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You searched for subject:(NHEJ). Showing records 1 – 30 of 82 total matches.

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University of Illinois – Chicago

1. Summerlin, Matthew Brock. Small Molecule And Protein Modifiers of The NHEJ Pathway.

Degree: 2018, University of Illinois – Chicago

 Non-Homologous End Joining (NHEJ) is a pathway for the repair of DNA doube-strand breaks (DSBs) that is active throughout the cell cycle and does not… (more)

Subjects/Keywords: NHEJ IP6 CYREN

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

APA (6th Edition):

Summerlin, M. B. (2018). Small Molecule And Protein Modifiers of The NHEJ Pathway. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/23046

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):

Summerlin, Matthew Brock. “Small Molecule And Protein Modifiers of The NHEJ Pathway.” 2018. Thesis, University of Illinois – Chicago. Accessed April 16, 2021. http://hdl.handle.net/10027/23046.

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

MLA Handbook (7th Edition):

Summerlin, Matthew Brock. “Small Molecule And Protein Modifiers of The NHEJ Pathway.” 2018. Web. 16 Apr 2021.

Vancouver:

Summerlin MB. Small Molecule And Protein Modifiers of The NHEJ Pathway. [Internet] [Thesis]. University of Illinois – Chicago; 2018. [cited 2021 Apr 16]. Available from: http://hdl.handle.net/10027/23046.

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

Council of Science Editors:

Summerlin MB. Small Molecule And Protein Modifiers of The NHEJ Pathway. [Thesis]. University of Illinois – Chicago; 2018. Available from: http://hdl.handle.net/10027/23046

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


Kyoto University / 京都大学

2. Yousif Ashraf Siddig. Differential regulation of S-region hypermutation and class switch recombination by noncanonical functions of uracil DNA glycosylase : ウラシルDNAグリコシラーゼのnoncanonicalな機能によるS-領域超変異と クラススイッチ組み換えに対する異なる制御.

Degree: 博士(医科学), 2014, Kyoto University / 京都大学

The final publication is available at http://dx.doi.org/10.1073/pnas.1402391111. Ashraf S. Yousif, Andre Stanlie, Samiran Mondal, Tasuku Honjo, and Nasim A. Begum. Differential regulation of S-region hypermutation and class-switch recombination by noncanonical functions of uracil DNA glycosylase. PNAS 2014 111 (11) E1016-E1024; published ahead of print March 3, 2014.

新制・課程博士

甲第18464号

医科博第55号

Subjects/Keywords: AID; UNG; SHM; CSR; NHEJ

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APA (6th Edition):

Siddig, Y. A. (2014). Differential regulation of S-region hypermutation and class switch recombination by noncanonical functions of uracil DNA glycosylase : ウラシルDNAグリコシラーゼのnoncanonicalな機能によるS-領域超変異と クラススイッチ組み換えに対する異なる制御. (Thesis). Kyoto University / 京都大学. Retrieved from http://hdl.handle.net/2433/189357 ; http://dx.doi.org/10.14989/doctor.k18464

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):

Siddig, Yousif Ashraf. “Differential regulation of S-region hypermutation and class switch recombination by noncanonical functions of uracil DNA glycosylase : ウラシルDNAグリコシラーゼのnoncanonicalな機能によるS-領域超変異と クラススイッチ組み換えに対する異なる制御.” 2014. Thesis, Kyoto University / 京都大学. Accessed April 16, 2021. http://hdl.handle.net/2433/189357 ; http://dx.doi.org/10.14989/doctor.k18464.

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

MLA Handbook (7th Edition):

Siddig, Yousif Ashraf. “Differential regulation of S-region hypermutation and class switch recombination by noncanonical functions of uracil DNA glycosylase : ウラシルDNAグリコシラーゼのnoncanonicalな機能によるS-領域超変異と クラススイッチ組み換えに対する異なる制御.” 2014. Web. 16 Apr 2021.

Vancouver:

Siddig YA. Differential regulation of S-region hypermutation and class switch recombination by noncanonical functions of uracil DNA glycosylase : ウラシルDNAグリコシラーゼのnoncanonicalな機能によるS-領域超変異と クラススイッチ組み換えに対する異なる制御. [Internet] [Thesis]. Kyoto University / 京都大学; 2014. [cited 2021 Apr 16]. Available from: http://hdl.handle.net/2433/189357 ; http://dx.doi.org/10.14989/doctor.k18464.

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

Council of Science Editors:

Siddig YA. Differential regulation of S-region hypermutation and class switch recombination by noncanonical functions of uracil DNA glycosylase : ウラシルDNAグリコシラーゼのnoncanonicalな機能によるS-領域超変異と クラススイッチ組み換えに対する異なる制御. [Thesis]. Kyoto University / 京都大学; 2014. Available from: http://hdl.handle.net/2433/189357 ; http://dx.doi.org/10.14989/doctor.k18464

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


University of Southern California

3. Li, Sicong. Mechanisms of nucleases in non-homologous DNA end joining.

Degree: PhD, Genetic, Molecular and Cellular Biology, 2013, University of Southern California

 DNA double-stranded breaks (DSB) can occur through programmed mechanisms such as V(D)J recombination and class switch recombination or pathological mechanisms such as ionizing radiation. To… (more)

Subjects/Keywords: NHEJ; Artemis; nuclease; DNA repair

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APA (6th Edition):

Li, S. (2013). Mechanisms of nucleases in non-homologous DNA end joining. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/342055/rec/4018

Chicago Manual of Style (16th Edition):

Li, Sicong. “Mechanisms of nucleases in non-homologous DNA end joining.” 2013. Doctoral Dissertation, University of Southern California. Accessed April 16, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/342055/rec/4018.

MLA Handbook (7th Edition):

Li, Sicong. “Mechanisms of nucleases in non-homologous DNA end joining.” 2013. Web. 16 Apr 2021.

Vancouver:

Li S. Mechanisms of nucleases in non-homologous DNA end joining. [Internet] [Doctoral dissertation]. University of Southern California; 2013. [cited 2021 Apr 16]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/342055/rec/4018.

Council of Science Editors:

Li S. Mechanisms of nucleases in non-homologous DNA end joining. [Doctoral Dissertation]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/342055/rec/4018


McMaster University

4. Lee, KY Wilson. CHARACTERIZATION OF THE OLIGOMERIZATION OF THE HUMAN XRCC4 DNA REPAIR PROTEIN: IMPLICATIONS TO NON-HOMOLOGOUS END JOINING.

Degree: MSc, 2013, McMaster University

If not efficiently repaired, DNA double-stranded breaks can result in cell death. A major contributor to the repair of this DNA damage is the… (more)

Subjects/Keywords: XRCC4; XLF; NHEJ; DNA repair; Biochemistry; Biochemistry

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APA (6th Edition):

Lee, K. W. (2013). CHARACTERIZATION OF THE OLIGOMERIZATION OF THE HUMAN XRCC4 DNA REPAIR PROTEIN: IMPLICATIONS TO NON-HOMOLOGOUS END JOINING. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/13012

Chicago Manual of Style (16th Edition):

Lee, KY Wilson. “CHARACTERIZATION OF THE OLIGOMERIZATION OF THE HUMAN XRCC4 DNA REPAIR PROTEIN: IMPLICATIONS TO NON-HOMOLOGOUS END JOINING.” 2013. Masters Thesis, McMaster University. Accessed April 16, 2021. http://hdl.handle.net/11375/13012.

MLA Handbook (7th Edition):

Lee, KY Wilson. “CHARACTERIZATION OF THE OLIGOMERIZATION OF THE HUMAN XRCC4 DNA REPAIR PROTEIN: IMPLICATIONS TO NON-HOMOLOGOUS END JOINING.” 2013. Web. 16 Apr 2021.

Vancouver:

Lee KW. CHARACTERIZATION OF THE OLIGOMERIZATION OF THE HUMAN XRCC4 DNA REPAIR PROTEIN: IMPLICATIONS TO NON-HOMOLOGOUS END JOINING. [Internet] [Masters thesis]. McMaster University; 2013. [cited 2021 Apr 16]. Available from: http://hdl.handle.net/11375/13012.

