Disease.” 2019. Web. 06 Apr 2020.

Vancouver:

Qiu B. Screening for Suppressors of Nemaline Myopathy in Zebrafish and Mouse Models of the Disease. [Internet] [Masters thesis]. University of Toronto; 2019. [cited 2020 Apr 06]. Available from: http://hdl.handle.net/1807/98318.

Council of Science Editors:

Qiu B. Screening for Suppressors of Nemaline Myopathy in Zebrafish and Mouse Models of the Disease. [Masters Thesis]. University of Toronto; 2019. Available from: http://hdl.handle.net/1807/98318


University of Sydney

24. Best, Heather Annette. Gene discovery and mechanism of disease in the myopathies .

Degree: 2018, University of Sydney

 Congenital myopathy and muscular dystrophy are two groups of inherited muscle diseases characterised by muscle weakness, and sub-classified by hallmark pathological features within a skeletal… (more)

Subjects/Keywords: Alpha-skeletal actin; leiomodin; PYROXD1; congenital myopathy; muscular dystrophy

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APA (6th Edition):

Best, H. A. (2018). Gene discovery and mechanism of disease in the myopathies . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/18940

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):

Best, Heather Annette. “Gene discovery and mechanism of disease in the myopathies .” 2018. Thesis, University of Sydney. Accessed April 06, 2020. http://hdl.handle.net/2123/18940.

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

MLA Handbook (7th Edition):

Best, Heather Annette. “Gene discovery and mechanism of disease in the myopathies .” 2018. Web. 06 Apr 2020.

Vancouver:

Best HA. Gene discovery and mechanism of disease in the myopathies . [Internet] [Thesis]. University of Sydney; 2018. [cited 2020 Apr 06]. Available from: http://hdl.handle.net/2123/18940.

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

Council of Science Editors:

Best HA. Gene discovery and mechanism of disease in the myopathies . [Thesis]. University of Sydney; 2018. Available from: http://hdl.handle.net/2123/18940

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


Tampere University

25. Sandell, Satu. DNAJB6 mutated LGMD1D - The clinical phenotype .

Degree: 2015, Tampere University

 Lihasrappeumasairaudet ovat perinnöllisiä sairauksia, joissa lihassyyt kuolevat ennenaikaisesti ja lihaskudos korvautuu rasva- ja sidekudoksella. Seurauksena on lihaksen surkastuminen ja heikkeneminen. Satu Sandellin väitöstutkimus käsittelee DNAJB6-geenin… (more)

Subjects/Keywords: lihasdystrofia; myopatia; DNAJB6; limb-girdle muscular dystrophy; myopathy

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APA (6th Edition):

Sandell, S. (2015). DNAJB6 mutated LGMD1D - The clinical phenotype . (Doctoral Dissertation). Tampere University. Retrieved from https://trepo.tuni.fi/handle/10024/97046

Chicago Manual of Style (16th Edition):

Sandell, Satu. “DNAJB6 mutated LGMD1D - The clinical phenotype .” 2015. Doctoral Dissertation, Tampere University. Accessed April 06, 2020. https://trepo.tuni.fi/handle/10024/97046.

MLA Handbook (7th Edition):

Sandell, Satu. “DNAJB6 mutated LGMD1D - The clinical phenotype .” 2015. Web. 06 Apr 2020.

Vancouver:

Sandell S. DNAJB6 mutated LGMD1D - The clinical phenotype . [Internet] [Doctoral dissertation]. Tampere University; 2015. [cited 2020 Apr 06]. Available from: https://trepo.tuni.fi/handle/10024/97046.

Council of Science Editors:

Sandell S. DNAJB6 mutated LGMD1D - The clinical phenotype . [Doctoral Dissertation]. Tampere University; 2015. Available from: https://trepo.tuni.fi/handle/10024/97046

26. Letter, M-A.C.J. Critical illness polyneuropathy and myopathy; a neuromuscular disorder encountered in the intensive care unit.

Degree: 2001, Erasmus University Medical Center

 textabstractPatients with neuromuscular disorders encountered on the ICU can be divided into two main categories. One category has been admitted to the intensive care unit… (more)

Subjects/Keywords: intensive care; myopathy; neurology; polyneuropathy

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APA (6th Edition):

Letter, M. C. J. (2001). Critical illness polyneuropathy and myopathy; a neuromuscular disorder encountered in the intensive care unit. (Doctoral Dissertation). Erasmus University Medical Center. Retrieved from http://hdl.handle.net/1765/23629

Chicago Manual of Style (16th Edition):

Letter, M-A C J. “Critical illness polyneuropathy and myopathy; a neuromuscular disorder encountered in the intensive care unit.” 2001. Doctoral Dissertation, Erasmus University Medical Center. Accessed April 06, 2020. http://hdl.handle.net/1765/23629.

