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You searched for subject:(replication inhibitor). Showing records 1 – 15 of 15 total matches.

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Vanderbilt University

1. Luzwick, Jessica Whitney. Regulation of the ATR Pathway in the Replication Stress Response.

Degree: PhD, Biochemistry, 2016, Vanderbilt University

 Every cell divisions cycle, over 6.8 billion base pairs of DNA must be accurately replicated. To further complicate this process, the DNA is damaged at… (more)

Subjects/Keywords: replication; ATR inhibitor; DNA damage response; replication stress; ATR; ATRIP

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APA (6th Edition):

Luzwick, J. W. (2016). Regulation of the ATR Pathway in the Replication Stress Response. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-07152016-092619/ ;

Chicago Manual of Style (16th Edition):

Luzwick, Jessica Whitney. “Regulation of the ATR Pathway in the Replication Stress Response.” 2016. Doctoral Dissertation, Vanderbilt University. Accessed January 18, 2020. http://etd.library.vanderbilt.edu/available/etd-07152016-092619/ ;.

MLA Handbook (7th Edition):

Luzwick, Jessica Whitney. “Regulation of the ATR Pathway in the Replication Stress Response.” 2016. Web. 18 Jan 2020.

Vancouver:

Luzwick JW. Regulation of the ATR Pathway in the Replication Stress Response. [Internet] [Doctoral dissertation]. Vanderbilt University; 2016. [cited 2020 Jan 18]. Available from: http://etd.library.vanderbilt.edu/available/etd-07152016-092619/ ;.

Council of Science Editors:

Luzwick JW. Regulation of the ATR Pathway in the Replication Stress Response. [Doctoral Dissertation]. Vanderbilt University; 2016. Available from: http://etd.library.vanderbilt.edu/available/etd-07152016-092619/ ;

2. Kalu, Nene Nwocha. Pharmacologically-induced cellular stress and herpesvirus replication.

Degree: 2014, Johns Hopkins University

 Herpesviruses are a family of DNA viruses that infect > 90% of the human population. The three classes of herpesviruses (alpha, beta and gamma) exhibit… (more)

Subjects/Keywords: Herpesvirus; Kaposi sarcoma; Nelfinavir; HIV protease inhibitor; Replication

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APA (6th Edition):

Kalu, N. N. (2014). Pharmacologically-induced cellular stress and herpesvirus replication. (Thesis). Johns Hopkins University. Retrieved from http://jhir.library.jhu.edu/handle/1774.2/37165

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):

Kalu, Nene Nwocha. “Pharmacologically-induced cellular stress and herpesvirus replication.” 2014. Thesis, Johns Hopkins University. Accessed January 18, 2020. http://jhir.library.jhu.edu/handle/1774.2/37165.

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

MLA Handbook (7th Edition):

Kalu, Nene Nwocha. “Pharmacologically-induced cellular stress and herpesvirus replication.” 2014. Web. 18 Jan 2020.

Vancouver:

Kalu NN. Pharmacologically-induced cellular stress and herpesvirus replication. [Internet] [Thesis]. Johns Hopkins University; 2014. [cited 2020 Jan 18]. Available from: http://jhir.library.jhu.edu/handle/1774.2/37165.

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

Council of Science Editors:

Kalu NN. Pharmacologically-induced cellular stress and herpesvirus replication. [Thesis]. Johns Hopkins University; 2014. Available from: http://jhir.library.jhu.edu/handle/1774.2/37165

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


University of Missouri – Columbia

3. Adedeji, Adeyemi. Mechanistic inhibition studies of SARS-CoV replication and entry.

Degree: 2012, University of Missouri – Columbia

 [ACCESS RESTRICTED TO THE UNIVERSITY OF MISSOURI AT AUTHOR'S REQUEST.] Severe acute respiratory syndrome (SARS) is an infectious and highly contagious disease that is caused… (more)

Subjects/Keywords: severe acute respiratory syndrome; helicase; nsp13; replication inhibitor

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APA (6th Edition):

Adedeji, A. (2012). Mechanistic inhibition studies of SARS-CoV replication and entry. (Thesis). University of Missouri – Columbia. Retrieved from http://hdl.handle.net/10355/36757

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):

Adedeji, Adeyemi. “Mechanistic inhibition studies of SARS-CoV replication and entry.” 2012. Thesis, University of Missouri – Columbia. Accessed January 18, 2020. http://hdl.handle.net/10355/36757.

