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You searched for subject:( Nucleoside reverse transcriptase inhibitor NRTI ). Showing records 1 – 30 of 4336 total matches.

[1] [2] [3] [4] [5] … [145]

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University of Bath

1. Mafuva, Christopher. Effect of ethinylestradiol and levonorgestrel on nucleoside reverse transcriptase inhibitor-induced apoptosis in human cervical epithelial cancer cells.

Degree: Thesis (D.Health), 2019, University of Bath

 Preliminary findings suggest an increase in cervical cancer among sub-Sahara African women on highly active antiretroviral treatment (HAART). There has been a sharp rise in… (more)

Subjects/Keywords: Nucleoside; reverse transcriptase inhibitor; apoptosis; cervical; cancer cells

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APA (6th Edition):

Mafuva, C. (2019). Effect of ethinylestradiol and levonorgestrel on nucleoside reverse transcriptase inhibitor-induced apoptosis in human cervical epithelial cancer cells. (Doctoral Dissertation). University of Bath. Retrieved from https://researchportal.bath.ac.uk/en/studentthesis/effect-of-ethinylestradiol-and-levonorgestrel-on-nucleoside-reverse-transcriptase-inhibitorinduced-apoptosis-in-human-cervical-epithelial-cancer-cells(9d6b72a6-62d5-4608-bb3e-a0d2b6685f8d).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.817805

Chicago Manual of Style (16th Edition):

Mafuva, Christopher. “Effect of ethinylestradiol and levonorgestrel on nucleoside reverse transcriptase inhibitor-induced apoptosis in human cervical epithelial cancer cells.” 2019. Doctoral Dissertation, University of Bath. Accessed March 08, 2021. https://researchportal.bath.ac.uk/en/studentthesis/effect-of-ethinylestradiol-and-levonorgestrel-on-nucleoside-reverse-transcriptase-inhibitorinduced-apoptosis-in-human-cervical-epithelial-cancer-cells(9d6b72a6-62d5-4608-bb3e-a0d2b6685f8d).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.817805.

MLA Handbook (7th Edition):

Mafuva, Christopher. “Effect of ethinylestradiol and levonorgestrel on nucleoside reverse transcriptase inhibitor-induced apoptosis in human cervical epithelial cancer cells.” 2019. Web. 08 Mar 2021.

Vancouver:

Mafuva C. Effect of ethinylestradiol and levonorgestrel on nucleoside reverse transcriptase inhibitor-induced apoptosis in human cervical epithelial cancer cells. [Internet] [Doctoral dissertation]. University of Bath; 2019. [cited 2021 Mar 08]. Available from: https://researchportal.bath.ac.uk/en/studentthesis/effect-of-ethinylestradiol-and-levonorgestrel-on-nucleoside-reverse-transcriptase-inhibitorinduced-apoptosis-in-human-cervical-epithelial-cancer-cells(9d6b72a6-62d5-4608-bb3e-a0d2b6685f8d).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.817805.

Council of Science Editors:

Mafuva C. Effect of ethinylestradiol and levonorgestrel on nucleoside reverse transcriptase inhibitor-induced apoptosis in human cervical epithelial cancer cells. [Doctoral Dissertation]. University of Bath; 2019. Available from: https://researchportal.bath.ac.uk/en/studentthesis/effect-of-ethinylestradiol-and-levonorgestrel-on-nucleoside-reverse-transcriptase-inhibitorinduced-apoptosis-in-human-cervical-epithelial-cancer-cells(9d6b72a6-62d5-4608-bb3e-a0d2b6685f8d).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.817805


University of Georgia

2. Blue, Shawn Kendale. Pharmacokinetics of anti-HIV agents in rodents.

Degree: 2014, University of Georgia

 The treatment of HIV/AIDS is one of, if not, the most challenging medical enigmas of the 20th and 21st centuries. At the time of its… (more)

Subjects/Keywords: HIV; Pharmacokinetics; Stavudine; Lamivudine; D4T; DDC; Placental Transport; NRTI; Nucleoside Reverse Transcriptase Inhibitors; HPLC; Antiviral Drugs; Integrase Inhibitors

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APA (6th Edition):

Blue, S. K. (2014). Pharmacokinetics of anti-HIV agents in rodents. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/26575

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):

Blue, Shawn Kendale. “Pharmacokinetics of anti-HIV agents in rodents.” 2014. Thesis, University of Georgia. Accessed March 08, 2021. http://hdl.handle.net/10724/26575.

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

MLA Handbook (7th Edition):

Blue, Shawn Kendale. “Pharmacokinetics of anti-HIV agents in rodents.” 2014. Web. 08 Mar 2021.

Vancouver:

Blue SK. Pharmacokinetics of anti-HIV agents in rodents. [Internet] [Thesis]. University of Georgia; 2014. [cited 2021 Mar 08]. Available from: http://hdl.handle.net/10724/26575.

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

Council of Science Editors:

Blue SK. Pharmacokinetics of anti-HIV agents in rodents. [Thesis]. University of Georgia; 2014. Available from: http://hdl.handle.net/10724/26575

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

3. Wang, Ruibin. The impact of tenofovir disoproxil fumarate on estimated glomerular filtration rate change and progression to end-stage renal disease among HIV-infected adults in North America.

Degree: 2015, Johns Hopkins University

 Background: Tenofovir disoproxil fumarate (TDF) was associated with an increased risk of renal toxicity, resulting in proximal tubular dysfunction, proteinuria, and chronic kidney disease (CKD).… (more)

Subjects/Keywords: HIV-infection; Tenofovir disoproxil fumarate (TDF); Nucleoside reverse transcriptase inhibitor (NRTI); End-stage renal Disease (ESRD); Glomerular filtration rate (GFR)

…disoproxil fumarate; NRTI, nucleoside reverse transcriptase inhibitor; ARV, antiretroviral drug; PI… …disease; TDF, tenofovir disoproxil fumarate; NRTI, nucleoside reverse transcriptase inhibitor… …nucleoside and nucleotide reverse transcriptase inhibitors (NRTIs) are excreted primarily… …containing TDF and a nonnucleotide reverse transcriptase inhibitor (NNRTI) in treatment… …active research. Tenofovir disoproxil fumartate (TDF) is a member of the NRTI class… 

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APA (6th Edition):

Wang, R. (2015). The impact of tenofovir disoproxil fumarate on estimated glomerular filtration rate change and progression to end-stage renal disease among HIV-infected adults in North America. (Thesis). Johns Hopkins University. Retrieved from http://jhir.library.jhu.edu/handle/1774.2/38064

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, Ruibin. “The impact of tenofovir disoproxil fumarate on estimated glomerular filtration rate change and progression to end-stage renal disease among HIV-infected adults in North America.” 2015. Thesis, Johns Hopkins University. Accessed March 08, 2021. http://jhir.library.jhu.edu/handle/1774.2/38064.

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

MLA Handbook (7th Edition):

Wang, Ruibin. “The impact of tenofovir disoproxil fumarate on estimated glomerular filtration rate change and progression to end-stage renal disease among HIV-infected adults in North America.” 2015. Web. 08 Mar 2021.

Vancouver:

Wang R. The impact of tenofovir disoproxil fumarate on estimated glomerular filtration rate change and progression to end-stage renal disease among HIV-infected adults in North America. [Internet] [Thesis]. Johns Hopkins University; 2015. [cited 2021 Mar 08]. Available from: http://jhir.library.jhu.edu/handle/1774.2/38064.

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

Council of Science Editors:

Wang R. The impact of tenofovir disoproxil fumarate on estimated glomerular filtration rate change and progression to end-stage renal disease among HIV-infected adults in North America. [Thesis]. Johns Hopkins University; 2015. Available from: http://jhir.library.jhu.edu/handle/1774.2/38064

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


University of KwaZulu-Natal

4. Nagiah, Savania. A biochemical assessment of stress response following acute and prolonged exposure to antiretroviral drugs (nucleoside reverse transcriptase inhibitors) in vitro.