Council of Science Editors:

Lee KW. CHARACTERIZATION OF THE OLIGOMERIZATION OF THE HUMAN XRCC4 DNA REPAIR PROTEIN: IMPLICATIONS TO NON-HOMOLOGOUS END JOINING. [Masters Thesis]. McMaster University; 2013. Available from: http://hdl.handle.net/11375/13012


Universidade Federal de Santa Maria

5. Marcos Henrique Barreta. CARACTERIZAÇÃO MOLECULAR DOS COMPONENTES DO SISTEMA ANGIOTENSINA-(1-7) DURANTE A DIVERGÊNCIA FOLICULAR E EXPRESSÃO DE GENES DE REPARO DA FITA DUPLA DE DNA EM EMBRIÕES BOVINOS.

Degree: 2012, Universidade Federal de Santa Maria

 O primeiro estudo caracterizou a expressão do receptor MAS e de enzimas responsáveis pela produção de Ang-(1-7), tais como, enzima conversora de angiotensina 2 (ACE2),… (more)

Subjects/Keywords: NHEJ; Recombinação homóloga; PEP; ECA2; MAS; MEDICINA VETERINARIA; ECA2; MAS; PEP; Homologous recombination; NHEJ

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APA (6th Edition):

Barreta, M. H. (2012). CARACTERIZAÇÃO MOLECULAR DOS COMPONENTES DO SISTEMA ANGIOTENSINA-(1-7) DURANTE A DIVERGÊNCIA FOLICULAR E EXPRESSÃO DE GENES DE REPARO DA FITA DUPLA DE DNA EM EMBRIÕES BOVINOS. (Thesis). Universidade Federal de Santa Maria. Retrieved from http://coralx.ufsm.br/tede/tde_busca/arquivo.php?codArquivo=4272

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):

Barreta, Marcos Henrique. “CARACTERIZAÇÃO MOLECULAR DOS COMPONENTES DO SISTEMA ANGIOTENSINA-(1-7) DURANTE A DIVERGÊNCIA FOLICULAR E EXPRESSÃO DE GENES DE REPARO DA FITA DUPLA DE DNA EM EMBRIÕES BOVINOS.” 2012. Thesis, Universidade Federal de Santa Maria. Accessed April 16, 2021. http://coralx.ufsm.br/tede/tde_busca/arquivo.php?codArquivo=4272.

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

MLA Handbook (7th Edition):

Barreta, Marcos Henrique. “CARACTERIZAÇÃO MOLECULAR DOS COMPONENTES DO SISTEMA ANGIOTENSINA-(1-7) DURANTE A DIVERGÊNCIA FOLICULAR E EXPRESSÃO DE GENES DE REPARO DA FITA DUPLA DE DNA EM EMBRIÕES BOVINOS.” 2012. Web. 16 Apr 2021.

Vancouver:

Barreta MH. CARACTERIZAÇÃO MOLECULAR DOS COMPONENTES DO SISTEMA ANGIOTENSINA-(1-7) DURANTE A DIVERGÊNCIA FOLICULAR E EXPRESSÃO DE GENES DE REPARO DA FITA DUPLA DE DNA EM EMBRIÕES BOVINOS. [Internet] [Thesis]. Universidade Federal de Santa Maria; 2012. [cited 2021 Apr 16]. Available from: http://coralx.ufsm.br/tede/tde_busca/arquivo.php?codArquivo=4272.

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

Council of Science Editors:

Barreta MH. CARACTERIZAÇÃO MOLECULAR DOS COMPONENTES DO SISTEMA ANGIOTENSINA-(1-7) DURANTE A DIVERGÊNCIA FOLICULAR E EXPRESSÃO DE GENES DE REPARO DA FITA DUPLA DE DNA EM EMBRIÕES BOVINOS. [Thesis]. Universidade Federal de Santa Maria; 2012. Available from: http://coralx.ufsm.br/tede/tde_busca/arquivo.php?codArquivo=4272

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

6. El Waly, Bilal. Contribution à l'étude des bases génétiques de la polymicrogyrie : Marqueurs pronostiques et prédictifs des cancers du sein - La voie de signalisation PI3K.

Degree: Docteur es, Pathologie humaine, 2012, Aix Marseille Université

La polymicrogyrie est un type de malformation corticale dans laquelle on retrouve un excès de gyrations et une surface corticale irrégulière. La polymicrogyrie peut être… (more)

Subjects/Keywords: Nhej; Polymicrogyrie; Malformation corticale; Génétique; Cortex cérébral; Nhej; Polymicrogyria; Cortical malformation; Genetics; Cerebral cortex

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APA (6th Edition):

El Waly, B. (2012). Contribution à l'étude des bases génétiques de la polymicrogyrie : Marqueurs pronostiques et prédictifs des cancers du sein - La voie de signalisation PI3K. (Doctoral Dissertation). Aix Marseille Université. Retrieved from http://www.theses.fr/2012AIXM5041

Chicago Manual of Style (16th Edition):

El Waly, Bilal. “Contribution à l'étude des bases génétiques de la polymicrogyrie : Marqueurs pronostiques et prédictifs des cancers du sein - La voie de signalisation PI3K.” 2012. Doctoral Dissertation, Aix Marseille Université. Accessed April 16, 2021. http://www.theses.fr/2012AIXM5041.

MLA Handbook (7th Edition):

El Waly, Bilal. “Contribution à l'étude des bases génétiques de la polymicrogyrie : Marqueurs pronostiques et prédictifs des cancers du sein - La voie de signalisation PI3K.” 2012. Web. 16 Apr 2021.

Vancouver:

El Waly B. Contribution à l'étude des bases génétiques de la polymicrogyrie : Marqueurs pronostiques et prédictifs des cancers du sein - La voie de signalisation PI3K. [Internet] [Doctoral dissertation]. Aix Marseille Université 2012. [cited 2021 Apr 16]. Available from: http://www.theses.fr/2012AIXM5041.

Council of Science Editors:

El Waly B. Contribution à l'étude des bases génétiques de la polymicrogyrie : Marqueurs pronostiques et prédictifs des cancers du sein - La voie de signalisation PI3K. [Doctoral Dissertation]. Aix Marseille Université 2012. Available from: http://www.theses.fr/2012AIXM5041

7. Benferhat, Karima. Etude structurale et fonctionnelle de complexes multi-protéiques impliqués dans la voie NHEJ humaine : Structural and Functional Study of Multi Protein Complexes Involved in Human non Homologous End Joining Pathway.

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie, 2018, Université Paris-Saclay (ComUE)

Chez les mammifères, la réparation des CDBs par la voie NHEJ (Non Homologous End Joining) implique plusieurs complexes multi-protéines : (i) de reconnaissance (ADN-Ku70/Ku80), (ii)… (more)

Subjects/Keywords: Réparation des CDBs d'ADN; NHEJ; Complexe de ligation; DSB repair; NHEJ; Ligation complex

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APA (6th Edition):

Benferhat, K. (2018). Etude structurale et fonctionnelle de complexes multi-protéiques impliqués dans la voie NHEJ humaine : Structural and Functional Study of Multi Protein Complexes Involved in Human non Homologous End Joining Pathway. (Doctoral Dissertation). Université Paris-Saclay (ComUE). Retrieved from http://www.theses.fr/2018SACLS271

Chicago Manual of Style (16th Edition):

Benferhat, Karima. “Etude structurale et fonctionnelle de complexes multi-protéiques impliqués dans la voie NHEJ humaine : Structural and Functional Study of Multi Protein Complexes Involved in Human non Homologous End Joining Pathway.” 2018. Doctoral Dissertation, Université Paris-Saclay (ComUE). Accessed April 16, 2021. http://www.theses.fr/2018SACLS271.

MLA Handbook (7th Edition):

Benferhat, Karima. “Etude structurale et fonctionnelle de complexes multi-protéiques impliqués dans la voie NHEJ humaine : Structural and Functional Study of Multi Protein Complexes Involved in Human non Homologous End Joining Pathway.” 2018. Web. 16 Apr 2021.

Vancouver:

Benferhat K. Etude structurale et fonctionnelle de complexes multi-protéiques impliqués dans la voie NHEJ humaine : Structural and Functional Study of Multi Protein Complexes Involved in Human non Homologous End Joining Pathway. [Internet] [Doctoral dissertation]. Université Paris-Saclay (ComUE); 2018. [cited 2021 Apr 16]. Available from: http://www.theses.fr/2018SACLS271.