MLA Handbook (7th Edition):

Letter, M-A C J. “Critical illness polyneuropathy and myopathy; a neuromuscular disorder encountered in the intensive care unit.” 2001. Web. 06 Apr 2020.

Vancouver:

Letter MCJ. Critical illness polyneuropathy and myopathy; a neuromuscular disorder encountered in the intensive care unit. [Internet] [Doctoral dissertation]. Erasmus University Medical Center; 2001. [cited 2020 Apr 06]. Available from: http://hdl.handle.net/1765/23629.

Council of Science Editors:

Letter MCJ. Critical illness polyneuropathy and myopathy; a neuromuscular disorder encountered in the intensive care unit. [Doctoral Dissertation]. Erasmus University Medical Center; 2001. Available from: http://hdl.handle.net/1765/23629


University of Illinois – Urbana-Champaign

27. Meador, Benjamin M. Statin-associated skeletal muscle damage and its interactions with novel or accustomed exercise.

Degree: PhD, 0351, 2011, University of Illinois – Urbana-Champaign

 Statin drugs are a very commonly prescribed medication, and their most common side effect is some degree of skeletal muscle myopathy. Unfortunately, this side effect… (more)

Subjects/Keywords: Statins; Myopathy; Exercise; Muscle Function; Heat Shock Proteins; Caspase

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

APA (6th Edition):

Meador, B. M. (2011). Statin-associated skeletal muscle damage and its interactions with novel or accustomed exercise. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/18603

Chicago Manual of Style (16th Edition):

Meador, Benjamin M. “Statin-associated skeletal muscle damage and its interactions with novel or accustomed exercise.” 2011. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed April 06, 2020. http://hdl.handle.net/2142/18603.

MLA Handbook (7th Edition):

Meador, Benjamin M. “Statin-associated skeletal muscle damage and its interactions with novel or accustomed exercise.” 2011. Web. 06 Apr 2020.

Vancouver:

Meador BM. Statin-associated skeletal muscle damage and its interactions with novel or accustomed exercise. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2011. [cited 2020 Apr 06]. Available from: http://hdl.handle.net/2142/18603.

Council of Science Editors:

Meador BM. Statin-associated skeletal muscle damage and its interactions with novel or accustomed exercise. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2011. Available from: http://hdl.handle.net/2142/18603

28. Kutchukian, Candice. Signalisation calcique et couplage excitation-contraction dans le muscle squelettique : modulation par certains phosphoinositides et altérations associées dans deux myopathies centronucléaires : Calcium signaling and excitation-contraction coupling in skeletal muscle : modulation by some phosphoinositides and related alterations in two centronuclear myopathies.

Degree: Docteur es, Physiologie, 2018, Lyon

Le couplage excitation-contraction (EC) du muscle squelettique correspond à l’efflux de Ca2+ par le réticulum sarcoplasmique (RS) suite à une dépolarisation sarcolemmale. Des mutations dans… (more)

Subjects/Keywords: Muscle squelettique; Couplage excitation-Contraction; Phosphoinositides; Myopathie myotubulaire; Myopathie centronucléaire; Calcium; Skeletal muscle; Excitation-Contraction Coupling; Phosphoinositides; Myotubular myopathy; Centronuclear myopathy; Calcium; 571

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

APA (6th Edition):

Kutchukian, C. (2018). Signalisation calcique et couplage excitation-contraction dans le muscle squelettique : modulation par certains phosphoinositides et altérations associées dans deux myopathies centronucléaires : Calcium signaling and excitation-contraction coupling in skeletal muscle : modulation by some phosphoinositides and related alterations in two centronuclear myopathies. (Doctoral Dissertation). Lyon. Retrieved from http://www.theses.fr/2018LYSE1148

Chicago Manual of Style (16th Edition):

Kutchukian, Candice. “Signalisation calcique et couplage excitation-contraction dans le muscle squelettique : modulation par certains phosphoinositides et altérations associées dans deux myopathies centronucléaires : Calcium signaling and excitation-contraction coupling in skeletal muscle : modulation by some phosphoinositides and related alterations in two centronuclear myopathies.” 2018. Doctoral Dissertation, Lyon. Accessed April 06, 2020. http://www.theses.fr/2018LYSE1148.

MLA Handbook (7th Edition):

Kutchukian, Candice. “Signalisation calcique et couplage excitation-contraction dans le muscle squelettique : modulation par certains phosphoinositides et altérations associées dans deux myopathies centronucléaires : Calcium signaling and excitation-contraction coupling in skeletal muscle : modulation by some phosphoinositides and related alterations in two centronuclear myopathies.” 2018. Web. 06 Apr 2020.