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

MLA Handbook (7th Edition):

Adedeji, Adeyemi. “Mechanistic inhibition studies of SARS-CoV replication and entry.” 2012. Web. 18 Jan 2020.

Vancouver:

Adedeji A. Mechanistic inhibition studies of SARS-CoV replication and entry. [Internet] [Thesis]. University of Missouri – Columbia; 2012. [cited 2020 Jan 18]. Available from: http://hdl.handle.net/10355/36757.

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

Council of Science Editors:

Adedeji A. Mechanistic inhibition studies of SARS-CoV replication and entry. [Thesis]. University of Missouri – Columbia; 2012. Available from: http://hdl.handle.net/10355/36757

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


University of Helsinki

4. Lillsunde, Katja-Emilia. Screening for marine-derived inhibitors of Chikungunya virus replication.

Degree: Farmaceutiska fakulteten, 2013, University of Helsinki

There is currently no vaccine or specific treatment available for diseases caused by alphaviruses. Marine organisms have attracted interest for the past decades as unexplored… (more)

Subjects/Keywords: Chikungunya; replikationsinhibitor; havsorganismer; sållning; antiviral; replication inhibitor; marine organisms; screening; Farmakognosi; Pharmacognosy; Farmakognosia; Chikungunya; replikationsinhibitor; havsorganismer; sållning; antiviral; replication inhibitor; marine organisms; screening

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APA (6th Edition):

Lillsunde, K. (2013). Screening for marine-derived inhibitors of Chikungunya virus replication. (Masters Thesis). University of Helsinki. Retrieved from http://hdl.handle.net/10138/38114

Chicago Manual of Style (16th Edition):

Lillsunde, Katja-Emilia. “Screening for marine-derived inhibitors of Chikungunya virus replication.” 2013. Masters Thesis, University of Helsinki. Accessed January 18, 2020. http://hdl.handle.net/10138/38114.

MLA Handbook (7th Edition):

Lillsunde, Katja-Emilia. “Screening for marine-derived inhibitors of Chikungunya virus replication.” 2013. Web. 18 Jan 2020.

Vancouver:

Lillsunde K. Screening for marine-derived inhibitors of Chikungunya virus replication. [Internet] [Masters thesis]. University of Helsinki; 2013. [cited 2020 Jan 18]. Available from: http://hdl.handle.net/10138/38114.

Council of Science Editors:

Lillsunde K. Screening for marine-derived inhibitors of Chikungunya virus replication. [Masters Thesis]. University of Helsinki; 2013. Available from: http://hdl.handle.net/10138/38114

5. Schiralli, Gillian M. A Novel Role For ITK, A Tec Family Tyrosine Kinase in HIV-1 Replication.

Degree: PhD, Immunology and Infectious Diseases, 2009, Penn State University

 HIV is highly dependent on T cell activation for its replication. The virus has evolved to hijack host machinery and signals to facilitate its entry,… (more)

Subjects/Keywords: HIV replication; ITK; Kinase inhibitor

…70 Fig. 3‐5: Inhibition of ITK by the chemical inhibitor BMS509744 disrupts co… …chemical inhibitor disrupts co‐localization with Gag in Jurkat T cells .72 Fig. 3‐7… …Inhibition of ITK by the chemical inhibitor BMS509744 disrupts F‐actin polymerization in infected… …inhibits HIV replication ….105 Fig. B‐1: Schematic of protocol for in… …114 viii Fig. D‐2: The inhibition of ITK by chemical inhibitor BMS509744 disrupts… 

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APA (6th Edition):

Schiralli, G. M. (2009). A Novel Role For ITK, A Tec Family Tyrosine Kinase in HIV-1 Replication. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/9456

Chicago Manual of Style (16th Edition):

Schiralli, Gillian M. “A Novel Role For ITK, A Tec Family Tyrosine Kinase in HIV-1 Replication.” 2009. Doctoral Dissertation, Penn State University. Accessed January 18, 2020. https://etda.libraries.psu.edu/catalog/9456.

MLA Handbook (7th Edition):

Schiralli, Gillian M. “A Novel Role For ITK, A Tec Family Tyrosine Kinase in HIV-1 Replication.” 2009. Web. 18 Jan 2020.

