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You searched for subject:(amyotrophic lateral sclerosis superoxide dismutase heterodimer homodimer stability conformation). Showing records 1 – 30 of 11428 total matches.

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Johannes Gutenberg Universität Mainz

1. Weichert, Anna. Der Einfluss einer wildtypischen SOD1-Untereinheit auf Konformation und Stabilität mutanter SOD1-Heterodimere.

Degree: 2012, Johannes Gutenberg Universität Mainz

Die Erkrankung Amyotrophe Lateralsklerose (ALS) ist gekennzeichnet durch eine progressive Degeneration der Motoneurone. Die hierdurch im Patienten hervorgerufene fortschreitende Paralyse kann von wenigen Wochen über… (more)

Subjects/Keywords: Amyotrophe Lateralsklerose, ALS, Superoxiddismutase, SOD1, Heterodimer, Homodimer, Stabilität, Konformation, A4V, G37R, G41D, G41S, G85R, G93C; amyotrophic lateral sclerosis, superoxide dismutase, heterodimer, homodimer, stability, conformation; Natural sciences and mathematics

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APA (6th Edition):

Weichert, A. (2012). Der Einfluss einer wildtypischen SOD1-Untereinheit auf Konformation und Stabilität mutanter SOD1-Heterodimere. (Doctoral Dissertation). Johannes Gutenberg Universität Mainz. Retrieved from http://ubm.opus.hbz-nrw.de/volltexte/2013/3561/

Chicago Manual of Style (16th Edition):

Weichert, Anna. “Der Einfluss einer wildtypischen SOD1-Untereinheit auf Konformation und Stabilität mutanter SOD1-Heterodimere.” 2012. Doctoral Dissertation, Johannes Gutenberg Universität Mainz. Accessed August 18, 2019. http://ubm.opus.hbz-nrw.de/volltexte/2013/3561/.

MLA Handbook (7th Edition):

Weichert, Anna. “Der Einfluss einer wildtypischen SOD1-Untereinheit auf Konformation und Stabilität mutanter SOD1-Heterodimere.” 2012. Web. 18 Aug 2019.

Vancouver:

Weichert A. Der Einfluss einer wildtypischen SOD1-Untereinheit auf Konformation und Stabilität mutanter SOD1-Heterodimere. [Internet] [Doctoral dissertation]. Johannes Gutenberg Universität Mainz; 2012. [cited 2019 Aug 18]. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2013/3561/.

Council of Science Editors:

Weichert A. Der Einfluss einer wildtypischen SOD1-Untereinheit auf Konformation und Stabilität mutanter SOD1-Heterodimere. [Doctoral Dissertation]. Johannes Gutenberg Universität Mainz; 2012. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2013/3561/


University of Waterloo

2. Doyle, Colleen. A Refined Method for Quantitation of Divalent Metal Ions in Metalloproteins and Local Stability and Conformational Heterogeneity of Amyotrophic Lateral Sclerosis-Associated Cu, Zn Superoxide Dismutase.

Degree: 2014, University of Waterloo

Amyotrophic lateral sclerosis (ALS) is a devastating and progressive disease that results in selective death of motor neurons in the cortex, brain stem and spinal… (more)

Subjects/Keywords: superoxide dismutase; amyotrophic lateral sclerosis; local stability; metal quantitation; nuclear magnetic resonance spectroscopy

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APA (6th Edition):

Doyle, C. (2014). A Refined Method for Quantitation of Divalent Metal Ions in Metalloproteins and Local Stability and Conformational Heterogeneity of Amyotrophic Lateral Sclerosis-Associated Cu, Zn Superoxide Dismutase. (Thesis). University of Waterloo. Retrieved from http://hdl.handle.net/10012/8440

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):

Doyle, Colleen. “A Refined Method for Quantitation of Divalent Metal Ions in Metalloproteins and Local Stability and Conformational Heterogeneity of Amyotrophic Lateral Sclerosis-Associated Cu, Zn Superoxide Dismutase.” 2014. Thesis, University of Waterloo. Accessed August 18, 2019. http://hdl.handle.net/10012/8440.

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

MLA Handbook (7th Edition):

Doyle, Colleen. “A Refined Method for Quantitation of Divalent Metal Ions in Metalloproteins and Local Stability and Conformational Heterogeneity of Amyotrophic Lateral Sclerosis-Associated Cu, Zn Superoxide Dismutase.” 2014. Web. 18 Aug 2019.

Vancouver:

Doyle C. A Refined Method for Quantitation of Divalent Metal Ions in Metalloproteins and Local Stability and Conformational Heterogeneity of Amyotrophic Lateral Sclerosis-Associated Cu, Zn Superoxide Dismutase. [Internet] [Thesis]. University of Waterloo; 2014. [cited 2019 Aug 18]. Available from: http://hdl.handle.net/10012/8440.

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

Council of Science Editors:

Doyle C. A Refined Method for Quantitation of Divalent Metal Ions in Metalloproteins and Local Stability and Conformational Heterogeneity of Amyotrophic Lateral Sclerosis-Associated Cu, Zn Superoxide Dismutase. [Thesis]. University of Waterloo; 2014. Available from: http://hdl.handle.net/10012/8440

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

3. Mackness, Brian C. The Identification and Targeting of Partially-Folded Conformations on the Folding Free-Energy Landscapes of ALS-Linked Proteins for Therapeutic Intervention: A Dissertation.

Degree: Biochemistry and Molecular Pharmacology, Biochemistry and Molecular Pharmacology, 2016, U of Massachusetts : Med

  The hallmark feature of many neurodegenerative diseases, including amyotrophic lateral sclerosis (ALS), is the accumulation of cytoplasmic inclusions of key disease-linked proteins. Two of… (more)

Subjects/Keywords: Amyotrophic Lateral Sclerosis; Mutation; DNA-Binding Proteins; Superoxide Dismutase; Proteostasis Deficiencies; Protein Folding; Protein Conformation; Biochemistry; Nervous System Diseases; Structural Biology

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APA (6th Edition):

Mackness, B. C. (2016). The Identification and Targeting of Partially-Folded Conformations on the Folding Free-Energy Landscapes of ALS-Linked Proteins for Therapeutic Intervention: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/826

Chicago Manual of Style (16th Edition):

Mackness, Brian C. “The Identification and Targeting of Partially-Folded Conformations on the Folding Free-Energy Landscapes of ALS-Linked Proteins for Therapeutic Intervention: A Dissertation.” 2016. Doctoral Dissertation, U of Massachusetts : Med. Accessed August 18, 2019. http://escholarship.umassmed.edu/gsbs_diss/826.

MLA Handbook (7th Edition):

Mackness, Brian C. “The Identification and Targeting of Partially-Folded Conformations on the Folding Free-Energy Landscapes of ALS-Linked Proteins for Therapeutic Intervention: A Dissertation.” 2016. Web. 18 Aug 2019.

Vancouver:

Mackness BC. The Identification and Targeting of Partially-Folded Conformations on the Folding Free-Energy Landscapes of ALS-Linked Proteins for Therapeutic Intervention: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2016. [cited 2019 Aug 18]. Available from: http://escholarship.umassmed.edu/gsbs_diss/826.

Council of Science Editors:

Mackness BC. The Identification and Targeting of Partially-Folded Conformations on the Folding Free-Energy Landscapes of ALS-Linked Proteins for Therapeutic Intervention: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2016. Available from: http://escholarship.umassmed.edu/gsbs_diss/826


University of Waterloo

4. Tong, Ming Sze. Stability and aggregation propensities of ALS-associated human superoxide dismutase mutants.

Degree: 2010, University of Waterloo

Amyotrophic lateral sclerosis (ALS) is the most common motor neuron disease and is characterized by progressive paralysis leading to death, typically, within 3-5 years of… (more)

Subjects/Keywords: Human copper zinc superoxide dismutase; amyotrophic lateral sclerosis

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APA (6th Edition):

Tong, M. S. (2010). Stability and aggregation propensities of ALS-associated human superoxide dismutase mutants. (Thesis). University of Waterloo. Retrieved from http://hdl.handle.net/10012/5036

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):

Tong, Ming Sze. “Stability and aggregation propensities of ALS-associated human superoxide dismutase mutants.” 2010. Thesis, University of Waterloo. Accessed August 18, 2019. http://hdl.handle.net/10012/5036.

