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You searched for subject:( POLG ). Showing records 1 – 9 of 9 total matches.

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University of Manitoba

1. Imperial, Robin John Lester. Identification of critical residues in the carboxyl-terminal extension of the mitochondrial DNA polymerase in Saccharomyces cerevisiae.

Degree: Microbiology, 2011, University of Manitoba

 Mip1p is the highly processive monomeric mitochondrial DNA polymerase in Saccharomyces cerevisiae. Despite differences in enzyme structure, substrate topology, and possible nucleoid interactions, Mip1p continues… (more)

Subjects/Keywords: mtDNA; polymerase; polg; cte

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APA (6th Edition):

Imperial, R. J. L. (2011). Identification of critical residues in the carboxyl-terminal extension of the mitochondrial DNA polymerase in Saccharomyces cerevisiae. (Masters Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/4798

Chicago Manual of Style (16th Edition):

Imperial, Robin John Lester. “Identification of critical residues in the carboxyl-terminal extension of the mitochondrial DNA polymerase in Saccharomyces cerevisiae.” 2011. Masters Thesis, University of Manitoba. Accessed January 22, 2021. http://hdl.handle.net/1993/4798.

MLA Handbook (7th Edition):

Imperial, Robin John Lester. “Identification of critical residues in the carboxyl-terminal extension of the mitochondrial DNA polymerase in Saccharomyces cerevisiae.” 2011. Web. 22 Jan 2021.

Vancouver:

Imperial RJL. Identification of critical residues in the carboxyl-terminal extension of the mitochondrial DNA polymerase in Saccharomyces cerevisiae. [Internet] [Masters thesis]. University of Manitoba; 2011. [cited 2021 Jan 22]. Available from: http://hdl.handle.net/1993/4798.

Council of Science Editors:

Imperial RJL. Identification of critical residues in the carboxyl-terminal extension of the mitochondrial DNA polymerase in Saccharomyces cerevisiae. [Masters Thesis]. University of Manitoba; 2011. Available from: http://hdl.handle.net/1993/4798


Université Paris-Sud – Paris XI

2. Pitayu, Laras. Mitochondrial Disorders Linked to mtDNA instability : From Therapy to Mechanism : Penyakit - penyakit Mitokondria terkait ketidakstabilan mtDNA : dari Terapi Obat menuju Mekanisme Molekuler.

Degree: Docteur es, Sciences de la vie et de la santé, 2015, Université Paris-Sud – Paris XI

L’instabilité d’ADN mitochondrial (ADNmt) peut être quantitative avec la déplétion de l’ADNmt ou qualitative avec des délétions de l’ADNmt. Ces anomalies sont une des causes… (more)

Subjects/Keywords: Instabilité de l’ADNmt; POLG; Clofilium tosylate; Repositionnement thérapeutique; MtDNA instability; POLG; Clofilium tosylate; Drug repurposing; Ketidakstabilan mtDNA; POLG; Clofilium tosylate; Reorientasi penggunaan obat

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APA (6th Edition):

Pitayu, L. (2015). Mitochondrial Disorders Linked to mtDNA instability : From Therapy to Mechanism : Penyakit - penyakit Mitokondria terkait ketidakstabilan mtDNA : dari Terapi Obat menuju Mekanisme Molekuler. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2015PA112233

Chicago Manual of Style (16th Edition):

Pitayu, Laras. “Mitochondrial Disorders Linked to mtDNA instability : From Therapy to Mechanism : Penyakit - penyakit Mitokondria terkait ketidakstabilan mtDNA : dari Terapi Obat menuju Mekanisme Molekuler.” 2015. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed January 22, 2021. http://www.theses.fr/2015PA112233.

MLA Handbook (7th Edition):

Pitayu, Laras. “Mitochondrial Disorders Linked to mtDNA instability : From Therapy to Mechanism : Penyakit - penyakit Mitokondria terkait ketidakstabilan mtDNA : dari Terapi Obat menuju Mekanisme Molekuler.” 2015. Web. 22 Jan 2021.

Vancouver:

Pitayu L. Mitochondrial Disorders Linked to mtDNA instability : From Therapy to Mechanism : Penyakit - penyakit Mitokondria terkait ketidakstabilan mtDNA : dari Terapi Obat menuju Mekanisme Molekuler. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2015. [cited 2021 Jan 22]. Available from: http://www.theses.fr/2015PA112233.

Council of Science Editors:

Pitayu L. Mitochondrial Disorders Linked to mtDNA instability : From Therapy to Mechanism : Penyakit - penyakit Mitokondria terkait ketidakstabilan mtDNA : dari Terapi Obat menuju Mekanisme Molekuler. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2015. Available from: http://www.theses.fr/2015PA112233

3. Correia, Renata de Luizi. Alterações metabólicas e o papel da mitocôndria no processo de tumorigênese de astrocitomas humanos.