Vancouver:

Schiralli GM. A Novel Role For ITK, A Tec Family Tyrosine Kinase in HIV-1 Replication. [Internet] [Doctoral dissertation]. Penn State University; 2009. [cited 2020 Jan 18]. Available from: https://etda.libraries.psu.edu/catalog/9456.

Council of Science Editors:

Schiralli GM. A Novel Role For ITK, A Tec Family Tyrosine Kinase in HIV-1 Replication. [Doctoral Dissertation]. Penn State University; 2009. Available from: https://etda.libraries.psu.edu/catalog/9456


University of Helsinki

6. Jokinen, Nora. Assay optimization and screening for hepatitis C virus replication inhibitors from marine-derived substances.

Degree: Farmaceutiska fakulteten, 2013, University of Helsinki

 Maailmassa on arviolta 180 miljoonaa hepatiitti C -viruksen kantajaa. C-hepatiitti aiheuttaa usein oireettomia maksasairauksia. Krooniset infektiot voivat aiheuttaa maksakirroosia, johtaa elinsiirtoon tai maksasyöpään. Lääkkeiden kehitys… (more)

Subjects/Keywords: Hepatitis C virus; replication inhibitor; antiviral screening; cell-based assay; luciferase reporter; Farmakognosi; Pharmacognosy; Farmakognosia

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APA (6th Edition):

Jokinen, N. (2013). Assay optimization and screening for hepatitis C virus replication inhibitors from marine-derived substances. (Masters Thesis). University of Helsinki. Retrieved from http://hdl.handle.net/10138/40773

Chicago Manual of Style (16th Edition):

Jokinen, Nora. “Assay optimization and screening for hepatitis C virus replication inhibitors from marine-derived substances.” 2013. Masters Thesis, University of Helsinki. Accessed January 18, 2020. http://hdl.handle.net/10138/40773.

MLA Handbook (7th Edition):

Jokinen, Nora. “Assay optimization and screening for hepatitis C virus replication inhibitors from marine-derived substances.” 2013. Web. 18 Jan 2020.

Vancouver:

Jokinen N. Assay optimization and screening for hepatitis C virus replication inhibitors from marine-derived substances. [Internet] [Masters thesis]. University of Helsinki; 2013. [cited 2020 Jan 18]. Available from: http://hdl.handle.net/10138/40773.

Council of Science Editors:

Jokinen N. Assay optimization and screening for hepatitis C virus replication inhibitors from marine-derived substances. [Masters Thesis]. University of Helsinki; 2013. Available from: http://hdl.handle.net/10138/40773

7. Tran, Tuan Anh. Screening against the dengue virus polymerase : Criblage contre la polymérase du virus de la dengue.

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

La dengue, une des maladies les plus largement émergents actuellement, avec 390 millions d'infections chaque année (OMS), est causée par le virus de la dengue… (more)

Subjects/Keywords: Virus de la dengue; Ns5; Polymérase; Réplication; Inhibiteur; Picogreen; Dengue virus; Ns5; Polymerase; Replication; Inhibitor; Picogreen; 570

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APA (6th Edition):

Tran, T. A. (2016). Screening against the dengue virus polymerase : Criblage contre la polymérase du virus de la dengue. (Doctoral Dissertation). Aix Marseille Université. Retrieved from http://www.theses.fr/2016AIXM4006

Chicago Manual of Style (16th Edition):

Tran, Tuan Anh. “Screening against the dengue virus polymerase : Criblage contre la polymérase du virus de la dengue.” 2016. Doctoral Dissertation, Aix Marseille Université. Accessed January 18, 2020. http://www.theses.fr/2016AIXM4006.

MLA Handbook (7th Edition):

Tran, Tuan Anh. “Screening against the dengue virus polymerase : Criblage contre la polymérase du virus de la dengue.” 2016. Web. 18 Jan 2020.

Vancouver:

Tran TA. Screening against the dengue virus polymerase : Criblage contre la polymérase du virus de la dengue. [Internet] [Doctoral dissertation]. Aix Marseille Université 2016. [cited 2020 Jan 18]. Available from: http://www.theses.fr/2016AIXM4006.