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

MLA Handbook (7th Edition):

Tong, Ming Sze. “Stability and aggregation propensities of ALS-associated human superoxide dismutase mutants.” 2010. Web. 18 Aug 2019.

Vancouver:

Tong MS. Stability and aggregation propensities of ALS-associated human superoxide dismutase mutants. [Internet] [Thesis]. University of Waterloo; 2010. [cited 2019 Aug 18]. Available from: http://hdl.handle.net/10012/5036.

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

Council of Science Editors:

Tong MS. Stability and aggregation propensities of ALS-associated human superoxide dismutase mutants. [Thesis]. University of Waterloo; 2010. Available from: http://hdl.handle.net/10012/5036

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

5. Aleandro Geraldo Alves. MUTAÇÕES DO GENE SOD-1 (SUPERÓXIDO DISMUTASE 1) NA FORMA FAMILIAR DA ESCLEROSE AMIOTRÓFICA LATERAL: REVISÃO SISTEMÁTICA.

Degree: 2011, Pontifícia Universidade Católica de Goiás

A esclerose amiotrófica lateral (EAL) é uma doença multifatorial que afeta os neurônios motores. Na maioria dos casos, a doença é esporádica, entretanto, 5 a… (more)

Subjects/Keywords: Esclerose Amiotrófica Lateral; Esclerose Amiotrófica Lateral Familiar; Superóxido Dismutase; SOD-1; Mutação; GENETICA; Amyotrophic lateral sclerosis (ALS); Amyotrophic lateral sclerosis familial (FALS); Superoxide Dismutase; SOD-1; Mutation

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APA (6th Edition):

Alves, A. G. (2011). MUTAÇÕES DO GENE SOD-1 (SUPERÓXIDO DISMUTASE 1) NA FORMA FAMILIAR DA ESCLEROSE AMIOTRÓFICA LATERAL: REVISÃO SISTEMÁTICA. (Thesis). Pontifícia Universidade Católica de Goiás. Retrieved from http://tede.biblioteca.ucg.br/tde_busca/arquivo.php?codArquivo=1304

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):

Alves, Aleandro Geraldo. “MUTAÇÕES DO GENE SOD-1 (SUPERÓXIDO DISMUTASE 1) NA FORMA FAMILIAR DA ESCLEROSE AMIOTRÓFICA LATERAL: REVISÃO SISTEMÁTICA.” 2011. Thesis, Pontifícia Universidade Católica de Goiás. Accessed August 18, 2019. http://tede.biblioteca.ucg.br/tde_busca/arquivo.php?codArquivo=1304.

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

MLA Handbook (7th Edition):

Alves, Aleandro Geraldo. “MUTAÇÕES DO GENE SOD-1 (SUPERÓXIDO DISMUTASE 1) NA FORMA FAMILIAR DA ESCLEROSE AMIOTRÓFICA LATERAL: REVISÃO SISTEMÁTICA.” 2011. Web. 18 Aug 2019.

Vancouver:

Alves AG. MUTAÇÕES DO GENE SOD-1 (SUPERÓXIDO DISMUTASE 1) NA FORMA FAMILIAR DA ESCLEROSE AMIOTRÓFICA LATERAL: REVISÃO SISTEMÁTICA. [Internet] [Thesis]. Pontifícia Universidade Católica de Goiás; 2011. [cited 2019 Aug 18]. Available from: http://tede.biblioteca.ucg.br/tde_busca/arquivo.php?codArquivo=1304.

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

Council of Science Editors:

Alves AG. MUTAÇÕES DO GENE SOD-1 (SUPERÓXIDO DISMUTASE 1) NA FORMA FAMILIAR DA ESCLEROSE AMIOTRÓFICA LATERAL: REVISÃO SISTEMÁTICA. [Thesis]. Pontifícia Universidade Católica de Goiás; 2011. Available from: http://tede.biblioteca.ucg.br/tde_busca/arquivo.php?codArquivo=1304

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


Oregon State University

6. Roberts, Blaine R. Structural studies of the antioxidant defense enzymes; copper, zinc superoxide dismutase and alkyl hydroperoxide reductase flavoprotein.

Degree: PhD, Biochemistry and Biophysics, 2007, Oregon State University

 Oxygen derived radicals are involved in many aspects of life from aging and cell signaling to disease states as diverse as heart disease, diabetes, neurodegeneration… (more)

Subjects/Keywords: Amyotrophic lateral sclerosis; Superoxide dismutase  – Structure

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APA (6th Edition):

Roberts, B. R. (2007). Structural studies of the antioxidant defense enzymes; copper, zinc superoxide dismutase and alkyl hydroperoxide reductase flavoprotein. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/5054

Chicago Manual of Style (16th Edition):

Roberts, Blaine R. “Structural studies of the antioxidant defense enzymes; copper, zinc superoxide dismutase and alkyl hydroperoxide reductase flavoprotein.” 2007. Doctoral Dissertation, Oregon State University. Accessed August 18, 2019. http://hdl.handle.net/1957/5054.

MLA Handbook (7th Edition):

Roberts, Blaine R. “Structural studies of the antioxidant defense enzymes; copper, zinc superoxide dismutase and alkyl hydroperoxide reductase flavoprotein.” 2007. Web. 18 Aug 2019.

Vancouver:

Roberts BR. Structural studies of the antioxidant defense enzymes; copper, zinc superoxide dismutase and alkyl hydroperoxide reductase flavoprotein. [Internet] [Doctoral dissertation]. Oregon State University; 2007. [cited 2019 Aug 18]. Available from: http://hdl.handle.net/1957/5054.

Council of Science Editors:

Roberts BR. Structural studies of the antioxidant defense enzymes; copper, zinc superoxide dismutase and alkyl hydroperoxide reductase flavoprotein. [Doctoral Dissertation]. Oregon State University; 2007. Available from: http://hdl.handle.net/1957/5054


Wright State University

7. Shurte, Leah A. Determining Protein-Protein Interactions of ALS-Associated SOD1.

Degree: MS, Biological Sciences, 2016, Wright State University

Amyotrophic Lateral Sclerosis (ALS) is a neurodegenerative disorder that occurs due to the death of motor neurons and leads to paralysis and death within three… (more)

Subjects/Keywords: Biology; Cellular Biology; SOD1; Superoxide Dismutase 1; ALS; Amyotrophic Lateral Sclerosis; Protein-Protein Interactions

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APA (6th Edition):

Shurte, L. A. (2016). Determining Protein-Protein Interactions of ALS-Associated SOD1. (Masters Thesis). Wright State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=wright1464283630

Chicago Manual of Style (16th Edition):

Shurte, Leah A. “Determining Protein-Protein Interactions of ALS-Associated SOD1.” 2016. Masters Thesis, Wright State University. Accessed August 18, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=wright1464283630.

MLA Handbook (7th Edition):

Shurte, Leah A. “Determining Protein-Protein Interactions of ALS-Associated SOD1.” 2016. Web. 18 Aug 2019.

Vancouver:

Shurte LA. Determining Protein-Protein Interactions of ALS-Associated SOD1. [Internet] [Masters thesis]. Wright State University; 2016. [cited 2019 Aug 18]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1464283630.

Council of Science Editors:

Shurte LA. Determining Protein-Protein Interactions of ALS-Associated SOD1. [Masters Thesis]. Wright State University; 2016. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1464283630


University of Texas Southwestern Medical Center

8. Day, Cameron E. A Role for BDNF-Trkb Signaling in the Modulation of Superoxide Dismutase-1 Expression.

Degree: 2014, University of Texas Southwestern Medical Center

Superoxide dismutase-1 (SOD1) has been implicated in the pathogenesis of familial amyotrophic lateral sclerosis (fALS), a degenerative motor neuron disease more commonly known as Lou… (more)

Subjects/Keywords: Amyotrophic Lateral Sclerosis; Brain-Derived Neurotrophic Factor; Motor Neuron Disease; Receptor, trkB; Superoxide Dismutase

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APA (6th Edition):

Day, C. E. (2014). A Role for BDNF-Trkb Signaling in the Modulation of Superoxide Dismutase-1 Expression. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/3310

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):

Day, Cameron E. “A Role for BDNF-Trkb Signaling in the Modulation of Superoxide Dismutase-1 Expression.” 2014. Thesis, University of Texas Southwestern Medical Center. Accessed August 18, 2019. http://hdl.handle.net/2152.5/3310.