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

As mitocôndrias desempenham um papel fundamental na sobrevivência e morte celular. Alterações do DNA mitocondrial (DNAmt) - como, por exemplo, amplificação, mutação homoplásmica, deleção e… (more)

Subjects/Keywords: Astrocitoma; Astrocytomas; DNA mitocondrial; Fatores de transcrição mitocondrial; Mitochondrial DNA; Mitochondrial transcription factors; POLG; POLG; Sobrevida; Survival; TFAM; TFAM

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APA (6th Edition):

Correia, R. d. L. (2010). Alterações metabólicas e o papel da mitocôndria no processo de tumorigênese de astrocitomas humanos. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5138/tde-25052010-162000/ ;

Chicago Manual of Style (16th Edition):

Correia, Renata de Luizi. “Alterações metabólicas e o papel da mitocôndria no processo de tumorigênese de astrocitomas humanos.” 2010. Doctoral Dissertation, University of São Paulo. Accessed January 22, 2021. http://www.teses.usp.br/teses/disponiveis/5/5138/tde-25052010-162000/ ;.

MLA Handbook (7th Edition):

Correia, Renata de Luizi. “Alterações metabólicas e o papel da mitocôndria no processo de tumorigênese de astrocitomas humanos.” 2010. Web. 22 Jan 2021.

Vancouver:

Correia RdL. Alterações metabólicas e o papel da mitocôndria no processo de tumorigênese de astrocitomas humanos. [Internet] [Doctoral dissertation]. University of São Paulo; 2010. [cited 2021 Jan 22]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5138/tde-25052010-162000/ ;.

Council of Science Editors:

Correia RdL. Alterações metabólicas e o papel da mitocôndria no processo de tumorigênese de astrocitomas humanos. [Doctoral Dissertation]. University of São Paulo; 2010. Available from: http://www.teses.usp.br/teses/disponiveis/5/5138/tde-25052010-162000/ ;


University of Toronto

4. Liyanage, Sanduni Umayanga. TARGETING THE MITOCHONDRIAL DNA POLYMERASE GAMMA IN ACUTE MYELOID LEUKEMIA.

Degree: PhD, 2017, University of Toronto

 Part I Mitochondrial DNA (mtDNA) biosynthesis requires replication factors and adequate nucleotide pools from the mitochondria and cytoplasm. We performed gene expression profiling analysis of… (more)

Subjects/Keywords: AML; mitochondria; mtDNA; nucleoside kinase; nucleotide salvage; POLG; 0307

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APA (6th Edition):

Liyanage, S. U. (2017). TARGETING THE MITOCHONDRIAL DNA POLYMERASE GAMMA IN ACUTE MYELOID LEUKEMIA. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/80704

Chicago Manual of Style (16th Edition):

Liyanage, Sanduni Umayanga. “TARGETING THE MITOCHONDRIAL DNA POLYMERASE GAMMA IN ACUTE MYELOID LEUKEMIA.” 2017. Doctoral Dissertation, University of Toronto. Accessed January 22, 2021. http://hdl.handle.net/1807/80704.

MLA Handbook (7th Edition):

Liyanage, Sanduni Umayanga. “TARGETING THE MITOCHONDRIAL DNA POLYMERASE GAMMA IN ACUTE MYELOID LEUKEMIA.” 2017. Web. 22 Jan 2021.

Vancouver:

Liyanage SU. TARGETING THE MITOCHONDRIAL DNA POLYMERASE GAMMA IN ACUTE MYELOID LEUKEMIA. [Internet] [Doctoral dissertation]. University of Toronto; 2017. [cited 2021 Jan 22]. Available from: http://hdl.handle.net/1807/80704.

Council of Science Editors:

Liyanage SU. TARGETING THE MITOCHONDRIAL DNA POLYMERASE GAMMA IN ACUTE MYELOID LEUKEMIA. [Doctoral Dissertation]. University of Toronto; 2017. Available from: http://hdl.handle.net/1807/80704


Universitat Autònoma de Barcelona

5. Blázquez Bermejo, Cora. Estimulación de la síntesis de nucleótidos como tratamiento de los defectos en la replicación del ADN mitocondrial.

