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You searched for subject:(DSBs). Showing records 1 – 12 of 12 total matches.

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1. Ishak, Layal. Etude de la Poly(ADP-ribosyl)ation dans un contexte des cassures double-brins des ADN nucléaire et mitochondriaux chez Drosophila melanogaster : Study of Poly(ADP-ribosyl)ation in response to mitochondrial and nuclear DNA strand breaks, in Drosophila melanogaster model.

Degree: Docteur es, Physiologie et Génétique Moléculaire, 2016, Université Blaise-Pascale, Clermont-Ferrand II

L’ADN cellulaire qu’il soit nucléaire ou mitochondrial est constamment soumis à l’action de stress d’origine exogène ou même endogène à la base d’altérations plus ou… (more)

Subjects/Keywords: Poly(ADP-ribosyl)ation (PARylation); PARP; PARG; ADN; ADNmt; DSBs; Poly(ADP-ribosyl)ation; PARP; PARG; DNA; ADNmt; DSBs

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

APA (6th Edition):

Ishak, L. (2016). Etude de la Poly(ADP-ribosyl)ation dans un contexte des cassures double-brins des ADN nucléaire et mitochondriaux chez Drosophila melanogaster : Study of Poly(ADP-ribosyl)ation in response to mitochondrial and nuclear DNA strand breaks, in Drosophila melanogaster model. (Doctoral Dissertation). Université Blaise-Pascale, Clermont-Ferrand II. Retrieved from http://www.theses.fr/2016CLF22685

Chicago Manual of Style (16th Edition):

Ishak, Layal. “Etude de la Poly(ADP-ribosyl)ation dans un contexte des cassures double-brins des ADN nucléaire et mitochondriaux chez Drosophila melanogaster : Study of Poly(ADP-ribosyl)ation in response to mitochondrial and nuclear DNA strand breaks, in Drosophila melanogaster model.” 2016. Doctoral Dissertation, Université Blaise-Pascale, Clermont-Ferrand II. Accessed December 02, 2020. http://www.theses.fr/2016CLF22685.

MLA Handbook (7th Edition):

Ishak, Layal. “Etude de la Poly(ADP-ribosyl)ation dans un contexte des cassures double-brins des ADN nucléaire et mitochondriaux chez Drosophila melanogaster : Study of Poly(ADP-ribosyl)ation in response to mitochondrial and nuclear DNA strand breaks, in Drosophila melanogaster model.” 2016. Web. 02 Dec 2020.

Vancouver:

Ishak L. Etude de la Poly(ADP-ribosyl)ation dans un contexte des cassures double-brins des ADN nucléaire et mitochondriaux chez Drosophila melanogaster : Study of Poly(ADP-ribosyl)ation in response to mitochondrial and nuclear DNA strand breaks, in Drosophila melanogaster model. [Internet] [Doctoral dissertation]. Université Blaise-Pascale, Clermont-Ferrand II; 2016. [cited 2020 Dec 02]. Available from: http://www.theses.fr/2016CLF22685.

Council of Science Editors:

Ishak L. Etude de la Poly(ADP-ribosyl)ation dans un contexte des cassures double-brins des ADN nucléaire et mitochondriaux chez Drosophila melanogaster : Study of Poly(ADP-ribosyl)ation in response to mitochondrial and nuclear DNA strand breaks, in Drosophila melanogaster model. [Doctoral Dissertation]. Université Blaise-Pascale, Clermont-Ferrand II; 2016. Available from: http://www.theses.fr/2016CLF22685


University of Georgia

2. Lu, Fang. A comparative genomic study of double-strand break repair in maize and rice.

Degree: 2014, University of Georgia

 Double-strand break (DSB) repair is essential for cell survival and for the maintenance of genome integrity. In this study, we utilized I-Sce I, an endonuclease… (more)

Subjects/Keywords: Comparative genomics; Double-strand breaks(DSBs); I-SceI; Maize; Rice

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APA (6th Edition):

Lu, F. (2014). A comparative genomic study of double-strand break repair in maize and rice. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/25549

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):

Lu, Fang. “A comparative genomic study of double-strand break repair in maize and rice.” 2014. Thesis, University of Georgia. Accessed December 02, 2020. http://hdl.handle.net/10724/25549.

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

MLA Handbook (7th Edition):

Lu, Fang. “A comparative genomic study of double-strand break repair in maize and rice.” 2014. Web. 02 Dec 2020.