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

MLA Handbook (7th Edition):

Day, Cameron E. “A Role for BDNF-Trkb Signaling in the Modulation of Superoxide Dismutase-1 Expression.” 2014. Web. 18 Aug 2019.

Vancouver:

Day CE. A Role for BDNF-Trkb Signaling in the Modulation of Superoxide Dismutase-1 Expression. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2014. [cited 2019 Aug 18]. Available from: http://hdl.handle.net/2152.5/3310.

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

Council of Science Editors:

Day CE. A Role for BDNF-Trkb Signaling in the Modulation of Superoxide Dismutase-1 Expression. [Thesis]. University of Texas Southwestern Medical Center; 2014. Available from: http://hdl.handle.net/2152.5/3310

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


University of Tasmania

9. Clark, JA. Targeting microtubules in the distal neuromuscular circuitry to improve outcomes in amyotrophic lateral sclerosis.

Degree: 2017, University of Tasmania

Amyotrophic lateral sclerosis (ALS), the most common form of motor neuron disease, is a disease that is characterised by the degeneration of motor neurons, their… (more)

Subjects/Keywords: Neuromuscular junctions; microtubule stabilisation; Amyotrophic Lateral Sclerosis; Superoxide Dismutase 1; cytoskeleton; spinal cord

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APA (6th Edition):

Clark, J. (2017). Targeting microtubules in the distal neuromuscular circuitry to improve outcomes in amyotrophic lateral sclerosis. (Thesis). University of Tasmania. Retrieved from https://eprints.utas.edu.au/23824/1/Clark_Jayden_whole_thesis.pdf ; Clark, JA ORCID: 0000-0003-1760-1489 <https://orcid.org/0000-0003-1760-1489> 2017 , 'Targeting microtubules in the distal neuromuscular circuitry to improve outcomes in amyotrophic lateral sclerosis', PhD thesis, University of Tasmania.

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):

Clark, JA. “Targeting microtubules in the distal neuromuscular circuitry to improve outcomes in amyotrophic lateral sclerosis.” 2017. Thesis, University of Tasmania. Accessed August 18, 2019. https://eprints.utas.edu.au/23824/1/Clark_Jayden_whole_thesis.pdf ; Clark, JA ORCID: 0000-0003-1760-1489 <https://orcid.org/0000-0003-1760-1489> 2017 , 'Targeting microtubules in the distal neuromuscular circuitry to improve outcomes in amyotrophic lateral sclerosis', PhD thesis, University of Tasmania..

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

MLA Handbook (7th Edition):

Clark, JA. “Targeting microtubules in the distal neuromuscular circuitry to improve outcomes in amyotrophic lateral sclerosis.” 2017. Web. 18 Aug 2019.

Vancouver:

Clark J. Targeting microtubules in the distal neuromuscular circuitry to improve outcomes in amyotrophic lateral sclerosis. [Internet] [Thesis]. University of Tasmania; 2017. [cited 2019 Aug 18]. Available from: https://eprints.utas.edu.au/23824/1/Clark_Jayden_whole_thesis.pdf ; Clark, JA ORCID: 0000-0003-1760-1489 <https://orcid.org/0000-0003-1760-1489> 2017 , 'Targeting microtubules in the distal neuromuscular circuitry to improve outcomes in amyotrophic lateral sclerosis', PhD thesis, University of Tasmania..

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

Council of Science Editors:

Clark J. Targeting microtubules in the distal neuromuscular circuitry to improve outcomes in amyotrophic lateral sclerosis. [Thesis]. University of Tasmania; 2017. Available from: https://eprints.utas.edu.au/23824/1/Clark_Jayden_whole_thesis.pdf ; Clark, JA ORCID: 0000-0003-1760-1489 <https://orcid.org/0000-0003-1760-1489> 2017 , 'Targeting microtubules in the distal neuromuscular circuitry to improve outcomes in amyotrophic lateral sclerosis', PhD thesis, University of Tasmania.

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


University of Melbourne

10. Hilton, James Benjamin William. Cuproenzyme dysfunction in the pathogenesis of amyotrophic lateral sclerosis and multiple sclerosis.

Degree: 2016, University of Melbourne

Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease characterised by the selective death of motor neurons within the spinal cord and brain. Although the… (more)

Subjects/Keywords: amyotrophic lateral sclerosis; multiple sclerosis; copper; cuproenzymes; superoxide dismutase; neurodegeneration; therapeutics; iron; ceruloplasmin; cytochrome c oxidase; biomarkers

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APA (6th Edition):

Hilton, J. B. W. (2016). Cuproenzyme dysfunction in the pathogenesis of amyotrophic lateral sclerosis and multiple sclerosis. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/123816

Chicago Manual of Style (16th Edition):

Hilton, James Benjamin William. “Cuproenzyme dysfunction in the pathogenesis of amyotrophic lateral sclerosis and multiple sclerosis.” 2016. Doctoral Dissertation, University of Melbourne. Accessed August 18, 2019. http://hdl.handle.net/11343/123816.

MLA Handbook (7th Edition):

Hilton, James Benjamin William. “Cuproenzyme dysfunction in the pathogenesis of amyotrophic lateral sclerosis and multiple sclerosis.” 2016. Web. 18 Aug 2019.

Vancouver:

Hilton JBW. Cuproenzyme dysfunction in the pathogenesis of amyotrophic lateral sclerosis and multiple sclerosis. [Internet] [Doctoral dissertation]. University of Melbourne; 2016. [cited 2019 Aug 18]. Available from: http://hdl.handle.net/11343/123816.

Council of Science Editors:

Hilton JBW. Cuproenzyme dysfunction in the pathogenesis of amyotrophic lateral sclerosis and multiple sclerosis. [Doctoral Dissertation]. University of Melbourne; 2016. Available from: http://hdl.handle.net/11343/123816


Texas Medical Center

11. McCarthy, Michael. STUDYING AGGREGATE FORMATION BY AMYOTROPHIC LATERAL SCLEROSIS-ASSOCIATED MUTANT SOD1 PROTEIN IN DROSOPHILA MODEL.

Degree: MS, 2013, Texas Medical Center

  A common pathological hallmark of most neurodegenerative disorders is the presence of protein aggregates in the brain. Understanding the regulation of aggregate formation is… (more)

Subjects/Keywords: Amyotrophic Lateral Sclerosis; Neurodegeneration; SOD1; Motor neuron disease; Aggregate; Excitotoxicity; Superoxide dismutase; Drosophila; ALS; GFP; Medicine and Health Sciences; Molecular Biology

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APA (6th Edition):

McCarthy, M. (2013). STUDYING AGGREGATE FORMATION BY AMYOTROPHIC LATERAL SCLEROSIS-ASSOCIATED MUTANT SOD1 PROTEIN IN DROSOPHILA MODEL. (Masters Thesis). Texas Medical Center. Retrieved from http://digitalcommons.library.tmc.edu/utgsbs_dissertations/381

Chicago Manual of Style (16th Edition):

McCarthy, Michael. “STUDYING AGGREGATE FORMATION BY AMYOTROPHIC LATERAL SCLEROSIS-ASSOCIATED MUTANT SOD1 PROTEIN IN DROSOPHILA MODEL.” 2013. Masters Thesis, Texas Medical Center. Accessed August 18, 2019. http://digitalcommons.library.tmc.edu/utgsbs_dissertations/381.

MLA Handbook (7th Edition):

McCarthy, Michael. “STUDYING AGGREGATE FORMATION BY AMYOTROPHIC LATERAL SCLEROSIS-ASSOCIATED MUTANT SOD1 PROTEIN IN DROSOPHILA MODEL.” 2013. Web. 18 Aug 2019.

Vancouver:

McCarthy M. STUDYING AGGREGATE FORMATION BY AMYOTROPHIC LATERAL SCLEROSIS-ASSOCIATED MUTANT SOD1 PROTEIN IN DROSOPHILA MODEL. [Internet] [Masters thesis]. Texas Medical Center; 2013. [cited 2019 Aug 18]. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/381.