Degree: 2015, University of KwaZulu-Natal

Nucleoside reverse transcriptase inhibitors (NRTIs) are the most extensively used antiretroviral (ARV) drugs in highly active antiretroviral therapy (HAART). The long term use of HAART… (more)

Subjects/Keywords: Medical biochemistry.; Nucleoside reverse transcriptase inhibitors.

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APA (6th Edition):

Nagiah, S. (2015). A biochemical assessment of stress response following acute and prolonged exposure to antiretroviral drugs (nucleoside reverse transcriptase inhibitors) in vitro. (Thesis). University of KwaZulu-Natal. Retrieved from http://hdl.handle.net/10413/14645

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):

Nagiah, Savania. “A biochemical assessment of stress response following acute and prolonged exposure to antiretroviral drugs (nucleoside reverse transcriptase inhibitors) in vitro.” 2015. Thesis, University of KwaZulu-Natal. Accessed March 08, 2021. http://hdl.handle.net/10413/14645.

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

MLA Handbook (7th Edition):

Nagiah, Savania. “A biochemical assessment of stress response following acute and prolonged exposure to antiretroviral drugs (nucleoside reverse transcriptase inhibitors) in vitro.” 2015. Web. 08 Mar 2021.

Vancouver:

Nagiah S. A biochemical assessment of stress response following acute and prolonged exposure to antiretroviral drugs (nucleoside reverse transcriptase inhibitors) in vitro. [Internet] [Thesis]. University of KwaZulu-Natal; 2015. [cited 2021 Mar 08]. Available from: http://hdl.handle.net/10413/14645.

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

Council of Science Editors:

Nagiah S. A biochemical assessment of stress response following acute and prolonged exposure to antiretroviral drugs (nucleoside reverse transcriptase inhibitors) in vitro. [Thesis]. University of KwaZulu-Natal; 2015. Available from: http://hdl.handle.net/10413/14645

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


University of Maryland

5. Achuthan, Vasudevan. HIV Reverse Transcriptase Fidelity And Inhibition Are Modulated By Divalent Cations In A Concentration-Dependent Manner In Vitro.

Degree: Cell Biology & Molecular Genetics, 2016, University of Maryland

 Human immunodeficiency virus (HIV) rapidly evolves through generation and selection of mutants that can escape drug therapy. This process is fueled, in part, by the… (more)

Subjects/Keywords: Biochemistry; Virology; Molecular biology; Divalent cations; Fidelity; HIV; Non-Nucleoside Reverse Transcriptase Inhibitors; Nucleoside Reverse Transcriptase Inhibitors; Reverse Transcriptase

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APA (6th Edition):

Achuthan, V. (2016). HIV Reverse Transcriptase Fidelity And Inhibition Are Modulated By Divalent Cations In A Concentration-Dependent Manner In Vitro. (Thesis). University of Maryland. Retrieved from http://hdl.handle.net/1903/18547

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):

Achuthan, Vasudevan. “HIV Reverse Transcriptase Fidelity And Inhibition Are Modulated By Divalent Cations In A Concentration-Dependent Manner In Vitro.” 2016. Thesis, University of Maryland. Accessed March 08, 2021. http://hdl.handle.net/1903/18547.

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

MLA Handbook (7th Edition):

Achuthan, Vasudevan. “HIV Reverse Transcriptase Fidelity And Inhibition Are Modulated By Divalent Cations In A Concentration-Dependent Manner In Vitro.” 2016. Web. 08 Mar 2021.

Vancouver:

Achuthan V. HIV Reverse Transcriptase Fidelity And Inhibition Are Modulated By Divalent Cations In A Concentration-Dependent Manner In Vitro. [Internet] [Thesis]. University of Maryland; 2016. [cited 2021 Mar 08]. Available from: http://hdl.handle.net/1903/18547.

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

Council of Science Editors:

Achuthan V. HIV Reverse Transcriptase Fidelity And Inhibition Are Modulated By Divalent Cations In A Concentration-Dependent Manner In Vitro. [Thesis]. University of Maryland; 2016. Available from: http://hdl.handle.net/1903/18547

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


Kwame Nkrumah University of Science and Technology

6. Sarfo, Fred S.; Zhang, Yuan; Egan, Deirdre; Tetteh, Lambert A.; Phillips, Richard O. Pharmacogenetic associations with plasma efavirenz concentrations and clinical correlates in a retrospective cohort of Ghanaian HIV-infected patients.

Degree: 2013, Kwame Nkrumah University of Science and Technology

Objectives: Efavirenz is widely used in first-line antiretroviral therapy in sub-Saharan Africa. However, exposure to efavirenz shows marked interindividual variability that is genetically mediated with… (more)

Subjects/Keywords: non-nucleoside reverse transcriptase inhibitors; Africa; pharmacokinetics; pharmacodynamics

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APA (6th Edition):

Sarfo, Fred S.; Zhang, Yuan; Egan, Deirdre; Tetteh, Lambert A.; Phillips, R. O. (2013). Pharmacogenetic associations with plasma efavirenz concentrations and clinical correlates in a retrospective cohort of Ghanaian HIV-infected patients. (Thesis). Kwame Nkrumah University of Science and Technology. Retrieved from http://dspace.knust.edu.gh:8080/jspui/handle/123456789/11869

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):

Sarfo, Fred S.; Zhang, Yuan; Egan, Deirdre; Tetteh, Lambert A.; Phillips, Richard O. “Pharmacogenetic associations with plasma efavirenz concentrations and clinical correlates in a retrospective cohort of Ghanaian HIV-infected patients.” 2013. Thesis, Kwame Nkrumah University of Science and Technology. Accessed March 08, 2021. http://dspace.knust.edu.gh:8080/jspui/handle/123456789/11869.

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

MLA Handbook (7th Edition):

Sarfo, Fred S.; Zhang, Yuan; Egan, Deirdre; Tetteh, Lambert A.; Phillips, Richard O. “Pharmacogenetic associations with plasma efavirenz concentrations and clinical correlates in a retrospective cohort of Ghanaian HIV-infected patients.” 2013. Web. 08 Mar 2021.

Vancouver:

Sarfo, Fred S.; Zhang, Yuan; Egan, Deirdre; Tetteh, Lambert A.; Phillips RO. Pharmacogenetic associations with plasma efavirenz concentrations and clinical correlates in a retrospective cohort of Ghanaian HIV-infected patients. [Internet] [Thesis]. Kwame Nkrumah University of Science and Technology; 2013. [cited 2021 Mar 08]. Available from: http://dspace.knust.edu.gh:8080/jspui/handle/123456789/11869.

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

Council of Science Editors:

Sarfo, Fred S.; Zhang, Yuan; Egan, Deirdre; Tetteh, Lambert A.; Phillips RO. Pharmacogenetic associations with plasma efavirenz concentrations and clinical correlates in a retrospective cohort of Ghanaian HIV-infected patients. [Thesis]. Kwame Nkrumah University of Science and Technology; 2013. Available from: http://dspace.knust.edu.gh:8080/jspui/handle/123456789/11869

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


Universiteit Utrecht

7. Kappelhoff, B.S. Clinical pharmacological investigations of antiretroviral drugs.

Degree: 2005, Universiteit Utrecht

 The major aim of all studies described in this thesis is to contribute to the optimisation of antiretroviral drug treatment in HIV-infected patients by the… (more)

Subjects/Keywords: Farmacie; HIV; antiretroviral drugs; non-nucleoside reverse transcriptase inhibitor; NNRTI; protease inhibitor; PI; (population) pharmacokinetics; (clinical) pharmacology; NONMEM; bioanalysis; 2NN study

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APA (6th Edition):

Kappelhoff, B. S. (2005). Clinical pharmacological investigations of antiretroviral drugs. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/29727

Chicago Manual of Style (16th Edition):

Kappelhoff, B S. “Clinical pharmacological investigations of antiretroviral drugs.” 2005. Doctoral Dissertation, Universiteit Utrecht. Accessed March 08, 2021. http://dspace.library.uu.nl:8080/handle/1874/29727.