Degree: Departament de Bioquímica i Biologia Molecular, 2019, Universitat Autònoma de Barcelona

 The mitochondrial DNA depletion and multiple deletions syndrome (mtDNA) (MDDS) comprises a group of rare diseases of autosomal recessive or dominant inheritance, due to alterations… (more)

Subjects/Keywords: Adnmt; Mtdna; Tk2; Polg; Ciències de la Salut; 57

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APA (6th Edition):

Blázquez Bermejo, C. (2019). Estimulación de la síntesis de nucleótidos como tratamiento de los defectos en la replicación del ADN mitocondrial. (Thesis). Universitat Autònoma de Barcelona. Retrieved from http://hdl.handle.net/10803/670111

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):

Blázquez Bermejo, Cora. “Estimulación de la síntesis de nucleótidos como tratamiento de los defectos en la replicación del ADN mitocondrial.” 2019. Thesis, Universitat Autònoma de Barcelona. Accessed January 22, 2021. http://hdl.handle.net/10803/670111.

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

MLA Handbook (7th Edition):

Blázquez Bermejo, Cora. “Estimulación de la síntesis de nucleótidos como tratamiento de los defectos en la replicación del ADN mitocondrial.” 2019. Web. 22 Jan 2021.

Vancouver:

Blázquez Bermejo C. Estimulación de la síntesis de nucleótidos como tratamiento de los defectos en la replicación del ADN mitocondrial. [Internet] [Thesis]. Universitat Autònoma de Barcelona; 2019. [cited 2021 Jan 22]. Available from: http://hdl.handle.net/10803/670111.

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

Council of Science Editors:

Blázquez Bermejo C. Estimulación de la síntesis de nucleótidos como tratamiento de los defectos en la replicación del ADN mitocondrial. [Thesis]. Universitat Autònoma de Barcelona; 2019. Available from: http://hdl.handle.net/10803/670111

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


Tampere University

6. Nurminen, Anssi. A Bioinformatics Approach to Analyzing the Pathogenicity of Mutations by Using Protein Structure Information : A Study on DNA Polymerase Gamma .

Degree: 2018, Tampere University

 Geneettisen testauksen kustannusten laskiessa, pullonkaulaksi saatavilla olevan tiedon hyödyntämiseen on muodostumassa tietämyksemme eri geneettisten variaatioiden ja mutaatioden merkityksestä. Jokaisella henkilöllä on satoja, yksilöllisiä variaatioita perimässään… (more)

Subjects/Keywords: DNA polymeraasi gamma ; POLG ; mutaatio ; proteiinirakenne ; patogeenisyys ; DNA polymerase gamma ; mutation ; protein structure ; pathogenicity

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APA (6th Edition):

Nurminen, A. (2018). A Bioinformatics Approach to Analyzing the Pathogenicity of Mutations by Using Protein Structure Information : A Study on DNA Polymerase Gamma . (Doctoral Dissertation). Tampere University. Retrieved from https://trepo.tuni.fi/handle/10024/102657

Chicago Manual of Style (16th Edition):

Nurminen, Anssi. “A Bioinformatics Approach to Analyzing the Pathogenicity of Mutations by Using Protein Structure Information : A Study on DNA Polymerase Gamma .” 2018. Doctoral Dissertation, Tampere University. Accessed January 22, 2021. https://trepo.tuni.fi/handle/10024/102657.

MLA Handbook (7th Edition):

Nurminen, Anssi. “A Bioinformatics Approach to Analyzing the Pathogenicity of Mutations by Using Protein Structure Information : A Study on DNA Polymerase Gamma .” 2018. Web. 22 Jan 2021.

Vancouver:

Nurminen A. A Bioinformatics Approach to Analyzing the Pathogenicity of Mutations by Using Protein Structure Information : A Study on DNA Polymerase Gamma . [Internet] [Doctoral dissertation]. Tampere University; 2018. [cited 2021 Jan 22]. Available from: https://trepo.tuni.fi/handle/10024/102657.

Council of Science Editors:

Nurminen A. A Bioinformatics Approach to Analyzing the Pathogenicity of Mutations by Using Protein Structure Information : A Study on DNA Polymerase Gamma . [Doctoral Dissertation]. Tampere University; 2018. Available from: https://trepo.tuni.fi/handle/10024/102657


University of Helsinki

7. Viitanen, Janne. Folate metabolic pathways in the mitochondrial recessive ataxia syndrome.

Degree: Medicinska fakulteten, 2016, University of Helsinki

 Objective Mitochondrial recessive ataxia syndrome (MIRAS) patients' phenotypes vary from early onset epileptic seizures to late onset ataxia and neuropathy. We aim to find possible… (more)

Subjects/Keywords: mitochondrial diseases; neuromuscular diseases; human POLG protein; Ataxia Neuropathy Spectrum; phenotype; Neurology; Neurologia; Neurologi

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APA (6th Edition):

Viitanen, J. (2016). Folate metabolic pathways in the mitochondrial recessive ataxia syndrome. (Masters Thesis). University of Helsinki. Retrieved from http://hdl.handle.net/10138/164165

Chicago Manual of Style (16th Edition):

Viitanen, Janne. “Folate metabolic pathways in the mitochondrial recessive ataxia syndrome.” 2016. Masters Thesis, University of Helsinki. Accessed January 22, 2021. http://hdl.handle.net/10138/164165.