Council of Science Editors:

Benferhat K. Etude structurale et fonctionnelle de complexes multi-protéiques impliqués dans la voie NHEJ humaine : Structural and Functional Study of Multi Protein Complexes Involved in Human non Homologous End Joining Pathway. [Doctoral Dissertation]. Université Paris-Saclay (ComUE); 2018. Available from: http://www.theses.fr/2018SACLS271


Université de Lorraine

8. Hoff, Grégory. Réparation des cassures double-brin et variabilité chromosomique chez Streptomyces : Double-strand break repair and chromosomal variability in Streptomyces.

Degree: Docteur es, Écotoxicologie, biodiversité, écosystèmes, 2016, Université de Lorraine

 Rayons ionisants, dessiccation, ou encore métabolites secondaires exogènes sont autant de facteurs qui peuvent engendrer des dommages à l’ADN chez les bactéries du sol, notamment… (more)

Subjects/Keywords: Streptomyces; NHEJ; Réparation de l’ADN; Cassure double-Brin; Streptomyces; NHEJ; DNA repair; Double-Strand break

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

APA (6th Edition):

Hoff, G. (2016). Réparation des cassures double-brin et variabilité chromosomique chez Streptomyces : Double-strand break repair and chromosomal variability in Streptomyces. (Doctoral Dissertation). Université de Lorraine. Retrieved from http://www.theses.fr/2016LORR0288

Chicago Manual of Style (16th Edition):

Hoff, Grégory. “Réparation des cassures double-brin et variabilité chromosomique chez Streptomyces : Double-strand break repair and chromosomal variability in Streptomyces.” 2016. Doctoral Dissertation, Université de Lorraine. Accessed April 16, 2021. http://www.theses.fr/2016LORR0288.

MLA Handbook (7th Edition):

Hoff, Grégory. “Réparation des cassures double-brin et variabilité chromosomique chez Streptomyces : Double-strand break repair and chromosomal variability in Streptomyces.” 2016. Web. 16 Apr 2021.

Vancouver:

Hoff G. Réparation des cassures double-brin et variabilité chromosomique chez Streptomyces : Double-strand break repair and chromosomal variability in Streptomyces. [Internet] [Doctoral dissertation]. Université de Lorraine; 2016. [cited 2021 Apr 16]. Available from: http://www.theses.fr/2016LORR0288.

Council of Science Editors:

Hoff G. Réparation des cassures double-brin et variabilité chromosomique chez Streptomyces : Double-strand break repair and chromosomal variability in Streptomyces. [Doctoral Dissertation]. Université de Lorraine; 2016. Available from: http://www.theses.fr/2016LORR0288

9. Gontier, Amandine. Etude d'interactions protéine-ADN : Interactions Ku70/Ku80-ADN au sein de la voie NHEJ et caractérisation d'inhibiteurs d'une interaction protéine-ADN cible dans un contexte de recherche de médicaments : Protein-DNA interaction study : Ku70/Ku80-DNA interactions in the NHEJ pathway and characterization of inhibitors of a target protein-DNA interaction in a drug search context.

Degree: Docteur es, Biochimie et biologie structurale, 2019, Université Paris-Saclay (ComUE)

 Pour qu’un organisme soit viable, il est essentiel que la molécule d’ADN soit dupliquée et transmise aux générations filles dans son intégralité avec le moins… (more)

Subjects/Keywords: SwitchSENSE; Biophysique; Ku70/80; Caractérisation de médicaments; Cristallographie; Nhej; SwitchSENSE; Nhej; Ku70/80; Drugs characterization; Biophysics; Crystallography

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APA (6th Edition):

Gontier, A. (2019). Etude d'interactions protéine-ADN : Interactions Ku70/Ku80-ADN au sein de la voie NHEJ et caractérisation d'inhibiteurs d'une interaction protéine-ADN cible dans un contexte de recherche de médicaments : Protein-DNA interaction study : Ku70/Ku80-DNA interactions in the NHEJ pathway and characterization of inhibitors of a target protein-DNA interaction in a drug search context. (Doctoral Dissertation). Université Paris-Saclay (ComUE). Retrieved from http://www.theses.fr/2019SACLS553

Chicago Manual of Style (16th Edition):

Gontier, Amandine. “Etude d'interactions protéine-ADN : Interactions Ku70/Ku80-ADN au sein de la voie NHEJ et caractérisation d'inhibiteurs d'une interaction protéine-ADN cible dans un contexte de recherche de médicaments : Protein-DNA interaction study : Ku70/Ku80-DNA interactions in the NHEJ pathway and characterization of inhibitors of a target protein-DNA interaction in a drug search context.” 2019. Doctoral Dissertation, Université Paris-Saclay (ComUE). Accessed April 16, 2021. http://www.theses.fr/2019SACLS553.

MLA Handbook (7th Edition):

Gontier, Amandine. “Etude d'interactions protéine-ADN : Interactions Ku70/Ku80-ADN au sein de la voie NHEJ et caractérisation d'inhibiteurs d'une interaction protéine-ADN cible dans un contexte de recherche de médicaments : Protein-DNA interaction study : Ku70/Ku80-DNA interactions in the NHEJ pathway and characterization of inhibitors of a target protein-DNA interaction in a drug search context.” 2019. Web. 16 Apr 2021.

Vancouver:

Gontier A. Etude d'interactions protéine-ADN : Interactions Ku70/Ku80-ADN au sein de la voie NHEJ et caractérisation d'inhibiteurs d'une interaction protéine-ADN cible dans un contexte de recherche de médicaments : Protein-DNA interaction study : Ku70/Ku80-DNA interactions in the NHEJ pathway and characterization of inhibitors of a target protein-DNA interaction in a drug search context. [Internet] [Doctoral dissertation]. Université Paris-Saclay (ComUE); 2019. [cited 2021 Apr 16]. Available from: http://www.theses.fr/2019SACLS553.

Council of Science Editors:

Gontier A. Etude d'interactions protéine-ADN : Interactions Ku70/Ku80-ADN au sein de la voie NHEJ et caractérisation d'inhibiteurs d'une interaction protéine-ADN cible dans un contexte de recherche de médicaments : Protein-DNA interaction study : Ku70/Ku80-DNA interactions in the NHEJ pathway and characterization of inhibitors of a target protein-DNA interaction in a drug search context. [Doctoral Dissertation]. Université Paris-Saclay (ComUE); 2019. Available from: http://www.theses.fr/2019SACLS553

10. Abello, Arthur. Spécialisation de Ku80c dans le couplage entre coupure et réparation de l’ADN lors des réarrangements programmés du génome chez Paramecium tetraurelia : Specialization of Ku80c in the coupling between DNA break and repair during programmed genome rearrangements in Paramecium tetraurelia.

Degree: Docteur es, Sciences de la vie et de la santé, 2019, Université Paris-Saclay (ComUE)

Au cours de son cycle sexuel, le cilié Paramecium tetraurelia procède à de massifs réarrangements programmés de son génome (RPG). Ils consistent, entre autres choses,… (more)

Subjects/Keywords: NHEJ; Réparation; Cassure double-Brin; Couplage; Paramécie; Ciliés; NHEJ; Repair; Double strand break; Coupling; Paramecia; Ciliates

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APA (6th Edition):

Abello, A. (2019). Spécialisation de Ku80c dans le couplage entre coupure et réparation de l’ADN lors des réarrangements programmés du génome chez Paramecium tetraurelia : Specialization of Ku80c in the coupling between DNA break and repair during programmed genome rearrangements in Paramecium tetraurelia. (Doctoral Dissertation). Université Paris-Saclay (ComUE). Retrieved from http://www.theses.fr/2019SACLS083

Chicago Manual of Style (16th Edition):

Abello, Arthur. “Spécialisation de Ku80c dans le couplage entre coupure et réparation de l’ADN lors des réarrangements programmés du génome chez Paramecium tetraurelia : Specialization of Ku80c in the coupling between DNA break and repair during programmed genome rearrangements in Paramecium tetraurelia.” 2019. Doctoral Dissertation, Université Paris-Saclay (ComUE). Accessed April 16, 2021. http://www.theses.fr/2019SACLS083.

MLA Handbook (7th Edition):

Abello, Arthur. “Spécialisation de Ku80c dans le couplage entre coupure et réparation de l’ADN lors des réarrangements programmés du génome chez Paramecium tetraurelia : Specialization of Ku80c in the coupling between DNA break and repair during programmed genome rearrangements in Paramecium tetraurelia.” 2019. Web. 16 Apr 2021.