Vancouver:

Lu F. A comparative genomic study of double-strand break repair in maize and rice. [Internet] [Thesis]. University of Georgia; 2014. [cited 2020 Dec 02]. Available from: http://hdl.handle.net/10724/25549.

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

Council of Science Editors:

Lu F. A comparative genomic study of double-strand break repair in maize and rice. [Thesis]. University of Georgia; 2014. Available from: http://hdl.handle.net/10724/25549

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

3. Beck, Carole. Caractérisation moléculaire et cellulaire du rôle de la poly(ADP-ribose) polymérase 3 (PARP3) dans la maintenance de l'intégrité du génome : Molecular and cellular characterization of the role of the poly(ADP-ribose) polymerase 3 (PARP3) in the maintenance of genome integrity.

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie, 2016, Université de Strasbourg

La poly(ADP-ribosyl)ation est une modification post-traductionnelle des protéines par les poly(ADP-ribose) polymérases (PARPs). PARP3 a été identifiée comme un nouvel acteur de la réparation des… (more)

Subjects/Keywords: PARP3; Ku80; BRCA1; 53BP1; Modifications d’histones; DSBs; Centrosomes; Cancer du sein; PARP3; Ku80; BRCA1; 53BP1; Histone modifications; DSBs; Centrosomes; Breast cancer; 572.8; 616.99

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APA (6th Edition):

Beck, C. (2016). Caractérisation moléculaire et cellulaire du rôle de la poly(ADP-ribose) polymérase 3 (PARP3) dans la maintenance de l'intégrité du génome : Molecular and cellular characterization of the role of the poly(ADP-ribose) polymerase 3 (PARP3) in the maintenance of genome integrity. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2016STRAJ075

Chicago Manual of Style (16th Edition):

Beck, Carole. “Caractérisation moléculaire et cellulaire du rôle de la poly(ADP-ribose) polymérase 3 (PARP3) dans la maintenance de l'intégrité du génome : Molecular and cellular characterization of the role of the poly(ADP-ribose) polymerase 3 (PARP3) in the maintenance of genome integrity.” 2016. Doctoral Dissertation, Université de Strasbourg. Accessed December 02, 2020. http://www.theses.fr/2016STRAJ075.

MLA Handbook (7th Edition):

Beck, Carole. “Caractérisation moléculaire et cellulaire du rôle de la poly(ADP-ribose) polymérase 3 (PARP3) dans la maintenance de l'intégrité du génome : Molecular and cellular characterization of the role of the poly(ADP-ribose) polymerase 3 (PARP3) in the maintenance of genome integrity.” 2016. Web. 02 Dec 2020.

Vancouver:

Beck C. Caractérisation moléculaire et cellulaire du rôle de la poly(ADP-ribose) polymérase 3 (PARP3) dans la maintenance de l'intégrité du génome : Molecular and cellular characterization of the role of the poly(ADP-ribose) polymerase 3 (PARP3) in the maintenance of genome integrity. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2016. [cited 2020 Dec 02]. Available from: http://www.theses.fr/2016STRAJ075.

Council of Science Editors:

Beck C. Caractérisation moléculaire et cellulaire du rôle de la poly(ADP-ribose) polymérase 3 (PARP3) dans la maintenance de l'intégrité du génome : Molecular and cellular characterization of the role of the poly(ADP-ribose) polymerase 3 (PARP3) in the maintenance of genome integrity. [Doctoral Dissertation]. Université de Strasbourg; 2016. Available from: http://www.theses.fr/2016STRAJ075


University of Tennessee – Knoxville

4. Hsu, Shih-Jui. Functional Study of the Suppressor of Hairy-­wing Insulator Protein in Drosophila melanogaster.

Degree: 2014, University of Tennessee – Knoxville

 Eukaryotic chromatin insulators play an essential role in regulating gene expression and modifying nuclear architecture by organizing the higher-order chromatin structure in response to cellular… (more)

Subjects/Keywords: insulator; oogenesis; DSBs; ring canal; and SUMO.; Cell Biology; Developmental Biology; Genetics

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APA (6th Edition):

Hsu, S. (2014). Functional Study of the Suppressor of Hairy-­wing Insulator Protein in Drosophila melanogaster. (Doctoral Dissertation). University of Tennessee – Knoxville. Retrieved from https://trace.tennessee.edu/utk_graddiss/2763

Chicago Manual of Style (16th Edition):

Hsu, Shih-Jui. “Functional Study of the Suppressor of Hairy-­wing Insulator Protein in Drosophila melanogaster.” 2014. Doctoral Dissertation, University of Tennessee – Knoxville. Accessed December 02, 2020. https://trace.tennessee.edu/utk_graddiss/2763.