MLA Handbook (7th Edition):

Viitanen, Janne. “Folate metabolic pathways in the mitochondrial recessive ataxia syndrome.” 2016. Web. 22 Jan 2021.

Vancouver:

Viitanen J. Folate metabolic pathways in the mitochondrial recessive ataxia syndrome. [Internet] [Masters thesis]. University of Helsinki; 2016. [cited 2021 Jan 22]. Available from: http://hdl.handle.net/10138/164165.

Council of Science Editors:

Viitanen J. Folate metabolic pathways in the mitochondrial recessive ataxia syndrome. [Masters Thesis]. University of Helsinki; 2016. Available from: http://hdl.handle.net/10138/164165


Tampere University

8. Rantamäki, Maria. New hereditary ataxia-disorders in Finland .

Degree: Lääketieteen laitos - Medical School, 2009, Tampere University

 Väitöskirjatutkimuksessa kuvattiin kaksi uutta perinnöllisen ataksian tautimuotoa ja selvitettiin niiden molekyyligeneettinen syy. Ataksia on neurologinen oire, joka tarkoittaa liikkeiden hallinnan ja tasapainon heikkenemistä. Toinen tässä… (more)

Subjects/Keywords: ataksia ; perinnölliset ataksiat ; mitokondriotaudit ; MIRAS ; POLG ; hereditary ataxias ; cerebellar ataxias ; mitochondrial diseases ; MIRAS ; POLG

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APA (6th Edition):

Rantamäki, M. (2009). New hereditary ataxia-disorders in Finland . (Doctoral Dissertation). Tampere University. Retrieved from https://trepo.tuni.fi/handle/10024/66520

Chicago Manual of Style (16th Edition):

Rantamäki, Maria. “New hereditary ataxia-disorders in Finland .” 2009. Doctoral Dissertation, Tampere University. Accessed January 22, 2021. https://trepo.tuni.fi/handle/10024/66520.

MLA Handbook (7th Edition):

Rantamäki, Maria. “New hereditary ataxia-disorders in Finland .” 2009. Web. 22 Jan 2021.

Vancouver:

Rantamäki M. New hereditary ataxia-disorders in Finland . [Internet] [Doctoral dissertation]. Tampere University; 2009. [cited 2021 Jan 22]. Available from: https://trepo.tuni.fi/handle/10024/66520.

Council of Science Editors:

Rantamäki M. New hereditary ataxia-disorders in Finland . [Doctoral Dissertation]. Tampere University; 2009. Available from: https://trepo.tuni.fi/handle/10024/66520


Tampere University

9. Rovio, Anja. DNA Polymerase Gamma Mutations in Male Infertility and Ageing .

Degree: Lääketieteellisen teknologian instituutti - Institute of Medical Technology, 2006, Tampere University

 Mitokondrio on solun energiaa tuottava organelli, jolla on oma genomi, mitokondriaalinen DNA (mtDNA). Mitokondrion DNA:ta monistaa yksi ainoa polymeraasi, polymeraasi gamma (POLG). Kirjallisuudessa on kuvattu… (more)

Subjects/Keywords: polymeraasi gamma ; miehen lapsettomuus ; vanheneminen ; POLG ; male infertility ; ageing ; mtDNA mutations

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APA (6th Edition):

Rovio, A. (2006). DNA Polymerase Gamma Mutations in Male Infertility and Ageing . (Doctoral Dissertation). Tampere University. Retrieved from https://trepo.tuni.fi/handle/10024/67615

Chicago Manual of Style (16th Edition):

Rovio, Anja. “DNA Polymerase Gamma Mutations in Male Infertility and Ageing .” 2006. Doctoral Dissertation, Tampere University. Accessed January 22, 2021. https://trepo.tuni.fi/handle/10024/67615.

MLA Handbook (7th Edition):

Rovio, Anja. “DNA Polymerase Gamma Mutations in Male Infertility and Ageing .” 2006. Web. 22 Jan 2021.

Vancouver:

Rovio A. DNA Polymerase Gamma Mutations in Male Infertility and Ageing . [Internet] [Doctoral dissertation]. Tampere University; 2006. [cited 2021 Jan 22]. Available from: https://trepo.tuni.fi/handle/10024/67615.

Council of Science Editors:

Rovio A. DNA Polymerase Gamma Mutations in Male Infertility and Ageing . [Doctoral Dissertation]. Tampere University; 2006. Available from: https://trepo.tuni.fi/handle/10024/67615

.