Vancouver:

Abello A. Spécialisation de Ku80c dans le couplage entre coupure et réparation de l’ADN lors des réarrangements programmés du génome chez Paramecium tetraurelia : Specialization of Ku80c in the coupling between DNA break and repair during programmed genome rearrangements in Paramecium tetraurelia. [Internet] [Doctoral dissertation]. Université Paris-Saclay (ComUE); 2019. [cited 2021 Apr 16]. Available from: http://www.theses.fr/2019SACLS083.

Council of Science Editors:

Abello A. Spécialisation de Ku80c dans le couplage entre coupure et réparation de l’ADN lors des réarrangements programmés du génome chez Paramecium tetraurelia : Specialization of Ku80c in the coupling between DNA break and repair during programmed genome rearrangements in Paramecium tetraurelia. [Doctoral Dissertation]. Université Paris-Saclay (ComUE); 2019. Available from: http://www.theses.fr/2019SACLS083

11. Montagne, Audrey. Etude de l'expression d'une transposase domestiquée : SETMAR : Study of the expression of a transposase domestical : SETMAR.

Degree: Docteur es, Sciences de la vie, 2015, Université François-Rabelais de Tours

SETMAR est un gène chimérique constitué d’un domaine SET (codant des fonctions d’histone méthylase) et du domaine MAR (ayant conservé certaines fonctions de la transposase… (more)

Subjects/Keywords: Éléments transposables; SETMAR; Épissage alternatif; NHEJ; Glioblastome multiforme; Transposable elements; SETMAR; Alternative splicing; NHEJ; Glioblastoma multiforme

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APA (6th Edition):

Montagne, A. (2015). Etude de l'expression d'une transposase domestiquée : SETMAR : Study of the expression of a transposase domestical : SETMAR. (Doctoral Dissertation). Université François-Rabelais de Tours. Retrieved from http://www.theses.fr/2015TOUR4017

Chicago Manual of Style (16th Edition):

Montagne, Audrey. “Etude de l'expression d'une transposase domestiquée : SETMAR : Study of the expression of a transposase domestical : SETMAR.” 2015. Doctoral Dissertation, Université François-Rabelais de Tours. Accessed April 16, 2021. http://www.theses.fr/2015TOUR4017.

MLA Handbook (7th Edition):

Montagne, Audrey. “Etude de l'expression d'une transposase domestiquée : SETMAR : Study of the expression of a transposase domestical : SETMAR.” 2015. Web. 16 Apr 2021.

Vancouver:

Montagne A. Etude de l'expression d'une transposase domestiquée : SETMAR : Study of the expression of a transposase domestical : SETMAR. [Internet] [Doctoral dissertation]. Université François-Rabelais de Tours; 2015. [cited 2021 Apr 16]. Available from: http://www.theses.fr/2015TOUR4017.

Council of Science Editors:

Montagne A. Etude de l'expression d'une transposase domestiquée : SETMAR : Study of the expression of a transposase domestical : SETMAR. [Doctoral Dissertation]. Université François-Rabelais de Tours; 2015. Available from: http://www.theses.fr/2015TOUR4017


Université de Lorraine

12. Zhang, Lingli. Vers la compréhension des mécanismes de réparation de l'ADN chez Streptomyces : identification d'acteurs de la recombinaison : Towards the understanding of DNA repair in streptomyces : identification of DNA recombination players.

Degree: Docteur es, Écotoxicologie, biodiversité et écosystèmes, 2014, Université de Lorraine

 Les cassures double brin de l’ADN sont des dommages pouvant engendrer la mort cellulaire. Deux mécanismes majeurs sont impliqués dans leur réparation chez les bactéries… (more)

Subjects/Keywords: Streptomyces; Réparation de DSB; Recombinaison homologue; NHEJ; Streptomyces; DNA repair; Homologous recombination; NHEJ; 572.864 59; 572.877

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APA (6th Edition):

Zhang, L. (2014). Vers la compréhension des mécanismes de réparation de l'ADN chez Streptomyces : identification d'acteurs de la recombinaison : Towards the understanding of DNA repair in streptomyces : identification of DNA recombination players. (Doctoral Dissertation). Université de Lorraine. Retrieved from http://www.theses.fr/2014LORR0104

Chicago Manual of Style (16th Edition):

Zhang, Lingli. “Vers la compréhension des mécanismes de réparation de l'ADN chez Streptomyces : identification d'acteurs de la recombinaison : Towards the understanding of DNA repair in streptomyces : identification of DNA recombination players.” 2014. Doctoral Dissertation, Université de Lorraine. Accessed April 16, 2021. http://www.theses.fr/2014LORR0104.

MLA Handbook (7th Edition):

Zhang, Lingli. “Vers la compréhension des mécanismes de réparation de l'ADN chez Streptomyces : identification d'acteurs de la recombinaison : Towards the understanding of DNA repair in streptomyces : identification of DNA recombination players.” 2014. Web. 16 Apr 2021.

Vancouver:

Zhang L. Vers la compréhension des mécanismes de réparation de l'ADN chez Streptomyces : identification d'acteurs de la recombinaison : Towards the understanding of DNA repair in streptomyces : identification of DNA recombination players. [Internet] [Doctoral dissertation]. Université de Lorraine; 2014. [cited 2021 Apr 16]. Available from: http://www.theses.fr/2014LORR0104.

Council of Science Editors:

Zhang L. Vers la compréhension des mécanismes de réparation de l'ADN chez Streptomyces : identification d'acteurs de la recombinaison : Towards the understanding of DNA repair in streptomyces : identification of DNA recombination players. [Doctoral Dissertation]. Université de Lorraine; 2014. Available from: http://www.theses.fr/2014LORR0104


Université Paris-Sud – Paris XI

13. Ghezraoui, Hind. Étude du mécanisme moléculaire de formation des translocations chromosomiques dans les cellules humaines : Understanding Chromosomal Translocation Formation in Human Cells.

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie, 2015, Université Paris-Sud – Paris XI

Les translocations chromosomiques qui consistent en l’échange de morceaux de chromosomes sont une des caractéristiques génétiques de nombreux cancers. Les séquences des jonctions des chromosomes… (more)

Subjects/Keywords: NHEJ; Complexe X4/L4; Fréquence de translocation; Délétion; Microhomologies; NHEJ; X4/L4 complex; Translocation frequency; Deletion; Microhomologies

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APA (6th Edition):

Ghezraoui, H. (2015). Étude du mécanisme moléculaire de formation des translocations chromosomiques dans les cellules humaines : Understanding Chromosomal Translocation Formation in Human Cells. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2015PA11T018

Chicago Manual of Style (16th Edition):

Ghezraoui, Hind. “Étude du mécanisme moléculaire de formation des translocations chromosomiques dans les cellules humaines : Understanding Chromosomal Translocation Formation in Human Cells.” 2015. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed April 16, 2021. http://www.theses.fr/2015PA11T018.

MLA Handbook (7th Edition):

Ghezraoui, Hind. “Étude du mécanisme moléculaire de formation des translocations chromosomiques dans les cellules humaines : Understanding Chromosomal Translocation Formation in Human Cells.” 2015. Web. 16 Apr 2021.

Vancouver:

Ghezraoui H. Étude du mécanisme moléculaire de formation des translocations chromosomiques dans les cellules humaines : Understanding Chromosomal Translocation Formation in Human Cells. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2015. [cited 2021 Apr 16]. Available from: http://www.theses.fr/2015PA11T018.

Council of Science Editors:

Ghezraoui H. Étude du mécanisme moléculaire de formation des translocations chromosomiques dans les cellules humaines : Understanding Chromosomal Translocation Formation in Human Cells. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2015. Available from: http://www.theses.fr/2015PA11T018


University of Pennsylvania

14. Gigi, Vered. The Rag2 C Terminus Participates in Repair Pathway Choice in Vivo and Suppresses Lymphomagenesis.

Degree: 2014, University of Pennsylvania

 THE RAG2 C TERMINUS PARTICIPATES IN REPAIR PATHWAY CHOICE IN VIVO AND SUPPRESSES LYMPHOMAGENESIS Vered Gigi Dr. David B Roth DNA double-stranded breaks (DSBs) can… (more)

Subjects/Keywords: alternative NHEJ; classical NHEJ; DNA repair; RAG2; VDJ recombination; Allergy and Immunology; Immunology and Infectious Disease; Medical Immunology

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APA (6th Edition):

Gigi, V. (2014). The Rag2 C Terminus Participates in Repair Pathway Choice in Vivo and Suppresses Lymphomagenesis. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/1284

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):

Gigi, Vered. “The Rag2 C Terminus Participates in Repair Pathway Choice in Vivo and Suppresses Lymphomagenesis.” 2014. Thesis, University of Pennsylvania. Accessed April 16, 2021. https://repository.upenn.edu/edissertations/1284.