MLA Handbook (7th Edition):

Hsu, Shih-Jui. “Functional Study of the Suppressor of Hairy-­wing Insulator Protein in Drosophila melanogaster.” 2014. Web. 02 Dec 2020.

Vancouver:

Hsu S. Functional Study of the Suppressor of Hairy-­wing Insulator Protein in Drosophila melanogaster. [Internet] [Doctoral dissertation]. University of Tennessee – Knoxville; 2014. [cited 2020 Dec 02]. Available from: https://trace.tennessee.edu/utk_graddiss/2763.

Council of Science Editors:

Hsu S. Functional Study of the Suppressor of Hairy-­wing Insulator Protein in Drosophila melanogaster. [Doctoral Dissertation]. University of Tennessee – Knoxville; 2014. Available from: https://trace.tennessee.edu/utk_graddiss/2763


University of Southern California

5. Li, Angela Ying-Jian. Molecular analysis of high mobility group A2 (HMGA2) oncogenic function.

Degree: PhD, Pharmaceutical Sciences, 2008, University of Southern California

 HMGA2 is located on chromosome 12q13-15, which is frequently amplified or subjected to chromosomal rearrangements in human cancers. However, the multitudinous tumorigenic roles of HMGA2… (more)

Subjects/Keywords: HMGA2; NHEJ; DNA-PK; DSBs; hTERT; telomere

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APA (6th Edition):

Li, A. Y. (2008). Molecular analysis of high mobility group A2 (HMGA2) oncogenic function. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/86635/rec/4176

Chicago Manual of Style (16th Edition):

Li, Angela Ying-Jian. “Molecular analysis of high mobility group A2 (HMGA2) oncogenic function.” 2008. Doctoral Dissertation, University of Southern California. Accessed December 02, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/86635/rec/4176.

MLA Handbook (7th Edition):

Li, Angela Ying-Jian. “Molecular analysis of high mobility group A2 (HMGA2) oncogenic function.” 2008. Web. 02 Dec 2020.

Vancouver:

Li AY. Molecular analysis of high mobility group A2 (HMGA2) oncogenic function. [Internet] [Doctoral dissertation]. University of Southern California; 2008. [cited 2020 Dec 02]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/86635/rec/4176.

Council of Science Editors:

Li AY. Molecular analysis of high mobility group A2 (HMGA2) oncogenic function. [Doctoral Dissertation]. University of Southern California; 2008. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/86635/rec/4176

6. Shen, Mingjuan. Characterization of the novel endonuclease Sae2 involved in DNA end processing.

Degree: PhD, Cell and Molecular Biology, 2011, University of Texas – Austin

 At the very center of sexual reproduction is meiosis. During meiosis, the formation of meiotic Double-Strand-Breaks (DBSs) and their repair by homologous recombination are widely… (more)

Subjects/Keywords: Spo11; Sae2; DSBs; Meiotic recombination; Endonuclease

…meiotic DSBs, forms physical connections between homologous chromosomes. These connections are… …recombination initiates at the sites of meiotic-specific DNA DSBs (Keeney 2001). The… …SPO11 AS THE CATALYST FOR MEIOTIC DSBS In budding yeast, SPO11 was first identified in a… …thought to create DSBs by forming dimers to coordinately break both strands of a DNA molecule… …Otero 2000) have also been shown to play an essential role in meiotic DNA DSBs initiation… 

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APA (6th Edition):

Shen, M. (2011). Characterization of the novel endonuclease Sae2 involved in DNA end processing. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/ETD-UT-2011-08-4169

Chicago Manual of Style (16th Edition):

Shen, Mingjuan. “Characterization of the novel endonuclease Sae2 involved in DNA end processing.” 2011. Doctoral Dissertation, University of Texas – Austin. Accessed December 02, 2020. http://hdl.handle.net/2152/ETD-UT-2011-08-4169.

MLA Handbook (7th Edition):

Shen, Mingjuan. “Characterization of the novel endonuclease Sae2 involved in DNA end processing.” 2011. Web. 02 Dec 2020.