Council of Science Editors:

Tran TA. Screening against the dengue virus polymerase : Criblage contre la polymérase du virus de la dengue. [Doctoral Dissertation]. Aix Marseille Université 2016. Available from: http://www.theses.fr/2016AIXM4006


University of Oxford

8. Pfister, Sophia Xiao. The three methyls : the function and therapeutic potential of histone H3K36 trimethylation.

Degree: PhD, 2014, University of Oxford

 DNA is wrapped around proteins called histones, whose modification regulates numerous cellular processes. Therefore it is not surprising that mutations in the genes that modify… (more)

Subjects/Keywords: 616.99; Medical Sciences; Biology (medical sciences); DNA damage signalling; Oncology; Radiation; Tumours; cancer; personalised cancer therapy; synthetic lethality; epigenetics; histone modification; H3K36me3; WEE1 inhibitor; ATR inhibitor; CHK1 inhibitor; DNA replication; DNA damage; homologous recombination

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APA (6th Edition):

Pfister, S. X. (2014). The three methyls : the function and therapeutic potential of histone H3K36 trimethylation. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:83cfd649-b75c-49f6-b881-1c1e96cafb08 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.658441

Chicago Manual of Style (16th Edition):

Pfister, Sophia Xiao. “The three methyls : the function and therapeutic potential of histone H3K36 trimethylation.” 2014. Doctoral Dissertation, University of Oxford. Accessed January 18, 2020. http://ora.ox.ac.uk/objects/uuid:83cfd649-b75c-49f6-b881-1c1e96cafb08 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.658441.

MLA Handbook (7th Edition):

Pfister, Sophia Xiao. “The three methyls : the function and therapeutic potential of histone H3K36 trimethylation.” 2014. Web. 18 Jan 2020.

Vancouver:

Pfister SX. The three methyls : the function and therapeutic potential of histone H3K36 trimethylation. [Internet] [Doctoral dissertation]. University of Oxford; 2014. [cited 2020 Jan 18]. Available from: http://ora.ox.ac.uk/objects/uuid:83cfd649-b75c-49f6-b881-1c1e96cafb08 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.658441.

Council of Science Editors:

Pfister SX. The three methyls : the function and therapeutic potential of histone H3K36 trimethylation. [Doctoral Dissertation]. University of Oxford; 2014. Available from: http://ora.ox.ac.uk/objects/uuid:83cfd649-b75c-49f6-b881-1c1e96cafb08 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.658441

9. Born, Erwin van den. RNA structures regulating nidovirus RNA synthesis.

Degree: 2006, Dept. of Medical Microbiology, Faculty of Medicine, LUMC, Leiden University

 Viruses depend on their host cell for the production of their progeny. The genetic information that is required to regulate this process is contained in… (more)

Subjects/Keywords: Discontinuous RNA synthesis; Arterivirus; Transcription; Hairpin; Inhibitor; SARS; Morpholino; Replication; Coronavirus; Discontinuous RNA synthesis; Arterivirus; Transcription; Hairpin; Inhibitor; SARS; Morpholino; Replication; Coronavirus

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APA (6th Edition):

Born, E. v. d. (2006). RNA structures regulating nidovirus RNA synthesis. (Doctoral Dissertation). Dept. of Medical Microbiology, Faculty of Medicine, LUMC, Leiden University. Retrieved from http://hdl.handle.net/1887/4285

Chicago Manual of Style (16th Edition):

Born, Erwin van den. “RNA structures regulating nidovirus RNA synthesis.” 2006. Doctoral Dissertation, Dept. of Medical Microbiology, Faculty of Medicine, LUMC, Leiden University. Accessed January 18, 2020. http://hdl.handle.net/1887/4285.

MLA Handbook (7th Edition):

Born, Erwin van den. “RNA structures regulating nidovirus RNA synthesis.” 2006. Web. 18 Jan 2020.

Vancouver:

Born Evd. RNA structures regulating nidovirus RNA synthesis. [Internet] [Doctoral dissertation]. Dept. of Medical Microbiology, Faculty of Medicine, LUMC, Leiden University; 2006. [cited 2020 Jan 18]. Available from: http://hdl.handle.net/1887/4285.

Council of Science Editors:

Born Evd. RNA structures regulating nidovirus RNA synthesis. [Doctoral Dissertation]. Dept. of Medical Microbiology, Faculty of Medicine, LUMC, Leiden University; 2006. Available from: http://hdl.handle.net/1887/4285

10. Kooloos, Wouter Michiel. Potential role of pharmacogenetics for optimalization of drug therapy in rheumatoid arthritis.