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

MLA Handbook (7th Edition):

Gigi, Vered. “The Rag2 C Terminus Participates in Repair Pathway Choice in Vivo and Suppresses Lymphomagenesis.” 2014. Web. 16 Apr 2021.

Vancouver:

Gigi V. The Rag2 C Terminus Participates in Repair Pathway Choice in Vivo and Suppresses Lymphomagenesis. [Internet] [Thesis]. University of Pennsylvania; 2014. [cited 2021 Apr 16]. Available from: https://repository.upenn.edu/edissertations/1284.

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

Council of Science Editors:

Gigi V. The Rag2 C Terminus Participates in Repair Pathway Choice in Vivo and Suppresses Lymphomagenesis. [Thesis]. University of Pennsylvania; 2014. Available from: https://repository.upenn.edu/edissertations/1284

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

15. Gelot, Camille. Rôle du complexe de cohésion sur la ligature d'extrémités d'ADN non homologues et la stabilité du génome : The cohesin complex protects against genome rearrangements by preventing the end-joining of distal DNA double-strand-ends.

Degree: Docteur es, Immunologie, 2014, Université Pierre et Marie Curie – Paris VI

Au cours de la réplication, la réparation des cassures double brin (CDB) par recombinaison homologue (RH), basée sur la synthèse d’ADN à partir de la… (more)

Subjects/Keywords: Cassures double-brin; Réparation; Nhej; Cohésines; Translocations; Mobilité des extrémités; DNA double-strand breaks; C-NHEJ; 616.079

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APA (6th Edition):

Gelot, C. (2014). Rôle du complexe de cohésion sur la ligature d'extrémités d'ADN non homologues et la stabilité du génome : The cohesin complex protects against genome rearrangements by preventing the end-joining of distal DNA double-strand-ends. (Doctoral Dissertation). Université Pierre et Marie Curie – Paris VI. Retrieved from http://www.theses.fr/2014PA066300

Chicago Manual of Style (16th Edition):

Gelot, Camille. “Rôle du complexe de cohésion sur la ligature d'extrémités d'ADN non homologues et la stabilité du génome : The cohesin complex protects against genome rearrangements by preventing the end-joining of distal DNA double-strand-ends.” 2014. Doctoral Dissertation, Université Pierre et Marie Curie – Paris VI. Accessed April 16, 2021. http://www.theses.fr/2014PA066300.

MLA Handbook (7th Edition):

Gelot, Camille. “Rôle du complexe de cohésion sur la ligature d'extrémités d'ADN non homologues et la stabilité du génome : The cohesin complex protects against genome rearrangements by preventing the end-joining of distal DNA double-strand-ends.” 2014. Web. 16 Apr 2021.

Vancouver:

Gelot C. Rôle du complexe de cohésion sur la ligature d'extrémités d'ADN non homologues et la stabilité du génome : The cohesin complex protects against genome rearrangements by preventing the end-joining of distal DNA double-strand-ends. [Internet] [Doctoral dissertation]. Université Pierre et Marie Curie – Paris VI; 2014. [cited 2021 Apr 16]. Available from: http://www.theses.fr/2014PA066300.

Council of Science Editors:

Gelot C. Rôle du complexe de cohésion sur la ligature d'extrémités d'ADN non homologues et la stabilité du génome : The cohesin complex protects against genome rearrangements by preventing the end-joining of distal DNA double-strand-ends. [Doctoral Dissertation]. Université Pierre et Marie Curie – Paris VI; 2014. Available from: http://www.theses.fr/2014PA066300

16. Lototska, Liudmyla. Le rôle de la protéine RAP1 dans la protection des télomères humains : Investigation into the role of human RAP1 in telomere protection.

Degree: Docteur es, Interactions moléculaires et cellulaires, 2018, Université Côte d'Azur (ComUE)

Les télomères sont des séquences d’ADN, généralement répétées en tandem, localisées à l’extrémité des chromosomes linéaires. Une des fonctions principales des télomères est de différencier… (more)

Subjects/Keywords: Télomères; RAP1; TRF2; Fusions inter-chromosomiques; Recombinaison non homologue (NHEJ); Sénescence réplicative; Telomeres; RAP1; TRF2; Chromosome fusions; NHEJ; Replicative senescence

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APA (6th Edition):

Lototska, L. (2018). Le rôle de la protéine RAP1 dans la protection des télomères humains : Investigation into the role of human RAP1 in telomere protection. (Doctoral Dissertation). Université Côte d'Azur (ComUE). Retrieved from http://www.theses.fr/2018AZUR4240

Chicago Manual of Style (16th Edition):

Lototska, Liudmyla. “Le rôle de la protéine RAP1 dans la protection des télomères humains : Investigation into the role of human RAP1 in telomere protection.” 2018. Doctoral Dissertation, Université Côte d'Azur (ComUE). Accessed April 16, 2021. http://www.theses.fr/2018AZUR4240.

MLA Handbook (7th Edition):

Lototska, Liudmyla. “Le rôle de la protéine RAP1 dans la protection des télomères humains : Investigation into the role of human RAP1 in telomere protection.” 2018. Web. 16 Apr 2021.

Vancouver:

Lototska L. Le rôle de la protéine RAP1 dans la protection des télomères humains : Investigation into the role of human RAP1 in telomere protection. [Internet] [Doctoral dissertation]. Université Côte d'Azur (ComUE); 2018. [cited 2021 Apr 16]. Available from: http://www.theses.fr/2018AZUR4240.

Council of Science Editors:

Lototska L. Le rôle de la protéine RAP1 dans la protection des télomères humains : Investigation into the role of human RAP1 in telomere protection. [Doctoral Dissertation]. Université Côte d'Azur (ComUE); 2018. Available from: http://www.theses.fr/2018AZUR4240

17. Barreta, Marcos Henrique. Caracterização molecular dos componentes do sistema angiotensina-(1-7) durante a divergência folicular e expressão de genes de reparo da fita dupla de dna em embriões bovinos.

Degree: 2012, Universidade Federal de Santa Maria; Programa de Pós-Graduação em Medicina Veterinária; UFSM; BR; Medicina Veterinária

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

The first study characterized the expression of MAS receptor and key enzymes for Ang-(1-7) production, such as,… (more)

Subjects/Keywords: MAS; ECA2; PEP; Recombinação homóloga; NHEJ; MAS; ECA2; PEP; Homologous recombination; NHEJ; CNPQ::CIENCIAS AGRARIAS::MEDICINA VETERINARIA

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APA (6th Edition):

Barreta, M. H. (2012). Caracterização molecular dos componentes do sistema angiotensina-(1-7) durante a divergência folicular e expressão de genes de reparo da fita dupla de dna em embriões bovinos. (Doctoral Dissertation). Universidade Federal de Santa Maria; Programa de Pós-Graduação em Medicina Veterinária; UFSM; BR; Medicina Veterinária. Retrieved from http://repositorio.ufsm.br/handle/1/4061

Chicago Manual of Style (16th Edition):

Barreta, Marcos Henrique. “Caracterização molecular dos componentes do sistema angiotensina-(1-7) durante a divergência folicular e expressão de genes de reparo da fita dupla de dna em embriões bovinos.” 2012. Doctoral Dissertation, Universidade Federal de Santa Maria; Programa de Pós-Graduação em Medicina Veterinária; UFSM; BR; Medicina Veterinária. Accessed April 16, 2021. http://repositorio.ufsm.br/handle/1/4061.

MLA Handbook (7th Edition):

Barreta, Marcos Henrique. “Caracterização molecular dos componentes do sistema angiotensina-(1-7) durante a divergência folicular e expressão de genes de reparo da fita dupla de dna em embriões bovinos.” 2012. Web. 16 Apr 2021.

Vancouver:

Barreta MH. Caracterização molecular dos componentes do sistema angiotensina-(1-7) durante a divergência folicular e expressão de genes de reparo da fita dupla de dna em embriões bovinos. [Internet] [Doctoral dissertation]. Universidade Federal de Santa Maria; Programa de Pós-Graduação em Medicina Veterinária; UFSM; BR; Medicina Veterinária; 2012. [cited 2021 Apr 16]. Available from: http://repositorio.ufsm.br/handle/1/4061.