MLA Handbook (7th Edition):

Kappelhoff, B S. “Clinical pharmacological investigations of antiretroviral drugs.” 2005. Web. 08 Mar 2021.

Vancouver:

Kappelhoff BS. Clinical pharmacological investigations of antiretroviral drugs. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2005. [cited 2021 Mar 08]. Available from: http://dspace.library.uu.nl:8080/handle/1874/29727.

Council of Science Editors:

Kappelhoff BS. Clinical pharmacological investigations of antiretroviral drugs. [Doctoral Dissertation]. Universiteit Utrecht; 2005. Available from: http://dspace.library.uu.nl:8080/handle/1874/29727

8. Kappelhoff, B.S. Clinical pharmacological investigations of antiretroviral drugs.

Degree: 2005, University Utrecht

 The major aim of all studies described in this thesis is to contribute to the optimisation of antiretroviral drug treatment in HIV-infected patients by the… (more)

Subjects/Keywords: HIV; antiretroviral drugs; non-nucleoside reverse transcriptase inhibitor; NNRTI; protease inhibitor; PI; (population) pharmacokinetics; (clinical) pharmacology; NONMEM; bioanalysis; 2NN study

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APA (6th Edition):

Kappelhoff, B. S. (2005). Clinical pharmacological investigations of antiretroviral drugs. (Doctoral Dissertation). University Utrecht. Retrieved from https://dspace.library.uu.nl/handle/1874/29727 ; URN:NBN:NL:UI:10-1874-29727 ; 1874/29727 ; urn:isbn:9039339317 ; URN:NBN:NL:UI:10-1874-29727 ; https://dspace.library.uu.nl/handle/1874/29727

Chicago Manual of Style (16th Edition):

Kappelhoff, B S. “Clinical pharmacological investigations of antiretroviral drugs.” 2005. Doctoral Dissertation, University Utrecht. Accessed March 08, 2021. https://dspace.library.uu.nl/handle/1874/29727 ; URN:NBN:NL:UI:10-1874-29727 ; 1874/29727 ; urn:isbn:9039339317 ; URN:NBN:NL:UI:10-1874-29727 ; https://dspace.library.uu.nl/handle/1874/29727.

MLA Handbook (7th Edition):

Kappelhoff, B S. “Clinical pharmacological investigations of antiretroviral drugs.” 2005. Web. 08 Mar 2021.

Vancouver:

Kappelhoff BS. Clinical pharmacological investigations of antiretroviral drugs. [Internet] [Doctoral dissertation]. University Utrecht; 2005. [cited 2021 Mar 08]. Available from: https://dspace.library.uu.nl/handle/1874/29727 ; URN:NBN:NL:UI:10-1874-29727 ; 1874/29727 ; urn:isbn:9039339317 ; URN:NBN:NL:UI:10-1874-29727 ; https://dspace.library.uu.nl/handle/1874/29727.

Council of Science Editors:

Kappelhoff BS. Clinical pharmacological investigations of antiretroviral drugs. [Doctoral Dissertation]. University Utrecht; 2005. Available from: https://dspace.library.uu.nl/handle/1874/29727 ; URN:NBN:NL:UI:10-1874-29727 ; 1874/29727 ; urn:isbn:9039339317 ; URN:NBN:NL:UI:10-1874-29727 ; https://dspace.library.uu.nl/handle/1874/29727


University of Kentucky

9. Fowler, Benjamin J. NUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITORS ARE ANTI-INFLAMMATORY AND TARGET DRY AGE-RELATED MACULAR DEGENERATION.

Degree: 2014, University of Kentucky

 Age-related macular degeneration (AMD) is a principal cause of blindness in the United States and other industrialized nations. An estimated 10 million Americans are afflicted… (more)

Subjects/Keywords: Nucleoside reverse transcriptase inhibitors; age-related macular degeneration; NLRP3 inflammasome; P2X7; Alu RNA; Ophthalmology

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APA (6th Edition):

Fowler, B. J. (2014). NUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITORS ARE ANTI-INFLAMMATORY AND TARGET DRY AGE-RELATED MACULAR DEGENERATION. (Doctoral Dissertation). University of Kentucky. Retrieved from https://uknowledge.uky.edu/physiology_etds/17

Chicago Manual of Style (16th Edition):

Fowler, Benjamin J. “NUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITORS ARE ANTI-INFLAMMATORY AND TARGET DRY AGE-RELATED MACULAR DEGENERATION.” 2014. Doctoral Dissertation, University of Kentucky. Accessed March 08, 2021. https://uknowledge.uky.edu/physiology_etds/17.

MLA Handbook (7th Edition):

Fowler, Benjamin J. “NUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITORS ARE ANTI-INFLAMMATORY AND TARGET DRY AGE-RELATED MACULAR DEGENERATION.” 2014. Web. 08 Mar 2021.

Vancouver:

Fowler BJ. NUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITORS ARE ANTI-INFLAMMATORY AND TARGET DRY AGE-RELATED MACULAR DEGENERATION. [Internet] [Doctoral dissertation]. University of Kentucky; 2014. [cited 2021 Mar 08]. Available from: https://uknowledge.uky.edu/physiology_etds/17.

Council of Science Editors:

Fowler BJ. NUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITORS ARE ANTI-INFLAMMATORY AND TARGET DRY AGE-RELATED MACULAR DEGENERATION. [Doctoral Dissertation]. University of Kentucky; 2014. Available from: https://uknowledge.uky.edu/physiology_etds/17


University of Missouri – Columbia

10. Michailidis, Eleftherios. Mechanisms of inhibition and resistance to antiviral drugs targeting human immunodeficiency virus type 1 (HIV-1) and hepatitis B virus (HBV).

Degree: 2012, University of Missouri – Columbia

 [ACCESS RESTRICTED TO THE UNIVERSITY OF MISSOURI AT AUTHOR'S REQUEST.] Although human immunodeficiency virus type 1 (HIV-1) and hepatitis B virus (HBV) are very different… (more)

Subjects/Keywords: reverse transcriptase; deoxyadenosine analog; translocation defective RT inhibitor; antiretroviral

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APA (6th Edition):

Michailidis, E. (2012). Mechanisms of inhibition and resistance to antiviral drugs targeting human immunodeficiency virus type 1 (HIV-1) and hepatitis B virus (HBV). (Thesis). University of Missouri – Columbia. Retrieved from https://doi.org/10.32469/10355/36771

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):

Michailidis, Eleftherios. “Mechanisms of inhibition and resistance to antiviral drugs targeting human immunodeficiency virus type 1 (HIV-1) and hepatitis B virus (HBV).” 2012. Thesis, University of Missouri – Columbia. Accessed March 08, 2021. https://doi.org/10.32469/10355/36771.

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

MLA Handbook (7th Edition):

Michailidis, Eleftherios. “Mechanisms of inhibition and resistance to antiviral drugs targeting human immunodeficiency virus type 1 (HIV-1) and hepatitis B virus (HBV).” 2012. Web. 08 Mar 2021.

Vancouver:

Michailidis E. Mechanisms of inhibition and resistance to antiviral drugs targeting human immunodeficiency virus type 1 (HIV-1) and hepatitis B virus (HBV). [Internet] [Thesis]. University of Missouri – Columbia; 2012. [cited 2021 Mar 08]. Available from: https://doi.org/10.32469/10355/36771.

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

Council of Science Editors:

Michailidis E. Mechanisms of inhibition and resistance to antiviral drugs targeting human immunodeficiency virus type 1 (HIV-1) and hepatitis B virus (HBV). [Thesis]. University of Missouri – Columbia; 2012. Available from: https://doi.org/10.32469/10355/36771

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


Queensland University of Technology

11. Morphet, Marilynn Norma. Method for identification of effective first-line treatment for HAART naïve HIV/AIDS patients.