Vancouver:

Shen M. Characterization of the novel endonuclease Sae2 involved in DNA end processing. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2011. [cited 2020 Dec 02]. Available from: http://hdl.handle.net/2152/ETD-UT-2011-08-4169.

Council of Science Editors:

Shen M. Characterization of the novel endonuclease Sae2 involved in DNA end processing. [Doctoral Dissertation]. University of Texas – Austin; 2011. Available from: http://hdl.handle.net/2152/ETD-UT-2011-08-4169

7. De Melo, Abinadabe Jackson. Molecular basis for the structural role of human DNA ligase IV : Base moléculaire pour le rôle structural de l'ADN humain Ligase IV.

Degree: Docteur es, Biologie, 2016, Aix Marseille Université

Les défauts dans la réparation des cassures double-brin de l'ADN (DSBs) peuvent avoir d'importantes conséquences pouvant entrainer une instabilité génomique et conduire à la mort… (more)

Subjects/Keywords: Cassures double-Brin de l'ADN (DSBs); Jonction des extrémités Non Homologues (NHEJ); DNA Ligase IV; Xrcc4; Xlf; DNA double-Strand breaks (DSBs); Non-Homologous End Joining (NHEJ); DNA Ligase IV; Xrcc4; Xlf; 570

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APA (6th Edition):

De Melo, A. J. (2016). Molecular basis for the structural role of human DNA ligase IV : Base moléculaire pour le rôle structural de l'ADN humain Ligase IV. (Doctoral Dissertation). Aix Marseille Université. Retrieved from http://www.theses.fr/2016AIXM4040

Chicago Manual of Style (16th Edition):

De Melo, Abinadabe Jackson. “Molecular basis for the structural role of human DNA ligase IV : Base moléculaire pour le rôle structural de l'ADN humain Ligase IV.” 2016. Doctoral Dissertation, Aix Marseille Université. Accessed December 02, 2020. http://www.theses.fr/2016AIXM4040.

MLA Handbook (7th Edition):

De Melo, Abinadabe Jackson. “Molecular basis for the structural role of human DNA ligase IV : Base moléculaire pour le rôle structural de l'ADN humain Ligase IV.” 2016. Web. 02 Dec 2020.

Vancouver:

De Melo AJ. Molecular basis for the structural role of human DNA ligase IV : Base moléculaire pour le rôle structural de l'ADN humain Ligase IV. [Internet] [Doctoral dissertation]. Aix Marseille Université 2016. [cited 2020 Dec 02]. Available from: http://www.theses.fr/2016AIXM4040.

Council of Science Editors:

De Melo AJ. Molecular basis for the structural role of human DNA ligase IV : Base moléculaire pour le rôle structural de l'ADN humain Ligase IV. [Doctoral Dissertation]. Aix Marseille Université 2016. Available from: http://www.theses.fr/2016AIXM4040


Indian Institute of Science

8. Pandey, Monica. Understanding the Sequence Dependence of NHEJ Mediated Double-strand Break Repair, and Identification of Novel DNA Ligase Inhibitors and their Potential Use as Cancer Therapeutics.

Degree: PhD, Faculty of Science, 2018, Indian Institute of Science

 Repair of DNA breaks is essential for maintenance of genomic integrity. DNA double-strand breaks (DSBs) are considered as the most harmful DNA lesions within the… (more)

Subjects/Keywords: DNA Ligase Inhibitors; Cancer Therapeutics; DNA Double-strand Breaks (DSBs); DNA Lesions; Ligase IV/XRCC4; Ligase I Inhibitors; Nonhomologous End Joining (NHEJ); Ligase IV Inhibitor SCR7; Biochemistry

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APA (6th Edition):

Pandey, M. (2018). Understanding the Sequence Dependence of NHEJ Mediated Double-strand Break Repair, and Identification of Novel DNA Ligase Inhibitors and their Potential Use as Cancer Therapeutics. (Doctoral Dissertation). Indian Institute of Science. Retrieved from http://etd.iisc.ac.in/handle/2005/4146

Chicago Manual of Style (16th Edition):

Pandey, Monica. “Understanding the Sequence Dependence of NHEJ Mediated Double-strand Break Repair, and Identification of Novel DNA Ligase Inhibitors and their Potential Use as Cancer Therapeutics.” 2018. Doctoral Dissertation, Indian Institute of Science. Accessed December 02, 2020. http://etd.iisc.ac.in/handle/2005/4146.