Council of Science Editors:

Barreta MH. Caracterização molecular dos componentes do sistema angiotensina-(1-7) durante a divergência folicular e expressão de genes de reparo da fita dupla de dna em embriões bovinos. [Doctoral Dissertation]. Universidade Federal de Santa Maria; Programa de Pós-Graduação em Medicina Veterinária; UFSM; BR; Medicina Veterinária; 2012. Available from: http://repositorio.ufsm.br/handle/1/4061

18. Valquiria Tiago dos Santos. Estudo dos mecanismos moleculares do reparo de quebra de duplas fitas no DNA mitocondrial.

Degree: 2015, University of São Paulo

 O DNA está constantemente exposto a danos causados tanto por agentes endógenos quanto exógenos. Estes podem causar diferentes tipos de lesões incluindo modificações de bases… (more)

Subjects/Keywords: Células de mamífero; DNA mitocondrial; HR; Mitocôndria; NHEJ; Reparo; HR; Mammalian cells; Mitochondria; Mitochondrial DNA; NHEJ; Repair

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APA (6th Edition):

Santos, V. T. d. (2015). Estudo dos mecanismos moleculares do reparo de quebra de duplas fitas no DNA mitocondrial. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/46/46131/tde-23092015-142853/

Chicago Manual of Style (16th Edition):

Santos, Valquiria Tiago dos. “Estudo dos mecanismos moleculares do reparo de quebra de duplas fitas no DNA mitocondrial.” 2015. Doctoral Dissertation, University of São Paulo. Accessed April 16, 2021. http://www.teses.usp.br/teses/disponiveis/46/46131/tde-23092015-142853/.

MLA Handbook (7th Edition):

Santos, Valquiria Tiago dos. “Estudo dos mecanismos moleculares do reparo de quebra de duplas fitas no DNA mitocondrial.” 2015. Web. 16 Apr 2021.

Vancouver:

Santos VTd. Estudo dos mecanismos moleculares do reparo de quebra de duplas fitas no DNA mitocondrial. [Internet] [Doctoral dissertation]. University of São Paulo; 2015. [cited 2021 Apr 16]. Available from: http://www.teses.usp.br/teses/disponiveis/46/46131/tde-23092015-142853/.

Council of Science Editors:

Santos VTd. Estudo dos mecanismos moleculares do reparo de quebra de duplas fitas no DNA mitocondrial. [Doctoral Dissertation]. University of São Paulo; 2015. Available from: http://www.teses.usp.br/teses/disponiveis/46/46131/tde-23092015-142853/

19. Wang, Jinglong. Insights into the mechanism of DNA double-strand breaks and classic NHEJ by single-molecule magnetic tweezers : Compréhension du mécanisme de la rupture des doubles brins de l'ADN et du NHEJ classique par des pinces magnétiques à molécule unique.

Degree: Docteur es, Biologie cellulaire et moléculaire, 2019, Université de Paris (2019-....)

La réparation des coupures de double brin (DSB) de l'ADN par une jonction d'extrémité non homologue (NHEJ) nécessite de multiples protéines pour reconnaître et lier… (more)

Subjects/Keywords: Pincettes magnétiques; Étude de molécule unique; Réparation de l’ADN; NHEJ; Magnetic tweezers; Single molecule study; DNA repair; NHEJ

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APA (6th Edition):

Wang, J. (2019). Insights into the mechanism of DNA double-strand breaks and classic NHEJ by single-molecule magnetic tweezers : Compréhension du mécanisme de la rupture des doubles brins de l'ADN et du NHEJ classique par des pinces magnétiques à molécule unique. (Doctoral Dissertation). Université de Paris (2019-....). Retrieved from http://www.theses.fr/2019UNIP7063

Chicago Manual of Style (16th Edition):

Wang, Jinglong. “Insights into the mechanism of DNA double-strand breaks and classic NHEJ by single-molecule magnetic tweezers : Compréhension du mécanisme de la rupture des doubles brins de l'ADN et du NHEJ classique par des pinces magnétiques à molécule unique.” 2019. Doctoral Dissertation, Université de Paris (2019-....). Accessed April 16, 2021. http://www.theses.fr/2019UNIP7063.

MLA Handbook (7th Edition):

Wang, Jinglong. “Insights into the mechanism of DNA double-strand breaks and classic NHEJ by single-molecule magnetic tweezers : Compréhension du mécanisme de la rupture des doubles brins de l'ADN et du NHEJ classique par des pinces magnétiques à molécule unique.” 2019. Web. 16 Apr 2021.

Vancouver:

Wang J. Insights into the mechanism of DNA double-strand breaks and classic NHEJ by single-molecule magnetic tweezers : Compréhension du mécanisme de la rupture des doubles brins de l'ADN et du NHEJ classique par des pinces magnétiques à molécule unique. [Internet] [Doctoral dissertation]. Université de Paris (2019-....); 2019. [cited 2021 Apr 16]. Available from: http://www.theses.fr/2019UNIP7063.

Council of Science Editors:

Wang J. Insights into the mechanism of DNA double-strand breaks and classic NHEJ by single-molecule magnetic tweezers : Compréhension du mécanisme de la rupture des doubles brins de l'ADN et du NHEJ classique par des pinces magnétiques à molécule unique. [Doctoral Dissertation]. Université de Paris (2019-....); 2019. Available from: http://www.theses.fr/2019UNIP7063


University of California – Irvine

20. Tat, Connie. Rad52 competes with Ku70/Ku86 for binding to switch region DSB ends to modulate immunoglobulin class switch DNA recombination.

Degree: Biomedical Sciences, 2015, University of California – Irvine

 Class switch DNA recombination (CSR) diversifies the biological effector functions of antibodies and is critical for the maturation of the antibody response. This process is… (more)

Subjects/Keywords: Medicine; Microbiology; Immunology; CSR; DSB; HR; Ku70/Ku86; NHEJ; Rad52

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APA (6th Edition):

Tat, C. (2015). Rad52 competes with Ku70/Ku86 for binding to switch region DSB ends to modulate immunoglobulin class switch DNA recombination. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/03f400k9

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):

Tat, Connie. “Rad52 competes with Ku70/Ku86 for binding to switch region DSB ends to modulate immunoglobulin class switch DNA recombination.” 2015. Thesis, University of California – Irvine. Accessed April 16, 2021. http://www.escholarship.org/uc/item/03f400k9.

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

MLA Handbook (7th Edition):

Tat, Connie. “Rad52 competes with Ku70/Ku86 for binding to switch region DSB ends to modulate immunoglobulin class switch DNA recombination.” 2015. Web. 16 Apr 2021.

Vancouver:

Tat C. Rad52 competes with Ku70/Ku86 for binding to switch region DSB ends to modulate immunoglobulin class switch DNA recombination. [Internet] [Thesis]. University of California – Irvine; 2015. [cited 2021 Apr 16]. Available from: http://www.escholarship.org/uc/item/03f400k9.

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

Council of Science Editors:

Tat C. Rad52 competes with Ku70/Ku86 for binding to switch region DSB ends to modulate immunoglobulin class switch DNA recombination. [Thesis]. University of California – Irvine; 2015. Available from: http://www.escholarship.org/uc/item/03f400k9

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


University of Toronto

21. Macrae, Chloe Jean. Characterization of APLF in the Nonhomologous End-joining Pathway.

Degree: 2008, University of Toronto

Nonhomologous end-joining (NHEJ) is a major DNA double-strand break (DSB) repair pathway. NHEJ is initiated through DSB recognition by the DNA end-binding heterodimer, Ku, while… (more)

Subjects/Keywords: DNA Repair; NHEJ; 0307

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APA (6th Edition):

Macrae, C. J. (2008). Characterization of APLF in the Nonhomologous End-joining Pathway. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/10435

Chicago Manual of Style (16th Edition):

Macrae, Chloe Jean. “Characterization of APLF in the Nonhomologous End-joining Pathway.” 2008. Masters Thesis, University of Toronto. Accessed April 16, 2021. http://hdl.handle.net/1807/10435.

MLA Handbook (7th Edition):

Macrae, Chloe Jean. “Characterization of APLF in the Nonhomologous End-joining Pathway.” 2008. Web. 16 Apr 2021.

Vancouver:

Macrae CJ. Characterization of APLF in the Nonhomologous End-joining Pathway. [Internet] [Masters thesis]. University of Toronto; 2008. [cited 2021 Apr 16]. Available from: http://hdl.handle.net/1807/10435.