Vancouver:

Kutchukian C. Signalisation calcique et couplage excitation-contraction dans le muscle squelettique : modulation par certains phosphoinositides et altérations associées dans deux myopathies centronucléaires : Calcium signaling and excitation-contraction coupling in skeletal muscle : modulation by some phosphoinositides and related alterations in two centronuclear myopathies. [Internet] [Doctoral dissertation]. Lyon; 2018. [cited 2020 Apr 06]. Available from: http://www.theses.fr/2018LYSE1148.

Council of Science Editors:

Kutchukian C. Signalisation calcique et couplage excitation-contraction dans le muscle squelettique : modulation par certains phosphoinositides et altérations associées dans deux myopathies centronucléaires : Calcium signaling and excitation-contraction coupling in skeletal muscle : modulation by some phosphoinositides and related alterations in two centronuclear myopathies. [Doctoral Dissertation]. Lyon; 2018. Available from: http://www.theses.fr/2018LYSE1148


University of Helsinki

29. Kleine, Iida-Marja. The role of fibroblast growth factor 21 in mediating altered metabolism of the Deletor mouse model for mitochondrial myopathy.

Degree: Medicinska fakulteten, 2018, University of Helsinki

 This study investigates the metabolic consequences of a biomarker for mitochondrial myopathies, using the mouse as a model organism. The studied biomarker is fibroblast growth… (more)

Subjects/Keywords: mitochondrial disease; myopathy; FGF21; biomarker; adPEO; Twinkle; metabolic pathway; one carbon metabolism; targeted metabolomics; MetaboAnalyst; mitochondrial disease; myopathy; FGF21; biomarker; adPEO; Twinkle; metabolic pathway; one carbon metabolism; targeted metabolomics; MetaboAnalyst

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

APA (6th Edition):

Kleine, I. (2018). The role of fibroblast growth factor 21 in mediating altered metabolism of the Deletor mouse model for mitochondrial myopathy. (Masters Thesis). University of Helsinki. Retrieved from http://hdl.handle.net/10138/236397

Chicago Manual of Style (16th Edition):

Kleine, Iida-Marja. “The role of fibroblast growth factor 21 in mediating altered metabolism of the Deletor mouse model for mitochondrial myopathy.” 2018. Masters Thesis, University of Helsinki. Accessed April 06, 2020. http://hdl.handle.net/10138/236397.

MLA Handbook (7th Edition):

Kleine, Iida-Marja. “The role of fibroblast growth factor 21 in mediating altered metabolism of the Deletor mouse model for mitochondrial myopathy.” 2018. Web. 06 Apr 2020.

Vancouver:

Kleine I. The role of fibroblast growth factor 21 in mediating altered metabolism of the Deletor mouse model for mitochondrial myopathy. [Internet] [Masters thesis]. University of Helsinki; 2018. [cited 2020 Apr 06]. Available from: http://hdl.handle.net/10138/236397.

Council of Science Editors:

Kleine I. The role of fibroblast growth factor 21 in mediating altered metabolism of the Deletor mouse model for mitochondrial myopathy. [Masters Thesis]. University of Helsinki; 2018. Available from: http://hdl.handle.net/10138/236397


University of Gothenburg / Göteborgs Universitet

30. Tajsharghi, Homa 1968-. Myosin myopathy. A new disease entity.

Degree: 2003, University of Gothenburg / Göteborgs Universitet

 By the discovery and characterization of two familial myopathies caused by mutations in myosin heavy chaingenes, we introduce a new entity within the field of… (more)

Subjects/Keywords: Neuromuscular disorders; Myosin myopathy; Myosin heavy chain; Myosin storage myopathy

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APA (6th Edition):

Tajsharghi, H. 1. (2003). Myosin myopathy. A new disease entity. (Thesis). University of Gothenburg / Göteborgs Universitet. Retrieved from http://hdl.handle.net/2077/16034

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):

Tajsharghi, Homa 1968-. “Myosin myopathy. A new disease entity.” 2003. Thesis, University of Gothenburg / Göteborgs Universitet. Accessed April 06, 2020. http://hdl.handle.net/2077/16034.

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

MLA Handbook (7th Edition):

Tajsharghi, Homa 1968-. “Myosin myopathy. A new disease entity.” 2003. Web. 06 Apr 2020.

Vancouver:

Tajsharghi H1. Myosin myopathy. A new disease entity. [Internet] [Thesis]. University of Gothenburg / Göteborgs Universitet; 2003. [cited 2020 Apr 06]. Available from: http://hdl.handle.net/2077/16034.

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

Council of Science Editors:

Tajsharghi H1. Myosin myopathy. A new disease entity. [Thesis]. University of Gothenburg / Göteborgs Universitet; 2003. Available from: http://hdl.handle.net/2077/16034

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

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