MLA Handbook (7th Edition):

Pandey, Monica. “Understanding the Sequence Dependence of NHEJ Mediated Double-strand Break Repair, and Identification of Novel DNA Ligase Inhibitors and their Potential Use as Cancer Therapeutics.” 2018. Web. 02 Dec 2020.

Vancouver:

Pandey M. Understanding the Sequence Dependence of NHEJ Mediated Double-strand Break Repair, and Identification of Novel DNA Ligase Inhibitors and their Potential Use as Cancer Therapeutics. [Internet] [Doctoral dissertation]. Indian Institute of Science; 2018. [cited 2020 Dec 02]. Available from: http://etd.iisc.ac.in/handle/2005/4146.

Council of Science Editors:

Pandey M. Understanding the Sequence Dependence of NHEJ Mediated Double-strand Break Repair, and Identification of Novel DNA Ligase Inhibitors and their Potential Use as Cancer Therapeutics. [Doctoral Dissertation]. Indian Institute of Science; 2018. Available from: http://etd.iisc.ac.in/handle/2005/4146


University of Adelaide

9. Cui, Jian. Research on Compound Kushen Injection (CKI): Anti-cancer Mechanism Pathway/Network structure.

Degree: 2018, University of Adelaide

 Traditional Chinese medicine (TCM) is built on a foundation of more than 2,500 years of Chinese medical practice with most therapies relying on herbal formulae.… (more)

Subjects/Keywords: systems biology approach; TCM,; CKI; multi-target medicine; anticancer; pathway/ network research; MCF-7; MDA-MB-231; Hep G2,; cell cycle; cancer metabolism; DSBs

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APA (6th Edition):

Cui, J. (2018). Research on Compound Kushen Injection (CKI): Anti-cancer Mechanism Pathway/Network structure. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/117801

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):

Cui, Jian. “Research on Compound Kushen Injection (CKI): Anti-cancer Mechanism Pathway/Network structure.” 2018. Thesis, University of Adelaide. Accessed December 02, 2020. http://hdl.handle.net/2440/117801.

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

MLA Handbook (7th Edition):

Cui, Jian. “Research on Compound Kushen Injection (CKI): Anti-cancer Mechanism Pathway/Network structure.” 2018. Web. 02 Dec 2020.

Vancouver:

Cui J. Research on Compound Kushen Injection (CKI): Anti-cancer Mechanism Pathway/Network structure. [Internet] [Thesis]. University of Adelaide; 2018. [cited 2020 Dec 02]. Available from: http://hdl.handle.net/2440/117801.

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

Council of Science Editors:

Cui J. Research on Compound Kushen Injection (CKI): Anti-cancer Mechanism Pathway/Network structure. [Thesis]. University of Adelaide; 2018. Available from: http://hdl.handle.net/2440/117801

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


The Ohio State University

10. Qin, Song. Acetylation of histone n-terminal tails contributes to DNA double strand break repair.

Degree: PhD, Molecular, Cellular, and Developmental Biology, 2006, The Ohio State University

 Acetylation of the N-terminal tails of newly synthesized histones H3 and H4 by type-B histone acetyltransferases (HATs) is thought to play a role in chromatin… (more)

Subjects/Keywords: Biology, Molecular; HISTONE; Hat1p; histones H3; DNA; chromatin; HAT1; DSBs

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APA (6th Edition):

Qin, S. (2006). Acetylation of histone n-terminal tails contributes to DNA double strand break repair. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1134575402

Chicago Manual of Style (16th Edition):

Qin, Song. “Acetylation of histone n-terminal tails contributes to DNA double strand break repair.” 2006. Doctoral Dissertation, The Ohio State University. Accessed December 02, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1134575402.

MLA Handbook (7th Edition):

Qin, Song. “Acetylation of histone n-terminal tails contributes to DNA double strand break repair.” 2006. Web. 02 Dec 2020.

Vancouver:

Qin S. Acetylation of histone n-terminal tails contributes to DNA double strand break repair. [Internet] [Doctoral dissertation]. The Ohio State University; 2006. [cited 2020 Dec 02]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1134575402.

Council of Science Editors:

Qin S. Acetylation of histone n-terminal tails contributes to DNA double strand break repair. [Doctoral Dissertation]. The Ohio State University; 2006. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1134575402

11. 정, 지민. Identification and characterization of ubiquitin-like modifiers involved in DNA repair for maintenance of genomic stability.