Degree: 2002, Queensland University of Technology

Subjects/Keywords: Drugs Effectiveness Mathematical models; AIDS (Disease) Treatment; HIV infections Treatment; Outcome assessment (Medical care); regimen; CD4+ cell count; viral load (VL); Highly Active Anti Retroviral Therapy (HAART); treatment effect; treatment compliance; protease inhibitor; nucleoside reverse transcriptase inhibitor; non nucleoside reverse transcriptase inhibitor; thesis; masters

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APA (6th Edition):

Morphet, M. N. (2002). Method for identification of effective first-line treatment for HAART naïve HIV/AIDS patients. (Thesis). Queensland University of Technology. Retrieved from http://eprints.qut.edu.au/37119/

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):

Morphet, Marilynn Norma. “Method for identification of effective first-line treatment for HAART naïve HIV/AIDS patients.” 2002. Thesis, Queensland University of Technology. Accessed March 08, 2021. http://eprints.qut.edu.au/37119/.

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

MLA Handbook (7th Edition):

Morphet, Marilynn Norma. “Method for identification of effective first-line treatment for HAART naïve HIV/AIDS patients.” 2002. Web. 08 Mar 2021.

Vancouver:

Morphet MN. Method for identification of effective first-line treatment for HAART naïve HIV/AIDS patients. [Internet] [Thesis]. Queensland University of Technology; 2002. [cited 2021 Mar 08]. Available from: http://eprints.qut.edu.au/37119/.

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

Council of Science Editors:

Morphet MN. Method for identification of effective first-line treatment for HAART naïve HIV/AIDS patients. [Thesis]. Queensland University of Technology; 2002. Available from: http://eprints.qut.edu.au/37119/

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


University of Gothenburg / Göteborgs Universitet

12. Sörstedt, Erik. Antiretroviral treatment of HIV-1 in Sweden with focus on virological aspects.

Degree: 2021, University of Gothenburg / Göteborgs Universitet

 From a clinical standpoint, there are many factors to consider when optimizing the care for people living with HIV (PLWH). With help from clinical guidelines,… (more)

Subjects/Keywords: HIV-1; antiretroviral therapy; transient viremia; viral blip; nucleoside transcriptase inhibitor resistance; dolutegravir; baseline viral load; HIV RNA; virological failure

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

APA (6th Edition):

Sörstedt, E. (2021). Antiretroviral treatment of HIV-1 in Sweden with focus on virological aspects. (Thesis). University of Gothenburg / Göteborgs Universitet. Retrieved from http://hdl.handle.net/2077/67127

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):

Sörstedt, Erik. “Antiretroviral treatment of HIV-1 in Sweden with focus on virological aspects.” 2021. Thesis, University of Gothenburg / Göteborgs Universitet. Accessed March 08, 2021. http://hdl.handle.net/2077/67127.

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

MLA Handbook (7th Edition):

Sörstedt, Erik. “Antiretroviral treatment of HIV-1 in Sweden with focus on virological aspects.” 2021. Web. 08 Mar 2021.

Vancouver:

Sörstedt E. Antiretroviral treatment of HIV-1 in Sweden with focus on virological aspects. [Internet] [Thesis]. University of Gothenburg / Göteborgs Universitet; 2021. [cited 2021 Mar 08]. Available from: http://hdl.handle.net/2077/67127.

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

Council of Science Editors:

Sörstedt E. Antiretroviral treatment of HIV-1 in Sweden with focus on virological aspects. [Thesis]. University of Gothenburg / Göteborgs Universitet; 2021. Available from: http://hdl.handle.net/2077/67127

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


University of Georgia

13. Li, Ting. Physiologically-based pharmacokinetic modeling approach for drug disposition in human and pregnant rat.

Degree: 2014, University of Georgia

 Physiologically-based pharmacokinetic (PBPK) modeling is a useful approach to investigate the absorption, distribution, metabolism and elimination (ADME) of a compound in animals as well as… (more)

Subjects/Keywords: physiologically-based pharmacokinetic model; dichloroacetic acid; nucleoside reverse transcriptase inhibitors; pregnancy; drug-drug interaction; suicide inhibition

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APA (6th Edition):

Li, T. (2014). Physiologically-based pharmacokinetic modeling approach for drug disposition in human and pregnant rat. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/24207

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):

Li, Ting. “Physiologically-based pharmacokinetic modeling approach for drug disposition in human and pregnant rat.” 2014. Thesis, University of Georgia. Accessed March 08, 2021. http://hdl.handle.net/10724/24207.

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

MLA Handbook (7th Edition):

Li, Ting. “Physiologically-based pharmacokinetic modeling approach for drug disposition in human and pregnant rat.” 2014. Web. 08 Mar 2021.

Vancouver:

Li T. Physiologically-based pharmacokinetic modeling approach for drug disposition in human and pregnant rat. [Internet] [Thesis]. University of Georgia; 2014. [cited 2021 Mar 08]. Available from: http://hdl.handle.net/10724/24207.

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

Council of Science Editors:

Li T. Physiologically-based pharmacokinetic modeling approach for drug disposition in human and pregnant rat. [Thesis]. University of Georgia; 2014. Available from: http://hdl.handle.net/10724/24207

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


University of Georgia

14. alnouti, yazen mohammed. The application of liquid chromatography and mass spectrometry for the determination of nucleoside analogues in biological matrices.

Degree: 2014, University of Georgia

 Multidrug therapy has become the standard treatment of acquired immunodeficiency syndrome (AIDS) caused by the human immunodeficiency virus (HIV). Nucleoside reverse transcriptase inhibitors (NRTIs) are… (more)

Subjects/Keywords: HPLC; CE; MS; SPE; LLE; Sample Preparation; liquid chromatography; Biological matrices; Nucleoside reverse transcriptase inhibitors; Lamivudine; 3TC; Zidovudine; AZT; placental transport

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APA (6th Edition):

alnouti, y. m. (2014). The application of liquid chromatography and mass spectrometry for the determination of nucleoside analogues in biological matrices. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/21743

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):

alnouti, yazen mohammed. “The application of liquid chromatography and mass spectrometry for the determination of nucleoside analogues in biological matrices.” 2014. Thesis, University of Georgia. Accessed March 08, 2021. http://hdl.handle.net/10724/21743.

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

MLA Handbook (7th Edition):

alnouti, yazen mohammed. “The application of liquid chromatography and mass spectrometry for the determination of nucleoside analogues in biological matrices.” 2014. Web. 08 Mar 2021.

Vancouver:

alnouti ym. The application of liquid chromatography and mass spectrometry for the determination of nucleoside analogues in biological matrices. [Internet] [Thesis]. University of Georgia; 2014. [cited 2021 Mar 08]. Available from: http://hdl.handle.net/10724/21743.

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

Council of Science Editors:

alnouti ym. The application of liquid chromatography and mass spectrometry for the determination of nucleoside analogues in biological matrices. [Thesis]. University of Georgia; 2014. Available from: http://hdl.handle.net/10724/21743

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

15. Braz, Valerie Ann. Binding of the Nonnucleoside Reverse Transcriptase Inhibitor Efavirenz to HIV-1 Reverse Transcriptase Monomers and Dimers.