Degree: 2009, Department of Clinical Pharmacy & Toxicology, Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University

 Results from this thesis have elucidated potential genetic markers, which were associated with treatment outcome to MTX and adalimumab. Furthermore, a model for predicting the… (more)

Subjects/Keywords: Adalimumab; Functionality; Methotrexate; Pharmacogenetics; Pharmacogenomics; Replication; Rheumatoid arthritis; Single nucleotide polymorphisms; TNF inhibitor; Adalimumab; Functionality; Methotrexate; Pharmacogenetics; Pharmacogenomics; Replication; Rheumatoid arthritis; Single nucleotide polymorphisms; TNF inhibitor

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APA (6th Edition):

Kooloos, W. M. (2009). Potential role of pharmacogenetics for optimalization of drug therapy in rheumatoid arthritis. (Doctoral Dissertation). Department of Clinical Pharmacy & Toxicology, Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University. Retrieved from http://hdl.handle.net/1887/14497

Chicago Manual of Style (16th Edition):

Kooloos, Wouter Michiel. “Potential role of pharmacogenetics for optimalization of drug therapy in rheumatoid arthritis.” 2009. Doctoral Dissertation, Department of Clinical Pharmacy & Toxicology, Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University. Accessed January 18, 2020. http://hdl.handle.net/1887/14497.

MLA Handbook (7th Edition):

Kooloos, Wouter Michiel. “Potential role of pharmacogenetics for optimalization of drug therapy in rheumatoid arthritis.” 2009. Web. 18 Jan 2020.

Vancouver:

Kooloos WM. Potential role of pharmacogenetics for optimalization of drug therapy in rheumatoid arthritis. [Internet] [Doctoral dissertation]. Department of Clinical Pharmacy & Toxicology, Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University; 2009. [cited 2020 Jan 18]. Available from: http://hdl.handle.net/1887/14497.

Council of Science Editors:

Kooloos WM. Potential role of pharmacogenetics for optimalization of drug therapy in rheumatoid arthritis. [Doctoral Dissertation]. Department of Clinical Pharmacy & Toxicology, Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University; 2009. Available from: http://hdl.handle.net/1887/14497

11. Aduri, Dasharatha Radha Krishna Chaitanya. Mechanistic Studies of Inhibitors of DNA Replication Restart Pathways in Neisseria Gonorrhoeae.

Degree: MS(M.S.), Chemistry, 2013, University of Dayton

 Complete and faithful replication of a cell's genetic information is an essential process. Many enzymes are involved in the process of successfully duplicating a cell's… (more)

Subjects/Keywords: Chemistry; Biochemistry; Replication Restart Pathways; Neisseria Gonorrhoeae; PriA; PriB; Inhibitor; Inhibition

…16 III-1 Effect of Inhibitor F0298-0039 …..16 III-2 Effect of Inhibitor F0359… …0046 …..18 III-3 Effect of Inhibitor F0683-0441 …..20 III-4… …Effect of Inhibitor F2018-1489 …..22 III-5 Effect of Inhibitor F0683-0207… …24 III-6 Mechanism of the Inhibition of DNA replication restart process of Neisseria… …Figure 1: DNA replication process …. …2 Figure 2a: Unwinding of duplex DNA by… 

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APA (6th Edition):

Aduri, D. R. K. C. (2013). Mechanistic Studies of Inhibitors of DNA Replication Restart Pathways in Neisseria Gonorrhoeae. (Masters Thesis). University of Dayton. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=dayton1380732786

Chicago Manual of Style (16th Edition):

Aduri, Dasharatha Radha Krishna Chaitanya. “Mechanistic Studies of Inhibitors of DNA Replication Restart Pathways in Neisseria Gonorrhoeae.” 2013. Masters Thesis, University of Dayton. Accessed January 18, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=dayton1380732786.

MLA Handbook (7th Edition):

Aduri, Dasharatha Radha Krishna Chaitanya. “Mechanistic Studies of Inhibitors of DNA Replication Restart Pathways in Neisseria Gonorrhoeae.” 2013. Web. 18 Jan 2020.

Vancouver:

Aduri DRKC. Mechanistic Studies of Inhibitors of DNA Replication Restart Pathways in Neisseria Gonorrhoeae. [Internet] [Masters thesis]. University of Dayton; 2013. [cited 2020 Jan 18]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=dayton1380732786.