Council of Science Editors:

Macrae CJ. Characterization of APLF in the Nonhomologous End-joining Pathway. [Masters Thesis]. University of Toronto; 2008. Available from: http://hdl.handle.net/1807/10435


Texas Medical Center

22. Tavana, Omid. Understanding the roles of Non-homologous end joining and p53 after DNA damage.

Degree: PhD, 2012, Texas Medical Center

  The inability to maintain genomic stability and control proliferation are hallmarks of many cancers, which become exacerbated in the presence of unrepaired DNA damage.… (more)

Subjects/Keywords: DNA damage; NHEJ; p53; senescence; diabetes; Medicine and Health Sciences

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APA (6th Edition):

Tavana, O. (2012). Understanding the roles of Non-homologous end joining and p53 after DNA damage. (Doctoral Dissertation). Texas Medical Center. Retrieved from https://digitalcommons.library.tmc.edu/utgsbs_dissertations/227

Chicago Manual of Style (16th Edition):

Tavana, Omid. “Understanding the roles of Non-homologous end joining and p53 after DNA damage.” 2012. Doctoral Dissertation, Texas Medical Center. Accessed April 16, 2021. https://digitalcommons.library.tmc.edu/utgsbs_dissertations/227.

MLA Handbook (7th Edition):

Tavana, Omid. “Understanding the roles of Non-homologous end joining and p53 after DNA damage.” 2012. Web. 16 Apr 2021.

Vancouver:

Tavana O. Understanding the roles of Non-homologous end joining and p53 after DNA damage. [Internet] [Doctoral dissertation]. Texas Medical Center; 2012. [cited 2021 Apr 16]. Available from: https://digitalcommons.library.tmc.edu/utgsbs_dissertations/227.

Council of Science Editors:

Tavana O. Understanding the roles of Non-homologous end joining and p53 after DNA damage. [Doctoral Dissertation]. Texas Medical Center; 2012. Available from: https://digitalcommons.library.tmc.edu/utgsbs_dissertations/227

23. Yuan, Ying. Modulation of DNA double strand breaks end-joining pathway choice by single stranded oligonucleotides in mammalian cells : Moduler le choix de la voie de réparation des cassures doubles brins de l'ADN entre la voie classique de jonction d'extrémité non homologue et la jonction d'extrémité alternative.

Degree: Docteur es, Cancérologie, 2015, Université Toulouse III – Paul Sabatier

En réponse aux dommages de son génome, le choix par la cellule de la voie de réparation de l'ADN est un crucial par ses conséquences… (more)

Subjects/Keywords: Réparation de l'ADN; Cassures double-brin; C-NHEJ; A-EJ

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APA (6th Edition):

Yuan, Y. (2015). Modulation of DNA double strand breaks end-joining pathway choice by single stranded oligonucleotides in mammalian cells : Moduler le choix de la voie de réparation des cassures doubles brins de l'ADN entre la voie classique de jonction d'extrémité non homologue et la jonction d'extrémité alternative. (Doctoral Dissertation). Université Toulouse III – Paul Sabatier. Retrieved from http://www.theses.fr/2015TOU30091

Chicago Manual of Style (16th Edition):

Yuan, Ying. “Modulation of DNA double strand breaks end-joining pathway choice by single stranded oligonucleotides in mammalian cells : Moduler le choix de la voie de réparation des cassures doubles brins de l'ADN entre la voie classique de jonction d'extrémité non homologue et la jonction d'extrémité alternative.” 2015. Doctoral Dissertation, Université Toulouse III – Paul Sabatier. Accessed April 16, 2021. http://www.theses.fr/2015TOU30091.

MLA Handbook (7th Edition):

Yuan, Ying. “Modulation of DNA double strand breaks end-joining pathway choice by single stranded oligonucleotides in mammalian cells : Moduler le choix de la voie de réparation des cassures doubles brins de l'ADN entre la voie classique de jonction d'extrémité non homologue et la jonction d'extrémité alternative.” 2015. Web. 16 Apr 2021.

Vancouver:

Yuan Y. Modulation of DNA double strand breaks end-joining pathway choice by single stranded oligonucleotides in mammalian cells : Moduler le choix de la voie de réparation des cassures doubles brins de l'ADN entre la voie classique de jonction d'extrémité non homologue et la jonction d'extrémité alternative. [Internet] [Doctoral dissertation]. Université Toulouse III – Paul Sabatier; 2015. [cited 2021 Apr 16]. Available from: http://www.theses.fr/2015TOU30091.

Council of Science Editors:

Yuan Y. Modulation of DNA double strand breaks end-joining pathway choice by single stranded oligonucleotides in mammalian cells : Moduler le choix de la voie de réparation des cassures doubles brins de l'ADN entre la voie classique de jonction d'extrémité non homologue et la jonction d'extrémité alternative. [Doctoral Dissertation]. Université Toulouse III – Paul Sabatier; 2015. Available from: http://www.theses.fr/2015TOU30091


University of Cambridge

24. Sivapalan, Rohan Pakiaraj. Investigating the regulation of DNA non-homologous end-joining through Ku70/80 interacting factors.

Degree: PhD, 2019, University of Cambridge

 DNA double-strand breaks are the most deleterious type of DNA damage that cells experience, which makes the study of double-strand break repair extremely important. Unrepaired… (more)

Subjects/Keywords: DNA repair; DNA damage; Molecular Biology; Cancer biology; NHEJ; HR; Ku

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

APA (6th Edition):

Sivapalan, R. P. (2019). Investigating the regulation of DNA non-homologous end-joining through Ku70/80 interacting factors. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/290644

Chicago Manual of Style (16th Edition):

Sivapalan, Rohan Pakiaraj. “Investigating the regulation of DNA non-homologous end-joining through Ku70/80 interacting factors.” 2019. Doctoral Dissertation, University of Cambridge. Accessed April 16, 2021. https://www.repository.cam.ac.uk/handle/1810/290644.

MLA Handbook (7th Edition):

Sivapalan, Rohan Pakiaraj. “Investigating the regulation of DNA non-homologous end-joining through Ku70/80 interacting factors.” 2019. Web. 16 Apr 2021.

Vancouver:

Sivapalan RP. Investigating the regulation of DNA non-homologous end-joining through Ku70/80 interacting factors. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2021 Apr 16]. Available from: https://www.repository.cam.ac.uk/handle/1810/290644.

Council of Science Editors:

Sivapalan RP. Investigating the regulation of DNA non-homologous end-joining through Ku70/80 interacting factors. [Doctoral Dissertation]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/290644


IUPUI

25. Beck, Brian Douglas. Functional Analysis of Two Novel DNA Repair Factors, Metnase and Pso4.

Degree: 2008, IUPUI

Indiana University-Purdue University Indianapolis (IUPUI)

Metnase is a novel bifunctional protein that contains a SET domain and a transposase domain. Metnase contains sequence-specific DNA binding… (more)

Subjects/Keywords: Metnase; NHEJ; Pso4; DNA repair

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APA (6th Edition):

Beck, B. D. (2008). Functional Analysis of Two Novel DNA Repair Factors, Metnase and Pso4. (Thesis). IUPUI. Retrieved from http://hdl.handle.net/1805/1705

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):

Beck, Brian Douglas. “Functional Analysis of Two Novel DNA Repair Factors, Metnase and Pso4.” 2008. Thesis, IUPUI. Accessed April 16, 2021. http://hdl.handle.net/1805/1705.

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

MLA Handbook (7th Edition):

Beck, Brian Douglas. “Functional Analysis of Two Novel DNA Repair Factors, Metnase and Pso4.” 2008. Web. 16 Apr 2021.

Vancouver:

Beck BD. Functional Analysis of Two Novel DNA Repair Factors, Metnase and Pso4. [Internet] [Thesis]. IUPUI; 2008. [cited 2021 Apr 16]. Available from: http://hdl.handle.net/1805/1705.