Degree: PhD, Chemistry, 2009, Case Western Reserve University School of Graduate Studies

 Human immunodeficiency virus type 1 (HIV-1) reverse transcriptase (RT) was the first target of antiretroviral therapy in the treatment of AIDS. RT converts single-stranded viral… (more)

Subjects/Keywords: Biochemistry; Biophysics; Chemistry; Nonnucleoside Reverse Transcriptase Inhibitor; Efavirenz; Reverse Transcriptase

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APA (6th Edition):

Braz, V. A. (2009). Binding of the Nonnucleoside Reverse Transcriptase Inhibitor Efavirenz to HIV-1 Reverse Transcriptase Monomers and Dimers. (Doctoral Dissertation). Case Western Reserve University School of Graduate Studies. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1257361654

Chicago Manual of Style (16th Edition):

Braz, Valerie Ann. “Binding of the Nonnucleoside Reverse Transcriptase Inhibitor Efavirenz to HIV-1 Reverse Transcriptase Monomers and Dimers.” 2009. Doctoral Dissertation, Case Western Reserve University School of Graduate Studies. Accessed March 08, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=case1257361654.

MLA Handbook (7th Edition):

Braz, Valerie Ann. “Binding of the Nonnucleoside Reverse Transcriptase Inhibitor Efavirenz to HIV-1 Reverse Transcriptase Monomers and Dimers.” 2009. Web. 08 Mar 2021.

Vancouver:

Braz VA. Binding of the Nonnucleoside Reverse Transcriptase Inhibitor Efavirenz to HIV-1 Reverse Transcriptase Monomers and Dimers. [Internet] [Doctoral dissertation]. Case Western Reserve University School of Graduate Studies; 2009. [cited 2021 Mar 08]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1257361654.

Council of Science Editors:

Braz VA. Binding of the Nonnucleoside Reverse Transcriptase Inhibitor Efavirenz to HIV-1 Reverse Transcriptase Monomers and Dimers. [Doctoral Dissertation]. Case Western Reserve University School of Graduate Studies; 2009. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1257361654


University of Toledo

16. Yang, Hui. Theoretical Studies of Molecular Recognition in Protein-Ligand and Protein-Protein Complexes.

Degree: PhD, Chemistry, 2010, University of Toledo

  Molecular recognition between protein and ligand is the foundation of a wide variety of biological processes. Non-bonded interactions are responsible for molecular recognition in… (more)

Subjects/Keywords: Chemistry; quantum chemical; molecular recognition; supermolecular approach; solvation correction; nonbonded interactions; HIV-1; Reverse Transcriptase; non-nucleoside inhibitor; trp 229; Botulinum neurotoxin B; synaptotagmin II; ASADH; structure-based drug design

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APA (6th Edition):

Yang, H. (2010). Theoretical Studies of Molecular Recognition in Protein-Ligand and Protein-Protein Complexes. (Doctoral Dissertation). University of Toledo. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=toledo1282339026

Chicago Manual of Style (16th Edition):

Yang, Hui. “Theoretical Studies of Molecular Recognition in Protein-Ligand and Protein-Protein Complexes.” 2010. Doctoral Dissertation, University of Toledo. Accessed March 08, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=toledo1282339026.

MLA Handbook (7th Edition):

Yang, Hui. “Theoretical Studies of Molecular Recognition in Protein-Ligand and Protein-Protein Complexes.” 2010. Web. 08 Mar 2021.

Vancouver:

Yang H. Theoretical Studies of Molecular Recognition in Protein-Ligand and Protein-Protein Complexes. [Internet] [Doctoral dissertation]. University of Toledo; 2010. [cited 2021 Mar 08]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=toledo1282339026.

Council of Science Editors:

Yang H. Theoretical Studies of Molecular Recognition in Protein-Ligand and Protein-Protein Complexes. [Doctoral Dissertation]. University of Toledo; 2010. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=toledo1282339026


University of Rochester

17. Operario, Darwin Joseph. The RT-dNTP interaction as a determinant for generation of retroviral genomic diversity and cell-type specificity.

Degree: PhD, 2009, University of Rochester

 Retroviruses contain two copies of a positive-sense single stranded RNA genome. Uniquely amongst RNA viruses, the retroviral lifecycle involves the replication of these RNA genomes… (more)

Subjects/Keywords: Reverse transcriptase

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APA (6th Edition):

Operario, D. J. (2009). The RT-dNTP interaction as a determinant for generation of retroviral genomic diversity and cell-type specificity. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/6525

Chicago Manual of Style (16th Edition):

Operario, Darwin Joseph. “The RT-dNTP interaction as a determinant for generation of retroviral genomic diversity and cell-type specificity.” 2009. Doctoral Dissertation, University of Rochester. Accessed March 08, 2021. http://hdl.handle.net/1802/6525.

MLA Handbook (7th Edition):

Operario, Darwin Joseph. “The RT-dNTP interaction as a determinant for generation of retroviral genomic diversity and cell-type specificity.” 2009. Web. 08 Mar 2021.

Vancouver:

Operario DJ. The RT-dNTP interaction as a determinant for generation of retroviral genomic diversity and cell-type specificity. [Internet] [Doctoral dissertation]. University of Rochester; 2009. [cited 2021 Mar 08]. Available from: http://hdl.handle.net/1802/6525.

Council of Science Editors:

Operario DJ. The RT-dNTP interaction as a determinant for generation of retroviral genomic diversity and cell-type specificity. [Doctoral Dissertation]. University of Rochester; 2009. Available from: http://hdl.handle.net/1802/6525


Rutgers University

18. Frahm, Stephanie A., 1983-. Functional quality control for human blood-based gene expression products.

Degree: MS, Microbiology and Molecular Genetics, 2012, Rutgers University

 Reliable and robust gene expression data generated by microarrays or quantitative real-time polymerase chain reaction (qPCR) is directly dependent upon use of high-quality input material,… (more)

Subjects/Keywords: RNA; Reverse transcriptase; Gene expression

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APA (6th Edition):

Frahm, Stephanie A., 1. (2012). Functional quality control for human blood-based gene expression products. (Masters Thesis). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000064089

Chicago Manual of Style (16th Edition):

Frahm, Stephanie A., 1983-. “Functional quality control for human blood-based gene expression products.” 2012. Masters Thesis, Rutgers University. Accessed March 08, 2021. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000064089.

MLA Handbook (7th Edition):

Frahm, Stephanie A., 1983-. “Functional quality control for human blood-based gene expression products.” 2012. Web. 08 Mar 2021.

Vancouver:

Frahm, Stephanie A. 1. Functional quality control for human blood-based gene expression products. [Internet] [Masters thesis]. Rutgers University; 2012. [cited 2021 Mar 08]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000064089.

Council of Science Editors:

Frahm, Stephanie A. 1. Functional quality control for human blood-based gene expression products. [Masters Thesis]. Rutgers University; 2012. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000064089

19. Braz, Valerie Ann. Binding of the Nonnucleoside Reverse Transcriptase Inhibitor Efavirenz to HIV-1 Reverse Transcriptase Monomers and Dimers.

Degree: PhD, Chemistry, 2010, Case Western Reserve University School of Graduate Studies

 Human immunodeficiency virus type 1 (HIV-1) reverse transcriptase (RT) was the first target of antiretroviral therapy in the treatment of AIDS. RT converts single-stranded viral… (more)

Subjects/Keywords: Biochemistry; Biophysics; Chemistry; Nonnucleoside Reverse Transcriptase Inhibitor; Efavirenz; Reverse Transcriptase; HIV-1

NRTI nucleoside reverse transcriptase inhibitor NNRTI nonnucleoside reverse transcriptase… …Binding of the Nonnucleoside Reverse Transcriptase Inhibitor Efavirenz to HIV-1 Reverse… …x28;HIV-1) reverse transcriptase (RT) was the first target of antiretroviral… …reverse transcription and replication. This work reports two novel functions of the inhibitor… …ribonucleic acid RT reverse transcriptase SDS/PAGE sodium dodecyl sulfate/polyacrylamide gel… 

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

APA (6th Edition):

Braz, V. A. (2010). Binding of the Nonnucleoside Reverse Transcriptase Inhibitor Efavirenz to HIV-1 Reverse Transcriptase Monomers and Dimers. (Doctoral Dissertation). Case Western Reserve University School of Graduate Studies. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1257363704

Chicago Manual of Style (16th Edition):

Braz, Valerie Ann. “Binding of the Nonnucleoside Reverse Transcriptase Inhibitor Efavirenz to HIV-1 Reverse Transcriptase Monomers and Dimers.” 2010. Doctoral Dissertation, Case Western Reserve University School of Graduate Studies. Accessed March 08, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=case1257363704.