Council of Science Editors:

Aduri DRKC. Mechanistic Studies of Inhibitors of DNA Replication Restart Pathways in Neisseria Gonorrhoeae. [Masters Thesis]. University of Dayton; 2013. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=dayton1380732786

12. Yang, Sherry W. (Sherry Wei). A TIMP2-armed conditionally-replicating adenovirus for the treatment of ovarian cancer.

Degree: PhD, 2010, University of Alabama – Birmingham

Ovarian cancer remains the most lethal gynecological malignancy in the U.S. Conventional therapies have limited therapeutic value due to advanced stage of the dis-ease at… (more)

Subjects/Keywords: Adenoviridae  – genetics<; br>; Adenoviridae  – physiology<; br>; DNA, Viral  – metabolism<; br>; Oncolytic Virotherapy  – methods<; br>; Ovarian Neoplasms  – pathology<; br>; Tissue Inhibitor of Metalloproteinase-2  – metabolism<; br>; Virus Replication  – physiology

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APA (6th Edition):

Yang, S. W. (. W. (2010). A TIMP2-armed conditionally-replicating adenovirus for the treatment of ovarian cancer. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1116

Chicago Manual of Style (16th Edition):

Yang, Sherry W (Sherry Wei). “A TIMP2-armed conditionally-replicating adenovirus for the treatment of ovarian cancer.” 2010. Doctoral Dissertation, University of Alabama – Birmingham. Accessed January 18, 2020. http://contentdm.mhsl.uab.edu/u?/etd,1116.

MLA Handbook (7th Edition):

Yang, Sherry W (Sherry Wei). “A TIMP2-armed conditionally-replicating adenovirus for the treatment of ovarian cancer.” 2010. Web. 18 Jan 2020.

Vancouver:

Yang SW(W. A TIMP2-armed conditionally-replicating adenovirus for the treatment of ovarian cancer. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2010. [cited 2020 Jan 18]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1116.

Council of Science Editors:

Yang SW(W. A TIMP2-armed conditionally-replicating adenovirus for the treatment of ovarian cancer. [Doctoral Dissertation]. University of Alabama – Birmingham; 2010. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1116


Duke University

13. Wang, XF. A novel, non-apoptotic role for Scythe/BAT3: a functional switch between the pro- and anti-proliferative roles of p21 during the cell cycle.

Degree: 2012, Duke University

 BACKGROUND: Scythe/BAT3 is a member of the BAG protein family whose role in apoptosis has been extensively studied. However, since the developmental defects observed in… (more)

Subjects/Keywords: Apoptosis; Blotting, Western; Bone Neoplasms; Cell Cycle; Cell Proliferation; Cyclin-Dependent Kinase Inhibitor p21; DNA Replication; Flow Cytometry; Fluorescent Antibody Technique; Humans; Molecular Chaperones; Osteosarcoma; Phosphorylation; RNA, Small Interfering; Tumor Cells, Cultured

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APA (6th Edition):

Wang, X. (2012). A novel, non-apoptotic role for Scythe/BAT3: a functional switch between the pro- and anti-proliferative roles of p21 during the cell cycle. (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/4958

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):

Wang, XF. “A novel, non-apoptotic role for Scythe/BAT3: a functional switch between the pro- and anti-proliferative roles of p21 during the cell cycle. ” 2012. Thesis, Duke University. Accessed January 18, 2020. http://hdl.handle.net/10161/4958.

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

MLA Handbook (7th Edition):

Wang, XF. “A novel, non-apoptotic role for Scythe/BAT3: a functional switch between the pro- and anti-proliferative roles of p21 during the cell cycle. ” 2012. Web. 18 Jan 2020.

Vancouver:

Wang X. A novel, non-apoptotic role for Scythe/BAT3: a functional switch between the pro- and anti-proliferative roles of p21 during the cell cycle. [Internet] [Thesis]. Duke University; 2012. [cited 2020 Jan 18]. Available from: http://hdl.handle.net/10161/4958.