Degree: 2019, Ajou University

Genetic mutations generated by intrinsic or extrinsic stimuli can result in diverse diseases, such as cancers and neurological disorders. Genomic stability is maintained by the… (more)

Subjects/Keywords: DNA damage response (DDR); Ubiquitin-like modifiers (ULMs); DNA double-strand breaks (DSBs); Autophagy-related genes (ATGs); 유전체 손상 및 복구 기전; 유비퀴틴 유사단백질 (ULMs); 유전체 이중가닥손상; 오토파지 관련 단백질 (ATGs)

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APA (6th Edition):

정, . (2019). Identification and characterization of ubiquitin-like modifiers involved in DNA repair for maintenance of genomic stability. (Thesis). Ajou University. Retrieved from http://repository.ajou.ac.kr/handle/201003/17883 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000028401

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):

정, 지민. “Identification and characterization of ubiquitin-like modifiers involved in DNA repair for maintenance of genomic stability.” 2019. Thesis, Ajou University. Accessed December 02, 2020. http://repository.ajou.ac.kr/handle/201003/17883 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000028401.

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

MLA Handbook (7th Edition):

정, 지민. “Identification and characterization of ubiquitin-like modifiers involved in DNA repair for maintenance of genomic stability.” 2019. Web. 02 Dec 2020.

Vancouver:

정 . Identification and characterization of ubiquitin-like modifiers involved in DNA repair for maintenance of genomic stability. [Internet] [Thesis]. Ajou University; 2019. [cited 2020 Dec 02]. Available from: http://repository.ajou.ac.kr/handle/201003/17883 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000028401.

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

Council of Science Editors:

정 . Identification and characterization of ubiquitin-like modifiers involved in DNA repair for maintenance of genomic stability. [Thesis]. Ajou University; 2019. Available from: http://repository.ajou.ac.kr/handle/201003/17883 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000028401

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


Indian Institute of Science

12. Mishra, Anup. Targeting RAD51C Pathological Mutants by Synthetic Lethality and Extended Functions of RAD51C/XRCC3 in Mitochondrial Genome Maintenance.

Degree: PhD, Faculty of Science, 2018, Indian Institute of Science

 To counteract the potentially calamitous effects of genomic instability in the form of double-strand breaks (DSBs), cells have evolved with two major mechanisms. First, DNA… (more)

Subjects/Keywords: DNA Single-strand Repair Pathway; Mitochondrial DNA; Nucleoid Organization; mtDNA Replisome; RAD51C/XRCC3; DNA Double-strand Breaks (DSBs); DNA Double-strand Break Repair (DSRB) Pathway; DNA Repair Pathway; PARP1 Inhibitors; Mitochondrial Genome; FANCJ DNA Helicase; RAD51; Biochemistry

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APA (6th Edition):

Mishra, A. (2018). Targeting RAD51C Pathological Mutants by Synthetic Lethality and Extended Functions of RAD51C/XRCC3 in Mitochondrial Genome Maintenance. (Doctoral Dissertation). Indian Institute of Science. Retrieved from http://etd.iisc.ac.in/handle/2005/4155

Chicago Manual of Style (16th Edition):

Mishra, Anup. “Targeting RAD51C Pathological Mutants by Synthetic Lethality and Extended Functions of RAD51C/XRCC3 in Mitochondrial Genome Maintenance.” 2018. Doctoral Dissertation, Indian Institute of Science. Accessed December 02, 2020. http://etd.iisc.ac.in/handle/2005/4155.

MLA Handbook (7th Edition):

Mishra, Anup. “Targeting RAD51C Pathological Mutants by Synthetic Lethality and Extended Functions of RAD51C/XRCC3 in Mitochondrial Genome Maintenance.” 2018. Web. 02 Dec 2020.

Vancouver:

Mishra A. Targeting RAD51C Pathological Mutants by Synthetic Lethality and Extended Functions of RAD51C/XRCC3 in Mitochondrial Genome Maintenance. [Internet] [Doctoral dissertation]. Indian Institute of Science; 2018. [cited 2020 Dec 02]. Available from: http://etd.iisc.ac.in/handle/2005/4155.

Council of Science Editors:

Mishra A. Targeting RAD51C Pathological Mutants by Synthetic Lethality and Extended Functions of RAD51C/XRCC3 in Mitochondrial Genome Maintenance. [Doctoral Dissertation]. Indian Institute of Science; 2018. Available from: http://etd.iisc.ac.in/handle/2005/4155

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