MLA Handbook (7th Edition):

Braz, Valerie Ann. “Binding of the Nonnucleoside Reverse Transcriptase Inhibitor Efavirenz to HIV-1 Reverse Transcriptase Monomers and Dimers.” 2010. Web. 08 Mar 2021.

Vancouver:

Braz VA. Binding of the Nonnucleoside Reverse Transcriptase Inhibitor Efavirenz to HIV-1 Reverse Transcriptase Monomers and Dimers. [Internet] [Doctoral dissertation]. Case Western Reserve University School of Graduate Studies; 2010. [cited 2021 Mar 08]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1257363704.

Council of Science Editors:

Braz VA. Binding of the Nonnucleoside Reverse Transcriptase Inhibitor Efavirenz to HIV-1 Reverse Transcriptase Monomers and Dimers. [Doctoral Dissertation]. Case Western Reserve University School of Graduate Studies; 2010. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1257363704


Arizona State University

20. Brown, Andrew. Exploring the Regulation of the Telomerase Reaction Cycle through Unique Protein, DNA, and RNA Interactions.

Degree: PhD, Chemistry, 2014, Arizona State University

 Telomerase is a unique reverse transcriptase that has evolved specifically to extend the single stranded DNA at the 3' ends of chromosomes. To achieve this,… (more)

Subjects/Keywords: Biochemistry; Molecular biology; Reverse transcriptase; Ribonucleoprotein; Telomerase

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APA (6th Edition):

Brown, A. (2014). Exploring the Regulation of the Telomerase Reaction Cycle through Unique Protein, DNA, and RNA Interactions. (Doctoral Dissertation). Arizona State University. Retrieved from http://repository.asu.edu/items/25104

Chicago Manual of Style (16th Edition):

Brown, Andrew. “Exploring the Regulation of the Telomerase Reaction Cycle through Unique Protein, DNA, and RNA Interactions.” 2014. Doctoral Dissertation, Arizona State University. Accessed March 08, 2021. http://repository.asu.edu/items/25104.

MLA Handbook (7th Edition):

Brown, Andrew. “Exploring the Regulation of the Telomerase Reaction Cycle through Unique Protein, DNA, and RNA Interactions.” 2014. Web. 08 Mar 2021.

Vancouver:

Brown A. Exploring the Regulation of the Telomerase Reaction Cycle through Unique Protein, DNA, and RNA Interactions. [Internet] [Doctoral dissertation]. Arizona State University; 2014. [cited 2021 Mar 08]. Available from: http://repository.asu.edu/items/25104.

Council of Science Editors:

Brown A. Exploring the Regulation of the Telomerase Reaction Cycle through Unique Protein, DNA, and RNA Interactions. [Doctoral Dissertation]. Arizona State University; 2014. Available from: http://repository.asu.edu/items/25104


University of Georgia

21. Underwood, Dana Elizabeth Hager. A genetic analysis of telomerase translocation and telomere function in L. lactis.

Degree: 2014, University of Georgia

 Telomeres are DNA-protein complexes that protect the ends of linear chromosomes. The non-genic DNA is typically composted of repetitive T/G-rich sequences, and maintained by telomerase,… (more)

Subjects/Keywords: Telomere; Telomerase; Repeat; Reverse transcriptase; Ribonucleoprotein; RAD52

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APA (6th Edition):

Underwood, D. E. H. (2014). A genetic analysis of telomerase translocation and telomere function in L. lactis. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/20694

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):

Underwood, Dana Elizabeth Hager. “A genetic analysis of telomerase translocation and telomere function in L. lactis.” 2014. Thesis, University of Georgia. Accessed March 08, 2021. http://hdl.handle.net/10724/20694.

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

MLA Handbook (7th Edition):

Underwood, Dana Elizabeth Hager. “A genetic analysis of telomerase translocation and telomere function in L. lactis.” 2014. Web. 08 Mar 2021.

Vancouver:

Underwood DEH. A genetic analysis of telomerase translocation and telomere function in L. lactis. [Internet] [Thesis]. University of Georgia; 2014. [cited 2021 Mar 08]. Available from: http://hdl.handle.net/10724/20694.

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

Council of Science Editors:

Underwood DEH. A genetic analysis of telomerase translocation and telomere function in L. lactis. [Thesis]. University of Georgia; 2014. Available from: http://hdl.handle.net/10724/20694

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


University of Missouri – Columbia

22. Flores, Jacqueline A. Biochemical characterization of clade B and non-B HIV-1 reverse transcriptase.

Degree: 2017, University of Missouri – Columbia

 [ACCESS RESTRICTED TO THE UNIVERSITY OF MISSOURI AT REQUEST OF AUTHOR.] Two classes of drugs: nucleos(t)ide reverse transcriptase inhibitors (NRTIs) and non-nucleoside RT inhibitors (NNRTIs)… (more)

Subjects/Keywords: Reverse transcriptase; Drug resistance; HIV (Viruses)

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APA (6th Edition):

Flores, J. A. (2017). Biochemical characterization of clade B and non-B HIV-1 reverse transcriptase. (Thesis). University of Missouri – Columbia. Retrieved from http://hdl.handle.net/10355/62017

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):

Flores, Jacqueline A. “Biochemical characterization of clade B and non-B HIV-1 reverse transcriptase.” 2017. Thesis, University of Missouri – Columbia. Accessed March 08, 2021. http://hdl.handle.net/10355/62017.

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

MLA Handbook (7th Edition):

Flores, Jacqueline A. “Biochemical characterization of clade B and non-B HIV-1 reverse transcriptase.” 2017. Web. 08 Mar 2021.

Vancouver:

Flores JA. Biochemical characterization of clade B and non-B HIV-1 reverse transcriptase. [Internet] [Thesis]. University of Missouri – Columbia; 2017. [cited 2021 Mar 08]. Available from: http://hdl.handle.net/10355/62017.

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

Council of Science Editors:

Flores JA. Biochemical characterization of clade B and non-B HIV-1 reverse transcriptase. [Thesis]. University of Missouri – Columbia; 2017. Available from: http://hdl.handle.net/10355/62017

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


Rutgers University

23. Hammond, Gifty Naa Ayeley, 1981-. Defining the nanoRNA regulon and the mechanism by which gene expression is controlled and manifested.

Degree: MS, Microbiology and Molecular Genetics, 2014, Rutgers University

 Gene transcription is mediated by the enzyme RNA polymerase (RNAP). RNAP is a multi subunit nucleotidyl transferase that polymerizes ribonucleotides at the 3’ end of… (more)

Subjects/Keywords: Gene expression; Genetic regulation; Reverse transcriptase

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APA (6th Edition):

Hammond, Gifty Naa Ayeley, 1. (2014). Defining the nanoRNA regulon and the mechanism by which gene expression is controlled and manifested. (Masters Thesis). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/42394/

Chicago Manual of Style (16th Edition):

Hammond, Gifty Naa Ayeley, 1981-. “Defining the nanoRNA regulon and the mechanism by which gene expression is controlled and manifested.” 2014. Masters Thesis, Rutgers University. Accessed March 08, 2021. https://rucore.libraries.rutgers.edu/rutgers-lib/42394/.

MLA Handbook (7th Edition):

Hammond, Gifty Naa Ayeley, 1981-. “Defining the nanoRNA regulon and the mechanism by which gene expression is controlled and manifested.” 2014. Web. 08 Mar 2021.