Council of Science Editors:

McCarthy M. STUDYING AGGREGATE FORMATION BY AMYOTROPHIC LATERAL SCLEROSIS-ASSOCIATED MUTANT SOD1 PROTEIN IN DROSOPHILA MODEL. [Masters Thesis]. Texas Medical Center; 2013. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/381


IUPUI

12. Fontanilla, Christine V. NEUROPROTECTIVE STUDIES ON THE MPTP AND SOD1 MOUSE MODELS OF NEURODEGENERATIVE DISEASES.

Degree: 2012, IUPUI

Indiana University-Purdue University Indianapolis (IUPUI)

The main, underlying cause of neurodegenerative disease is the progressive loss of neuronal structure or function, whereby central and/or peripheral… (more)

Subjects/Keywords: ALS; MPTP; SOD1; neurodegeneration; Nervous system  – Degeneration  – Treatment  – Research; Nervous system  – Diseases  – Treatment  – Research; Amyotrophic lateral sclerosis; Methylphenyltetrahydropyridine; Superoxide dismutase

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APA (6th Edition):

Fontanilla, C. V. (2012). NEUROPROTECTIVE STUDIES ON THE MPTP AND SOD1 MOUSE MODELS OF NEURODEGENERATIVE DISEASES. (Thesis). IUPUI. Retrieved from http://hdl.handle.net/1805/2724

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):

Fontanilla, Christine V. “NEUROPROTECTIVE STUDIES ON THE MPTP AND SOD1 MOUSE MODELS OF NEURODEGENERATIVE DISEASES.” 2012. Thesis, IUPUI. Accessed August 18, 2019. http://hdl.handle.net/1805/2724.

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

MLA Handbook (7th Edition):

Fontanilla, Christine V. “NEUROPROTECTIVE STUDIES ON THE MPTP AND SOD1 MOUSE MODELS OF NEURODEGENERATIVE DISEASES.” 2012. Web. 18 Aug 2019.

Vancouver:

Fontanilla CV. NEUROPROTECTIVE STUDIES ON THE MPTP AND SOD1 MOUSE MODELS OF NEURODEGENERATIVE DISEASES. [Internet] [Thesis]. IUPUI; 2012. [cited 2019 Aug 18]. Available from: http://hdl.handle.net/1805/2724.

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

Council of Science Editors:

Fontanilla CV. NEUROPROTECTIVE STUDIES ON THE MPTP AND SOD1 MOUSE MODELS OF NEURODEGENERATIVE DISEASES. [Thesis]. IUPUI; 2012. Available from: http://hdl.handle.net/1805/2724

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


University of Illinois – Urbana-Champaign

13. Dietrich, Alicia. Role of estrogen receptor α and oxidative stress response proteins in the central nervous system.

Degree: PhD, 0325, 2014, University of Illinois – Urbana-Champaign

 Cellular metabolism results in the production of reactive oxygen species (ROS) as byproducts and can damage proteins, lipids, and DNA. Cells utilize a number of… (more)

Subjects/Keywords: Oxidative stress; Estrogen receptor α; Cu/Zn superoxide dismutase; Amyotrophic lateral sclerosis; Apurinic endonuclease 1; Neuroprotection; Hypoxia; Estrogen

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APA (6th Edition):

Dietrich, A. (2014). Role of estrogen receptor α and oxidative stress response proteins in the central nervous system. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/50567

Chicago Manual of Style (16th Edition):

Dietrich, Alicia. “Role of estrogen receptor α and oxidative stress response proteins in the central nervous system.” 2014. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed August 18, 2019. http://hdl.handle.net/2142/50567.

MLA Handbook (7th Edition):

Dietrich, Alicia. “Role of estrogen receptor α and oxidative stress response proteins in the central nervous system.” 2014. Web. 18 Aug 2019.

Vancouver:

Dietrich A. Role of estrogen receptor α and oxidative stress response proteins in the central nervous system. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2014. [cited 2019 Aug 18]. Available from: http://hdl.handle.net/2142/50567.

Council of Science Editors:

Dietrich A. Role of estrogen receptor α and oxidative stress response proteins in the central nervous system. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2014. Available from: http://hdl.handle.net/2142/50567

14. Medinas, Danilo Bilches. Atividade peroxidásica da enzima superóxido dismutase 1 humana: produção do radical carbonato, dimerização covalente da enzima e implicações para a esclerose lateral amiotrófica.

Degree: PhD, Bioquímica, 2010, University of São Paulo

 A esclerose lateral amiotrófica (ELA) é uma doença neurodegenerativa que afeta os neurônios motores levando a atrofia muscular e morte por insuficiência respiratória. Esta patologia… (more)

Subjects/Keywords: Amyotrophic lateral sclerosis; Atividade peroxidásica; Carbonate radical; Ditriptofano; Ditryptophan; Doenças neurodegenerativas; Esclerose lateral amiotrófica; Free radicals; Neurodegenerative diseases; Peroxidase activity; Radicais livres; Radical carbonato; Superoxide dismutase 1; Superóxido dismutase 1

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APA (6th Edition):

Medinas, D. B. (2010). Atividade peroxidásica da enzima superóxido dismutase 1 humana: produção do radical carbonato, dimerização covalente da enzima e implicações para a esclerose lateral amiotrófica. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/46/46131/tde-26042010-102014/ ;

Chicago Manual of Style (16th Edition):

Medinas, Danilo Bilches. “Atividade peroxidásica da enzima superóxido dismutase 1 humana: produção do radical carbonato, dimerização covalente da enzima e implicações para a esclerose lateral amiotrófica.” 2010. Doctoral Dissertation, University of São Paulo. Accessed August 18, 2019. http://www.teses.usp.br/teses/disponiveis/46/46131/tde-26042010-102014/ ;.

MLA Handbook (7th Edition):

Medinas, Danilo Bilches. “Atividade peroxidásica da enzima superóxido dismutase 1 humana: produção do radical carbonato, dimerização covalente da enzima e implicações para a esclerose lateral amiotrófica.” 2010. Web. 18 Aug 2019.

Vancouver:

Medinas DB. Atividade peroxidásica da enzima superóxido dismutase 1 humana: produção do radical carbonato, dimerização covalente da enzima e implicações para a esclerose lateral amiotrófica. [Internet] [Doctoral dissertation]. University of São Paulo; 2010. [cited 2019 Aug 18]. Available from: http://www.teses.usp.br/teses/disponiveis/46/46131/tde-26042010-102014/ ;.

Council of Science Editors:

Medinas DB. Atividade peroxidásica da enzima superóxido dismutase 1 humana: produção do radical carbonato, dimerização covalente da enzima e implicações para a esclerose lateral amiotrófica. [Doctoral Dissertation]. University of São Paulo; 2010. Available from: http://www.teses.usp.br/teses/disponiveis/46/46131/tde-26042010-102014/ ;

15. Rotunno, Melissa S. Identifying, Targeting, and Exploiting a Common Misfolded, Toxic Conformation of SOD1 in ALS: A Dissertation.

Degree: Biochemistry and Molecular Pharmacology, Neurology, 2015, U of Massachusetts : Med

Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease characterized by a loss of voluntary movement over time, leading to paralysis and death. While 10%… (more)

Subjects/Keywords: Amyotrophic Lateral Sclerosis; Biological Markers; Mutation; Superoxide Dismutase; Post-Translational Protein Processing; Proteostasis Deficiencies; Biochemistry, Biophysics, and Structural Biology; Genetics and Genomics; Nervous System Diseases; Neuroscience and Neurobiology

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

APA (6th Edition):

Rotunno, M. S. (2015). Identifying, Targeting, and Exploiting a Common Misfolded, Toxic Conformation of SOD1 in ALS: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/781

Chicago Manual of Style (16th Edition):

Rotunno, Melissa S. “Identifying, Targeting, and Exploiting a Common Misfolded, Toxic Conformation of SOD1 in ALS: A Dissertation.” 2015. Doctoral Dissertation, U of Massachusetts : Med. Accessed August 18, 2019. http://escholarship.umassmed.edu/gsbs_diss/781.

MLA Handbook (7th Edition):

Rotunno, Melissa S. “Identifying, Targeting, and Exploiting a Common Misfolded, Toxic Conformation of SOD1 in ALS: A Dissertation.” 2015. Web. 18 Aug 2019.