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

Council of Science Editors:

Beck BD. Functional Analysis of Two Novel DNA Repair Factors, Metnase and Pso4. [Thesis]. IUPUI; 2008. Available from: http://hdl.handle.net/1805/1705

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


Brandeis University

26. Chu, Pingjin. Generation of 4EBP1 knock out stable HEK 293T cell lines.

Degree: 2020, Brandeis University

 Translation is complicated and poorly understood. Translation initiation is most commonly regulated by scientists. Various proteins play important roles in two types of translation initiation;… (more)

Subjects/Keywords: 4EBP; CRISPR/Cas9-coupled NHEJ repair; HEK293T cell lines

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

APA (6th Edition):

Chu, P. (2020). Generation of 4EBP1 knock out stable HEK 293T cell lines. (Thesis). Brandeis University. Retrieved from http://hdl.handle.net/10192/37513

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):

Chu, Pingjin. “Generation of 4EBP1 knock out stable HEK 293T cell lines.” 2020. Thesis, Brandeis University. Accessed April 16, 2021. http://hdl.handle.net/10192/37513.

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

MLA Handbook (7th Edition):

Chu, Pingjin. “Generation of 4EBP1 knock out stable HEK 293T cell lines.” 2020. Web. 16 Apr 2021.

Vancouver:

Chu P. Generation of 4EBP1 knock out stable HEK 293T cell lines. [Internet] [Thesis]. Brandeis University; 2020. [cited 2021 Apr 16]. Available from: http://hdl.handle.net/10192/37513.

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

Council of Science Editors:

Chu P. Generation of 4EBP1 knock out stable HEK 293T cell lines. [Thesis]. Brandeis University; 2020. Available from: http://hdl.handle.net/10192/37513

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


University of Southern California

27. Watanabe, Go. X-ray structural studies on DNA-dependent protein kinase catalytic subunit:DNA co-crystals.

Degree: PhD, Genetic, Molecular and Cellular Biology, 2017, University of Southern California

 Nonhomologous DNA end joining (NHEJ) is the major repair mechanism for double‐strand DNA breaks. One of the key components in human NHEJ is DNA‐dependent protein… (more)

Subjects/Keywords: DNA repair; NHEJ; DNA-PKcs; X-ray crystallography

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

APA (6th Edition):

Watanabe, G. (2017). X-ray structural studies on DNA-dependent protein kinase catalytic subunit:DNA co-crystals. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/583888/rec/7982

Chicago Manual of Style (16th Edition):

Watanabe, Go. “X-ray structural studies on DNA-dependent protein kinase catalytic subunit:DNA co-crystals.” 2017. Doctoral Dissertation, University of Southern California. Accessed April 16, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/583888/rec/7982.

MLA Handbook (7th Edition):

Watanabe, Go. “X-ray structural studies on DNA-dependent protein kinase catalytic subunit:DNA co-crystals.” 2017. Web. 16 Apr 2021.

Vancouver:

Watanabe G. X-ray structural studies on DNA-dependent protein kinase catalytic subunit:DNA co-crystals. [Internet] [Doctoral dissertation]. University of Southern California; 2017. [cited 2021 Apr 16]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/583888/rec/7982.

Council of Science Editors:

Watanabe G. X-ray structural studies on DNA-dependent protein kinase catalytic subunit:DNA co-crystals. [Doctoral Dissertation]. University of Southern California; 2017. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/583888/rec/7982


California State University – Northridge

28. Long, Joseph. Characterization of Chromosomal Alterations Using a Zinc-Finger Nuclease Targeting the Beta-globin Gene Locus in Hematopoietic Stem/Progenitor Cells.

Degree: MS, Biology, 7, California State University – Northridge

 The use of engineered nucleases for targeted gene correction of the sickle mutation in hematopoietic stem and progenitor cells (HSPCs) combined with a homologous DNA… (more)

Subjects/Keywords: NHEJ; Dissertations, Academic  – CSUN  – Biology.

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APA (6th Edition):

Long, J. (7). Characterization of Chromosomal Alterations Using a Zinc-Finger Nuclease Targeting the Beta-globin Gene Locus in Hematopoietic Stem/Progenitor Cells. (Masters Thesis). California State University – Northridge. Retrieved from http://hdl.handle.net/10211.3/193728

Chicago Manual of Style (16th Edition):

Long, Joseph. “Characterization of Chromosomal Alterations Using a Zinc-Finger Nuclease Targeting the Beta-globin Gene Locus in Hematopoietic Stem/Progenitor Cells.” 7. Masters Thesis, California State University – Northridge. Accessed April 16, 2021. http://hdl.handle.net/10211.3/193728.

MLA Handbook (7th Edition):

Long, Joseph. “Characterization of Chromosomal Alterations Using a Zinc-Finger Nuclease Targeting the Beta-globin Gene Locus in Hematopoietic Stem/Progenitor Cells.” 7. Web. 16 Apr 2021.

Vancouver:

Long J. Characterization of Chromosomal Alterations Using a Zinc-Finger Nuclease Targeting the Beta-globin Gene Locus in Hematopoietic Stem/Progenitor Cells. [Internet] [Masters thesis]. California State University – Northridge; 7. [cited 2021 Apr 16]. Available from: http://hdl.handle.net/10211.3/193728.

Council of Science Editors:

Long J. Characterization of Chromosomal Alterations Using a Zinc-Finger Nuclease Targeting the Beta-globin Gene Locus in Hematopoietic Stem/Progenitor Cells. [Masters Thesis]. California State University – Northridge; 7. Available from: http://hdl.handle.net/10211.3/193728


University of Cambridge

29. Sivapalan, Rohan Pakiaraj. Investigating the regulation of DNA non-homologous end-joining through Ku70/80 interacting factors.

Degree: PhD, 2019, University of Cambridge

 DNA double-strand breaks are the most deleterious type of DNA damage that cells experience, which makes the study of double-strand break repair extremely important. Unrepaired… (more)

Subjects/Keywords: DNA repair; DNA damage; Molecular Biology; Cancer biology; NHEJ; HR; Ku

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Sivapalan, R. P. (2019). Investigating the regulation of DNA non-homologous end-joining through Ku70/80 interacting factors. (Doctoral Dissertation). University of Cambridge. Retrieved from https://doi.org/10.17863/CAM.37852 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.774623

Chicago Manual of Style (16th Edition):

Sivapalan, Rohan Pakiaraj. “Investigating the regulation of DNA non-homologous end-joining through Ku70/80 interacting factors.” 2019. Doctoral Dissertation, University of Cambridge. Accessed April 16, 2021. https://doi.org/10.17863/CAM.37852 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.774623.

MLA Handbook (7th Edition):

Sivapalan, Rohan Pakiaraj. “Investigating the regulation of DNA non-homologous end-joining through Ku70/80 interacting factors.” 2019. Web. 16 Apr 2021.

Vancouver:

Sivapalan RP. Investigating the regulation of DNA non-homologous end-joining through Ku70/80 interacting factors. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2021 Apr 16]. Available from: https://doi.org/10.17863/CAM.37852 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.774623.

Council of Science Editors:

Sivapalan RP. Investigating the regulation of DNA non-homologous end-joining through Ku70/80 interacting factors. [Doctoral Dissertation]. University of Cambridge; 2019. Available from: https://doi.org/10.17863/CAM.37852 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.774623


Kyoto University

30. Yousif Ashraf Siddig. Differential regulation of S-region hypermutation and class switch recombination by noncanonical functions of uracil DNA glycosylase .

Degree: 2014, Kyoto University

Subjects/Keywords: AID; UNG; SHM; CSR; NHEJ

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

APA (6th Edition):

Siddig, Y. A. (2014). Differential regulation of S-region hypermutation and class switch recombination by noncanonical functions of uracil DNA glycosylase . (Thesis). Kyoto University. Retrieved from http://hdl.handle.net/2433/189357

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):

Siddig, Yousif Ashraf. “Differential regulation of S-region hypermutation and class switch recombination by noncanonical functions of uracil DNA glycosylase .” 2014. Thesis, Kyoto University. Accessed April 16, 2021. http://hdl.handle.net/2433/189357.

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

MLA Handbook (7th Edition):

Siddig, Yousif Ashraf. “Differential regulation of S-region hypermutation and class switch recombination by noncanonical functions of uracil DNA glycosylase .” 2014. Web. 16 Apr 2021.

Vancouver:

Siddig YA. Differential regulation of S-region hypermutation and class switch recombination by noncanonical functions of uracil DNA glycosylase . [Internet] [Thesis]. Kyoto University; 2014. [cited 2021 Apr 16]. Available from: http://hdl.handle.net/2433/189357.

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

Council of Science Editors:

Siddig YA. Differential regulation of S-region hypermutation and class switch recombination by noncanonical functions of uracil DNA glycosylase . [Thesis]. Kyoto University; 2014. Available from: http://hdl.handle.net/2433/189357

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

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