Vancouver:

Hammond, Gifty Naa Ayeley 1. Defining the nanoRNA regulon and the mechanism by which gene expression is controlled and manifested. [Internet] [Masters thesis]. Rutgers University; 2014. [cited 2021 Mar 08]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/42394/.

Council of Science Editors:

Hammond, Gifty Naa Ayeley 1. Defining the nanoRNA regulon and the mechanism by which gene expression is controlled and manifested. [Masters Thesis]. Rutgers University; 2014. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/42394/


Universiteit Utrecht

24. Cohen Stuart, J.W.T. (James Willem Theodoor). HIV and the immune system during highly active antiretroviral therapy.

Degree: 2000, Universiteit Utrecht

 Het humaan immuundeficiëntie virus (HIV) is de veroorzaker van het verworven immuundeficiëntie syndroom (Acquired Immunodeficiency Syndrome, AIDS). Een infectie met HIV leidt tot een afname… (more)

Subjects/Keywords: Geneeskunde; HIV; antiretroviral therapy; reverse transcriptase inhibitor; protease inhibitor; CD4/CD8; lymphocyte; plasma drug levels; EC; reconstitution; thymus

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APA (6th Edition):

Cohen Stuart, J. W. T. (. W. T. (2000). HIV and the immune system during highly active antiretroviral therapy. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/370

Chicago Manual of Style (16th Edition):

Cohen Stuart, J W T (James Willem Theodoor). “HIV and the immune system during highly active antiretroviral therapy.” 2000. Doctoral Dissertation, Universiteit Utrecht. Accessed March 08, 2021. http://dspace.library.uu.nl:8080/handle/1874/370.

MLA Handbook (7th Edition):

Cohen Stuart, J W T (James Willem Theodoor). “HIV and the immune system during highly active antiretroviral therapy.” 2000. Web. 08 Mar 2021.

Vancouver:

Cohen Stuart JWT(WT. HIV and the immune system during highly active antiretroviral therapy. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2000. [cited 2021 Mar 08]. Available from: http://dspace.library.uu.nl:8080/handle/1874/370.

Council of Science Editors:

Cohen Stuart JWT(WT. HIV and the immune system during highly active antiretroviral therapy. [Doctoral Dissertation]. Universiteit Utrecht; 2000. Available from: http://dspace.library.uu.nl:8080/handle/1874/370

25. Cohen Stuart, J.W.T. (James Willem Theodoor). HIV and the immune system during highly active antiretroviral therapy.

Degree: 2000, University Utrecht

 Het humaan immuundeficiëntie virus (HIV) is de veroorzaker van het verworven immuundeficiëntie syndroom (Acquired Immunodeficiency Syndrome, AIDS). Een infectie met HIV leidt tot een afname… (more)

Subjects/Keywords: HIV; antiretroviral therapy; reverse transcriptase inhibitor; protease inhibitor; CD4/CD8; lymphocyte; plasma drug levels; EC; reconstitution; thymus

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APA (6th Edition):

Cohen Stuart, J. W. T. (. W. T. (2000). HIV and the immune system during highly active antiretroviral therapy. (Doctoral Dissertation). University Utrecht. Retrieved from https://dspace.library.uu.nl/handle/1874/370 ; URN:NBN:NL:UI:10-1874-370 ; URN:NBN:NL:UI:10-1874-370 ; https://dspace.library.uu.nl/handle/1874/370

Chicago Manual of Style (16th Edition):

Cohen Stuart, J W T (James Willem Theodoor). “HIV and the immune system during highly active antiretroviral therapy.” 2000. Doctoral Dissertation, University Utrecht. Accessed March 08, 2021. https://dspace.library.uu.nl/handle/1874/370 ; URN:NBN:NL:UI:10-1874-370 ; URN:NBN:NL:UI:10-1874-370 ; https://dspace.library.uu.nl/handle/1874/370.

MLA Handbook (7th Edition):

Cohen Stuart, J W T (James Willem Theodoor). “HIV and the immune system during highly active antiretroviral therapy.” 2000. Web. 08 Mar 2021.

Vancouver:

Cohen Stuart JWT(WT. HIV and the immune system during highly active antiretroviral therapy. [Internet] [Doctoral dissertation]. University Utrecht; 2000. [cited 2021 Mar 08]. Available from: https://dspace.library.uu.nl/handle/1874/370 ; URN:NBN:NL:UI:10-1874-370 ; URN:NBN:NL:UI:10-1874-370 ; https://dspace.library.uu.nl/handle/1874/370.

Council of Science Editors:

Cohen Stuart JWT(WT. HIV and the immune system during highly active antiretroviral therapy. [Doctoral Dissertation]. University Utrecht; 2000. Available from: https://dspace.library.uu.nl/handle/1874/370 ; URN:NBN:NL:UI:10-1874-370 ; URN:NBN:NL:UI:10-1874-370 ; https://dspace.library.uu.nl/handle/1874/370

26. Cohen Stuart, J.W.T. (James Willem Theodoor). HIV and the immune system during highly active antiretroviral therapy.

Degree: 2000, University Utrecht

 Het humaan immuundeficiëntie virus (HIV) is de veroorzaker van het verworven immuundeficiëntie syndroom (Acquired Immunodeficiency Syndrome, AIDS). Een infectie met HIV leidt tot een afname… (more)

Subjects/Keywords: HIV; antiretroviral therapy; reverse transcriptase inhibitor; protease inhibitor; CD4/CD8; lymphocyte; plasma drug levels; EC; reconstitution; thymus

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

APA (6th Edition):

Cohen Stuart, J. W. T. (. W. T. (2000). HIV and the immune system during highly active antiretroviral therapy. (Doctoral Dissertation). University Utrecht. Retrieved from https://dspace.library.uu.nl/handle/1874/370 ; URN:NBN:NL:UI:10-1874-370 ; 1874/370 ; URN:NBN:NL:UI:10-1874-370 ; https://dspace.library.uu.nl/handle/1874/370

Chicago Manual of Style (16th Edition):

Cohen Stuart, J W T (James Willem Theodoor). “HIV and the immune system during highly active antiretroviral therapy.” 2000. Doctoral Dissertation, University Utrecht. Accessed March 08, 2021. https://dspace.library.uu.nl/handle/1874/370 ; URN:NBN:NL:UI:10-1874-370 ; 1874/370 ; URN:NBN:NL:UI:10-1874-370 ; https://dspace.library.uu.nl/handle/1874/370.

MLA Handbook (7th Edition):

Cohen Stuart, J W T (James Willem Theodoor). “HIV and the immune system during highly active antiretroviral therapy.” 2000. Web. 08 Mar 2021.

Vancouver:

Cohen Stuart JWT(WT. HIV and the immune system during highly active antiretroviral therapy. [Internet] [Doctoral dissertation]. University Utrecht; 2000. [cited 2021 Mar 08]. Available from: https://dspace.library.uu.nl/handle/1874/370 ; URN:NBN:NL:UI:10-1874-370 ; 1874/370 ; URN:NBN:NL:UI:10-1874-370 ; https://dspace.library.uu.nl/handle/1874/370.

Council of Science Editors:

Cohen Stuart JWT(WT. HIV and the immune system during highly active antiretroviral therapy. [Doctoral Dissertation]. University Utrecht; 2000. Available from: https://dspace.library.uu.nl/handle/1874/370 ; URN:NBN:NL:UI:10-1874-370 ; 1874/370 ; URN:NBN:NL:UI:10-1874-370 ; https://dspace.library.uu.nl/handle/1874/370

27. Azevedo, Filipe Costa. A transcriptase reversa como alvo terapêutico em doenças retrovirais.

Degree: 2013, Universidade Fernando Pessoa

Projeto de Pós-Graduação/Dissertação apresentado à Universidade Fernando Pessoa como parte dos requisitos para obtenção do grau de Mestre em Ciências Farmacêuticas

O impacto imediato da… (more)

Subjects/Keywords: Transcriptase reversa; VIH; Retrovírus; Terapia antirretroviral; Transcrição reversa; Reverse transcriptase; HIV; Retroviruses; Antiretroviral therapy; Reverse transcription

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

APA (6th Edition):

Azevedo, F. C. (2013). A transcriptase reversa como alvo terapêutico em doenças retrovirais. (Thesis). Universidade Fernando Pessoa. Retrieved from http://www.rcaap.pt/detail.jsp?id=oai:bdigital.ufp.pt:10284/4082

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):

Azevedo, Filipe Costa. “A transcriptase reversa como alvo terapêutico em doenças retrovirais.” 2013. Thesis, Universidade Fernando Pessoa. Accessed March 08, 2021. http://www.rcaap.pt/detail.jsp?id=oai:bdigital.ufp.pt:10284/4082.