Vancouver:

Rotunno MS. Identifying, Targeting, and Exploiting a Common Misfolded, Toxic Conformation of SOD1 in ALS: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2015. [cited 2019 Aug 18]. Available from: http://escholarship.umassmed.edu/gsbs_diss/781.

Council of Science Editors:

Rotunno MS. Identifying, Targeting, and Exploiting a Common Misfolded, Toxic Conformation of SOD1 in ALS: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2015. Available from: http://escholarship.umassmed.edu/gsbs_diss/781


University of Florida

16. Roberts, Brittany-Lee. Effect of Charge and Polarity Changes on the Propensity of Inclusion Formation by Mutant SOD1.

Degree: 2013, University of Florida

 The present study investigated the relationship between changes in charge and polarity on the propensity of aggregate formation by mutant SOD1. Two different mutation sites… (more)

Subjects/Keywords: Aggregation; Amyotrophic lateral sclerosis; Cell aggregates; Charge separation; Genetic mutation; Inclusion bodies; Motor neurons; Plasmids; Point mutation; Superoxides; Amino acids; Mutation (Biology); Polarity (Biology); Superoxide dismutase

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APA (6th Edition):

Roberts, B. (2013). Effect of Charge and Polarity Changes on the Propensity of Inclusion Formation by Mutant SOD1. (Thesis). University of Florida. Retrieved from http://ufdc.ufl.edu/AA00060949

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):

Roberts, Brittany-Lee. “Effect of Charge and Polarity Changes on the Propensity of Inclusion Formation by Mutant SOD1.” 2013. Thesis, University of Florida. Accessed August 18, 2019. http://ufdc.ufl.edu/AA00060949.

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

MLA Handbook (7th Edition):

Roberts, Brittany-Lee. “Effect of Charge and Polarity Changes on the Propensity of Inclusion Formation by Mutant SOD1.” 2013. Web. 18 Aug 2019.

Vancouver:

Roberts B. Effect of Charge and Polarity Changes on the Propensity of Inclusion Formation by Mutant SOD1. [Internet] [Thesis]. University of Florida; 2013. [cited 2019 Aug 18]. Available from: http://ufdc.ufl.edu/AA00060949.

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

Council of Science Editors:

Roberts B. Effect of Charge and Polarity Changes on the Propensity of Inclusion Formation by Mutant SOD1. [Thesis]. University of Florida; 2013. Available from: http://ufdc.ufl.edu/AA00060949

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


Oregon State University

17. Robinson, Kristine M. The detection of superoxide and implications for amyotrophic lateral sclerosis.

Degree: PhD, Biochemistry, 2007, Oregon State University

 Mutations to superoxide dismutase were the first proven cause of Lou Gehrig’s disease (amyotrophic lateral sclerosis; ALS) implicating superoxide in the selective death of motor… (more)

Subjects/Keywords: superoxide; Amyotrophic lateral sclerosis

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

APA (6th Edition):

Robinson, K. M. (2007). The detection of superoxide and implications for amyotrophic lateral sclerosis. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/5003

Chicago Manual of Style (16th Edition):

Robinson, Kristine M. “The detection of superoxide and implications for amyotrophic lateral sclerosis.” 2007. Doctoral Dissertation, Oregon State University. Accessed August 18, 2019. http://hdl.handle.net/1957/5003.

MLA Handbook (7th Edition):

Robinson, Kristine M. “The detection of superoxide and implications for amyotrophic lateral sclerosis.” 2007. Web. 18 Aug 2019.

Vancouver:

Robinson KM. The detection of superoxide and implications for amyotrophic lateral sclerosis. [Internet] [Doctoral dissertation]. Oregon State University; 2007. [cited 2019 Aug 18]. Available from: http://hdl.handle.net/1957/5003.

Council of Science Editors:

Robinson KM. The detection of superoxide and implications for amyotrophic lateral sclerosis. [Doctoral Dissertation]. Oregon State University; 2007. Available from: http://hdl.handle.net/1957/5003


Macquarie University

18. Parakh, Sonam. Role of protein disulphide isomerase and its family members in amyotrophic lateral sclerosis.

Degree: 2016, Macquarie University

Theoretical thesis.

Bibliography: pages 239-279.

General introduction  – Chapter 2. Methods and materials  – Chapter 3. PDI is protective against major familial ALS causing proteins… (more)

Subjects/Keywords: Amyotrophic lateral sclerosis  – Pathogenesis; Protein disulfide isomerase; Superoxide dismutas; amyotrophic lateral sclerosis; protein disulphide isomerase; SODI

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

APA (6th Edition):

Parakh, S. (2016). Role of protein disulphide isomerase and its family members in amyotrophic lateral sclerosis. (Doctoral Dissertation). Macquarie University. Retrieved from http://hdl.handle.net/1959.14/1115418

Chicago Manual of Style (16th Edition):

Parakh, Sonam. “Role of protein disulphide isomerase and its family members in amyotrophic lateral sclerosis.” 2016. Doctoral Dissertation, Macquarie University. Accessed August 18, 2019. http://hdl.handle.net/1959.14/1115418.

MLA Handbook (7th Edition):

Parakh, Sonam. “Role of protein disulphide isomerase and its family members in amyotrophic lateral sclerosis.” 2016. Web. 18 Aug 2019.

Vancouver:

Parakh S. Role of protein disulphide isomerase and its family members in amyotrophic lateral sclerosis. [Internet] [Doctoral dissertation]. Macquarie University; 2016. [cited 2019 Aug 18]. Available from: http://hdl.handle.net/1959.14/1115418.

Council of Science Editors:

Parakh S. Role of protein disulphide isomerase and its family members in amyotrophic lateral sclerosis. [Doctoral Dissertation]. Macquarie University; 2016. Available from: http://hdl.handle.net/1959.14/1115418

19. Cerqueira, Fernanda Menezes. Conseqüências da expressão da enzima Cu,Zn-superóxido dismutase (SOD1) e sua mutante G93A em neuroblastomas. Implicações para a esclerose lateral amiotrófica.

Degree: Mestrado, Bioquímica, 2007, University of São Paulo

Cerca de 20 % dos casos familiares de esclerose lateral amiotrófica (ELAf) são causados por mutações na enzima Cu,Zn-superóxido dismutase (SOD1). Inicialmente se supôs que… (more)

Subjects/Keywords: Agregação protéica; Amyotrophic Lateral Sclerosis (ALS); CuZn-superoxide dismutase (SOD1); CuZn-superóxido dismutase citosólica (SOD1); Dímero covalente de SOD; Disulfide bond; Esclerose Lateral Amiotrófica (ELA); Ligação dissulfeto; Protein aggregation; SOD covalent dimer

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

APA (6th Edition):

Cerqueira, F. M. (2007). Conseqüências da expressão da enzima Cu,Zn-superóxido dismutase (SOD1) e sua mutante G93A em neuroblastomas. Implicações para a esclerose lateral amiotrófica. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/46/46131/tde-25042007-075453/ ;

Chicago Manual of Style (16th Edition):

Cerqueira, Fernanda Menezes. “Conseqüências da expressão da enzima Cu,Zn-superóxido dismutase (SOD1) e sua mutante G93A em neuroblastomas. Implicações para a esclerose lateral amiotrófica.” 2007. Masters Thesis, University of São Paulo. Accessed August 18, 2019. http://www.teses.usp.br/teses/disponiveis/46/46131/tde-25042007-075453/ ;.

MLA Handbook (7th Edition):

Cerqueira, Fernanda Menezes. “Conseqüências da expressão da enzima Cu,Zn-superóxido dismutase (SOD1) e sua mutante G93A em neuroblastomas. Implicações para a esclerose lateral amiotrófica.” 2007. Web. 18 Aug 2019.

Vancouver:

Cerqueira FM. Conseqüências da expressão da enzima Cu,Zn-superóxido dismutase (SOD1) e sua mutante G93A em neuroblastomas. Implicações para a esclerose lateral amiotrófica. [Internet] [Masters thesis]. University of São Paulo; 2007. [cited 2019 Aug 18]. Available from: http://www.teses.usp.br/teses/disponiveis/46/46131/tde-25042007-075453/ ;.