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

Council of Science Editors:

Wang X. A novel, non-apoptotic role for Scythe/BAT3: a functional switch between the pro- and anti-proliferative roles of p21 during the cell cycle. [Thesis]. Duke University; 2012. Available from: http://hdl.handle.net/10161/4958

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


Leiden University

14. Eijk, van, H.W. The replication machinery of Clostridium difficile: a potential target for novel antimicrobials.

Degree: 2019, Leiden University

 This thesis provides an overview of DNA replication proteins that potentially may serve as targets for antimicrobials in drug-resistant pathogens and includes the in silico… (more)

Subjects/Keywords: Clostridium difficile; DNA replication proteins; Antibiotic resistant bacteria; Protein protein interactions; Primase; Helicase; RNAseq; Novel targets antimicrobials; DNA polymerase inhibitors; PolC inhibitor; Clostridium difficile; DNA replication proteins; Antibiotic resistant bacteria; Protein protein interactions; Primase; Helicase; RNAseq; Novel targets antimicrobials; DNA polymerase inhibitors; PolC inhibitor

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

APA (6th Edition):

Eijk, van, H. W. (2019). The replication machinery of Clostridium difficile: a potential target for novel antimicrobials. (Doctoral Dissertation). Leiden University. Retrieved from http://hdl.handle.net/1887/73422

Chicago Manual of Style (16th Edition):

Eijk, van, H W. “The replication machinery of Clostridium difficile: a potential target for novel antimicrobials.” 2019. Doctoral Dissertation, Leiden University. Accessed January 18, 2020. http://hdl.handle.net/1887/73422.

MLA Handbook (7th Edition):

Eijk, van, H W. “The replication machinery of Clostridium difficile: a potential target for novel antimicrobials.” 2019. Web. 18 Jan 2020.

Vancouver:

Eijk, van HW. The replication machinery of Clostridium difficile: a potential target for novel antimicrobials. [Internet] [Doctoral dissertation]. Leiden University; 2019. [cited 2020 Jan 18]. Available from: http://hdl.handle.net/1887/73422.

Council of Science Editors:

Eijk, van HW. The replication machinery of Clostridium difficile: a potential target for novel antimicrobials. [Doctoral Dissertation]. Leiden University; 2019. Available from: http://hdl.handle.net/1887/73422

15. Mishra, Akaash K. Developing small molecule inhibitors targeting Replication Protein A for platinum-based combination therapy.

Degree: 2014, IUPUI

Indiana University-Purdue University Indianapolis (IUPUI)

All platinum (Pt)-based chemotherapeutics exert their efficacy primarily via the formation of DNA adducts which interfere with DNA replication, transcription… (more)

Subjects/Keywords: replication protein a, platinum, cisplatin, protein-DNA interaction, small molecule inhibitor; DNA replication  – Research  – Methodology; DNA-protein interactions; DNA  – Synthesis; DNA damage  – Research; Cisplatin  – Research; Binding sites (Biochemistry)  – Research; Cellular signal transduction  – Research  – Methodology; Tissue culture  – Research  – Methodology; Platinum  – Therapeutic use; Molecules  – Research; Epithelial cells  – Cancer; Ovaries  – Cancer  – Molecular aspects; Molecular theory  – Research; Small cell lung cancer  – Research; Chemotherapy  – Research

…12 5. Role of RPA in NER, HRR and DNA replication… …platinum Rad51 Rad51 recombinase RPA replication… …RPA inhibitor RPMI Roswell park memorial institute… …small molecule inhibitor SSB single stranded DNA binding… …DNA lesions. Pt-­‐DNA adducts interfere with DNA replication… 

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

APA (6th Edition):

Mishra, A. K. (2014). Developing small molecule inhibitors targeting Replication Protein A for platinum-based combination therapy. (Thesis). IUPUI. Retrieved from http://hdl.handle.net/1805/6466

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):

Mishra, Akaash K. “Developing small molecule inhibitors targeting Replication Protein A for platinum-based combination therapy.” 2014. Thesis, IUPUI. Accessed January 18, 2020. http://hdl.handle.net/1805/6466.

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

MLA Handbook (7th Edition):

Mishra, Akaash K. “Developing small molecule inhibitors targeting Replication Protein A for platinum-based combination therapy.” 2014. Web. 18 Jan 2020.

Vancouver:

Mishra AK. Developing small molecule inhibitors targeting Replication Protein A for platinum-based combination therapy. [Internet] [Thesis]. IUPUI; 2014. [cited 2020 Jan 18]. Available from: http://hdl.handle.net/1805/6466.

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

Council of Science Editors:

Mishra AK. Developing small molecule inhibitors targeting Replication Protein A for platinum-based combination therapy. [Thesis]. IUPUI; 2014. Available from: http://hdl.handle.net/1805/6466

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

.