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

MLA Handbook (7th Edition):

Azevedo, Filipe Costa. “A transcriptase reversa como alvo terapêutico em doenças retrovirais.” 2013. Web. 08 Mar 2021.

Vancouver:

Azevedo FC. A transcriptase reversa como alvo terapêutico em doenças retrovirais. [Internet] [Thesis]. Universidade Fernando Pessoa; 2013. [cited 2021 Mar 08]. Available from: http://www.rcaap.pt/detail.jsp?id=oai:bdigital.ufp.pt:10284/4082.

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

Council of Science Editors:

Azevedo FC. A transcriptase reversa como alvo terapêutico em doenças retrovirais. [Thesis]. Universidade Fernando Pessoa; 2013. Available from: http://www.rcaap.pt/detail.jsp?id=oai:bdigital.ufp.pt:10284/4082

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


Université Montpellier II

28. Abidi-Azzouz, Naïma. Élaboration d'Intrabodies ciblant l'organisation conformationnelle du complexe de reverse transcription de VIH-1 : Intrabodies targeting conformational organization of the HIV-1 reverse transcriptase as potent new HIV inhibitors.

Degree: Docteur es, Biologie Santé, 2013, Université Montpellier II

Les traitements actuels dirigés contre le VIH ne sont que partiellement efficaces en raison de l'apparition de mutations qui confèrent au virus une grande capacité… (more)

Subjects/Keywords: Vih; Reverse transcriptase; Phage display; Nanobodies; Intrabodies; Peptides vecteurs; Vhh; Phase display; Cell penetrating peptide; Reverse transcriptase; Hiv-1; Nanobodies

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

APA (6th Edition):

Abidi-Azzouz, N. (2013). Élaboration d'Intrabodies ciblant l'organisation conformationnelle du complexe de reverse transcription de VIH-1 : Intrabodies targeting conformational organization of the HIV-1 reverse transcriptase as potent new HIV inhibitors. (Doctoral Dissertation). Université Montpellier II. Retrieved from http://www.theses.fr/2013MON20050

Chicago Manual of Style (16th Edition):

Abidi-Azzouz, Naïma. “Élaboration d'Intrabodies ciblant l'organisation conformationnelle du complexe de reverse transcription de VIH-1 : Intrabodies targeting conformational organization of the HIV-1 reverse transcriptase as potent new HIV inhibitors.” 2013. Doctoral Dissertation, Université Montpellier II. Accessed March 08, 2021. http://www.theses.fr/2013MON20050.

MLA Handbook (7th Edition):

Abidi-Azzouz, Naïma. “Élaboration d'Intrabodies ciblant l'organisation conformationnelle du complexe de reverse transcription de VIH-1 : Intrabodies targeting conformational organization of the HIV-1 reverse transcriptase as potent new HIV inhibitors.” 2013. Web. 08 Mar 2021.

Vancouver:

Abidi-Azzouz N. Élaboration d'Intrabodies ciblant l'organisation conformationnelle du complexe de reverse transcription de VIH-1 : Intrabodies targeting conformational organization of the HIV-1 reverse transcriptase as potent new HIV inhibitors. [Internet] [Doctoral dissertation]. Université Montpellier II; 2013. [cited 2021 Mar 08]. Available from: http://www.theses.fr/2013MON20050.

Council of Science Editors:

Abidi-Azzouz N. Élaboration d'Intrabodies ciblant l'organisation conformationnelle du complexe de reverse transcription de VIH-1 : Intrabodies targeting conformational organization of the HIV-1 reverse transcriptase as potent new HIV inhibitors. [Doctoral Dissertation]. Université Montpellier II; 2013. Available from: http://www.theses.fr/2013MON20050


University of Southern California

29. Upton, Thomas George. Design and synthesis of a series of methylenebisphosphonates: a nucleotide analogue toolkit to probe nucleic acid polymerase structure and function.

Degree: PhD, Chemistry, 2009, University of Southern California

 A stereoelectronically varied series of alpha-substituted methylenebisphosphonic acids (X,Y = H, F, Cl, Br, CH3) was synthesized and used to prepare corresponding dNTP beta,y-CXY and… (more)

Subjects/Keywords: DNA polymerase beta; bisphosphonates; titrations; fluorination; trifluoromethylation; halogenation; nucleotide analogues; stereoselectivity; autodock; docking; inhibitor design; HIV reverse transcriptase; polymerase kinetics

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

APA (6th Edition):

Upton, T. G. (2009). Design and synthesis of a series of methylenebisphosphonates: a nucleotide analogue toolkit to probe nucleic acid polymerase structure and function. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/109922/rec/1862

Chicago Manual of Style (16th Edition):

Upton, Thomas George. “Design and synthesis of a series of methylenebisphosphonates: a nucleotide analogue toolkit to probe nucleic acid polymerase structure and function.” 2009. Doctoral Dissertation, University of Southern California. Accessed March 08, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/109922/rec/1862.

MLA Handbook (7th Edition):

Upton, Thomas George. “Design and synthesis of a series of methylenebisphosphonates: a nucleotide analogue toolkit to probe nucleic acid polymerase structure and function.” 2009. Web. 08 Mar 2021.

Vancouver:

Upton TG. Design and synthesis of a series of methylenebisphosphonates: a nucleotide analogue toolkit to probe nucleic acid polymerase structure and function. [Internet] [Doctoral dissertation]. University of Southern California; 2009. [cited 2021 Mar 08]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/109922/rec/1862.

Council of Science Editors:

Upton TG. Design and synthesis of a series of methylenebisphosphonates: a nucleotide analogue toolkit to probe nucleic acid polymerase structure and function. [Doctoral Dissertation]. University of Southern California; 2009. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/109922/rec/1862


NSYSU

30. Tai, Chun-pao. Detection of microRNA expression in the blood of CCl4-induced liver fibrotic mice.

Degree: Master, Biological Sciences, 2013, NSYSU

 Abstract MiRNAs are an emerging class of highly conserved non-coding small RNAs that regulate gene expression at the post-transcriptional level. Most miRNAs are generated by… (more)

Subjects/Keywords: liver fibrosis; miRNA; Drosha; gene-specific reverse transcriptase-PCR; Dicer

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

APA (6th Edition):

Tai, C. (2013). Detection of microRNA expression in the blood of CCl4-induced liver fibrotic mice. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0810113-130547

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):

Tai, Chun-pao. “Detection of microRNA expression in the blood of CCl4-induced liver fibrotic mice.” 2013. Thesis, NSYSU. Accessed March 08, 2021. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0810113-130547.

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

MLA Handbook (7th Edition):

Tai, Chun-pao. “Detection of microRNA expression in the blood of CCl4-induced liver fibrotic mice.” 2013. Web. 08 Mar 2021.

Vancouver:

Tai C. Detection of microRNA expression in the blood of CCl4-induced liver fibrotic mice. [Internet] [Thesis]. NSYSU; 2013. [cited 2021 Mar 08]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0810113-130547.

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

Council of Science Editors:

Tai C. Detection of microRNA expression in the blood of CCl4-induced liver fibrotic mice. [Thesis]. NSYSU; 2013. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0810113-130547

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

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