Council of Science Editors:

Cerqueira FM. Conseqüências da expressão da enzima Cu,Zn-superóxido dismutase (SOD1) e sua mutante G93A em neuroblastomas. Implicações para a esclerose lateral amiotrófica. [Masters Thesis]. University of São Paulo; 2007. Available from: http://www.teses.usp.br/teses/disponiveis/46/46131/tde-25042007-075453/ ;


Baylor University

20. [No author]. Electrostatic control of Cu, Zn superoxide dismutase aggregation in Amyotrophic Lateral Sclerosis : from lysine modification to interaction with lipid membranes.

Degree: 2018, Baylor University

 Cu, Zn superoxide dismutase (SOD1) is a ubiquitous metalloprotein, which is responsible for protecting living cells from oxidative stress via disproportionation of superoxide ions. Misfolding… (more)

Subjects/Keywords: Amyotrophic lateral sclerosis.

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APA (6th Edition):

author], [. (2018). Electrostatic control of Cu, Zn superoxide dismutase aggregation in Amyotrophic Lateral Sclerosis : from lysine modification to interaction with lipid membranes. (Thesis). Baylor University. Retrieved from http://hdl.handle.net/2104/10435

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):

author], [No. “Electrostatic control of Cu, Zn superoxide dismutase aggregation in Amyotrophic Lateral Sclerosis : from lysine modification to interaction with lipid membranes. ” 2018. Thesis, Baylor University. Accessed August 18, 2019. http://hdl.handle.net/2104/10435.

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

MLA Handbook (7th Edition):

author], [No. “Electrostatic control of Cu, Zn superoxide dismutase aggregation in Amyotrophic Lateral Sclerosis : from lysine modification to interaction with lipid membranes. ” 2018. Web. 18 Aug 2019.

Vancouver:

author] [. Electrostatic control of Cu, Zn superoxide dismutase aggregation in Amyotrophic Lateral Sclerosis : from lysine modification to interaction with lipid membranes. [Internet] [Thesis]. Baylor University; 2018. [cited 2019 Aug 18]. Available from: http://hdl.handle.net/2104/10435.

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

Council of Science Editors:

author] [. Electrostatic control of Cu, Zn superoxide dismutase aggregation in Amyotrophic Lateral Sclerosis : from lysine modification to interaction with lipid membranes. [Thesis]. Baylor University; 2018. Available from: http://hdl.handle.net/2104/10435

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

21. Duffy, Amanda Marie. Deep Phenotyping of ALS and ALS-FTD Mouse Models Using Automated Continuous Behavioral Monitoring.

Degree: Department of Neuroscience, 2018, Brown University

Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease of the upper and lower motor neurons resulting in weakness, paralysis and death within two to five… (more)

Subjects/Keywords: Amyotrophic lateral sclerosis

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APA (6th Edition):

Duffy, A. M. (2018). Deep Phenotyping of ALS and ALS-FTD Mouse Models Using Automated Continuous Behavioral Monitoring. (Thesis). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:792852/

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):

Duffy, Amanda Marie. “Deep Phenotyping of ALS and ALS-FTD Mouse Models Using Automated Continuous Behavioral Monitoring.” 2018. Thesis, Brown University. Accessed August 18, 2019. https://repository.library.brown.edu/studio/item/bdr:792852/.

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

MLA Handbook (7th Edition):

Duffy, Amanda Marie. “Deep Phenotyping of ALS and ALS-FTD Mouse Models Using Automated Continuous Behavioral Monitoring.” 2018. Web. 18 Aug 2019.

Vancouver:

Duffy AM. Deep Phenotyping of ALS and ALS-FTD Mouse Models Using Automated Continuous Behavioral Monitoring. [Internet] [Thesis]. Brown University; 2018. [cited 2019 Aug 18]. Available from: https://repository.library.brown.edu/studio/item/bdr:792852/.

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

Council of Science Editors:

Duffy AM. Deep Phenotyping of ALS and ALS-FTD Mouse Models Using Automated Continuous Behavioral Monitoring. [Thesis]. Brown University; 2018. Available from: https://repository.library.brown.edu/studio/item/bdr:792852/

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


Baylor University

22. [No author]. Aggregation of Cu, Zn superoxide dismutase in amyotrophic lateral sclerosis : kinetic, mechanistic, and therapeutic approaches.

Degree: 2017, Baylor University

 Investigating in vitro kinetics of protein aggregation using high-throughput microplate-based assays provides open venues for obtaining valuable information regarding mechanism(s) of pathogenesis of protein aggregates… (more)

Subjects/Keywords: Cu; Zn superoxide. Amyotrophic lateral sclerosis. Amyloid. Fibril. Stochasticity. Acylation. Aspirin. Bead. Aggregation.

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APA (6th Edition):

author], [. (2017). Aggregation of Cu, Zn superoxide dismutase in amyotrophic lateral sclerosis : kinetic, mechanistic, and therapeutic approaches. (Thesis). Baylor University. Retrieved from http://hdl.handle.net/2104/10185

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):

author], [No. “Aggregation of Cu, Zn superoxide dismutase in amyotrophic lateral sclerosis : kinetic, mechanistic, and therapeutic approaches. ” 2017. Thesis, Baylor University. Accessed August 18, 2019. http://hdl.handle.net/2104/10185.

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

MLA Handbook (7th Edition):

author], [No. “Aggregation of Cu, Zn superoxide dismutase in amyotrophic lateral sclerosis : kinetic, mechanistic, and therapeutic approaches. ” 2017. Web. 18 Aug 2019.

Vancouver:

author] [. Aggregation of Cu, Zn superoxide dismutase in amyotrophic lateral sclerosis : kinetic, mechanistic, and therapeutic approaches. [Internet] [Thesis]. Baylor University; 2017. [cited 2019 Aug 18]. Available from: http://hdl.handle.net/2104/10185.

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

Council of Science Editors:

author] [. Aggregation of Cu, Zn superoxide dismutase in amyotrophic lateral sclerosis : kinetic, mechanistic, and therapeutic approaches. [Thesis]. Baylor University; 2017. Available from: http://hdl.handle.net/2104/10185

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

23. Jones, Page. Enzymatic and proteomic analysis of spinal cord in a G93A ALS mouse model.

Degree: PhD, 2008, University of Alabama – Birmingham

Mutations to copper,zinc superoxide dismutase (Cu,Zn SOD or SOD1) are the only known causes of amyotrophic lateral sclerosis (ALS), a neurodegenerative disorder characterized primarily by… (more)

Subjects/Keywords: Amyotrophic Lateral Sclerosis  – enzymology <; br>; Copper  – metabolism <; br>; Disease Progression <; br>; Nerve Degeneration  – enzymology <; br>; Neurons  – metabolism <; br>; Spinal Cord  – enzymology <; br>; Superoxide Dismutase  – metabolism

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APA (6th Edition):

Jones, P. (2008). Enzymatic and proteomic analysis of spinal cord in a G93A ALS mouse model. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,370

Chicago Manual of Style (16th Edition):

Jones, Page. “Enzymatic and proteomic analysis of spinal cord in a G93A ALS mouse model.” 2008. Doctoral Dissertation, University of Alabama – Birmingham. Accessed August 18, 2019. http://contentdm.mhsl.uab.edu/u?/etd,370.

MLA Handbook (7th Edition):

Jones, Page. “Enzymatic and proteomic analysis of spinal cord in a G93A ALS mouse model.” 2008. Web. 18 Aug 2019.

Vancouver:

Jones P. Enzymatic and proteomic analysis of spinal cord in a G93A ALS mouse model. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2008. [cited 2019 Aug 18]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,370.

Council of Science Editors:

Jones P. Enzymatic and proteomic analysis of spinal cord in a G93A ALS mouse model. [Doctoral Dissertation]. University of Alabama – Birmingham; 2008. Available from: http://contentdm.mhsl.uab.edu/u?/etd,370


Kyoto University / 京都大学

24. Murayama, Shuuhei. Development of solution NMR method for observation and analysis of proteins inside cells : 核磁気共鳴法による細胞内タンパク質の観測及び手法開発.

Degree: 博士(工学), 2015, Kyoto University / 京都大学

新制・課程博士

甲第19003号

工博第4045号

Subjects/Keywords: in-cell NMR; 19F NMR; protein-drug interaction; Amyotrophic lateral sclerosis (ALS); Superoxide dismutase 1 (SOD1); disulfide bond

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APA (6th Edition):

Murayama, S. (2015). Development of solution NMR method for observation and analysis of proteins inside cells : 核磁気共鳴法による細胞内タンパク質の観測及び手法開発. (Thesis). Kyoto University / 京都大学. Retrieved from http://hdl.handle.net/2433/199327 ; http://dx.doi.org/10.14989/doctor.k19003

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):

Murayama, Shuuhei. “Development of solution NMR method for observation and analysis of proteins inside cells : 核磁気共鳴法による細胞内タンパク質の観測及び手法開発.” 2015. Thesis, Kyoto University / 京都大学. Accessed August 18, 2019. http://hdl.handle.net/2433/199327 ; http://dx.doi.org/10.14989/doctor.k19003.

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

MLA Handbook (7th Edition):

Murayama, Shuuhei. “Development of solution NMR method for observation and analysis of proteins inside cells : 核磁気共鳴法による細胞内タンパク質の観測及び手法開発.” 2015. Web. 18 Aug 2019.

Vancouver:

Murayama S. Development of solution NMR method for observation and analysis of proteins inside cells : 核磁気共鳴法による細胞内タンパク質の観測及び手法開発. [Internet] [Thesis]. Kyoto University / 京都大学; 2015. [cited 2019 Aug 18]. Available from: http://hdl.handle.net/2433/199327 ; http://dx.doi.org/10.14989/doctor.k19003.

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

Council of Science Editors:

Murayama S. Development of solution NMR method for observation and analysis of proteins inside cells : 核磁気共鳴法による細胞内タンパク質の観測及び手法開発. [Thesis]. Kyoto University / 京都大学; 2015. Available from: http://hdl.handle.net/2433/199327 ; http://dx.doi.org/10.14989/doctor.k19003

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


The Ohio State University

25. Likhite, Shibi B. Therapeutic suppression of mutant SOD1 by AAV9-mediated gene therapy approach in Amyotrophic Lateral Sclerosis.

Degree: PhD, Molecular, Cellular and Developmental Biology, 2014, The Ohio State University

Amyotrophic Lateral Sclerosis is one of the most common, adult-onset neurodegenerative disorder, characterized by progressive and fatal loss of motor neurons in spinal cord, motor… (more)

Subjects/Keywords: Biology; Biomedical Research; Immunology; Molecular Biology; Neurosciences; Neurobiology; Neurology; Virology; Amyotrophic Lateral Sclerosis, ALS; Superoxide Dismutase 1, SOD1; Adeno-associated vector 9, AAV9; short hairpin RNA, shRNA; Astrocytes; Neuroinflamation; Galectin 1, Gal1; Microglia

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

APA (6th Edition):

Likhite, S. B. (2014). Therapeutic suppression of mutant SOD1 by AAV9-mediated gene therapy approach in Amyotrophic Lateral Sclerosis. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1417394084

Chicago Manual of Style (16th Edition):

Likhite, Shibi B. “Therapeutic suppression of mutant SOD1 by AAV9-mediated gene therapy approach in Amyotrophic Lateral Sclerosis.” 2014. Doctoral Dissertation, The Ohio State University. Accessed August 18, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1417394084.

MLA Handbook (7th Edition):

Likhite, Shibi B. “Therapeutic suppression of mutant SOD1 by AAV9-mediated gene therapy approach in Amyotrophic Lateral Sclerosis.” 2014. Web. 18 Aug 2019.

Vancouver:

Likhite SB. Therapeutic suppression of mutant SOD1 by AAV9-mediated gene therapy approach in Amyotrophic Lateral Sclerosis. [Internet] [Doctoral dissertation]. The Ohio State University; 2014. [cited 2019 Aug 18]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1417394084.

Council of Science Editors:

Likhite SB. Therapeutic suppression of mutant SOD1 by AAV9-mediated gene therapy approach in Amyotrophic Lateral Sclerosis. [Doctoral Dissertation]. The Ohio State University; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1417394084

26. 森, 麗; モリ, アキラ. Derlin-1過剰発現は変異SOD1蓄積軽減により小胞体ストレスを軽減する : Derlin 1 カジョウ ハツゲン ワ ヘンイ SOD 1 チクセキ ケイゲン ニ ヨリ ショウホウタイ ストレス オ ケイゲン スル; Exogenous Derlin-1 ameliorates endoplasmic reticulum stress by reduction of mutant SOD1 accumulation.

Degree: Kumamoto University / 熊本大学

stress sensor kinase, chaperone, やapoptotic mediatorの惹起をもたらすUnfolded protein responseは, 変異Cu/Zn superoxide dismutase (SOD1)が関与する家族性筋萎縮性側索硬化症(familial amyotrophic lateralsclerosis: FALS)モデルや孤発性筋萎縮性側索硬化症(Sporadic amyotrophiclateral sclerosis: SALS)に関与している. 我々は, 小胞体局在の分子であるDerlin-1が変異SOD1の引き起こす, ミスフォールディング蛋白を減少させる上で, 極めて重要な役割を担っているのではないかと仮説を立てた. 我々はDerlin-1過剰発現が小胞体ストレス経路である, immunoglobulin-bindingprotein, activating transcription factor 6 p50, and C/EBP homologousproteinを抑制することにより, 変異SOD1による細胞毒性の軽減や細胞活性の促進をもたらすことを示す. 興味深いことに, 外因性Derlin-1は, 遺伝子導入した培養細胞内の変異SOD1の蛋白発現を減少させ, それに比べ程度は少ないが,野生型SOD1蛋白発現も減少させていた. そのSOD1蛋白発現減少は, マイクロゾーム分画においては, 野生型や変異SOD1蛋白両方にみられていた. さらに我々の結果は, Derlin-1がプロテアソームやオートファジーにおける分解により, SOD1の代謝回転を促進していることを示唆するものであったが, 変異SOD1のmRNAレベルを減少させるものではなかった. 変異SOD1におけるDerlin-1果の知見はALSに関与する, 運動ニューロン変性における治療を前進させるものであるかもしれない.

Subjects/Keywords: amyotrophic lateral sclerosis (ALS); Cu/Zn superoxide dismutase (SOD1); endoplasmic reticulum (ER) stress; Derlin-1; ER-associated degradation (ERAD); autophagy

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APA (6th Edition):

森, 麗; モリ, . (n.d.). Derlin-1過剰発現は変異SOD1蓄積軽減により小胞体ストレスを軽減する : Derlin 1 カジョウ ハツゲン ワ ヘンイ SOD 1 チクセキ ケイゲン ニ ヨリ ショウホウタイ ストレス オ ケイゲン スル; Exogenous Derlin-1 ameliorates endoplasmic reticulum stress by reduction of mutant SOD1 accumulation. (Thesis). Kumamoto University / 熊本大学. Retrieved from http://hdl.handle.net/2298/21709

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):

森, 麗; モリ, アキラ. “Derlin-1過剰発現は変異SOD1蓄積軽減により小胞体ストレスを軽減する : Derlin 1 カジョウ ハツゲン ワ ヘンイ SOD 1 チクセキ ケイゲン ニ ヨリ ショウホウタイ ストレス オ ケイゲン スル; Exogenous Derlin-1 ameliorates endoplasmic reticulum stress by reduction of mutant SOD1 accumulation.” Thesis, Kumamoto University / 熊本大学. Accessed August 18, 2019. http://hdl.handle.net/2298/21709.

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):

森, 麗; モリ, アキラ. “Derlin-1過剰発現は変異SOD1蓄積軽減により小胞体ストレスを軽減する : Derlin 1 カジョウ ハツゲン ワ ヘンイ SOD 1 チクセキ ケイゲン ニ ヨリ ショウホウタイ ストレス オ ケイゲン スル; Exogenous Derlin-1 ameliorates endoplasmic reticulum stress by reduction of mutant SOD1 accumulation.” Web. 18 Aug 2019.

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

Vancouver:

森, 麗; モリ . Derlin-1過剰発現は変異SOD1蓄積軽減により小胞体ストレスを軽減する : Derlin 1 カジョウ ハツゲン ワ ヘンイ SOD 1 チクセキ ケイゲン ニ ヨリ ショウホウタイ ストレス オ ケイゲン スル; Exogenous Derlin-1 ameliorates endoplasmic reticulum stress by reduction of mutant SOD1 accumulation. [Internet] [Thesis]. Kumamoto University / 熊本大学; [cited 2019 Aug 18]. Available from: http://hdl.handle.net/2298/21709.

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:

森, 麗; モリ . Derlin-1過剰発現は変異SOD1蓄積軽減により小胞体ストレスを軽減する : Derlin 1 カジョウ ハツゲン ワ ヘンイ SOD 1 チクセキ ケイゲン ニ ヨリ ショウホウタイ ストレス オ ケイゲン スル; Exogenous Derlin-1 ameliorates endoplasmic reticulum stress by reduction of mutant SOD1 accumulation. [Thesis]. Kumamoto University / 熊本大学; Available from: http://hdl.handle.net/2298/21709

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


Kyoto University

27. Murayama, Shuuhei. Development of solution NMR method for observation and analysis of proteins inside cells .

Degree: 2015, Kyoto University

Subjects/Keywords: in-cell NMR; 19F NMR; protein-drug interaction; Amyotrophic lateral sclerosis (ALS); Superoxide dismutase 1 (SOD1); disulfide bond

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

APA (6th Edition):

Murayama, S. (2015). Development of solution NMR method for observation and analysis of proteins inside cells . (Thesis). Kyoto University. Retrieved from http://hdl.handle.net/2433/199327

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):

Murayama, Shuuhei. “Development of solution NMR method for observation and analysis of proteins inside cells .” 2015. Thesis, Kyoto University. Accessed August 18, 2019. http://hdl.handle.net/2433/199327.

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

MLA Handbook (7th Edition):

Murayama, Shuuhei. “Development of solution NMR method for observation and analysis of proteins inside cells .” 2015. Web. 18 Aug 2019.

Vancouver:

Murayama S. Development of solution NMR method for observation and analysis of proteins inside cells . [Internet] [Thesis]. Kyoto University; 2015. [cited 2019 Aug 18]. Available from: http://hdl.handle.net/2433/199327.

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

Council of Science Editors:

Murayama S. Development of solution NMR method for observation and analysis of proteins inside cells . [Thesis]. Kyoto University; 2015. Available from: http://hdl.handle.net/2433/199327

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


University of Miami

28. Garcia-Chacon, Luis Ernesto. On the Role of Mitochondria in the Regulation of Calcium in Motor Nerve Terminals During Repetitive Stimulation.

Degree: PhD, Physiology and Biophysics (Medicine), 2008, University of Miami

 During repetitive stimulation of motor nerve terminals, mitochondrial Ca2+ uptake limits increases in free cytosolic [Ca2+] and helps ensure faithful neuromuscular transmission. Changes in cytosolic… (more)

Subjects/Keywords: Superoxide Dismutase; Amyotrophic Lateral Sclerosis; Levator Auris; Acetylcholine; Neurotransmitter Release; Oregon Green; Rhod; Rhodamine 123

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

APA (6th Edition):

Garcia-Chacon, L. E. (2008). On the Role of Mitochondria in the Regulation of Calcium in Motor Nerve Terminals During Repetitive Stimulation. (Doctoral Dissertation). University of Miami. Retrieved from https://scholarlyrepository.miami.edu/oa_dissertations/82

Chicago Manual of Style (16th Edition):

Garcia-Chacon, Luis Ernesto. “On the Role of Mitochondria in the Regulation of Calcium in Motor Nerve Terminals During Repetitive Stimulation.” 2008. Doctoral Dissertation, University of Miami. Accessed August 18, 2019. https://scholarlyrepository.miami.edu/oa_dissertations/82.

MLA Handbook (7th Edition):

Garcia-Chacon, Luis Ernesto. “On the Role of Mitochondria in the Regulation of Calcium in Motor Nerve Terminals During Repetitive Stimulation.” 2008. Web. 18 Aug 2019.

Vancouver:

Garcia-Chacon LE. On the Role of Mitochondria in the Regulation of Calcium in Motor Nerve Terminals During Repetitive Stimulation. [Internet] [Doctoral dissertation]. University of Miami; 2008. [cited 2019 Aug 18]. Available from: https://scholarlyrepository.miami.edu/oa_dissertations/82.

Council of Science Editors:

Garcia-Chacon LE. On the Role of Mitochondria in the Regulation of Calcium in Motor Nerve Terminals During Repetitive Stimulation. [Doctoral Dissertation]. University of Miami; 2008. Available from: https://scholarlyrepository.miami.edu/oa_dissertations/82


University of Debrecen

29. Buseinipirima, Tamunomiebaka Michael. Pharmacotherapy of Amyotrophic lateral sclerosis .

Degree: DE – Gyógyszerésztudományi Kar, University of Debrecen

 Abstract Although the exact pathway that leads to this motor neuron disease – amyotrophic lateral sclerosis remains unclear and thus the treatment is not yet… (more)

Subjects/Keywords: Amyotrophic lateral sclerosis (ALS); Superoxide dismutase 1 (SOD1); TAR DNA- binding protein 43 (TDP-43; transactive response DNA binding proteins).

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

APA (6th Edition):

Buseinipirima, T. M. (n.d.). Pharmacotherapy of Amyotrophic lateral sclerosis . (Thesis). University of Debrecen. Retrieved from http://hdl.handle.net/2437/263052

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):

Buseinipirima, Tamunomiebaka Michael. “Pharmacotherapy of Amyotrophic lateral sclerosis .” Thesis, University of Debrecen. Accessed August 18, 2019. http://hdl.handle.net/2437/263052.

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):

Buseinipirima, Tamunomiebaka Michael. “Pharmacotherapy of Amyotrophic lateral sclerosis .” Web. 18 Aug 2019.

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

Vancouver:

Buseinipirima TM. Pharmacotherapy of Amyotrophic lateral sclerosis . [Internet] [Thesis]. University of Debrecen; [cited 2019 Aug 18]. Available from: http://hdl.handle.net/2437/263052.

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:

Buseinipirima TM. Pharmacotherapy of Amyotrophic lateral sclerosis . [Thesis]. University of Debrecen; Available from: http://hdl.handle.net/2437/263052

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

30. Kayatekin, Can. The Coupling Between Folding, Zinc Binding, and Disulfide Bond Status of Human Cu, Zn Superoxide Dismutase: A Dissertation.

Degree: Biochemistry and Molecular Pharmacology, Biochemistry and Molecular Pharmacology, 2010, U of Massachusetts : Med

  Cu, Zn superoxide dismutase (SOD1) is a dimeric, β-sandwich, metalloenzyme responsible for the dismutation of superoxide. Mutations covering nearly 50% of the amino acid… (more)

Subjects/Keywords: Superoxide Dismutase; Amyotrophic Lateral Sclerosis; Zinc; Protein Folding; Proteostasis Deficiencies; Disulfides; Amino Acids, Peptides, and Proteins; Biochemical Phenomena, Metabolism, and Nutrition; Biochemistry, Biophysics, and Structural Biology; Enzymes and Coenzymes; Genetic Phenomena; Inorganic Chemicals; Nervous System Diseases; Nutritional and Metabolic Diseases; Organic Chemicals

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

APA (6th Edition):

Kayatekin, C. (2010). The Coupling Between Folding, Zinc Binding, and Disulfide Bond Status of Human Cu, Zn Superoxide Dismutase: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/515

Chicago Manual of Style (16th Edition):

Kayatekin, Can. “The Coupling Between Folding, Zinc Binding, and Disulfide Bond Status of Human Cu, Zn Superoxide Dismutase: A Dissertation.” 2010. Doctoral Dissertation, U of Massachusetts : Med. Accessed August 18, 2019. https://escholarship.umassmed.edu/gsbs_diss/515.

MLA Handbook (7th Edition):

Kayatekin, Can. “The Coupling Between Folding, Zinc Binding, and Disulfide Bond Status of Human Cu, Zn Superoxide Dismutase: A Dissertation.” 2010. Web. 18 Aug 2019.

Vancouver:

Kayatekin C. The Coupling Between Folding, Zinc Binding, and Disulfide Bond Status of Human Cu, Zn Superoxide Dismutase: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2010. [cited 2019 Aug 18]. Available from: https://escholarship.umassmed.edu/gsbs_diss/515.

Council of Science Editors:

Kayatekin C. The Coupling Between Folding, Zinc Binding, and Disulfide Bond Status of Human Cu, Zn Superoxide Dismutase: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2010. Available from: https://escholarship.umassmed.edu/gsbs_diss/515

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